@article {2493, title = {Andrographolide and Resveratrol as Potential Modulators of AIM2 and IFI16 Inflammasomes in Periodontitis: A Docking Study}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {April 2025}, pages = {179-187}, type = {Original Article}, chapter = {179}, abstract = {

Background: Proinflammatory cytokines play a critical role in the destruction of periodontal tissues. DNAsensing inflammasomes, such as AIM2 and IFI16, are key mediators in the secretion of IL-1 and IL-18 and facilitate pyroptosis in periodontitis. Andrographolide and resveratrol are phytocompounds known for their anti-inflammatory effects, though their precise mechanisms of action remain uncertain. This study aimed to elucidate the molecular interactions of andrographolide and resveratrol with AIM2 and IFI16 inflammasomes using a computational approach. Methods: Ten phytocompounds were selected and analyzed via molecular docking. Protein-ligand docking was conducted with AutoDock 4.2.6. Binding affinities and hydrogen bond interactions were assessed. Andrographolide and resveratrol complexes with AIM2 and IFI16 were further subjected to 100 ns molecular dynamics simulations using GROMACS software to assess complex stability. Results: Both andrographolide and resveratrol complexes demonstrated stability throughout the simulations, with adequate inter-hydrogen bonding. Molecular Mechanics Poisson-Boltzmann Surface Area (MMPBSA) analysis revealed that AIM2-andrographolide (-112.100 {\textpm} 18.106 kJ/mol) and IFI16-andrographolide (-50.047 {\textpm} 27.076 kJ/mol) complexes exhibited higher binding energies compared to AIM2-resveratrol (-15.328 {\textpm} 2.539 kJ/mol) and IFI16-resveratrol (-12.534 {\textpm} 20.184 kJ/mol) complexes. Conclusion: Molecular docking and dynamics analyses indicate that andrographolide demonstrates a stronger binding affinity to AIM2 and IFI16 inflammasomes compared to resveratrol. This suggests andrographolide as a promising host modulatory candidate for the therapeutic management of periodontitis.

}, keywords = {AIM2 inflammasome, Andrographolide, IFI16 inflammasome, Molecular docking, Periodontitis, Resveratrol}, doi = {10.5530/pj.2025.17.22}, author = {Lalitha Tanjore Arunachalam and Snophia Suresh and Vamsi Lavu and Shankarram Vedamanickam and Nissanthe Nagarajan} } @article {2531, title = {A Comprehensive Review on the Pharmacological Potential of Dioscorea bulbifera and its Potential Hepatotoxicity}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {August 2025}, pages = {520-530}, type = {Review Article}, chapter = {520}, abstract = {

Dioscorea bulbifera, or the air potato has been studied and used in traditional medicine for centuries particularly in countries like China and India. It is loaded in different secondary metabolites such as steroidal saponins, flavonoids, diterpenoids, tannins, and carotenoids, which all play a major role in its pharmacological activities. Researchers have shown that it can be useful in the treatment of inflammation, microbial infections, oxidative stress, cancer, and liver diseases. even with these benefits there remains a shortage of clinical trials, toxicity assessment, and standardized extraction procedures to facilitate its application in herbal drug industry in a safe manner. One of the most striking features of Dioscorea bulbifera is its antimicrobial activity especially in the fight against antibiotic-resistant bacteria. also, studies done on anticancer activity are actively being conducted with some compounds being reported to induce apoptosis in cancer cells and suppress the growth of tumour. However, talking about its drawbacks some diterpenoid compounds such as diosbulbin A have been reported to show hepatotoxicity in humans and hence further studies are required to determine its safety for therapeutic purposes. The other significant challenge to developing this plant as a standard drug is its variability in chemical composition. The bioactive content is dependent on its cultivation, so it is quite a challenge to control for consistent potency. Sophisticated analytical methods such as HPLC and LC-MS could be utilized to overcome this and contemporary drug delivery systems like nano-formulations could enhance its absorption and bioavailability. Bringing together the ancient herbal knowledge and new scientific inquiry might reveal even greater therapeutic applications of the plant constituents. In the future the studies need to penetrate deeply into its safety, carry out extensive clinical trials, and explore sustainable mechanisms for massproducing its major compounds. With additional studies, Dioscorea bulbifera could become a prominent natural medicine, providing solutions for numerous health conditions while maintaining its traditional medicinal significance.

}, keywords = {air potato, Anticancer, Antimicrobial, Bioactive compounds, Dioscorea bulbifera, Medicinal plants}, doi = {10.5530/pj.2025.17.65}, author = {Rudresh Adarkar and Chandrashekar K S and Vasudev Pai and Richard Lobo and Aswatharam H N and Vamshi Krishna Tippavajhala and Ullas Prakash D{\textquoteright}Souza and Rajesh Kaverikana Shankara} } @article {2562, title = {Cytotoxic Activity of Annona Muricata L, Momordica Charantia L. and Launaea Taraxacifolia Willd. from Benin: A Flow Cytometric Approach}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {727-732}, type = {Original Article}, chapter = {727}, abstract = {

Background: Cancer is rising worldwide, causing approximately 9.7 million deaths in 2022. Treatments are costly, have significant side effects, and are sometimes unavailable in Benin. Medicinal plants offer promising avenues for new therapeutic agents. Objective: This study uses flow cytometry method to evaluate the cytotoxic activity of Annona muricata (Annonaceae), Momordica charantia (Cucurbitaceae) and Launaea taraxacifolia (Asteraceae), three plants from the Beninese pharmacopoeia known for their anti-cancer properties. Materials and Methods: The leaves of A. muricata, L. taraxacifolia and whole plants of M. charantia were collected in southern Benin. Extracts were prepared by aqueous decoction and sequential extraction with solvents of increasing polarity (dichloromethane, ethyl acetate, methanol). The phytochemical profiles of the extracts were determined using TLC and tube tests. The cytotoxicity of the extracts was evaluated on THP-1 cancer cells and PBMC healthy cells. After treatment with the extracts, cell viability was measured by flow cytometry after staining with Thiazole Orange and Hoechst 33258. Results: The dichloromethane extracts of A. muricata and M. charantia, and the ethyl acetate extract of M. charantia and L. taraxacifolia showed significant cytotoxic effects on THP-1 cells. Their half-maximal inhibitory concentrations (IC50) were 139.6 μg/mL, 72.89 μg/mL, 81.88 μg/mL and 106.3 μg/ mL, respectively. These extracts also demonstrated good selectivity toward normal cells. Phytochemical screening revealed the presence of alkaloids, coumarins, flavonoids, anthracene glycosides and triterpenes in the active extracts. Conclusion: This study demonstrated the cytotoxic potential of three medicinal plants from the Beninese pharmacopoeia which may serve to develop further new anticancer therapies.

}, keywords = {Benin, Cancer, Cytotoxicity, Plant extracts, selectivity, THP-1 cells}, doi = {10.5530/pj.2025.17.91}, author = {Habib Ganfon and Axel Ahouansou and Celia Dechavanne and Callinice Capo-Chichi and Latifou Lagnika and Agnes Aubouy and Sebastien Dechavanne and Achille Massougbodji} } @article {2536, title = {Effect of PHELA, an African traditional drug, on levels of selected inflammatory cytokines in mammalian cells infected with SARSCoV- 2}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {September 2025}, pages = {552-565}, type = {Original Article}, chapter = {552}, abstract = {

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes a severe illness, often characterized by an excessive release of proinflammatory cytokines, leading to a cytokine storm associated with disease severity. In this study the effect of PHELA, an accepted herbal combination of four exotic African medicinal plants, namely; Clerodendrum glabrum E. Mey. Lamiaceae, Gladiolus dalenii van Geel, Rotheca myricoides (Hochst.) Steane \& Mabb, and Senna occidentalis (L.) Link, was investigated to determine the effect on viral replication of SARS-CoV-2 Omicron infected mammalian cells and the effect on cytokine release. PHELA has previously been proposed for use as an immune booster. In this study mammalian cells were treated with plant extracts before or after infection with SARS-CoV-2. Viral RNA was measured at intervals and selected cytokine levels (IL-1β, IL-2Rα, IL-6, TNF-α, IFN-γ) were monitored. No significant difference in viral RNA was observed between infected cells treated with plant extracts and untreated infected cells. However, PHELA-treated cells showed a delay in viral RNA increase. Infected cells treated with PHELA exhibited significantly lower levels of IL-1β, IL-2Rα, and TNF-α compared to untreated infected cells at 48- and 72-hours post-infection. Post-treatment was more effective in reducing proinflammatory cytokine production than pre-treatment, highlighting the potential of PHELA and its constituents in modulating cytokine responses during SARS-CoV-2 infection.

}, keywords = {African traditional medicine, immune-modulating, PHELA, proinflammatory, SARS-CoV-2}, doi = {10.5530/pj.2025.17.69}, author = {MM Litabe and M Matsabisa and FJ Burt} } @article {2560, title = {The Effectiveness of Beltfish (Trichiurus lepturus) Protein Intake and Physical Activity on Muscle Mass Growth}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {714-717}, type = {Original Article}, chapter = {714}, abstract = {

Malnutrition cases have increased every year. One of the causes is insufficient food intake, marked by a decrease in muscle mass. Preventing malnutrition can be done by increasing muscle mass through providing daily protein intake according to needs and engaging in physical activity. The fish species Trichiurus lepturus is a high-protein source from the sea. The protein content in this fish can help promote muscle mass growth. This study aims to determine the effectiveness of protein intake from Trichiurus lepturus combined with physical activity on increasing muscle mass. The research method is experimental, using test animals (Rattus norvegicus) given protein intake and physical activity for 28 days. The animals were divided into six groups: three control groups and three treatment groups receiving different protein levels. Muscle growth was assessed by observing the enlargement of the cruris muscle using HE (hematoxylin and eosin) staining under a 4x microscope magnification. The data obtained were analyzed using ANOVA with an Bonferroni test. The results showed a significant difference between all groups (p=0.000). The treatment groups receiving protein intake and physical activity had larger muscle sizes compared to the control groups (P<=0.05). The conclusion is that protein intake accompanied by physical activity causes changes in muscle mass. Additionally, the amount of protein intake is directly proportional to the increase in muscle size.

}, keywords = {Malnutrition, Muscle Mass, Physical Activity, Protein Intake, Trichiurus lepturus}, doi = {10.5530/pj.2025.17.89}, author = {Rivan Virlando Suryadinata and Gabriel Tirtawijaya and Sawitri Boengas and Priscilla Keshia Jayasaputri and Henriette Milda Latuputty and Nisa Kirania Dianti Mulyadi and Nawal Fajril Haya} } @article {2554, title = {Ethnomedicinal survey, phytochemical, isolation and identification of bioactive compounds from Elephantorrhiza elephantina, Pentanisia prunelloides and Dioscorea sylvatica used in the treatment of elephantiasis}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {662-675}, type = {Original Article}, chapter = {662}, abstract = {

Introduction: More than 200 diseases can be transmitted to people through ingesting food contaminated with microorganisms (bacteria, viruses and parasites) or chemicals. Other pathogens for example those causing malaria, tuberculosis and leprosy, as well as parasitic worms can be as chronic infections and impaired nutrition, growth, cognitive development and fertility. Objective: The aim of this research was to screen extracts from the three plants for phytochemicals. This includesthe isolation and identification of bioactive compounds of Elephantorrhiza elephantina. Methods:In this study, an ethnomedicinal survey, phytochemical analysis, isolation, and identification of bioactive compounds were conducted in Elephantorrhiza elephantina, Pentanisia prunelloides and Dioscorea sylvatica plant species used in the treatment of elephantiasis in most parts of the eastern Free State using standard methods. Results:The ethnobotanical survey documented 12 medicinal plants that are used to treat lymphatic filariasis. Elephantorrhiza elephantina, Pentanisia prunelloides and Dioscorea sylvatica were the three most used plant species. All three plants tested positive for the presence of tannins, saponins, flavonoids, steroids, terpenoids, glycosides, anthraquinones and alkaloids. Four compounds: acetyl salicylic acid, benzoic acid, resorcinol and nonanedioic acid were identified from E. elephantina rhizome. Discussion:Amongst 12 documented plant species, E. elephantina, P. prunelloides and D. sylvatica were the most frequently used plants and were selected for isolation and characterisation of bioactive compounds. Acetyl salicylic acid, benzoic acid, resorcinol and nonanediotic acid were isolated and identified from the methanol extract from E. elephantina rhizome. Conclusion:The presence or existence of isolated phenolic-flavonoids in E. elephantin demonstrated the basis for utilising it based on the isolated compounds

}, keywords = {Bioactive compounds, elephantiasis, Elephantorrhiza elephantina, ethnomedicinal survey, Phytochemicals, Traditional medicinal plants}, doi = {10.5530/pj.2025.17.83}, author = {Selloane G. Lehasa and Siphamandla Q.N. Lamula and Lisa V. Buwa-Komoreng} } @article {2564, title = {Hepatoprotective Potential of Coffea arabica Extract Against Carbon Tetrachloride Induced Liver Damage: Ultrasonographic and Cytokine Evaluation}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {742-750}, type = {Original Article}, chapter = {742}, abstract = {

Carbon tetrachloride (CCl$_{4}$) is a hepatotoxic agent widely used to model liver injury in experimental animals, and coffee (Coffea arabica) extract is known to contain various bioactive compounds with antioxidant and anti-inflammatory potential. This study aimed to evaluate the hepatoprotective activity of Coffea arabica extract in male Wistar rats induced with CCl$_{4}$ through phytochemical analysis, liver biochemical parameters (albumin, bilirubin, SGOT, SGPT), inflammatory cytokines (TNF-α, IL-6, CRP), and liver morphology observations using ultrasonography and histopathology. The extract contained alkaloids, flavonoids, triterpenoids, saponins, and glycosides, with total phenolic and flavonoid contents of 51.32 mg GAE/g and 1.25 mg QE/g extract, respectively, and moderate antioxidant activity (IC$_{5}$$_{0}$ = 124.36 ppm). Administration of the extract at 300 mg/kg BW significantly improved liver structure, reduced TNF-α (120.62 {\textpm} 21.78 pg/mL), IL-6 (68 {\textpm} 14.44 pg/mL), CRP (199.0 {\textpm} 41.5 pg/mL), SGOT (147.0 {\textpm} 34.28 g/dL), and SGPT (69.6 {\textpm} 9.94 g/dL) levels, while increasing albumin (2.94 {\textpm} 0.34 g/dL) and reducing bilirubin (0.09 {\textpm} 0.04 mg/dL), approaching normal conditions. The 300 mg/kg BW dose showed the most optimal protective effect compared to other treatment groups, as evidenced by improvements in biochemical parameters, liver morphology, and hepatic histology, indicating that Coffea arabica extract has strong potential as an effective hepatoprotective agent against CCl$_{4}$-induced liver damage

}, keywords = {CCl$_{4}$, Coffea arabica, Cytokines, Hepatotoxicity, liver protection, Ultrasonographic}, doi = {10.5530/pj.2025.17.93}, author = {Desi Novianti and I Nyoman Ehrich Lister and Ali Napiah Nasution} } @article {2517, title = {Mechanistic Insights on the Neuro-Modulatory Potential of Cannabis sativa: A Network Pharmacology- and Molecular Dynamics Simulation-Based Approach}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {August 2025}, pages = {407-419}, type = {Original Article}, chapter = {407}, abstract = {

Background: Although, studies have reported the use of cannabis as a temporary antidepressant and implicated its chronic use in neurological diseases, the exact mechanisms through which these happen remain elusive. Objective: This study aims to investigate the neuro-modulatory potential of cannabis as antidepressant and its role in neurological disorders Methodology: Network pharmacology and molecular dynamics simulation were employed to unveil the mechanism of cannabis as a temporary antidepressant and potential agent implicated in neurological disorders. Results: A total of 156 cannabis metabolites were retrieved from data mining. 22 genes were common in cannabis metabolites and central nervous system (CNS) neurotransmitters{\textquoteright} genes. Glutamate receptor activity and neuroactive ligand receptor activity (NALR) were the most enriched biological process and signalling pathway, respectively, with cannabinoid receptor 1 (CNR1) and glutamate metabotropic receptor 2 (GRM2) being the hub targets in the NALR pathway. A probe into the structural stability of top-ranked metabolites identified cholesterol- CNR1 (-73.88 kcal/mol) and campesterol-CNR1 (-65.96 kcal/mol) with lower free binding energy than reference antidepressant drug (anandamide) (-65.08 kcal/mol), whereas for GRM2, the binding free energy of nerolidol (-43.57 kcal/mol) which was the least among the top ranked metabolites was higher compared to anandamide (-58.78 kcal/mol). Conclusion: Data from this study shows that the profiled cannabis metabolites displayed modulatory effects on key neurotransmitters of the CNS and their receptors and formed stable binding interaction with genes implicated in brain functioning suggestive of the mechanistic effect of cannabis on brain activity during depression and chronic use.

}, keywords = {Cannabinoid receptors, Cannabis, Depression, Neurological diseases, Neurotransmitters}, doi = {10.5530/pj.2025.17.51}, author = {Christina Peter and Halimat Yusuf Lukman and Nosipho Wendy S{\textquoteright}thebe and Usman Abiola Sanni and Saheed SABIU} } @article {2484, title = {Phytochemical Analysis and Antimicrobial Activity of Medicinal Plants Commonly Used in the Treatment of Tuberculosis in the Eastern Free State, South Africa}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {April 2025}, pages = {155-163}, type = {Original Article}, chapter = {155}, abstract = {

Background: Tuberculosis (TB), an airborne infectious disease that mainly infects the lungs, caused by Mycobacterium tuberculosis. South Africa is one of the countries with the highest TB and multi-drugresistant TB burden. Objective: This study aimed at screening eight medicinal plants that are frequently used by herbalists and traditional healers of the eastern Free State for the treatment of TB. Methods: Thirty-two plant extracts were screened for the presence of phytochemicals, antibacterial, antifungal and antimycobacterial activities using standard methods. Results: Extracts prepared from Hermannia depressa and Senecio harveianus displayed the best antibacterial activity against all test microorganisms ranging between 0.098 and 0.781 mg/ml while Drimia depressa and Lotononis lanceolata extracts displayed the best antifungal activity between 0.049 and 0.781 mg/ml. The good antimycobacterial activity was observed with organic extracts prepared from Dicoma anomala, H. depressa, L. lanceolata and S. harveianus between 0.195 and 0.781 mg/ml. Discussion: All plants displayed the presence of tannins and saponins and the absence of alkaloids, anthraquinones and steroids. Plants under this study demonstrated significant antibacterial, antifungal and antimycobacterial activities, with extracts prepared from H. depressa and S. harveianus displaying the best activity against all the test microorganisms with MIC values ranging between 0.098 and 0.781 mg/ml, respectively. Conclusion: The selected medicinal plants that are used in the treatment of TB and related respiratory ailments in the eastern Free State revealed the presence of phytochemicals and significant antimicrobial activities, which explain and justify their frequent use by traditional healers.

}, keywords = {Dicoma anomala, Drimia depressa, Eucomis autumnalis, Hermannia depressa, Lotononis lanceolata, Senecio harveianus, Thesium angulosum, Xysmalobium undulatum}, doi = {10.5530/pj.2025.17.19}, author = {Mandla Hlongwane and Siphamandla Lamula and Lisa Buwa-Komoreng} } @article {2464, title = {Preconception Posyandu Performance Assessment Instrument with Europan Foundation Quality Management (EFQM) Method: Indicators, Validity and Reliability}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {January 2025}, pages = {40-46}, type = {Original Article}, chapter = {40}, abstract = {

Preconception Posyandu is one of the preconception women{\textquoteright}s health services created to help reduce MMR, IMR and stunting prevalence in Banggai District. This study aims to create a performance assessment instrument for the Preconception Posyandu so that it can maintain the existence of the service. The development of performance assessment indicators through Focus Discussion Group (FGD) activities using the Europan Foundation Quality Management (EFQM) method consists of using 9 variables. We involved 30 village midwives and 30 preconception women at three health centers within Luwuk City to test the performance assessment instrument. Internal reliability was assessed with Cronbach{\textquoteright}s alpha and criterion validity. The performance appraisal instrument using the EFQM method obtained development results, namely from 52 indicator questions made into 92 questions, then after testing the validity of the instrument, 81 questions were declared valid and 11 questions were invalid. The results of Cronbach{\textquoteright}s alpha value, there are 5 variables with strong reliability (alpha\> 0.80), namely leadership variables, strategic policies, staff management and partnerships and resources, while there is 1 variable with perfect reliability (alpha\> 0.90), namely process variables, and 3 variables with sufficient reliability (alpha \> 0.70), namely performance outcome variables, customer satisfaction and impact on society. The questions generated from the development of indicators can be used to measure performance. The service of the Preconception Posyandu Program that has been running so far, this is evidenced by the average value of the reliability test which is 0.83, which means strong reliability.

}, keywords = {EFQM, Instrument, Performance Appraisal, Preconception Health Post}, doi = {10.5530/pj.2025.17.5}, author = {Fitrianty Sutadi Lanyumba and Muhammad Syafar and Darmawansyah D and Apik Indarty Moedjiono and Healthy Hidayanty and Wahiduddin W and Faizal Fahmi and Anang S Otoluwa and Anwar Mallongi} } @article {2565, title = {Ultrasonographic and Biochemical Evaluation of the Hepatoprotective Effect of Cinnamomum burmannii Bark Extract in Carbon Tetrachloride{\textendash}Induced Liver Injury}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {751-759}, type = {Original Article}, chapter = {751}, abstract = {

This study aimed to evaluate the hepatoprotective activity of ethanolic extract of cinnamon (Cinnamomum burmannii) in male Wistar rats induced with carbon tetrachloride (CCl$_{4}$). Cinnamon extract is known to contain bioactive compounds such as flavonoids and polyphenols, which play significant roles in antioxidant and anti-inflammatory mechanisms. Phytochemical analysis revealed that the extract contained total phenolic content of 71.55 mg GAE/g and flavonoid content of 0.41 mg QE/g, with a potent antioxidant activity indicated by an IC$_{5}$$_{0}$ value of 18.19 ppm. Administration of the extract for 28 days at a dose of 300 mg/kg body weight resulted in a significant reduction (P\<0.05) in pro-inflammatory cytokines TNF-α, IL-6, and CRP levels compared to the negative control group. The 300 mg/kg dose showed the highest efficacy, with TNF-α levels approaching those of the normal group. Furthermore, liver function parameters improved, as evidenced by significant reductions in SGOT and SGPT enzyme levels, an increase in serum albumin (2.96 {\textpm} 0.52 g/dL), and a decrease in serum bilirubin to 0.102 {\textpm} 0.040 mg/dL. Ultrasonographic examination showed improved liver parenchymal homogeneity and a reduction in the number of nodules. Histopathological findings revealed a decrease in liver tissue damage score from moderate to mild. These findings suggest that Cinnamomum burmannii extract has potential hepatoprotective effects through antiinflammatory, antioxidant, and hepatocellular recovery mechanisms. Therefore, this extract holds promise as a phytopharmaceutical candidate for complementary therapy in liver function disorders; however, further studies are required to isolate the active compounds and evaluate long-term toxicity.

}, keywords = {Anti-inflammatory, Antioxidant, Cinnamon, Cytokine, Hepatoprotective, Histopathology}, doi = {10.5530/pj.2025.17.94}, author = {Inda Kania Meilani and Ermi Girsang and Yolanda Eliza Putri Lubis} } @article {2354, title = {Analysis of the Implementation of the Use of Hospital Management Information Systems (Simrs) in Hospitals Kindergarten IV Dr Sumantri Parepare}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {888-894}, type = {Research Article}, chapter = {888}, abstract = {

Background: TK Hospital management information system . IV DR Sumantri Parepare is not yet fully integrated and SIMRS must be developed to meet the criteria. Objective: This research aims to analyze the use of the Hospital Management Information System (SIMRS) at TK Hospital. IV DR. Sumantri Parepare, Parepare City. Method: The type of research used in this research is qualitative research and data collection using interviews, observation, documentation. With key informants and supporting informants using purposive sampling techniques. Results: The research results show that in terms of HR input the number of officers is sufficient and training has been given to officers regarding SIMRS, there are funds available, the availability of computers is not sufficient, SIMRS is not yet integrated , the infrastructure inadequate , inadequate implementation of SOPs and socialization Not yet done. The ability of medical records staff to use SIMRS is not optimal , there is incompleteness in filling out medical resumes and informed consent in SIMRS and reporting is carried out every month, quarterly and annually, but experiences delays. Conclusion: Improvement efforts that can be made include disseminating information about the importance or benefits of SIMRS in backing up and searching for data that is entered routinely.

}, keywords = {Hospital, Management, Reporting, SIMRS}, doi = {10.5530/pj.2024.16.144}, author = {Suparno and Muhammad Alwy Arifin and Sukri Palutturi and Darmawansyah and Yahya Thamrin and Ida Leida} } @article {2452, title = {Antioxidant Activity of Senna (Senna alexandrina MILL.) Leaf Extracts}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1355-1358}, type = {Research Article}, chapter = {1355}, abstract = {

Senna leaf plant (Senna alexandrina Mill.) is empirically effective in treating several diseases. Senna leaves contain saponins, alkaloids, glycosides, flavonoids, phenols, sesquiterpenes, tannins, and phytosterols. This study aims to assess Senna leaf extract{\textquoteright}s antioxidant activity, flavonoid, and phenolic content (Senna alexandrina Mill.) with various extraction methods and solvent variations.\ Read more . . .\ 

}, keywords = {Antioxidant, Flavonoid, Senna leaf; Maceration; Phenolic}, doi = {10.5530/pj.2024.16.218}, author = {Aktsar Roskiana Ahmad and Abd. Malik and Selpida Handayani and Iskandar Zulkarnain and Amliati A and Nur Lailatulqadri and Mardatilla Mamas} } @article {2260, title = {Anxiety Levels, Cortisol, Blood Gluc Ose and Sodium Levels in Working Wives: Comparison Between Husbands Who Were Hospitalized and Husbands Who Were Not Hospitalized}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {382-387}, type = {Research Article}, chapter = {382}, abstract = {

Background:\ Anxiety affects balance and physiological changes in the body. The research aims to investigate the comparison of anxiety levels, blood cortisol levels, blood glucose levels and blood sodium levels between working wives of husbands who are hospitalized and working wives of husbands who are not hospitalized. Methods: The research design uses statistical group comparison. The research subjects were 40 people divided into 2 groups, namely 20 subjects, working wives, husbands who were hospitalized, 20 subjects, working wives, husbands, who were not hospitalized. Data was collected using the HARS (Hamilton Anxiety Rating Scale) questionnaire instrument, laboratory examination of blood cortisol levels, blood glucose levels and blood sodium levels. Results: Unpaired t test with a significant value of p \< 0.05 if the data is normally distributed or Mann Whitney U Test with a significant value of p \< 0.05 if the data is not normally distributed was carried out to analyze the comparison of anxiety levels, blood cortisol levels, sugar levels blood and blood sodium levels. Data processing with the help of statistical software. The results of the analysis showed that there were differences in anxiety levels (p\<0.05), blood cortisol levels (p\<0.05) and blood glucose levels (p\<0.05) but there were no differences in blood sodium levels (p\>0.05). between working wives whose husbands are hospitalized and working wives whose husbands are not hospitalized. Conclusion: blood cortisol levels and blood sugar levels in working wives of husbands who were hospitalized were higher than working wives of husbands who were not hospitalized and based on statistical tests, significant differences were found in HARS values, blood cortisol levels and blood sugar levels between the group of working wives whose husbands were hospitalized. hospitalized and the wife works, the husband is not hospitalized.

}, keywords = {Anxiety, blood cortisol levels, blood glucose levels, blood sodium levels, HARS, working wife}, doi = {10.5530/pj.2024.16.59}, author = {Rudi Mahruzar and I Nyoman Ehrich Lister and OK Yulizal and Hamzah Shatri and Gusbakti Rusip} } @article {2247, title = {Assessment of Anti-tyrosinase, Antioxidant and Cytotoxic Activities of Trigonostemon reidioides Extracts on Mouse Fibroblast (L929) Cells}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {302-306}, type = {Original Article}, chapter = {302}, abstract = {

Background: Trigonostemon reidioides (Kurz) Craib is a plant traditionally used for its whitening properties, although previous studies have reported some adverse effects associated with its use. Objectives: The objective of this study were to investigate the antityrosinase activity, antioxidant activity, and toxicity on Mouse Fibroblast (L929) Cells of the T. reidioides extracts. The antityrosinase activity was determined using the dopachrome method, while the antioxidant activity was evaluated using the DPPH method. The cytotoxicity was assessed using the MTT assay. Results: The results revealed that the ethanol extract exhibited strong antityrosinase activity, with an IC50 value of 5.38 μg/ml. Furthermore, Fraction 3 and Fraction 4, which were further separated from the ethanol extract, demonstrated high antioxidant activity, with IC50 values ranging from 1.65 to 2.10 μg/ml. The hexane extract, as well as Fraction 4 and Fraction 5, exhibited low toxicity, with IC50 values ranging from 11.82 to 40.12 μg/ml. Conclusions: These findings indicate that Fraction 4 and Fraction 5 of T. reidioides possess potent antityrosinase and antioxidant activities, while displaying low cytotoxicity against the mouse fibroblast (L929) cell line. Therefore, Fraction 4 and Fraction 5 hold considerable potential for further development as skin whitening agents derived from T. reidioides extracts.

}, keywords = {antioxidant activity, Antityrosinase activity, Cytotoxicity activity, Trigonostemon reidioides (Kurz) Craib}, doi = {10.5530/pj.2024.16.45}, author = {Issara Chummalee and Methin Phadungkit and Pornpun Laovachirasuwan} } @article {2343, title = {Association of CRP, Procalcitonin, Lactate, and Albumin Levels with In-Hospital Mortality Post-Definitive Laparotomy in Patients with Complicated Intra-Abdominal Infections}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {805-808}, type = {Original Article}, chapter = {805}, abstract = {

Introduction: Complicated intra-abdominal infection (cIAI) still has a high mortality rate due to organ dysfunction despite advances in supportive care. Unlike other sources of septicemia, cIAI requires source control surgery, which is crucial for improving outcomes. The strategy for source control varies depending on the degree of inflammation associated with cIAI; the more severe the inflammation, the less aggressive the surgery needs to be. Therefore, we need a reliable parameter to predict the degree of inflammation before any physiological rearrangement or organ dysfunction occurs due to excessive inflammation from surgery. The literature shows that CRP, procalcitonin, lactate, and albumin are associated with the degree of inflammation. Thus, it{\textquoteright}s necessary to study about mentioned parameters for being reference determination strategy of surgery in cIAI, classical definitive laparotomy, or rapid source control laparotomy (RSCL). Methods: We have collected data from CIAI patients at Dr. Soetomo Regional General Hospital in Surabaya, Indonesia, covering November 2022 to April 2024. Our primary focus is assessing the inflammation level associated with the compensated or decompensated phase. The decompensated phase signifies an excessive inflammatory response, with one indication being in-hospital mortality. Subsequently, we performed univariate and multivariate analyses using the SPSS program to determine which laboratory parameters (CRP, Procalcitonin, Lactate, and Albumin) are most associated with in-hospital mortality. Results: Between November 2022 and April 2024, there were 309 patients with complicated intra-abdominal infections (cIAI). Among the patients, 61.8\% were male and 38.2\% were female. The majority of patients (27.17\%) were aged 61-70. The causes of cIAI included perforated appendicitis (22.65\%), perforated peptic ulcer (21.69\%), complications from previous surgeries (18.13\%), large bowel perforation (12.29\%), small bowel perforation (11.33\%), intraperitoneal abscess (11.33\%), and other causes (2.58\%). Statistically, lactate was found to be the most accurate predictor of intraoperative hemodynamic instability (p-value \< 0.001; correlation coefficient of 0.481), followed by albumin (p-value \< 0.001; correlation coefficient of 0.357). CRP and Procalcitonin were less accurate, with correlation coefficients of 0.182 and 0.272, respectively. The determined cut-off points for lactate and albumin were 1.94 and 2.73, for CRP and Procalcitonin were 23,24 and 47,95. Abnormal laboratory finding in our study mean CRP above cut off point, Procalcitonin above cut off point, lactate above cut off point and albumin below cut off point. More than 2 laboratories finding, in-hospital mortality 66,7\%, 2 laboratory finding in-hospital mortality 42,8\% and only 1 laboratory finding in-hospital mortality 28,4\%. Conclusions: CRP, Procalcitonin, Lactate and Albumin have relation statistically significant with in-hospital mortality. Lactate and albumin are better than CRP and procalcitonin in our study, and consider RSCL for more than 2 parameter abnormal laboratory findings CRP, procalcitonin, lactate or albumin.

}, keywords = {Complicated intraabdominal infection, Damage control laparotomy, Inflammatory mediators}, doi = {10.5530/pj.2024.16.133}, author = {Mochamad Syahroni Fardiansyah and Tomy Lesmana and Edwin Danardono and Denny Septarendra and Ismu Nugroho and Adhitya Angga Wardhana and Anton Sugianto and Rena Normasari} } @article {2225, title = {Bioguided Assay of Polyphenols Isolated from Medicinal Mayan Species and its Activity Against Leishmania mexicana.}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {174-180}, type = {Research Article}, chapter = {174}, abstract = {

Objective: This study underlines the in vitro leishmanicidal activity of the methanol extracts (MeOH), fractions of n-hexane (n-Hex), chloroform (TCM) and ethyl acetate (EtOAc), and compounds isolated from plant species used in the Mayan traditional medicine. Materials and Methods: Extracts of medicinal species collected in the Mayan Peninsula such as Hylocerus undatus, Bauhinia divaricate, Euphorbia hirta, Ruellia nudiflora and Cedrela odorata, were tasted in a bio guided assays against amastigotes of Leishmania mexicana. Different chromatographic techniques were applied in order to isolated the most active compounds. Additionally, spectroscopic experiments 1H-NMR, 13C-NMR, LC-MS and FT-IR were stablished to determine the chemical structure of the chemical compounds. Results: Euphorbia hirta and Cedrella odorata, showed good bioactivity with 14.81 {\textpm} 2.63 g/mL and IC50 = 18.39 {\textpm} 0.88 μg/mL respectively, meanwhile Bauhinia divaricata not show activity and Ruellia nudiflora showed poor activity with IC50 = 92.18 {\textpm} 3.64 μg/mL, followed by Hylocerus undatus with IC50 = 122.5 {\textpm} 20.99 μg/mL, when tasted against amastigotes of Leishmania mexicana. Spectroscopic data confirmed the presence of quercetin, myricetin, kempherol and scopoletin, with IC50 = 2.92 {\textpm} 0.42 μM, 12.30 {\textpm} 0.57 μM, 20.22 {\textpm} 4.66 μM and 4.05 {\textpm} 0.68 μM respectively. Conclusion: The bioguided assays guided us, to the purification and isolation of four different metabolites, mainly flavonoids and structurally related compounds, some of them show good activity, however, their low bioavailability indicates the need for detailed structural relation activity studies, together with the development of formulations and delivery systems.

}, keywords = {Coumarins, Flavonoids, Leishmania mexicana, NMR structural determination, Polyphenols}, doi = {10.5530/pj.2024.16.24}, author = {Horacio Larqu{\'e} and Abelardo Ch{\'a}vez Montes and Jaime Zamora-Chimal and Moises Looh-Hern{\'a}ndez and Joel H. Elizondo Luevano and Esther del Olmo} } @article {2443, title = {Comparison of Asiatic Acid and Dexamethasone Effect on Interleukin-4 Expression and Eosinophile Cell Count Following Strabismus Surgery: An Experimental Study in New Zealand Rabbit}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1411-1417}, type = {Research Article}, chapter = {1411}, abstract = {

Introduction: Postoperative strabismus inflammation can lead to fibrotic tissue formation. Dexamethasone, while generally effective as an anti-inflammatory post-surgery medication, can increase IOP and blood sugar levels. Research on asiatic acid suggests its potential as an anti-inflammatory and anti-fibrotic agent. Methods: Superior rectus recession was conducted on 20 rabbits, which were divided into five groups based on the subconjunctival injection substance: aquadest, dexamethasone, asiatic acid at a concentration of 0.4 mg/0.5 mL, 0.8 mg/0.5 mL, and 1.6 mg/0.5 mL. After three days, exenteration was performed, and an immunohistochemical examination was performed to assess interleukin-4 expression. Hematoxylin and eosin staining was performed to assess eosinophile cell count. SPSS 26.0 facilitated the data analysis using the Kruskal-Wallis and Wilcoxon Mann-Whitney tests. P\<0.05 was considered significant statistically. Results: This study showed that interleukin-4 expression in the asiatic acid 0.4 mg/0.5 mL group was significantly decreased compared to the aquadest group (P = 0.029) and dexamethasone group (P = 0.029). Higher-dose groups did not exhibit a significant decrease. Dexamethasone also did not exhibit a significant decrease compare to aquadest. There was no significant reduction of eosinophile cell count among all groups. Conclusions: This study highlighted the potential of asiatic acid, particularly at the concentration of 0.4 mg/0.5 mL, in reducing the inflammatory response, specifically interleukin-4 expression, after strabismus surgery in New Zealand rabbits.

}, keywords = {Asiatic acid, Dexamethasone, Eosinophil, Interleukin-4, Strabismus}, doi = {10.5530/pj.2024.16.227}, author = {Harris Kristanto Gunawan and Evelyn Komaratih and Rozalina Loebis and Djoko Agus Purwanto and Luki Indriaswati and Wimbo Sasono} } @article {2294, title = {The Effect of Cryopreservation on the Sperm Ultrastructure of Mus Musculus Albinus Strain DDY: Comparison of Nakagata vs Modified vs Kitazato Cryoprotectants}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {563-569}, type = {Original Article}, chapter = {563}, abstract = {

Introduction: Sperm morphology analysis is very necessary to understand male fertility and the etiology of infertility. Currently, scanning electron microscopy (SEM) has been widely used to determine surface topology. In this study, we will compare the effects of spermatozoa cryopreservation using three different types of cryoprotectants, namely Nakagata, modification and Kitazato. The cryoprotectant compositions used are Nakagata (raffinose and skim milk), modified (glycerol and raffinose) and Kitazato (glycerol and trehalose). Methods: SEM analysis was carried out on 8 sperm samples before cryopreservation and after the freeze-thaw process. Results: The results obtain showed that cryoprotectant modification was able to protect spermatozoa morphology better than Nakagata and Kitazato. Analysis revealed damage to plasma membrane, acrosome and loss of mitochondria in all treatment groups compared to fresh sperm. SEM showed obvious signs of post-thaw damage such as missing plasma membranes, sperm showing damaged acrosomes and mitochondria in the middle showing structural disorganization. Conclusion: SEM revealed that cryopreservation caused ultrastructural damage to mice sperm due to freezing and thawing. These details provide valuable data for further research to minimize the damage caused by cryopreservation to mice sperm. Apart from that, further examination using TEM is recommended to obtain a more comprehensive picture.

}, keywords = {cryopreservation, glycerol, mice sperm, raffinose, Scanning electron microscope, Trehalose}, doi = {10.5530/pj.2024.16.88}, author = {Manggiasih Dwiayu Larasati and Silvia W. Lestari and Mulyoto Pangestu and Andon Hestiantoro and Kusmardi Kusmardi} } @article {2293, title = {Effect of Glutathione Supplementation in Cryoprotectant Modification on Tyrosine Phosphorylation, Acrosin Expression and Acrosome Reaction of Post-Thawing Spermatozoa Quality}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {554-562}, type = {Original Article}, chapter = {554}, abstract = {

Background: Tyrosine phosphorylation, acrosin, and acrosome reaction play an important role in fertilisation. However, cryopreservation causes changes in tyrosine phosphorylation, acrosin expression, and acrosome reaction which affect the quality of spermatozoa. Cryoprotectant media added with antioxidants is needed to protect Spermatozoa from the effects of cryopreservation so that the quality of spermatozoa can be maintained. Objectives: This research examined the effect of glutathione (GSH) supplementation in cryopreservation media on tyrosine phosphorylation, acrosin expression, and acrosome reaction. In this research, pure modified Cryoprotectant (CPA) was compared with CPA supplemented with GSH in three different concentrations. Materials and Methods: The research sample was male mus musculus albinus strain Deutchland Denken Yoken (DDY). Mice spermatozoa was cryopreserved and several parameters were measured including tyrosine phosphorylation, acrosin expression, and acrosome reaction. Results: The addition of GSH to the modified CPA increased tyrosine phosphorylation, acrosin expression, and acrosome reaction (maintaining acrosome integrity). The group with 1.00 mM GSH obtained the highest results among the other groups. Significant increases were found in tyrosine phosphorylation, acrosin expression, and acrosome reaction after the addition of 1.00 mM GSH. Conclusion: Glutathione supplementation in modified CPA can increase tyrosine phosphorylation, acrosin expression, and acrosome reaction of frozen-thawed spermatozoa. Treatment using GSH at a dose of 1.00 mM is the most effective and modification of CPA with the addition of glutathione can improve the tyrosine phosphorylation, acrosin expression and acrosome reaction in cryopreserved spermatozoa.

}, keywords = {acrosin expression, acrosome reaction, CPA modification, glutathione (GSH), spermatozoa cryopreservation, tyrosine phosphorylation}, doi = {10.5530/pj.2024.16.87}, author = {Zuraida and Silvia Werdhy Lestari and Mulyoto Pangestu and Andon Hestiantoro and Kusmardi Kusmardi} } @article {2299, title = {Effect of Propofol TIVA Compared Sevoflurane Inhalation Anesthesia on Triglyceride Levels After Elective Craniotomy Surgery}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {597-601}, type = {Research Article}, chapter = {597}, abstract = {

Background: Propofol TIVA has been shown to be more effective than sevoflurane in craniotomy surgery. Propofol TIVA offers the benefit of giving better brain relaxation during surgery while also being less expensive than sevoflurane. Nonetheless, it is important to highlight that propofol has side effects that should be considered. Large doses and prolonged anesthesia may result in increased triglycerides (lipids) as well as Propofol Infusion Syndrome (PRIS). As part of their investigation into the detrimental effects of propofol, researchers discovered the necessity for controls to avoid confusing the effects of the surgery itself. Therefore, sevoflurane was chosen as the control group to comprehend and analyze the effects of propofol more accurately. Methods: A prospective observational study analysis was conducted on elective craniotomy patients at RSUD Dr. Soetomo from November to December 2023. 52 subjects were divided into two groups, namely the TIVA Propofol and Sevoflurane Inhalation groups. Each group will be examined for preoperative triglyceride levels and postoperative triglyceride levels while already in the ICU. Results: Postoperative triglyceride levels in the Propofol TIVA group were significantly higher. In the comparison test between the two anesthesia methods on triglyceride levels, there was a significant effect in the Propofol TIVA group. In the test of the relationship between the duration of anesthesia in both groups, there was no significant relationship. In the test of the relationship between the total dose of propofol and triglyceride levels, it was found that the greater the dose of propofol used, the higher the increase in triglyceride levels. In the test of the relationship between the total amount of sevoflurane and triglyceride levels, it was found that the greater the dose of sevoflurane used, the greater the decrease in triglyceride levels, which was statistically not significant. Conclusion: TIVA Propofol increases triglyceride levels compared to sevoflurane inhalation in patients undergoing elective craniotomies.

}, keywords = {Craniotomy, Sevoflurane, TIVA propofol, Triglycerides}, doi = {10.5530/pj.2024.16.93}, author = {Andika Perdani Somawi and Nancy Margarita Rehatta and Prihatma Kriswidyatomo and Kohar Hari Santoso and Hamzah and Pudji Lestari} } @article {2396, title = {Effective Dose of Cocoa as a Preemptive Analgesic and Anti- Inflammatory Agent Assessed through Pain Scale and Tumor Necrosis Factor Alpha (TNF-α) in an Acute Pain Animal Model}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1134-1137}, type = {Research Article}, chapter = {1134}, abstract = {

Background: Pain is a significant issue for 40-50\% of hospital patients, with 10-50\% of acute pain cases potentially progressing to chronic pain. Pain-associated inflammation often involves the release of mediators, including Tumor Necrosis Factor Alpha (TNF-α). Cocoa beans contain polyphenols, catechins, anthocyanidins, and proanthocyanidins, compounds believed to possess analgesic properties. This study aims to assess cocoa{\textquoteright}s potential as an oral preemptive analgesic agent in an acute pain mouse model, with an emphasis on its impact on inflammation through TNF-α levels. Methods: This true experimental study involved 24 male white mice split into four groups: a control group (K0) receiving a placebo, a treatment group receiving 15 mg/kg BW oral paracetamol (Kpct), a treatment group receiving 0.5 mg/g BW cocoa (K1), and a treatment group receiving 1 mg/g BW cocoa (K2). Pain response was measured using TNF-α levels and the von Frey test. The Kruskal-Wallis test and One-Way ANOVA were employed for statistical analysis. Results: Cocoa at doses of 0.5 mg/g BW and 1 mg/g BW substantially reduced TNF-α levels (75.82 {\textpm} 7.77 and 70.79 {\textpm} 11.50, respectively) compared to the control and paracetamol groups (98.22 {\textpm} 14.74 and 92.81 {\textpm} 2.64). On the first day, compared to the control group{\textquoteright}s 1.82 {\textpm} 0.78 von Frey values, the cocoa-treated groups{\textquoteright} values (6.20 {\textpm} 2.72 and 7.63 {\textpm} 4.11) were notably higher. There were no notable variations in von Frey values across the groups on the second day. However, a correlation was found between von Frey values on the first and second days. Conclusion: Cocoa can potentially serve as an effective preemptive analgesic agent, reducing pain and inflammation primarily by reducing TNF-α levels. These results provide validity to the use of cocoa as an alternative therapy in acute pain management.

}, keywords = {Cocoa, Pain, Pain Degree Analgesia, TNF-α}, doi = {10.5530/pj.2024.16.185}, author = {Herry Cahya Fathani and Herdiani Sulistyo Putri and Prananda Surya Airlangga and Christrijogo Sumartono Waloejo and Ira Sari Yudaniayanti and Pudji Lestari} } @article {2405, title = {Effects of Bacteriophage in Postoperative Endophthalmitis Caused by Staphylococcus aureus}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1188-1191}, type = {Research Article}, chapter = {1188}, abstract = {

Postoperative endophthalmitis is a serious complication of cataract surgery. It may leads to vision loss. The most common organism cause endophthalmitis is gram-positive bacteria, mainly Staphylococcus aureus (S. aureus). To prevent postoperative endophthalmitis, eye drops or intracameral administration of antibiotic agents are universally used. In recent years, the trend of endophthalmitis treatment has grown rapidly. Administration of bacteriophage is a subject of research for the treatment and prophylaxis of postoperative endophthalmitis. This literature review investigates the potential of bacteriophage to provide a rapid, effective alternative to antibiotic treatments for postoperative endophthalmitis caused by S. aureus

}, keywords = {bacteriophage, postoperative endophthalmitis, Staphylococcus aureus}, doi = {10.5530/pj.2024.16.194}, author = {Herdina Ramadhani and Indri Wahyuni and Ismi Zuhria and Firman Setiawan and Annise Proboningrat and Djoko Legowo and Diah Indriani} } @article {2214, title = {Evaluating the Therapeutic Potential of Vernonia amygdalina: A Promising Antidiabetic Agent in STZ and Nicotinamide-Induced Rat Model}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {94-99}, type = {Original Article}, chapter = {94}, abstract = {

Background: Vernonia amygdalina, commonly known as bitter leaf, has been traditionally used for its potential antidiabetic properties. This study aimed to evaluate the therapeutic potential of Vernonia amygdalina extract (VAE) in ameliorating hyperglycemia using a streptozotocin (STZ) and high-fat diet (HFD)-induced rat model of diabetes. Methods: Sixty male Wistar rats were divided into six groups: normal control, diabetic control, and four treatment groups receiving different doses of VAE (100, 300, and 500 mg/kg body weight) orally for eight weeks. Diabetes was induced in rats by a single intraperitoneal injection of STZ (55 mg/kg) after four weeks of Nicotinamid feeding. Body weight, fasting blood glucose levels, HbA1c, serum insulin levels, superoxide dismutase (SOD) activity, and malondialdehyde (MDA) levels were measured. Results: Treatment with VAE significantly reduced fasting blood glucose levels in a dose-dependent manner compared to the diabetic control group (p \< 0.05). VAE administration also led to a significant decrease in HbA1c levels and an increase in serum insulin levels in a dosedependent manner (p \< 0.05). Furthermore, VAE supplementation restored SOD activity and reduced MDA levels, indicating improved antioxidant status in the treated groups (p \< 0.05). Conclusion: This study demonstrates the therapeutic potential of Vernonia amygdalina as an antidiabetic agent in the STZ and HFD-induced rat model of diabetes. VAE supplementation effectively reduced fasting blood glucose levels, improved glycemic control as indicated by reduced HbA1c levels, and enhanced insulin secretion. Moreover, VAE exhibited antioxidant activity by restoring SOD activity and reducing MDA levels. These findings suggest that Vernonia amygdalina could be a promising natural remedy for the management of diabetes. Further investigations are warranted to elucidate the underlying mechanisms and evaluate its long-term safety and efficacy in humans.

}, keywords = {Diabetes, HbA1c, Insulin, MDA, SOD, Vernonia amygdalina}, doi = {10.5530/pj.2024.16.13}, author = {Muhammad Faridz Syahrian and I Nyoman Ehrich Lister and Chrismis Novalinda Ginting} } @article {2251, title = {Evaluation of the Acute Toxicity of the Ethanolic Extract of the Rhizome of Zingiber officinale Roscoe in Rats}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {323-331}, type = {Original Article}, chapter = {323}, abstract = {

Background: Ginger has pharmacological activities such as anticancer, antidiabetic, antioxidant, antimicrobial, anti-neuroinflammatory, and chemotherapy-induced nausea and vomiting. Objective: The research aims to evaluate the acute toxicity of the ethanolic extract of the rhizome of Zingiber officinale Roscoe in rats. Materials and Methods: The extract was administrated at doses of 300 and 2000 mg/ Kg/day to female and male rats. Changes in body weight were determined during the 14-day treatment period, and on the last day of treatment, blood was drawn, and euthanasia was performed, removing organs for histological analysis. Biochemical parameters were measured. Results: The body weight of the research specimens not show statistically significant variation. In the liver, mild lymphocytic portal inflammation and moderate hepatic steatosis occurred at doses of 2000 mg/kg/day. The kidneys exhibited a mild infiltration around the renal tubules and glomeruli at the same dose. The brain showed a slight increase in the count of astrocytes with focal glial reaction at the highest dose. The stomach and heart also showed mild inflammatory processes at the dose of 2000 mg/kg/day. In biochemical parameters, statistically significant differences were observed between the dose of 2000 mg/Kg/day and the control group. Conclusion: The ethanolic extract of the rhizome of Z. officinale in rats revealed histopathological changes in the liver, kidneys, brain, stomach, and heart, besides changes in biochemical parameters at doses of 2000 mg/Kg/day.

}, keywords = {Acute toxicity test, Biochemical parameters, Histopathology, Rats, Zingiber officinale}, doi = {10.5530/pj.2024.16.49}, author = {V{\'\i}ctor E. Villarreal-La Torre and Juana E. Chávez-Flores and Carmen R. Silva-Correa and Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo-Villalaz and Julio Hilario-Vargas and Maria J. Abanto-Vaella and C{\'e}sar D. Gamarra-S{\'a}nchez and Yuri F. Curo-Vallejos and Marco L. Salazar-Castillo and Icela M. Rodriguez-Haro and Flor Soriano-L{\'o}pez and Renato Cueva- Veneros and Jos{\'e} L. Cruzado-Razco} } @article {2353, title = {Evaluation of the Program to Overcome Undernutrition in the Working Area of Cendrawasih City Health Center, Makassar}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {880-887}, type = {Research Article}, chapter = {880}, abstract = {

Poor or insufficient nutrition can have serious impacts, especially on vulnerable groups such as toddlers, pregnant women and the elderly. Malnutrition not only has a direct impact on physical health conditions, but can also hinder optimal growth and development, both physically and mentally. Objective: The aim of this study to evaluate the implementation of the malnutrition prevention program in the Cendrawasih Health Center work area, Makassar City in 2023. Method: This type of research is qualitative research. The samples for this research are community health center staff, stakeholders and program users. Results: Evaluation of the malnutrition prevention program in the Cendrawasih Health Center working area, Makassar City is based on Context, Input, Process and Product analysis. The research results show that in terms of social and cultural conditions, some communities pay less attention to children{\textquoteright}s nutrition. Input is in the form of funds used, namely BOK funds and funds from the local government. Apart from that, the availability of human resources is inadequate. The facilities and infrastructure used are quite complete with the availability of anthropometric tools. Process Growth monitoring is carried out by community health center officers and posyandu cadres every 10 days. Product The nutritional status of toddlers is starting to improve, this is proven by the number of cases which has decreased. Mothers{\textquoteright} knowledge about the characteristics or signs that children are experiencing malnutrition is still lacking. Apart from that, mothers still don{\textquoteright}t fully understand parenting patterns for toddlers. Conclusion: The evaluation of the malnutrition prevention program at the Cendrawasih Community Health Center in 2023 is still not going well because the input is not adequate, the process has not been carried out optimally so that the product produced does not meet the achievement targets. Efforts that can be made include active cadres in socializing children{\textquoteright}s nutrition. Apart from that, counseling efforts regarding malnutrition among pregnant women also continue to be increased.

}, keywords = {Evaluation, Malnutrition., Program}, doi = {10.5530/pj.2024.16.143}, author = {Armiaty Octavia and Muhammad Alwy Arifin and Indar and Darmawansyah and M. Furqaan Naiem and Ida Leida} } @article {2320, title = {Expression of Matrix Metalloproteinase-9, Transforming Growth Factor Beta and Fibroblast in The Simblefaron Due to Alkali Burn: Literature Review}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {687-690}, type = {687-690}, chapter = {687}, abstract = {

Simblefaron is one of the most challenging complications in the late stages of an alkali burn. Symblepharon characteristically resembles connective tissue or bands that protrude from the eyelid{\textquoteright}s interior surface (palpebral conjunctiva) to the surface of the eyeball (bulbar conjunctiva). This literature review was conducted to see the molecular mechanism of symblepharon formation. Matrix metalloproteinase (MMP- 9), transforming growth factor (TGF-β), and Fibroblast played a significant part in the healing of conjunctival wounds. MMP-9, TGF-β, and fibroblast overexpressed are suspected to cause excessive inflammation and fibrosis, which results in symblepharon. By knowing this, it is hoped that it can become a basis for developing appropriate management for the occurrence of simblepharon.

}, keywords = {Alkali, Burn, Conjunctiva, Symblepharon}, doi = {10.5530/pj.2024.16.115}, author = {Dian Mayangsari and Lukisiari Agustini and Susy Fatmariyanti and Ridholia and Pudji Lestari} } @article {2316, title = {Implementation of Preconception Health Services in Some Southeast Asian Countries: A Literature Review}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {677-681}, type = {Review Article}, chapter = {677}, abstract = {

Objective: This literature discusses various forms of implementation of preconception health services in Indonesia, Malaysia, Singapore, Thailand, Vietnam, and the Philippines. Methods: This literature uses a narrative review with a time limit of 10 years (2011{\textendash}2021) and sources from online database journals that provide free journal articles in PDF format. These include Q1{\textendash}Q4 open access journals, Google Scholar, PubMed, Elsevier, and other sources, such as data from the Ministry of Health of the Republic of Indonesia. Of the 52 studies identified in the search phase, 17 were eligible for inclusion in this review. The keywords used in the literature search are preconception, health services, and Southeast Asia. The analysis carried out in this study is to group and combine the same types of preconception services from each country. Results: There is literature showing the implementation of preconception health services in some countries in Southeast Asia. These services include increasing preconception knowledge (in couples of childbearing age and adolescents), providing preconception care in the form of micronutrients, iron administration, use of contraceptives, counseling, screening for infectious diseases, increasing the participation of health workers in the village, and developing web-based preconception electronic modules and platforms. Conclusions: Providing micronutrients to women of childbearing age is a preconception service that is carried out in almost every country in Southeast Asia; some countries have developed preconception health service information systems, and other countries have not. It is necessary to evaluate the performance of existing preconception health services.

}, keywords = {Health Services, Preconception, Southeast Asia}, doi = {10.5530/pj.2024.16.113}, author = {Fitrianty Sutadi Lanyumba and Muhammad Syafar and Darmawansyah and Apik Indarty Moedjiono and Anang S Otoluwa} } @article {2390, title = {Improving Tuberculosis Detection: A Comprehensive Evaluation of Contact Investigation Implementation}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1103-1109}, type = {Research Article}, chapter = {1103}, abstract = {

Background: Tuberculosis (TB) is the leading cause of death. Indonesia is currently ranked 2nd globally, and the incidence rate increases yearly. TB is highly contagious to risk groups, especially to those who live in one house. Purpose. This study aims to evaluate the implementation of tuberculosis contact investigation by health workers and health cadres in Samarinda City, Indonesia. Methods: This study was conducted with an exploratory qualitative design to explore the implementation of Active Case Finding through contact investigation in Samarinda. As research informants, there are five managers of the tuberculosis program of the Samarinda City Health Office and Public Health Center, four Health Cadres, and ten household contacts of tuberculosis patients. Results: The results of the in-depth interviews identified three domains, eight themes, and 22 sub-themes. We found several obstacles in investigating the TB patient case index contacts, including a lack of resources, low awareness of household contacts, and difficulty meeting targets. Conclusion: Lack of resources and use of conventional instruments indicate less effective coverage of contact investigations. Low awareness of household contact for screening is due to a lack of understanding of TB, shame as a family of TB sufferers, denying the existence of TB symptoms, and not wanting others to know about their health conditions.

}, keywords = {Contact Investigation, Evaluation, Tuberculosis Detection}, doi = {10.5530/pj.2024.16.179}, author = {Joko Sapto Pramono and Ridwan Amiruddin and Ida Leida and Aminuddin Syam and Anwar Mallongi} } @article {2292, title = {Inventory of Medicinal Plants for Male and Female Reproductive Health by Ethnic Javanese and Ethnic Dayak Seberuang in Balai Harapan Village, Tempunak District, Sintang Regency}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {545-553}, type = {Original Article}, chapter = {545}, abstract = {

Introduction: Knowledge of the use of plants as medicine is one of the local wisdom of the Javanese and Dayak ethnic communities of Seberuang, Balai Harapan Village, which has been passed down from generation to generation by their ancestors. This research aims to inventory plants that have medicinal properties for male and female reproductive health which are used by the people of Balai Harapan Village, especially the Javanese and Dayak Seberuang ethnic groups. Methods: This research used a triangulation technique which is a combination of interviews, observation, and documentation of plant types for male and female reproductive health. The data obtained in this research analyzed and presented narratively for each plant and accompanied by pictures and tables. Results: There are 26 types of medicinal plants used by the Javanese and Dayak Seberuang ethnic groups to support reproductive health. Conclusion: The plants used as medicine for male and female reproductive health by the Javanese and Dayak Seberuang ethnic groups in Balai Harapan Village come from several families, namely Zingiberaceae, Asteraceae, Poaceae, Lamiaceae, Fabaceae, Polypodiaceae, Rubiaceae, Caricaceae, Melastomataceae, Gleicheniaceae, Dilleniaceae, Phylanthaceae, Blechnaceae, Schizaeaceae, Piperaceae, Moraceae, and Asparagaceae. The most common types of plants used come from the Zingiberaceae family.

}, keywords = {Local wisdom; Medicinal plants; Reproduction health}, doi = {10.5530/pj.2024.16.86}, author = {Ruqiah Ganda Putri Panjaitan and Risma Nurkholifah and Eko Sri Wahyuni and Kurnia Ningsi and Liya Angga Lestari} } @article {2373, title = {Juglans regia L.: Source of Bioactive Compounds with Potential Anticancer Activity}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {998-1003}, type = {Original Article}, chapter = {998}, abstract = {

Background: Juglans regia L., commonly known as {\textquotedblleft}walnut{\textquotedblright}, belongs to the Juglandaceae family, with antioxidant, anti-inflammatory, and hypoglycemic medicinal properties. Objective: Describe the anticancer potential of the bioactive compounds present in Juglans regia L. Method: Recent scientific studies were reviewed on the effects of bioactive compounds from Juglans regia L. on inhibiting tumor growth and cancer development in several experimental models. To do this, a scientific literature search was carried out, using databases such as PubMed, Scopus, and Science Direct. Results: Regarding the selected articles, it was found that some bioactive compounds from Juglans regia L. exhibit mechanisms of anticancer action, among which the following stand out: induction of apoptosis, suppression of angiogenesis, and modulation of cell signaling pathways related to cell proliferation and survival. Conclusion: It is concluded that Juglans regia L. contains active metabolites with potential anticancer effects.

}, keywords = {Angiogenesis, Antitumor, Apoptosis, Cancer, Juglans regia L.}, doi = {10.5530/pj.2024.16.161}, author = {Carla Y. Requejo-Rodr{\'\i}guez and Elmer M. Roncal-Alayo and Carmen R. Silva-Correa and V{\'\i}ctor E. Villarreal-La Torre and William A. Sag{\'a}stegui-Guarniz and William A. Sag{\'a}stegui-Guarniz and Walter E. Janampa-Castillo and Jos{\'e} E. Alvarez- Trujillo and Glenda J. Vela-Urbina and Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo-Villalaz and Mar{\'\i}a E. Cotrina-Le{\'o}n and Julio A. Casta{\~n}eda-Carranza and Deivy Y. Dionicio-Rosado} } @article {2239, title = {Occupational Diseases in Female Workers in the Industrial World, Indonesia: Hazard Types and Exposure Mechanisms {\textendash} Literature Review}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {263-267}, type = {Review Article}, chapter = {263}, abstract = {

Background: Occupational diseases are diseases caused by work and the work environment. Specifically gender, women have a double burden, namely domestic work in the household and the burden of being a breadwinner who works outside the home, women are also faced with reproductive tasks, namely pregnancy, childbirth and breastfeeding, and bioanatomically women have physical strength different from men, so that women are specifically more vulnerable to health risks due to their work, both physically, mental and social. This research will review the types and mechanisms of the spread of Occupational Diseases (OD) in female workers in the industrial world. Methods: The writing of this research was carried out using the Literature Review method which is a literature review method in which scientific articles are selected by researchers related to the research topic. Results: According to the results of the study, the specific risk of occupational diseases in the female worker community is pregnancy and childbirth disorders, Anemia and Sexuall Transmitted Disease (STD), while other accompanying diseases are Pulmonary Obstruction Disease, Tinea pedis, Neurotoksic Symptoms, Noice Induce Hearing Loss (NIHL), Low Back Pain (LBP), MSDs, and Work Stress. Conclusion: Every female worker has a susceptibility to occupational diseases according to the conditions and work environment experienced. The industry must pay attention to programs to improve occupational health by making anticipatory efforts so that occupational diseases do not become a life threat to female workers.

}, keywords = {Female Worker, Hazard, Industry, Occupational Disease}, doi = {10.5530/pj.2024.16.38}, author = {Mirawati Tongko and Yahya Thamrin and Syamsiar S. Russeng and Lalu Muhammad Saleh and Sukri Palutturi and Ridwan Amiruddin and Irwandy and Anwar Mallongi and Maria Kanan and Fahrudin Lahay and Almustari} } @article {2440, title = {Optimizing Emergency Cesarean Section Response Times in Category I Fetal Distress: A Pharmacological Perspective}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1396-1403}, type = {Research Article}, chapter = {1396}, abstract = {

Backgrounds: Cesarean section (CS) is a common procedure globally, often performed due to fetal distress, which requires delivery within 30 minutes According to data from Airlangga University Hospital, the achievement rate of emergency CS is only 80-82\%, this causes the activation of the obstetric operating room to increase the achievement of emergency CS \<30 minutes. Objective: To improve the quality of service regarding response time emergency CS for fetal distress at Airlangga University Hospital. Methods: This retrospective descriptive study analyzed medical records of emergency CS cases due to fetal distress in the central surgical operating room in 2022 and the obstetric operating room in 2023. Total sampling was used, and data were tabulated using Microsoft Excel. Results: From the results of the study, in 2022, the number of cesarean deliveries was 699 patients, of which 22 patients of fetal distress (3.1\%) underwent emergency CS in the operating room of the central surgical building from a total of 47 emergency CS (7.6\%). In 2023, the number of CS was 631 patients, of which 23 patients with fetal distress (3.6\%) underwent emergency CS in the obstetric operating room from a total of 58 emergency CS operations (9.1\%). Conclusion: Data from 2023 indicate improved response times for emergency CS, with the dedicated obstetric operating room significantly enhancing service quality.

}, keywords = {Activation Obstetric operating room, Emergency CS, Fetal Distress, Response Time}, doi = {10.5530/pj.2024.16.224}, author = {Evania Nita Oetama and Muhammad Ardian Cahya Laksana and Rizki Pranadyan1} } @article {2276, title = {Phytochemical Analysis of Curry Leaf Extract (Murraya koenigii L.) as a Potential Animal Feed and Medicinal Ingredient}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {471-477}, type = {Research Article}, chapter = {471}, abstract = {

Herbal plants have been used for centuries as traditional medicine to treat various diseases. Green plants generally contain phytochemical compounds, such as vegetables and plants that add aroma to dishes, one of which is curry leaves (Murraya Koenigii). This research aims to identify the phytochemical compounds contained in curry leaves. This research was carried out from August 2023 to October 2023. The curry leaves that were obtained were converted into extract form and then the extract was tested for the content of alkaloids, flavonoids, saponins, phenolics and tannins. The research results showed that curry leaf extract contained 23.73\% alkaloids, 1.24\% flavonoids, 8.74\% saponins, 4.4\% phenolics, and 5.2\% tannins. Alkaloids in plants have a role as a defense against biotic and abiotic disorders. The benefits of flavonoids in plants include anti-mutagenic, anti-inflammatory, antioxidant and anti-carcinogenic. Saponins have various benefits in the health sector, including being able to reduce cholesterol concentrations in the blood. Polyphenols have good antioxidant power because this group can provide electrons to neutralize free radical electrons formed in the body. Tannins also consist of polyphenolic compounds which have antibacterial, antioxidant and astringent activities. The results of the analysis regarding the content of secondary metabolite compounds in curry leaf extract play an important role in the development of future medicines and need to be carried out to provide knowledge to the public. This study can be a basis for bioactive content for further research to expand the use of medicinal plants in the future, especially curry plants.

}, keywords = {Curry leaf extract, Human health, Medicine, Phytochemicals, Plant}, doi = {10.5530/pj.2024.16.75}, author = {Mohammad Anam Al Arif and Sunaryo Hadi Warsito and Mirni Lamid and Widya Paramita Lokapirnasari and Aswin Rafif Khairullah and Siti Rani Ayuti and Sugito and Intan Permatasari Hermawan and Oky Setyo Widodo and Rakhi Gangil} } @article {2213, title = {Phytochemical Screening, Thin Layer Chromatography and Fourier Transform Infra-Red Spectroscopy Analysis of Eleutherine Bulbous (Mill.) Urb Bulb Extract}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {88-93}, type = {Original Article}, chapter = {88}, abstract = {

Background: Many traditional medicinal plants were studied for their phytochemical components. Dayak onions (Eleutherine bulbous (Mill.) Urb) is one of traditional medicinal plant in Indonesia. Analysis of the phytochemical compounds in the extract of the plant would help in determining various biological activities of the plant. Objective: This study was primarily aimed to identify the phytochemical profile of Dayak onions extract and its fractions. Methods: The Dayak onion bulbs were collected from Pancur Batu District, North Sumatra Province, Indonesia. Multiple solvents used to for extraction and analysis of phytochemical compound by chemical reactions, thin layer chromatography (TLC) profiling, and Fourier Transform Infrared Spectrophotometer (FTIR) profiling. Results: The phytochemical screening of Dayak onions ethanol extract showed it contained alkaloids, flavonoids, glycosides, tannins, and triterpenes/ steroids. The n-hexane fraction contained flavonoids and triterpenes/steroids, while the ethyl acetate fraction contains flavonoids and glycosides. The water fraction contained alkaloids, flavonoids, glycosides and tannins. By TLC profiling, the bioactive compounds in ethanol extract of the Dayak onion contain steroids, tannins, flavonoids and alkaloids. The bioactive compound in ethyl acetate fraction contains steroids, tannins, triterpenes, flavonoids and glycosides. The bioactive compound in n-hexan fraction contains steroids. The bioactive compound in water fraction fraction contains steroids and tannins. The FTIR demonstrated the presence of C-H alkanes, =C-H alkenes (aliphatic), C-O alcohol, ether, esters and carboxy acid in the ethanol extract, en-hexan fractions and ethyl acetate fractions. Conclusion: The phytochemical qualitative profiling showed that Dayak onion bulb as a rich source of bioactive compounds and have medicinal potential as therapeutic agent. A higher content of bioactive compounds of Dayak onion bulbs found in the ethanol and ethyl acetate extracts. The FTIR demonstrated the presence of C-H alkanes, =C-H alkenes (aliphatic), C-O alcohol, ether, esters and carboxy acid in the ethanol extract, enhexan fractions and ethyl acetate fractions.

}, keywords = {Dayak onion, Eleutherine bulbous, Extract, Fraction, FTIR, TLC}, doi = {10.5530/pj.2024.16.12}, author = {Lokot Donna Lubis and Muhammad Fidel Ganis Siregar and Farhat and Iqbal Pahlevi Adeputra Nasution and Dedy Syahrizal and Kamal Basri Siregar and Putri Chairani Eyanoer and Ichwanul Adenin and Muhammad Rusda and Mustafa M. Amin} } @article {2340, title = {The Protective Effects of UV-blocking Spectacle Lenses and Class 1 UV-blocking Contact Lenses (Senofilcon A) on Superoxide Dismutase-2 and Catalase Expression in Lens Epithelial Cells Following UVB Radiation Exposure: An Experimental Study in Animal Model}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {785-790}, type = {Original Article}, chapter = {785}, abstract = {

Introduction: To determine SOD2 and CAT expression in lens epithelial cells with the protection of UVblocking spectacle lens and UV-blocking contact lenses after UVB radiation. Methods: 32 eyes of Rattus norvegicus mice were subjected to UVB radiation from Philips PL-S 9W/01 narrowband 311 nm lamps at a distance of 18 cm for 30 minutes. Divided into four groups: a control group, P1 group exposed to radiation, P2 group wearing UV-blocking spectacle lens, and P3 group wearing UV-blocking contact lens. The mice were euthanized three days later and had their eyes removed. Immunohistochemistry analysis was used to evaluate the expression of SOD2 and CAT. Results: P1 demonstrated a statistically significant SOD2 expression (p=0.002) compared to the control group. Neither P2 nor P3 exhibited significant differences in SOD2 expression (p=0.693; p=0.365). The SOD2 of the P1 group was significantly different compared to the P2 and P3 groups (p=0.007; p=0.023). No statistically significant difference between groups P2 and P3 (p=0.606). The CAT levels in the P1 group significantly differed from the control group (p=0.001). The differences between the P2 and P3 groups and the control groups were statistically insignificant (p=0.894; p=0.120). CAT P1 group had a significant difference with P2 and P3 groups (p=0.001; p=0.033). No statistically significant difference was observed between groups P2 and P3 (p=0.154). Conclusions: UV-B exposure decreases the expression of SOD2 and CAT. Both protection can provide equally good protection.

}, keywords = {CAT, epithelial lens, SOD2, UV-blocking contact lens., UV-blocking spectacles, UVB}, doi = {10.5530/pj.2024.16.130}, author = {Made Dessy Gangga Ayu Cinthiadewi and Nurwasis and Muhammad Firmansjah and Djoko Legowo and Ni Putu Ayu Reza Dhiyantari and Rifat Nurfahri} } @article {2285, title = {The Role of α-SMA, Type 1 Collagen, and Myofibroblasts in Cicatrizing Conjunctivitis by Alkali Chemical Trauma}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {May 2024}, pages = {591-596}, type = {Research Article}, chapter = {591}, abstract = {

Introduction: Chemical trauma to the eye is a serious condition in the field of ophthalmology and a leading factor contributing to global blindness. Cicatrizing conjunctivitis (CC) is a term used to describe conditions marked by inflammation and the formation of scars on the conjunctiva. CC can have various causes, with one of them being chemical injury to the eye. The development of CC involves the participation of several cytokines and cells, such as α-SMA, Type 1 collagen, and Myofibroblasts. Myofibroblasts have the ability to contract through the utilization of diverse cytoskeletal proteins, which are commonly present in smooth muscle cells, including α-SMA. Actin filaments contribute to mechanically supporting cells, defining cell morphology, and facilitating cell mobility. Actin, in conjunction with myosin, participates in the muscle contraction process within muscle cells. Subsequently, type 1 collagen contributes to the healing of conjunctival wounds by providing a tensile force that aids in the closure of such wounds. As a significant constituent of the extracellular matrix, type 1 collagen plays a crucial role in maintaining the integrity of tissues.

}, keywords = {Cicatrizing conjunctivitis, Myofibroblasts, Type 1 collagen, α -SMA}, doi = {10.5530/pj.2024.16.92}, author = {Henu Hadiyantama and Lukisiari Agustini and Sutjipto and Evelyn Komaratih and Ismi Zuhria and Pudji Lestari and Ridholia} } @article {2219, title = {Screening and Identification of Metabolites from Sambiloto (Andrographis paniculata) Ethanol Extract for Pro-Inflammatory Cytokines Inhibitory through In Silico and In Vitro Approaches}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {131-140}, type = {Research Article}, chapter = {131}, abstract = {

Objective: Andrographis paniculata has long been a traditional medicinal plant in Indonesia. This study is intended to evaluate the anti-pro-inflammatory cytokines of 98\% ethanol extract of A. paniculata by in vitro and in silico approaches. Inhibition of pro-inflammatory cytokines is also one of the therapies in treating COVID-19. Methods: The molecular docking approach was utilized as a first screening to evaluate the potential for suppression of macrophage cell activation; an ADMET prediction test was performed to determine the pharmacological, pharmacokinetic, and toxicity as a therapeutic target. TNF-α, IL-1{\ss}, and IL-6 levels were measured using an ELISA method to investigate anti-cytokine pro-inflammatory activity in LPS-induced RAW 264.7 macrophage cells. LC-MS/MS was used to identify additional metabolite compounds. Results: Ethanol extract containing particular metabolites 14-Deoxyandrographoside and 14-Deoxy-17-hydroxyandrographolide inhibited TNF-α and IL-1β by 100\% and IL-6 by 85.59\%, respectively. While compared to the Dexamethasone molecule as a positive control, preliminary screening and ADMET prediction for the metabolite compound 14-Deoxyandrographoside exhibited relatively high binding stability to the CD14 receptor by -7.5 kcal/mol and was safe against various ADMET indications. Conclusions: This study reveals that the compound 14-Deoxyandrographoside in pure ethanol extract is a potential anticytokine agent candidate for treating pro-inflammatory cytokines, including COVID-19 infection.

}, keywords = {LC-MS/MS, Molecular docking, Pro-inflammatory cytokines, Sambiloto}, doi = {10.5530/pj.2024.16.18}, author = {Evul Winoto Lukito and Dyah Iswantini and Budhi Antariksa and Mohamad Rafi and Setyanto Tri Wahyudi} } @article {2233, title = {Test of Antihyperuricemia Activity of Methanol Extract of Plantain Peel (Musa Paradisiaca Var. Sapientum) Against Caffeine- Induced Mice (Mus Musculus)}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {226-230}, type = {Research Article}, chapter = {226}, abstract = {

Background: Hyperuricemia occurs when serum uric acid levels rise above the normal range, typically exceeding 7.0 mg/dl for adults and 6.0 mg/dl for women. This condition can lead to various health issues, including gout, kidney stones, and renal failure. Objective: This study aims to verify the effectiveness of the methanol extract from plantain peel (Musa paradisiaca var. sapientum) in reducing uric acid levels in mice (Mus musculus) and to establish the optimal dosage for maximum efficacy. Materials and Methods: This analytical experimental research utilized a paired sample T-test Pretest-Posttest design. The mice were divided into five groups: a Negative Control of Na.CMC 0.5\%, a Positive Control of allopurinol at 100 mg/kg body weight, and groups receiving plantain peel methanol extract at 100 mg/kg, 200 mg/kg, and 400 mg/kg body weight. Uric acid levels were measured initially, post-caffeine induction on day 7, and post-extract induction on day 14. Results: The study found that plantain peel methanol extract exhibited an anti-hyperuricemic effect in male mice. Among the dosages tested, 400 mg/kg body weight of the plantain peel methanol extract was the most effective in reducing uric acid levels, followed by the 200 mg/kg and 100 mg/kg doses. Conclusion: Plantain peel methanol extract is effective in reducing uric acid levels in male mice, with 400 mg/kg being the most efficacious dosage. This suggests potential for further exploration of plantain peels as a treatment for hyperuricemia.

}, keywords = {Anti-hyperuricemic effect, Hyperuricemia, Methanol extract, Mus musculus, Optimal dosage, Plantain peel, Uric acid levels}, doi = {10.5530/pj.2024.16.32}, author = {Ratna Umi Nurlila and Jumarddin La Fua and Toto Surianto S and Titi Purnama and Muh Ikhsan Idrus and Armayani and Anwar Mallongi} } @article {2245, title = {Wound Healing Activity of an Essential Oil-Based Cream of Origanum vulgare L. on Mice}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {292-295}, type = {Original Article}, chapter = {292}, abstract = {

Background and Aim: The objective was to evaluate the effect of a cream based on the essential oil of Origanum vulgare on skin lesions induced in Mus musculus Balb/c. Materials and Methods: The experimental animals were divided into four groups of 6 specimens each, in which skin lesions of approximately 1 cm in diameter were induced. Group I (Control) received no treatment, Group II (0.1\% Origanum vulgare cream), Group III (0.5\% Origanum vulgare cream), and Group IV (1\% Origanum vulgare cream) received treatment for eight days. Skin lesions were measured on days 4 and 7. At the end of treatment, they were euthanized using sodium pentobarbital 60 m/kg v.ip. Skin samples were obtained and preserved in 10\% formalin for histopathological analysis. Results: When measuring the size of the skin lesions induced in the study groups, it was observed that in the control group, the decrease in the length of the lesions occurred on the fifth day; in group II, III, and IV, the lesions length decrease occurs on the second day. At the end of the experience, the measurements of the lesions were much smaller for the III and IV groups (0.33 and 0.41, respectively) compared to the control group (0.40 cm). On day seven, statistically significant difference was found on skin lesion measure between Group IV and the Control, with a significance level of p\<0.05. Conclusion: It is concluded that the 1\% Origanum vulgare essential oil-based cream has a healing effect on dermal lesions induced in Mus musculus Balb/c.

}, keywords = {Cream, Essential oil, Origanum vulgare, Skin, Wound Healing}, doi = {10.5530/pj.2024.16.43}, author = {Laurente-Pachamango Katherine G and Cruzado-Razco Jos{\'e} L and Silva-Correa Carmen R and Villarreal-La Torre V{\'\i}ctor E and Sag{\'a}stegui-Guarniz William Antonio and Gamarra-S{\'a}nchez C{\'e}sar D and Ricardo M Gomez-Arce and Deivy Y Dionicio-Rosado and Julio A. Casta{\~n}eda-Carranza and Calder{\'o}n-Pe{\~n}a Abhel A and Aspajo-Villalaz Cinthya L and Ch{\'a}vez- Flores Juana E} } @article {1967, title = {Alkaloids from Pandanus amaryllifolius Roxb Leaf as Promising Candidates for Antidyslipidemic Agents: An in silico study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {106-111}, type = {Original Article }, chapter = {106}, abstract = {

Introduction: The plant Pandanus amaryllifolius Roxb (pandan), has been shown to have antidyslipidemic potency. This study explored the potential of several alkaloids from pandan leaf as antidyslipidemia as well as their safety profile in silico. Methods: Analyses were carried out by studying the binding affinity of the alkaloids to 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, peroxisome proliferator activator receptor (PPAR) alpha and Niemann Pick C1 Like 1 (NPC1L1). The structures of the alkaloids were downloaded from the Pubchem database and optimized using the ChemDraw Professional 16.0 to obtain 3D structures in protein data bank (PDB) format. The in silico testing was based on the interactions of the alkaloids with the HMG-CoA reductase (PDB ID 1HW9), PPAR alpha (PDB ID 6LX4) and NPC1L1 (PDB ID 7DFZ) proteins, downloaded from the Research Collaboratory for Structural Bioinformatics (RSCB) PDB website (http://www.rcsb.org/pdb). The preparation of protein structures was performed using the Discovery studio 2021 client and Gromacs applications, while optimization of the 3D structure of the alkaloids was carried out with the ChemDraw professional 16.0. Finally, validation was completed using AutoDock application. The safety profile was assessed by pkCSM online tool. Results: The respective root mean square deviation (RMSD) values of the 1HW9, 6LX4 and 7DFZ proteins were 1.677, 0.918 and 1.706, respectively. The alkaloids pandanusine B, pandamarilactonine A, pandamarilactonine B had respective values of binding energy for HMG-CoA of -5.52, -5.51 and -5.46 kcal/mol. The binding energy of pandamarilactonine B, pandamarilactonine A and pandanamine for PPAR alpha were -9.14, -9.10 and -8.48 kcal/mol, respectively, with the corresponding energy for t NPC1L1 of -9.63, -9.71 and -8.54 kcal/mol. The toxicity tests indicated that the alkaloids were safe, pandamarilactonines had the highest LD50 (2.736 mol/ kg). Conclusion: The studied pandan alkaloids have potential antidyslipidemic activity by interacting with HMG-CoA reductase, PPAR alpha, and NPC1L1, with good safety profile.

}, keywords = {Alkaloids, Dyslipidemia, In Silico., Pandan, Pandanus amaryllifolius}, doi = {10.5530/pj.2023.15.14}, author = {Martohap Parotua Lumbanraja and Kusnandar Anggadiredja and Hubbi Nashrullah Muhammad and Neng Fisheri Kurniati} } @article {1990, title = {An Analysis of Local Knowledge of Phit-Samdaeng in Yang Sisurat District, Maha Sarakham Province and The Medicinal Plants Used to Relieve Its Symptoms}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {259-265}, type = {Original Article }, chapter = {259}, abstract = {

Introduction: {\textquotedblleft}Phit-Samdaeng{\textquotedblright} is a Thai term often used to refer to an illness of eating unsuitable foods. However, its use in a diagnosis is limited due to the unclear definition and description. This study aimed to compare knowledge of Phit-Samdaeng symptoms and treatments in Northeastern folk medicine, Thai Traditional Medicine, and medicinal plants in the Yang Sisurat District of Thailand. Methods: Semistructured interviews and participatory observations were used to collect data from 12 folk healers. Questions were designed to obtain local knowledge of Phit-Samdaeng and medicinal plants. The data was analyzed using descriptive statistics, comparison and interpretation. Results: Some symptoms of Phit-Samdaeng in the nine scriptures of Thai Traditional Medicine, Tumraya Silajaruek Watprachethupon, and of Kin-Phit and Phit-Kaboon, in Tamraya Boran Isan, were similar in Yang Sisurat. However, the names were different. There were also differences in species and the recipes of herbal remedies among folk healers and in the textbooks. The most used plants to treat Phit-Samdaeng by folk healers were Clerodendrum paniculatum L. and Clausena wallichii Oliv. var. guillauminii (Tanaka) Molino. Only nine species had pharmacological effects relating to Phit-Samdaeng treatment. Conclusions: The knowledge of Phit-Samdaeng symptoms in Yang Sisurat District were consistent with the Northeast folk medicine and Thai Traditional Medicine. The most commonly used species were native plants of Thailand. However, information on the medicinal taste and property from scriptures and pharmacological evidence is lacking. Therefore, the pharmacological activity and toxicity of herbal remedies should be further investigated for efficacy and safety.

}, keywords = {Alternative medicine, Folk knowledge, Herbal medicine, Phit-Samdaeng.}, doi = {10.5530/pj.2023.15.37}, author = {Hatthapan Wipanso and Bhanubong Bongcheewin and Suppachai Tiyaworanant and Suksalin Booranasubkajorn and Natchagorn Lumlerdkij and Pravit Akarasereenont} } @article {2015, title = {Analysis of the Metabolite Compound of the Ethanol Extract of Chrysanthemum cinerariifolium Stem and Activity for inhibition of Oral Squamous Cell Carcinoma (OSCC) in silico study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {393-398}, type = {Research Article}, chapter = {393}, abstract = {

Background: Oral cancer is a deadly disease that is expected to increase yearly. Current cancer treatment methods have side effects. C. cinerariifolium plants have potential as anticancer agents. Objective: To evaluate the anti-OSCC properties of the ethanol extract of C. cinerariifolium stems via an in-silico study. Materials and Methods: Analysis of active compounds in ethanol extracts of C. cinerariifolium stems using TLC and UPLC-QToF-MS/MS metabolic profiling. The data were analysed statistically using principal component analysis (PCA). In silico of C. cinerariifolium compounds on protein (PI3K and Cyclin D) from OSCC. Results: TLC procedures utilizing UV light with λ 366 nm after spraying with H2SO4 revealed multiple-colored spots, indicating that H2SO4 is a specific spray detector for terpenoid and carotene. Metabolic profiling in ethanol extract of C. cinerariifolium stem included Pronethalol (3.96\%), 1-(4-Methoxyphenyl)-N-(1 naphthylmethyl) methanamine (7.34\%), Orphenadrine (24.27\%), Pentazocine (5.09\%), 4-(Dodecyloxy) aniline (6.30\%), Linoleamide (4.95\%), and Pheophorbide A (8.05\%). Orphenadrine had the highest percentage. Based on the Lipinski rule of five, pronethalol has the potential to be used as a drug-like therapy for OSCC. The anticancer activity profile is predicted by PASS online with a likely range of 0.065 to 0.385. An in-silico study showed that the strongest binding affinity is pronethalol to Cyclin D1 and pheophorbide A to the PI3K protein. Conclusion: The active metabolite of the ethanolic extract of C. cinerariifolium stem exhibits potency against oral squamous cell carcinoma via the downregulation of the cell cycle (cyclin D1) and P13K, especially pronethalol.

}, keywords = {Chrysanthemum cinerariifolium, Cyclin D1, OSCC, P13K.}, doi = {10.5530/pj.2023.15.61}, author = {Anik Listiyana and Yuanita Lely Rachmawati and Hani Susianti and Nurdiana and Hidayat Sujuti and Roihatul Mutiah and Agustina Tri Endharti} } @article {2124, title = {Analysis of the Phytochemical and Antibacterial Properties of the Indigenous Mizo Medicinal Plant, Helicia Excelsa}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {823-828}, type = {Research Article}, chapter = {823}, abstract = {

Background: Helicia excelsa (Roxb.) Bl. is a scarcely known medicinal plant and is native to Southeast Asia. It is most notably used for the treatment of gastric problems in the Mizo traditional medicine in India. Method: The leaves of H. excelsa were collected from Aizawl, Mizoram, India. An extract was prepared using chloroform. Qualitative phytochemical tests were performed to detect the important phytocompounds. The antioxidant activity was determined by total phenolic content, total flavonoid content, total antioxidant content, DPPH- and ferric-reducing antioxidant power. Antibacterial activity was evaluated by agar well-diffusion method. Results: H. excelsa leaf contains amino acids, alkaloids, carbohydrates, glycosides, phenols, phytosterols, proteins, and tannins. It showed inhibition in selected Gram-negative and Gram-positive bacteria. The phenol, flavonoid and total antioxidant contents were 4.52{\textpm}0.09 gallic acid equivalent (GAE mg/g), 64.27{\textpm}1.04 quercetin equivalent (QE mg/g), 11.39{\textpm}0.45 ascorbic acid equivalent (AAE mg/g) respectively. IC50 value of DPPH-scavenging activity was 5.67{\textpm}0.36. The ferric ion-reducing power showed concentration-dependent activity. The plant extract showed growth-inhibitory actions against Gram-negative bacterium, Escherichia coli, and Gram-positive species, Bacillus cereus and Staphylococcus aureus. :Conclusion H. excelsa leaf contains important bioactive compounds that need to be identified. The antioxidant and antibacterial activities support the basis of its medicinal application.

}, keywords = {Antibacterial activity, Antioxidant, Helicia excelsa, Mizo traditional medicine., Plant extract}, doi = {10.5530/pj.2023.15.157}, author = {Lalbiakngheti Tlau and Lucy Lalawmpuii and P.B. Lalthanpuii and K. Lalchhandama} } @article {2044, title = {Anti-Gastritis Activity of Cloves (Eugenia caryophyllata Thunberg) and Lime (Citrus aurantifolia) Leaf Extracts Combination in Absolute Alcohol Induced-Gastric Injury Mice}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {378-384}, type = {Research Article}, chapter = {378}, abstract = {

Background: Clove (Eugenia caryophyllata Thunberg) and lime (Citrus aurantifolia) are medicinal plants traditionally used to treat various diseases such as gastritis. Some studies reported that cloves leaf and lime leaf extract showed a gastroprotective effect by decreasing the gastric acid secretion and increasing the gastric mucus. Aim: This study aims to investigate the anti-gastritis activity of the combination of ethanolic extract of cloves leaf and lime leaf extract in alcohol absolute-induced mice. Methods: Mice were treated with the combination extract 0.7 g/kg BW, 1.4 g/kg BW, and 2.8 g/kg BW. Famotidine was used as a positive control, and Na CMC suspension was used as a negative control. After 45 minutes of oral administration, 0.14 ml/20g BW alcohol absolute was given to all mice. All groups were sacrificed one hour later. The evaluation showed that extract combination in all doses significantly decreased ulcer index (UI) compared to a negative control group (p\<0.005) in macroscopic evaluation. Results: In histopathologic evaluation, all doses significantly decreased mucosal edema and epithelial cell loss (p\<0.005), but in gastric bleeding evaluation, only 0.7 and 1.4 g/kg BW doses showed a significant decrease. Conclusion: This study showed that a combination of clove and lime leaf extracts has anti-gastritis activity and could be a possible therapeutic of anti-gastritis. The most effective dose is 1.4 g/kg BW in mice which showed the lowest ulcer index and gastric mucosal edema, bleeding and epithelial cells loss reduction on histopathological observation.

}, keywords = {Citrus aurantifolia, Clove, Eugenia caryophyllata, Gastritis, Lime, Ulcer}, doi = {10.5530/pj.2023.15.88}, author = {Herra Studiawan and Sukardiman and Indana Lazulfa and Rosita Handayani} } @article {2142, title = {Briefly Describe the Traditional Preparation Method of Mercury in Mongolian Medicine}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {921-923}, type = {Research Article}, chapter = {921}, abstract = {

Objective: This study aims to review the traditional preparation methods and clinical applications of mercury in Mongolian medicine through a literature review. Methods: Ancient and modern literature on the preparation of mercury were reviewed, and the recorded preparation methods in the literature were summarized and organized. The clinical applications were also briefly described. Results: The traditional preparation methods of mercury in Mongolian medicine can be divided into two parts: preparation before processing and specific processing methods. The preparation before processing includes steps such as removing impurities and reducing the weight of mercury. The "Four Parts Ganlu" emphasizes the toxicity of mercury due to its rust (impurities) and weight. Specific processing methods include hot processing, cold processing, slow processing, and quick processing. According to the clinical application records in the literature, hot processing is widely used and still in use today. As a commonly used mineral medicine in Mongolian medicine, mercury is found in various compound formulations recorded in the literature, with a focus on diseases such as "bile", lymphatic, and brain diseases. The proportion of mercury used varies significantly. For example, the preparation of mercury in the Mongen Wusu-18 pill has a higher content and is widely used with significant effects. In addition, mercury is also used in formulations such as Qishiwu Pearl Pill, Ershiwu Songshi Pill, and Ershiwu Coral Pill. Conclusion: The review and study of the traditional preparation methods of mercury in Mongolian medicine can contribute to the standardization and normalization of processing techniques and provide reference materials for the safe application and formulation of mercury processing products.

}, keywords = {Literature research., Mercury, Traditional processing methods}, doi = {10.5530/pj.2023.15.175}, author = {Qimuge and Terbish L and Bold Sharavyn} } @article {2164, title = {Comparison of the Anti-Inflammatory Activity of Flavonoid Bioactive Compounds Acetone Fraction and Steroid Fraction Ethyl Acetate Sungkai Leaves In Vivo and In Silico Studies}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1068-1076}, type = {Original Article}, chapter = {1068}, abstract = {

One of the medicinal plants that is widely used by traditional communities is sungkai (Peronema canescens Jack), which is known to contain secondary metabolite compounds of flavonoids, saponins, tannins, steroids, terpenoids, alkaloids, and phenols. This research aims to isolate secondary metabolite compounds from acetone and ethyl acetate fractions, which act as anti-inflammatory agents in vivo and in silico. Acetone and ethyl acetate fractions were isolated and characterized using UV-Vis and FT-IR. The In Vivo test was carried out on Mus musculus, while the In Silico test was carried out using the IL-10 and IFN-γ receptors, which play a role in inflammation and immunity. Our research results showed that the ethanolic (F1) and n-hexane (F2) fractions of P. canescens extract had good anti-inflammatory activity with percent inhibition values of 58.12\% and 56.59\%, respectively. The characterization results showed that isolate F1 was a flavonoid group, Naringenin compound, while isolate F2 was a steroid group, β-Sitosterol compound. Moreover, from the scoring docking results, β-Sitesterol has tremendous potential as an anti-inflammatory than the compound naringenin.

}, keywords = {Anti-inflamatory; β-Sitesterol; Naringenin, P. canescens Jack}, doi = {10.5530/pj.2023.15.196}, author = {Madyawati Latief and Rahmani and Arliangga Fahrezi and Sutrisno and Indra Lasmana Tarigan} } @article {2066, title = {Computational Evaluation of the Potential of Salicylate Compound from Syzygium aromaticum on Carbonic Anhydrase I as a Gastric Acid Stimulant}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {489-493}, type = {Original Article }, chapter = {489}, abstract = {

This article explores the potential of the salicylate compound (Syzygium Aromaticum) as a stimulant for Carbonic Anhydrase I in gastric acid secretion, using a computational approach. The research methods include molecular modeling with Pymol and Pyrex, determination of compound structure and interactions with Protein Plus, and examination of physicochemical properties using the Lipinski Rule. The results show that the Binding Affinity of salicylate with Carbonic Anhydrase I ranges from -7.3 to -6.5, with RMSD values of 0, 2.102, and 2.212, indicating good modeling quality. The interaction between salicylate and Carbonic Anhydrase I is also supported by the findings from Protein Plus. Furthermore, the salicylate compound complies with the Lipinski Rule, with a molecular weight of 137, 1 hydrogen bond donor, 3 hydrogen bond acceptors, a log P value of 0.34, and a molar reactivity of 34.16. This study highlights the prospect of salicylate as a potential modulator of Carbonic Anhydrase I.

}, keywords = {Carbonic Anhydrase I, Gastric Acid Stimulant, Molecular docking, Salicylate, Syzygium Aromaticum.}, doi = {10.5530/pj.2023.15.107}, author = {Rahadian Zainul and Rismi Verawati and Rauza Sukma Rita and Fadhli Ranuharja and Musa Ghufron and Agariadne Dwinggo Samala and Herland Satriawan and Muhammad Raffi Ghifari and Devi Purnamasari and Riso Sari Mandeli and Amalia Putri Lubis and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {1999, title = {The Effect of Moringa Leaf Extract Intervention Since Preconception Period on the Prevention of Oxidative Stress in Pregnant Women and Adverse Pregnancy Outcomes}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {310-314}, type = {Original Article }, chapter = {310}, abstract = {

Background: Oxidative stress occurs due to an imbalance of oxidants and anti-oxidants and is often associated with poor pregnancy outcomes. Therefore, additional supplementation is needed since the preconception period to prevent oxidative stress and poor pregnancy outcomes. This study aims to examine the effect of supplementing Moringa leaf extract on the prevention of oxidative stress in pregnant women and poor pregnancy outcomes. Methods: This study is an observational study with a prospective cohort study design. The research subjects were third trimester pregnant women consisting of 2 groups, namely the control group who only received Iron-Folic Acid (IFA) supplements (n = 30) and the group that received moringa leaf extract and IFA supplements (n = 26). Then an examination of Malondialdehyde (MDA) levels as a biomarker of oxidative stress was carried out using the ELISA (enzyme-link immune sorbent) method, followed by pregnancy outcomes including birth weight and birth length. Data were analyzed by unpaired t test. Results: The results showed that there were no significant differences in the levels of MDA, birth weight and birth length in the two groups with a p value \> 0.05. Nevertheless, MDA level in IFA group was 49.25 nmol/ml higher than Moringa + IFA group which was 47.58 nmol/ml. Likewise, the average of birth weight and birth length in Moringa group were 3042.3 grams and 48.62 cm higher than IFA group which were 2993.7 grams and 48.23 cm. Malondialdehyde levels were also higher in women who had babies with birth weight \< 2500 grams was 49.48 nmol/ml and birth length \< 48 cm was 49.13 nmol/l compared to birth weight >= 2500 grams was 48.50 nmol/ml and birth length >= 48 cm was 48.62 nmol/ml but there was no significant difference in the two groups (p\>0.05). Conclusion: Oxidative stress in pregnant women tends to be associated with poor pregnancy outcomes. Moringa leaf extract supplementation since preconception can prevent increased oxidative stress and improve pregnancy outcomes.

}, keywords = {Malondialdehyde, Moringa oleifera, Oxidative stress, Pregnancy outcomes.}, doi = {10.5530/pj.2023.15.45}, author = {Rahma and Veni Hadju and A. Arsunan Arsin and Aminuddin Syam and Anwar Mallongi and Abd. Farid Lewa and Haerani Harun and Miranti} } @article {2029, title = {The Effect Supplementation of Microbiota Inoculant in the Early Laying Hens Feed on High Density Lipoprotein (HDL) and Low- Density Lipoprotein (LDL) in Egg Yolk}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {270-273}, type = {Original Article }, chapter = {270}, abstract = {

Laying hens (Gallus gallus) are one of the poultries kept for their eggs. Eggs produced by chickens are used as a source of human food that contains a lot of nutrition and is affordable. Eggs also contain high levels of cholesterol in the yolk, so if consumed in large quantities, they will pose a risk of disease. This study aims to determine the effect of giving probiotics in the early layer laying hen feed on the levels of high-density lipoprotein and low-density lipoprotein in egg yolks. This study has four treatments, namely P1 = control, P2 = feed + AGP, and P3 and P4 = feed + probiotics. The probiotic used is a combination of three bacteria, namely Lactobacillus plantarum, Lactobacillus acidophilus, and Bifidobacterium sp. The sample used in this study was egg yolk, which was collected in the last week of the study. Testing for HDL and LDL levels in egg yolks was carried out using the Quantitative Colorimetric/Fluorometric Determination of HDL and LDL/VLDL method. Testing HDL and LDL levels in this study showed that the administration of probiotics had an effect in the form of increasing HDL levels but did not have an effect in the form of a significant decrease in egg yolk LDL levels during the four-week treatment period in laying hens in the early layer phase, aged 18{\textendash}22 weeks. The best probiotic dose used among the three probiotic doses is 3 ml/kg of feed.

}, keywords = {High Density Lipoprotein, Laying hens, Low Density Lipoprotein, Probiotics.}, doi = {10.5530/pj.2023.15.73}, author = {Bodhi Agustono and Rini Apriliawati and Sunaryo Hadi Warsito and Maya Nurwartanti Yunita and Widya Paramita Lokapirnasari and Sri Hidanah and Emy Koestanti Sabdoningrum and Mohammad Anam Al-Arif and Mirni Lamid and Gandul Atik Yuliani and Shekhar Chhetri and Sarasati Windria} } @article {2133, title = {The Effectiveness of SI-DINI Mobile App (an Education and Early Detection of Leprosy App) on Changes in Community Behavior}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {868-872}, type = {Research Article}, chapter = {868}, abstract = {

Most leprosy case detection in Indonesia is based on passive surveillance. This condition impacts the high number of new cases of leprosy and the disability rate of leprosy. Data from the Ministry of Health of the Republic of Indonesia stated that for 2021, there were 7,201 new cases of leprosy with a disability proportion of 84.6\%. The community{\textquoteright}s reluctance to make early contact is due to low knowledge and fear of stigma. SI-DINI is an android-based application that contains information about leprosy, videos on identifying the characteristics and symptoms of leprosy, and reporting suspected leprosy so that it is hoped that it can change people{\textquoteright}s behavior in a positive direction. This study aims to see the effectiveness of the SI-DINI App in changing people{\textquoteright}s behavior. This study used a quasi-experimental design with a pre and post-test design with intervention and control groups. The use of the SI-DINI App has been proven effective in changing people{\textquoteright}s behavior in terms of knowledge, attitudes and actions. There is a significant increase in the knowledge aspect with p-value = 0.000 (p\<0,05), the attitude aspect p-value = 0.000 (p\<0,05), and the action aspect p-value = 0.000 (p\<0,05). It is hoped that the application of education and surveillance for early detection of leprosy (SI-DINI) can be applied on a broader scope and can be used sustainably and in the future.

}, keywords = {Attitude, Behavior., knowledge, Leprosy, SI-DINI App}, doi = {10.5530/pj.2023.15.166}, author = {Maspa Lapui and Wahiduddin and Ida Leida Maria and A Arsunan Arsin and Ridwan M Thaha and Syamsuar Manyullei and Anwar Mallongi} } @article {2179, title = {Elucidating the Use of the Plant Paeonia Anomala from the Ancient Medical Books Kept in Mongolia}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1163-1165}, type = {Research Article}, chapter = {1163}, abstract = {

Background: It is important to determine and study in detail the action of the main chemical and secondary components contained in Paeonia anomala against diseases. In particular, it is of great practical significance to clarify the use of the plant from ancient medical books and scriptures and to determine which of the six main diseases were used in traditional medicine. Purpose: To compare the information of the ancient medical books written by Mongolian doctors and scientists, who wrote about Paeonia anomala L. and to clarify the taste, potency, strength, and quality. Research materials and methods: Research materials: Sumbe khamba Ishbaljir. {\textquotedblleft}gso dpyad bdud rtsi {\textquoteright}i chu rgyun gyi cha lag gi nang tshan gyi sman so so{\textquoteright}i mngon brjod dang ngos {\textquoteright}dzin shel dkar me long{\textquotedblright}. Wooden printing block with Tibetan script. Toin Jambaldorj. {\textquotedblleft}gso byed bdud rtsi{\textquoteright}i {\textquoteright}khrul med ngos {\textquoteright}dzin bzo rig me long du rnam par shar ba mdzes mtshar mig rgyan zhes bya ba bzhugs so{\textquotedblright}. Wooden printing block with Tibetan script. Research methods: Methods of textual analysis for ancient medical books and checklists were used in the study. Conclusion: The use of Paeonia anomala has been enriched with indications for use in traditional Mongolian medicine, Mongolian folk medicine, Russian folk medicine, and Chinese, Japanese, and Korean traditional medicine. In his book "ngos {\textquoteright}dzin shel dkar me long", the ancient medical scientist Sumbe khamba Ishbaljir wrote the name of the Paeonia anomala plant in Sanskrit as shogandha and in Tibetan as baspru. On the other hand, Toin Jambaldorj noted in his book "mtshar mig rgyan" wrote Paeonia anomala has a warm and equable quality, thus it can create potency. Therefore, it is appropriate to note that this plant in traditional Mongolian medicine is mainly used to treat back pain caused by cold conditions, chronic kidney disease, arthritis, uterine benign tumors, and bladder stones.

}, doi = {10.5530/pj.2023.15.211}, author = {Ariunjargal Tudev and Sansarkhuyag Enkhtur and Khurelbaatar Luvsan and Odontuya Gendaram and Bold Sharav and Ulambayar Lkhamsuren} } @article {2138, title = {Elucidating the Uses of the Plant Veronica Incana from the Ancient Medical Books}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {901-904}, type = {Research Article}, chapter = {901}, abstract = {

Background: Medicinal plant research has been successfully carried out in the field of pharmacy and pharmacology in Mongolia, and dozens of research projects are still being carried out. However, there are still fewer studied medicinal plants of practical importance growing in Mongolia. Therefore, there is a need to register and study the ancient medicinal books written by ancient Mongolian doctors about the relatively little-studied Veronica Incana plant. In addition, taking into account that scientific research on Veronica Incana, which grows in Mongolia, has not been done in the field of medicine. Therefore, the topic was selected for research in this field. Purpose: Comparing the information of the ancient medical books written by Mongolian doctors and scientists, who wrote about Veronica Incana, to clarify the taste, power, and quality. Research materials and methods: 1. Research materials: Sumbe khamba Ishbaljir. gso dpyad bdud rtsi {\textquoteright}i chu rgyun gyi cha lag gi nang tshan gyi sman so so{\textquoteright}i mngon brjod dang ngos {\textquoteright}dzin shel dkar me long. Wooden printing block with Tibetan script. Toin Jambaldorj. gso byed bdud rtsi{\textquoteright}i {\textquoteright}khrul med ngos {\textquoteright}dzin bzo rig me long du rnam par shar ba mdzes mtshar mig rgyan zhes bya ba bzhugs so. Wooden printing block with Tibetan script. 2. Research methods: Methods of textual analysis for ancient books and checklist methods were used in the study. Conclusion: Gandhabhatra plant is used in traditional Mongolian medicinal practices from ancient times, the plant is called Veronica Incana in Latin. Also called Buural gandbadraa in Mongolian. On the other hand, the traditional medical doctors of China{\textquoteright}s Inner Mongolia and Tibet use Gandbadraa, the Latin name Gnaphalium affine D. Don. The appearance, shape, and color of the flowers of these two plants are different. According to the research of the source, the main instruction and usage of the plants are the same: to destroy benign tumors, to remove poison, to treat colds, and to stop cough.

}, keywords = {Ancient medicinal books., Medicinal plants, Traditional Mongolian medicine, Veronica Incana}, doi = {10.5530/pj.2023.15.171}, author = {Sansarkhuyag Enkhtur and Ariunjargal Tudev and Tungalag Dagdanbazar and Selenge Erdenechimeg and Odontuya Gendaram and Ulambayar Lkhamsuren and Bold Sharav} } @article {2165, title = {Immunomodulatory and Acute Toxicity Tests of Rhizome Ethanol Extract of Etlingera Flexuosa Poulsen (Zingiberaceae) on Male Mice (Mus Musculus)}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1077-1083}, type = {Original Article}, chapter = {1077}, abstract = {

Introduction: Immunomodulators are molecules of synthetic or biological origin that help to regulate the immune system. Many studies have focuses on exploring for phytochemical compounds that used as immunomodulatory properties in Indonesia, as well as in Sulawesi. The immunomodulatory activity of rhizome extract of E. flexuosa, an endemic flowering plant of Sulawesi on male mice were studied. Methods: 25 male mice (Mus musculus) used were randomly divided into 5 groups and Staphylococcus aureus (ATCC 25923) was used as inducer. The negative control group was given 0.5\% Na-CMC (Carboxymethyl Cellulosa Sodium), positive control group was given stimuno{\textregistered} and treatment groups were an ethanol extract of E. flexuosa with successive doses of 200, 400 and 800 mg/kg body weight (BW) respectively. Each group was given the preparation orally for 7 days and on the 8th day the test animals were induced by Staphylococcus aureus bacteria intraperitoneally. The mice were dissected and the peritoneal fluid was taken to determine the activity of the macrophage cells. Meanwhile, Thomson and Weil method was used to study the acute toxicity test and determine the lethal dose 50 (LD50). Results: The percentage of macrophage activity in each group of negative control, positive control, extract doses of 200, 400 and 800 mg/kg BW respectively were 40.40\%, 82.65\%, 53.05\%, 69.38\% and 82.06\%. Based on the results obtained, it was shown that the E. flexuosa rhizome extract has an optimum dose of 800 mg/kg BW, which was not significantly different from the positive control. Meanwhile, the symptoms of toxicity began to appear from a dose of 600 mg/kg BW to a dose of 2400 mg/kg BW including decreased motor activity, tremor, ataxia, lids and writhing. LD50 expressed in LD50 within the criteria of being practically non-toxic. Conclusions: The E. flexuosa rhizome ethanolic extract showed the immunomodulatory activity at optimum dose of 800 mg/kg BW by the increasing of macrophage phagocytosis activity. Moreover, the extract was also practically non-toxic based on LD50 value.

}, keywords = {Etlingera flexuosa, Immunomodulators, Immunostimulants, Lethal Dose 50, Macrophages, Phagocytosis, Toxicity}, doi = {10.5530/pj.2023.15.197}, author = {Ramadanil Pitopang and Nadhirah Nur Azizah Lubis and Mifthahul Jannah Tahapary Zubair and Puti Andalusia Sarigando Banilai and Nurhaeni and Ihwan} } @article {2180, title = {Immunomodulatory and Antiallergic Potentials of the Bioactive Compounds of Ginger}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1166-1176}, type = {Research Article}, chapter = {1166}, abstract = {

Background: Allergy is an ever-increasing immune disorder and is often fatal under certain circumstances. Lack of total curative medication prompts the search for various compounds as the lead molecules. Ginger, Zingiber officinale Roscoe, is a well-established medicinal plant in different traditional practices. Its use as antiallergic or anti-inflammatory agent has been vindicated but the underlying mechanism of action is yet unknown. Method: In this study, we analyzed the phytocompounds characterized from ginger for their binding affinities on cysteinyl leukotriene receptor 1 (CysLTR1) and histamine H1 receptor (H1R) by molecular docking. The molecular interactions were compared against known agonists and antagonists of the two receptors. Results: The data indicate that ginger compounds have high binding affinity for both LTR1 and H1R comparable to those of antiallergic medications. The highest binding affinities were recorded for gingerenone-A (-7.3 kcal/mol) and zingiberol (-7.2 kcal/mol) on LTR1; and gingerenone-A (-8.7 kcal/mol) and α-curcumene (-8.0 kcal/mol) on H1R. Conclusion: In addition to antiallergic activity, molecular predications on the probable biological activities of the ginger compounds show that they can have a variety of medicinal applications including immunomodulatory and anticancer activities.

}, keywords = {Allergy, Ginger, Histamine Receptor; Leukotriene Receptor, Molecular Modelling}, doi = {10.5530/pj.2023.15.212}, author = {B. Lalruatfela and P. B. Lalthanpuii and C. Lalrinmawia and K. Lalchhandama} } @article {2081, title = {In Silico Study on the Inhibition of Sitogluside from Clove Plant (Syzygium aromaticum) on Interleukin 2 in B and T Cell Proliferation}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {575-580}, type = {Research Article}, chapter = {575}, abstract = {

This research discusses an in-silico study of sitogluside found in the clove plant (Syzygium aromaticum) as a potential inhibitor of B and T cell proliferation through interaction with Interleukin-2. This study utilizes methods such as Swiss Target Prediction, Pymol, Pyrex, Protein Plus, and Lipinski{\textquoteright}s Rule to predict the biological activity and pharmacokinetic characteristics of sitogluside. From the docking simulation results, sitogluside exhibited strong interactions with interleukin-2 with RMSD values of 0, 1.637, and 2.299, and Binding Affinities of -5.7, -5.5, and -5.5, indicating its potential effectiveness as an inhibitor. In addition, sitogluside fulfills Lipinski{\textquoteright}s rule with a molecular mass of 520, 4 hydrogen bond donors and acceptors, a log P value of 2.3, and a molar reactivity of 133, indicating a high potential for good bioavailability in biological systems. These results suggest that sitogluside from the clove plant holds potential as a new therapy in inhibiting B and T cell proliferation, however further research is needed to validate these findings and explore its potential in clinical treatments.

}, keywords = {Cell Proliferation, Interleukin-2, Molecular docking, Sitogluside, Syzygium.}, doi = {10.5530/pj.2023.15.122}, author = {Linda Rosalina and Devi Purnamasari and Rismi Verawati and Okta Suryani and Muhammad Arya Ghifari and Amalia Putri Lubis and Rahadian Zainul and Riso Sari Mandeli and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2067, title = {In Silico Study on the Potential of Guaiacol Extract from Green Tea (Camellia sinensis) as a Stimulant for Carbanoic Anhydrase II in Renal Tubular Acidosis}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {494-499}, type = {Original Article }, chapter = {494}, abstract = {

This study explores the potential of Guaiacol, a green tea extract from Camellia sinensis, as a stimulant in renal tubular acidosis through in-silico investigation on the Carbanoic Anhydrase II enzyme. Utilizing comprehensive computational tools including PyMOL, PyRx, Protein Plus, and the Lipinski{\textquoteright}s Rule of Five, a detailed examination of the molecular structure and its interactions with the target enzyme was conducted. The results from Protein Plus revealed interactions between Guaiacol and Carbanoic Anhydrase II. Quantitative parameters were determined with Binding Affinity values of -5, -4.7, and -4.5, along with RMSD values of 0, 0.956, and 1.412. The Lipinski{\textquoteright}s Rule of Five was employed to evaluate the compound{\textquoteright}s drug-like properties, with the findings indicating a molecular weight of 124, one hydrogen bond donor, two hydrogen bond acceptors, a log P of 1.4, and a molar reactivity of 34.65. Overall, these findings suggest that Guaiacol holds promising therapeutic potential in the treatment of renal tubular acidosis.

}, keywords = {Camellia sinensis., Carbanoic Anhydrase II, Guaiacol, Molecular docking, Renal Tubular Acidosis}, doi = {10.5530/pj.2023.15.108}, author = {Rahadian Zainul and Rismi Verawati and Agus Suprijono and Riso Sari Mandeli and Asri Peni Wulandari and Dony Novaliendry and Ritmaleni and Linda Rosalina and Muhammad Arya Ghifari and Amalia Putri Lubis and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2161, title = {The Influence of Vitamin D3 Administration on the Levels of CGRP, Glutamate, and NLRP3 during the Ictal Phase in Chronic Migraine Patients}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1052-1058}, type = {Original Article}, chapter = {1052}, abstract = {

Background: Migraine is a primary headache disorder that ranks as the third leading cause of disability. Various prophylactic therapies have been developed for migraine treatment, including vitamin D3 supplementation. The mechanism of action of vitamin D3 supplementation in the pathophysiology of migraine has not been extensively studied. Objective: This study assesses the impact of vitamin D3 administration on the levels of the biomarkers CGRP, Glutamate, and NLRP3 and its effect on reducing the frequency and intensity of migraine attacks in chronic migraine patients. Methods: This experimental study (single-blind clinical trial) observes two groups: a group given vitamin D3 at 2000 IU for 12 weeks and a placebo group. This study involved 61 chronic migraine subjects. At the end of the study, after excluded 31 subjects, there were 12 subjects in each of the two groups. Results: A significant relationship was found between vitamin D3 administration and the reduction in the frequency and duration of migraine attacks in both the vitamin D3 group (p\<0.001) and the placebo group (p=0.078). No significant relationship was found between vitamin D3 administration and changes in CGRP levels (p=0.633), but there were significant changes in glutamate (p\<0.001) and NLRP3 (p=0.016) levels following vitamin D3 administration. Conclusion: Vitamin D3 supplementation has an impact on reducing the frequency and duration of migraine attacks in chronic migraine patients, and there is a significant association with changes in glutamate and NLRP3 levels, but not with changes in CGRP levels.

}, keywords = {CGRP, Chronic Migraine, Glutamate, NLRP3, Vitamin D3}, doi = {10.5530/pj.2023.15.193}, author = {Restu Susanti and Yuliarni Syafrita and Afriwardi and Rauza Sukma Rita and Eryati Darwin and Nur Indrawaty Lipoeto and Hirowati Ali and Fika Tri Anggraini} } @article {2063, title = {Interaction of Masilinic Acid from Clove Plant (Syzygium aromaticum) with CD81 Antigen in Inhibiting HIV Virus Regulation In Silico}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {484-488}, type = {Original Article }, chapter = {484}, abstract = {

This research explores the interaction of Masilinic Acid from the clove plant (Syzygium aromaticum) with the CD81 antigen to inhibit HIV virus regulation in silico. Using computational methods such as Pymol, Pyrex, and Protein Plus, we demonstrate that Masilinic Acid can significantly interact with the CD81 antigen. The obtained data shows binding affinities of -6.4, -6.2, and -5.7, and RMSD values of 0, 1.885, and 1.952. Further detailed interaction analysis with Protein Plus strengthens these findings, providing evidence of a strong interaction between Masilinic Acid and the CD81 antigen. This study also includes the testing of the Lepinski Rule of Five to assess the potential of Masilinic Acid as a drug candidate, with results indicating a mass of 472, three hydrogen bond donors, four hydrogen bond acceptors, a log P value of 6.2, and a molar reactivity of 134. These results indicate that Masilinic Acid has the potential as an inhibitor of the CD81-HIV interaction, which can be utilized as an effective antiviral strategy. Key words: Masilinic Acid, Clove plant, CD81 antigen, HIV virus, In silico.

}, keywords = {CD81 antigen, Clove plant, HIV virus, In Silico., Masilinic Acid}, doi = {10.5530/pj.2023.15.106}, author = {Rahadian Zainul and Elsa Yanuarti and Siti Amiroch and Muhammad Thoriq Albari and Rismi Verawati and Amalia Putri Lubis and AAA Murtadlo} } @article {2187, title = {Intravitreal Resveratrol as Anti Apoptotic Agent Against Retinal Ganglion Cell Loss in Ischemic Reperfusion Injury}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1207-1212}, type = {Research Article}, chapter = {1207}, abstract = {

Background: Glaucoma is an optic neuropathy caused by the apoptosis of retinal ganglion cells and results in progressive retinal ganglion cell injury. A decrease in intraocular pressure (IOP) is a modifiable risk factor for slowing the progression of the disease, and can be accomplished through medication, laser therapy, or surgery. Even though the intraocular pressure has decreased and attained normal levels, the injury to the retinal ganglion cells continues in some cases. It is believed that neuroprotective administration has a positive effect on preventing the loss of retinal ganglion cells. Methods: Bax and Caspase-3 expression were measured involving 20 eyeballs of Rattus Norvegicus by immunohistochemistry examination. I-R injury was developed by increasing intraocular pressure (IOP) through the intracameral balanced salt solution (BSS) injection, then lowered after 60 minutes. Samples were divided into 4 groups: control, no further injection group, phosphate-buffered saline (PBS)-injected group and resveratrol-injected group. Each group was enucleated at days 7, 0, 7, and 7, respectively. Data with a non-normal distribution were examined using the Kruskal-Wallis test, and if the outcome was significant, the Mann-Whitney test. Results: The highest mean Bax and Caspase-3 expression was found in PBS injected and enucleated at day 7 group (G2), 0.96{\textpm}0.40 and 0.72 {\textpm} 0.30, respectively. When compared to PBS injection, the expression of Bax and Caspase-3 was lower in the resveratrol-injected group. Conclusion: Bax and Caspase-3 expressions were lower in the intravitreal injection of Resveratrol in the dose of 100 {\textmu}M following the I-R injury group compared to the group without intravitreal Resveratrol injection.

}, keywords = {Apoptosis, Glaucoma, Ischemic-reperfusion injury, Neuroprotective, Resveratrol}, doi = {10.5530/pj.2023.15.219}, author = {Amelia Shinta Prasetya and Evelyn Komaratih and Wimbo Sasono and Mercia Chrysanti and Maria Debora Niken Larasati and I Ketut Sudiana} } @article {2122, title = {Knowledge and Perception of the Risk of Respiration Disorders in COVID-19 Pandemic in COPD Patient: A Mixed-Method Study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {801-810}, chapter = {801}, abstract = {

Introduction: Chronic obstructive pulmonary disease (COPD) have a higher risk for COVID-19-related complications. Knowledge and perception will greatly influence the behavior of a COPD patient in dealing with a problem, such as the risk of COVID-19 infection. The purpose of the study was to determine knowledge and perceptions about the risk of respiration disorders during the COVID-19 pandemic in COPD patients. This research was a mixed methods research with an explanatory sequential research design. The location was conducted in Rungkut District in Surabaya City, East Java, from May-October 2022. Sampling by purposive sampling method, and analyzed descriptively. The research sample was 116 people. On the knowledge, the most correct answers were the COVID-19 virus was contagious (112 of 116). On the perception, the answer with the most positive level is a question regarding the use of masks. Some respondents had a low knowledge category (54 of 116), and the most positive perception category (57 of 116). The respondents{\textquoteright} knowledge of the COVID-19 virus showed COVID-19 virus was a contagious disease and was transmitted through air. But many respondents didn{\textquoteright}t know about the type of COVID-19 virus. Therefore, it was necessary to develop a strategy to increase knowledge about COVID-19 and related COPD treatment.

}, keywords = {COPD, COVID-19, knowledge, Perception.}, doi = {10.5530/pj.2023.15.155}, author = {Amelia Lorensia and Rivan Virlando Suryadinata and Dita Sukmaya Prawitasari} } @article {2068, title = {Molecular Docking of Thaflavine from Camellia sinensis in Inhibiting B-Cell Lymphoma Through BCl2 Apoptosis Regulator: An In Silico Study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {500-505}, type = {Original Article }, chapter = {500}, abstract = {

This study aims to analyze the potential of Thaflavine, a compound found in green tea (Camellia sinensis), as an inhibitor in inhibiting B-cell lymphoma through its interaction with the BCl2 apoptosis regulator using an in-silico approach. The research methodology involved the use of software tools such as PyMOL, PyRx, Protein Plus, and the Lepinski Rule. Through molecular docking analysis using PyMOL and PyRx, the findings of this study demonstrate significant interactions between Thaflavine and BCl2, with Binding Affinity values of -5.5, -4.6, and -4.6, and RMSD values of 0, 1.436, and 2.292. The analysis using Protein Plus indicates the presence of interactions between Thaflavine and BCl2. Additionally, the analysis using the Lepinski Rule of Five reveals that Thaflavine meets the criteria as a potential drug compound, with a molecular weight of 549, 9 hydrogen bond donors, 12 hydrogen bond acceptors, a log P value of -2.5, and a molar reactivity of 119.17. The findings of this study provide important contributions to the development of therapies for B-cell lymphoma through an in-silico approach. However, further research is needed for in vitro and in vivo validation.

}, keywords = {Apoptosis Regulator BCl2, B-cell Lymphoma, Camellia sinensis., In-Silico Thaflavine, Molecular docking}, doi = {10.5530/pj.2023.15.109}, author = {Rahadian Zainul and Rismi Verawati and Herland Satriawan and Teresa Liliana Wargasetia and Devi Purnamasari and Amalia Putri Lubis and Bahrun and Riso Sari Mandeli and Muhammad Thoriq Albari and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2037, title = {Nonmotoric Symptoms Scale (NMSS) Validity and Reliability Test in Patients with Parkinson{\textquoteright}s Disease in Dr. Soetomo General Hospital, Surabaya, Indonesia: A Questioner Validation Study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {316-320}, type = {Original Article }, chapter = {316}, abstract = {

Background: Nonmotor symptoms are common but less reported in Parkinson{\textquoteright}s disease. it{\textquoteright}s the cause of decreased quality of life and disability in many patients with Parkinson{\textquoteright}s disease compared to the motor symptom. Our study aimed to translate the original English-language version of the nonmotor symptom scale (NMSS) into the Indonesian version of the NMSS. And also to evaluate its validity and reliability for use in Indonesian-speaking Parkinson{\textquoteright}s disease patients. This for better and valid usage of NMSS scale in the Indonesian patient and health care provider Material and Method: This was descriptive-analytic study. Cross-cultural adaptation of NMSS and psychometric analysis of the Indonesian version of NMSS was carried out from 2 Teaching Hospital centers in Surabaya, East Java. Several other scales were also examined, including MMSE, ESS, BDI, and Scopa-Aut. A reliability test was performed using Alpha Cronbach. Results: A total of 35 patients were included in this study. the average age was 64.03{\textpm}12.92 with the female sex 42.9\% (n=15) and the male 57.1\% (n=20), and Hoehn and Yahr stage II 57.1\% (n=20). The total average NMSS is 11.64. The validity of contents and constructs of the NMSS on each domain has been proven valid. Internal reliability of internal consistency in these tools with an alpha Cronbach value of 0.836. Each domain correlates with several other scores including MMSE, BDI, ESS, and Scopa-aut. Conclusion: The Indonesian version of NMSS has good validity and reliability in assessing nonmotor symptoms in Parkinson{\textquoteright}s disease patients in Indonesia.

}, keywords = {Nonmotoric Symptoms Scale, Parkinson{\textquoteright}s disease, Validation, Validity}, doi = {10.5530/pj.2023.15.81}, author = {Muhammad Hamdan and Priya Nugraha and Pramitha Nayana Librata and Cindy Cecilia} } @article {2099, title = {Optimization of Osteopontin Recombinant Protein as a Candidate Supplementation for Semen Preservation}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {668-673}, type = {Research Article}, chapter = {668}, abstract = {

The recombinant protein of heterologous proteins in Escherichia coli strains K12 has various and different systems tested and demands a detailed insight into the multiple factors affecting the encoded protein. One of the crucial factors is the acceptable quality of the DNA copies inserted inside the bacteria. Firstly, the amplification procedure needed to be performed well; thus, designing the primer and selecting the optimum annealing temperature are the focus indicators in this study. This study obtained a reference gene from the NCBI data bank with Reference Sequence: NM_174187.2. Two types of primers (SPP1FSPP1R and OPN1F - OPN1R) with different targeted bands were designed and selected after being reconstructed using the software. Online software such as addgene.org is also used to identify the right restriction site. The annealing temperature distinguished the PCR system used to amplify each primer. The result of this study revealed the best annealing at 65{\textordmasculine}C successfully amplified 820 bp of the targeted band. The phenomenon not following the theory of blue-white screening is the empty plasmid control, where not a single colony grows on the media. Competent cells inserted with empty plasmids should still be able to expand on LB-Amp agar media because the presence of these plasmids is capable of providing resistance to antibiotics (in this case, ampicillin). This discrepancy is thought to have been caused by the improper insertion of the empty plasmid so that the plasmid did not enter the competent cell.

}, keywords = {DNA clone, Osteopontin, PCR amplification., Primer}, doi = {10.5530/pj.2023.15.135}, author = {Tatik Hernawati and Tita Damayanti Lestari and Suzanita Utama and Rimayanti} } @article {2117, title = {Phytochemical Profile, Antioxidant and Antibacterial Activity of the Essential Oil of Luma Chequen (Molina) A. Gray from Peru}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {777-780}, type = {Original Article}, chapter = {777}, abstract = {

Background: Luma chequen belongs to Myrtaceae family and it is known as {\textquotedblleft}arrayan{\textquotedblright}. In the traditional medicine from Peru, L chequen is used as aromatic plant, anti-inflammatory and hypocholesterolemic. Objective: To determine the phytochemical profile, evaluate the antioxidant and the antibacterial activity of L. chequen essential oil. Material and Methods: In the analysis of the volatile components a Gas Chromatography coupled to Mass Spectrometry (GC-MS) was used to identify the content of terpenes and sesquiterpenes. 2,2-diphenyl-1-picrylhydrazyl (DPPH) was the method used to determine the antioxidant activity and obtain the half inhibitory concentration (IC50). For the antibacterial activity, a colorimetric macrodilution method was carried out to evaluate the effect of the essential oil of L. chequen against Staphylococcus aureus ATCC 25923 and Escherichia coli ATCC 25922. Results: The analysis by GC-MS showed two major components alpha-pinene (62.89\%) followed by 1,8-cineole (11.94\%), and propanoic acid, 2-methyl-, 2-methylpropyl ester with 8.67\%. In the antioxidant activity against DPPH radical, the essential oil of L. chequen showed an IC50 equivalent to124.60 {\textpm} 2.0 μg/mL. In the antibacterial activity, L. chequen had an MIC (minimum inhibitory concentration) for Staphylococcus aureus ATCC 25923 and Escherichia coli ATCC 25922 of 4.35 {\textpm} 0 μg/mL and 8.71 {\textpm} 0 μg/mL respectively. Conclusion: L. chequen presented monoterpene compounds as main phytoconstituents as well as antioxidant and antibacterial activity in vitro. The essential oil might be used as antimicrobial agent in the future overall against S. aureus.

}, keywords = {Antibacterial., Antioxidant, Aromatic plant, Essential oil, Luma chequeen, Medicinal plant}, doi = {10.5530/pj.2023.15.151}, author = {Julio Luis D{\'\i}az-Uribe and Mar{\'\i}a Elena Salazar-Salvatierra and Julio Reynaldo Ruiz-Quiroz and Oscar Herrera- Calderon and Eddie Loyola-Gonzales and Freddy Emilio Tataje-Napuri and Jos{\'e} Francisco Kong-Chirinos} } @article {2119, title = {Phytochemical Screening and Antiinflammatory Activity of the Extract from the Leaves of Desmodium molliculum (Kunth) DC (Fabaceae) in Rats with Acute Inflammation}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {786-790}, type = {Original Article}, chapter = {786}, abstract = {

Inflammation and pain are the initial response mechanisms to environmental aggression on the human body. The traditional use of plants such as Desmodium Molliculum (Kunth) DC, among the Peruvian population for the treatment of inflammatory diseases, has occurred since ancient times. The objective of this research was to determine the presence of secondary metabolites and evaluate the antiinflammatory activity of Desmodium molliculum (EDM) leaves in rats with acute inflammation induced using carrageenan. The phytochemical profile was performed for the main secondary metabolites with biological activity. Subsequently, 25 rats were divided into 5 groups and treated as follows: Group I and II: Physiological Saline Solution (PSS) by oral administration. Group III: Sodium Diclofenac (25 mg/kg body weight) by intraperitoneal administration. Group IV and V: EDM at 250 mg/kg bw and 500 mg/kg bw by oral administration, respectively; 30 minutes after administration, acute inflammation was induced in Groups II, III, IV, and V using the subplantar edema technique with 1\% w/v carrageenan. The volume displaced by the hind paw was evaluated in all 5 groups using a digital plethysmometer every 60 minutes for 5 hours. The results were obtained from the displaced volume (Mean {\textpm} SD), with the most representative values obtained at 240 minutes, where EDM at 250 mg/kg (0.57 {\textpm} 0.07 ml) bw and 500 mg/kg bw (0.578 {\textpm} 0.051 ml) showed significant anti-inflammatory activity (ANOVA p\<0.05). We concluded that Desmodium Molliculum has anti-inflammatory activity at doses of 250 mg/kg bw and 500 mg/kg bw.

}, keywords = {Acute inflammation, Carrageenan, Desmodium, Dog{\textquoteright}s Paw, Edema Subplantar, Fabaceae.}, doi = {10.5530/pj.2023.15.153}, author = {Karyn Olascuaga-Castillo and Olga Castillo-Medina and Marleni Villacorta-Zavaleta and Dan Altamirano- Sarmiento and Elena Caceres-Andonaire and Maria Llontop and Fatima Malca and Sebastian Noe and Cyntia Blanco-Olano} } @article {2025, title = {The Role of Cyclooxigenase-2 Inhibitor in Basal Cell Carcinoma: A Literature Review}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {233-238}, type = {Review Article}, chapter = {233}, abstract = {

Basal cell carcinoma (BCC) is the most common skin malignancy worldwide. It has low mortality but can cause significant morbidity primarily due to local destruction. The incidence and associated cost are rising in recent years causing a burden in healthcare system. BCC incidence are continue to increase due to lack of effective chemopreventive option. Several risk factors are associated with the pathogenesis of BCC. One of the major risk factors of BCC is exposure to ultraviolet (UV) rays, hence the prevention strategy for this malignancy include avoidance of natural and artificial sources of UV radiation. However, these methods are still less than optimal in inhibiting the emergence of basal cell carcioma. In recent years, there is accumulating evidence that cyclooxygenase-2 (COX-2), may be involved in the pathogenesis of BCC. Several recent studies have shown that the use of cyclooxygenase-2 (COX-2) inhibitor drugs can prevent the development of nonmelanoma skin tumors including BCC. In this review, we described the potential of COX-2 inhibitors as chemoprevention for BCC.

}, keywords = {Basal cell carcinoma., Cancer, Chemoprevention, Cox-2 inhibitor, Cyclooxygenase, Skin malignancy}, doi = {10.5530/pj.2022.15.35}, author = {Maylita Sari and Kartika Misalina and M. Yulianto Listiawan} } @article {2127, title = {Total Phenolic and Flavonoid Contents, Anti-tyrosinase and Antioxidant Activities of Pachyrhizus erosus Extracts}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {839-842}, type = {Research Article}, chapter = {839}, abstract = {

Background: The storage roots of Pachyrhizus erosus (PE) have been traditionally used as a skin whitening agent in Indonesia and are also consumed fresh in many Southeast Asian countries, including Thailand. However, research on the biological activities of PE is limited. Objective: This study aimed to measure the total phenolic and flavonoid contents and to test the anti-tyrosinase and antioxidant activities of PE extracts. The Folin-Ciocalteu colorimetric, the Aluminium chloride colorimetric, the DPPH scavenging, and the Dopachrome assays were used for the experiments. Results: The dichloromethane extract had the highest anti-tyrosinase activity (IC50= 2.08 {\textpm} 0.40 mg/mL), total flavonoid content (9.93 {\textpm} 0.02 mg QE/g extract), and antioxidant activity (IC50= 40 {\textpm} 0.02 μg/mL). The largest total phenolic concentration was found in the 80\% ethanol extract, albeit (11.97 {\textpm} 0.55 mg GAE/g extract). Conclusion: Based on its remarkable activities, the dichloromethane extract is recommended for future development in skinlightening products. The study{\textquoteright}s findings conclude that PE extracts may be used as an alternate source of antioxidants and anti-tyrosinase agents

}, keywords = {Anti-tyrosinase, Free radical scavenging., Pachyrhizus erosus, total flavonoid content, total phenolic content}, doi = {10.5530/pj.2023.15.160}, author = {Pornpun Laovachirasuwan and Methin Phadungkit} } @article {1805, title = {Alpha-Mangostin Enhances Proliferation in Sorafenib-Surviving HepG2 Liver Cancer Cells by Increasing Anti-Apoptosis and Antioxidant Markers Expressions}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {584-590}, type = {Research Article}, chapter = {584}, abstract = {

Background: Sorafenib is the first-line systemic option for treatment in advanced liver cancer. However, sorafenib resistance may develop rapidly, which may involve apoptosis and oxidative stress dysregulations. Several alternative treatments have been suggested to alleviate the delayed resistance of cancer cells to sorafenib, including alpha mangostin (AM). According to an earlier study, AM might be able to overcome doxorubicin resistance in hepatocellular cancer cells. Objective: The aim of this study was to investigate the effects of AM in sorafenib-surviving HepG2 cells, a hepatocellular carcinoma (HCC) cell line. Methods: Sorafenib 10 μM was used to treat HepG2 to obtain sorafenib-surviving cells. Subsequently, sorafenib surviving cells were treated with DMSO -(vehicle) or sorafenib (SF) 10 μM or AM 20 μM, or SF 10 μM + AM 20 μM. Afterward, the cells were counted, collected and extracted for RNA. The mRNA expressions of Ki-67, c-Jun, Bcl-2, Bax, Caspase-3 and -9, GPx, and MnSOD were then quantified using qRT-PCR. Results: Treatment of alpha-mangostin, alone or in combination with sorafenib combined enhanced the expressions of proliferation markers, Ki-67 and c-Jun. In addition, there was a marked increase in mRNA expressions of Bax and BCl2, but not Caspase-3 and -9. There were amplifications of antioxidant markers expressions, GPx, and MnSOD after AM or a combination of sorafenib and AM. Conclusion: Treatment of alpha mangostin in sorafenib-surviving HCC cells caused an increase in proliferation markers, which might be explained by the reduced expressions of apoptosis markers and enhancement of antioxidant markers.

}, keywords = {Anti-cancer drug resistance, Caspase, Hepatocellular carcinoma, Ki-67, Oxidative stress.}, doi = {10.5530/pj.2022.14.75}, author = {Melva Louisa and Meuthia Faralita Annisa and Pamela Basuki and Brigitta Cindy Lauren and Syarinta Adenina} } @article {1920, title = {Ameliorative Effects of Moringa (Moringa Oleifera Lam.) Leaves Extract on Lead-Induced Oxidative Stress, Hepcidin and δ-Alad Levels in Rat{\textquoteright}s Blood}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {856-862}, type = {Research Article }, chapter = {856}, abstract = {

Introduction: Lead (Pb) is a toxic heavy metal that cause a lot health problem. Blood, especially hemoglobin and erythrocyte, is the main target of lead poisoning. Literatures explain that moringa has phytochemical contents to reduce heavy metal poisoning. This study aimed to examine ameliorative effects of moringa leaves extract on oxidative stress, hepcidin increasement and δ-alad level decline induced by lead poisoning in the blood of rat model. Methods: This study was completely randomized posttest-control group design. Forty-eight males Rattus norvegicus Wistar strain rat were divided into 4 groups. The control group or G0 (given Pb orally doses of 750 mg/kgBW/day for 7 days and was not given 50\% ethanol extract of moringa leaves/MLEE). Three treatment groups (G1, G2 and G3), all were given Pb at a dose of 750 mg/kgBW/day orally for 7 days, followed by administration of MLEE for 14 days at a dose of 250 mg/kgBW/day, 500 mg/kgBW/day and 1,000 mg/kg/day orally, respectively. Blood samples were taken one day after 14 days of MLEE treatment. Pb levels was examined by AAS and δ-ALAD levels, GSH levels, MDA levels and hepcidin levels examined by ELISA. Results: MLEE doses 1,000 mg/kgBW/day for 14 days increased δ-ALAD levels, GSH levels, hepcidin levels and reduce MDA levels significantly compared to the control group. Conclusion: Moringa leaves ameliorate lead-induced poisoning by reducing oxidative stress, declining hepcidin, and increasing δ-ALAD in the blood of male Rattus norvegicus Wistar strains rats. Moringa leaves is beneficial to address Pb poisoning in the blood through antioxidants, anti-inflammation, and improving δ-ALAD level in the blood of Wistar strain rats.

}, keywords = {Blood, Hepcidin, Lead poisoning, Moringa, Oxidative stress., δ-ALAD}, doi = {10.5530/pj.2022.14.179}, author = {Agung Saprasetya Dwi Laksana and Harianto Notopuro and Arifa Mustika} } @article {1863, title = {Antioxidant Activity of DPPH, CUPRAC, and FRAP Methods, as well as Activity of Alpha-Glucosidase Inhibiting Enzymes from Tinospora crispa (L.) Stem Ultrasonic Extract}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {511-520}, type = {Original Article}, chapter = {511}, abstract = {

Aims: The goal of this work was to get the stem extract of Tinospora crispa (L.) using ultrasoundassisted extraction (UAE) with duration and amplitude changes to achieve optimal extraction conditions. The antioxidant potential of the extract as measured by 2,2-diphenyl-1-picrylhydrazyl (DPPH), CUPRAC (Cupric Ion Reducing Antioxidant Capacity), FRAP (Ferric Reducing Ability of Plasma), and its antidiabetic potential. Results: The third test of antioxidant methods showed that the measurement of antioxidant activity with, DPPH, CUPRAC, and FRAP gave significantly different results, but CUPRAC and FRAP gave the same response to the ethanol extract of Tinospora crispa stems, it can be concluded that the extract of Tinospora crispa stems in all treatments had strong antioxidant activity using either the CUPRAC or methods FRAP. In addition, it is very active as an antidiabetic by inhibiting alpha glucosidase. The optimum extract selected was extract B (extraction time was 35 minutes and amplitude 65\%) with IC50 values for antioxidant activity in the CUPRAC method of 72.53 {\textpm} 0.18 mg/L and the FRAP method of 152.29 {\textpm} 2.16 mg/L, while the inhibition of alpha glucosidase was 0.30 {\textpm} 0.006 mg/L.

}, keywords = {Antidiabetic, Antioxidant, Tinospora crispa (L.), Ultrasound-assisted extraction.}, doi = {10.5530/pj.2022.14.128}, author = {Candra Irawan and Imalia Dwi Putri and Maman Sukiman and Andita Utami and Ismail and Ratna Komala Putri and Anisa Lisandi and Andrean Nur Pratama} } @article {1882, title = {Antioxidants, Total Phenolic and Flavonoid Content and Toxicity Assay of Ampelas (Tetracera macrophylla Wall.Ex Hook.F.\& Thoms) From Kalimantan-Indonesia}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {642-648}, type = {Research Article}, chapter = {642-648}, abstract = {

Background: High Reactive Oxygen Species (ROS) contribute to disease pathogenesis. Phenolic compounds and flavonoids are effective as antioxidants. Objective: This research aimed to measure the antioxidant activity, total phenolic and flavonoid content and leaf toxicity of Tetracera macrophylla. Methods: DPPH and FRAP were used to determine antioxidants, and the Folin{\textendash}Ciocalteu method was used for total phenolic content, total flavonoid content with AlCl3 and toxicity with MTT assay against RAW 264.7 cells. Results: Methanol extract has antioxidant activity with IC50 = 81.582 μg/mL (DPPH) and 11840 mol/g (FRAP), total phenolic content of 353.781 mg GAE/g dry weight, and flavonoid content of 279.2 mg QE/g dry weight. The ethyl acetate and n-hexane extracts had weaker antioxidant activity than the methanol extracts. The IC50 toxicity assay methanol extract and ethyl acetate extract respectively showed 288.792 μg/mL and 541.472 μg/mL. Conclusion: The methanol extract of Tetracera macrophylla showed the highest yield, total phenolic content and total flavonoid content and had the highest antioxidant activity. Methanol extract has low toxicity to RAW 264.7 cells.

}, keywords = {Antioxidants, Tetracera macrophylla, total flavonoid, total phenolic, Toxicity}, doi = {10.5530/pj.2022.14.147}, author = {Vera Ladeska and Berna Elya and Muhammad Hanafi and Kusmardi} } @article {1763, title = {Anti-Ulcer Activity of Spray-dried Powders Prepared from Aerial Parts Extracts of Ampelopsis cantoniensis}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {276-281}, type = {Original Article}, chapter = {276}, abstract = {

Introduction: Ampelopsis cantoniensis is called {\textquotedblleft}Che day{\textquotedblright} in Vietnam and has been used as a traditional treatment for inflammatory diseases. Methods: Plant material and hydroalcoholic extract were processed and analyzed for their physicochemical characteristics. A method using HPLC was validated to quantify ampelopsin. Hydroalcoholic extract was spray dried and the powder obtained was characterized in terms of its physicochemical parameters and potential for antiulcerogenic activity. Results: The analytical method proved to be selective, linear, accurate, sensitive. A. cantoniensiss pray dried extract (ACP) was obtained using colloidal silicon dioxide as adjuvant and was shown to possess 25.94 \% ampelopsisn. It showed significant antiulcer activity in a model of an indomethacin-induced gastric lesion in rats and also produced a gastroprotective effect.

}, keywords = {Ampelopsis cantoniensis, Antiulcer, Spray drying, Vitaceae}, doi = {10.5530/pj.2022.14.34}, author = {Duc Minh Nguyen and Quang Canh Tran and Minh Trung Do and Duc Thinh Pham and Thi Hong Hanh Le and Duy Bac Nguyen and Van Thu Nguyen} } @article {1772, title = {Determination Antioxidant Activity of Coffea Arabica, Coffea Canephora, Coffea Liberica and Sunscreens Cream Formulation for Sun Protection Factor (SPF)}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {335-342}, type = {Research Article }, chapter = {335}, abstract = {

Coffee is a highly consumed and popular beverage consumed in many countries. Its ingredients have a powerful antioxidant capacity and have the potential as sunscreen to protect the skin. This study aimed to examine the antioxidant activity of Arabica, robusta and liberica coffee extracts and the SPF activity of the coffee extract cream formulation. Coffee were macerated with three types of solvents with polarity gradients. The fraction of each coffee was analyzed for antioxidant activity using DPPH and formulated into the cream. Furthermore, the cream was analyzed for its SPF activity. The results of this study indicated that the methanol fraction of Robusta and Arabica coffee has the best antioxidant activity with IC50 values of 8.98 (ppm) and 13.13, respectively. Meanwhile, Liberica coffee has the best antioxidant in the ethyl acetate fraction, IC50 = 10.90 (ppm). In addition, the best SPF values for Robusta, Liberica and Arabica coffees were found in F3 cream with the category of Very Good Protection; 36.087 {\textpm} 0.0005; 35.007 {\textpm} 0.0005; 36,867 {\textpm} 0.0005 respectively.

}, keywords = {Antioxidant, Coffee, Cream, SPF}, doi = {10.5530/pj.2022.14.43}, author = {Madyawati Latief and Muhaimin and Heriyanti and Indra Lasmana Tarigan and Sutrisno} } @article {1737, title = {Determination of Phytochemical Constituent, Antioxidant Activity, Total Phenol and Total Flavonoid of Extract Ethanol Phyllanthus emblica Fruit}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {February 2022}, pages = {63-67}, type = {Original Article}, chapter = {63}, abstract = {

Introduction: Phyllanthus emblica (PE) is a plant that grows widely in Indonesia, particularly on Sumatra island. In India, it is known as Indian gooseberry and is frequently used in ayurvedic medicine. PE fruit is well-known for its high antioxidant activity and a variety of pharmacological properties. The purpose of this study was to ascertain the phytochemical composition, antioxidant activity, total phenol, and total flavonoid concentrations. Methods: The fruits were harvested in the Indonesian town of Padang Sidimpuan. Up to 700 g of dry PE fruit powder was dissolved in 96 percent ethanol and macerated for seven days, with periodic steering daily. The solution was then filtered using Whatman paper no 1, and the filtered result was evaporated under reduced pressure using a rotary evaporator until a crude extract/ethanol extract of PE (EEPE) was obtained, and the phytochemical constituents, antioxidant activity, total phenol, and flavonoid were analysed. Results: The result shows that EEPE contains some flavonoids such as quercetine, betaine, Trigonelline, Myricitrin, Myricetin, Leucine, and Kaempferol. EEPE as an antioxidant of 7.626 {\textpm} 0.41 μg/dL. It shows that the antioxidant activity of the ethanol extract of Phyllanthus emblica is strong ethanol extract of Phyllanthus emblica contains Total Flavonoid was 5.816 {\textpm} 2.81(mg QE/g extract) and total phenol was 274.590 {\textpm} 13.61(mg GAE/g extract). Conclusions: In summary, extract ethanol of Pyllanthus emblica contains flavonoid and have antioxidant activity and high total phenol and flavonoid levels.

Key words: Antioxidant, Total flavonoid, Total phenol, Phyllanthus emblica..

}, doi = {10.5530/pj.2022.14.9}, author = {B Halim and RA Syahputra and I Adenin and HP Lubis and F Mendrofa and S Lie and SE Nugraha} } @article {1925, title = {Differences in interleukin-6 and interleukin-17 expression in covid-19 post-mortem lung tissue biopsy compared with noncovid- 19}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {887-892}, type = {Original Article }, chapter = {887}, abstract = {

Background: COVID-19 has spread rapidly around the world. It is necessary to study lung tissue of postmortem COVID19 patients to determine the molecular alteration particularly the role of IL-6 and IL-17 in causing fatality. Objective: This study aims to determine the differences in the expressions of IL-6 and IL-17 in lung tissue of post-mortem COVID-19 patients compared to non-COVID-19 patients. This study also aimed to analyze the correlation between the expressions of IL-6 and IL-17 in lung tissue of post-mortem COVID-19 patients. Methods: This research is an observational analytic study with crosssectional approach. The samples were 15 paraffin blocks of post-mortem lung tissue biopsy of COVID-19 patients, and 15 paraffin blocks of inflammatory lung tissue biopsy or surgery of non-COVID-19 patients. IL-6 and IL-17 expressions were evaluated by immunohistochemical procedure. Result: There was a significant difference in the expression of IL-6 in the COVID-19 group and the non-COVID-19 group with a p-value = 0.001 (p \< 0.05). There was a significant difference in the expression of IL-17 in the COVID-19 group and the non-COVID-19 group with p-value = 0.001 (p \< 0.05). There was a significant correlation between the expressions of IL-6 and IL-17 in the COVID-19 group, with the Spearman coefficient value (rs) of 0.548 with p = 0.034 (p \< 0.05). Conclusion: There are differences in the expression of IL-6 and IL-17 between COVID-19 and non-COVID-19 lung tissue. There is a significant correlation between the expressions of IL-6 and IL-17 in post-mortem lung tissue of COVID-19 patients.

}, keywords = {Biopsy, COVID-19, IL-17, IL-6, Post mortem lung tissue.}, doi = {10.5530/pj.2022.14.184}, author = {Etty Hary Kusumastuti and Priangga Adi Wiratama and Grace Ariani and Stephanie Natasha Djuanda and Alphania Rahniayu and Nila Kurniasari and Dyah Fauziah and Anny Setijo Rahaju and Isnin Anang Marhana and Alfian Nur Rosyid and Dwi Wahyu and Gilang Muhammad Setyo Nugroho and Adhitri Anggoro and I Komang Rusgi Yandi and Bambang Pujo Semedi and Jilientasia Godrace Lilihata and Ummi Maimunah and Supriadi and Achmad Lefi and Lalu Galih Pratama Rinjani and Edi Suyanto and Ricardo Ardian Nugraha} } @article {1746, title = {Does Soybean (Glycine max) Supplementation Increase Oocyte Viability, Decrease Oocyte Apoptosis and Improve Embryo Development Quality? An Experimental Study}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {February 2022}, pages = {133-140}, type = {Original Article}, chapter = {133}, abstract = {

Introduction: One of the important factors in Assisted Reproductive Technology (ART) is embryo quality that depends on oocyte quality. Maternal nutrition in form of soybean supplementation is thought to have benefits in oocyte quality. To determine the effect soybean supplementation to the embryo quality from oocyte side. Methods: This experimental study involved female mice from Swiss strain aged 6 weeks that were divided into two groups, group with soybean (soybean group/SG) and group without soybeans (pellet group/PG). Follicles were collected and denuded to get oocytes. The oocytes were stained with MitoTracker for assessing the mitochondrial membrane potential and TUNEL for assessing the apoptotic level. Colour intensity was assessed using a confocal microscope and determined using ImageJ software. Sperms were extracted surgically from the epididymis-vas deferens and performed preparation prior to intra cytoplasmic sperm injection (ICSI) procedure. Then, the embryos were cultured and observed for the quality. Result: In TUNEL test, the average colour intensity of the SG was lower compared to the PG, significantly (p=0.03). While in the Mito Tracker test, the average colour intensity for the SG was higher compared to PG, not significantly (p=1.08). In addition, the embryo development on Day-1 and Day-3 showed more good embryo quality of SG compared to PG, significantly (p=0.03). Conclusion: Soybean supplementation improved embryo quality at the cleavage stage by decreasing apoptosis of the oocytes rather than increasing the viability the oocytes.

Key words: Oocyte, Soybean, Apoptosis, Embryo development, Embryo quality.

}, doi = {10.5530/pj.2022.14.18}, author = {Silvia W Lestari and Khairunnisa F Ilato and M. Iqbal A Pratama and Husna Qonitah and Gito Wasian and Amandanu Bramantya and Firda A Husna and Ria Margiana and Gita Pratama} } @article {1898, title = {Effect of Bajakah Tea Extract (Spatholobus littoralis Hassk) on High Density Lipoprotein, Triglyceride and Total Cholesterol Levels in Male Wistar Rats}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {687-691}, type = {Original Article}, chapter = {687}, abstract = {

Hyperlipidemia is the high concentrations of low-density lipoprotein, cholesterol, and triglycerides in the blood. Furthermore, hyperlipidemia has a risk factor for cardiovascular complications through atherosclerosis that triggers coronary heart disease (CHD). Spatholobus littoralis Hassk known as Bajakah tea is a plant with high antioxidant content and acts as an HMG-CoA reductase inhibitor to suppress lipid metabolism disorders, increase HDL levels, and reduce triglycerides and total cholesterol. Experimental and posttest control group design methods were used to obtain 24 male Wistar rats. Furthermore, the experimental animals were randomly divided into 4 groups, namely K1 (normal rats), K2 (hyperlipidemia rats), K3 (hyperlipidemic rats + pirated tea extract dose 9 mg/200gramBW/day), and K4 (hyperlipidemic rats + simvastatin dose 0.18 mg/200 gBW/day). The study was conducted at the Center for Food and Nutrition Studies Laboratory, Gajah Mada University, Yogyakarta. Data levels of HDL, triglycerides, and total cholesterol were analyzed using the One Way Anova test and LSD post hoc to determine between groups. The results showed that an increase in triglyceride and total cholesterol and a decrease in HDL levels in the K2 group compared to the K1. Triglyceride and total cholesterol decreased in groups K3 and K4 compared to K2, and HDL levels increased in groups K3 and K4 compared to K2. Meanwhile, the results of the analysis obtained p value \<0.05. This study concluded that the administration of Bajakah tea extract at a dose of 9 mg/200gram BW/day for 14 days increase HDL, reduce triglyceride and total cholesterol levels (p\<0,05).

}, keywords = {HDL levels, Hyperlipidemia, Pirated tea extract, Total cholesterol., Triglycerides}, doi = {10.5530/pj.2022.14.155}, author = {Sampurna and Andin Putri Aulia and Eka Puji Liashari and Happy Hapsari and Syafrie Sahrul Gibran and Siti Thomas Zulaikhah} } @article {1834, title = {Effects of Golden Sea Cucumber Extract (Stichopus hermanni) on Hyphae, Neutrophils and TNF-α in BALB/c Mice Inoculated with C. albicans Intravaginally}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {278-285}, type = {Original Article }, chapter = {278}, abstract = {

Introduction: Candidal vaginitis is an inflammatory disease that caused mainly by Candida albicans. Yeast transitions to filamentous hyphae considered the most important virulence factor. Neutrophils are the first line of defense of the immune system, but in patients with Candidal vaginitis the recruitment of neutrophils into the vaginal lumen is positively correlated with symptoms of the disease. This is supported by the release of proinflammatory cytokines such as TNF-α. Standard treatment is considered less effective in relieving symptoms, so other alternative/adjunctive treatments are needed. Golden sea cucumber (Stichopus hermanni) extract has been widely studied, especially for anti-fungal and anti-inflammatory. This study aims to analyze the mechanism of decreasing number of hyphae and neutrophils, and proinflammatory cytokine TNF-α in BALB/c mice inoculated intravaginally with C. albicans after administration of golden sea cucumber extract (S. hermanni). Methods: Experimental research uses a post-test only control group design. The experimental unit consisted of 36 BALB/c mice that were inoculated intravaginally with C. albicans and divided into 4 groups, group that did not receive treatment (K-), group that received standard treatment fluconazole (K+), group that received treatment with golden sea cucumber extract (S. hermanni) (P1) and group that received standard treatment with fluconazole plus extract of golden sea cucumber (S. hermanni) (P2). The hyphae and neutrophils number were seen microscopically on vaginal mucosal tissue. Cytokine levels of TNF-α were seen from the ELISA blood samples. Results: Results showed from the vaginal mucosal tissue of mice, there was significant difference in the number of hyphae (p = 0.001) between groups and no significant difference in the number of neutrophils (p = 0.070) between groups. From the blood serum of mice, there were significant differences in TNF-α levels (p=0.001) between groups. From the path analysis obtained a significant relationship from the number of hyphae to the number of neutrophils (p = 0.034) and the number of neutrophils to TNF-α levels (p = 0.021). The strength of the pathway from number of hyphae to number of neutrophils (β= 0.354) and number of neutrophils to TNF-α levels (β= 0.382) with positive interactions all. Conclusion: In summary, the administration of S. hermanni extract was able to reduce the number of hyphae, neutrophils and TNF-α levels through the hyphae, neutrophil and TNF-α pathway.

}, keywords = {Candida vaginitis, Hyphae, Neutrophils, Stichopus hermanni extract, TNF-α}, doi = {10.5530/pj.2022.14.97}, author = {Varidianto Yudo and Widjiati and Harianto Notopuro and Yulianto Listiawan and Budi Utomo and Purwo Sri Rejeki and Prawesty Diah Utami and Aryati} } @article {1902, title = {Efficacy of Combined Relaxed Deep-Breathing with Chest Mobilization Exercise and Vernonia cinerea-Hard Candy on Smoking Cessation and Oxidative Stress in Active Teenage Smokers}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {720-727}, type = {Original Article}, chapter = {720}, abstract = {

Background: Smoking cessation is very important worldwide. Chronic smoking can induce oxidative stress and inflammatory status and induce dangerous diseases such as hypertension and lung cancer. Standardized counseling is an important process in a routine program for smoking cessation. Withdrawal symptoms from smoking cessation are a significant barrier to a successful result, and they can be relieved by relaxed deep-breathing exercise. At present, the Thai herb, Vernonia cinerea (VC), has been claimed to reduce cigarette smoking because of its antioxidant compounds and nicotine that are modified and used as lozenges, gum, and hard candy. However, its efficacy in smoking cessation has not been confirmed. Furthermore, the efficacy of relaxed deep-breathing (rDB) during the chest mobilization exercise (CME) with VC hard candy on smoking cessation and oxidative stress is unclear. Objective: This study aimed to evaluate the combined effects of rDB/CME and VC-hard candy on smoking cessation and oxidative stress status in active teenage smokers. Methods: Hard candy with honey and VC powder from whole mixed parts of the stem, flowers and leaves was developed industrially under the spray dry technique. Thirty active smokers were randomized into three groups; product group (rDB/CME+ product) (aged 25.0 {\textpm} 3.0 years, n = 10), placebo group (rDB/CME + placebo) (aged 26.9 {\textpm} 3.7 years, n = 10), and a control group with no product or placebo administered (aged 25.6 {\textpm} 2.7 years, n=10). All of the groups received consultation on specific smoking cessation and two weeks of strict observation, which was followed up for 8 weeks. The 7-day point prevalence abstinence rates (7-day PAR) and continuous abstinence rate (CAR) were reported at week 2, 4, 6 and 8. In addition, the oxidative stress status with lipid peroxide and glutathione (GSH) in blood was evaluated before the program and after 2 weeks. Results: The results of 7-day PARs in the control group showed no statistical changes at week 2 (0\%), 4 (10\%), 6 (20\%) and 8 (20\%), which was the same in the rDB/CME + placebo group (10\%, 20\%, 30\% and 40\%, respectively). Whereas, a significant difference was presented in the rDB/CME+ product group (20\%, 60\%, 80\% and 90\% respectively). When comparing between the groups, 7-day PARs at week 2 was not statistically different, but it was in the follow-up period at week 4, 6 and 8. There was no statistical difference at week 4 between the three groups, but there was between the rDB/CME+ product, control and rDB/CME+ placebo groups at week 6 and 8. The results of CAR showed no statistical difference between the control and rDB/CWE+ placebo group in any of the periods. Whereas the rDB/CWE+ product group showed a significant difference after week 4. The CAR was statistically different between the groups after week 6 and 8. At week 6, the CAR of the rDB/CWE+ product group was different to the control group. There was no difference between the control and rDB/CWE+ placebo groups, or between the rDB/CWE+ product and placebo groups. At week 8, the CAR of the rDB/CWE+ product group was different from that of the control, but not from the rDB/CWE+ placebo group. Finally, the GSH level increased significantly in the rDB/CWE + product group when compared to the rDB/CWE+placebo group. Moreover, malondialdehyde (MDA) levels decreased significantly in both the placebo and product groups. In addition, MDA levels showed a significant difference between baseline and after 2 weeks in the rDB/CWE + placebo and product groups. Conclusion: Integrating relaxed-deep breathing with chest mobilization exercise and VC hard candy for 2 weeks can help smoking cessation during consultation, and possibly reduce oxidative stress status among active teenage smokers.

}, keywords = {7-day point prevalence abstinence rate, Chest mobilization exercise, Continuous abstinence rate, Oxidative stress, Relaxation deep-breathing, Smoking cessation, Vernonia cinerea-hard candy.}, doi = {10.5530/pj.2022.14.159}, author = {Rungtiwa Kanthain and Jirakrit Leelarungrayub and Surinporn Likhitsathian and Surapol Natakankitkul} } @article {1819, title = {Evaluation of Antiviral Effects and Toxicity of Herbal Medicine Vipdervir Capsules}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {681-689}, type = {Research Article}, chapter = {681}, abstract = {

Background: Antiviral vaccine is not effective, synthetic antiviral drugs are highly toxic, leading to increased interest in herbal medicines as promising antiviral drugs. Recently, Vipdervir has been developed from medicinal herbs with the aim to support and treat diseases caused by viruses such as H5N1 and SARSCoV- 2. In the present study, we assessed Vipdervir{\textquoteright}s antiviral activity against H5N1 and SARS-CoV-2. In addition, we also evaluated the acute toxicity and repeated dose toxicity of Vipdervir in mice and rabbits, respectively. Methods: H5N1 inhibitory effect of Vipdervir was assessed using hemagglutination inhibition assay. Vipdervir{\textquoteright}s SARS-CoV-2 inhibitory effect was evaluated by Plaque Reduction Neutralization assay. Acute and repeated dose oral toxicities of Vipdervir were determined according to OECD 423 and OECD 407 guidelines, respectively. Results: Data show that Vipdervir is effective against both H5N1 and SARSCoV- 2. At concentrations of 3 mg/mL and 5 mg/mL Vipdervir completely inhibits H5N1. At a concentration of 50 μg/mL Vipdervir showed an inhibitory effect on SARS-CoV-2. Acute toxicity data revealed that the LD50 of Vipdervir is greater than 35200 mg/kg, b.wt. in mice. Repeated toxicity data indicated that Vipdervir did not induce significant differences in body weight gain, hematology and clinical biochemistry in compared to the control group. The No Observed Adverse Effect Level of Vipdervir is greater than 613.8 mg/kg b.wt./day in rabbits. No delayed toxicity effects of Vipdervir were observed. Conclusion: Vipdervir capsules were found to be antiviral effective and relatively safe in the tested doses and experimental conditions.

}, keywords = {Antiviral, COVID-19, H5N1, Herbal, SARS-CoV-2.}, doi = {10.5530/pj.2022.14.87}, author = {Thi-Lien Nguyen and Huong Ha Thi Thanh and Kiet Ngo Tuan and Doan Cao Son and Thao Le Quang and Hang Nguyen Thi and Tien Vuong Duy and Quyen Doan Thi Tam and Huan Le Quang} } @article {1951, title = {Histopathological Perspectives of Multiple Organs in a Red- Footed Tortoise (Chelonoidis carbonaria) with Suspected Metabolic Bone Disease: A Case Report}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {1075-1078}, type = {Case Report}, chapter = {1075}, abstract = {

Introduction: Exotic pet lovers{\textquoteright} interest in keeping tortoises is increasing all over the world, including Indonesia. However, this trend cannot be separated from the potential emergence of various health problems in tortoises. One of the problems that often affects tortoises is metabolic bone disease. Metabolic bone disease (MBD) is a disorder related to the mechanisms of vitamin D and calcium metabolism, which generally occurs in reptiles, especially Chelonia and Lizards. Case Presentation: A 3-month-old redfooted tortoise, which was clinically suspected to have a MBD, was necropsied as an effort to support the provisional diagnosis through histopathological evaluation. The purpose of this examination was to analyze the impact of the disease on various organs microscopically in patients with suspected MBD. The results showed a decrease in the number of trabeculae and hematopoietic cells in the metatarsal bones; moderate myonecrotic changes and atrophy in the skeletal muscle; inflammation of the perineuron; acute tubular necrosis and mild edema of the renal cortex; congestion and an increase in the number of melanomacrophages in the liver; as well as epicarditis and myocarditis in the heart. Conclusion: Several forms of the histopathological changes seem to indicate a pathophysiological relationship between the suspected metabolic bone disease and the multiple organs examined.

}, keywords = {Hematoxylin-eosin, MBD, Septicemia., Tortoise}, doi = {10.5530/pj.2022.14.212}, author = {Hani Plumeriastuti and Annise Proboningrat and Djoko Legowo and Bilqisthi Ari Putra and Gracia Angelina H and Agung Budianto Achmad} } @article {1808, title = {In Silico Phytochemical Compounds Screening of Allium sativum Targeting the Mpro of SARS-CoV-2}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {604-609}, type = {Research Article}, chapter = {604}, abstract = {

The global pandemic of coronavirus disease is still widely spread across the world causing catastrophic effect in both human life and global economy. By the end of year 2021, it has caused a total of 5.437.636 deaths across the world. Indonesia has rich plant biodiversity including medicinal plants that may be used for combating the virus. One of the commonly used medicinal plants comes from Allium species and it has been proved to have antiviral activity. Conducting an in silico study, we screened bioactive compounds that came from Allium sativum to fight against coronavirus through the inhibition of 3CL-Pro, one of the major protease that have an active role for viral replication. Molecular docking of compounds from Allium sativum to 3CL-Pro resulting in the discovery of 5 compounds that have the best binding affinity to 3CL-Pro, which are squalene, 1,4-dihydro-2,3-benzoxathiin 3-oxide, 1,2,3-propanetriyl ester, trans-13-octadecenoic acid and methyl-11-hexadecenoate with binding affinity of -7, -6.5, -5.9, -5.7 and -5.6 kcal/mol, respectively. It is very likely that these compounds can be candidates for therapeutic agents and these candidates need to be studied further.

}, doi = {10.5530/pj.2022.14.78}, author = {Priscilla Listiyani and Viol Dhea Kharisma and Arif Nur Muhammad Ansori and Muhammad Hermawan Widyananda and Rasyadan Taufiq Probojati and Ahmad Affan Ali Murtadlo and Dora Dayu Rahma Turista and Md. Emdad Ullah and Vikash Jakhmola and Rahadian Zainul} } @article {1873, title = {In Silico Screening of Bioactive Compounds from Garcinia mangostana L. Against SARS-CoV-2 via Tetra Inhibitors}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {575-579}, type = {Research Article}, chapter = {575}, abstract = {

The global COVID-19 pandemic caused by SARS-CoV-2 has been the resulted of massive human deaths since early 2020. The purpose of this study was to determine the potential of mangosteen (Garcinia mangostana L.) as an inhibitor of RBD spike, helicase, Mpro, and RdRp activity of SARS-CoV-2 with an in silico approach. The samples were obtained from PubChem and RCSB PDB. Analysis of the similarity of the drug was carried out with the Swiss ADME on the basis of Lipinski rule of five. Prediction of antivirus probabilities was carried out using PASS Online. Molecular screening was performed using PyRx through molecular docking. Discovery Studio was used for visualization. The bioactive compounds with the highest antiviral potential were indicated with the lowest binding affinity to the targeted proteins RBD spike, helicase, Mpro, and RdRp of SARS-CoV-2. The results indicated that mangiferin has the greatest potential as a potential antiviral. However, more research is required to validate the results of these computational predictions.

}, keywords = {Antiviral agent, Garcinia mangostana L., in silico, SARS-CoV-2}, doi = {10.5530/pj.2022.14.138}, author = {Nur Sofiatul Aini and Viol Dhea Kharisma and Muhammad Hermawan Widyananda and Ahmad Affan Ali Murtadlo and Rasyadan Taufiq Probojati and Dora Dayu Rahma Turista and Muhammad Badrut Tamam and Vikash Jakhmola and Elsa Yuniarti and Saddam Al Aziz and Muhammad Raffi Ghifari and Muhammad Thoriq Albari and Riso Sari Mandeli and Muhammad Arya Ghifari and Devi Purnamasari and Budhi Oktavia and Amalia Putri Lubis and Fajriah Azra and Fadhilah Fitri and ANM Ansori and Maksim Rebezov and Rahadian Zainul} } @article {1741, title = {In Silico Studies of Sesquiterpene Lactones from Vernonia amygdalina Delile on the Expression of EGFR and VEGFR as a New Anticancer Potential}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {February 2022}, pages = {91-97}, type = {Original Article}, chapter = {91}, abstract = {

Objective: To assess the inhibition activity of sesquiterpene lactones from Vernonia amygdalina Delile as a new anticancer potential on the expression of cancer therapeutic target-proteins, namely: epidermal growth factor receptor (EGFR), and vascular endothelial growth factor receptor (VEGFR). Methods: The in silico screening, target-based approach (docking) was performed by the Prediction of Activity Spectra for Substances (PASS) website and AutoDock Vina program. The therapeutic cancer target proteins model of EGFR and VEGFR were downloaded from Research Collaboratory for Structural Bioinformatics (RCSB) protein data bank (PDB) with 5HG7 and 4AG8 as their respective codes. Results: The test compounds have anticancer activity as predicted by the Prediction of Activity Spectra for Substances (PASS) website and AutoDock Vina program. The molecular docking analysis of the test compounds showed strong interactions and good inhibition activity with the targeted proteins with a low docking score value predicted by the AutoDock Vina program. Conclusion: The test compounds have the potential to be used in anticancer drugs through the inhibitory qualities of EGFR and VEGFR.

Key words: In silico, Sesquiterpene lactones, EGFR, VEGFR, Vernonia amygdalina Delile.

}, doi = {10.5530/pj.2022.14.13}, author = {N Nerdy and P Lestari and F Fahdi and EDL Putra and SAB Amir and F Yusuf and TK Bakri} } @article {1872, title = {In Silico Study of Entry Inhibitor from Moringa oleifera Bioactive Compounds against SARS-CoV-2 Infection}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {565-574}, type = {Research Article}, chapter = {565}, abstract = {

The aim of this study is to screen the content of bioactive compounds of Moringa oleifera and to identify its potential as an antiviral against COVID 19 through an entry inhibitor mechanism using bioinformatics tools. The sample was obtained from PubChem database. Amino acis sequences were obtained from the NCBI. Protein modeling is made through the SWISSMODEL site. The target proteins for this study were SARS-CoV-2 Mpro and RdRp. The protein-inhibitory interaction of the drug from M. oleifera bioactive compounds to SARS-CoV-2 was predicted by molecular docking with PyRx software. The result shows that M. oleifera was a potential antiviral candidate for SARS-CoV-2 with an entry inhibitor mechanism through a compound, especially quercetin. The RFMS value of both interactions between Mpro and quercetion and RdRp with quercetin were not higher than 1.05. This result still needed further research to prove this prediction.

}, keywords = {Active site, COVID-19, Moringa oleifera, Mpro, RdRp}, doi = {10.5530/pj.2022.14.137}, author = {Nala Mawaddani and Ekris Sutiyanti and Muhammad Hermawan Widyananda and Viol Dhea Kharisma and Dora Dayu Rahma Turista and Muhammad Badrut Tamam and Vikash Jakhmola and Syamsurizal and Bayu Ramadhani Fajri and Muhammad Raffi Ghifari and Muhammad Thoriq Albari and Muhammad Arya Ghifari and Amalia Putri Lubis and Dony Novaliendry and Dwi Hilda Putri and Fadhilah Fitri and Devni Prima Sari and Alexander Patera Nugraha and ANM Ansori and Maksim Rebezov and Rahadian Zainul} } @article {1900, title = {Influence of Chitosan Concentration on Characteristic of Microspheres Delivery System Prepared from Eleutherine palmifolia (L.) Merr. Extract}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {702-709}, type = {Original Article}, chapter = {702}, abstract = {

Background: Eleutherine palmifolia (L.) Merr. (E.palmifolia) is a medicinal plant containing naphthoquinone, isoliquiritigenin, and oxyresveratrol compound. This study aims to formulate and characterize the E. palmifolia microspheres delivery system using chitosan variation as the polymer. Methods: The preparation method was the solvent evaporation method. The microspheres delivery system was performed by variation of chitosan concentration in each formulation 0.637\% (F1), 1.275\% (F2), and 1.912\% (F3). The physical and chemical characterizations include Entrapment Efficiency (EE), yield percentage, particle size, particle morphology, FTIR analysis, X-Ray Diffraction (XRD) analysis, and Differential Thermal Analysis (DTA) had been evaluated. Results: The results showed that chitosan concentration variation affected the microsphere{\textquoteright}s physical and chemical characteristics. Variations in the concentration of chitosan polymer (0.637\%, 1.275\% and 1.912\%) had an effect on the physical characteristics of the microspheres of the resulting Dayak onion bulb extract. The higher the concentration of chitosan used, the higher the entrapment efficiency and the yield yield will increase. Meanwhile, in observing the particle size, the higher the concentration of chitosan used, the smaller the particle size produced. The optimal concentration of chitosan as a polymer at concentration variations of 0.637\%, 1.275\% and 1.912\% to provide good physical characteristics of the Dayak onion bulb extract microspheres was shown in formula 3 with a chitosan concentration of 1.912\%. Conclusion: The better characteristic was obtained upon higher chitosan concentration. The best physical characteristics of E.palmifolia extract microspheres were obtained from chitosan concentration at 1.912\% (F3).

}, keywords = {Characteristic, Chitosan, Delivery system., Eleutherine palmifolia, Microspheres}, doi = {10.5530/pj.2022.14.157}, author = {Roihatul Mutiah and Wirda Ardania and Arief Suryadinata and Dewi Sinta Megawati and Anik Listiyana and Abdul Wafi and Rahmi Annisa} } @article {1905, title = {Isolation of a Flavone Apigenin and a Steroids Squalene from Peronema canescens Jack Leaves with Anti-Inflammatory Activities}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {744-752}, type = {Original Article}, chapter = {744}, abstract = {

The leaves of the P. canescens are ethnobotanically used by the community as a remedy for bruises and fever. This study aims to isolate both of ethanol and n-hexane fractions of P. canescens Jack leaves. Isolate then characterized and determined their anti-inflammatory activity with male white mice. Anti- Inflammatory was determined by the volume of exudate and \% inflammation inhibition. The isolates with good anti-inflammatory activity were characterized using UV-Vis and IR spectrophotometry. Our findings showed that the ethanolic (F1) and n-hexane (F2) fractions of P. canescens extract had a good anti-inflammatory activity with percent inhibition values of 58.12\% and 56.59\%, respectively. The characterization results showed that isolate F1 was a flavonoid group, Apigenin compound, while isolate F2 was a steroid group, Squalene compound.

}, keywords = {Anti-inflammatory., Apigenin, P. canescens, Squalene}, doi = {10.5530/pj.2022.14.162}, author = {Indra Lasmana Tarigan and Sutrisno and Rumaida and Indah Pramana Sari Aini and Madyawati Latief} } @article {1910, title = {Nano Transdermal Delivery Potential of Fucoidan from Sargassum sp. (Brown Algae) as Chemoprevention Agent for Breast Cancer Treatment}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {789-795}, type = {Research Article }, chapter = {789}, abstract = {

Conventional chemotherapy substances are associated with mild to severe side effects that affect both healthy and cancer cells. It is presumed to improve therapeutic efficacy in coexistence reducing chemotherapy{\textquoteright}s side effects. Fucoidan is an anticancer bioactive compound derived from Sargassum sp. that has low cytotoxic activity. The purpose of this study was to explore the effectiveness of anticancer activities of fucoidan from Sargassum sp. against breast cancer then analyze the suitability of nano transdermal patch of fucoidan and blueprint the long-term research design of nano transdermal patch as a chemoprevention agent in the chemotherapeutic management of breast cancer. This research was performed through a literature study and in silico study by imposing carbonic anhydrase IX (CA IX) as a marker of hypoxia and metastatic state of cancer cells. The results showed that the fucoidan from Sargassum sp. effectively induced apoptosis and prevented metastasis of breast cancer cells through the Bcl-2, Bcl-w, and bad pathways. Fucoidan, in addition, was predicted to inhibit CA IX by Glu4 Glu5, Leu7, Pro8, and Asp6 residues. Therefore, the delivery of fucoidan is favored to have a local effect on the site of breast cancer cells by nano transdermal patch preparations using fucoidan nanoparticle polymer. Further nano transdermal patch development as a treatment for breast cancer is suggested through the stages of formulation optimization, optimum formula activity testing, patent filing, and distribution in health services.

}, keywords = {Anticancer, Breast cancer, Fucoidan, Nano transdermal, Sargassum sp. .}, doi = {10.5530/pj.2022.14.169}, author = {Syeftyan Muhammad Ali Hamami and Michelle Fai and Ahmad Fariduddin Aththar and M Nizam Zulfi Zakaria and Viol Dhea Kharisma and Ahmad Affan Ali Murtadlo and Muhammad Badrut Tamam and Vikash Jakhmola and Muhammad Hermawan Widyananda and Dora Dayu Rahma Turista and Maksim Rebezov and Nikolai Maksimiuk and Nataliya Kulmakova and Evgeniya Latynina and ANM Ansori and Rahadian Zainul and Riso Sari Mandeli and Devi Purnamasari and Oski Illiandri and Khoirun Nisyak and Ernarisa Fitri} } @article {1769, title = {Pasuchaca (Geranium ruizii Hieron.): A Medicinal Plant of the Geraniaceae Family with Hypoglycemic Effect on Alloxan-Induced Hyperglycemia in Mice}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {315-321}, type = {Original Article}, chapter = {315}, abstract = {

Objective: The current study aims to evaluate the hypoglycemic effect of the hydroalcoholic extract of Geranium ruizii on alloxan-induced hyperglycemia in albino mice. Material and Methods: Geranium ruizii was collected in Huancayo, Junin, Peru. A phytochemical analysis was carried out to confirm the chemical groups. In the pharmacological study, hyperglycemia was induced with alloxan at doses of 170 mg/kg in male albino mice, animals with blood sugar levels above 250 mg/dL were included in the protocol. Mice were randomized into five groups (I: Alloxan 170 mg/Kg; II, III and IV (Geranium ruizii extract: 50; 150 and 300 mg/Kg body weight); and V: glibenclamide, 5mg/Kg B.W. Results: Phytochemical analysis confirmed the presence of tannins, flavonoids, alkaloids, terpenes, saponins and phenolic compounds. It is observed that at doses of 50, 150 and 300 mg/kg reduced blood glucose at 14 days of treatment. Conclusion: The hypoglycemic effect of the hydroalcoholic extract of Geranium ruizii, administered orally in mice with alloxan-induced hyperglycemia was effective with 150 mg/Kg body weight.

}, keywords = {Antidiabetic drugs, Antioxidants, Geranium ruizii, Herbal therapy, Medicinal plants, Pasuchaca}, doi = {10.5530/pj.2022.14.40}, author = {Oscar Herrera-Calderon and Renan Dilton Ha{\~n}ari-Quispe and Johnny Aldo Tinco-Jayo and Josefa Bertha Pari-Olarte and Luz Josefina Chacaltana-Ramos and Eddie Loyola-Gonzales and Melva Iparraguirre-Meza and Mildred Hilda C{\'o}ndor- Privat and Beatriz Lilian Galdos-Vadillo and Jenny Mendoza-Vilcahuaman and Rossibel Juana Mu{\~n}oz-de-la-Torre} } @article {1810, title = {Pharmacobotany, Phytochemical Analysis and Anti-inflammatory effect of the Ethanolic Extract of Luffa operculata}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {622-628}, type = {Research Article}, chapter = {622}, abstract = {

Background: Luffa operculata is a vegetable species well known in the traditional peruvian medicine for its many medicinal properties and cosmetic applications. Objective: The aim objective was to determine the pharmacognostic characteristics of L. operculata as well as observing the pharmacological effect of the ethanol extract of L. operculata fruit on chronic inflammation in rats. Materials and Method: Phytochemical analysis was carried out by using specific chemical reagents for each constituent chemical, the pharmacobotanical study was done with a histological tinction (fruit, steam and leaves), which were stained with Safranin 1\% and Toluidine blue 1\%; the chronical inflammation was assessed by air bag method in Holztman male rats. Doses of 100, 250 and 500 mg/Kg were tested in order to determine the anti-inflammatory effect, which was demonstrated with histopathological evaluation and lymphocytes reduction. Results: The main findings indicate that the ethanolic extract presented saponins, alkaloids, carbohydrates, terpenes and steroids. The efficiency of lymphocyte reduction per field in the histopathological study of the granuloma was 58.4\% with the middle dose of 250 mg/kg (p \< 0.0001), which gives a dose-independent anti-inflammatory effect in rats. Conclusion: Luffa operculata presented anti-inflammatory effect at 250 mg/Kg by oral administration in a chronical experimental model of inflammation in rats.

}, keywords = {Anti-inflammatory., Luffa operculata, Pharmacobotany, Saponins}, doi = {10.5530/pj.2022.14.80}, author = {Jorge Alejandro Arroyo-Sandoval and Manuel Jes{\'u}s Marin-Bravo and Jorge Luis Arroyo-Acevedo and Hugo Jes{\'u}s Justil-Guerrero and Roberto Jes{\'u}s Ch{\'a}vez-Asmat and Josefa Bertha Pari-Olarte and Javier Hern{\'a}n Ch{\'a}vez-Espinoza and Jaime David Torres-L{\'e}vano and Eddie Loyola-Gonzales and Jos{\'e} Santiago Almeida-Galindo and Oscar Herrera-Calderon} } @article {1935, title = {Phytochemical Analysis and Antioxidant Activity of Water Hyacinth Flowers (Eichhornia Crassipes) Extract}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {955-957}, type = {Research Article }, chapter = {955}, abstract = {

The purpose of this research was to know about phytochemical compounds and antioxidant activity of water hyacinth flowers extract and its potential use as a natural antioxidant. Data analysis was performed descriptively. Research consisted of several stages including sampling, sample preparation, sample extraction, yield of extract, phytochemical analysis (phenols, tannins, alkaloids, flavonoids and saponins), antioxidant activity test with DPPH method and reducing power. The results showed that extracts yield of water hyacinth flowers with n-hexane solvent was 4.95\%, ethyl acetate solvent was 1.69\%, and highest extracts yiled obtained from methanol was 26.06\%. Results of phytochemical compounds analysis showed positive results for phenolic compounds, tannins, flavonoids and saponins. Result of antioxidant activity with DPPH method interpreted within parameters of IC50. IC50 of Hyacinth flower extract were 1085.31 ppm for n-hexane, 950.71 ppm for ethyl acetate and 35.83 ppm for methanol. Small IC50 showed that higher antioxidant activity.

}, keywords = {Antioxidant, Phytochemical, Reducing ability., Water Hyacinth Flowers}, doi = {10.5530/pj.2022.14.196}, author = {Ace Baehaki and Shanti Dwita Lestari and Wiwira Agustina and Sintya Dwika Putri} } @article {1816, title = {Potential Anticancer Activity of Bioactive Compounds from Ipomoea batatas}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {650-659}, type = {Research Article}, chapter = {650}, abstract = {

Ipomoea batatas L. (Lam.) known as "sweet potato" is a plant species of great importance in the human diet due to the contribution of nutrients and also for its bioactive compounds that have various medicinal properties. Its anticancer activity is one of the properties that attract the attention of researchers in the study of plant species. This review aims to make a critical compilation of current information on research that evaluated the antitumor and antiproliferative activity of Ipomoea batatas. The studies included in this review show a diversity of bioactive compounds present in Ipomoea batatas such as phenolic compounds, anthocyanins, flavonoids, coumarins and sterols; also isolated compounds such as pectin, peptides and glycoproteins that can be related to their biological activity. It is concluded that there are positive results about Ipomoea batatas and its anticancer activity evaluated through in vitro and in vivo tests. In humans, safety and efficacy trials are still lacking to support its future use and allow drug development. Further research evaluating the safety and efficacy of reported bioactive compounds in Ipomoea batatas is important for the development of this promising area.

}, keywords = {Antiproliferative, Antitumoral., Cancer, Sweet potato}, doi = {10.5530/pj.2022.14.84}, author = {Carmen R. Silva-Correa and Julio Hilario-Vargas and V{\'\i}ctor E. Villarreal-La Torre and Abhel A. Calder{\'o}n-Pe{\~n}a and Anabel D. Gonz{\'a}lez-Siccha and Cinthya L. Aspajo-Villalaz and Jos{\'e} L. Cruzado-Razco} } @article {1762, title = {The Potential Effect of Nigericin from Streptomyces hygroscopicus subsp. Hygroscopicus Against the Syndemic of Malaria and COVID-19 through Molecular Docking Perspective}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {268-275}, type = {Original Article}, chapter = {268}, abstract = {

Background: Malaria is a constantly challenging problem, notably in the Coronavirus Disease-19 (COVID-19) pandemic. The syndemic condition, malaria-COVID-19 co-infections, had been reported. Our previous study successfully revealed several compounds from Streptomyces hygroscopicus subsp. Hygroscopicus, including nigericin that has both antimalarial and antiviral effects. In malaria infection, Plasmodium falciparum Chloroquine Resistance Transporter (PfCRT) is the potential target for eliminating Plasmodium. Meanwhile, for SARS-CoV-2 infection, MPro is an essential protein for SARS-CoV-2 survival. This research aims to examine the potential effect of nigericin towards Plasmodium and SARS-CoV-2 by assessing its molecular interaction with PfCRT and MPro through molecular docking study. Methods: The protein target PfCRT and MPro were obtained from Protein Data Bank. Nigericin and the control ligand (chloroquine and N3) were obtained from PubChem. The pharmacokinetic analysis was done using SwissADME. Specific molecular docking was conducted using PyRx 0.9 and was visualized using LigPlot and PyMOL. Results: Nigericin has a large molecular weight, leading to the non-fulfillment of the Lipinski rule for oral administration. Through molecular docking study, the binding affinity of the Nigericin-PfCRT complex was -8.1 kcal/mol, and Nigericin-MPro was -8.6 kcal/mol. These binding affinities were stronger than the control ligand. The interaction between Nigericin-PfCRT and Nigericin-MPro share a similar pocket-site and amino acid residues as the control ligands. Conclusion: Nigericin has potential antimalarial and anti-coronavirus effects through molecular docking perspective by assessing the binding affinity and similarity of amino acid residues compared to control. Administration of systemic route can be an option in giving nigericin.

}, keywords = {COVID-19, Malaria, Molecular docking, Nigericin}, doi = {10.5530/pj.2022.14.33}, author = {Faratisha IFD and Cahyono AW and Erwan NE and Putri AM and Ariel DG and Yunita KC and Nugraha RYB and Mardhiyyah K and Fitri LE} } @article {1757, title = {Potential Pharmacokinetics and Pharmacodynamics (PK-PD) Drug-Herbs Interactions (DHI) from Metformin and Traditional Medicines: A Literature Review}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {February 2022}, pages = {235-244}, type = {Review Article}, chapter = {235}, abstract = {

Introduction: Metformin given together with herbs in order to optimizing its mechanism of actions. The effect might be positive and vice versa. Interaction might occur pharmacokinetics or pharmacodynamically. The study aimed to review potential interaction of metformin and some herbs with various pharmacological activities. Methods: This literature review was conducted by collecting articles with keywords Metformin, Herb-drug Interaction, drug interaction, pharmacokinetics, pharmacodynamics, and pharmacology from international databases such as Science Direct, PubMed, Springer Link, and Scopus up to 2021. Results: Metformin with its various uses such as antidiabetic agent, an agent for reducing weight for patients that sensitive or even resistant to insulin, patients with obesity, anti-tumor agent, anti-cancer potential agent, and also has anti-aging potential. Metformin could interacted with drugs, herbs, and also some bioactive isolate. The interaction might occurs pharmacokinetically or pharmacodynamically. Pharmacokinetics interactions occurred during distribution and also excretion via transporters that metformin transported with. This was shown as the elevated or lowered metformin levels in blood. Pharmacodynamic interactions can be seen as the lowering or elevated levels of glucose, HbA1c and even the lipid profile in blood or plasma. Conclusion: According to this literature review, Metformin have potential interaction with drugs, herbs, and also some bioactive isolate. The interactions occur pharmacokinetically or pharmacodynamically. This study can be used as a established familiarity with and understanding the potential HDIs from Metformin and herbal products.

Key words: Drug-Herbs Interactions (DHIs), Metformin, Pharmacokinetics, Pharmacodynamics.

}, doi = {10.5530/pj.2022.14.29}, author = {Asri Dwi Endah Dewi Pramesthi and Endang Lukitaningsih and Agung Endro Nugroho} } @article {1865, title = {Potential Role of Mitragynine as Lipolysis Stimulator via Adrenergic Signalling: Docking Model Study}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {527-531}, type = {Original Article}, chapter = {527}, abstract = {

Backgrounds: Mitragynine is the most popular of the more than 50 alkaloids contained in M.Speciosa. In particular, the Mitragynine alkaloid has the potential to increase lipid (fats) metabolism through specific pathways such as adenylyl cyclase signaling via adrenergic receptors. In this case, Asp Amino acid and Ser are the types of residues that can activate adenylyl cyclase to initiate a series of activities in cells. Methods: This study used Mitragynine ligand and adrenergic receptors (α1b, α2a, α2b, α2c dan β1). The receptor candidates were tested using Autodock whose test results were presented in the form of tables and 3-dimensional images using the Biovia Discovery Studio. Results: Hydrogen bonds were formed between Mitragynine and the amino acids Asp and Ser at the β1-adrenergic receptor. The binding amino acids were found in Ser20 and Asp21 with energy bond of -5.26 kcal/mol and IC50: 111.35 ppm. Meanwhile, at the adrenergic receptor α2b there was only Asp residue that formed hydrogen bond with Mitragynine namely Asp218A. The energy bond formed between the two was -5.19 kcal/mol and IC50: 125.04 ppm. Conclusion: Mitragynine has the potential to stimulate lipolysis through the pathways of α2b and β1-adrenergic receptors.

}, keywords = {Adrenergic, Docking, Lipolysis, Mitragynine}, doi = {10.5530/pj.2022.14.130}, author = {Khoirul Rista Abidin and Ronny Lesmana and Mas Rizky Anggun Adipurna Syamsunarno and Kelana Kusuma Dharma} } @article {1782, title = {Preliminary Data on the Antibacterial Activity of Coffea Arabica, Coffea Canephora and Coffea Liberica}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {413-424}, type = {Research Article}, chapter = {413}, abstract = {

The continuous use of synthetic antibiotics will not only kill bacteria but also can accelerate the emergence of resistant pathogenic races. In addition, it can also cause the death of normal flora. Coffee extract is reported to have the potential as a naturally active and non-toxic antibacterial compound suitable for biomedical applications. Extraction using methanol was carried out on green coffee and which had been roasted for three types of Jambi coffee, namely Arabica, Robusta and Liberica coffee and continued with fractionation using hexane and ethyl acetate. The results of the analysis using FTIR showed that OH, C-H, C = C, C = O, C-O, C-N and N-H groups were detected. These functional groups are probably the functional groups that belong to caffeine, trigonelline, nicotinic acid and dehydrocafestol, which are believed to have bacteriostatic effects on some bacteria. The SEM-EDX analysis results of the three types of coffee showed that the dominant elements were O, K and Mg. Potassium and magnesium minerals bind with chlorogenic acid to form salt complexes of chlorogenic acid and magnesium chlorogenic acid complex. The antibacterial activity of the coffee extract and fraction was still low with the diameter of the inhibition zone was still low (0-10 mm). Furthermore, further characterization and tests are needed to confirm the antibiotic potency of the Arabica, Robusta and Liberica coffee ethanol extracts.

}, keywords = {Antibiotics, Coffee, E. coli}, doi = {10.5530/pj.2022.14.53}, author = {Madyawati Latief and Heriyanti and Indra Lasmana Tarigan and Sutrisno} } @article {1936, title = {Research on External Signs and Chemical Composition of Medicinal Plant Raw Material -Leaves of Ficus Elastica}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {958-972}, type = {Research Article }, chapter = {958}, abstract = {

Ficus elastica is a species of the plant in the genus Ficus, from the family Moraceae. Ficus elastica, which is the object of our study, has been used for many years in phytodesign, however in terms of medicine, it remains a poorly studied plant. While studying the external signs and chemical composition of medicinal plant raw materials of leaves F{\'\i}cus elastica, chromato-mass spectrometry was used. During the process of studying, some diagnostic signs of Ficus elastica were identified. Chromato-mass spectrometry was used to identify 68 compounds. The maximum amount was accounted for б-D-Glucopyranoside, methyl (28,99\%), Phytol (9,90\%), 2-Hydroxy-3-methylsuccinic acid (6,93\%), Lanosterol (6,13\%), Hydroquinone (5,55\%), 9,12,15-Octadecatrienoic acid, ethyl ester, (Z,Z,Z)- (4,86\%), Lup-20(29)-en-3- one (4,17\%), 1,2-Benzenediol (3,33\%), Lupeol (2,95\%), 16-Allopregnene-3б,9а-diol-20-one 3-O-acetate (2,77\%), 9-Octadecenamide, (Z)- (2,67\%), 9,12,15-Octadecatrienoic acid, (Z,Z,Z)- (2,05\%), з-Sitosterol (1,84\%), а-d-Lyxofuranoside, methyl (1,57\%), Dasycarpidan-1-methanol, acetate (ester) (1,52\%), n-Hexadecanoic acid (1,45\%), Hexadecanoic acid, ethyl ester (1,33\%), 1,8-Dioxacyclohexadecane-2,10- dione, 5,6:12,13-diepoxy-8,16-dimethyl- (1,15\%), Vitamin E (0,64\%). Identified morphological features of the leaves of Ficus elastica can be used in diagnosis of this species and may help to develop indicators of authenticity for promising medicinal leaves. As mentioned earlier, by means of chromato-mass spectrometry were identified 68 compounds, and the relative percentage of identified compounds was determined using a simple normalization method.

}, keywords = {Chromato-mass spectrometry, Ficus elastic, Methyl, Phytol, Vitamin E., б-D-Glucopyranoside}, doi = {10.5530/pj.2022.14.197}, author = {Angelina V. Strelyaeva and Anna G. Kharitonova and Larisa B. Vaskova and Alexander N. Luferov and Dmitry O. Bokov and Alina A. Bondar and Natalia V. Bobkova and Nevena Jeremic and Yulia B. Lazareva and Alla M. Antsyshkina and Tatiana V. Prostodusheva and Roman M. Kuznetsov} } @article {1931, title = {Risk Factors for Hepatotoxicity From L-Asparaginase Chemotherapy In Children With Acute Lymphoblastic Leukemia}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {921-927}, type = {Original Article }, chapter = {921}, abstract = {

Introduction: L-asparaginase chemotherapy often causes hepatotoxicity and affects complete remission in pediatric acute lymphoblastic leukemia (ALL). This study aims to investigate the risk factors that affect the incidence of hepatotoxicity caused by L-asparaginase chemotherapy in ALL children. Methods: An observational study with prospective sampling was conducted at Dr. Soetomo Hospital, Surabaya. The inclusion criteria included ALL children aged 1-18 years, undergoing ALL Induction phase chemotherapy based on the 2018 Indonesian Children{\textquoteright}s ALL protocol as evidenced by bone marrow aspiration, receiving L-asparaginase chemotherapy, and obtaining written consent from parents or guardians. Each child had 3 ml of blood drawn from a peripheral vein to assess their complete blood count, alanine transaminase (ALT) levels, and albumin level. Results: Thirty-two children with ALL were collected. Two of them were excluded due to allergic reaction and enable to continue the L-asparaginase chemotherapy. Thirty of them were eligible participants. Approximately 53.3\% of ALL children aged <= seven years. Fourteen (47\%) children with ALL were included in the standard-risk group and 16 (53\%) of them included high-risk group. There were significant differences in ALT levels between the four stages of observation (p=\<0.001). Twenty-two ALL children had hepatotoxicity (73.3\%), while 8 had non-hepatotoxicity (26.7\%). Two risk factors had a significant influence on the occurrence of hepatotoxicity due to L-asparaginase chemotherapy including age and hypoalbuminemia (p=0.045, p=0.028). Conclusion: Age and hypoalbuminemia were the risk factors that might affect the incidents of hepatotoxicity. Clinical monitoring before and after treatment needs to be done to prevent poor outcomes.

}, keywords = {Acute lymphoblastic leukemia, Children, Hepatotoxicity, L-asparaginase}, doi = {10.5530/pj.2022.14.190}, author = {Agniya Ali Fahmi Hikmat and Mia Ratwita Andarsini and Bagus Setyoboedi and Maria Christina Shanty Larasati and Andi Cahyadi and I Dewa Gede Ugrasena} } @article {1906, title = {Risk Factors of Acute and Chronic Erythema Nodosum Leprosum in Dr. Soetomo General Academic Hospital Surabaya}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {766-770}, type = {Original Article}, chapter = {766}, abstract = {

Background: Leprosy is a chronic granulomatous infection and is one of the neglected diseases caused by Mycobacterium leprae. ENL is a complex syndrome, that caused inflammation of the skin, nerves, and other organs due to an inflammatory immune response to Mycobacterium leprae antigens. Acute ENL was defined as the first episode of ENL with a duration of less than 24 weeks. Chronic ENL was defined as ENL that persisted for more than 24 weeks. These types of ENL can have different risk factors and require different therapeutic interventions. Purpose: The onset of ENL is acute, but may progress to a chronic or recurrent phase and require long-term therapy. Early detection of leprosy is very important, because the infection is curable and prompt treatment can reduce nerve damage and associated stigma. Chronic ENL patients require prolonged high doses of corticosteroids to control inflammation in ENL and cause severe complications and side effects associated with morbidity and mortality. Methods: This retrospective study was conducted using a non-probability sampling technique consecutively using a casecontrol formula in leprosy patients with ENL in the Leprosy Division of the Outpatient Dermatology and Venereology Unit RSUD Dr. Soetomo Surabaya for the period 2015 {\textendash} 2020, using secondary data in the form of medical record data. Result: The results of this study obtained leprosy patients with ENL as many as 234 patients, 56 patients with acute ENL and 89 patients with chronic ENL. 45 patients with acute ENL and 45 patients with chronic ENL were obtained from the case-control minimal sample size formula. Conclusion: The results of the bivariate analysis test showed that there was a relationship between risk factors for coinfection and steroid therapy with the type of ENL. The presence of coinfection and steroid therapy showed that patients tend to be chronic ENL, conversely, in the absence of coinfection and without steroid therapy, patients tend to be acute ENL. The multivariate logistic regression analysis test showed a significant association between risk factors for ENL onset before MDT and the presence of coinfection with chronic ENL, whereas ENL onset after MDT and absence of coinfection were associated with acute ENL.

}, keywords = {Acute ENL, Chronic ENL, ENL, Leprosy, Neglected disease., Risk factors}, doi = {10.5530/pj.2022.14.165}, author = {Ditya Indrawati and Linda Astari and Afif Nurul Hidayati and Sawitri, Damayanti and Budi Utomo and Bagus Haryo Kusumaputra and Medhi Denisa Alinda and Cita Rosita Sigit Prakoeswa and M. Yulianto Listiawan} } @article {1786, title = {Ten Commonly Available Medicinal Plants in Malaysia with Potential Sun Protection Factor and Antioxidant Properties {\textendash} A Review}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {444-455}, type = {Review Article}, chapter = {444}, abstract = {

Background: Malaysia has a diverse range of medicinal plants that utilized to make effective nutritional, folk medicine, and cosmetic preparations. Natural antioxidants obtained from medicinal plant extracts have recently gained popularity as protective ingredients in sunscreen formulations due to their safety, wide range of biological effects on skin, and environmental sustainability in absorbing Ultraviolet (UV) radiation and preventing skin damage. Prolonged exposure to UV rays may cause skin damages like sunburn, photoaging, erythema, edema, wrinkle, and skin cancer. Natural sunscreen products are becoming more popular among consumers who are becoming more aware of the risks of excessive UV and chemicals in beauty and personal care products. Objective: This review aimed to provide brief information about ten commonly available medicinal plants in Malaysia with potential sun protection factor and antioxidant properties. Methods: In the present review, the relevant literatures were an extensive search from various scientific database including Pubmed, Google Scholar, ScienceDirect and Scopus. Ten commonly available medicinal plants in Malaysia such as Graptophyllum pictum, Moringa oleifera, Mangifera indica, Zanthoxylum rhetsa, Andrographis paniculata, Sonneratia caseolaris, Camellia sinensis, Morinda citrifolia, Nephelium lappaceum and Murraya koenigii were included based on its potential sun protection factor (SPF) and antioxidant properties. Results: All the ten medicinal plants reported in this review found to have potential antioxidant activities due to the presence of phenolic and flavonoid content in the extracts. All of these findings well correlated to their potential SPF. The M. indica extracts had the highest SPF value among the ten plant extracts reported in this review, with a value of >=30. This is considered high sun protection action. Extracts of A. paniculata, M. citrifolia, C. sinensis, and G. pictum have a moderate photoprotective effect (SPF value of >=15). Sun protection activity was low in M. oleifera and S. caseolaris (SPF value <= 2). Conclusion: The identification of natural antioxidant and photoprotective ingredients from medicinal plants has demonstrated as a potential natural sunscreen product in protecting UV radiation against damaging UV rays, and therefore recommended to utilize them to replace synthetic chemicals in cosmetics development in the future.

}, keywords = {Antioxidant, Medicinal plants, Sun protection factor, total flavonoid, Total phenol}, doi = {10.5530/pj.2022.14.57}, author = {Noor Diyana Ibrahim and Lay Jing Seow and Mahendran Sekar and Nur Najihah Izzati Mat Rani and Pei Teng Lum} } @article {1835, title = {Uncover Itchy Leaves Ethnomedicine Usage: A Preliminary Study on Characterization and Bioactivity of Laportea Spp}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {286-295}, type = {Original Article }, chapter = {286}, abstract = {

Background: Laportea decumana (Roxb.) Wedd. and Laportea stimulans (L.f.) Miq. (Urticaceae) or itchy leaves are endogenous plants from The Maluku Islands, Indonesia, which are used topically as analgesics by local people. Objective: As part of a preliminary investigation on the itchy leaves, this study was conducted to provide information on their macroscopic and microscopic characteristics, phytochemical profiles, and bioactivities according to the ethnomedicinal usages. Materials and Methods: The macroscopic examination was carried out on fresh leaves. The microscopic examination was carried out on leaf powder under a light microscope. The phytochemical analyses using TLC were conducted on those crude extracts and fractions. The bioactivity assays were conducted in vitro as Cox-2 inhibitory and DPPH radical scavenging activities. Results: reveal similar characteristics in the macroscopic and microscopic properties of both Laportea spp. leaves. Calcium oxalate crystals were observed in L. decumana but not found in L. stimulans. Both species have stomata with anisocytic type. More trichomes are found in the leaves of L. decumana, yet smaller and easily detachable. TLC analyses exhibited slightly different profiles. The crude extracts and fractions at 10 μg/ml showed similar inhibitory percentages on Cox-2. The DPPH scavenging activities of the crude extracts and fractions of L. decumana showed active moderate activity with an IC50 value \< 250 μg/ml, while those of L. stimulans showed moderate to weak potency with an IC50 value \< 500 μg/ml. Conclusion: Further exploration on Laportea spp. pharmacological activity is recommended to provide stronger evidence for its ethnomedicinal usage.

}, keywords = {Characterization, Cox-2 inhibitor, DPPH radical scavenging activity., Itchy leaves, Laportea decumana (Roxb.) Wedd, Laportea stimulans (L.f.) Gaud, Phytochemical profiles}, doi = {10.5530/pj.2022.14.98}, author = {Lukman La Basy and Djoko Santosa and Retno Murwanti and Triana Hertiani} } @article {1395, title = {The Acute Toxicity of Ki Hampelas Leaves (Sterculia rubiginosa Zoll. Ex Miq)}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {570-576}, type = {Research Article}, chapter = {570}, abstract = {

Background: Ki Hampelas (Sterculia rubiginosa Zoll. Ex Miq) is a medicinal plant with antioxidant and nephroprotective activity. Objective: This research aims to prove that Ki Hampelas leaves extract through an acute toxicity test. Materials and Methods: This study used white male rats of the Sprague-Dawley strain divided into four groups, the normal group and the 50 mg/ kg, 1000 mg/kg, 2000 mg/kg dose groups. For the acute toxicity test, a single dose with an observation of 14 days. After that, the surgery was done to see changes in the histopathology of the liver and kidneys. Results: The administration of Ki Hampelas leaf extract in the acute toxicity test did not cause death in the tested animals. There were no significant liver and kidney changes seen from the SGOT, SGPT, creatinine, urea, and histopathology. Conclusion: Ki Hampelas leaves extract did not cause death and toxic effects in the acute toxicity test.

}, keywords = {Acute toxicity, Ki Hampelas ( Sterculia rubiginosa Zoll. Ex Miq), Kidney, Liver}, doi = {10.5530/pj.2021.13.71}, author = {Rini Prastiwi and Ema Dewanti and Cut Mauliza and Ester Hidayati and Ita Anggraini and Riska Anggraini and Vera Ladeska} } @article {1656, title = {Amelioration of Cisplatin-Induced Kidney Injury by Pometia pinnata}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1257-1268}, type = {Research Article}, chapter = {1257}, abstract = {

Introduction: Cisplatin is one of the most effective anticancer drugs. But using cisplatin can cause very serious nephrotoxicity and acute kidney injury (AKI). Pometia pinnata (PE) or commonly referred to as matoa is a typical plant, especially Papua, Indonesia. Pometia pinnata belongs to the Sapindaceae family. This study aimed to determined the nephroprotective activity of the extract ethanol pometia pinnata on rats induced cisplatin. Methods: 30 rats are divided into six groups, each group were contained 5 rats. Group I was a normal group which rats only given CMC (carboxy methyl celluloce). Group II was a negative group which rats injected 7 mg / kgbw of Cisplatin in day 3. Group III was a positive group which rats given vitamin C 1\% from day 1 to 7 and in day 3 rats were injected cisplatin. Group IV-VI were extract groups (100 mg / kgbb, 200 mg / kgb, 400 mg / kgbb) which rats orally given extract from day 1 to 7 and in day 3 rats were injected cisplatin. On day 8 rats were injected ketamine 1\% which directly took the blood from the heart. Results: The result shows that EEPE on rats biochemical parameters including urea, creatinine, uric acid. Group II showed that there was a significant increase (p \<0.05) compared to the normal group that was not given cisplatin and extracts. Whereas in the group given the extract in groups IV, V, and VI there was a reduction in biochemical parameters because the Pometia leaf extract had high antioxidant activity so that it had nephroprotective activity. extract ethanol pometia pinnata can reduced the level of sodium, potassium and chloride of each group after receiving cisplatin. Statistically group II that only given cisplatin has significantly different with group I (p\<0,05) and also statically different with group VI (p\<0,05).

}, keywords = {Cisplatin, Kidney injury, Pometia pinnata}, doi = {10.5530/pj.2021.13.159}, author = {Adrian and RA Syahputra and Sukirman Lie and SE Nugraha and PC Situmorang} } @article {1325, title = {Analysis of Heavy Metal Contents of Marsilea crenata Presl. Leaves and Soils from East Java Province, Indonesia}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {17-22}, type = {Original Article}, chapter = {17}, abstract = {

Introduction: Marsilea crenata Presl. grows in East Java Province, Indonesia, and showed several pharmacological activities due to its phytoestrogen content. Research indicated its phytoremediation property, and therefore has an impact on heavy metal accumulation in the plants. Lead, cadmium, and mercury are amongst heavy metals that are toxic to the human body. This study aimed to determine and compare Pb, Cd, and Hg mineral contents of soils and leaves of the plants grew in Batu, Pasuruan, Surabaya, and Kediri cities in the province. Method: 10 g of dried powdered leaves and soils were put in separate crucible porcelains, and add 2ml of nitric acid. All were burnt in low heat until white smoke were not formed, and then stood to cool. Ashes obtained were examined using AA 6200 Atomic Absorption Spectrometer (AAS). Result: Showed that leaves samples from the areas showed no Pb and Hg mineral contents that exceeded the permissible limit. Batu City leaf sample had Cd heavy metal content of 2.79 {\textpm} 0.01 ppm, which exceeded the permissible limit. Conclusion: Analysis of heavy metal contents of soils from all of the areas showed no exceed limit of Pb and Hg mineral concentrations. Cd soil contents of Surabaya and Kediri cities, were 0.73 {\textpm} 0.00 and 2.61 {\textpm} 0.08 ppm respectively.

}, keywords = {Aas, Clover, Phytoremediation}, doi = {10.5530/pj.2021.13.3}, author = {Mangestuti Agil and Hening Laswati and Neny Purwitasari and Burhan Ma{\textquoteright}arif} } @article {1637, title = {Antibacterial Activities of Cationic Porphyrins and Porphyrin Encapsulated Gold Nanorods on Bacterial Cell Lines}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1086-1096}, type = {Original Article}, chapter = {1086}, abstract = {

Bacterial infections form part of the major causes of mortality and morbidity around the world more especially in developing and under-developed countries. Cationic porphyrins have been reported to display better efficacy in antimicrobial photodynamic therapy activity. The purpose of this study was to synthesise the cationic porphyrins; (TAP) and (TPyP) and evaluate their pharmacokinetics and metabolic interactions with the DNA gyrase subunit A. The antibacterial activity of the nano-conjugates was evaluated against Staphylococcus aureus (ATCC 25925), Enterococcus faecalis (ATCC 29212) and Klebsiella pneumoniae (ATCC 4352) using the micro-dilution assay without light. AutoDock Vina was used to assess the molecular interactions between ligands and the DNA gyrase subunit A. The SwissADME online tool was used to assess the pharmacokinetic properties of the nano-conjugates, while the ADMETlab online tool was used to assess the ability to inhibit the hERG gene, human hepatotoxicity and mutagenicity. The test nano-conjugates showed broad-spectrum antibacterial activity against all tested bacterial strains with the MIC values in a range of 0.42 {\textpm} 0.1 to2.6 {\textpm} 0.7 mg/ml. The nano-conjugates revealed good molecular interaction with DNA gyrase subunit A with their binding free energy in the range of -8.3 to -8.7 kcal/ mol. They are predicted to be P-glycoprotein (P-gp) substrates, able to penetrate the blood-brain barrier and non-inhibitors of cytochrome P450 (CYP) isomers (CYP 2C19, CYP 2C9 and CYP 2D6). Both nanoconjugates have the potential to cause cardiotoxic and mutagenic effects but not hepatotoxic effects. The results show that the synthesized compounds have the potential as anti-bacterial PDT agents.

}, keywords = {Antimicrobial, Bacteria, Porphyrin}, doi = {10.5530/pj.2021.13.141}, author = {Hlapisi N and Maliehe TS and Oluwafemi OS and Songca SP and Linganiso L and Motaung TE} } @article {1386, title = {Anti-Cancer Activity of Cayratia Auriculata Ethanolic Extracts Against Cancer Cell Line A549 An In Vitro Analysis}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {495-499}, type = {Research Article}, chapter = {495}, abstract = {

Background: The purpose of this study was to evaluate the anticancer activity of ethanolic cayratia auriculata extracts using the A549 cell line MTT assay. Materials and Methods: Using Soxhlet apparatus, ethanolic extracts from cayratia auriculata were prepared. The cancer cells were exposed to 12.5, 25, 50 , 100 , 150, 200 μg / mL and incubated for 24 h at different concentrations. Compared with control, C. auriculata exhibited a cytotoxic effect. Results: At 150 and 200μg / ml concentrations, with 61 percent and 73.7 percent respectively, the highest cytotoxicity was identified. The findings show that cytotoxicity is directly proportionate to the concentration of the extract. IC50 of the ethanolic extract value of C. auriculata was found to be 102.9μg / ml against the A549 cell line. Conclusion: In the present analysis, C.auriculata ethanolic extract was shown to be a strong suppressant for cell division and proliferation. As for anti-tumor medicine, it can be a new source and can be effectively used as an immunological anti-malignant compound.

}, keywords = {Activity against cancer, Cell line cancer, Ethanol Extract, MTT Assay}, doi = {10.5530/pj.2021.13.62}, author = {S Lalitha and D Anusha and Yogeshkumar Murkunde and Viji Devanand and K Maheshkumar} } @article {1667, title = {Anti-Inflammatory Effects of Methanol Extract, Hexane, Ethyl Acetate, and Butanol Fraction of Piper crocatum Ruiz \& Pav Leaves on Lipopolysaccharide-induced RAW 264.7 Cells}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1341-1346}, type = {Original Article}, chapter = {1341}, abstract = {

Piper crocatum Ruiz \& Pav is a traditional Indonesian plant that is empirically used to treat various diseases. Several studies have stated that Piper crocatum leaves extract has anti-inflammatory effects. Piper crocatum leaves contain different secondary metabolites alkaloids, flavonoids, tannin-polyphenols, steroids, terpenoids, and saponins. The purpose of this study was to determine the anti-inflammatory effect of Piper crocatum leaves extract and fraction on the production of nitric oxide in lipopolysaccharideinduced RAW 264.7 cells. Anti-inflammatory effect of methanol extract of Piper crocatum leaves (MEPC), n-hexane fraction of Piper crocatum leaves (HFPC), ethyl acetate fraction of Piper crocatum leaves (EAFPC), and n-butanol fraction of Piper crocatum leaves (BFPC) against RAW 264 cell macrophages, 7 Lipopolysaccharide-induced (LPS). Extraction of Piper crocatum leaves was the maceration method. Cell viability was determined by the MTT method in the concentration range of 12.5;25;50;100;200 ug/ mL. The anti-inflammatory effects of MEPC, HFPC, EAFPC and BFPC were tested against nitric oxide (NO) production inhibition in LPS-induced RAW 264.7 macrophage cells. NO levels were determined by the NO Colorimetric Assay Kit as measured by the ELISA plate reader. The viability test of MEPC, HFPC, EAFPC, and BFPC from Piper crocatum leaves showed the concentrations that gave the percentage of viability above 80\% were concentrations of 100, 50, and 25 g/mL. MEPC, HFPC, EAFPC, and BFPC at concentrations of 100, 50, 25 μg/mL could significantly inhibit NO production with p\<0.05 (p=0.000). The highest NO production inhibition effect was on EAFPC. MEPC, HFPC, EAFPC, and BFPC have antiinflammatory effects, with the highest effect on EAFPC.

}, keywords = {Anti-inflammatory Effect, LPS, Nitric oxide, Piper crocatum}, doi = {10.5530/pj.2021.13.169}, author = {Nilda Lely and Helmi Arifin and Yufri Aldi and Fatma Sri Wahyuni} } @article {1707, title = {Antioxidant Activity of Methanol Fractions Stem Bark of Kayu Sarampa (Xylocarpus moluccensis (Lam.) M. Roen))}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1694-1701}, type = {Research Article}, chapter = {1694}, abstract = {

Introduction: Methanol extract of X. moluccensis was found to be significantly effective in scavenging DPPH method. Therefore, this research is a follow-up research study from Budiarso et al (2020).. The methanol extract was then fractionated and tested for antioxidant activity. Objective: To assess antioxidants activity of methanolic fractions from stem bark of Kayu Sarampa. Method: The Stem bark was extracted with Reflux method using hexane, ethyl acetate, and methanol as solvent. The methanolic extract was fractionated using a chromatographic column were subjected to the antioxidant activity assay by the 2.2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging and the ferric-reducing antioxidant power (FRAP) method. Results: F3 Fractions IC50 of X. moluccensis exhibits the highest DPPH scavenging activity compared with F2, F3, ascorbic acis as control positif, F5, and F4, wich are 4.64, 6.79, 9.69, 10.49, and 227.44 respectively and Ferric reducing power from methanolic fraction of X. moluccensis stembark F3 exhibits higher antioxidant power compared to F2, F1, F5, ascorbic acid and F4, respectively which are 667.8 μmol/gr, 607.8 μmol/gr, and 573.8 340.48 and 309.8 μmol/gr, respectively

}, keywords = {Antioxidant., DPPH, FRAP, Kayu Sarampa}, doi = {10.5530/pj.2021.13.218}, author = {Fitri Santy Budiarso and Berna Elya and Muhammad Hanafi and Andy Howard Limengan and Ratika Rahmasari} } @article {1607, title = {Antioxidant and Hepatoprotective Activity of Ethanol Extract of Annona cherimola Mill. On Paracetamol-Induced Liver Toxicity in Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {874-882}, type = {Original Article}, chapter = {874}, abstract = {

Background: Annona cherimola Mill. (A. cherimola) is mainly characterized by its antioxidant and cytoprotective properties due to their content of phenolic compounds. Objective: To evaluate antioxidant and hepatoprotective activity of ethanol extract of leaves from A. cherimola against induced toxicity by paracetamol in rats. Methods: Amount of total phenolics compounds of ethanol extract of A. cherimola Mill. was determined by the Folin-Ciocalteu method and antioxidant activity was evaluated by DPPH method. Three doses of the ethanol extract of leaves of A. cherimola (250, 500 and 750 mg/Kg/day) were administered to rats and it was evaluated biochemical blood parameters: aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) were measured, liver tissue was removed for histopathological analysis. Results: Ethanol extract of leaves from A. cherimola had 41.26 mg GAE/g extract and antioxidant DPPH Scavenging Activity had 85.51\%. A. cherimola reduced blood levels of ALT, AST and ALP, compared to control group Paracetamol, ethanol extract, being more effective at doses of 750 mg/Kg/day. Histopathological evaluation suggested that A. cherimola decreased hepatic necrosis and degenerative process induced by paracetamol. Conclusions: Hepatoprotective activity of ethanol extract of leaves of A. cherimola was demonstrated, being hepatoprotective activity dose dependent and the mechanism may involve antioxidant activity and total polyphenols found in extract of this plant.

}, keywords = {Antioxidants, DPPH, Liver, Paracetamol, Rat}, doi = {10.5530/pj.2021.13.112}, author = {Carmen R. Silva-Correa and V{\'\i}ctor E. Villarreal-La Torre and Jos{\'e} L. Cruzado-Razco and William Antonio Sag{\'a}stegui- Guarniz and Mar{\'\i}a V. Gonz{\'a}lez-Blas and Anabel D. Gonz{\'a}lez-Siccha and Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo- Villalaz and Luz M. Guerrero-Espino and Jorge Del Rosario-Ch{\'a}varri and Julio Hilario-Vargas} } @article {1703, title = {Comparative Modulatory Assessment of the Sperm Quality and Testicular Function by Solvent Fractions of the Cannabis Extract in Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1678-1687}, type = {Research Article}, chapter = {1678}, abstract = {

Background: The bioactive ingredients present in medicinal plants have various pharmacological activities which have explored for therapeutic and management of disease conditions like infertility. Objective: This study evaluated the comparative modulations on semen quality and testicular function in the rat by solvents soluble portions of ethanolic leaf extract in varying polar solvents. Methods: Thirty Wistar rats were randomly placed into five groups (A, B, C, D, E and F) with five rats per group: A, control: 0.2 ml 2 \% DMSO was administered, B (vitamin C): 90 mg/kg body weight, 4.4 mg/kg body weight of n-hexane, 3.65 mg/kg body weight of ethyl acetate, 0.52 mg/kg body weight of n-butanol and 0.18 mg/kg body weight of the residual portion of Cannabis leaf extract were given to groups C, D, E and F, respectively. The rats were sacrificed 24 hours after the last day of 60 days of treatment. Results: Sperm indices, testosterone, FSH, LH, and HDL showed significant increase (p <= 0.05) across the treatment groups compared to normal control. Similarly, there was a significant increase in activity (p <= 0.05) of ALP, ACP, SOD, and CAT across the treatment groups compared to normal control. In addition, there were significant increases in GSH, MDA, triglyceride, cholesterol, total protein concentration levels across the treatment groups compared to normal control. The n-butanol soluble portion showed normal histomorphology with typical seminiferous tubule with spermatogonia lying on the basement membrane. Conclusion: Testicular integrity and improved sperm quality were pronounced in rats administered n-butanol solvent portion.

}, keywords = {Cannabis, Fertility, Medicinal., Sperm, Testis}, doi = {10.5530/pj.2021.13.216}, author = {Nwonuma Charles O and Favours God{\textquoteright}slove Oluwafemi and Rotimi Damilare E and Alejolowo Omokolade O and Ojo Oluwafemi A and Afolabi Boluwatife L and Irokanulo Emenike O} } @article {1658, title = {Determination of Urinary Methyl Hippuric Acid Using Shimadzu UV-Visible Spectrophotometer Among Petroleum Employees}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1277-1281}, type = {Research Article}, chapter = {1277}, abstract = {

Xylene is a significant part of petroleum and a broadly considered as a natural impure material. About 98\% of Xylene is extracted from the petrochemical and petrol refining factories. It is one of the major genotoxicant part in petroleum, which may initiate various diseases but malignancy is questionable. Taking into consideration, we intend to identify the urinary methyl hippuric acid level which is metabolic product of xylene among petroleum station employees as well as in healthy persons. Aims and Objectives: To identify the occupational exposure of xylene in petrol station employees by assessing urinary methyl hippuric acid level. To determine and compare the level of urinary methyl hippuric acid among healthy individuals and petrol station employees. Materials and Methods: Urine samples were collected from 30 healthy individual (control) and 30 petroleum employees (case) working in petroleum station who are above 18 years of age. The urinary methyl hippuric acid (MHA) level was analysed by using Shimadzu UV-Visible Spectrophotometer method. Results: The urinary Methyl hippuric acid level was significantly higher in petroleum station employees than in healthy individuals (p\<0.001). Conclusion: The urinary MHA level is a helpful tool to identify the occupational exposure of people who work in petrol and petroleum product. Subsequently, our investigation accentuates that proper precautionary measure and efficiently bio-observing should be taken among petrol station employees which will assist with reducing their likely degrees of risk related with the occupation. It might start the cancer-causing disease through the cellular DNA changes and induce genotoxic effects.

}, keywords = {Occupational Exposure, Urine Methyl Hippuric Acid Level, UV Spectrophotometry, Xylene}, doi = {10.5530/pj.2021.13.161}, author = {Vidya Gowdappa Doddawad and B.M. Gurupadayya and Shivananda S and Vidya CS and Azhar Mohammed and Bhuyan L} } @article {1715, title = {Effect of a Gel Based on Ipomoea batatas (Purple Sweet Potato) on Dermal Wound Healing in Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1720-1726}, type = {Research Article}, chapter = {1720}, abstract = {

Background: Ipomoea batatas (L.) Lam. (I. batatas) is a root native from South America that is characterized by its antioxidant, antimicrobial and anti-inflammatory properties. These properties contribute to the wound healing process. Objective: To evaluate the healing activity of a gel based on I. batatas on dermal wound healing in mice. Material and methods: An acid ethanolic extract (1.5 N hydrochloric acid: Ethanol 96 {\textdegree} 15:85, v / v) was prepared with the peels of the roots of I. batatas "purple sweet potato", which was incorporated into the formulations 0.5\% and 1\% gel. Mus musculus Balb / c with induced injury were distributed in four experimental groups: Group I (Control), which did not receive any treatment. Group II (Gel base), Group III (Gel I. batatas 0.5\%) and Group IV (Gel I. batatas 1\%) received the daily administration of topical treatments for 14 days. Wound closure was determined during the experimentation time, then they were euthanized with sodium pentobarbital 60 mg / kg / pc v.ip. to obtain skin samples for histopathological analysis. Results: Group IV shows a higher percentage of wound closure, which is also evidenced in histopathological changes. Conclusions: The 1\% gel based on the ethanolic extract of the peels of the roots of Ipomoea batatas (L.) Lam. they show healing activity in wounds induced in mice, being the most effective treatment.

}, keywords = {Histology, Ipomoea batatas, Skin., Wound Healing}, doi = {10.5530/pj.2021.13.222}, author = {Carmen R. Silva-Correa and Cristel M. Ortiz-Noriega and V{\'\i}ctor E. Villarreal-La Torre and Abhel A. Calder{\'o}n-Pe{\~n}a} } @article {1714, title = {Effect of a Gel Based on Ipomoea batatas (Purple Sweet Potato) on Dermal Wound Healing in Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1720-1726}, type = {Research Article}, chapter = {1720}, abstract = {

Background: Ipomoea batatas (L.) Lam. (I. batatas) is a root native from South America that is characterized by its antioxidant, antimicrobial and anti-inflammatory properties. These properties contribute to the wound healing process. Objective: To evaluate the healing activity of a gel based on I. batatas on dermal wound healing in mice. Material and methods: An acid ethanolic extract (1.5 N hydrochloric acid: Ethanol 96 {\textdegree} 15:85, v / v) was prepared with the peels of the roots of I. batatas "purple sweet potato", which was incorporated into the formulations 0.5\% and 1\% gel. Mus musculus Balb / c with induced injury were distributed in four experimental groups: Group I (Control), which did not receive any treatment. Group II (Gel base), Group III (Gel I. batatas 0.5\%) and Group IV (Gel I. batatas 1\%) received the daily administration of topical treatments for 14 days. Wound closure was determined during the experimentation time, then they were euthanized with sodium pentobarbital 60 mg / kg / pc v.ip. to obtain skin samples for histopathological analysis. Results: Group IV shows a higher percentage of wound closure, which is also evidenced in histopathological changes. Conclusions: The 1\% gel based on the ethanolic extract of the peels of the roots of Ipomoea batatas (L.) Lam. they show healing activity in wounds induced in mice, being the most effective treatment.

}, keywords = {Histology, Ipomoea batatas, Skin., Wound Healing}, doi = {10.5530/pj.2021.13.222}, author = {Carmen R. Silva-Correa and Cristel M. Ortiz-Noriega and V{\'\i}ctor E. Villarreal-La Torre and Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo-Villalaz and Luz M. Guerrero-Espino and William A. Sag{\'a}stegui-Guarniz and Anabel D. Gonz{\'a}lez- Siccha and Mar{\'\i}a V. Gonz{\'a}lez-Blas and Jos{\'e} L. Cruzado-Razco and Jorge Del Rosario-Ch{\'a}varri and Patricia Contreras- Vera and Julio Hilario-Vargas} } @article {1670, title = {The Effect of Sambiloto and Spirulina Combination on Mucin-1 Protein Expression in Medial Colon of Plasmodium berghei ANKA Infected Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1359-1365}, type = {Original Article}, chapter = {1359}, abstract = {

Malaria still be health problem in the world, especially in Eastern Indonesia. Malaria{\textquoteright}s inflammation and metabolism defect can cause colonic damage, such as enhancement Muc-1 protein expression and goblet cells hyperplasia. Sambiloto and spirulina combination as antiinflammatory and antioxidative agent can prevent medial colon damage Plasmodium berghei ANKA infected mice. The aim of the study to show the effect of sambiloto and spirulina combination on Muc-1 protein activity in medial colon Plasmodium berghei ANKA infected mice. This study use preserve male Swiss Webser mice colonic tissue which has inoculated by Plasmodium berghei ANKA, whose treatment group include positive control (dehyroartemisin piperaquine), negative control (carboxymethil cellulose), AP (sambiloto), AP+ES (sambiloto+spirulina extract), and AP+PS (sambiloto+spirulina powder) and terminated after 28 days of treatment. Colonic tissue was stained with immunohistochemistry and observed using light microscope (400x) in five different field and was analyzed with ImageJ{\textregistered} sowtware, and statisitcal analysis was done with SPSS 20.0. According to One Way ANOVA and Duncan posthoc test, only AP+PS(120,98 {\textpm}3,37), which significantly difference between negative control, AP, and AP+ES group. Meanwhile, between DHP, AP+PS group not significantly differenece. Sambiloto extract and spirulina powder combination can reduce Muc-1 protein expression in medial colon Plasmodium berghei ANKA infected mice.

}, keywords = {Medial colon, Muc-1, Plasmodium berghei Anka, Sambiloto, Spirulina}, doi = {10.5530/pj.2021.13.172}, author = {Kusmardi Kusmardi and Baiqi Nur Hairi and Nadar Sukri Lubis and Tri Wahyuni Lestari and Putri Reno Intan} } @article {1646, title = {Evaluation of the Anticonvulsant, Anxiolytic, Sedative, and Neuroprotective Activities of Polysaccharides from Mycelium of Two Ganoderma Species}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1161-1173}, type = {Research Article}, chapter = {1161}, abstract = {

Background: Ganoderma lucidum has been used as a medicinal mushroom since centuries in East Asia. Recent reports have shown that metabolites isolated from Ganoderma species have shown effects on central nervous system. Objective:\ To determine the neuroprotective, anticonvulsant, anxiolytic, and sedative effects of Ganoderma sp. and Ganoderma curtisii polysaccharides. Methods: Polysaccharides (Gsp-PS2 or Gc-PS2) were isolated from two Ganoderma mycelia submerged cultures. Acute toxicity effects of Gc-PS2 or Gsp-PS2 on mice were treated orally with doses of 50 - 2000 mg/kg. Anticonvulsant activity was determined using three chemoconvulsants: kainic acid (KA), strychnine, or pentylenetetrazole (PTZ). Anxiolytic-like effects were determined using the elevated plus maze test on mice. GABA release evoked by GC-PS2 or Gsp-PS2 content was determined by HPLC. Neuroprotective effects of Gsp-PS2 or Gc-PS2 were determined by glial activation, histopathological changes, and immunohistochemistry. Results: Gc-PS2 or Gsp-PS2 showed neuroprotective activity by diminishing neuronal death, reducing glial activation and Neu-N expression levels. Gsp-PS2 or Gc-PS2 inhibited convulsions in the KA model. An anxiolytic-like, but not a sedative effect was reported in mice treated with Gc-PS2 or Gsp-PS2. Polysaccharides Gc-PS2 or Gsp-PS2 evoked endogenous GABA release and increased its concentration within the incubation medium. Pretreatment with Gsp-PS2 or Gc-PS2 showed a reduction of the LPSinduced NO production. Gc-PS2 or Gsp-PS2 did not produce toxic effects. Conclusion:\ Ganoderma sp. or Ganoderma curtisii polysaccharides showed neuroprotective and anticonvulsant activities in animal models. The anticonvulsant activity may involve the GABAergic neurotransmision.

}, keywords = {a- and b-glucan, Anticonvulsant, GABA, Ganoderma curtissi, Ganoderma sp, Neuroprotective}, doi = {10.5530/pj.2021.13.149}, author = {Veronica Nunez-Urquiza and Juana Villeda-Hernandez and Elizur Montiel-Arcos and Isaac Tello and Victoria Campos-Pena and Maribel Herrera-Ruiz and Mar{\'\i}a del Carmen Guti{\'e}rrez and Vera Petricevich and Mar{\'\i}a Ang{\'e}lica Santana and Martha Navarro and Ang{\'e}lica Berenice Aguilar-Guadarrama and Gabriel Navarrete-V{\'a}zquez and Irene Perea-Arango and Ismael Leon-Rivera} } @article {1364, title = {Hepatoprotective Activity of Cordia lutea Lam Flower Extracts Against Paracetamol-Induced Hepatotoxicity in Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {309-316}, type = {Original Article}, chapter = {309}, abstract = {

Background: Paracetamol or acetaminophen overdose leads to hepatotoxicity. This study evaluates the effect of Cordia lutea extract on paracetamol-induced hepatotoxicity in rats. Methods: Three different doses of dry fluid extract of C. lutea (200, 400 and 600 mg / Kg) were evaluated and compared with Silymarin 200 mg / Kg. Biochemical parameters such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), direct bilirubin, indirect bilirubin, total bilirubin, albumin, globulin and total proteins were evaluated, and histopathological changes in the liver were studied and evaluated. Results: C. lutea reduced the levels of ALT, AST, ALP and increases proteins significantly, although the reduction of bilirubin was not significant, the extract at 400 mg / Kg reduced the levels better than the extract at 600 mg / Kg. The histopathological evaluation suggested that C. lutea extract reduced paracetamol-induced liver necrosis. Conclusions: The extract of C. lutea has a marked hepatoprotective effect, significantly reducing the levels of ALT, AST and ALP, in addition to increasing the levels of albumin, globulin and total proteins, in Rattus norvegicus var. albinus. C. lutea extract is an excellent candidate for use in paracetamol-induced liver diseases.

}, keywords = {Acetaminophen, Biochemical parameters, Cordia lutea, Hepatoprotection, Histopathology, Paracetamol}, doi = {10.5530/pj.2021.13.40}, author = {Ruiz-Reyes SG and Villarreal-La Torre V{\'\i}ctor E and Silva-Correa Carmen R and Sag{\'a}stegui Guarniz William Antonio and Cruzado-Razco Jos{\'e} L and Gamarra-S{\'a}nchez C{\'e}sar D and Venegas Casanova Edmundo A and Miranda-Leyva Manuel and Valdiviezo Campos Juan Ernesto and Cuellar-Cuellar Armando} } @article {1331, title = {Immunomodulatory Effect of Methanolic Extract and Ethyl Acetate Fraction of Bengkoang (Pachyrhizus erosus (L.) Urban) Tuber in Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {59-65}, type = {Original Article}, chapter = {59}, abstract = {

Background: Recently, interest in the use of herbal medicine that can modulate the immune system is increasing in the pandemic situation. One plant that can be developed as an immunomodulator is bengkoang (Pachyrhizus erosus (L.) Urban). Objectives: To evaluate the immunomodulatory effect of a methanolic extract of bengkoang (MEB) and the ethyl acetate fraction of bengkoang (EAFB) in mice induced by the hepatitis B vaccine. Materilas and Methods: Thirty healthy male mice were divided into six groups namely, control, standard levamisole, MEB (100 and 200 mg/kg BW), and EAFB at 100 and 200 mg/kg body weight (BW). The treatments were given for 18 days, and hepatitis B vaccine was injected intraperitoneally twice during the treatment. Assessment of the immunomodulatory effect was carried out against nonspecific and specific immune response parameters. Results: The MEB and EAFB could significantly increase phagocytic capacity, the spleen index, and lymphocyte proliferation. MEB stimulated IgG production, while EAFB, 100 mg/kg BW suppressed immunoglobulin G (IgG) production; otherwise, at the higher dose, EAFB increased IgG production. EAFB also increases nitric oxide production, while MEB had no effect. The higher dose of MEB tended to increase tumor necrosis factor (TNF)-α levels and decrease interleukin (IL)-10, while EAFB tended to decrease TNF-α and increase IL-10, but these changes were not significant. Conclusion: Based on this study, MEB and EAFB could increase the innate immune response and stimulate the humoral immune response but had no effect on cytokine production, which may have potential usefulness of bengkoang to treat immunomodulatory-related disease.

}, keywords = {Bengkoang (Pachyrizus erosus (L.) Urban), Dietary fiber fraction, Immunomodulatory effect, Lymphocyte proliferation, Phagocytic macrophages activity}, doi = {10.5530/pj.2021.13.9}, author = {Tanti Azizah Sujono and Arief Nurrochmad and Endang Lukitaningsih and Agung Endro Nugroho} } @article {1371, title = {Immunostimulatory Activities of Pegagan Embun (Hydrocotyle sibthorpioides Lam.) in White Male Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {368-375}, type = {Original Article}, chapter = {368}, abstract = {

Introduction: Pegagan embun (Hydrocotyle sibthorpioides L.) has many pharmacological activies, such as improving the immune system. Aim: This research aims to study the immunomodulatory effect of Pegagan embun herbs ethanol extract (Hydrocotyle sibthorpioides L.) determined by phagocytic activity and capacity of macrophages, total and percentage of leukocytes. Methods: 25 male white mice were divided into 5 equal groups. Negative control group were given Na CMC 0.5\%, the extract treated group were given Pegagan embun ethanol extract at doses of 10, 50, 200 mg/kgbw, and the positive control group was given Stimuno 50 mg/kgbw orally for 7 days. On the 8th day, the total and percentage of leukocytes were counted through blood sample taken intravenously. The mice were then induced with Staphylococcus aureus suspension. After one hour, the peritoneal fluids was taken to determine the macrophages activity and capacity. The macrophages phagocytic activity and capacity, total and percentage of leukocytes were analyzed by One-Way Anova followed by Duncan Multiple Range Test (p\<0.05). Results: The results show significant increase of concentration (p\<0.05) towards macrophages phagocytic activity and capacity, and total leukocytes count. Percentage of leukocytes show that lymphocytes increase significantly (p\<0.05), meanwhile neutrophils segments decrease significantly (p\<0.05). Conclusion: It can be concluded that ethanol extract of Pegagan embun herb at doses of 10, 50, 200 mg/kgbw shows immunostimulatory activity.

}, keywords = {Hydrocotyle sibthorpioides Lam., Leukocytes, Macrophage, Phagocytosis, Staphylococcus aureus}, doi = {10.5530/pj.2021.13.47}, author = {Afriwardi and Yufri Aldi and Dwisari Dillasamola and Yolanda Alfiyyah Larakhansa and Elsa Badriyya} } @article {1348, title = {Liver Organ Impairment Due to the Consumption of Kratom Leaves (Mitragyna speciosa Korth.)}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {179-184}, type = {Research Article}, chapter = {179}, abstract = {

This study was aimed to evaluate the administration effects of kratom leaves extracts on the liver of mice (Mus musculus). The total of 25 mice was divided into five groups, respectively; (A) without treatment, (B) treatment with distilled water at 0.50 ml/20 g body weight, (C) treatment of kratom leaves extracts with a dosage of 0.15 mg/20 g body weight, (D) treatment of kratom leaves extracts with a dosage to 0.30 mg/20 g body weight and (E) treatment with a dosage of silymarin at 0.70 mg/20 g body weight. All those treatments were completed in seven consecutive days. On day 8, blood withdrawal and liver dissection were executed. The average levels of AST enzyme in the treatment groups respectively showed 22.81 U/L (A), 23.30 U/L (B), 34.86 U/L (C), 40.68 U/L (D), and 25.44 U/L (E), (p\<0.05). Whereas, the average levels of ALT exposed respectively at 17.96 U/L (A), 18.35 U/L (B), 29.13 U/L (C), 33.59 U/L (D), and 20.68 U/L (E), (p\<0.05). The average scoring for the treatment groups resulted in 0.33, 0.67, 1.33, 1.67, and 0.67, respectively, with p\<0.05. Hence, it was concluded that the higher doses of the extracts of kratom leaves administered during the treatment, the more severe damage the liver organ became.

}, keywords = {ALT, AST, Kratom leaves, Liver organ}, doi = {10.5530/pj.2021.13.25}, author = {Ruqiah Ganda Putri Panjaitan and Linda Liridah} } @article {1653, title = {Phytochemical Screening and Anti-Inflammatory Potential of the Organic Extracts from Cleoserrata serrata (Jacq.) Iltis.}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1225-1241}, type = {Research Article}, chapter = {1225}, abstract = {

Cleoserrata serrata is used in Mexican-south traditional medicine to treat chicleros ulcer. The phytochemical profile and the anti-inflammatory effect from four extracts obtained by maceration proccess and of the primary fractions from two extracts are described. In addition, the antioxidant, leishmanicidal and antimycobaterial activities and LD50 from active extracts are reported. Anti-inflammatory activity was evaluated in TPA and carrageenan assays. Ethyl palmitate and γ-sitosterol were detected in Hexanic and CH2Cl2 extracts. Same compounds and stigmasta-3,5-dien-7-one, palmitic acid, phytol acetate and phytol were detected in primary fractions from CH2Cl2:EtOH extract. In this and in MeOH extracts a polyphenolmixture was obtained. The MeOH extract was subjected to acid hydrolysis, and kaempferol, quercetin and scopoletin were detected in organic-phase. Polyphenol-mixture and organic-phase (IC50=3730 and 2338 μg/mL) showed moderate antioxidant activity; meanwhile MeOH extract exhibited scarce activity. In carrageenan model, Hexanic extract and polyphenol-mixture showed ED50=131.46 and 64.89 mg/ kg, respectively. Three extracts were active but not-dose-dependent. In TPA-model, CH2Cl2 extract and polyphenol-mixture showed ED50 \<0.79 mg/ear, and three extracts were active, however the effect was not-dose-dependent. CH2Cl2:EtOH showed antimycobacterial and leishmanicidal activities. The LD50 was \>2 g/kg for all extracts.

}, keywords = {Anti-inflammatory Effect, Antimycobacterial activity, antioxidant activity, Cleoserrata serrata, DL50, Leishmanicidal activity, Organic extract}, doi = {10.5530/pj.2021.13.156}, author = {Mar{\'\i}a del Carmen Ju{\'a}rez-V{\'a}zquez and Alejandro Zamilpa A and Rosalba Le{\'o}n-D{\'\i}az and Mariano Mart{\'\i}nez-V{\'a}zquez and Adolfo L{\'o}pez-Torres and Julieta Luna-Herrera and Lilian Y{\'e}pez-Mulia and Francisco Alarc{\'o}n-Aguilar and Mar{\'\i}a Adelina Jim{\'e}nez-Arellanes} } @article {1358, title = {Potential Activity of Medicinal Plants as Pain Modulators: A Review}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {248-263}, type = {Review Article}, chapter = {248}, abstract = {

This review aims to demonstrate the relevance that medicinal plants and their promising results have in prevention and treatment of pain. The neurophysiological bases of pain have been analyzed and the potential mechanisms of action have been proposed, it has also been determined that the main experimental models used for the evaluation of the analgesic potential are: acetic acid-induced writhing test, formalin test, hot-plate test, capsaicin-induced nociception, cinnamaldehyde-induced nociception, glutamate-induced nociception, tail{\textendash}flick test and tail immersion test. There are countless medicinal plants with potential analgesic activity, in some of them main responsible compounds for the activity are flavonoids (vitexin, quercetin, naringenin, astragalin, eupatilin), alkaloids (scotanamine B, bullatine A, S-(+)- dicentrine, stephalagine, lappaconitine), terpenoids (p-cymene, thymol, menthol, citronellol, myrcene, carvacrol, linalool) and saponins (siolmatroside I, cayaponoside D, cayaponoside B4, cayaponoside A1); however, all studies have only been carried out up to pre-clinical stages. Therefore, it is recommended to carry out kinetic studies of the most remarkable natural compounds, evaluate mixtures of active compounds for diminishing doses to avoide possible side effects, and continue with clinical studies of medicinal plants whose safety has already been reported.

}, keywords = {Analgesic, Antinociceptive, Extract, Natural product, Pain}, doi = {10.5530/pj.2021.13.35}, author = {Carmen R Silva-Correa and Jorge L Campos-Reyna and V{\'\i}ctor E Villarreal-La Torre and Abhel A Calder{\'o}n-Pe{\~n}a and Mar{\'\i}a V Gonz{\'a}lez Blas and Cinthya L Aspajo-Villalaz and Jos{\'e} L Cruzado-Razco and William Antonio Sag{\'a}stegui- Guarniz and Luz M Guerrero-Espino and Julio H} } @article {1647, title = {The Potential Interaction of Ethionamide-Thyroid Hormone Receptor Induces Hypothyroidism}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1174-1179}, type = {Research Article}, chapter = {1174}, abstract = {

Background: Hypothyroidism is a common side effect found in patients with multidrug-resistant tuberculosis taking ethionamide. The mechanism of ethionamide-induced hypothyroidism is potentially caused by the structure of ethionamide compounds chemically similar to thioamide, such as propylthiouracil (C7H8N2S), which inhibits thyroid hormone synthesis. However, hypothyroidism is caused not only by a lack of production but also by signaling alteration. Thyroid hormone action is mediated by thyroid hormone receptors (TRs), members of the nuclear receptor superfamily that regulate their target genes. Unfortunately, there are limited studies on the potential interaction of ethionamide with TRs. Objective: In the present study, we want to elaborate on the potential interaction of ethionamide with TRs which might alter the thyroid hormone genomic regulation. Methods: Molecular docking studies were used to evaluate the potential interaction between ethionamide with TRα and TRβ. Results: The molecular docking results on TRα showed more than one hydrogen bond{\textendash}steric interaction formed from the ethionamide{\textendash}amino acid residue interaction. Ethionamide{\textendash}TRβ interaction showed more than one steric interaction, but the hydrogen bonds are not visualized. The docking score between ethionamide and TRα is -7.373 kcal/ mol and higher than its interaction with TRβ. Conclusion: These findings indicate that ethionamide can interact with TRα and TRβ. However, the ethionamide{\textendash}TRα interaction is stronger than ethionamide{\textendash}TRβ interaction. Our study reports a novel mechanism of action of ethionamide-induced hypothyroidism.

}, keywords = {Ethionamide, Hypothyroidism, Molecular docking, TRα, TRβ}, doi = {10.5530/pj.2021.13.150}, author = {Ronny Lesmana and Firyali Rahmani Shidqi and Hanna Goenawan and Iwan Setiawan and Marisca Evalina Gondokesumo and Farida Suhud and Nasrul Wathoni} } @article {1663, title = {Potential Neuroprotective Activity of Essential Oils in Memory and Learning Impairment}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1312-1322}, type = {Review article}, chapter = {1312}, abstract = {

Memory and learning is negatively affected by many factors. Alzheimer{\textquoteright}s disease is a progressive and irreversible neurological disorder that occurs gradually, a sickness that is increasingly common, and multiple scientific articles suggest that essential oils improve memory and learning and are useful in the treatment of various neurodegenerative diseases, including Alzheimer{\textquoteright}s disease. This review aims to conduct a critical collection of current information on research into both memory and learning impairment, as well as essential oils that are able to avoid this neurodegenerative disease. Currently, different animal models have been useful for the study of neurodegenerative problems that alter memory and learning, experimental pharmacological, genetic and toxicological models that can simulate specific cognitive deficit syndromes. In addition, research in this review show several essential oil compounds that present positive results in animal studies, but still lack human clinical trials. Therefore, the assessment of the safety and efficacy of these phytochemical compounds in diseases that cause memory impairment and learning, remain a promising area for future research.

}, keywords = {Alzheimer disease, Animal model, Essential oil, Learning, Memory, Neurodegenerative diseases}, doi = {10.5530/pj.2021.13.166}, author = {Carmen R. Silva-Correa and Jorge L. Campos-Reyna and V{\'\i}ctor E. Villarreal-La Torre and Abhel A. Calder{\'o}n-Pe{\~n}a and William Antonio Sag{\'a}stegui-Guarniz and Luz M. Guerrero-Espino and Anabel D Gonz{\'a}lez-Siccha and Cinthya L. Aspajo-Villalaz and Mar{\'\i}a V. Gonz{\'a}lez-Blas and Jos{\'e} L. Cruzado-Razco and Julio Hilario-Vargas} } @article {1428, title = {A Review of the Traditional Uses, Medicinal Properties and Phytochemistry of Centaurea benedicta L.}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {798-812}, type = {Review Article}, chapter = {798}, abstract = {

Centaurea benedicta L. is an annual herbaceous plant which belongs to the Asteraceae family. It is native to the Mediterranean region and western Asia and is commonly known as blessed thistle, holy thistle, St Benedict{\textquoteright}s thistle or spotted thistle. Traditionally, it has been used to treat bubonic plague and possesses diuretic, galactagogue, liver-strengthening and wound healing properties. Recent research studies have investigated its anticancer, antiinflammatory, antioxidant and other therapeutic properties. Several studies have also reported its antimicrobial activity against a range of bacterial pathogens. However, most of these studies were preliminary and only tested relatively high concentrations of the extracts. Additionally, most studies screened a limited number of pathogens. Cnicin is the main chemical compound present in C. benedicta and it has been widely investigated. However, few other compounds from this plant have been identified and/or investigated, and further phytochemical studies are warranted. Interestingly, pure cnicin has good anticancer activity, whilst the crude extracts lack cytotoxic properties. Phytochemical analyses of C. benedicta extracts reveal the presence of multiple flavonoids, tannins, terpenoids and lactones, although few specific phytochemicals within these phytochemical classes have been identified. A limited number of research studies have determined the toxicity profile of C. benedicta in order to evaluate its safety for human use. Substantially more detailed studies are required to rigorously investigate the therapeutic properties and phytochemistry of C. benedicta, which may ultimately lead to the development of new plant-based therapeutic medicines.

}, keywords = {Asteraceae, Blessed thistle, Flavonoids, St Benedict{\textquoteright}s thistle, Tannins, Terpenoids}, doi = {10.5530/pj.2021.13.102}, author = {Gagan Tiwana and Jiahe Fua and Lanping Lu and Matthew J Cheesman and IE.Cock} } @article {1635, title = {Total Phenol Content and Gastric Anti-Ulcer Activity of Hydroalcoholic Extract of Persea caerulea (Ruiz \& Pav.) Mez. Bark}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1072-1078}, type = {Original Article}, chapter = {1072}, abstract = {

Objective: Determine the content of total phenols and evaluate the gastroprotective effect of the extract of Persea caerulea (Ruiz \& Pav.) Mez. in mice with induced gastric ulcer. Material and Methods: The bark of Persea caerulea was macerated in 70\% ethanol and the phenol content was determined using the Folin-Ciocalteu method. The female Mus musculus Balb/c specimens were distributed in the following groups: White Control Group, without indomethacin dosing; Negative Control Group, dosing with indomethacin; Positive Control Group treated with ranitidine at a dose of 50 mg/kg; Groups P. caerulea treated with extract at doses of 50 mg/kg, 100 mg/kg and 200 mg/kg. Gastric ulcer was induced with indomethacin orally at a dose of 50 mg/kg, the procedure was repeated 12 hours later; Gastroprotective treatment was administered 60 minutes after each dose of indomethacin, 6 hours after the last dose, sodium pentobarbital was euthanized and the stomach was resected to determine ulceration using the Marhuenda Scale. Results: Higher percentages of gastric ulcer inhibition were obtained in the P. caerulea 100 mg/kg (80\%) and P. caerulea 200 mg/kg (85.71\%) groups. Conclusions: Extract of Persea caerulea (Ruiz \& Pav.) Mez., At doses of 100 and 200 mg/kg of body weight, has a gastric antiulcerative effect which is related to its content of total polyphenols.

}, keywords = {Gastric ulcer, Indomethacin, Mice}, doi = {10.5530/pj.2021.13.139}, author = {Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo-Villalaz and Carmen R. Silva-Correa and V{\'\i}ctor E. Villarreal-La Torre and Mar{\'\i}a V Gonz{\'a}lez-Blas and Orlando E Pretel-Sevillano and Marco L Salazar-Castillo and Maricielo Vaella-Alarc{\'o}n and Franco Huaccha-C{\'a}ceres and Jonatam Le{\'o}n-Soto and Whendy Alaya-Davir{\'a}n and Anabel D. Gonz{\'a}lez-Siccha and William Antonio Sag{\'a}stegui-Guarniz and Luz M. Guerrero-Espino and Julio Hilario-Vargas} } @article {1111, title = {Anticholesterol Activity of Okra Fruit Extract (Abelmoschus esculentus (L) Moench) and Its Nanoemulsion in vivo}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {316-320}, type = {Original Article}, chapter = {316}, abstract = {

Background: Okra fruit has phytosterol, pectin that has the potential as an anticholesterol. Objective: The purpose of this study was to obtain 70\% (v/v) ethanol extract of okra fruit and its nanoparticles and to evaluate their anti-cholesterol activity in vivo. Material and Methods: Okra fruit was extracted by kinetic maceration and the produced extract was tested for phytochemical screening and anti-cholesterolemi activity in vivo. The nanoparticles was prepared using a cosolvention method. In this study, DDY white mice was divided into 5 groups, namely normal control, negative control, positive control (simvastatin), the extract (400 mg /kg BW), and the nanoparticles (~ 400 mg /kg BW) group. All groups except normal were fed for 14 days with high cholesterol diet. After 14 days, the induction of hypercholesterolemia was stopped and simvastatin was administrated to positive control and the test groups were treated with the extract and the nanoparticles for 7 days. Measurement of total cholesterol level was carried out by cholesterol stripe test method. Results: The nanoparticles used demonstrated particle size of 134.7 nm and zeta potential of -26.72. The results showed a decrease in total cholesterol levels in positive control, the extract and the nanoparticles group as many as 48.68\%; 32.44\% and 42.95\%, respectively. Conclusion: The nanoparticles can increase the activity of the extract.

}, keywords = {Abelmoschus esculentus L. Moench, Hypercholesterolemia, Nanoparticles, Okra fruits, Total cholesterol level}, doi = {10.5530/pj.2020.12.50}, author = {Ratna Djamil and Deni Rahmat and Sarah Zaidan and Maya Nur latifah} } @article {1179, title = {Antidiabetic Activity with N-Hexane, Ethyl-Acetate and Ethanol Extract of Halodule uninervis Seagrass}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {805-808}, type = {Original Article}, chapter = {805}, abstract = {

The purpose of this research was to observe the antidiabetic activity from N-hexane, ethylacetate and ethanol extract of Halodule uninervis seagrass. The antidiabetic activity with extract concentrations of 125 ppm, 250 ppm, 500 ppm, 1000 ppm and 2000 ppm from seagrass extract with ethanol solvent showed that it had the ability as an anti-diabetic agent stronger than seagrass extract with n-hexane and ethyl acetate solvents. Calculation of IC50 of Halodule uninervis seagrass with ethanol extract was 74.99 ppm and ethyl acetate was 1,517,05 ppm. Glukobay as control was 0.27 ppm.

}, keywords = {Antidiabetic, Extract, Haludule uninervis, Seagrass}, doi = {10.5530/pj.2020.12.115}, author = {Ace Baehaki and Herpandi and Susi Lestari and Muhammad Hendri and Febri Ariska} } @article {1110, title = {Antidiabetic and Antioxidant Effect Combination Vasconcellea pubescens A.DC. and Momordica charantia L. Extract in Alloxan- Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {311-315}, type = {Original Article}, chapter = {311}, abstract = {

Introduction: Mountain papaya (Vasconcellea pubescens A.DC.) and bitter melon (Momordica charantia L.) fruit extract have total flavonoids and some metabolite from its contains. The use of a single dose in the treatment of diabetes is often considered to lack a strong effect. Giving a combination of the compound is a solution to provide a synergistic effect in treatment. Material and Methods: Rat were divided into eight groups (normal, negative control, glibenclamide as a positive control, and five dose extract group). The single dose mountain papaya extract (MPE) and bitter melon extract (BME) were given at 174 mg/kg b.w of MPE, and 380 mg/kg b.w of BME in oral administration. Combination of MPE:BME (25:75, 50:50, 75:25)\% or (87:190; 44:285 and 130:95) mg/kg b.w in oral administration. Induction of diabetes used alloxan dose of 150 mg/kg b.w intraperitoneally. The treatment was performed for 21 days with a frequency of once a day. Blood sugar level was measured at pretest, 7th, 14th, and 21st days. At the end of the test, measurements of malondialdehyde (MDA), glutathione (GSH), and pancreatic morphology were measured. Data were analyzed by ANOVA statistic. Results: The single and combination of MPE-BME showed an decrease in blood glucose levels significantly compared with the negative control (p <= 0.05). The same results from measurements of levels of malondialdehyde (MDA), glutathione (GSH), and pancreatic morphology. Conclusions: Based on the research, a combination of the MPE-BME had antidiabetic and antioxidant activity, but the activity was not significantly different from both single-dose extract (p\> 0.05).

}, keywords = {Antidiabetic, Antioxidant, Flavonoids, Momordica, Synergistic, Vasconcellea}, doi = {10.5530/pj.2020.12.49}, author = {Heru Sasongko and Ratih Guswinda Lestari and Adi Yugatama and Yeni Farida and Sugiyarto} } @article {1254, title = {Anti-inflammatory and Cytotoxic Effect of Arrow Root Mediated Selenium Nanoparticles}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1363-1367}, type = {Research Article}, chapter = {1363}, abstract = {

Nanoparticles serve to reduce toxicity, enhance bioactivity and improve targeting. Selenium nanoparticles (SeNPs) are explored because of it{\textquoteright}s unique characteristics and various known therapeutic benefits such as antioxidants activities and reducing risk of cancer. In this study, arrow root which is a starch obtained from tapioca or cassava is mediated with SeNPs and studied for it{\textquoteright}s anti-inflammatory and cytotoxic effect. The plant extract of arrow root was prepared and mixed with the sodium selenite solution. The solution is kept in a magnetic stirrer while being observed for any colour change. The synthesis of nanoparticles is observed using UV-vis spectrophotometry. Then the anti-inflammatory activity is observed using albumin denaturation assay and cytotoxic analysis conducted on brine shrimp nauplii. The results showed that there was a lower toxicity rate of SeNPs and significant anti-inflammatory activity which concludes that these nanoparticles can be used in various drug designing aspects in future.

}, keywords = {Anti-inflammatory, Brine shrimp, Green synthesis, Selenium nanoparticles}, doi = {10.5530/pj.2020.12.188}, author = {Twinkle Francis and S Rajeshkumar and Anita Roy and T Lakshmi} } @article {1089, title = {Antimicrobial Activity and Chemical Composition of Momordica Charantia: A Review}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {213-222}, type = {Review Article }, chapter = {213}, abstract = {

Momordica charantia L. (bitter melon) is a plant belonging to the Cucurbitaceae family and is widely distributed in tropical and subtropical areas around the world, mainly in Asia, India, China and Brazil, where it is traditionally used as a medicinal plant, and the fruits of some varieties of M. charantia are consumed as food. Studies have determined that this plant contains a great diversity of bioactive compounds with therapeutic potential like charantin, α-momorcharin and MAP30, and highlighting its properties as antidiabetic, antiulcer, antioxidant, antimicrobial, anthelmintic, antihyperglycemic and anticancer. Review shows the complete botanical description of the plant (fruits, leaves, stem, etc.), the bioactive chemical compounds reported in the plant species, the antimicrobial activity of the extracts or fractions of M. charantia, emphasizing the antibacterial and antifungal activities, with respective values of MIC (Minimum Inhibitory Concentration) reported according to the methodology used in each study. The review seeks to update the phytochemical and pharmacological knowledge of M. charantia, which would be useful for researchers in their search for new chemical compounds of the plant, studies of its safety and efficacy, as well as the evaluation of its possible synergistic action in combination with other antimicrobials, in order to find new therapeutic alternatives against bacterial resistance.

}, keywords = {Antibacterial, Antifungal, Charantin, Cucurbitaceae, Cucurbitane, Phytochemicals}, doi = {10.5530/pj.2020.12.32}, author = {V{\'\i}ctor Eduardo Villarreal-La Torre and William Sag{\'a}stegui Guarniz and Carmen Silva-Correa and Lizardo Cruzado- Razco and Ra{\'u}l Siche} } @article {1084, title = {Beautyberry (Callicarpa arborea) as an Antiparasitic Agent Against Raillietina echinobothrida, an Intestinal Tapeworm}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {66-70}, type = {Original Article}, chapter = {66}, abstract = {

Background: The beautyberry (Callicarpa arborea Roxb.) is member of the family Lamiaceae and is native to Asia. It is used in different traditional medicines for the treatment of debilitating ailments including cancer, dermatitis, diabetes mellitus, gastritis, helminthiasis, and pyrexia. A couple of pentacyclic triterpenes and phytosterols have been reported from this plant. Objective: We aimed to investigate the antiparasitic potentials of C. arborea bark extract. We used an intestinal tapeworm, Raillietina echinobothrida, for its convenience in handling and established nature as a model helminth parasite. Materials and Methods: The extract of the stem bark was prepared using methanol. Tapeworms were treated in vitro with varying concentrations of the extract. Survival values were statistically analysed. Treated tapeworms were fixed and processed for scanning electron microscopy. Results: C. arborea bark extract showed dose-dependent antiparasitic similar to that of albendazole. Scanning electron microscopy revealed damaging effects all over the body of the tapeworm. There was general shrinkage of the tegument on the scolex, neck region and strobila. Microtriches were completely removed throughout the tegument. Suckers and rostellum on the scolex were also deformed. Conclusion: Our data shows that C. arborea is a promising source of antiparasitic principles.

}, keywords = {Callicarpa arborea, Scanning electron microscopy, Tapeworm, Tegument}, doi = {10.5530/pj.2020.12.11}, author = {P.B. Lalthanpuii and Kholhring Lalchhandama} } @article {1193, title = {Capsaicin Bioactive in Cabai (Capsicum Annum L.) as Anticancer Through Inhibition of over Ekspresi Protein Target RAC-alpha serine/threonine-protein kinase (AKT1) and Mitogen-activated protein kinase 1 (MAPK1) on Hepatocyt Cell Mice (mus musculus)}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {911-915}, type = {Research Article}, chapter = {911}, abstract = {

Capsaicin is a secondary metabolite of the Chilean plant. In the pharmaceutical field in addition to relieving pain or pain, capsaicin is also known to have anticancer activity because it inhibits certain oncogenic proteins. Screening of components in Capsicum Annum L. against the target proteins AKT1 and MAPK1 is needed as an initial stage of drug discovery. Further screening of Capsaicin compounds for oncogenic proteins produced in Hepatocellular carcinoma (HCC) pathogenesis signaling. In silico data that have been obtained, Capsaicin in chili (Capsicum Annum L.) has a high affinity for MAPK1 and AKT1 receptor/protein targets with energy and potential activity score (Pa) 0.690 for preneoplastic treatment, 0.590 for apoptotic agonists, and 0.366 for antineoplastic activity. Statistical data using Kruskal Wallis obtained information that Capsaicin can inhibit the expression of AKT 1 and MAPK 1 on mice hepatocyte cells induced by AFB1 in vivo administration, therefore it can be a candidate for anticancer drugs.

}, keywords = {AKT1, Anticancer, Capsaicin, Hepatocellular carcinoma (HCC), MAPK1}, doi = {10.5530/pj.2020.12.129}, author = {Mohammad Sukmanadi and Sri Agus Sudjarwo and Mustofa Helmi Effendi and Pudji Srianto and Aulanni{\textquoteright}am and Rr Sri Pantja Madyawati and Mirni Lamid and Hani Plumeriastuti} } @article {1231, title = {Cytotoxicity of Lactobacillus plantarum KK518 Isolated from Pak-Sian Dong (Thai Fermented Gynandropsis pentaphylla DC.) Against HepG2, MCF-7 and HeLa Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1050-1057}, type = {Original Article}, chapter = {1050}, abstract = {

Background: Pak-Sian Dong is a fermented vegetable product of Thailand prepared from aerial parts of Pak-Sian (Gynandropsis pentaphylla DC.). Lactobacillus plantarum KK518 was isolated from Pak-Sian Dong and already assessed for its probiotic attributes. Objective: The aim of this work was to determine the untapped cytotoxic effects of L. plantarum KK518 extract against HepG2 (liver cancer), MCF-7 (breast cancer) and HeLa (cervical cancer) cells. Materials and Methods: The bacterial extracts were prepared from whole cultures; containing cells and broths using ethyl acetate as extracting solvent and the dried extracts were redissolved in ethanol before use. Cytotoxic, antiproliferative and antimigratory effects of the bacterial extracts on three types of cancer cells were determined using 3-(4,5-dimethylthiazolyl-2)-2, 5-diphenyltetra zolium bromide (MTT) assay, clonogenic formation and wound healing assays, respectively. Results: L. plantarum KK518 extract showed the highest cytotoxicity at 90.88\% at 1,000 μg/mL against HeLa cells (IC50 of 371.97 μg/mL) over 48 h of exposure. Anti-colony formation test showed that the bacterial extracts at 600, 800 and 1,000 μg/mL over 48 h led to a complete inhibition of colony formation of HeLa cells; however the highest IC50 of 418.52 μg/mL was found in HepG2 cells suggesting that HepG2 was least affected by bacterial extract. Likewise, HepG2 cells seemed to be most resistant to antimigratory effects as observed by highest relative area of the wound at most time intervals and most extract concentrations. Conclusion: L. plantarum KK518 offers a potential use as a bio-therapeutic with chemopreventive effects against cervical, breast and liver cancers.

}, keywords = {HeLa, HepG2, L. plantarum KK518, MCF-7, Pak-Sian-Dong}, doi = {10.5530/pj.2020.12.148}, author = {Vijitra Luang-In and Worachot Saengha and Benjaporn Buranrat and Sutisa Nudmamud-Thanoi and Arjan Narbad and Supaporn Pumriw and Wannee Samappito} } @article {1163, title = {Cytotoxicity of Selenium-Enriched Chinese Kale (Brassica oleracea var. alboglabra L.) Seedlings Against Caco-2, MCF-7 and HepG2 Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {674-681}, type = {Original Article}, chapter = {674}, abstract = {

Background: The Selenium-enriched Chinese kale (Brassica oleracea var. alboglabra L.) seedlings (Se-KS) have been known for its antioxidant activities, however its cytotoxic effects on various cancer cells are yet to be reported. Objective: The objective of this work was to study the cytotoxic effects of Se-KS on Caco-2, MCF-7 and HepG2 cancer cells. Materials and Methods: Freeze-dried seedlings were ground and incubated in 0.1 M citrate phosphate buffer pH 7.0 for 1 h at 37{\textdegree}C and extracted with dichloromethane to obtain total isothiocyanate (ITC) content which was quantified using the 1,2-benzenedithiole (BDT)-based cyclocondensation assay. The extracts from fresh seedlings were used to determine the cytotoxic effect on Caco- 2, MCF-7 and HepG2 cancer cells. Results: Se-KS was found to contain total ITC content at 1.02 mmol/100 g dry weight (DW) which was significantly lower than that of 7-day old broccoli microgreens (1.60 mmol/100 g DW) as reference Cruciferous vegetables. In addition, Se-KS extract exhibited cytotoxic effects in a dose- and time-dependent manners. The lowest IC50 value of 82.83 μg/mL at 72 h was derived from HepG2 cells and the highest IC50 value of 164.00 μg/mL at 72 h was from MCF-7 cells suggesting that the Se-KS extract was most effective against HepG2 cells. Cancer cells showed signs of apoptotic bodies over 72 h and DNA fragmentations at 24 h indicating that the Se-KS extract was able to induce apoptosis in cancer cells in addition to cytotoxic effect. Conclusion: Thus, Se-KS could be a novel source of organo selenium with chemopreventive benefits for functional food development.

}, keywords = {Caco-2, HepG2, Isothiocyanate, Kale, MCF-7, Selenium}, doi = {10.5530/pj.2020.12.99}, author = {Vijitra Luang-In and Worachot Saengha and Benjaporn Buranrat and Anut Chantiratikul and Nyuk Ling Ma} } @article {1192, title = {The Development of Phyllanthus emblica Extract in Ethosomes for Hair Loss Prevention}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {905-910}, type = {Research Article}, chapter = {905}, abstract = {

Background: Hair loss is not a serious health problem but leads to decreased self- confidence, personality, and psychological problems. According to Thai traditional medical wisdom, Phyllanthus emblica has the property to prevent hair loss. Ethosomes are a drug delivery system, which can increase drug delivery to deep skin layers and enhance the effectiveness of the active ingredient. Objective: This research aims to develop ethosomes of Phyllanthus emblica extract with beneficial properties. Materials and Methods: Phyllanthus emblica was extracted by a maceration method with 95\% ethanol as a solvent. The total phenolic content of the extracts was determined using the Folin-Ciocalteu method. The antioxidation activity was evaluated by DPPH assay. Ethosomes were formulated by a cold method and their properties were observed. Results: The results showed that the total phenolic content of Phyllanthus emblica extract was 406.37{\textpm}2.39 mg GAE/g extract. The IC50 of antioxidant activity was 7.05{\textpm}0.17 μg/ml. Ethosomes with 0.03\% of Phyllanthus emblica extract, 2\% of soya phosphatidylcholine, and 20\% of ethanol had the highest percentage of entrapment efficiency (65.26\%{\textpm}1.80\%). The ethosomes of Phyllanthus emblica extract was the spherical shape and white colloid. The particle size, polydispersity index, zeta potential, and pH of ethosomes were 0.43{\textpm}0.00 μm, 0.44{\textpm}0.03, -10.40{\textpm}0.28 mV, and 4.06{\textpm}0.03, respectively. Conclusion: The ethosomes of Phyllanthus emblica extract had good properties and area possible alternative product for hair loss prevention.

}, keywords = {Entrapment efficiency, Ethosomes, Phyllanthus emblica}, doi = {10.5530/pj.2020.12.128}, author = {Pornpun Laovachirasuwan and Wutthichart Fuangbangluang and Atchariyaporn Phanichanaphan and Issarapong Nasomroop and Methin Phadungkit} } @article {1169, title = {An Endangered Medicinal Plant, Ilex khasiana Exhibits Potent Antiparasitic Activity Against Intestinal Tapeworm}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {725-730}, type = {Original Article}, chapter = {725}, abstract = {

Background: A species of holly, Ilex khasiana Purk. (family Aquifoliaceae) is one of a few critically endangered medicinal plants in India. It is endemic to Khasi Hills, Meghalaya, and Aizawl, Mizoram. In the traditional medicines of Khasi and Mizo people, the leaves are used as a panacea for all sorts of infections. Nothing is known about its true pharmacological potentials. Objective: We aimed to assess the extract of I. khasiana leaves for its purported antiparasitic property. To test the antiparasitic activity, we collected intestinal tapeworms, Raillietina tetragona. Materials and Methods: I. khasiana leaves were dried and extracted in methanol. The plant extract was used to treat the tapeworms at different concentrations. The efficacy was recorded as survival values and were analysed by Student{\textquoteright}s t-test. The plant extracttreated tapeworms were fixed, dehydrated and observed under scanning electron microscopy for studying the structural details. Results: The methanol extract of I. khasiana leaf showed dose-dependent antiparasitic effect as that of albendazole. The treated tapeworms developed massive structural damages. The scolex was deformed, with its tegument extensively damaged. The suckers had their spines clumped. The body segments severely contracted and some portions were eroded. Hair-like microtriches were completely lost. Conclusion: Our findings indicate that I. khasiana has antiparasitic activity and requires further investigations, and that there is a need to foster its conservation and propagation.

}, keywords = {Medicinal plant, Parasite, Scanning electron microscopy, Tapeworm, Tegument}, doi = {10.5530/pj.2020.12.105}, author = {Charles Lalnunfela and PB Lalthanpuii and TC Lalhriatpuii and K Lalchhandama} } @article {1227, title = {Green Algae Halimeda macroloba in Spermonde Archipelago: Phytochemical and in vitro Antibacterial Studies}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1000-1004}, type = {Original Article}, chapter = {1000}, abstract = {

Background: Green algae Halimeda macroloba compounds active against human, fish, and shrimp pathogenic bacteria. It is one of the marine natural organisms (MNO) which is a diverse source of secondary metabolites. Objective: We have set our goal towards determining the antimicrobial potential of crude extracts of green algae H. macroloba. Materials and Methods: Three crude mixtures of Marine Natural Product (MNP) were obtained from macroalgae Halimeda macroloba (Lae-Lae island, Spermonde Archipelago) by extraction (n-hexane, ethyl acetate, and methanol were used as solvents). Results: Theses mixtures (phytochemical tests showed they contained steroids, terpenoids, and alkaloids) were screened for their activity against shrimp pathogenic bacteria (Vibrio harveyi (M-120), Aeromonas hydrophilla\ and Vibrio parahaemolyticus (T-170)). The obtained results confirmed weak antibacterial activity of studied extracts of H. macroloba. The ethyl acetate extract was the most potent antimicrobial agent at a concentration of 4 μg/25 μl. The inhibition zones for the growth of A. hydrophilla (the most susceptible microorganism) and V. harveyi were at 8.27 mm and 8.23 mm, respectively (inhibition zone was 15.2 mm for ciprofloxacin which was used as a positive control). Conclusion: They might be even used in the future as alternatives to conventional drugs in aquaculture.

}, keywords = {Antibacterial activity, Halimeda macroloba, Phytochemical screening, Shrimp Pathogenic Bacteria}, doi = {10.5530/pj.2020.12.141}, author = {Lulu Adilla Latifah and Nunuk Hariani Soekamto and Akbar Tahir} } @article {1229, title = {Hepatoprotective and Nephroprotective Activity of Artemisia absinthium L. on Diclofenac-induced Toxicity in Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1032-1041}, type = {Original Article}, chapter = {1032}, abstract = {

Background: Artemisia absinthium L. is known for its antimalarial activity however, hepatoprotective activity of aqueous extracts has also been reported but, nephroprotective activity not yet evaluated. Objective: To evaluate the hepatoprotective and nephroprotective activities of A. absinthium against diclofenac-induced toxicity on rats. Materials and Methods: Three different doses of methanol and ethyl acetate extract of A. absinthium (50, 100 and 200 mg/kg/day) were evaluated and compared with silymarin 100 mg/kg. Rats received these doses for 5 days and on the 3rd and 4th day diclofenac (50 mg/kg i.p.) was administered 1 h after treatment. Animals were sacrificed 48 h after the last injection of diclofenac. Biochemical blood parameters like aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), urea and creatinine, and histopathologic changes of liver and kidney were studied and evaluated. Results: A. absinthium reduced the elevated blood levels of ALT, AST, ALP, urea and creatinine with the methanol extract to 200 mg/kg/day being more effective. The histopathologic evaluation suggested that A. absinthium decreased hepatic and renal necrosis induced by diclofenac. Conclusions: Hepatoprotective and nephroprotective activities of methanol and ethyl acetate extract of A. absinthium were demonstrated, being methanol extract to 200 mg/kg/day the most effective. This provides scientific support for the use of medicinal plants such as A. absinthium in the treatment of liver and kidney disorders.

}, keywords = {Artemisia absinthium, Biochemical parameters, Diclofenac, Hepatoprotective, Histopathology, Nephroprotective}, doi = {10.5530/pj.2020.12.146}, author = {Sag{\'a}stegui-Guarniz William Antonio and Silva-Correa Carmen R and Villarreal-La Torre V{\'\i}ctor E and Cruzado-Razco Jos{\'e} L and Calder{\'o}n-Pe{\~n}a Abhel A and Aspajo-Villalaz Cinthya L and Gamarra-S{\'a}nchez C{\'e}sar D and Ruiz-Reyes Segundo G and Ch{\'a}vez-Flores Juana E} } @article {1178, title = {Human Umbilical Cord Blood-derived Secretome Enhance Endothelial Progenitor Cells Migration on Hyperglycemic Conditions}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {793-797}, type = {Original Article}, chapter = {793}, abstract = {

Hyperglycemia state is harmful to body{\textquoteright}s homeostasis. Uncontrolled hyperglycemic patients, especially patients with diabetes mellitus have a higher mortality risk of heart disease 2 to 4 times compared to non-hyperglycemic patients. Vascular endothelial impairment always been observed and found as a key feature of hyperglycemia state, which is correlated with reduced numbers and dysfunction of endothelial progenitor cells (EPCs). Objective: This paper aims to investigate the effect of hUCB-MSCs derived secretome treatment on the EPCs migration under hyperglycemia state. Materials and Methods: EPCs were isolated and cultured from peripheral blood samples and cultured for three days. Cultured EPCs were cultivated in 6-well plates until confluence and incubated with high glucose for 5 days, then placed in the modified Boyden chamber at the upper chamber with basal media. The lower chamber was supplemented with basal media and secretome at 2\%, 10\%, and 20\% concentration and VEGF treated group as a control. EPCS migration was evaluated using a Boyden chamber assay. Statistical analysis was performed using SPS 25.0. Results: EPCs migration were significantly higher when hUCB-MSCs-derived secretome was given in high glucose concentrations compared to the and control group (79.80 {\textpm} 5.07 vs 51.00 {\textpm} 5.15, p\<0.000). This study also showed that hUCB-MSCs-derived secretome increase EPCs migration under high glucose concentrations in a dose-dependent manner (p\<0.05). Conclusion: hUCB-MSCsderived secretome enhances EPCs migration under hyperglycemic state. This result may be of relevance for cell-free and regenerative therapeutic modality for a diabetic patient with coronary artery disease (CAD).

}, keywords = {Endothelial progenitor cells, Hyperglycemia state, Mesenchymal stem cells, Migration, Secretome}, doi = {10.5530/pj.2020.12.113}, author = {Yudi Her Oktaviono and Melly Susanti and Achmad Lefi and Ferry Sandra} } @article {1291, title = {Lutein: A Comprehensive Review on its Chemical, Biological Activities and Therapeutic Potentials}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1769-1778}, type = {Review Article}, chapter = {1769}, abstract = {

Background: Lutein is a naturally occurring carotenoid found in high amounts in flowers, grains, fruits and green vegetables with green leaves include spinach, kale and carrots. The market for lutein encompasses pharmaceutical, dietary supplement, food, animal and fish feed industries. Objective: The present review aimed to provide an updated and comprehensive analysis of lutein, including its chemistry, biological properties and therapeutic potentials. Methods: Relevant literatures were collected from several scientific databases, include Google Scholar, Pubmed and ScienceDirect between 2000 to till date. Following a detailed inclusion and exclusion screening process, the information obtained was summarized. Results: Information on the sources, chemistry and biological properties including antioxidant, anti-arthrisits, antiinflammatory, hepatoprotective, cardioprotective, anti-cataract, antidiabetic, anticancer and bone remodelling activities, as well as food industry processing for lutein were tabled. Lutein can be considered powerful antioxidants along with multifaceted molecular targets, such as NF-ҡB, PI3K/Akt, Nrf-2, HO-1 and SIRT-1 signaling pathways in various pathological conditions. Conclusion: The present review observe the chemical, pharmacological properties, in addition to the therapeutic potentials of lutein. It is hoped that the information can provide a good reference to aid in the development and utilization of lutein in phytopharmaceuticals and food industries.

}, keywords = {Antioxidant, Inflammatory cytokines, Lutein, Molecular targets, Pharmacology, Transcription factors}, doi = {10.5530/pj.2020.12.239}, author = {Nurul Iman Nurul Fuad and Mahendran Sekar and Siew Hua Gan and Pei Teng Lum and Jaishree Vaijanathappa and Subban Ravi} } @article {1168, title = {Microencapsulation of Macaranga gigantea Leaf Extracts: Production and Characterization}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {716-724}, type = {Original Article}, chapter = {716}, abstract = {

Introduction: The aim of this research was to formulate the microcapsules of Macaranga gigantea leaves extract with solvent evaporation method using Ethocel 10 cP and Eudragit E100 as matrix. Methods: M. gigantea leaves were extracted using ethanol 96\%. This extract was dried by rotary evaporator. The microencapsulation process of M. gigantea leaves extract was conducted by solvent evaporation method (O/W: oil in water). The formula of M. gigantea leaves extract microcapsules were designed into six formulas (Eudragit E100: FA1, FA2, FA3 and Ethocel 10 cP: FB1, FB2, FB3). Microcapsules of M. gigantea leaves extract were characterized for particle size, in terms of surface morphology by scanning electron microscope (SEM) and encapsulation efficiency. Antioxidant activity of the formulation have been evaluated by DPPH method. Physical characterization on microparticles were performed by conducting entrapment efficiency and SEM picture. Results: In this research, the micoparticles containing M. gigantea extract has been developed by using ethyl cellulose (Ethocel 10 cP ) and eudragit (Eudragit E100) as polymer matrix. The results showed that high concentration of polymer (Ethocel 10 cP and Eudragit E100) used in microencapsulation resulted in better M. gigantea leaves extract microcapsules in terms of physical characteristics. Particle size of microcapsules containing M. gigantea leaves extract were in the range of 3.564 to 5.887 μm. Encapsulation efficiency (\% EE) was categorized as good because the value were >= 80\% to which 85.978\% (FA3) and 88.992\% (FB3). SEM picture of FA3 (Eudragit E100) revealed that the surface of microcapsule were rough and porous. When Ethocel 10 cP used as polymer, a smoother surface and less visible pores of microcapsule were obtained. The antioxidant ability of M. gigantea leaves extract microcapsule showed that IC50 values was 64.51 ppm. Conclusion: It can be concluded that microcapsules of M. gigantea leaves extract can be prepared by solvent evaporation method by using Eudragit E100 and Ethocel 10 cP as polymer matrix. M. gigantea leaves has potent antioxidant activity either as extract or after formulated into microcapsules.

}, keywords = {Antioxidant, Ethocel 10 cP, Eudragit E100, Macaranga gigantea, Microencapsulation, Solvent evaporation method}, doi = {10.5530/pj.2020.12.104}, author = {Muhaimin Muhaimin and Yusnaidar Yusnaidar and Wilda Syahri and Madyawati Latief and Anis Yohana Chaerunisaa} } @article {1197, title = {Molecules of Interest {\textendash} Karanjin {\textendash} A Review}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {938-945}, type = {Review Article}, chapter = {938}, abstract = {

Background: At the present time, several plants are largely contributing to the medical field due to its valuable use. Scientific evidence generated with their special inherent compounds gave more confidence to the scientific community. Pongamia pinnata (Linn.) is an Indian native plant and well exploited in Ayurvedic medicinal system. Concurrently, a few pieces of scientific research have been done to prove the therapeutic activity of this medicinal plant. The medicinal properties of this plant are most likely due to its principal active compound, karanjin. As a molecule of interest, karanjin is an antioxidant and also exerts other biological benefits. Karanjin has also been recognized to be used in agricultural and environmental management other than medicinal purposes. Objectives: This review aimed to provide a brief information on the chemical and biological properties of karanjin along with its traditional uses. It is also discusses the scientific evidences available for its various biological properties. Materials and Methods: Various databases such as Google, Google Scholar Scopus, Web of Science, Pubmed had been searched and the data was obtained. Results: The chemistry and reported biological properties of karanjin were highlighted. Karanjin revealed antidiabetic, anticancer, antioxidant, gastroprotective, anti-inflammatory, antibacterial and anti-Alzheimer{\textquoteright}s activities, and thus has several possible applications in clinical research. Conclusion: Therefore, further research may help in exploiting its properties and emergent phytopharmaceuticals based on it.

}, keywords = {Chemistry, Flavonoid, Karanja, Karanjin, Pharmacology, Pongam oil tree, Pongamia pinnata}, doi = {10.5530/pj.2020.12.133}, author = {Aina Akmal Mohd Noor and Siti Nurul Najiha Othman and Pei Teng Lum and Shankar Mani and Mohd Farooq Shaikh and Mahendran Sekar} } @article {1185, title = {The Nephroprotective And Antioxidant Activity of Sterculia rubiginosa Zoll. Ex Miq. Leaves}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {843-849}, type = {Research Article}, chapter = {843}, abstract = {

Background: Sterculia has an antioxidant activity. The Sterculia genus has phenols and flavonoids content, and this chemical content may be have an nephroprotective activity. Objective: The study was to investigate the in vitro study of antioxidant activity with DPPH and FRAP study and nephroprotective activity of Sterculia rubiginosa Zoll. Ex Miq. Leaves extract. Materials and Methods: The leaves was extracted using ethanol. This extract was determined for antioxidant activity by in vitro study with DPPH and FRAP methods, determined the content of total phenols, total flavonoids, and also identification of chemical content. Nephrotoxicity study done by induced gentamycin. The groups divided 6 group, consist: negative control, positive control, normal control, and the extract with dose 50 mg/kg, 100 mg/kg, and 200 mg/ kg. The parameter for nephroprotective activity was tubular necrosis, the presence of tubules casts and glomerular damage, creatinine serum, and urea. Results: The ethanol extract has IC50 162.34 μg/ml for DPPH scavenging activity and 18.65 {\textpm} 3.53 FeEAC (Mol/g) for FRAP. The secondary metabolite presence flavonoids, tannins, terpenes, alkaloids, and glycosides. The total phenols 462.36 {\textpm} 9.23 mg GAE/gr, total flavonoids content 59.44 {\textpm} 0.11 mg QE/gr extract. All the dose have an nephroprotective activity, but the best dose was 50 mg/kg. Conclusion: The ethanol extract of Sterculia rubiginosa showed antioxidant activity and nephroprotective activity.

}, keywords = {Antioxidant, Gentamicin, Nephroprotective, Sterculia rubiginosa Zoll Ex. Miq.}, doi = {10.5530/pj.2020.12.121}, author = {Rini Prastiwi and Ema Dewanti and Inka Nurul Fadliani and Nessa Aqilla and Salwaa Salsabila and Vera Ladeska} } @article {1299, title = {A Perspective Overview on Hygrophila auriculata}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1748-1752}, type = {Review Article}, chapter = {1748}, abstract = {

Hygrophila auriculata, belonging to the family Acanthaceae, is a promising medicinal plant with great economic potential. The medicinal value of H. auriculata has been appreciated in the ancient medical literature. The plant contains terpenoids, alkaloids, flavonoids, and is traditionally known as an aphrodisiac, renal tonic, and for its health-promoting properties. The plant is cultivated throughout India. However, systematic information on the different aspects of this species is not available. In this review, an attempt has been made to present this information.

}, keywords = {Hygrophila auriculata, Pharmacological activity, Phytochemistry}, doi = {10.5530/pj.2020.12.237}, author = {S Dhanalakshmi and N Harikrishnan and N Srinivasan and P Pandian and BA Tanisha and M Tharun Kumar and V Lokesh and N Yuvashri and S Supriya} } @article {1120, title = {Phenolic Compounds from Caesalpinia sappan}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {410-414}, type = {Research Article}, chapter = {410}, abstract = {

Introduction: Caesalpinia sappan L., a traditional ingredient of food and beverages in South East Asia, was investigated for its chemical constituents. Methods: The compounds were isolated by column chromatography and their chemical structures were elucidated by NMR spectroscopy and confirmed by comparison of their NMR data with literature data. Results: Repeated column chromatography of the EtOAc-soluble fraction from the heartwood of C. sappan resulted in the isolation of sappanchalcone (1), caesalpiniaphenol G (2), and quercetin (3). Conclusion: Three phenolic compounds have been successfully isolated from C. sappan.

}, keywords = {Analgesic, Caesalpinia sappan, Caesalpiniaceae, Homoisoflavonoids}, doi = {10.5530/pj.2020.12.63}, author = {Van Ba Nguyen and Binh Duong Vu and Gia Khanh Pham and Bach Quang Le and Van Chuyen Nguyen and Chu Van Men and Van Thu Nguyen} } @article {1071, title = {Potential of Hard Candy Containing Spray-Dried Vernonia cinerea Extract with Total Phenolic Compounds, Total Flavonoids and Nicotine Replacement as an Anti-Smoking Aid}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {35-43}, type = {Original Article}, chapter = {35}, abstract = {

Backgound: Vernonia cinerea (VC) is a natural plant claimed to reduce cigarette smoking. Some pilot anti-smoking products with nicotine replacement, such as lozenges or gum, have been presented, but with some adverse effects. Thus, application of VC as a new-anti-smoking product is very challenging. Objectives: The aims of this study were to compare the active compounds; total phenolic compounds, total flavonoids and nicotine, and study antioxidant activity on scavenging 2,2{\textquoteright}-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) and 1,1-diphenyl-2-picryl hydrzayl (DPPH) radicals of extracts prepared by spray drying (SD) and freeze drying (FD) techniques for pilot hard candy. Methods: Raw VC materials of mixed parts, i.e., the stem, flowers and leaves, were made to form extracts by FD and SD techniques. Then, extract from the SD technique was manufactured industrially into hard candy containing glucose syrup and refined glucose. Total phenolic compounds, total flavonoids, nicotine, scavenging activity of extracts, VC hard candy and placebo candy were evaluated by folin-ciocalteau reagent, aluminum chloride colorimetric assay, high-performance liquid chromatography, ABTS cation decolorization and DPPH protocols. Results: Total phenolic compounds were significantly different between extracts, but total flavonoids and nicotine were slightly higher in SD extract. Antioxidant activity of both extracts on ABTS radicals was not significantly different, but the half-maximal inhibitory concentration (IC50) on DPPH radicals was significantly higher in SD extract when compared to the FD extract. Finally, total phenolic compounds, total flavonoids and nicotine, as well as scavenging activity could be detected in hard candy. Conclusion: VC can be used as an anti-smoking aid with nicotine replacement and anti-oxidant compounds in pilot hard candy.

}, keywords = {antioxidant activity, Hard candy, Nicotine, Total flavonoids, Total phenolic compounds, Vernonia cinerea}, doi = {10.5530/pj.2020.12.7}, author = {Rungtiwa Kanthain and Supawatchara Singhatong and Surapol Natakankitkul and Nathupakorn Dechsupa and Jirakrit Leelarungrayub} } @article {1211, title = {Protective Effect of Natural Products against Chemotherapy-Induced Cardiotoxicity: A Review}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1180-1189}, type = {Review Article}, chapter = {1180}, abstract = {

Background: Cancer is one of the diseases with high mortality rate recorded each year across the world. Its mainstay treatment is chemotherapy although they are largely toxic, causing severe adverse reactions including cardiotoxicity, nephrotoxicity and genotoxicity. Cardiotoxicity is unique to certain chemotherapeutic agents and occur via several mechanisms. It has been hypothesized that co-administration of natural products which may be cardioprotectant, together with chemotherapy can alleviate cardiotoxicity-induced by chemotherapy. Objectives: This review aimed to provide a brief information about the protective effect of natural products against chemotherapy-induced cardiotoxicity Methods: To complete this review, relevant literatures were searched from several scientific databases including Google, Google Scholar, Scopus, Web of Science and Pubmed. Results: In this paper, we have reviewed ten natural products (curcumin, mangiferin, naringenin, quercetin, 6-gingerol, lycopene, resveratrol, apigenin, proanthocyanidins and indole-3-carbinol), which have major influences in attenuating chemotherapy-drug induced cardiotoxicity. Apart from the cardioprotective effects, they tend to confer some synergistic effects with chemotherapeutic agents and therefore have the potential to be used as an adjunct. Conclusion: Though a panel of natural products demonstrate protective effects against cardiotoxicity in cells and animal models, their therapeutic potentials for clinical needs further investigation.

}, keywords = {Anticancer drugs, Cardioprotective, Cardiotoxicity, Chemotherapy, Natural products}, doi = {10.5530/pj.2020.12.166}, author = {Siti Nurul Najiha Othman and Pei Teng Lum and Siew Hua Gan and Shankar Mani and Mahendran Sekar} } @article {1228, title = {Prototype Star Fruit-Honey Product and Effectiveness on Antixidants, Inflammation and Walking Distance in Participants with Stable Chronic Obstructive Pulmonary Disease (COPD)}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1121-1134}, type = {Research Article}, chapter = {1121}, abstract = {

Background: Star fruit (Averrhoa carambola L.) is a seasonal fruit, which has proven antioxidant and inflammation activities in vitro. However, sweet-type is more available than sour-type. Therefore, developing a new product from sweet-type star fruit, and evaluating its effectiveness on antioxidants and inflammation have been very challenging. Objectives: The aims were to develop a prototype product from sweet-type star fruit and evaluate its effectiveness with or without walking exercise on participants with stable chronic obstructive pulmonary disease (COPD). Methods: The prototype product of sweet-type star fruit was prepared industrially by mixing with honey before nutrients such as L-ascorbic acid (Vit C) and total phenolic compound, and contaminants like chemicals, microbials and oxalic acid were evaluated. Effectiveness of this product on antioxidents, inflammation and physical function was evaluated in participants with stable COPD with and without walking exercise, and compared to walking exercise and control participants. Two spoons of the product (20 g) in sterile warm water (150 mL) were guided and consumed twice daily for 4 weeks, whereas the walking exercise was prescribed with moderate intensity at home for 30 min 3 days per week. Plasma Vit C, total antioxidant capacity (TAC), malondialdehyde (MDA), tumor necrotic factoralpha (TNF-∝) and 6-minutes walking distance (6MWD) were evaluated before and after the 4-week study period. Results: The prototype product composed of star fruit juice with honey (1:1, v:v). Main nutrients were composed of ash (0.4 g), carbohydrate (74.59 g), lipid (2.88 g), protein (0.57 g) and 326.56 kcal of total energy, whereas Vit C and total phenolic compound were equivalent to 0.25 {\textpm} 0.11 mg and 144.89 {\textpm} 2.51 μg gallic acid equivalent in a 100 gram of product. The results of chemicals and microbials showed safety under food conditions. The results of study compared the ages of stable COPD participants between those of the controls (n=10, 69.20{\textpm}1.40 years), and those with star fruit juice and honey supplement (n=20, 71.25 {\textpm} 6.01 years), walking exercise (n=15, 60.60{\textpm}3.38 years), and supplement with walking exercise (n=15, 64.40{\textpm}1.63 years) and no statistical difference was shown in any parameters in the control group. Whereas, the plasma Vit C and TAC levels increased, and MDA and TNF-∝ levels reduced significantly, in the supplement consumption group, which was in contrast to the Vit C, MDA and TNF-∝ levels in the walking exercise group. However, the TAC level increased significantly when the walking exercise was completed. When the prototype product was applied to the walking exercise, the levels of Vit C and TAC increased, and MDA and TNF-∝ levels reduced significantly. Whereas, the supplement levels increased significantly in all of the groups, especially in the 6MWD. Conclusion: This study proposed that sweet-type star fruit can be prepared industrially by mixing with honey, and be developed as a new commercial product with antioxidant and inflammation activities for participants suffering with chronic lung disease.

}, keywords = {6MWD, Antioxidant, COPD, Oxidative stress, Star fruit product, TNF-∝}, doi = {10.5530/pj.2020.12.159}, author = {Yothin Pothasak and Jirakrit Leelarungrayub and Surapol Natakankitkul and Supawatchara Singhatong} } @article {1076, title = {Qualitative and Quantitative Assay of Hydroxycinnamates of Prunus spinosa L.}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {157-161}, type = {Research Article}, chapter = {157}, abstract = {

Background: Blackthorn (Prunus spinosa L.) is a plant commonly found in the Russian Federation on the roadsides, forest margins, and meadows. Despite lack of recognition by the official medicine, blackthorn fruits possess antioxidant properties and are used in homeopathic preparations. They may also demonstrate antibacterial and anticancer potential due to hydroxycinnamic acids. The aim of present study was to identify and assay hydroxycinnamates in fruits of P. spinosa cultivated in Moscow Region. Materials and Methods: Fresh and dried fruits of P. spinosa, gathered from plants cultivated in Moscow Region in the harvest maturity stage, were used in the study. Qualitative composition of hydroxycinnamic acids was assessed by high performance liquid chromatography, using reversed phase C18 column. Total hydroxycinnamic acids (THA) content was assessed spectrophotometrically. Results: Similar chromatographic profiles were obtained for both fresh and dried blackthorn fruits, the two most abundant compounds being epicatechin (2.91\%) and chicoric acid (2.90\%). Fruits gathered in Chekhovsky District had lower content of hydroxycinnamates (0.798 {\textpm} 0.89) than those coming from Klinsky District (0.886 {\textpm} 0.92). However, the THA content in dried fruits grown in both districts was found to be similar (0.540 {\textpm} 0.71 and 0.557 {\textpm} 0.74, respectively). Conclusions: It can be concluded that blackthorn fruits can be considered as a source of hydroxycinnamic acids, as both fresh and dried fruits contain at least eleven hydroxycinnamates. It was found that the dried fruits have similar content of hydroxycinnamic acids, independently of their origin. Future research should be aimed at drying method optimization.

}, keywords = {Blackthorn, Herbal raw material, HPLC, Hydroxycinnamic acids, Prunus Spinosa L., Spectrophotometry}, doi = {10.5530/pj.2020.12.23}, author = {Sergey Kondrashev and Nadezhda Nesterova and Alexey Luzin and Vitaliy Kochanov and Anna Luzina and Alexey Matyushin} } @article {1292, title = {Resveratrol: Latest Scientific Evidences of its Chemical, Biological Activities and Therapeutic Potentials}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1779-1791}, type = {Review Article}, chapter = {1779}, abstract = {

Background: Resveratrol is a non-flavonoid polyphenol possesses many biological properties with great potential to develop into various products. In order to cure a wide variety of diseases, resveratrol has attracted a great deal of attention for medicinal purposes. Objective: The present review aimed to provide a comprehensive literature summary of latest scientific evidences on the chemistry, biological properties and therapeutic potentials of resveratrol. Methods: To complete this review, relevant literatures were collected from several scientific databases, including Google Scholar, Pubmed and ScienceDirect, using keywords {\textquotedblleft}source{\textquotedblright}, {\textquotedblleft}chemistry{\textquotedblright}, {\textquotedblleft}bioavailability{\textquotedblright}, {\textquotedblleft}pharmacokinetics{\textquotedblright}, {\textquotedblleft}isolation{\textquotedblright}, {\textquotedblleft}anticancer{\textquotedblright}, {\textquotedblleft}analgesic{\textquotedblright}, {\textquotedblleft}antiinflammatory{\textquotedblright}, {\textquotedblleft}antidiabetic{\textquotedblright}, {\textquotedblleft}nephroprotective activity{\textquotedblright}, {\textquotedblleft}neuroprotective activity{\textquotedblright}, {\textquotedblleft}antiobesity{\textquotedblright}, {\textquotedblleft}cardioprotective effects{\textquotedblright}, {\textquotedblleft}antioxidant{\textquotedblright}, {\textquotedblleft}anti-aging{\textquotedblright} with resveratrol. After a detailed screening process for inclusion and exclusion, the information obtained was summarised. Results: The information on the source, chemistry, bioavailability, biological and therapeutic potentials of resveratrol were tabled. In various pathological conditions, resveratrol can be considered as powerful antioxidants along with multidimensional molecular targets such as NF-ҡB, MAPK, AMPK, SIRT-1, Nrf-2, m-TOR, PI3K/Akt and PPAR-γ signaling pathways. Conclusion: Based on the existing knowledge, we may believe that resveratrol has a significant therapeutic potential for the treatment of various diseases. To accelerate the development and utilization of resveratrol as promising products, in-depth studies should be focused on exploiting its properties and developing phytopharmaceuticals.

}, keywords = {Bioavailability, Inflammatory cytokines, Molecular targets, Pharmacology, Resveratrol, Toxicity}, doi = {10.5530/pj.2020.12.240}, author = {Nur Mursyida Saad and Mahendran Sekar and Siew Hua Gan and Pei Teng Lum and Jaishree Vaijanathappa and Subban Ravi} } @article {1202, title = {A Review on Phaseolus vulgaris Linn}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1160-1164}, type = {Review Article}, chapter = {1160}, abstract = {

Medicinal herbs have been discovered and used in traditional medicine practices since antiquated times. Phaseolus vulgaris Linn. (Family-Fabaceae) commonly known as French bean, is a most consuming carbohydrate and protein rich food crop having medicinal values. This plant having diverse compounds like carbohydrate, proteins, flavonoids, Saponins, tannins and phenolic acid. The seeds of Phaseolus vulgaris Linn. Possess having anti-urolithiatic activity and anti- obesity activity. This review provides a summary of phytochemistry and pharmacological effect of Phaseolus vulgaris Linn., The plant can be further investigated for other pharmacological activities as it contains variety of chemical constituents and it is a commonly using food crop and medical remedies of this plant are sync with nature.

}, keywords = {Food crop, Obesity, Phaseolus vulgaris Linn, Urolithiasis}, doi = {10.5530/pj.2020.12.163}, author = {M Devi and S Dhanalakshmi and GE Thillai Govindarajan and BA Tanisha and Talluri Sonalika and JE Ruth and T Avinash and C Jethendra Sri and K Logeswaran and M Nithish Ramasamy} } @article {1119, title = {The Study of External Signs, Microscopy and Chemical Composition of Medicinal Plant Materials of Verоnica beccabunga L. Herb}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {391-403}, type = {Research Article}, chapter = {391}, abstract = {

Introduction: Veronica beccabunga L. belongs to the class dicotyledons, order Lami{\'a}les, family Scrophulariaceae. Representatives of the genus Veronica have long been used in folk medicine as antiinflammatory, antibacterial, antiseptic, wound healing, hemostatic, choleretic and antispasmodic drugs. Widely studied species are Veronica officinalis and Veronica chamaedrys. Veronica beccabunga L., which is the object of our study, remains a poorly studied plant. Aim: The study of external signs, microscopy and chemical composition of medicinal plant materials of Verоnica beccabunga L. herb. Materials and Methods: Chromato-mass spectrometry was used in the work. Results and Discussion: When describing external signs and microscopy, diagnostic signs of Verоnica beccabunga were revealed. 27 compounds were identified by chromatography-mass spectrometry. The maximum content falls on: Citronellol epoxide (R or S) (30.5 \%), Linolenic acid, ethyl ester (15.18), Diethyl succinate (12.17\%), Ethyl palmitate (6.43\%), Phytol (4.89\%), Acetaldehyde ethyl amyl acetal (3.94\%), Dibenzylamine (3.01\%), Oleamide (2.77\%), 2-(1-Methylbutyl)oxirane (2.7\%), Butyl octyl phthalate(1.7\%), Ethyl 10-bromodecanoate (1.68), Valeric acid, 4-methyl-, ethyl ester (1.58). Glycoside detected : 1-Benzyl-1Hbenzimidazole 3-oxide (0.76\%). Conclusion: The revealed morphological and anatomical signs of Verоnica beccabunga herb can be used to diagnose this species and develop authenticity indicators for promising medicinal herbs. 27 compounds were identified by chromatographymass spectrometry. Using the method of simple normalization, the relative percentage of identified compounds was determined.

}, keywords = {1-Benzyl-1H-benzimidazole 3-oxide, Verоnica beccabunga L.}, doi = {10.5530/pj.2020.12.61}, author = {Angelina V Strelyaeva and Olga A Larina and Alla M Antsyshkina and Roman M Kuznetsov and Alina A Bondar and Vladimir A Sorokin} } @article {1216, title = {Tacrolimus Therapeutic Drug Monitoring in Vietnamese Renal Transplant Recipients}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {984-992}, type = {Original Article}, chapter = {984}, abstract = {

Background: Use of tacrolimus (Tac) is pivotal to renal transplant (RT) immunosuppressive maintenance regiments. The most frequently used means of Tac monitoring is the measurement of the trough concentration (C0) in whole blood to maintain drug efficacy and minimize the consequences of overexposure. Most previous studies focused on therapeutic drug monitoring of Tac in renal transplant recipients and assessed the clinical response of patients. Our study aimed to describe a real Tacrolimus therapeutic drug monitoring transplantation and determine the clinical outcomes in Vietnamese adult renal transplant recipients. Methods: This retrospective study including 114 adult renal transplant patients (89 men and 25 women) with a mean age of 35.4 {\textpm} 8.98 years has been performed from August 2012 to March 2018 at Military Hospital 103 (Vietnam). Tac trough concentrations were adjusted according to the target range proposed by the European consensus conference on tacrolimus optimization. Samples for determination of tacrolimus blood levels were subdivided according to the posttransplantation period into three groups (0- 3 months (G1), 3-12 months (G2) and over 1 year (G3). Median Years of follow-up was 15.4 months [range 0.233 to 68.4 months]. Results: A total of 3037 blood samples for the determination of tacrolimus trough concentration were obtained. Median concentrations were 6.7 (4.5 {\textendash} 10.2) ng/ml, 6.4 (5.1 {\textendash} 8.3) and 5.6 (4.5 to 7.1) ng/ml for G1, G2, G3, respectively. After transplantation, three acute rejection (AR) events were documented (Cellular AR: 2, Humoral AR: 1). Cytomegalovirus, BK polyomavirus, Hepatitis B virus and Hepatitis C virus were detected in 7, 4, 7 and 3 renal post- transplant recipients, respectively. There were 5 patients with post-transplant diabetes (NODAT) and all of them had to convert to cyclosporine. 6 patients developed chronic kidney disease (CKD) after transplantation and 2 case with Tac-associated nephrotoxicity with proven biopsy. This observational study provided a real Tacrolimus therapeutic drug monitoring transplantation in Vietnamese renal transplant recipients. Main outcomes were acute rejection, post-transplant viral infections, neurotoxicity, NODAT, CKD, and Tac-associated nephrotoxicity.

}, keywords = {Renal transplantation, Tacrolimus, Therapeutic drug monitoring, Vietnam}, doi = {10.5530/pj.2020.12.139}, author = {Van Anh T Nguyen and Thang Viet Le and Manh Van Bui and Toan Quoc Pham and Son The Trinh and Binh Nhu Do and Lien Huong T Nguyen} } @article {1242, title = {Wound Healing Activity of an Ointment from Solanum tuberosum L. "Tumbay Yellow Potato" on Mus musculus Balb/c}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1268-1275}, type = {Original Article}, chapter = {1268}, abstract = {

Background: Solanum tuberosum L. is an Andean tuber that is mainly characterized by its antioxidant properties. Objective: To evaluate the healing activity of an S. tuberosum-based ointment on wounds induced in mice. Material and methods: Ethanolic extracts of peel and pulp of tubers of S. tuberosum "Tumbay yellow potato" were prepared, which were incorporated into 1\% and 2\% ointment formulations. Mus musculus Balb/c with induced wound were distributed in the following working groups: Group I (Negative Control), Group II (Positive Control: Neomycin, Polymyxin B and Bacitracin Ointment) and Groups III and IV (Ointment at 1 \% and 2\% of S. tuberosum extract, respectively), daily administration of topical treatments were carried out for 07 days. Wound closure was determined during the experimentation time, then euthanized with sodium pentobarbital 60 mg/kg b.w. (i.p.) to obtain skin samples for histopathological analysis. Results: Groups III and IV showed that better evidence of wound closure and scarring in the histopathological analysis, the greatest effect being in Group IV. Conclusions: S. tuberosum ointments show healing activity in induced wounds in mice, the most effective treatment being the 2\% ointment formulation.

}, keywords = {Histology, Skin, Solanum tuberosum, Wound Healing, Yellow potato}, doi = {10.5530/pj.2020.12.175}, author = {Galy P Rosas-Cruz and Carmen R Silva-Correa and Abhel A Calder{\'o}n-Pe{\~n}a and V{\'\i}ctor E Villarreal-La Torre and Cinthya L Aspajo-Villalaz and Jos{\'e} L. Cruzado-Razco and Jorge Del Rosario-Ch{\'a}varri and Juan C Rodr{\'\i}guez-Soto and Orlando E Pretel-Sevillano and William Antonio Sag{\'a}stegui-Guarniz and Anabel D Gonz{\'a}lez-Siccha} } @article {1044, title = {Anthelmintic Activity of Millettia pachycarpa Root Bark Extract on an Intestinal Roundworm, Ascaridia galli}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1428-1433}, type = {Original Article}, chapter = {1428}, abstract = {

Background: Millettia pachycarpa Benth. is member of the family Fabaceae and is a wellknown traditional medicinal plant used for different health conditions. Its roots and seeds are rich in bioactive compounds such as chalcones, isoflavones and rotenoids, which are attributed to the anticancer, antiparasitic and insecticidal properties of the plant. In Mizo traditional medicine, the root bark is also used for parasitic infections. Objective: The study was designed to understand the anthelmintic efficacy and effects of M. pachycarpa on an intestinal roundworm, Ascaridia galli. Materials and Methods: The methanolic extract of the root bark was prepared and survival test was performed against A. galli. The structural effects were studied using scanning electron microscopy and histological preparations. Results: The roundworm showed extensive structural changes and damages. The cuticle showed extensive shrinkage and cracks. Lacerations and scars distorted the fine transverse rings. The mouthparts collapsed with shrunken lips and degenerated denticles. Internal tissues such as musculature and reproductive organs were also impaired. Conclusion: The findings indicate that the plant extract is effective against parasitic roundworms.

}, keywords = {Ascaridia galli, Cuticle, microscopy, Millettia pachycarpa, Roundworm}, doi = {10.5530/pj.2019.11.221}, author = {Kholhring Lalchhandama} } @article {856, title = {Antibacterial Activity of Carica papaya Leaves and Allium sativum Cloves Alone and in Combination against Multiple Strains}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {600-602}, type = {Original Article}, chapter = {600}, abstract = {

Aim: Screening of natural extracts is a focused intensive study that aims to find active principles sorted from plant resources both safe and environmental friendly. The present study was aimed to evaluate the antibacterial activity of direct crude extracts of Carica papaya leaves and Allium sativum cloves alone and in combination against multiple drug resistant strains. Methods: Two Gram positive (Staphylococcus aureus and Bacillus cereus) and three strains of Gram negative (Escherichia coli, Salmonella typhi and Pseudomonas aeruginosa) bacteria were used to evaluate the antibacterial activity of Carica papaya leaves and Allium sativum using Agar Disk Diffusion Method. Results: The results of this study showed that both extracts showed moderate antibacterial activity against the test bacterial strains and the potency of the extracts was increased when these two extracts were combined. Conclusion: These extracts directly can be used as natural alternative preventives to control various food poisoning diseases and preserve food stuff avoiding healthy hazards of chemically antimicrobial agent applications.

}, keywords = {Allium sativum cloves, Antibacterial activity, Bacillus cereus, Carica papaya leaves, crude extract, Escherichia coli, Pseudomonas aeruginosa, Salmonella typhi, Staphylococcus aureus}, doi = {10.5530/pj.2019.11.95}, author = {Srividya Lonkala and A. Rama Narsimha Reddy} } @article {902, title = {Anti-inflammatory Effect of the Aqueous Fruit Pulp Extract of Tamarindus indica Linn in Lipopolysaccharide-Stimulated Macrophages}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {669-673}, type = {Original Research Study}, chapter = {669}, abstract = {

Aim: The aim of the present study was to evaluate the effect of the aqueous fruit pulp extract of Tamarind indica Linn on NO production and iNOS expression in LPS stimulated RAW 264.7 macrophages. Material\ and Method: The efficacy of tamarind extract on nitric oxide production was determined using RAW macrophages. RT - PCR was used to examine the expression of the iNOS gene in activated macrophages. The Statistical analysis for multiple comparisons was evaluated by one way ANOVA followed by the Dunnett{\textquoteright}s test when significant differences were detected. The data were considered to be statistically significant at p \< 0.001, p \< 0.01 and p \< 0.05. Results: LPS stimulated RAW macrophages strongly up regulated the iNOS gene expression levels. The iNOS levels were significantly suppressed in the presence of different concentrations of tamarind extract, compared to LPS treatment alone. The tamarind extract also exhibited dose {\textendash} dependent decrease in the production of NO. The IC50 was found to be 35.69 μg/ml. LPS stimulated group showed 89.61 {\textpm} 0.47 \% of NO. Conclusion: Nitric oxide production is found to be more in conditions such as periodontitis, oral squamous cell carcinoma and many other diseases. This study could prove the ability of tamarind fruit pulp extract to inhibit the production of nitric oxide and the iNOS gene expression. Hence, Tamarind indica Linn pulp extract may be used as a good anti-inflammatory agent in periodontitis as well as in conditions associated with over production of nitric oxide in different cancers such as oral squamous cell carcinoma.

}, keywords = {iNOS expression, Nitric oxide, Oral squamous cell carcinoma, Periodontitis, Tamarind indica}, doi = {10.5530/pj.2019.11.105}, author = {Mathews Meriam Leya and Roy Anitha} } @article {930, title = {Antioxidant Activity of Cumin Oil Mediated Silver Nanoparticles}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {787-789}, type = {Original Research Study}, chapter = {787}, abstract = {

Aim: The aim of the study was to employ cumin oil in the synthesis of silver nanoparticles and check the antioxidant activity of the cumin oil mediated silver nanoparticles. Background: The introduction of Nanoparticles (NPs) has revolutionized every field including medicine, nutrition and energy. The use of nanotechnology in medicine especially for drug delivery is shown to have various benefits. Nanoparticles are being used to reduce toxicity and side effects that drugs may impose to the patient. Cumin (Cuminum cyminum) is a common spice used for its distinct aromatic effect. Plant mediated biological synthesis of nanoparticles has been gaining importance due to its simplicity and eco friendliness. This study therefore was aimed to synthesize cumin oil mediated silver nanoparticles and assess its antioxidant activity. Materials and Methods: Cumin oil mediated silver nanoparticles were initially synthesised and characterised by UV-Visible spectrophotometer and TEM. Further the cumin oil mediated AgNPs were subjected to DPPH assay to determine the antioxidant activity. Results: Cumin oil mediated AgNPs were biosynthesised with ease and showed good antioxidant activity compared to standard. Conclusion: This study conclude that cumin seed oil mediated silver nanoparticles have the potential to be used as an effective antioxidant. Hence, it may be employed in large scale production and may be used in many medicinal applications where there is a need for antioxidant.

}, keywords = {AgNP, antioxidant activity, Biosynthesis, Cumin oil, Nanoparticles}, doi = {10.5530/pj.2019.11.125}, author = {Nagarajan Keerthiga and Roy Anitha and S Rajeshkumar and Thangavelu Lakshmi} } @article {910, title = {Antioxidant and Cytotoxic Attributes of Paris polyphylla Smith from Sikkim Himalaya}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {705-711}, type = {Original Article}, chapter = {705}, abstract = {

Introduction: Paris polyphylla Smith is a high value medicinal plant available in Sikkim Himalaya which is well known in local traditional medicine system. Scientific study to ascertain its claimed biological activity is lacking. The objective of this work was to determine the antioxidant and anticancer activity of Paris polyphylla rhizomes. Methods: Phytochemical analysis were carried out by standard methods. Antioxidant activity of the methanolic extract was carried out by DPPH, ABTS, OH-radical and Fe2+chelating activity assays. Cytotoxicity of the extract was determined by MTT assay on three cancer cell lines: HeLa, HepG2 and PC3. Results: Of the P. polyphylla from two altitudinal zones, P. polyphylla from Tholung (PPT), the one from the higher altitude showed higher total phenolic contents in methanolic extracts of rhizomes as compraed to that from the lower altitude i.e., P. polyphylla from Uttaray (PPU). PPT also showed a higher content of total falvonoid and total flavonols. Both types of plant were excellent scavenger of DPPH and ABTS radical and Fe2+ chelator. A trend of a relatively greater antioxidant activity of PPT was established through these assay methods. In MTT assay, both the extract showed significant dose-dependent inhibition of HeLa cell growth after 72 hrs of treatment, while the extract had a moderately positive effect on the inhibition of PC3 and HepG2 cells growth. Conclusion: The study suggested a strong antioxidant activity and appreciable cytotoxic activity of P. polyphylla from Sikkim Himalaya. Of the two varieties, PPT was more pronounced in both type of activities.

}, keywords = {Anticancer, Antioxidant, Cytotoxicity, Paris polyphylla, Phytochemicals, Sikkim Himalaya}, doi = {10.5530/pj.2019.11.112}, author = {Dawa Lhendup Lepcha and Abhijit Chhetri and Dhani Raj Chhetri} } @article {1004, title = {Antiplasmodial Activity of Ethanolic Extract of Macaranga Gigantea Leaf and Its Major Constituent}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1181-1188}, type = {Original Article}, chapter = {1181}, abstract = {

Introduction: This research main goal is to study the antiplasmodial activity of Macaranga gigantea leaf ethanolic extract and its major components on malaria parasites using ex vivo model. Methods: This study was conducted by extraction of M. gigantea leaves using ethanol and isolation of its major constituent. The extract and isolate were tested ex vivo on Balb-C mice{\textquoteright}s blood after i.p. administration of Plasmodium berghei strain ANKA. Antiplasmodial activity was observed from mice blood treated by various concentration of either extract or isolate and the parasitaemia percentage were determined by calculating infected blood cell after 24 h of the treatment. It is expressed as decreased of parasitaemia levels and percent of inhibition. Qualitative analysis of active fraction were tested by HPLC method. Chemical structure of isolate were characterized by using UV, IR, 1H-NMR, 13C-NMR and MS spectrophotometry. Results: Ex vivo antiplasmodial study gave the percent inhibition as much as 92.1; 85.7; 64.1; 41.5 and 21.7\% at extract concentrations of 300, 100, 30, 10 and 3 μg/ mL respectively. The IC50 values of the extract was 27.1 μg/ml. With respect to the percent of inhibition, at the same concentration, the isolate showed activity as much as 70.2; 62.5; 39.1; 21.7 and 10.8\%. The IC50 value of the isolate was 60.2 μg/ml. At the same concentration with extract and Isolate, Pyrimethamine as positive control gave percent inhibition of 94; 87.5; 44.8; 15.; and 12\%, with IC50 of 31.4 μg/ml. The results showed that major constituent of M. gigantea leaves is flavonoid. HPLC analysis using a photo diode-array detector showed that the active fraction have same retention time with that of apigenin as standard. Based on instrumental analysis data and compared with literature, a flavonoid derivate known as apigenin can be said has been isolated. Conclusion: It can be concluded that either M. gigantea leaves extract or isolated active constituent known as apigenin have potent antiplasmodial property.

}, keywords = {Antiplasmodial, Ex vivo, Flavonoid, Macaranga gigantea, Plasmodium berghei}, doi = {10.5530/pj.2019.11.183}, author = {Muhaimin Muhaimin and Yusnaidar Yusnaidar and Wilda Syahri and Madyawati Latief and Riski Dwimalida Putri and Andita Utami and Anis Yohana Chaerunisaa and Andreas Yoga Aditama and Josephine Elizabeth Siregar} } @article {956, title = {Antiplasmodial Activity of Methanolic Leaf Extract of Mangrove Plants against Plasmodium berghei}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {929-935}, type = {Original Article}, chapter = {929}, abstract = {

Introduction: A mosquito-borne disease infected by Plasmodium is named as Malaria. Some drugs subjected to be active againts protozoans has developed resistance. It is very urgent to find alternative sources of new antimalarial agent. The main aim of this research was to study the activity of methanolic extracts of the leaf from mangrove plants on Plasmodium berghei by using ex vivo model. Method: Screening of antiplasmodial activity from methanolic leaf extracts of Sonneratia alba, Acanthus ilicifolius and Sonneratia caseolaris against Plasmodium berghei was carried out in this study. Antiplasmodial study was subjected ex vivo against P. berghei strain ANKA infected into Balb-C mice. Calculation of the percentage of parasitemia after 24 h observed in the model and a decrease in parasitemia level and inhibitory propagation were defined as the results. Results: Potential antiplasmodial activity shown by a decrease in parasitemia level and high inhibitory percentage was revealed by S. alba leaf methanolic extract at concentrations of 300, 100, 30, 10 and 3 μg/mL which provide the inhibition percentage of 95.5; 92,9; 78.7; 42.7 and 18.8\%, respectively. Antiplasmodial activity can also be identified by the life cycle inhibition of plasmodium. Methanolic leaf extract of S. alba showed inhibition activity in the development of ring stage at minimum extract concentration of 300 μg/mL. At lower concentrations, trophozoites and schizones persisted with defects in morphological conditions. Moreover, Antiplasmodial activity of methanolic extracts of S. alba leaf was better than methanol extracts of A. Ilicifolius and S. caseolaris leaf. Conclusion: The results of this study indicated that among the mangrove plants have been studied, S. alba mangrove exhibited the highest antisplasmodial activity which moreover assumed as a potential source for natural antimalarial drug candidate.

}, keywords = {Antimalaria, Ex vivo, Mangrove, Plasmodium berghei, Sonneratia alba}, doi = {10.5530/pj.2019.11.148}, author = {Muhaimin Muhaimin and Madyawati Latief and Riski Dwimalida Putri and Anis Yohana Chaerunisaa and Andreas Yoga Aditama and Normalita Eka Pravitasari and Josephine Elizabeth Siregar} } @article {801, title = {The Anti-proliferative and Anti-bacterial Activity of Argan oil and Crude Saponin Extract from Argania spinosa (L.) Skeels}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {26-31}, type = {Original Article}, chapter = {26}, abstract = {

Introduction: Argan oil is a well-known cosmeceutical that is commercially available. It is traditionally used for the treatment of acne and skin inflammation among others. The objective of this study was to assess the anti-proliferative and antibacterial activities of argan oil and a crude saponin extract from the argan tree (Argania spinosa (L.) Skeels) that is endemic to Morocco. Materials and Methods: The anti-proliferative activity of argan oil and the crude saponin extract was assessed by the 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium- 5-carboxanilide (XTT) assay on A431; HaCat; HeLa; MCF-7 and UCT-Mel 1 cells. The antibacterial activity was evaluated by the broth microdilution method against two species of bacteria: Cutibacterium acnes and Prevotella intermedia. Results: The results of this study indicated that the argan oil sample did not inhibit the cell growth of the specified cell lines up to 1000μg/ml, while the crude saponin extract had low anti-proliferative activity. The minimal inhibitory concentration (MIC) values for both the argan oil and the crude saponin extract were found to be 500μg/ml against Cutibacterium acnes. No antibacterial activity from the argan oil or the crude saponin extract was evident against Prevotella intermedia up to a concentration of 12.5mg/ml. Conclusion: The results of this study indicated that argan oil and the crude saponin extract might have direct inhibitory effects on the growth and proliferation of Cutibacterium acnes. This finding supports the use argan oil as a treatment for acne vulgaris.

}, keywords = {Acne, Broth microdilution method, Cutibacterium acnes, Prevotella intermedia, XTT assay}, doi = {10.5530/pj.2019.1.5}, author = {Namrita Lall and Marco Nuno De Canha and Karina Szuman and Zoubida Charrouf and Lester M. Davids and Sunelle Rademan} } @article {952, title = {The Assay of Quercetin Solid Dispersion as a Potential Nephronprotector in Acute Renal Failure Induced Mice}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {907-912}, type = {Original Article}, chapter = {907}, abstract = {

Quercetin has been used with other nutraceutical components to improve renal function. Its potential to be developed as an active pharmaceutical ingredient, however, is limited by poor aqueous solubility and low rate of dissolution leading to low bioavailability in rats (\< 17\%) and in human (1\%). Solid dispersion of quercetin with PVP K30 has increased its solubility 13.24 times and the amount dissolved (95.12 {\textpm} 1.83\%) in comparison to pure quercetin. This study aimed to determine the nephron-protection effect of the solid dispersion on Acute Renal Failure (ARF) mice. The animals were divided into 6 groups, normal mice as a negative control group (G1), ARF induced mice as a positive control group (G2), ARF induced mice given pure quercetin 50 mg/kg BW (G3), ARF induced mice given solid dispersion containing 10 mg/ kg BW (G4), 5 mg/kg BW (G5) and 2.5 mg/kg BW (G6) quercetin respectively. The ARF was induced by injection of gentamycin sulphate 100 mg/kg BW for 7 days consecutively. Renal function was monitored by measuring the serum creatinine at day 8th. The protection effect was also observed from the histopathology score of the nephrons. Results showed that ARF induction increased serum creatinine above normal. Solid dispersion doses variations significantly influence the serum creatinine (p \< 0.05). The stage of renal impairment based on histopathology score was significantly influenced by the doses of quercetin in solid dispersion (p \< 0.05). It was concluded that solid dispersion containing quercetin at doses 2.5 and 5.0 mg/ kg BW respectively did not effective as a nephron-protector. The solid dispersion containing quercetin 10.0 mg/kg BW was effective to reduce the serum creatinine and showed a nephronprotection effect on the ARF induced mice.

}, keywords = {Acute renal failure mice, Nephron-protector, Quercetin, Solid dispersion}, doi = {10.5530/pj.2019.11.145}, author = {Henny Lucida and Poppy Agustin and Suhatri} } @article {1008, title = {Comparative Free Radical Scavenging Efficacy of Leaves Extract of Moringa Oleifera and Petals Extract of Hibiscus Sabdariffa}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1342-1346}, type = {Original Article}, chapter = {1342}, abstract = {

Background: Use of molecules with antioxidant properties have evolved as effective strategy for preventing oxidative damage caused by reactive oxygen species. Moringa oleifera and Hibiscus sabdariffa are ancient plants with antioxidant properties, and have served numerous therapeutic purposes, in addition to their nutritional benefits. Aim: This in vitro study compared the free radical scavenging efficacy of ethylacetate leaves extract of Moringa oleifera and ethylacetate petal extract of Hibiscus sabdariffa. Method: Determinations were carried out following standard procedures for analytical experiments. The leaves of Moringa oleifera and petals of Hibiscus sabdariffa were extracted by cool maceration with distilled water and ethylacetate, independently for 48 hours using soxhlet extractor. The free radical scavenging activities of the extracts were determined spectrophotometrically. DPPH free radical was used to determine the free radical scavenging activities of the extracts. The reducing power efficacy of the extracts was determined by their ability to reduce Fe3+ to Fe2+ ions using FERAP. Results: Ethylacetate extract of Hibiscus sabdariffa petals had higher free radical scavenging efficacy and more reducing power with an inhibitory concentration (IC50) of 1.57 mg/ml compared to the ethylacetate extract of Moringa oleifera leaves which had an IC50 of 2.60 mg/ml. Phytochemical profile revealed that the predominant compounds in both extracts were flavonoids, phenols, and amino acids. Conclusion: This study has established that ethylacetate extract of the Petals of Hibiscus sabdariffa has more reducing power and free radical scavenging efficacy compared to ethylacetate extract of Moringa oleifera leaves. These plant parts could serve as novel sources for clinically efficient antioxidants.

}, keywords = {Antioxidant, Free radical scavenger, Hibiscus sabdariffa, Moringa oleifera, Oxidative stress, Oxygen-free radicals}, doi = {10.5530/pj.2019.11.207}, author = {Garba Auwalu and Emeka John Dingwoke and Adamude Fatima Amin and Nwobodo Ndubuisi Nwobodo and Mohammed Mohammed Lawan} } @article {916, title = {Cytoprotective Effect of the Eryngium foetidum "Sacha Culantro" Methanolic Leaf Extract Versus Sodium Fluoride Exposed Mice using the Micronucleus Test and the Comet Assay}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {461-465}, type = {Original Article}, chapter = {461}, abstract = {

Introduction: Eryngium foetidum, commonly known as sacha culantro, is a plant that grows in the Peruvian Amazonian jungle, studied for its high concentration of antioxidant substances and various ethnopharmacological properties. The main goal of the study is to observe the cytoprotective and antioxidant effect of the extract from its leafs in Mus musculus previously administered with Sodium fluoride (NaF) using the Micronucleus test and the Comet assay. Methods: The extract was administrated orally in four different concentrations: 180, 360, 720, 1440 mg/Kg for ten days, at the 11th day a single dose of NaF was administrated via intraperitoneal at 20 mg/Kg. The genotoxicity study was made with mice from the strain BALB/c, using the Micronucleus test on bone marrow and the Comet assay on peripheral blood according the OECD guides 474 and 489 respectively. The statistical analysis was made by the media{\textquoteright}s analysis with ANOVA. Results: Significant differences were found in Micronucleus frequency between the highest concentrations of Eryngium foetidum and NaF. The Comet assay showed significant reduction in NaF induced damage according to different concentrations of the extract. Conclusion: The Eryngium foetidum extract has cytoprotective activity against oxidant substances such as NaF.

}, keywords = {Comet assay, Cytoprotective, Eryngium foetidum, Genotoxicity, Micronucleus test, Toxicity}, doi = {10.5530/pj.2019.11.72}, author = {Paola Raunelli and Danae Liviac and Rafael Alvis and Silvio Puente and Ivan Best and Oscar Reategui} } @article {1031, title = {The Effect of Ultraviolet-B Radiation Exposure on Hibiscus cannabinus Linn with its Phytochemical and Pharmacological Responses}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1540-1543}, type = {Research Article}, chapter = {1540}, abstract = {

Aim: Exposure of UV-B Radiation on\ Hibiscus cannabinus Linn and to evaluate both Phytochemical and Pharmacological responses. Objective: UV-B can increase the nutrients contents from plants, plants become tastier and increases the yield and UV-will make plants resistant to fungal infections and stimulate the production of phytomarkers. Material and Methods: Hibiscus cannabinus Linn seeds were soaked with 50\% H2O2 for 12 hours and then inoculated with the Azospirillum. UV-B radiation cabinet was provided by UV lamps which are above 15 cm from control maintained. Normal daylight exposed control group Seedlings irradiated for 2 hour per day (12.30 pm to 2.30 pm) for 20 days. Results and Discussion: 20 days treatment increases total phenolic contents and sugars content were decreased in uncovered leaf tissue. Protein content was at first diminished but expanded on the 20 day of UV-B treatment. Also, perform pharmacological studies no toxic elements are observed 20 days treatment and pharmacological activity by using anticancer activity by using human colon HT-29 cancer cell line. UV light exposed plants shows good anticancer activity when compared with non UV exposed Plant.

}, keywords = {Cancer cells line HT-29, Hibiscus cannabinus Linn, Total Phenolic Contents, UV-B radiation}, doi = {10.5530/pj.2019.11.235}, author = {T Sundarrajan and V Velmurugan and MK Kathiravan and K Manikandan and KS Lakshmi and MR Ganesh} } @article {960, title = {Evaluation of Antioxidant Activity and Phytochemical Screening of Leaves, Barks, Stems and Fruits of Alphitonia philippinensis (Rhamnaceae) From Brunei Darussalam}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {951-961}, type = {Original Article}, chapter = {951}, abstract = {

Phytochemical screening of Alphitonia philippinensis extracts revealed the presence of cardiac glycosides, tannins, saponins and steroids in different plant parts. Total phenolic content (TPC), total flavonoid content (TFC) and total flavonol content (TFlC) were measured using spectrophotometric methods where gallic acid and quercetin were the standards. Antioxidant activity of extracts was assessed using 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,2̉-azino-bis(3- ethylbenzothiazoline-6-sulfonic acid) (ABTS), free radical scavenging and ferric reducing antioxidant power (FRAP) assays using ascorbic acid and trolox were used as standards. Among the four different crude methanol extracts studies, leaves showed highest antioxidant capacity. EC50 values of the leaves extract from DPPH and ABTS method found 32 and 45 μg/mL respectively. The higher antioxidant activity of the leaves extract could be correlated with the presence of higher total phenolic content, total flavonoid, and total flavonol contents. According to antioxidant contents and assay results leaves extract possesses highest antioxidant property following fruits, barks and stems.

}, keywords = {Antioxidant property, philippinensis, Phytochemical investigation, Total Phenolic Contents}, doi = {10.5530/pj.2019.11.151}, author = {Jamiuddin Ahmed and Kamariah Abu Salim and Linda B.L. Lim and Abdalla Mohamed Jama} } @article {899, title = {The Evaluation of Dietary Black Soybean and Purple Sweet Potato on Insulin Sensitivity in Streptozotocin - Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {639-646}, type = {Original Article}, chapter = {639}, abstract = {

Introduction: Hyperglycemia mediates the production of excess free radicals and reduces endogenous antioxidant in type 2 diabetes mellitus (T2DM). Black soybean (BSB) is rich in antioxidant mainly from isoflavones, whereas the antioxidant of purple sweet potato (PSP) comes from high anthocyanin. The study aimed to evaluate the efficacy of BSB, PSP, and its combination on malondialdehyde (MDA), superoxide dismutase (SOD) concentrations, insulin and insulin receptor substrate-1 (IRS-1) expression in T2DM rats. Methods: T2DM induced by high-calorie diet for five weeks and then injected with a low dose of streptozotocin (30 mg/kg BW) intraperitoneally. The DM rats then treated with black soybean (DM + BSB), purple sweet potato (DM + PSP) and the combination of BSB and PSP 1:3, 2:2, 3:1 respectively (DM + C1- 3). Treatments were given for thirty days. The effect of BSB, PSP and its combination evaluated by measuring SOD and MDA, necrosis in pancreas evaluated through hematoxylin-eosin (HE) and insulin and IRS-1 expression in pancreas through immunohistochemistry-fluorescence (IHC-F). Results: Our result indicated that there were no significant differences of BSB and the combination in decreasing MDA concentrations. The ratio of BSB and PSP combination of 2:2 increase SOD towards near normal, decrease necrosis, and improve insulin and IRS-1. Conclusion: The combination of BSB and PSP had the potential to improve insulin sensitivity through the increase of SOD, reduce necrosis, and improve insulin and IRS-1 expression.

}, keywords = {Antioxidant, Malondialdehyde, Necrosis, Superoxide dismutase, T2DM}, doi = {10.5530/pj.2019.11.102}, author = {Abdul Gofur and Agung Witjoro and Erni Widya Ningtiyas and Evi Setyowati and Siti Aminatul Mukharromah and Mochammad Fitri Atho{\textquoteright}illah and Sri Rahayu Lestari} } @article {895, title = {Extraction and Identification of Cactus Opuntia dillenii Seed Oil and its added Value for Human Health Benefits}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {579-587}, type = {Original Article}, chapter = {579}, abstract = {

Cactus Opuntia dillenii presents multiple health benefits. The current study aims to investigate the seed composition and content of prickly pear fruits from Iraq. Results obtained showed that Opuntia dillenii contained 9.5\% of seeds of the entire fruit while extracted oil presented 6.5\% of total seed composition. Fatty acid analysis revealed that the polyunsaturated linoleic acid (72.9\%), the saturated palmitic acid (15.12\%) and stearic acid (7.51\%) presented the main seed fatty acids of Opuntia dilleniid. Other essential oils were detected but at low percentage. Interestingly, stearic acid content in Cactus oil presented 7.51\%, which is much higher than soybeans (~3\%) that are considered as the largest source of animal protein feed and the second largest source of vegetable oil worldwide. Stearic acid presents neutral effects on the concentration of blood serum LDL cholesterol and does not exhibit cholesterolemic effects on human health. The analysis of cactus seed oil demonstrated a strong antioxidant ability estimated by their capability to reduce oxidation. Treated cake with BHT (butylated hydroxytoluene) at concentration of 0.02 mg/100g of butter from cactus seed-oil exhibited lower peroxide values ranging from 0.67 to 1.5 milli-equivalents (meq) peroxide per 1 kg of oil throughout 15 days of storage time at 4 {\textdegree}C. In contrast, treated cake with 0.11 mg/100g of butter from cactus seed-oil presented lower peroxide values ranged from 0.69 to 2.5 meq peroxide per 1 kg of oil among all treatments. Because of its high-saturated fatty acid composition (\>22\%) and rich linoleic acid (72.9\%) composition, Opuntia dillenii present an alternative source with several health benefits by lowering cholesterol risks and for biodiesel production.

}, keywords = {Cactus, Cake, Fatty Acid, GC-MS, Peroxide value, Seed-oil}, doi = {10.5530/pj.2019.11.92}, author = {Alya Jameel Ali Alsaad and Ammar B. Altemimi and Salah Naji Aziz and Naoufal Lakhssassi} } @article {835, title = {Gymnema sylvestre (Gurmar): A Potent Herb with Anti-diabetic and Antioxidant Potential}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {201-206}, type = {Review Article}, chapter = {201}, abstract = {

Introduction: Diabetes Mellitus is a metabolic disorder with high blood sugar level. Type 2 is the common form. The herbal remedies for diabetes treatment is an area of research with a huge potential for the progress in the growth of inexpensive alternative medicine with low or no side effects. In this paper, reviews mainly focused on traditionally used medicinal herb, Gymnema sylvestre and its bioactive components and their mode of actions. Method: Relevant information was collected from scientific journals, research papers, books and various medicinal reviews. Result: This review provides a comprehensive report on Gymnema sylvestre having antidiabetic and antioxidant activity due to its bioactive compounds like oleanines (gymnemic acid, gymnema saponins), dammarenes (gymnemasides), anthraquinones, flavones, hentriacontane, pentatriacontane, phytin, resin, tartaric acid, formic acid, butyric acid, lupeol, β-amyrene related glycosides and anthraquinones, alkaloid like gymnamine, flavonoids, cinnamic acid, folic acid, ascorbic acid etc. Conclusion: Considering the presence of bioactive compounds present in Gymnema sylvestre, this review is aimed to summarize the information of the chemical constituents and their antidiabetic activities and specially to detect the relation between antioxidants and antidiabetic compounds regarding blood sugar reduction in diabetes.

}, keywords = {Alternative medicine, Anti- diabetic, Antioxidant, Bioactive compounds, Gymnema sylvestre}, doi = {10.5530/pj.2019.11.33}, author = {Suparna Laha and Santanu Paul} } @article {925, title = {Macroscopic and Microscopic Studies of Polyscias guilfoylei L. H. Bailey Leaves (Araliaceae)}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {824-827}, type = {Original Article}, chapter = {824}, abstract = {

Introduction: The leaves of Polyscias guilfoylei L. (Araliaceae) were reported to have medicinal value. Therefore, authentication of the leaves of Polyscias guilfoylei L. is important to ensure the reproducible quality of herbal raw materials. Objective: This study aims to evaluate macroscopic and microscopic parameters of the leaves of Polyscias guilfoylei L. Methods: Organoleptic, macroscopy, and microscopy of fresh leaves and microscopy parameters of leaves powder were observed. Results: Organoleptic and macroscopic studies found that the leaves had a smooth surface with green color, pinnate venation, elonged to lanceolate shape, cuspidate apex, serrated margin, broad base steam, a bit of distinctive smell, and characteristic taste. The leaves microscopy indicated the presence of anisocytic and paracytic stomata, druses type of calcium oxalate crystals, spiral type xylem, and essential oil were found. Conclusion: The results obtained can be used as quality control parameters, especially diagnostic features for the herbal raw material of Polyscias guilfoylei L.

}, keywords = {Araliaceae, Morphological studies, Plant anatomy, Polyscias guilfoylei, Puding leaves}, doi = {10.5530/pj.2019.11.132}, author = {Siti Marwah Lestari and Berna Elya and Sutriyo} } @article {935, title = {Medicinal Plants in Basic Care: A Study of Clinical Practice}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {796-802}, type = {Original Article}, chapter = {796}, abstract = {

According to World Health Organization, 80\% of world population uses traditional practices for primary health care, and 85\% of this shares the use of medicinal plants or plants-based preparations. Thus, the present work had as objective to investigate the profile of herbal medicine use as well as the conditions to the alive pharmacy implementation in four basic health units in the city of Aracaju, Sergipe, Brazil. For such, 84 family health professionals were interviewed about the use of medicinal plants. Concerning the indication of medicinal plants, 41.67\% of the health staff prescribes medicinal plants, 55.95\% reported never having prescribed medicinal plants and 2.4\% abstained from responding. Despite the intention to use phytotherapy as a therapeutic practice, this practice is not yet fully inserted in the analyzed units due to factors such as lack of training and specific protocols to assist professionals in the use of medicinal plants and phytotherapics.

}, keywords = {Brazilian Unified Health System, Healthcare Unit, Phytotherapy, Traditional and Complementary Medicine}, doi = {10.5530/pj.2019.11.127}, author = {Carlos A.S. Souza and Wesley M.G. Andrade and Tha{\'\i}s S. Ramos and Alex J. S. Filho and Anderson L. Freitas and Tamires C. Lima and {\^A}ngelo R. Antoniolli and Wellington B. Silva and Francilene A. Silva} } @article {988, title = {Neuroprotective Effects of Ganoderma curtisii Polysaccharides After Kainic Acid-Seizure Induced}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1046-1054}, type = {Original Article}, chapter = {1046}, abstract = {

Background: Epilepsy is one of the major neurological disorders affecting world population. Although, some Ganoderma species have shown neuroprotective activities, the effects of polysaccharides isolated from Ganoderma curtisii on epileptic seizures have not been reported. Objective: The aims of the present study were to determine whether treatment with a polysaccharide fraction (GCPS-2) from a Mexican Ganoderma curtisii strain can reduce seizures, and the increases in the levels of apoptotic molecules and inflammatory cytokines in kainic acid-induced seizure mouse model. Materials and Methods: Rats were separated in groups: Control group received 2.5\% Tween 20 solution; GCPS-2 groups were administered GCPS-2 (10, 40, or 80 mg/kg); KA group received KA 10 mg/kg; GCPS-2+KA received GCPS- 2 and 30 min later KA. Pathological changes in neuronal morphology, expression of B-cell lymphoma-2, and pro-inflammatory cytokines (interleukin1-β and tumor necrosis factor-α) in the rat hippocampus and cortex were determined by immunohistochemistry. Results: Ganoderma curtisii soluble polysaccharides (GCPS-2) inhibited convulsions in rats. Moreover, treatment with GCPS-2 reduced the increased levels of apoptotic signaling molecules (Bcl-2) and proinflammatory mediators (in the kainic acid-treated hippocampus and cortex). Conclusion: Ganoderma curtisii soluble polysaccharides have a neuroprotective potential against epilepsy, partially through its ability to inhibit neurotoxic events in the in vivo hippocampus and cortex.

}, keywords = {Anti-inflammatory, Anticonvulsant, Ganoderma curtisii, Neuroprotective, β-glucan}, doi = {10.5530/pj.2019.11.164}, author = {Ismael Leon-Rivera and Juana Villeda-Hernandez and Elizur Montiel-Arcos and Isaac Tello and Maria Yolanda Rios and Samuel Estrada-Soto and Angelica Berenice Aguilar and Veronica Nunez-Urquiza and Jazmin Mendez-Miron and Victoria Campos-Pena and Sergio Hidalgo-Figueroa and Eva Hernandez and Gerardo Hurtado} } @article {786, title = {Pharmacognostic Studies of the Leaves, Stem and Root of Capparis erythrocarpos Isert (Capparaceae)}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {112-118}, type = {Original Article}, chapter = {112}, abstract = {

Introduction: The roots of Capparis erythrocarpos are used traditionally across Africa for the management of pain, arthritis and other forms of inflammatory conditions. Owing to its proven efficacy, it has gained commercial value, particularly as a key ingredient in several herbal products and alcoholic beverages. The increased scarcity owing to demand outstripping supply lend the roots of C. erythrocarpos to adulteration. This paper presents a detailed pharmacognostic evaluation of the leaf, stem and root of C. erythrocarpos which will be used in its identification and consequent standardization. Methods: The leaf, stem and root were evaluated for their macroscopic and microscopic features as were the physicochemical parameters and phytochemical screening done. Results: Leaves are alternately arranged, have collateral vascular bundle, crystal sheaths and a pericyclic fibre. Actinocytic stomata and secretory cells were contained in powdered leaves. The stem showed lenticels and thorns, stellate and branched trichomes which leave off cicatrices in older stems. The powdered stem and roots contained stone cells, secretory cells and scalariform vessels. However, the roots lacked thorns, trichomes and had smaller secretory cells. Aqueous and ethanolic extracts of the leaves, stem and roots were slightly acidic to neutral. Ash values of leaves, stem and roots are (16.58 {\textpm} 0.09) \% w/w, (5.01 {\textpm} 0.09) \% w/w and (6.53 {\textpm} 0.19) \% w/w respectively. Preliminary phytochemical screening of the leaves, stem and roots showed the presence of glycosides, flavonoids and tannins. Conclusion: The determined parameters for the leaf, stem and root of C. erythrocarpos constitute quality parameters for their unequivocal identification.

}, keywords = {Capers, Cicatrices, crystal sheaths, Herbal medicine, Morphological features, Physicochemical parameters}, doi = {10.5530/pj.2019.1.19}, author = {Twumasi Mary A and Ekuadzi Edmund and Mante Priscilla K and Boakye-Gyasi Mariam E and Mensah Merlin LK and Woode Eric} } @article {1026, title = {Pharmacognostical Studies and Determination of Total Flavonoids of Paitan (Tithonia diversifolia (Hemsl.) A. Gray}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1256-1261}, type = {Original Article}, chapter = {1256}, abstract = {

Tithonia diversifolia (Hemsl.) A. Gray is one of the plants used in traditional medicine and belongs to Compositae family. In different parts of Indonesia, it is commonly known as {\textquotedblleft}paitan and kembang bulan{\textquotedblright}. The study provides an early description of Tithonia diversifolia (Hemsl.) A. Gray) and complete the monographs data extract. This plant prospects to the main source of the raw material for the herb-drug product and some parameters identified were needed to ensure the safety, quality and efficacy of the product. The present study is to evaluate macrosand microscopic characteristic of the Indonesian plant and its quality parameter including fluorescence, physicochemical characteristics and phytochemical screening. Moisture content, ethanol and water-soluble extract was determined, and were discovered to be 11,27\%, 4,73\% and 18,01\%. Total ash value and acid insoluble ash value were determined which was 10.29 and 0.72 \% respectively. Phytochemical screening of aqueous ethanol extract of Tithonia diversifolia showed the presence of alkaloids, flavonoids, tannins, saponins and triterpenoids. The result showed that average content of flavonoid total is 69.1653 mg QE/g extract.

}, keywords = {Pharmacognostical, Physicochemical, Phytochemical, Tithonia diversifolia (Hemsl.) A. Gray)}, doi = {10.5530/pj.2019.11.195}, author = {Vera Ladeska and Ema Dewanti and Deviana Indah Sari} } @article {840, title = {Phytochemical Analysis, In vitro Antioxidant Capacity and Toxicity Assessment of Copaifera paupera Oleoresin}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {March 2019}, pages = {374-378}, type = {Original Article}, chapter = {374}, abstract = {

Introduction: The present study was taken to determine the phytochemical analysis, the antioxidant activity in vitro (FRAP and TBARS methodologies), the oral acute toxicity and antigenotoxicity of the oleoresin Copaifera paupera. Methods: The oleoresin was tested for in vivo cytoprotective capacity using the Micronucleus Test and the Comet Assay in mice bone marrow cells and mice erythrocytes cells, respectively. Results: The oleoresin had low levels of total flavonoids and phenol content and also of antioxidant capacity. Orally, the LD50 appeared to be \> 5000 mg/kg (no toxic or low toxic). The results showed all the doses evaluated (180 360, 720 and 1440 mg/kg) antigenotoxic effect by reduce the DNA damage induced by cyclophosphamide, being a 100 \% DNA damage reduction at the highest dose evaluated. Conclusion: According to the Micronucleus test, the oleoresin Copaifera paupera had the ability of increase the cell proliferation despite the exposition of cyclophosphamide. (abstract is not arranged properly, improper sentences)

}, keywords = {Antigenotoxicity, Comet assay, Copaifera paupera, Micronucleus test, Oleoresin, Phytochemical analysis}, doi = {10.5530/pj.2019.11.57}, author = {Danae Liviac and Paola Raunelli and Rafael Alvis and Silvio Puente and Ivan Best and Oscar Reategui} } @article {987, title = {Phytosomal Nanoparticles Preparation of Curcuminoids to Enhance Cellular Uptake of Curcuminoids on Breast Cancer Cell Line MCF-7}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1037-1045}, type = {Original Article}, chapter = {1037}, abstract = {

Objective: Curcuminoids, the bioactive compounds extracted from Curcuma longa consisting of Curcumin (CUR), demethoxycurcumin (DMC) and bisdemethoxycurcumin (BDMC), have shown promising biological effects, including anticancer activity. This study sought to prepare a physically stable phytosomal nanoparticles of curcuminoids (Curs-Phyto) to facilitate uptake of curcuminoids on breast cancer cells line, and further increase the cytotoxicity against cancer cells. Methods: The evaporation combined extrusion technique was employed to prepare phytosomal curcuminoids nanoparticles. The interaction between curcuminoids and phospholipid by a hydrogen bond was confirmed by differential scanning calorimetry (DSC), powder X-ray diffraction (XRD), fourier transform infrared (FT-IR), and 1H nuclear magnetic resonance (1H-NMR). Their physicochemical characterizations and stability in simulated gastric and intestinal media were investigated. The effects of Curs-Phyto on MCF-7 cells were evaluated by flow cytometry, MTS assay and cell cycle analysis. Results: We found that the Curs-Phyto were formed at a spherical shape with good size (~ 180 nm), a narrow size distribution (PDI \< d0.2), high complexation rate (~ 87\%, 95\%, and 90\% for BDMC, DMC, and CUR respectively) and high loading capacity of curcuminoids. More importantly, the Curs-Phyto showed the increased cellular uptake and enhanced cytotoxicity against MCF- 7 cancer cells, compared to free curcuminoids. Conclusion: These results indicated that the phytosome could be a promising oral delivery system for curcuminoids for cancer treatment.

}, keywords = {Cellular uptake, Curcuminoids, FACS analysis, Nanoparticle, Phytosome}, doi = {10.5530/pj.2019.11.163}, author = {Nguyen Van Long and Bui Thi Thu Ha and Anh Vu Tuan and Hoang Van Luong and Nguyen Tung Linh and Thanh Chu Duc and Phung Cao Dai and Chul Soon Yong and Chu Van Men} } @article {919, title = {Tetrahydroxy Flavone from Acacia auriculiformis A. Cunn Ex Benth. (Fabaceae) with Novel Kinase Activity}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {559-563}, type = {Original Article}, chapter = {559}, abstract = {

Background: The decoctions of the bark of Acacia auriculiformis are used in folkloric medicine to relieve pain and inflammation and as remedy for cancer. Objective: The aim of this work is to screen the extract and fractions of Acacia auriculiformis for protein kinase inhibitory activity and also to isolate and characterize chemical entities from this plant and evaluate their protein kinase inhibitory activity. Materials and Methods: Kinase inhibitory activity were assayed in appropriate buffer, with either protein or peptide as substrate in the presence of 15μM (33-P) ATP (3,000Ci/mmol; 10mCi/ml) in a final volume of 30μL. Controls were performed with appropriate dilutions of dimethyl sulphoxide. A portion of the Chloroform extract, ethylacetate and n-butanol soluble fractions of the stem bark of Acacia auriculiformis were screened against a panel of disease-related protein kinases and the active fractions was tested over a wide range of concentrations from 0.016 to 50μg/ml and the IC50 values were determined from the dose response curve. The most active fraction was subjected to chromatographic separation using Silica gel G column chromatography and sephadex LH-20 to give compound I. The structure of the isolated compound was elucidated using NMR and LCMS. Results: The Primary screening of the extract and fractions showed that the chloroform extract was inactive against all the protein kinases investigated, while the ethylacetate and n-butanol soluble fractions inhibited all the protein kinases tested. Compound I also inhibited all the kinases tested. The IC50 of the active fractions and compound were also evaluated. Ethylacetate fraction inhibited all the kinases tested with the highest activity against Haspine kinase with IC50 of 1.0 μg/ml, while n-butanol also gave the highest activity against Haspine kinase with 1C50 of 1.3 μg/ml. From the active ethylacetate fractions 3, 4{\textquoteright}, 7, 8- tetrahydroxy flavone was isolated. The Compound exhibited the maximal activity against DYRK1A kinase with an IC50 of 2.05 μg/ml followed by CDK9 with an IC50 of 2.28 μg/ml. Conclusion: 3, 4{\textquoteright},7, 8- tetrahydroxy flavone was isolated was found to be a DYRK1A and CDK9 inhibitor which might justify the anticancer potential of this plant.

}, keywords = {CDK9, DYRK1A, Protein kinases, Tetrahydroxyflavone}, doi = {10.5530/pj.2019.11.89}, author = {Augustine A. Ahmadu and Bilqis A. Lawal and Anas Haruna and Lukman Mustapha} } @article {683, title = {Antibacterial and Cytotoxic Activities of Sponges Collected off the Coast of Togean Islands, Indonesia}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {988-992}, type = {Original Article}, chapter = {988}, abstract = {

Context: Marine sponges (Porifera: Demospongia) have astonishing structural diversity and broad biological activities. Aims: To evaluate the antibacterial and cytotoxic activities of five sponges collected off the coast of Togean Islands, Indonesia, identified as Spheciospongia inconstan, Melophlus sarasironum, Oceanapia amboinensis, Biemna sp and Axinella sp. Methods and Material: All dried sponges materials were extracted by maceration method using methanol and then evaporated by the rotary evaporator to obtain viscous extracts. The determination of antibacterial activity was performed by well agar diffusion method against Staphylococcus aureus and Escherichia coli while the cytotoxic activity was determined by MTT methods on human breast adenocarcinoma (MCF-7) and human colon colorectal carcinoma (HCT-116), followed by determination of the apoptosis mechanism by Annexin V-FTIC assay. Results: M. sarasinorum and Axinella sp showed strong inhibition against S.aureus and E.coli with the diameter of inhibition of 14.21 \± 0.92 mm and 14.36 \± 0.92 mm, and 10.01 \± 2.65 mm and 12.07 \± 1.54 mm, respectively. Moreover, they also exhibited potent cytotoxicity on HCT-116 with IC50 values of 0.002 and 8.518 \μg/mL, respectively. Meanwhile, on MCF-7, only M. sarasinorum showed moderate inhibition with an IC50 value of 87.35 \μg/mL. Annexin V-FTIC assay clearly showed that the cytotoxic mechanism of M. sarasinorum and Axinella sp on HCT-116 and MCF-7 was via apoptosis induction. Conclusion: The sponges of M. Sarasinorum and Axinella sp are undergoing further analysis to identify the active constituents which could be developed as potential antibacterial and anticancer agents.

}, keywords = {Antibacterial, Cytotoxicity, MTT, Sponges, Togean Islands}, doi = {10.5530/pj.2018.5.168}, author = {Muhammad Sulaiman Zubair and Subehan Lallo and Masteria Yunovilsa Putra and Tri Aryono Hadi and Ibrahim Jantan} } @article {753, title = {Antidepressant and Antipsychotic-like Activity of the Ethanolic Extract of the Leaves of Maytenus macrocarpa}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s33-s37}, type = {Original Article}, chapter = {s33}, abstract = {

Introduction: Maytenus macrocarpa (Chuchuhuasi) is an Amazonian Peruvian traditional plant, traditionally used as anti-inflammatory, antipyretic, antihemorrhagic and antidiarrheic agent. Also, chuchuhuasi is known as a master plant, attributing to it properties in the central nervous system. In addition, depression is a disorder of the mood that cause disability to millions of people around the world. For this reason, the aim of this study was to determinate the antidepressant and antipsychotic-like activity of the ethanolic extract of Maytenus macrocarpa. Methods: It was used the ethanolic extract of the leaves of Maytenus macrocarpa (EELMM) in female mice at the experimental model of the Forced Swim Test described by Porsolt. As control, it was used distillate water, fluoxetine and haloperidol. Results: The immobility time of the groups of EELMM has a mean of 38.26 \± 21.57, 84.32 \± 26.68 and 32.17 \± 25.55 for the doses of 750, 1000 and 1250 mg/Kg respectively; and the immobility time had a median of 7.5 [4.07 \– 20.3] and 20.93 \± [17.63 \– 23.75] for the doses of 500 mg/Kg and 1500 mg/Kg. It was seen a positive dose-response between the dose of 500 to 1000 mg/Kg (Pearson correlation of r=0.8339 and R=0.6954) and a negative dose-response between the dose of 1000 to 1500 mg/Kg. (Pearson correlation of r= -0.7590 and R= 0.5760). Conclusion: It was demonstrated the antidepressant-like activity of the ethanolic extract of the leaves of Maytenus macrocarpa with a dose of 500 mg/kg and an antipsychotic-like activity with a dose of 1000 mg/kg.

}, keywords = {Chuchuhuasi, Depression, Fluoxetine, Forced swim test, Haloperidol}, doi = {10.5530/pj.2018.6s.6}, author = {T{\'a}cuna-Calder{\'o}n Ana Lucia and Huaccho-Rojas Juan Jesus and Zimic-Zare Carolina and Pante-Medina Carlos and Salazar-Granara Alberto} } @article {487, title = {Characteristics of Thai Pigmented Rice Milk Kefirs with Potential as Antioxidant and Anti-Inflammatory Foods}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {154-161}, type = {Original Article}, chapter = {154}, abstract = {

Aims: The characteristics, antioxidant property of Hawm Nil rice (Purple rice), Red Hawm rice (Red rice), Khao Dawk Mali 105 rice (White rice) milk kefirs and mixing of three color rice milk kefir in different ratios were investigated. Then, anti-inflammatory activity of Hawm Nil rice kefir was studied. Methodology: The physiochemical properties, total phenolic compounds and antioxidant activities of these rice milk kefirs were investigated. Anti-inflammatory measurements were performed to study blood chemistry, hematological values and tumor necrosis factor-a (TNF-a) level in colitis rats compared with rats treated with prednisolone (positive control) and cow\’s milk kefir. Results: All the rice kefir formulas had lower pH values than the cow\’s milk kefir. Moreover, they all exhibited no changing viscosity. Lactic acid concentrations increased in cow\’s milk kefir during 24-48 h. Alcohol concentrations in all the rice formulas increased within 24-48 h, while cow\’s milk only increased at 72 h. Antioxidant activity, most of the rice milk kefirs had antioxidant activity higher than cow\’s milk by DPPH assay. In addition, the Hawm Nil rice milk kefir had high antioxidant activity by DPPH assay and FRAP assay. Blood chemistry, hematological values and tumor necrosis factor-\α (TNF-\α) levels in colitis rats treated with Hawm Nil rice milk kefir did not differ from those treated with prednisolone and cow\’s milk kefir. TNF-\α in the serum of colitis rats treated with Hawm Nil rice milk kefir was significantly reduced when compared to the PBS buffer. Conclusion: The findings indicated that color rice kefirs may offer protection against chemically induced tissue injury. Hawm Nil rice milk kefir exerted potential antioxidant and anti-inflammatory activities and was safe for human consumption. Other Thai colored rice will be used to develop Thai rice milk kefir products as new and antioxidant-rich beverages and functional foods for human health benefits in the future.

}, keywords = {Anti-inflammatory, Antioxidant, Lactic acid, Rice kefir, Thai color rice}, doi = {10.5530/pj.2018.1.26}, url = {http://fulltxt.org/article/412}, author = {Sirirat Deeseenthum and Vijitra Luang-In and Supaporn Chunchom} } @article {586, title = {Effect of Gynura procumbens Extracts on Anti-Proliferative Activity and its Associated Morphological Changes of Human Glioblastoma multiforme Cell Line (U-87)}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {492-496}, type = {Original Article}, chapter = {492}, abstract = {

Objective: Gynura procumbens (Lour.) Merr is a well-known traditional herb and is widely used for traditional medicine by human. Previous clinical studies have shown the benefit effect of this leaves with inflammation, high blood pressure and others. This study aims to investigate the effect of methanol, ethanol, and ethyl acetate extracts of Gynura procumbens on U-87 cell line, human Glioblastoma multiforme cell line. Methods: In the present study, effect of methanol, ethanol and ethyl acetate extracts on U-87 cell line was determined by MTT-based anti-proliferative assay and any significant changes to the cells towards apoptotic changes was observed under a light microscope. Results: The ethanol and methanol extracts of Gynura procumbens was found to have high anti-proliferative effect on U-87 cell line with IC50 less than 20\μg/ml. By comparing IC50 value, ethanol and methanol extracts of Gynura procumbens had high potential for anti-proliferative effect on U- 87 cell line. Therefore, ethanol and methanol extracts can be a potential anti-proliferative effect on U-87 cell line. Conclusion: To the best of our knowledge, this is the first study of exploring the effect of Gynura procumbens extracts using three different polarity (methanol, ethanol, ethyl acetate) effect on U-87 cell line, Human Glioblastoma multiforme cells.

}, keywords = {Antiproliferative, Ethanol, Gynura procumbens, Methanol, U87 cell line}, doi = {10.5530/pj.2018.3.81}, url = {http://fulltxt.org/article/514}, author = {Mohd Adzim Khalili Rohin and Mimie Noratiqah Jumli and Norhaslinda Ridzwan and Atif Amin Baig and Ahmad Zubaidi Abdul Latif and Norhayati Abd Hadi} } @article {555, title = {Effect of Gynura procumbens Extracts on Anti-Proliferative Activity and its Associated Morphological Changes of Human Glioblastoma multiforme Cell Line (U-87)}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {x}, pages = {XX-XX}, type = {x}, chapter = {XX}, abstract = {

Objective: Gynura procumbens (Lour.) Merr is a well-known traditional herb and is widely used for traditional medicine by human. Previous clinical studies have shown the benefit effect of this leaves with inflammation, high blood pressure and others. This study aims to investigate the effect of methanol, ethanol, and ethyl acetate extracts of Gynura procumbens on U-87 cell line, human glioblastoma multiforme cell line. Methods: In the present study, effect of methanol, ethanol and ethyl acetate extracts on U-87 cell line was determined by MTT-based anti-proliferative assay and any significant changes to the cells towards apoptotic changes was observed under a light microscope. Results: The ethanol and methanol extracts of Gynura procumbens was found to have high anti-proliferative effect on U-87 cell line with IC50 less than 20\μg/ml. By comparing IC50 value, ethanol and methanol extracts of Gynura procumbens had high potential for anti-proliferative effect on U- 87 cell line. Therefore, ethanol and methanol extracts can be a potential anti-proliferative effect on U-87 cell line. Conclusion: To the best of our knowledge, this is the first study of exploring the effect of Gynura procumbens extracts using three different polarity (methanol, ethanol, ethyl acetate) effect on U-87 cell line, Human glioblastoma multiforme cells.

Key words: Gynura procumbens, Ethanol, Methanol, U87 cell line, Antiproliferative.

}, keywords = {Antiproliferative., Ethanol, Gynura procumbens, Methanol, U87 cell line}, doi = {10.5530/jppcm.2018.2s.xx}, author = {Mohd Adzim Khalili Rohin and Mimie Noratiqah Jumli and Norhaslinda Ridzwan and Atif Amin Baig and Ahmad Zubaidi Abdul Latif and Norhayati Abd Hadi} } @article {720, title = {Effect of Lutein on Cytochrome P450 (Isoform CYP3A4) - An in vitro Study}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1093-1095}, type = {Original Article}, chapter = {1093}, abstract = {

Background: Lutein is a carotenoids vitamin rich in many fruits and vegetables and also available in multivitamin products. It is consumed for its effect on eye disease, cancer, diabetes and other health conditions. Recently, herbal preparations are increasingly used in healthcare systems and concomitant administration of synthetic medications may cause pharmacokinetic or pharmacodynamic interactions leading to very serious medical problems. Understanding the ability of herbal extracts and preparations to modulate the metabolizing enzymes can help the health system for proper treatment of patients and thereby can avoid many adverse effects associated with it. The aim of the study was to find the effect of lutein isolated from Tagetes erecta L on cytochrome P450 isoform CYP3A4. Materials and Methods: The different concentrations of lutein (5 \– 100\μg/ml), potassium phosphate buffer, CYP450 reagent and substrate 7-Benzyloxy-4-trifluoromethylcoumarin (BFC) were added to a 96-well plate. The fluorescent intensities of the products were measured by Perkin Elmer Enspire fluorescence reader using an excitation and emission wavelength of 405 nm and 460 nm, respectively to examine the effect of lutein on Cytochrome P 450 isoform CYP3A4 and the IC50 was calculated by plotting concentrations of lutein against the corresponding percent inhibition. Results: All the tested concentrations of lutein showed potent inhibition against CYP3A4 in a dose \– dependent manner. The IC50 value was found to be 35.27\μg/ml. Conclusion: The inhibitory effect of lutein indicates the possibilities of herb-drug interaction if it is co \– administered with prescribed drugs that are normally metabolised by CYP3A4 enzyme.

}, keywords = {CYP3A4, Cytochrome P450, Inhibitory assay, Lutein, Marigold}, doi = {10.5530/pj.2018.6.185}, author = {Murthy Meenapriya and Roy Anitha and Thangavelu Lakshmi} } @article {704, title = {Effects of Kefir Fermentation on Antioxidation Activities (in vitro) and Antioxidative Stress (in vivo) of Three Thai Rice Milk Varieties Prepared by Ultrasonication Technique}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1061-1066}, type = {Original Article}, chapter = {1061}, abstract = {

Aims: The effects of kefir fermentation were investigated on antioxidation activities (in vitro) and antioxidative stress (in vivo) for different Thai rice; Hawm Nil rice, Red Hawm rice and Khao Dawk Mali 105 rice. Methodology: Antioxidant activity (in vitro) was investigated using ferric reducing antioxidant power and 2, 2\´-diphenyl-1-picrylhydrazyl assays. In addition, antioxidative stress (in vivo) was performed using colitis rat models to study nitric oxide (NO), lipid peroxidation (LPO) and superoxide dismutase (SOD) compared with rats treated with prednisolone and cow\’s milk kefir. Results: Antioxidant activity of rice kefir powder from both assays had higher antioxidant activity than cow\’s milk kefir powder. NO levels of colitis rats received Hawm Nil rice kefir powder (HNKP) was reduced when compared to phosphate buffered saline (PBS) group. Moreover, colitis rats received HNKP did not differ in NO levels from colitis rats that received prednisolone and non-colitis rats. The result of LPO product malondialdehyde (MDA) indicated that colitis rats treated with HNKP had reduced TBARS compared to PBS group, and did not differ in TBARS levels from rats that received prednisolone and non-colitis rats. Surprisingly, increase in SOD activity was observed in colitis rats that received HNKP compared to PBS, with similar results of increased SOD in rats that received prednisolone and cow\’s milk kefir powder. Conclusion: Hawm Nil rice kefir may offer a protective effect for antioxidative stress resulting from chemical induction; it has potential as a supplementary food with high antioxidant activity and is regarded as safe for consumer health.

}, keywords = {Antioxidant, Antioxidative stress, Lactic acid, Rice kefir, Thai rice}, doi = {10.5530/pj.2018.5.179}, author = {Sirirat Deeseenthum and Vijitra Luang-In and Stephen Moses John and Pheeraya Chottanom and Supaporn Chunchom} } @article {559, title = {In vitro Antimicrobial Activity Evaluation of Mangrove Fruit (Sonneratia caseolaris L.) Extract}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {598-601}, type = {Original Article}, chapter = {598}, abstract = {

Introduction: Mangrove fruit (Sonneratia caseolaris L) from Sonneratiaceae family known with local name \“Pidada Merah\” has bioactive components. The present study aimed to evaluate the antimicrobial activity of this plant. Method: The sample was macerated using methanol, the antimicrobial activity assay was performed using agar disc diffusion method against Escherichia coli ATTC9637, Staphylococcus aureus ATTC6538, and Candida albicans ATTC10231. Results: Antimicrobial activity of Mangrove fruit methanol extract were obtained the optimum concentration of S. aureus of 80\%, E. coli of 15\%, and C. albicans of 30\%. Conclusion: based on the results, the sample has antimicrobial properties, and this is a preliminary data for further study.

Key words: Sonneratia caseolaris L, Mangrove fruit, Antimicrobial activity, Agar disc diffusion method.

}, keywords = {Agar disc diffusion method, Antimicrobial activity, Mangrove fruit, Sonneratia caseolaris L.}, doi = {10.5530/pj.2018.3.98}, url = {http://fulltxt.org/article/531}, author = {Islamudin Ahmad and Neneng Siti Silfi Ambarwati and Arif Lukman and Muhammad Amir Masruhim and Laode Rijai and Abdul Mun{\textquoteright}im} } @article {618, title = {Inhibition of Advanced Glycation End-Product Formation by Lutein from Tagetes erecta}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {734-737}, type = {Original Article}, chapter = {734}, abstract = {

Background: Advanced glycation end products(AGEs) are formed by non-enzymatic glycation of proteins that enhance vascular permeability in both micro and macro vascular structures by binding to specific macrophage receptors. AGEs affect nearly every type of cells and molecule in the body and play causative role in the vascular complication in diabetes mellitus. Materials and Method: AGE reaction solution was constituted with 10mg/ml bovine serum albumin in 50mM sodium phosphate buffer (pH 7.4) and 0.02\% sodium benzoate into 0.2M fructose and 0.2M of glucose. 2.5 ml of the reaction mixture was treated with lutein (10, 20, 40, 60, 60, 80, 100, 120, 140 \μ g/ml in methanol). Amino guanidine was used as the positive control. After incubating at 37\°C for 7 days, the fluorescence intensity of the reaction was determined at excitation and emission wavelength of 350 nm and 450 nm, respectively, using a multimode reader. The percentage activity was calculated with respect to solvent control. Result: 7 days of exposure to lutein showed a maximum inhibition of 89.27\±0.24 \% at 140\μg/ml and Amino guanidine exhibited 90\% of inhibition. The IC50 of Lutein for AGE inhibition was found to be 77.78\μg/ml and for AG, 72.66\μg/ml.Conclusion: The non-enzymatic adduct formation between the keto group of sugar and amino group of proteins is one of the molecular basis of diabetic complications in hyperglycaemic state. Inhibition of this process will be useful in the management of diabetic complications. Lutein showed dose dependent inhibitory effect on the protein glycation.Hence, it may be used for the management of diabetic complication.

}, keywords = {Advance glycation end product, Amino-guanidine, Diabetes mellitus, Lutein}, doi = {10.5530/pj.2018.4.123}, url = {http://fulltxt.org/article/661}, author = {Karan Rajpurohit Gayathri and Roy Anitha and Thangavelu Lakshmi} } @article {485, title = {Nephroprotective Activity of Methanolic Extract of Lantana camara and Squash (Cucurbita pepo) on Cisplatin-Induced Nephrotoxicity in Rats and Identification of Certain Chemical Constituents of Lantana camara by HPLC-ESI- MS}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {136-147}, type = {Original Article}, chapter = {136}, abstract = {

Introduction: Cisplatin is a highly effective chemotherapeutic agent; its clinical use is severely limited by serious side effects as nephrotoxicity. The aim of this study is to evaluate the nephroprotective activity of defatted methanolic extract of two Egyptian plants: Lantana camara and Cucurbita pepo and certain fractions derived from the defatted methanolic extract of L. camara on cisplatin-induced nephrotoxicity in rats. Also, identification of certain chemical constituents of L. camara by HPLC-ESI- MS. Methods: Nephrotoxicity was induced in rats by single dose of cisplatin. The effect of plants extract at doses 100-400 mg/kg.b.wt comparing with standard; ascorbic acid; was determined using serum urea, creatinine and some ions. Furthermore, the effect of these extracts on some renal antioxidant enzymes and histopathological examination of kidneys were examined. Results: The defatted methanolic extract and ethyl acetate fraction of L. camara showed the highest improvement of renal parameters. Also, HPLC-ESI-MS analysis of L. camara extracts exhibited bioactive phenolic compounds including phenyl ethanoid, flavonoids and phenolic acids. Conclusion: The phytochemical constituents of L. camara are responsible for their nephroprotective activity.

}, keywords = {Antioxidant enzymes, Ascorbic acid, Creatinine, Flavonoids, Histological studies, Phenyl etanoid.}, doi = {10.5530/pj.2018.1.24}, url = {http://fulltxt.org/article/410}, author = {Heba Abdel-Hady and Mortada Mohamed El-Sayed and Afaf Ahmed Abdel-Hady and Maher Mahmoud Hashash and Ahmed Mohamed Abdel-Hady and Tarek Aboushousha and El-Sayed Saleh Abdel-Hameed and Ezzat El-Sayed Abdel- Lateef and Eman Abdalla Morsi} } @article {511, title = {Pharmacodynamic and Pharmacokinetic Interactions of Piperine on Gliclazide in Animal Models}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {221-225}, type = {Original Article}, chapter = {221}, abstract = {

Back Ground: The objective of the present study was to find out the pharmacodynamic and pharmacokinetic interactions of piperine on gliclazide in rats and rabbits. Methods: Influence of piperine on the activity of gliclazide was determined by conducting single- and multipledose interaction studies in rats (normal and diabetic) and diabetic rabbits. Blood samples collected at predetermined time intervals from experimental animals were used for the estimation of glucose and insulin levels by using automated clinical chemistry analyzer and radioimmunoassay method, respectively. \β-cell function was determined by homeostasis model assessment. Additionally, serum gliclazide levels in rabbits were analyzed by highperformance liquid chromatography. Results: Gliclazide showed significant reduction in blood glucose levels in diabetic rats and rabbits. Similarly, piperine also showed significant reduction in blood glucose levels in animals. Additionally, , samples analyzed from all time points in combination with piperine showed peak reduction in blood glucose in diabetic rats and rabbits. The pharmacokinetics of gliclazide was also altered by single- or multiple-dose piperine treatments in rabbits. Conclusion: The interaction of piperine with gliclazide upon single and multiple-dose treatment was pharmacodynamic and pharmacokinetic in nature, indicating the need for periodic monitoring of glucose levels and dose adjustment as necessary when this combination is prescribed to diabetic patients.

}, keywords = {Diabetes, Drug interaction, Gliclazide, Piperine}, doi = {10.5530/pj.2018.2.38}, url = {http://fulltxt.org/article/468}, author = {Umachandar Lagisetty and Habibuddin Mohammed and Sivakumar Ramaiah} } @article {533, title = {Pharmacognostic Studies of Psychotria rubra(Lour.)Poir.}, journal = {Pharmacog Journal}, volume = {10}, year = {2018}, month = {January-2018}, pages = {249-255}, type = {Original Article}, chapter = {249}, abstract = {

Objective: Various traditional systems of medicine enlightened the importance of Psychotria rubra (Lour.) Poir to have a great medicinal value. The present study was carried out to provide a scientific basis of the identification and the authenticity of Psychotria rubra (Lour.) Poir with the help of pharmacognostic parameters, which is not done before. Methods: Roots, stems, and leaves of P. rubra were collected for Pharmacognostic studies involving macros, microscopic evaluation, histochemistry and physicochemical parameters analysis like Ash value, Moisture content, Fluorescence analysis and Thin Layer Chromatography et al. Results: Transverse section of root was found like stone cells, calcium oxalate crystal and vessels in circular shape. Transverse section of stem showed the presence of lenticels and stone cell bands. Transverse section of leaf vein revealed the presence of shaft type of porosity. Powder microscopy revealed the presence of cork cells, stone cells, crystals and resin, fibers, needle crystal beam, thread tracheid and scalariform tracheid. Phytochemical investigation was found like alkaloids, flavones, carbohydrates, saponins, tannins and volatile oils. Results obtained in physicochemical parameters like Total ash value, acid insoluble ash and moisture content were 9.77\%, 0.68\% and 1.28\%, respectively. The leaching degree of P. rubra was higher in ethanol(75\%, v/v) and methanol solutions than that in chloroform, petroleum ether, and tetrachloromethane solutions. Thin Layer Chromatography (TLC) of the extract revealed 4 spots with the Rf values 0.47, 0.46, 0.46, 0.47 with the solvent system of chloroform: methanol: water: formic acid(7:3:1:0.1). Conclusion: The observations confirmed that P. rubra has an obvious Pharmacognostic characteristics, which will be useful towards providing a reliable basis for identification, purity, quality and classification of the plant.

}, keywords = {Histochemistry, Identification, Pharmacognostic, Physicochemical, Poir, Psychotria rubra(Lour.)}, doi = {10.5530/pj.2018.2.44}, url = {http://fulltxt.org/article/474}, author = {Gengqiu Tang and Xiaojing Lin and Xiudi Lai and Xue Gong and Shengguo Ji} } @article {598, title = {Purified Anthocyanin from in vitro Culture of Bridelia retusa (L.) Spreng. Capable of Inhibiting the Growth of Human Oral Squamous Cell Carcinoma Cells}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {559-566}, type = {Original Article}, chapter = {559}, abstract = {

The present study aims in vitro cell suspension culture of Bridelia retusa, isolation of anthocyanin, purification, fractionation and its anti-metastatic potential against oral squamous carcinoma cells. Experimental results reveal that 2, 4-D either alone or in combination with kinetin supplemented in MS medium showed significant initiation of callus from leaf explants than stem. Growth hormones, pH, light, and carbon source influence anthocyanin synthesis. Maximum callus induction was noticed with 2.5 mg/L N6-benzyladenine (BA) + 2 mg/L 2, 4-dichlorophenoxyacetic acid (2, 4-D) (98.9\%). Fresh and dry weight of the calli were i.e., 1.9 \± 0.04 and 0.45 \± 0. 03 g respectively. Optimal response was seen with light on MS medium contain 4\% glucose + 2.5 mg/L BA and 2 mg/L 2, 4-D at pH 3.5 yielded 2.8 mg /g of anthocyanins. Suspension culture medium fortified with 2, 4-D (2.5 mg/L) + BA (2 mg/L) at pH 5.0 induced anthocyanin production at pH 4.4 \– 4.6. HCl-ethanol extraction for 90 min yielded the maximum anthocyanin content. Fractionation of anthocyanin using HPLC coupled with mass spectrometry revealed 07 fractions such as acylated cyanidins, two peonidins, cyanidin 3-p-coumaroyl and feruloyl diglucoside-5-glucosides. In the search of novel therapeutic drugs against cancer, cytotoxicity effect of B.retusa anthocyanin extracts on human oral squamous cell carcinoma (SCC4, SCC9 and SCC25) cells using cell adhesion and cell viability assay was carried. The morphological alterations in SCCs cells after treatment with B.retusa anthocyanin includes nuclear condensation, fragmentation and apoptotic cells as revealed by Hoechst stain. Flow cytometry showed arresting of SCC25 cells mostly in the G0/G1 and S-G2/M stages with a concomitant up regulation of sub-G1 fraction, indicating cell death by apoptosis. Apoptosis was further substantiated by the activation of caspase-3 expression in the SCC25 cells treated with B.retusa anthocyanin. Thus, it is possible to suggest that B.retusa anthocyanin cause apoptosis of SCCs and warrant further investigation using animal models.

}, keywords = {Anthocyanin, Anti-metastatic potential, Apoptosis, Bridelia retusa, Cell suspension, in vitro culture, Purification}, doi = {10.5530/pj.2018.3.91}, url = {http://fulltxt.org/article/524}, author = {Aswathy Jayasree Madanakumar and Bosco Lawarence and Manoj GS and Murugan Kumaraswamy} } @article {751, title = {A Triterpene and a Depside from Parmotrema austrocetratum Elix and J. Johnst.}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s27-s29}, type = {Original Article}, chapter = {s27}, abstract = {

Introduction: Parmotrema austrocetratum Elix and J. Johnst. (syn. Rimelia austrocetrata Elix and J. Johnst.) which belongs to a large genus of lichenized fungi, Parmotrema Massalongo under family Parmeliaceae was investigated for its chemical constituents. Methods: The compounds were isolated by silica gel chromatography and their chemical structures were elucidated by NMR spectroscopy. Results: Chemical investigation of the dichloromethane extract of Parmotrema austrocetratum Elix and J. Johnst. has led to the isolation of zeorin (1) and atranorin (2). Conclusion: P. austrocetratum shares similar chemical characteristic with other Parmotrema species which afforded atranorin. This work highlights the first reported isolation of 1 from P. austrocetratum and the genus Parmotrema.

}, keywords = {Atranorin, Parmeliaceae, Parmotrema austrocetratum, Rimelia austrocetrata, Zeorin}, doi = {10.5530/pj.2018.6s.4}, author = {Consolacion Y. Ragasa and Maria Carmen S. Tan and Virgilio C. Linis and Chien-Chang Shen} } @article {267, title = {ACE Inhibitory Activity, Total Phenolic and Flavonoid Content of Pereskia saccharose Griseb. Leaves Extract}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {285-287}, type = {Original Article}, chapter = {285}, abstract = {

Introduction: Angiotensin-converting enzyme inhibitors (ACEi) are drugs that can control hypertension. Pereskia saccharose Griseb. leaves have been used traditionally as antihypertensive. Objective: The objective of this study was to determine the antihypertensive activity through inhibition of ACE activity, the total phenolic content and total flavonoid content of the ethanolic extract of Pereskia saccharose Griseb. leaves and its fractions. Methods: Extraction was done by maceration with 80\% ethanol and fractionation performed by liquid-liquid partition. Results: In vitro ACE inhibitory activity assay of the ethanolic extract using ACE Kit-WST Dojindo had IC50 value of 3.448 \μg/mL and ethyl acetate fraction had IC50 value of 1.714 x 10-3 \μg/mL. Ethyl acetate contained the highest amounts of both TPC (72.991 \± 0.932 mg GAE/g sample) and TFC (61.337 \± 1.612 mg QE/g sample). Conclusion: The results suggest that Pereskia saccharose Griseb. possess ACE inhibitory activity.

}, keywords = {ACE inhibitor, Flavonoid, Pereskia saccharose Griseb, phenolic}, doi = {10.5530/pj.2017.2.49}, url = {http://phcogj.com/fulltext/316}, author = {Sarlina Jihan Lusiyanti and Katrin and Rissyelly and Nuraini Puspitasari and Putu Gita Maya Widyaswari Mahayasih} } @article {328, title = {Alpha-Glucosidase Inhibitory Activity and Fractionation of Bioactive Compounds from bark Extracts of Sibucao (Caesalpinia sappan L.) In the Philippines}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017 }, pages = {356-360}, type = {Original Article}, chapter = {356}, abstract = {

Diabetes is a chronic disease that affects millions of people around the world. Although conventional medicine is available, it is usually accompanied by serious side effects such as gastrointestinal problem. Thus, the search for alternative medicine from natural sources is of primary importance. Context: The study is concerned with Caesalpinia sappan L. found in the vicinity of Baybay City, Leyte Philippines. Furthermore, it deals with ethanolic and aqueous extracts of the bark only. It was conducted to determine the alpha-glucosidase inhibitory activity of C. sappan to provide evidence to support its efficacy as a folkloric medicinal plant. Aims: This work aimed to evaluate the alpha-glucosidase inhibitory activity of aqueous and ethanolic bark extracts of Sibucao (Caesalpinia sappan L.) and to partially fractionate its bioactive compounds. Settings and Design: Extracts were prepared in increasing concentration to get IC50 values. Samples were analysed in triplicate both for extracts and fractions collected from chromatography. Methods and Material: Caesalpinia sappan L. bark samples were collected from the vicinity of Visayas State University. Plant materials were dried, weighed and stored. Aqueous and ethanolic bark extracts were prepared using water and 20\% ethanol. The total phenolic content of the extracts were determined and the \α-glucosidase inhibitory activity of crude bark and aqueous extracts were measured using the method of Kim et al., 2011. Partial fractionation of bioactive compounds was done successively using gradient elution. The \α-glucosidase inhibitory activity of fractions were then determined and Rf values of active compounds were measured using thin layer chromatography (TLC). Results: Results revealed that aqueous extract (2000 ppm) and ethanolic extract (2000 ppm) show high \α-glucosidase inhibitory activity of 100\% and 59\% respectively. IC50 values of aqueous and ethanolic extract were found to be 300.52 \± 1.467 ppm and 1560.81 \± 2.582 ppm, respectively. TLC of fractions show 7 peaks for aqueous extract and 6 peaks for ethanolic extract in which compound with Rf value 0.70 had the highest inhibitory activity of 65\%. Conclusions: Taken together, the high \α-glucosidase inhibitory activity of aqueous extracts support the effectiveness of C. sappan L. bark decoctions. In addition, results from bioassay-guided fractionation can be used as an effective tool for further isolation and characterization of \α-glucosidase inhibitors from Caesalpinia sappan L. in the Philippines.

}, keywords = {Caesalpinia sappan, Flavonoids, Fractionation, Type II diabetes, α-glucosidase}, doi = {10.5530/pj.2017.3.60}, url = {/files/PJ-9-3/10.5530pj.2017.3.60}, author = {Ea Kristine Clarisse B. Tulin and Ma Theresa P. Loreto and Edgardo E. Tulin} } @article {226, title = {Anti-inflammatory activity of isolated compounds from the stem bark of Garcinia cowa Roxb}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {December 2016}, pages = {55-57}, type = {Original Article}, chapter = {55}, abstract = {

Objective: To find the anti inflammatory active compounds from methanol extract of Garcinia cowa. Methods: To evaluate the inhibitory activity of isolated compounds on nitric oxide (NO) production, culture media was assayed using Griess reaction. An equal volume of Griess reagent (1\% sulphanilamide and 0.1\% N-(L-naphthyl)-ethylene diamine dihydrochloride, dissolved in 2.5\% H3PO4) was mixed with culture supernatant and color development was measured at 550 nm using a micro plate reader. The amount of nitrite in the culture supernatant was calculated from a standard curve (0\–100 \μM) of sodium nitrite freshly prepared in deionized water. Percentage of the NO inhibition was calculated by using nitrate level of IFN-\γ/LPS-induced group as the control. Results: Isolated compounds, tetraprenyltoluquinone, rubraxanthone and \α-mangostin from stem bark of Garcinia cowa Roxb were evaluated for their anti-inflammatory activity. Only \α-mangostin exhibited strong anti-inflammatory activity with 83.42 \% inhibition of NO and without inducing severe cytotoxicity at 50M. Rubraxanthone showed weak inhibition of NO with 23.86 \% inhibition of NO while maintained 77.32 \% of cell viability. TPTQ also showed the strong inhibition of NO with 80.98 \% inhibition but unfortunately this compound also induced severe cytotoxicity with 39.62\% viability. Conclusion: \α-Mangostin exhibited strong anti-inflammatory activity without inducing severe cytotoxicity at 50 M. Rubraxanthone showed weak inhibition of NO while Tetraprenyltoluquinone also showed the strong inhibition of NO however this compound also induced severe cytotoxicity.

}, keywords = {Anti-inflammatory, Garcinia cowa, Nitric oxide, rubraxanthone, tetrapreniltoluquinone, α-mangostin}, doi = {10.5530/pj.2017.1.10}, author = {Fatma Sri Wahyuni and Daud Ahmad Israf Ali and Nordin Hj. Lajis and Dachriyanus} } @article {265, title = {Antioxidant Activity and Lipoxygenase Enzyme Inhibitory Assay with Total Flavonoids Content from Garcinia hombroniana Pierre Stem Bark Extract}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {276-279}, type = {Original Article}, chapter = {276}, abstract = {

Introduction: Garcinia has been known as a rich source of xanthones, flavonoids, and phenols. The aim of this research is to obtain data of antioxidant activity and to observe potential inhibition of lipoxygenase activity that most active from methanolic, ethyl acetate and n-hexane extracts with total flavonoids content from most active extracts from the bark of Garcinia hombroniana Pierre. Methods: The antioxidant activity was measured using the ferric reducing antioxidant power (FRAP), the anti-inflammatory assay was measured using inhibition of lipoxygenase activity test, qualitative analysis of flavonoids using thin layer chromatography, and total flavonoids content was measured using AlCl3 colorimetric method. Results: The results showed that the ethyl acetate extract from G. hombroniana Pierre stem bark as the most active extract for antioxidant and lipoxygenase inhibition activity with EC50 and IC50 value consecutively 15.34 \μg /ml; 0.26 \μg /ml. Total flavonoids content of ethyl acetate is 7.430 mg QE/g extract. The results of this study showed bark extract Garcinia hombroniana Pierre has antioxidant activity and potent to inhibit lipoxygenase activity. Conclusion: Based on the research for methanolic, ethyl acetate and n-hexane extract, it can be concluded that the ethyl acetate extract of G. hombroniana Pierre as the most active extract for antioxidant and lipoxygenase inhibition activity.

}, keywords = {Antioxidant, Garcinia hombroniana Pierre, Inflammation, Lipoxygenase, Total flavonoids content}, doi = {10.5530/pj.2017.2.47}, url = {http://phcogj.com/fulltext/314}, author = {Amanda Listiyani and Berna Elya and Nuraini Puspitasari} } @article {378, title = {Comprehensive Evaluation of Antioxidant Potential of Selected Osbeckia species and their in vitro Culture, Purification and Fractionation}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {July 2017}, pages = {674-682}, type = {Original Article}, chapter = {674}, abstract = {

Background: Health-benefit properties of natural pigments have been intensely studied, especially the anthocyanins. In the last few decades, research on anthocyanins has attracted biologists by the increasing evidence of their health beneficial effects. Osbeckia, belongs to Melastomataceae and is well-known for colouring pigments and other bioactive compounds. In the present study, total anthocyanin and antioxidant capacity indicators were evaluated from 8 Osbeckia spp. and anthocyanin was extracted from in vitro cultures of O. aspera and O. reticulata. Materials and Methods: The antioxidant effect was studied using ABTS (2, 2\’-azino-bis-3-ethyl benzthiazoline-6-sulphonic acid) radical cation decolourisation assay, the FRAP, the scavenging ability of hydroxyl radicals and the superoxide anion scavenging activity. Anthocyanin extracted from in vitro cultures were purified and fractionated using column chromatography and LC-MS MS analysis. Results: In vitro cultures of O. aspera was obtained in MS medium fortified with various combinations of Benzyl Adenine (BA), Naphthalene acetic acid (NAA) and 2, 4-D. The chromatograms of O. aspera revealed the presence of malvidin-3 -diglucoside, peonidin, delphinidin and cyanindin whereas O. reticulata cultures accumulated large amounts of malvidin, cyanindin and cyanidin aglycone. The purified anthocyanins of these species were evaluated for their antioxidant potential and was found more remarkable than the crude extracts. Conclusion: Osbeckia species are rich in anthocyanin and therefore display potential AOX power. O. aspera and O. reticulata callus was induced in vitro production of anthocyanins. The pool of anthocyanins was purified and fractionated by LCMS/ MS and AOX assays were performed with the purified anthocyanin which showed higher level activities.

}, keywords = {Anthocyanins, Antioxidant Capacity, Free Radicals, Osbeckia Spp., Reactive Oxygen Species}, doi = {10.5530/pj.2017.5.107}, url = {/files/pj-9-5/10.5530pj.2017.5.107/index.html}, author = {Bosco Lawarence and Murugan K} } @article {219, title = {Cytotoxicity of Fucoidan from Three Tropical Brown Algae Against Breast and Colon Cancer Cell Lines}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {December 2016}, pages = {14-20}, type = {Original Article}, chapter = {14}, abstract = {

Introduction: Fucoidan is a sulfated polysaccharide that has a wide range of bioactivities including anti-cancer. This polysaccharide commonly is extracted from marine brown seaweed. There is lack of information on the fucoidan extracted from tropical brown algae and its anti-cancer activity. Objectives: The objectives of this study were to purify fucoidan from Sargassum sp., Turbinaria sp. and Padina sp., and to evaluate their cytotoxicity against breast cancer (MCF-7) and colon cancer cells (WiDr). Materials and Methods: Fucoidan extraction was conducted by using acid extraction method. Purified fucoidans were obtained by DEAE cellulose column chromatography and confirmed by HPLC and FT-IR spectrometry. The cytotoxicity was evaluated by using the MTT (3-[4,5-dimethylthiazol-2-yl] -2,5- diphenyltetrazolium bromide) assay. Results: Fucoidan from Sargassum sp. and Turbinaria sp. showed low cytotoxicity with IC50 ranging between 461-663 \μg/mL. Higher cytotoxicity against MCF-7 and WiDr was showed by fucoidan from Padina sp. with IC50 of 144 and 118 \μg/mL, respectively. While its IC50 against Vero cells was 501 \μg/mL.Standard fucoidan from Fucus vesiculosus exhibited IC50 of 60, 63 and 211 \μg/mL against MCF-7, WiDr and Vero Cells, respectively. Although the IC50 was higher than that of standard fucoidan, Padina sp. fucoidan showed cytotoxicity comparable with standard fucoidan at concentrations below 100 \μg/mL. Conclusion: These results indicated that Padina sp.fucoidan showed potential selective cytotoxicity, and promising for the development of an anti-cancer compound.

}, keywords = {Breast cancer, Colon cancer, Cytotoxicity., Fucoidan, Phaeophyta}, doi = {10.5530/pj.2017.1.3}, author = {Alim Isnansetyo and Fadilah Nor Laili Lutfia and Muhammad Nursid and Trijoko and Ratna Asmah Susidarti} } @article {341, title = {Effects of Rainfall on the Antimicrobial Activity and Secondary Metabolites Contents of Leaves and Fruits of Anadenanthera colubrina from Caatinga Area.}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {May 2017}, pages = {435-440}, type = {Original Article}, chapter = {435}, abstract = {

Background: Anadenanthera colubrina (Vell.) Brenan var. cebil (Griseb) is a plant widely used for medicinal proposes in Brazilian Northeast. Objective: This study aimed to analyze the influence of rainfall indexes (RI) in antimicrobial activity and phytochemical constituents of extracts from leaves and fruits of A. colubrina. Material and Methods: Samples were collected in Catimbau National Park (Bu\íque, Pernambuco, Brazil) at September 2010 (RI: 75 mm) and January (RI: 65 mm), April (RI: 162 mm) and June 2011 (RI: 73 mm). The extracts were prepared by Soxhlet extraction using cyclohexane, chloroform, ethyl acetate and methanol. The antimicrobial activity was determined by MIC and MBC values. Results: All extracts showed antimicrobial activity, but ethyl acetate extracts (from all periods) were more active. Strong correlations were found between the RI and the average MIC of MLE (\ρ: -0.99), EALE (\ρ: -0.81), CHFE (\ρ: -0.81), EAFE (\ρ: -0.80); while moderate and weak correlations were found for other extracts. Through a HPLC analysis was possible to reveal that the samples collected from dry periods had more chemical diversity (as they presented more peaks). Gallic acid and quercetin (and derivative compounds) were identified. The levels of quercetin were enhanced in extracts from dry months. Conclusion: Our results showed that the rainfall has a positive effect on the antimicrobial activity of leaves and fruits of A. colubrina, however these extracts showed more chemical diversity during dry months.

}, keywords = {Antimicrobial agents, Medicinal plants, Natural products, Semi arid area}, doi = {10.5530/pj.2017.4.73}, url = {/files/PJ-9-4/10.5530pj.2017.4.73}, author = {Daniel Rodrigo Cavalcante de Ara{\'u}jo and Lu{\'\i}s Cl{\'a}udio Nascimento da Silva and Wolfgang Harand and J{\'u}lia Morais Fernandes and Thaciane da Cunha Soares and Silvana Maria Zucolotto Langassner and Raquel Brandt Giordani and Rafael Matos Ximenes and Alexandre Gomes da Silva and M{\'a}rcia Vanusa da Silva and Maria Tereza dos Santos Correia} } @article {371, title = {GC-MS analysis of Tasmannia lanceolata Extracts which Inhibit the Growth of the Pathogenic Bacterium Clostridium perfringens}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {July 2017}, pages = {626-637}, type = {Original Article}, chapter = {626}, abstract = {

Introduction: Clostridium perfringens is the etiological agent of clostridial myonecrosis and enteritis necroticans. Infections result in exotoxin production, tissue necrosis and unless promptly treated, often result in death. Methods: Tasmannia lanceolata extracts were investigated for C. perfringens growth inhibitory activity by disc diffusion analysis and MIC determination. Toxicity was evaluated by Artemia nauplii bioassay and the most potent extracts were phytochemically evaluated by GC-MS headspace analysis. Results: All T. lanceolata berry and leaf extracts displayed potent C. perfringens growth inhibition. The berry extracts were more potent growth inhibitors than the corresponding leaf extracts, although the leaf extracts were also potent growth inhibitors. The berry aqueous, methanolic and ethyl acetate extracts were particularly potent growth inhibitors, with MIC values of 654, 65 and 329 \μg/mL respectively. T. lanceolata leaf also displayed good efficacy, with an MIC of 839, 1255 and 625 \μg/mL for the aqueous, methanolic and ethyl acetate extracts respectively. All extracts were nontoxic in the Artemia franciscana bioassay, with LC50 values substantially \> 1000 \μg/mL. Non-biased GC-MS analysis of the aqueous, methanolic and ethyl acetate berry extracts revealed the presence of high relative levels of a diversity of terpenoids. Conclusions: The lack of toxicity of the T. lanceolata extracts and their potent growth inhibitory bioactivity against C. perfringens indicates their potential as medicinal agents in the treatment and prevention of clostridial myonecrosis and enteritis necroticans. GC-MS metabolomic profiling studies indicate that these extracts contained a diversity of terpenoids, with monoterpenoids being particularly abundant.

}, keywords = {Enteritis necroticans, Gas gangrene, Myonecrosis, Tasmannia Lanceolata, Winteraceae}, doi = {10.5530/pj.2017.5.100}, url = {/files/pj-9-5/10.5530pj.2017.5.100/index.html}, author = {Mitchell Henry Wright and Cameron Jay Lee and Megan Sarah Jean Arnold and Joseph Shalom and Alan White and Anthony Carlson Greene and Ian Edwin Cock} } @article {240, title = {HPLC Fingerprint Analysis and Content Determination of Extract with Anticancer Activities of Sedi Linearis Herba}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {128-134}, type = {Original Article}, chapter = {128}, abstract = {

Aims: The purpose of this paper was to develop a HPLC fingerprint analysis method, compare the chromatographic fingerprints characteristics of the ethyl acetate extract with anticancer activity from Sedi Linearis Herba (Sedum lineare Thumb.) collected in different seasons and environments, determine the contents of active ingredients hyperoside, isoquercetin and astragalin of each sample by HPLC, provide believable scientific foundations for quality control and evaluation of Sedi Linearis Herba. Methods: The analyte was analyzed using BDS Hypersil C18 as chromatographic column, acetonitrile -0.1\% acetic acid solution as the mobile phase (gradient elution). Results: The results showed that the major active ingredient contents of the samples collected in different seasons but at the same environment all had obvious differences. These ingredient contents of the samples collected in the end of April were much more than those in mid-August in general. Moreover, the major active ingredient contents of the samples picked in the same season but different environments were different too. For instance, the major ingredient contents of the sample in damp environment in August were more than those in sunny environment. Conclusion: All of these indicated that the HPLC fingerprint analysis and contents determination method established were very useful for quality analysis and control of Sedi Linearis Herba.

}, keywords = {Anticancer Activity Ingredients, Content Determination, HPLC Fingerprint, Sedum lineare Thunb.}, doi = {10.5530/pj.2017.2.22}, url = {http://phcogj.com/fulltext/289}, author = {Diangang Liu and Qing Mei and Weifang Long and Xiangluan Wan and Dingrong Wan and Luyao Wang} } @article {261, title = {Inhibition Activity of Angiotensin Converting Enzyme (ACE) and Determination of Total Phenolic and Flavonoid Compound from Bitter Melon Leaves (Momordica charantia L.)}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {252-256}, type = {Original Article}, chapter = {252}, abstract = {

Introduction: Hypertension is a leading problem in Indonesia, because of the high prevalence and the long term effect. Bitter melon leaves (Momordica charantia L.) has been traditionally utilized to treat hypertension, yet not many studies explained the antihypertension effect of this plant. Methods: This study was conducted to test the benefit of bitter melon leaves as antihypertension using angiotensin converting enzyme inhibition activity in 80\% ethanolic extract and its fractions (n-hexane, ethyl acetate, and n-butanol) using ACE kit-WST (Dojindo, Japan). Then the antihypertension activity was associated with the phenolic content which was expressed in gallic acid equivalent (GAE) and total flavonoid in quercetin equivalent (QE). Results: Result of the study showed that the IC50 value obtained from the ethanolic extract to inhibit ACE activity was 7.52 \μg/mL and the highest inhibition obtained in ethyl acetate fraction with IC50 value was 4,29 \μg/mL. Phenolic total and flavonoid total determination also showed that the highest content obtained in ethyl acetate fraction with 18.752 mg GAE/gr extract and 8.310 mg QE/gr extract, respectively. Conclusion: According to the study, it could be concluded that bitter melon (Momordica charantia L.) leaves provide inhibition activity against Angiotensin Converting Enzyme (ACE) and chemical compounds that were expected to play an active role in inhibiting ACE were flavonoid and tannin.

}, keywords = {Angiotensin converting enzyme, antihypertension, Momordica charantia L., total flavonoid., total phenolic}, doi = {10.5530/pj.2017.2.43}, url = {http://phcogj.com/fulltext/310}, author = {Putri Lestari and Katrin and Rissyelly and Putu Gita Maya Widyaswari Mahayasih} } @article {443, title = {Isolation, Purification of Quercetin from in vitro Cell Suspension Culture of Caesalpinia pulcherrima and its Analysis by HPLC-DAD and NMR}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {November 2017}, pages = {s44-s51}, type = {Original Article}, chapter = {s44}, abstract = {

Background: Caesalpinia pulcherrima, belongs to Caesapiniaceae, is a known medicinal plant widely distributed in India and is used in traditional medicine for the treatment of various ailments. Many phytochemicals are reported from the plant as potential source of crude drug. Materials and Methods: An efficient and simple reproducible protocol was developed for callus production using leaf explants of C. pulcherrima. The combination of 2, 4-D, kin and BA, was used for the callus induction. Subsequently, cell suspension culture and quercetin synthesis from in vitro callus was attempted. Role of effect of elicitors (Sucrose, ABA and salicylic acid) in cell suspension culture was carried in MS medium containing 2,4-D + BA + kinetin. Flavonoids was purified, fractionated by HPLC-DAD and NMR. Results: 2, 4-D (2.5 mg/L), BA (2.5 mg/L) + kin (1 mg/mL) was effective for maximum callus induction from leaf explants. Significant cell suspension culture was noticed with liquid MS medium containing 2,4-D (2 mg/L)+ BA (1mg/L)+ kinetin (1.5 mg/L). Sucrose, ABA and salicylic acid (SA) at different concentrations influenced cell biomass and quercetin accumulation. The addition of ABA/SA along with sucrose was found to have no remarkable effect on cell biomass and also quercetin synthesis. However, cells cultured in the medium fortified with 45 g/L sucrose without ABA/ SA showed the highest quercetin content (16.5 mg/g). Flavonoids was purified, fractionated by HPLC-DAD and NMR revealed the presence of 9 components such as quercetin, isoquercetin, quercetrin, rutin, quercetin 3-O-\β-D-xyloside, quercetin 3-Oarabinopyranoside, quercetin 3-O- \α-arabinopyranosyl (1\→2) \β-galactopyranoside, isorhamnetin 3-O-rutinoside and an unknown compound. Conclusion: C. pulcherima reveals significant synthesis of quercetin. Quercetin content recorded in cell suspension culture was significantly higher compared with in vivo plants grown in fields and the compounds were identified by NMR.

}, keywords = {Caesalpinia pulcherrima, Callus, Cell suspension culture, Elicitors; growth hormones, Quercetin}, doi = {10.5530/pj.2017.6s.156}, url = {http://fulltxt.org/article/380}, author = {Aswathy Jayasree Madanakumar and Greeshma Murukan and Bosco Lawarence and Murugan Kumaraswamy} } @article {251, title = {Screening of Ethanolic Extracts of Medicinal Herbal Drugs Against Oral Microbes}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {201-203}, type = {Original Article}, chapter = {201}, abstract = {

Aim: The aim of the present study is to screen the ethanolic extracts of medicinal herbal drugs against oral microbes. Objective: In this study, 3 medicinal herbs were evaluated for antimicrobial activity against five common oral bacteria as a screen for potential candidates for the development of natural antibiotics. Methods: Ethanolic extracts of medicinal herbs were tested for activity against Enterococcus faecalis, Lactobacillus acidophilus, Streptococcus mutans, and Streptococcus sanguis grown in brain heart infusion (BHI) broth. A broth microdilutionassay was used to determine the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). A disk diffusion assay was performed by inoculating bacterial cultures on BHI agar plates with paper disks soaked in each of the medicinal herb extracts. Results: The ethanolic extracts of many of the 3 medicinal herbs showed antimicrobial activity against the five types of pathogenic oral bacteria. The extracts of Caralluma fimbriata, Hemidesmus indicus, and Grape seed effectively inhibited the growth of oral bacteria and showed distinct bactericidal activity. Conclusion: These results suggest that alternative medicines with proven antimicrobial effects, such as Caralluma fimbriata, Hemidesmus indicus, and Grape seed may be useful for the treatment of dental diseases.

}, keywords = {Anti cariogenic, Dental caries, Natural products Pathogenic, Oral bacteria}, doi = {10.5530/pj.2017.2.33}, url = {http://phcogj.com/fulltext/300}, author = {Harsha L and Lakshmi Thangavelu} } @article {165, title = {Anti-anemia Effect of Chlorophyll from Katuk (Sauropus androgynus) Leaves on Female Mice Induced Sodium Nitrite}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {June/2016}, pages = {375-379}, type = {Original Article}, chapter = {375}, abstract = {

Context: Sodium nitrite (NaNO2) in blood is highly reactive with haemoglobin (Hb), thus affecting hematopoiesis and induction of methemoglobinemia. Aim: This study was conducted to determine the effect of chlorophyll from katuk (Sauropus androgynus) leaves on the level of Hb, Malondialdehyde (MDA), ferritin, and schistocytes percentage in female mice induced NaNO2. Settings and Design: Experimental research was conducted using 24 female mice strain Balb-c. Methods and Material: NaNO2 0.3 ml/head/day given during 18 days, while the chlorophyll or Cu-chlorophyllin as much as 0.7 ml/head/day given the following day for 14 days. Statistical analysis used: Results are reported as mean values \± SD and statistically analyzed by One Way Anova test with 95\% significance level. Results: The Hb levels of blood plasma in the control group, NaNO2 induction, induction NaNO2 and chlorophyll of katuk leaves (NaNO2+katuk), induction of NaNO2 and Cu-chlorophyllin from K-LiquidTM (NaNO2+Cu-chlorophyllin) in sequence is 13.29 g/dl; 11.83 g/dl; 14.54 g/dl; 13.99 g/dl, whilst the MDA levels in each group is 2.10 \± 0.11 mol/L, 3.44 \± 0.38 mol/L, 2.31 \± 0.18 mol/L, 2.31 \± 0.13 mol/L, and the ferritin levels is 62.71 \± 6.42 ng/ml; 63.22 \± 7.59 ng/ml; 67.45 \± 8.03 ng/ml, and 64.74 \± 7.80 ng/ml, respectively. The fragment schistocytes ocyte percentage\’s in each group is 0\%, 0.11\%, 0.01\%, 0.03\%. The ferritin levels tend to increase in NaNO2+katuk. Mann Whitney test results obtained no significant difference in Hb, MDA level and schistocytes percentage between the groups of mice that received NaNO2+katuk NaNO2+Cu-chlorophyllin (p\>0.05). This indicates that chlorophyll from S. androgynus leaves as effective as Cu-chlorophyllin in decrease the MDA levels after NaNO2 treatment, and although not significant, it can increase ferritin levels. Conclusion:\ The antioxidant activity of chlorophyll from katuk leaves are able to decrease schistocytes percentage\’s and MDA level. The increasing of Hb and ferritin level indicates its potential in the treatment of haemolityc anaemia. Further studies aimed at the mechanisms of action of this chlorophyll are needed.

}, keywords = {Anemia, Chlorophyll, Ferritin, Schistocytes., Sodium nitrite}, doi = {10.5530/pj.2016.4.10}, author = {Suparmi Suparmi and Sampurna Sampurna and Nur Anna C.S and Alvenia Meilina Ednisari and Galuh Dea Urfani and Iqrommatul Laila and Heavin Rakhmat Saintika} } @article {102, title = {The Anticancer Potential of Pavonia odorata extract on Human Breast (MD-MB-231), Prostate (PC-3) and Lung (Calu-6) Cancer cell lines}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {28-30}, type = {Original Article}, chapter = {28}, abstract = {

Introduction: A huge reservoir of bioactive compounds exists in many species of plants, only a small percentage of which have been examined and continued to be an important source of anticancer agents. Worldwide effects are ongoing to identify new anticancer compounds from plants. With the current decline in the number of new molecular entities from the pharmaceutical industry, novel anticancer agents are being sought from traditional medicines. Objective: In the present study we investigated the efficacy of methanol extracts of Pavonia odorata, for its clonogenic inhibition on Human Breast cancer (MD-MB-231), Prostate cancer (PC-3) and Lung cancer (Calu-6) cell lines. Materials and Methods: The cytotoxic effect was evaluated by MTT assay. Results: The methanol extract of P. odorata showed significant cytotoxicity against MD-MB-231 and Calu-6, when compared to PC-3cells. Conclusion: The methanol extracts of P. odorata, showed effective cytotoxic activities in a dose dependent manner. Future work will be interesting to know the chemical composition and also better understanding the mechanism of action will help in developing it as drug for therapeutic application.

}, keywords = {Alternative medicine, Anti-cancer, Drugs, Indian Medicinal plants, Inhibition.}, doi = {10.5530/pj.2016.1.6}, author = {Girish H V and Vinod A B and Dhananjaya B L and Satish Kumar D and Senthil Duraisamy} } @article {213, title = {Awareness of Complimentary and Alternative Medicine- A Cross Sectional Survey Among Pharmacists}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {593-594}, type = {Original Article}, chapter = {593}, abstract = {

Aim: To determine the prevalence of complementary and alternative medicine among pharmacists. Materials and method: This survey was a cross sectional study. A set of 30 questionnaires containing 15 questions where given to various pharmacists of different colleges. Datas were collected and statistics was done using SPSS software and represented in graph form. Background: Use of complementary and alternative medicine (CAM) by the U.S. population increased significantly in the past 2 decades. The purpose of this study was to determine, among the Indian community, the prevalence and utilisation patterns of complementary and alternative medicine (CAM), attitudes associated with CAM use and communication patterns of CAM users. Conclusion: The knowledge about and use of CAM is wide among pharmacists . In- depth studies on the knowledge and use of CAM among other health care professionals and among ethnic minorities are urgently needed and may help to better manage the treatment of minor disorders as well as chronic diseases.

}, keywords = {awareness, Complementary and alternative medicine, knowledge, pharmacist}, doi = {10.5530/pj.2016.6.12}, author = {Reshmi B and Thangavelu Lakshmi} } @article {152, title = {Fingerprint Of Tiger Balm{\textregistered} By Thermal Desorption Gas Chromatography Mass Spectroscopy}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {February 2016}, pages = {230-233}, type = {Original Article}, chapter = {230}, abstract = {

Introduction: Tiger Balmis a blend of volatile oils used for many years in control of muscle cramps and headache. Objectives: To establish a quick and accurate method of analysis for Tiger Balm. Materials and Methods: GC-MS and TD GC-MS were used in parallel to define the metabolites available in Tiger Balm blend, high quality standards were help in confirmation of the metabolites identities. Results: TD GC-MS was more\ efficient in showing the 1:1 relative abundance of camphor and menthol\ which can be taken as a chemical marker of this herbal medicine. Conclusion:\ In this work we applied efficiently the use of TD GC-MS in quality\ analysis of semisolid herbal medicine with volatile scents without the\ need of tedious pre-treatment with organic solvents, which is required\ by using GC-MS.

}, keywords = {Camphor, GC-MS, Menthol., TD GC-MS, Tiger Balm{\textregistered}}, doi = {10.5530/pj.2016.3.9}, author = {Omar A. Aldulaimi and Wen W. Li} } @article {105, title = {Induction of hairy roots and plant regeneration from the medicinal plant Pogostemon Cablin}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {50-55}, type = {Original Article}, chapter = {50}, abstract = {

An efficient transformation system for the medicinal and aromatic plant, Pogostemon cablin Benth was developed by using Agrobacterium rhizogenes ATCC15834 and C58C1. Hairy roots formed directly from the cut edges of leaf explants after infection for 2 days. The highest frequency of leaf explant transformation by A. rhizogenes ATCC15834 and C58C1 were 83.3\% and 80.5\% after pre culture about 2 days and infection by the bacterium containing 15 mg l-1 acetosyringone about 25 min. The PCR amplification showed that rolB genes of Ri plasmid of A. rhizogenes were integrated and expressed into the genome of transformed hairy roots. The optimum medium for callus induction of hairy roots consisted of 2.0 mg l-1 benzyladenine (BA) and 0.1 mg l-1 a-naphthaleneacetic acid (NAA); while optimum medium for adventitious shoot regeneration from these cultures consisted of 0.1 mg l-1 BA and 0.1 mg l-1 NAA. Adventitious shoots could be rooted on 1/2MS. PCR analysis confirmed that rol genes of TL-DNA of Ri plasmid was integrated with at least three copies into the genome of hairy roots-regenerated P. cablin plants. The results presented provide a possibility for breeding of a new cultivar of P. cablin.

}, keywords = {Agrobacterium rhizogenes, ATCC15834., C58C1, Plant regeneration, Pogostemon cablin.}, doi = {10.5530/pj.2016.1.11}, author = {Han-jing Yan and Meng-ling He and Wei-Jian Huang and Dong-mei Li and Xiao-fang Yu} } @article {156, title = {Phytochemical and Antidiabetic Evaluation of the Methanolic Stem Bark Extract of Spathodea campanulata (P. Beauv.) Bignoniaceae}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Jan/2016}, pages = {243-249}, type = {Original Article}, chapter = {243}, abstract = {

Background: Spathodea campanulata (P. Beauv.) Bignoniaceae extract\ (SCE) is one of many herbal medicines\ used widely in Ugandan traditional\ medicine for various ailments. Generally most of these herbal\ medicines\ are yet to be standardized or have their phytochemical content characterized.\ Method: This study identified the secondary metabolites in the stem bark\ methanolic extract and quantified them. The same extract was subjected\ to serial solvent fractionation, TLC characterization and antidiabetic testing.\ Results: The secondary metabolites were found to comprise of 7.5\% alkaloids,\ 10\% flavonoids, 13\% tannins and 17\% saponins per gram of plant material.\ The TLC characteristics of the fractions (hexane (HX), ethylacetate (EA)\ and methanol (ME)) viewed under UV light revealed spots with the following\ Rf values; the hexane partition gave HX7EA3 (0.96 and 0.68) HX9EA1\ (0.68 and 0.3), EA1ME9 (0.86 and 0.58), EA3ME7 (0.87), EA7ME3 (0.85)\ and EA9ME1 (0.85). The ethylacetate partition gave the following HX1EA9 (0.53, 0.34 and 0.18), HX3EA7 (0.59, 0.40 and 0.26). Discussion: All the\ fractions produced nominal reduction of hyperglycemia. Except hexane\ fraction at 50 mg/kg and ethylacetate fraction at 200 mg/kg all the fractions\ had percentage reductions of glucose greater than that of the control at\ the experimental doses. Although the values of percentage reductions of\ hyperglycemia by the hexane fraction were apparently dose-dependent,\ the greatest margin of reduction of hyperglycemia was observed in the\ residual aqueous fraction. Conclusion: It was found that SCE contains\ valuable phytochemicals in appreciable quantities which are antidiabetic.\ The residual aqueous fraction is the most potent antihyperglycemic of the\ solvent fractions.

}, keywords = {Flavonoids, Saponins, Spathodea campanulata (P. Beauv.) Bignoniaceae, TLC Tannins, Uganda.}, doi = {10.5530/pj.2016.3.12}, author = {Tanayen Julius Kihdze and Ajayi Abayomi Mayowa and Oloro Joseph and Ezeonwumelu Joseph OC and Tanayen Grace Ghaife and Adzu Bulus and Arthur van Aerschot and Gert Laekeman and Agaba Amon Ganafa} } @article {85, title = {Assessment of Acute and Subacute Toxicity of the Total Dichloromethane-Ethanol Extract of Morinda morindoides (Baker) Milne-Redh (ETDE) on Rats}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {Nov-Dec 2015}, pages = {372-377}, type = {Original Article}, chapter = {372}, abstract = {

Context: ETDE shown good antihypertensive and antioxidant activities in rats made hypertensive. This present study aims to assess its toxicity. Aims: This study was designed to study the toxicity of dichloromethaneethanol extract of Morinda morindoides. Settings and Design: Toxicological activity in vivo. Methods and Material: Alkaloids were characterized from reagents of Bouchardat, flavonoids by reacting the cyanidrine, tannins by the reagent Stiasny, polyphenols by reacting ferric chloride, quinones by the reagent Bornstra\ëgen, sterols and polyterpenes by the reaction of Libermann and saponins by observing the foam after agitation of the extract. Acute and subacute toxicity were studied using respectively 423 and 407 OECD guidelines for testing of chemicals. Statistical analysis used: The graphical representation of the data was performed using the Graph Pad Prism 5.0. The mean value is accompanied by the standard error of the mean (Mean \± SEM). The difference between the two values is considered significant when P\<0.001. Statistical analysis of results was performed using analysis of variance (ANOVA). Results: The phytochemical screening showed the presence in the ETDE of polyphenols, alkaloids, flavonoids, sterols and polyterpenes. The toxicological study shows that ETDE has a LD50 between 2000 and 5000 mg/kg bw therefore classified in the hazard category 5. The administration of ETDE at repeated dose for 28 days did not significantly affect the weight gain, hematological and biochemical parameters of rats. Conclusion: ETDE toxicity is relatively low with LD50 between 2000 and 5000 mg/kg bw. It does not cause damage to the heart, liver and kidney. ETDE can be used without risk of intoxication.

}, keywords = {Acute toxicity, Damage, Morinda morindoides, Subacute toxicity, Weight gain.}, doi = {10.5530/pj.2015.6.10}, author = {Boga Gogo Lucien and Bahi Calixte and Yapi Houphou{\"e}t F{\'e}lix and N{\textquoteright}Guessan Jean David}, editor = {Konkon N{\textquoteright}Dri Gilles} } @article {57, title = {Dynamic Comparison of Free Radical Scavenging Abilities of Hypericum Perforatum L., Herba Verbenae Officinalis, and Valeriana Officinalis L. Extracts}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {198-204}, type = {Original Article}, chapter = {198}, abstract = {

Objectives: The purpose of this research was to compare the dynamic antioxidant activities and the free radical scavenging abilities of three botanical supplements, Hypericum perforatum L. (HPL), Herba Verbena Officinalis (HVO), and Valeriana officinalis L. (VO), which have been reported to effectively treat menopause symptoms. Methods: The antioxidant activities of the three supplements were determined by the ferric reducing ability of plasma (FRAP) assay. In addition, their free radical scavenging abilities were studied by ftheir interactions with the stable radicals of 2, 2\’-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH). Results: The results indicated that the HPL ethanolic extract exhibited greater antioxidant activity (1.2688 \± 0.01 mmol Trolox/g) than the HVO ethanolic extract (1.1686\± 0.043 mmol Trolox/g) and the VO ethanolic extract (0.2579 \± 0.0031 mmol Trolox/g) as compared to Nilestriol (0.0026\±0.0012), a positive control agent in the experiment. Moreover, the HPL extract showed remarkable free radical scavenging activity against ABTS\•+, and the HVO extract was the most potent against DPPH\•. Conclusion: These activities may be attributed to the total flavonoid or phenolic acid contents of among these extracts.

}, keywords = {ABTS{\textbullet}+, DPPH{\textbullet}, Herba Verbena Officinalis, Hypericum perforatum L., Menopause Oxidative Stress, Valeriana officinalis L.}, doi = {10.5530/pj.2015.3.9}, author = {Yi-ming Li and Yan-Ru Liu and Bing-Kun Xiao and Jian-Yun Yang and Rong-Qing Huang} } @article {1476, title = {Dynamic Comparison of Free Radical Scavenging Abilities of Hypericum Perforatum L., Herba Verbenae Officinalis, and Valeriana Officinalis L. Extracts}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {09th Mar, 2015}, pages = {198-204}, type = {Original Article}, chapter = {198}, abstract = {

Objectives: The purpose of this research was to compare the dynamic antioxidant activities and the free radical scavenging abilities of three botanical supplements, Hypericum perforatum L. (HPL), Herba Verbena Officinalis (HVO), and Valeriana officinalis L. (VO), which have been reported to effectively treat menopause symptoms. Methods: The antioxidant activities of the three supplements were determined by the ferric reducing ability of plasma (FRAP) assay. In addition, their free radical scavenging abilities were studied by ftheir interactions with the stable radicals of 2, 2\’-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH). Results: The results indicated that the HPL ethanolic extract exhibited greater antioxidant activity (1.2688 \± 0.01 mmol Trolox/g) than the HVO ethanolic extract (1.1686\± 0.043 mmol Trolox/g) and the VO ethanolic extract (0.2579 \± 0.0031 mmol Trolox/g) as compared to Nilestriol (0.0026\±0.0012), a positive control agent in the experiment. Moreover, the HPL extract showed remarkable free radical scavenging activity against ABTS\•+, and the HVO extract was the most potent against DPPH\•. Conclusion: These activities may be attributed to the total flavonoid or phenolic acid contents of among these extracts.

Key words: ABTS\•+, DPPH\•, Hypericum perforatum L.,Herba Verbena Officinalis, Menopause Oxidative Stress, Valeriana officinalis L.

}, keywords = {ABTS{\textbullet}+, DPPH{\textbullet}, Herba Verbena Officinalis, Hypericum perforatum L., Menopause Oxidative Stress, Valeriana officinalis L.}, author = {Yi-ming Li and Yan-Ru Liu and Bing-Kun Xiao and Jian-Yun Yang and Rong-Qing Huang} } @article {86, title = {Preliminary Phytochemical Analysis and In vitro Anti-helmenthic activity of Achyranthes aspera Leaf extract}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {397-399}, type = {Original Article}, chapter = {397}, abstract = {

Objective: To evaluate the preliminary phytochemical analysis and in vitro- Antihelmenthic activity of leaf extract of Achyranthes aspera. Background: Achyranthes aspera is an annual, stiff-erect herb found commonly as a weed throughout India. The leaf ethyl acetate extract showed high larvicidal activity on the tick larvae of Rhipicephalus. It strengthen the liver and kidneys, strengthening muscles, tendons and bones, anti-inflammatory, anti-toxin, urine laxative, normalize menstruation, hemostatic, ease childbirth. Chemical Ingredients includes Akirantin, glokosa, galactose, reilosa, ramnosa, and alkaloids. Hentriakontan, sapogenin, Betaine, ecdysterone, triterpenoid saponins. Methods: Preliminary phytochemical analysis was done by adopting the method of Evans. Antihelmenthic assay is performed by standard protocol. Result: The present study reveals the presence of few secondary metabolites and the extract exhibitspotent Antihelmenthic activity. Conclusion: From the present study it can be concluded that Achyranthes aspera leaf extract possessed marked in vitro Anti helminthic effect.

}, keywords = {Achyranthes aspera, Anti-helmenthic, Anti-inflammatory, Laxative, Phytochemical.}, doi = {10.5530/pj.2015.6.14}, author = {Kamal Hasan and Thangavelu Lakshmi and Thirumalai Kumaran Rathinam} } @article {79, title = {Preliminary Phytochemical analysis and In vitro Antioxidant, FTIR Spectroscopy, Anti-diabetic activity of Acacia catechu ethanolic seed extract}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {Nov-Dec 2015}, pages = {356-362}, type = {Original Article}, chapter = {356}, abstract = {

Objective: To evaluate the preliminary phytochemical analysis and in vitro antioxidant activity, anti-diabetic effect of ethanolic seed extract of Acacia catechu against the alpha amylase and alpha glucosidase digestive enzymes in the pancreas and small intestine. Methods: Preliminary phytochemical analysis was done by adopting the method of Evans. Antioxidant assay is performed by DPPH, ABTS and FRAP assay, Anti diabetic activity was determined by modified method of miller, the extract at different concentrations was tested for mammalian alpha amylase and alpha glucosidase enzyme inhibitory assay under the controlled experimental conditions and subjected to determination of absorbance. Results: The present study reveals the presence of few secondary metabolites and the extract exhibits potent Antioxidant activity and a concentration dependent inhibition of Alpha amylase and Alpha glucosidase. Conclusion: From the present study it can be concluded that ethanolic seed extract of Acacia catechu possessed marked in vitro antioxidant and anti-diabetic effect. The effect was plausibly due to the presence of phenolic contents of Acacia catechu

}, keywords = {Acacia catechu seed, Alpha glucosidase, Alpha-amylase, Antidiabetic, Antioxidant, FTIR Spectroscopy, Phytochemical}, doi = {10.5530/pj.2015.6.7}, author = {Thangavelu Lakshmi and Rajendran Ramasamy and Rathinam Thirumalaikumaran} } @article {87, title = {Quantitative Determination and Variation Tendencies of Flavonoids in Five Selaginella Plant Drugs}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {Nov-Dec 2015}, pages = {378-382}, type = {Original Article}, chapter = {378}, keywords = {Amentoflavone content, HPLC, Selaginella, Total flavonoids content, UV-Vis spectrophotometry, Variation tendencies}, doi = {10.5530/pj.2015.6.11}, author = {Weifang Long and Qi Ding and Yujie Chen and Jiqing Hu and Luyang Li and Fei Zhang and Dingrong Wan} } @article {1487, title = {Chemical Constituents of Dendrobium williamsonii}, journal = {Pharmacognosy journal}, volume = {6}, year = {2014}, month = {8th April 2014}, pages = {36-41}, type = {Original Article}, abstract = {

Objective: Isolation of compounds from Dendrobium williamsonii and evaluation of each isolates for its free radical scavenging, antiherpetic and cytotoxic activities. Results: Six phenolic compounds were isolated including tetratriacontanyltrans- p-coumarate (1), trans-docosanoylferulate (2), 3,3\′-dihydroxy-4,5-dimethoxybibenzyl (3), moscatilin (4), apigenin (5) and vanillic acid (6). Among these isolates, compounds 3, 4 and 5 exhibited recognizable DPPH free radical scavenging potential.Only 3 exhibited weak activity against Herpes simplex virus, whereas 3 and 4 showed cytotoxicity against KB and MCF-7 cancer cells. Conclusion: This study is the first report on the chemical and biological properties of D. williamsonii.Compounds 3, 4 and 5 are responsible for free radical scavenging activity of this plant. Compound 4 showed the strongest cytotoxic effect on KB cancer cells.

Key words:Dendrobium williamsonii, Orchidaceae, Anti-herpetic Cytotoxicity, Free radical scavenging activity.

}, keywords = {Anti-herpetic Cytotoxicity, Dendrobium williamsonii, Free Radical Scavenging Activity, Orchidaceae}, author = {Pathrapa Rungwichaniwat and Boonchoo Sritularak and Kittisak Likhitwitayawuid} } @article {1531, title = {Sterols and triterpenes from the non-polar antitubercular fraction of Abutilon indicum}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {26th May 2014}, pages = {49-52}, type = {Research Article}, abstract = {

Introduction:Abutilon indicum Sweet (Malvaceae) is used in Filipino folk medicine as demulcent, diuretic, sedative, aphrodisiac and antidiabetic remedy. It is also effective in the treatment of leprosy. It is also used as a laxative for patients having hemorrhoids and in the treatment of coughs, puerperal disease, urinary disorders, chronic dysentery and fever. Methods: Air-dried powdered leaves of A. indicum were initially extracted with DCM-methanol (1:1) to afford a crude extract which was fractionated on a silica gel column to afford four fractions. The first fraction which showed antimycobacterial activity was further chromatographed in a silica gel column to afford bioactive fractions from which four compounds were obtained. The crude extract, fractions and isolated compounds were screened for their inhibitory effect against Mycobacterium tuberculosis H37Rv (ATCC) using the colorimetric Microplate Alamar Blue Assay (MABA) method. Results: The fractions obtained after silica gel chromatography of the crude DCMmethanol (1:1) revealed the first fraction (MIC=64 mg/mL) to exert the highest inhibition against M. tuberculosis H37Rv. Further separation of this fraction afforded sub-fractions with moderately strong inhibitory activity against the test organism (MIC up to 64 mg/mL). Chromatographic purification of sub-fraction 1 afforded four compounds which were spectroscopically identified as \β-amyrin 3-palmitate (1), squalene (2) and a 1:1 mixture of the sterols \β-sitosterol (3) and stigmasterol (4). Evaluation of the antimycobacterial activity of 1\–4 showed insignificant inhibitory activity against the test organism (MIC = \>128 mg/mL). Conclusion: The present results demonstrate the potential of Abutilon indicum as a plant source of compounds that may exhibit promising antituberculosis activity. While the known compounds isolated for this plant did not show antimycobacterial activity, the obtained results are considered sufficient reason for further study to isolate the metabolites from A. indicum responsible for the antitubercular activity.

Key words:Abutilon indicum, Malvaceae, antitubercular, squalene, \β-amyrin 3-palmitate, \β-sitosterol, stigmasterol.

}, keywords = {Abutilon indicum, Antitubercular, Malvaceae, Squalene, Stigmasterol., β-amyrin 3-palmitate, β-sitosterol}, author = {Allan Patrick G. Macabeo and Christopher A. Lee} } @article {1238, title = {In vitro Evaluation of Acetylcholinesterase Inhibitory and Neuroprotective Activity in Commiphora species: A Comparative Study}, journal = {Pharmacognosy Journal}, volume = {12}, year = {202}, month = {September 2020}, pages = {1223-1231}, type = {Original Article}, chapter = {1223}, abstract = {

Introduction: Herbal medicines are widely used in the therapeutic intervention that could delay the onset of Neurodegenerative diseases like, Alzheimer{\textquoteright}s disease. Despite intensive advancements in the field of research currently available therapeutic strategies are often limited due to their adverse effects. Hence there is a need for the search for novel compounds for effective medications to treat neurocognitive deficits. Objective: The present study focused on acetylcholinesterase inhibitory and neuroprotective activity of Commiphora species plant for their possible use in Alzheimer{\textquoteright}s disease. Methods: Phytochemical screening, TLC bioautographic and colourimetric assay was performed to quantify their acetylcholinesterase inhibitory activity of ethanolic extracts of the Commiphora species. The MTT assay was carried to evaluate the neuroprotective effect against the Aβ-induced cytotoxicity in SHSY5Y cell lines. Results: The bark of Commiphora berryi, leaves of Commiphora caudata and Commiphora pubescens were found abundant in flavonoids, glycosides, steroids and terpenoids. Further, the ethanol extract of Commiphora berryi (65.48\% {\textpm} 0.10) showed the highest acetylcholinesterase inhibitory activity. The Aβ25-35 induced cell damage was as evidenced at a concentration of 20μM. The neuroprotective effect of the ethanol extracts was examined in neurodegenerative cells induced by Aβ25-35. On pretreatment with plant extracts, significant improvement in cell viability was observed as 63.42 {\textpm} 2.02\% (25μg/ml) for Commiphora berryi. The maximum percentage of in-vitro AChE inhibition and neuroprotective effect was effective in the ethanol bark extract of Commiphora berryi. Conclusion: The results are very rousing to continue the screening of more unexplored plant species could be used for the development of novel bioactive compounds to treat the many diseases, especially for Alzheimer{\textquoteright}s disease.

}, keywords = {Acetylcholinesterase, Aβ25-35, Commiphiora pubescens, Commiphora berryi, Commiphora caudata, Neuroprotective, SH-SY5Y Cell line}, doi = {10.5530/pj.2020.12.171}, author = {PS Dhivya and P Selvamani and S Latha and Vasudevan Mani and Nur Syamimi Mohd Azahan} }