@article {2228, title = {Evaluation of Tumor Necrosis Factor Alpha, Insulin, glucose, HbA1c\% and HOMA-IR as Predictors for Cardiovascular Diseases in Patients with Type 2 Diabetes}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {195-201}, type = {Research Article}, chapter = {195}, abstract = {

Objective: Comparison of the blood level of TNFα in patients with and without type 2 diabetes who have cardiovascular diseases. Examine the connection between the amount of serum TNFα and insulin resistance in patients with type 2 diabetes who have cardiovascular diseases. Method: The present study included 60 patients with Diabetes Mellitus (DM) with a mean age of 56.02{\textpm}1.395 years and an age range of (40 - 80)years and 60 patients with cardiovascular diseases and diabetes (CVD and DM) with a mean age of 59.20{\textpm}1.478 and an age range of (40-80) years, Who visited Al-Basrah Teaching Hospital in Basrah. in addition, the study included 60 healthy controls mean age of healthy control subjects was 54.72{\textpm}1.405years. All patients in this study were diagnosed by specialized doctors and the diagnosis was verified by clinical and laboratory tests, during the period from September 2022 to September 2023. All Subjects signed a written informed consent form. The BMI was calculated as body weight (kg) and was divided by squared height in meters. Results: The results of this study showed an increase in the level of glucose, haemoglobin A1c\%, insulin, and HOMA IR (in CVD and DM patients as compared with DM patients and control and there was a significant difference in concentrations among study groups (p-value \<0.0001). Also, The results of this study showed an increase in the level of tumor necrosis factor-alpha in CVD and DM patients as compared with DM and control and there was a significant difference in concentrations of TNFα among study groups (p-value \<0.0001). Conclusion: Based on the findings of this research, it can be inferred that TNFα and HbA1c have the potential to serve as practical and straightforward indicators for predicting the coexistence of insulin resistance, dysglycemia, and Cardiovascular Diseases in seemingly healthy individuals within the young (\<50 years) Al-Basra community.

}, keywords = {Cardiovascular Disease, Diabetes Mellitus and Inflammation, HOMA-IR, Insulin, TNFα}, doi = {10.5530/pj.2024.16.27}, author = {Haider Nasser Jabber and Bassem Charfeddine and Hamed Jaddoa Abbas} } @article {2229, title = {New Insights of Oxidative Stress and Thalassemia May Lead to Antioxidant Therapy}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {202-204}, type = {Research Article}, chapter = {202}, abstract = {

Background: Because of chronic hemolysis, thalassemic patients are under oxidative cell injury caused by secondary iron overload. This provokes oxidative damage to the cellular membranes of organs that accumulate excess iron. Several researchers studied the oxidative stress in patients with thalassemia during chelation therapy and repeated blood transfusion periods, and they found that β-thalassemia patients are under oxidative stress, but they did not focus on before the chelating therapy period. Objective: To evaluate the total antioxidant capacity (TAOC) and oxidative stress (OS) in newly diagnosed patients with β-thalassemia before chelating therapy. Methodology: In the present case-control study, twenty patients newly diagnosed with β-thalassemia before receiving chelating agents, and another 30 healthy individuals, sex-matched with patients, considered as a control, were included in the study. Total antioxidant capacity (TAOC) and Malondialdehyde (MDA) were assessed in the studied groups. Results: The TAOC values of the thalassemic group (35{\textpm}0.11 u/ml ) were significantly (p\<0.001) lower than that of the control group (79{\textpm}7.2 u/ml). MDA values of the thalassemic group (7.9 {\textpm}2.35nmol/l) were significantly (p\<0.001) more than that of the control group (0.57{\textpm}0.25 nmol/l). Conclusion: The present study demonstrated that patients with β thalassemia have decreased values of TAOC, and increased values of MDA when compared with the control group.

}, keywords = {Antioxidants, Oxidative stress, Thalassemia}, doi = {10.5530/pj.2024.16.28}, author = {Kassim SA Al Neaimy and Maes MK Alkhyatt and Israa A Jarjess} } @article {2217, title = {Pharmacognostic Profile and Antidiabetic Activity of Eleutherine bulbosa Mills. Bulbs from East Kalimantan, Indonesia}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {118-125}, type = {Research Article}, chapter = {118}, abstract = {

Background: Eleutherine bulbosa (Mill.) Urb., known as Bawang Dayak, is commonly found growing in Kalimantan, Indonesia. The characteristics of the environment in which the plant grows greatly influence the characteristics of the plant and its biological activity. Objective: This study aimed to determine the pharmacognostic profile and evaluate the antidiabetic activity of E. bulbosa bulb extract obtained from Kota Bangun, Kutai Kertanegara, Indonesia. Methods: The dried powdered of E. bulbosa bulbs was extracted using two different methods (maceration and microwave-assisted extraction). The evaluation of the sample fluorescence and non-specific parameters was done. The antidiabetic activity of the extracts was conducted using streptozocin-induced mice and histopathology analysis. Results: The fluorescence evaluation indicated various secondary metabolites contained in E. bulbosa simplicia. Non-specific parameters include drying loss (8.83{\textpm}0.2611\%), water content in simplicia (8.04{\textpm}0.7481\%), specific gravity (1.04{\textpm}0.0058\%), total ash content (20.3{\textpm}0.1583\%), acid insoluble ash content (1.70{\textpm}0.0608\%), ethanol content in extract (0.99{\textpm}0.0017\%), lead content (0.010 mg/g), cadmium (0.091 mg/g), Arsenic (0.0003 mg/g), aflatoxin (not detected), and mold/yeast (0.8 {\texttimes} 105 colonies/g) meet the established regulations. Meanwhile, the antidiabetic assay showed that both extracts decreased the blood glucose levels in mice during the 14 days of treatments in a dose-dependent manner. This activity is correlated with the increased repair of pancreatic beta cells as observed by histopathological analysis. Conclusion: The dried bulbs of E. bulbosa obtained from Kota Bangun, Kutai Kertanegara, East Kalimantan, Indonesia meet the standards set as raw materials for antidiabetic herbal medicines.

}, keywords = {Antidiabetic activity, Bawang Dayak, contaminant levels evaluation, Eleutherine bulbosa (Mill.) Urb, pharmacognostic profile}, doi = {10.5530/pj.2024.16.16}, author = {Herman Herman and Arsyik Ibrahim and Junaidin Junaidin and M. Arifuddin and Baso Didik Hikmawan and Siska Siska and Tahyatul Bariroh and Reza Yuridian Purwoko and Lizma Febrina and Muhammad Faisal and Iswahyudi Iswahyudi and Marissa Angelina and Erwin Samsul and Laode Rijai and Islamudin Ahmad} } @article {2235, title = {Safety Assessment of Oral Lysiphyllum strychnifolium Aqueous Extract in Healthy Volunteers}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {235-240}, type = {Research Article}, chapter = {235}, abstract = {

Background: Lysiphyllum strychnifolium (LS), widely known as Ya nang daeng in Thailand, is a traditional herbal remedy that has long been used to promote health and treat diverse health conditions, especially detoxification, by alleviating the severity of symptoms and lowering the risks associated with toxic exposures. Although it is extensively used in Thailand, human safety studies have been lacking. Thus, this study aimed to examine the safety of using LS capsules in healthy participants through a Phase I clinical trial. Objective: This study aimed to investigate the safety of aqueous extract of LS in twenty-four healthy Thai participants. Method: The participants were received 1,000 mg of LS aqueous extract each morning before their meals for seven days. All participants were examined safety assessment including history taking, physical examination, and laboratory tests at day 0, 8 and 14 (follow-up). Results: The findings showed that there were no significant side effects or abnormalities found during the history taking, physical examination, or laboratory evaluation. Particularly, when compared to baseline, participants who received LS experienced statistically significant reductions in blood sugar, triglyceride, LDL cholesterol, and creatinine (P \< 0.05), but still within normal ranges. Conclusions: Dietary supplementation with 1,000 mg of LS aqueous extract per day may have a beneficial effect on blood sugar and cholesterol management while remaining safe for healthy people.

}, keywords = {Clinical study, Healthy volunteers, Lysiphyllum strychnifolium, Safety, Yanang Daeng}, doi = {10.5530/pj.2024.16.34}, author = {Piracha Jumpa-ngern and Parunkul Tungsukruthai and Chuntida Kamalashiran and Somboon Kietinun and Kesara Na- Bangchang and Kusuma Sriyakul} } @article {2114, title = {Activity of Pegagan Embun (Hydrocotyle sibthorpioides Lam.) Extracts in Capsule Dosage Form to IgM and IgG Levels in Humans}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {756-760}, type = {Original Article}, chapter = {756}, abstract = {

Objective: Traditionally, Pegagan embun (Hydrocotyle sibthorpiodes Lam.) has been used to enhance the immune system. Previous studies confirmed that Hydrocotyle sibthorpiodes Lam. enhanced antibody titers and was practically non-toxic by animal tests. This study aimed to determine the effect of Hydrocotyle sibthorpioides Lam. extract on IgM and IgG levels in humans. Methods: The participants involved 20 healthy volunteers aged 20-25 years were divided into two groups with a placebo as a comparison. The capsules containing Hydrocotyle sibthorpiodes Lam extract were in the treatment group at a dose of 67 mg and the placebo group was given capsules containing lactose orally for three days. IgM and IgG levels were measured before and after consuming the capsules. The ELISA method tested IgM and IgG levels and detected them using specific antibodies that form complexes with enzymes and substrates. Results: The results showed the average baseline IgM level of 1.480 mg/mL and after consumption of 1.405 mg/mL for placebo. For Hydrocotyle sibthorpiodes Lam. extract capsules, the baseline was 1.492 mg/mL and 1.854 mg/mL after consumption. For IgG, before given 8.941 mg/mL and after given 8.710 mg/mL for placebo, while before given Hydrocotyle sibthorpiodes Lam. extract capsules 8.946 mg/mL and after given Hydrocotyle sibthorpiodes Lam. extract capsules was 10.234 mg/mL. Statistical results showed a significant increase in IgM and IgG levels after consuming Hydrocotyle sibthorpiodes Lam. extract capsules for three days (p\<0.05). Conclusion: It can be concluded that 67 mg of Hydrocotyle sibthorpiodes Lam. extract capsules can increase IgM and IgG levels in humans.

}, keywords = {ELISA, Extract, Hydrocotyle sibthorpioides Lam, IgG, IgM, Volunteers.}, doi = {10.5530/pj.2023.15.148}, author = {Afriwardi Afriwardi and Adinny Julmiza and Salman Umar and Yufri Aldi} } @article {2140, title = {The Analysis of Matrix Metalloproteinase-9 and Tissue Inhibitor Matrix Metalloproteinase-1 Levels in the Amniochorion Membrane Patients on Premature Rupture of Membranes}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {910-912}, type = {Research Article}, chapter = {910}, abstract = {

Introduction: MMP-9 is essential for extracellular matrix remodeling, which affects the incidence of premature rupture of membranes. In addition, decreased and increased levels of TIMP-1, a preferential MMP-9 inhibitor, have been reported to be associated with premature rupture of membranes because it showed an imbalance in the MMP-9 or TIMP-1 levels. This study aims to analyze MMP-9 and TIMP-1 levels in amniochorion membrane patients on premature rupture of membranes. Methods: An analytic observational study was conducted on 70 subjects. The MMP-9 and TIMP-1 levels in the amniochorion membrane were determined by ELISA. Results: The results of this study indicate that the amniochorion membrane in the incidence of premature rupture of membranes is characterized by increased levels of MMP-9, while TIMP-1 levels do not differ between the incidence of premature rupture of membranes. Conclusion: Based on the research that has been done, it can be concluded that there are differences in protein levels of MMP-9 but there are no differences in protein levels of TIMP-1 in premature rupture of membranes

}, keywords = {MMP-9, Premature rupture of membranes., TIMP-1}, doi = {10.5530/pj.2023.15.173}, author = {Meidrin Joni and Eryati Darwin and Herlambang Herlambang and Aisyah Elliyanti} } @article {1960, title = {Analysis of The Effect of Leptin, AMPK, Adiponectin, and NPY Markers on Changes in Body Weight of Childhood Epileptic Using Valproic Acid Monotherapy}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {150-153}, type = {Research Article}, chapter = {150}, abstract = {

Introduction: Epilepsy is a neurological disorder that occurs due to abnormal neurons in the brain and an imbalance between excitation and inhibition in the central nervous system. The first line of OAE in children is VPA (Valproate Acid). However, long-term use can cause weight gain with a frequency of 10-70\%. The underlying mechanism of weight gain in patients remains unclear. Purpose: This study aimed to analyze the relationship between levels of biomarkers AMPK, NPY, Leptin, and Adiponectin on changes in body weight in patients with epileptic seizures using VPA monotherapy. Method: This study is an observational cohort design. Data collection in April-June 2019. Inclusion criteria were children aged 2-10 years who used VPA requirement less than two years, not taking any drugs that affect body weight, not diagnose systemic lupus, nephrotic syndrome, and diabetes mellitus. Bodyweight and all biomarkers measurement on subjects who came to the clinic at the time of study and at least after one month of taking VPA. A total of 17 subjects participated in this study. Result: The results of the statistical multivariate analysis test of VPA dosage on changes in body weight and biomarker levels found that Leptin, AMPK, Adiponectin did not significantly increase in body weight (p\>0.05), but NPY significant increase in body weight (p\<0.05). Conclusion: NPY is the most potent for appetite enhancing, preferential effect on carbohydrate intake, weight regulation, energy storage, and expenditure. Increase production of NPY, there is an increase in energy intake and then increases fat storage and body weight.

}, keywords = {Adiponectin, AMPK, Childhood., Epilepsy, Leptin, NPY, Valproic acid, Weight gain}, doi = {10.5530/pj.2023.15.21}, author = {Wardah Rahmatul Islamiyah and Nasronudin and Abdulloh Machin and Iin Ernawati and Yunita Dwi Tanti and Nur Jaya and Farah Medina and Fathia Faza Rahmadanita and Paulus Sugianto} } @article {1969, title = {Anticancer and Neuroprotective Effects of the Triterpene Glycosides From Sea Cucumber Holothuria imitans}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {119-127}, type = {Research Article}, chapter = {119}, abstract = {

Introduction: Sea cucumbers has gained notoriety because possess a wide range of biological and pharmacological activities. In this sense, the aim of this work was to evaluate the anticancer and neuroprotective effects of the triterpene glycosides from sea cucumber Holothuria imitans. Methods: Triterpene glycosides were separated and purified by Reversed-phase high-performance liquid chromatography (RP-HPLC). Their structures were deduced by spectral analysis and chemical evidence. Cytotoxic activity was evaluated using normal African green monkey kidney epithelial cell line (VERO) and three cancer cell lines: cancer gastric (MKN-28), breast adenocarcinoma (MCF-7) and lung carcinoma (A-549). Besides, the neuroprotective effect was studied using the Cath.a-differentiated (CAD) cell line and human glial (Oligodendrocytic) hybrid cell line (MO3.13). Results: Two triterpene glycosides (Fuscocineroside C and Scabraside D) were isolated, which showed low cytotoxic activity against VERO cell line, and high cytotoxic activity against lines MKN-28, MCF-7 and A-549 cells, with IC50 between the ranges of 0.92 μmol/L to 2.61 μmol/L. The isolated triterpene glycosides showed the ability to regain mitochondrial viability in CAD and MO3.13 cells treated with neurotoxin (C2-ceramide) with statistically significant results (p\<0.05). Conclusion: The triterpene glycosides Fuscocineroside C and Scabraside D isolated from sea cucumber Holothuria imitans show anticancer and neuroprotective potential and may be considered promising active principles for anticancer and neuroprotective drugs.

}, keywords = {Anticancer, Holothuria imitans, Neuroprotective., Triterpene glycosides}, doi = {10.5530/pj.2023.15.16}, author = {Maril{\'u} Roxana Soto-V{\'a}squez and Paul Alan Arkin Alvarado-Garc{\'\i}a and Demetrio Rafael Jara-Aguilar and Elda Maritza Rodrigo-Villanueva and Jos{\'e} Gilberto Gavidia-Valencia and Iris Melina Alfaro-Beltr{\'a}n and Bertha Mirella Alfaro-Ttito} } @article {2087, title = {Antioxidant, Total Phenolic, and Total Flavonoid of 70\% Ethanol Extract of Avocado Seeds (Persea americana Mill.)}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {599-605}, type = {Research Article}, chapter = {599}, abstract = {

Avocado seeds (Persea americana Mill.) are high in phytochemicals and are utilized in herbal medicine. The objective of this study is to analyze the antioxidant activities, total phenolics and flavonoids of the P. americana seed extract. P. americana seed extraction was obtained through maceration and reflux using a 70\% ethanol solvent. The results obtained were compared in terms of yield productivity, with yields of 43.07 (\%) and 39.58 (\%) respectively. Phytochemical compounds extracted from P. americana seeds were tested using the phytochemical screening method, the antioxidant activity assay, the total phenolic analysis, and the total flavonoid analysis. The phytochemical screening showed that P. americana seeds contain flavonoids, saponins, phenols, tannins, alkaloids, and quinones. The antioxidant activity of the 70\% ethanol extract of P. americana seeds obtained by maceration and reflux method was 77.298 g/mL and 98.626 g/mL, respectively, meanwhile the IC50 values of vitamin C were 12.883 g/mL. The 70\% ethanol extract of P. americana seeds obtained by maceration and reflux method had total phenolic content of 276.96 mgGAE/g and 294.96 mgGAE/g, and total flavonoid content of 1.73 mgQE/g and 12.70 mgQE/g respectively. This simply implies that the 70\% ethanolic extracts from P. americana seeds obtained through maceration and reflux have strong antioxidant activity.

}, keywords = {Antioxidants, Avocado seeds, DPPH, Persea americana Mill., Total flavonoids, Total phenolics.}, doi = {10.5530/pj.2023.15.126}, author = {Sri Wahyu Ningsih Munthe and Riskianto Riskianto and Denny Juvi and Jessica Novia} } @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 {2052, title = {The Effect of Family-Based Empowerment in Preventing Overweight and Obesity in Elementary School Children in Kupang}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {428-434}, type = {Research Article}, chapter = {428}, abstract = {

Background: The prevalence of overweight and obesity continues to increase in both developing and developed countries and occurs in all age groups. As well as being the biggest threat to public health, especially non-communicable diseases. Childhood is the most special period in life. It is almost certain that many health problems/illnesses experienced during this period will be carried on into adulthood. The causes of obesity in children are very complex; genetic, biological, psychosocial, behavioral and sociocultural factors. The impact of overweight and obesity on children is related to physical and psychological effects. Lifestyle modification which includes increasing knowledge, diet, physical activity, sedentary behavior, socio-cultural aspects is believed to be a strategy in preventing and controlling overweight and obesity. This study aims to examine the effect of family empowerment on the prevention of overweight and obesity in elementary school children. This research is a quasy experiment that is pre-test and posttest with control group design. Parallel design with one treatment group and one control group. The sample is determined by purposive random sampling. The research sample was overweight/obese children in elementary school grades 4, 5 and 6, totaling 112 people. Data were obtained through a structured questionnaire covering family abilities, knowledge, physical activity and nutritional intake. Nutritional status was measured after measuring body weight and height using digital scales. Eating patterns were measured using a food frequency questionnaire and a 24-hour recall formula. Results: The results showed that there were differences in family ability (p\<0.016), knowledge (p\<0.001), physical activity (p\<0.015) and nutritional intake (p\<0.000) in the treatment group and the control group after implementing the family empowerment intervention. Conclusion: Family-centered empowerment interventions through health education about overweight and obesity management have a positive impact on increasing family capacity, family knowledge, physical activity and changes in family eating patterns. It is necessary to implement lifestyle modifications in preventing and controlling overweight and obesity. Family-centered empowerment interventions through health education about overweight and obesity management have a positive impact on increasing family capacity, family knowledge, physical activity and changes in family eating patterns. It is necessary to implement lifestyle modifications in preventing and controlling overweight and obesity. Family-centered empowerment interventions through health education about overweight and obesity management have a positive impact on increasing family capacity, family knowledge, physical activity and changes in family eating patterns. It is necessary to implement lifestyle modifications in preventing and controlling overweight and obesity.

}, keywords = {Elementary School Children., Empowerment, Family, Obesity, Overweigh}, doi = {10.5530/pj.2023.15.96}, author = {Fransiskus Geroda Mado and Nurhaedar Jafar and Masyta Muis and Ida Leida Maria and Muhammad Syafar and Darmawansyah and Muhammad Alwi Arifin and Anwar Mallongi and Toto Sudargo and Agustina} } @article {2079, title = {Effect of Naphthaleneacetic Acid (NAA) and 6-Benzylamino Purine (BAP) on In-Vitro Propagation of "Mashua" (Tropaeolum tuberosum Ru{\'\i}z \& Pav{\'o}n) Morphotypes from Peru}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {563-568}, type = {Original Article }, chapter = {563}, abstract = {

Background: Tropaeolum tuberosum Ru{\i}z \& Pav{\'o}n {\textquotedblleft}mashua{\textquotedblright} is a native species of the central Andes and different propagation methods in vitro have been evaluated. However, this research has studied the in vitro propagation of 15 mashua (Tropaeolum tuberosum Ru{\'\i}z \& Pav{\'o}n) morphotypes from the Ayacucho and Apur{\'\i}mac regions (Peru) Objective: To evaluate the effect of the additives naphthaleneacetic acid (NAA) and 6-benzylamino purine (BAP) on the micro-propagation rate of T. tuberosum. Material and Methods: For in vitro establishment, seedlings were used after disinfection with sodium hypochlorite, propagated in Murashige and Skoog (MS) medium. For the evaluation of the effect of NAA and BAP additives, nodes were isolated from in vitro seedlings after 30 days of cultivation and transferred to MS medium supplemented with 3\% sucrose, pH 5.6 and 7 g/L of agar according to T1 (MS + NAA 1ppm) and T2 (MS + BAP 1ppm) treatments. The samples were cultivated for 28 days at 19 {\textdegree}C {\textpm} 2 {\textdegree}C with photoperiods of 16 h/light and 8 h/darkness. Results: After evaluating 20 repetitions for each of the three treatments, the addition of NAA or BAP does not improve the micropropagation rate of practically all the morphotypes studied. Furthermore, BAP behaved as an inhibitor of the development of mashua seedlings. Conclusion: The best micropropagation medium of Tropaeolum tuberosum Ru{\'\i}z \& Pav{\'o}n (mashua) is the basic Murashige and Skoog (MS) medium without the NAA or BAP additives.

}, keywords = {BAP., Mashua, Micropropagation, NAA, Tropaeolum tuberosum}, doi = {10.5530/pj.2023.15.120}, author = {Gilmar Pe{\~n}a-Rojas and Luz Quispe-Calle and Vidalina And{\'\i}a-Ayme and Alex Pereda-Medina and Rolando Estrada- Jimenez and Josefa Bertha Pari-Olarte and Elizabeth Julia Melgar-Merino and Jos{\'e} Santiago Almeida-Galindo and Oscar Herrera-Calderon} } @article {2006, title = {Effect of Rosmarinus Officinalis Essential Oil On Anxiety, Depression, And Sleep Quality}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {343-349}, type = {Research Article}, chapter = {343}, abstract = {

Introduction: The objective of this investigation was to evaluate the effect of Rosmarinus officinalis essential oil on anxiety, depression, and sleep quality. Methods: The essential oils were extracted by hydro-distillation using a modified Clevenger-type apparatus and the chemical composition was performed by Gas chromatography with flame ionization detection (GC-FID) and Gas chromatography mass spectrometry (GC{\textendash}MS). Furthermore, a quasi-experimental study was conducted, where 81 participants were divided into two groups, comprising a waiting list control group and an experimental group treated with essential oils. Anxiety and depression indexes were evaluated using the Zung Self-Rating Anxiety Scale (SAS) and the Zung Self-Rating Depression Scale (SDS), and sleep quality was measured with the Pittsburgh Sleep Quality Inventory (PSQI). Results: Chemical analysis showed that 1,8 cineole (37.6\%), α-pinene (19.9\%), and linalool (15.8\%) were the main components. Anxiety, depression, and sleep quality scores showed a decrease in the post-test study phase compared to the pre-test in the experimental group (p\<0.05). A large size effect was found in the case of anxiety (d = 1.491; g= 1.490) with 1-β=0.996, while medium size effects were observed for depression (d = 0.581; g= 0.582) with 1-β=0.585; and sleep quality (d = 0.586; g = 0.588) with 1-β=0.638. Conclusion: Essential oils extracted from Rosmarinus officinalis are more effective in calming anxiety and show moderate changes in depression and sleep quality.

}, keywords = {Anxiety, Depression, Essential oils, Rosmarinus officinalis, Sleep quality}, doi = {10.5530/pj.2023.15.52}, author = {Paul Alan Arkin Alvarado-Garc{\'\i}a and Maril{\'u} Roxana Soto-V{\'a}squez and Luis Enrique Rosales-Cerquin and Santiago M. Benites and Taniht Lisseth Cubas-Romero and Demetrio Rafael Jara-Aguilar and Jos{\'e} Gilberto Gavidia-Valencia and Iris Melina Alfaro-Beltr{\'a}n} } @article {2080, title = {The Effectiveness of the Si-DBD Application in Increasing the Number of Households in Conducting Periodic Larvae Examination at the Health Center in Bantaeng Regency}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {569-574}, type = {Original Article }, chapter = {569}, abstract = {

Background: Vector-borne diseases, namely DHF, are estimated to infect 100-400 million people each year. Until now there is no specific drug or vaccine for DHF that can be done to avoid or prevent mosquitoes, which focuses on prevention efforts by eradicating mosquito nests. This study aims to see the effectiveness of the application system in carrying out periodic inspections by households. Method: Quasi-experimental research type with design "The Nonrandomized Control Group Pretest Posttest Design{\textquotedblright}. There are 112 samples with a ratio of 1:1 treatment (application system) and control (manual). Data collection using observation sheets (secondary data) and data from larvae inspection results through the application. Seeing the difference before and after the Mc test. Nemar and Chi-Square to see the difference between the treatment and control groups. Results: Periodic larvae inspection by the household before and after manually had no difference, while the system with the application had a significant difference with a value of P=0.000. The comparison between the treatment and control groups with a value of P = 0.000 indicates that there is a difference in the number of households that carry out periodic larva inspections through an application compared to the manual method. The system with the Si-DBD application is simpler, more acceptable, and timelier in carrying out periodic larvae inspections by households with a value of P=0.000. Conclusion: The implementation of periodic larvae inspections that is modeled by an application-based information system via a smartphone has an influence on the number of households that carry out larvae inspections compared to the manual system that is running. Follow-up testing can be carried out on a large scale of household respondents covering the entire work area of the health center and with a cohort research design.

}, keywords = {Application, DHF., Periodic larva inspection}, doi = {10.5530/pj.2023.15.121}, author = {Muhammad Firdaus and Ida Leida Maria and Ansariadi and Andi Zulkifli and Nurhaedar Jafar and Shanti Riskiyani and Anwar Mallongi} } @article {2057, title = {Effects of Melissa officinalis essential oil on state and trait anxiety}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {454-460}, type = {Research Article}, chapter = {454}, abstract = {

Introduction: Essential oils are complex substances used extensively in aromatherapy and phytotherapy, some of them as anxiety and stress-relieving agents. In order to evaluate the effects of Melissa officinalis essential oil on state and trait anxiety, this study was conducted. Methods: The essential oil was extracted by steam distillation and the chemical composition was investigated by Gas chromatographymass spectrometry (GC{\textendash}MS). In addition, a Quasi experimental study with measures at pretest-posttest was conducted, where 58 participants were divided into two groups, a waiting-list (WL) control group, and an experimental group (EG)treated with aromatherapy based on Melissa officinalis essential oil. The anxiety index was evaluated by State-Trait Anxiety Inventory (STAI). Measures were taken at two times: pretest and posttest. Results: The chemical analysis showed that β-cubebene (26.3\%), β-caryophyllene (25.4\%) and geranial (12.5\%) were de main components. Both state and trait anxiety levels decreased in the experimental group during the posttest phase; however, only state anxiety demonstrated statistically significant differences (p\<0.05). A moderate size effect was found for state anxiety (d = 0.799; g= 0.797) with 1-β=0.803; but none for trait anxiety. Conclusion: Melissa officinalis essential oil was moderately effective on state anxiety but has no effect on trait anxiety.

}, keywords = {Essential oil, Melissa officinalis., State anxiety, Trait anxiety}, doi = {10.5530/pj.2023.15.101}, author = {Paul Alan Arkin Alvarado-Garc{\'\i}a and Maril{\'u} Roxana Soto-V{\'a}squez and Francisco Mercedes Infantes Gomez and Natalia Mavila Guzm{\'a}n Rodr{\'\i}guez and Yolanda Elizabeth Rodr{\'\i}guez de Guzm{\'a}n and Demetrio Rafael Jara-Aguilar and Roger Antonio Rengifo-Penadillos and Jos{\'e} Gilberto Gavidia-Valencia and Iris Melina Alfaro-Beltr{\'a}n} } @article {2022, title = {Health Literacy Brisk Walking Exercise on Clinical Outcomes of Blood Sugar in Patients with Type 2 Diabetes Mellitus in Indonesia}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {433-438}, type = {Research Article}, chapter = {433}, abstract = {

Background: Regular Physical activity (PA) is recommended for patients with type 2 diabetes because it has a beneficial effect on metabolic risk factors for the development of diabetic complications. This study was designed to determine the effect of health literacy (HL) brisk walking on clinical outcomes (HbA1c) and PA in patients with DMT2. Method: In using the Quasi Experimental method using the Two group pre-posttest design approach. Research subjects were allocated for the provision of Health literacy Brisk walking (n-30, 30 completed) and the usual care group (n = 30,30 completed). Health literacy brisk walking participants received weekly scheduled information via WhatsApp group with monitoring to walk 3-5 times for 150 minutes/week, while the control group only received regular care from the Chronic Disease Management (Prolanis) program. Results: Sixty T2DM patients (thirty in the intervention group and thirty in the control group) were examined. The results showed that Health literacy Brisk walking with Whatsapp Group Monitoring in the intervention group was significantly higher than usual care from the Chronic Disease Management program (Prolanis) in the control group towards changes in HbA1c and PA after 3 months (p\<0.05). Conclusion: Health literacy brisk walking related to diabetes can be a modifiable factor related to HbA1c for DMT2 patients. The findings indicate the need for health care providers to be able to consider brisk walking PA as a solution in controlling blood sugar (HbA1c).

}, keywords = {Blood Sugar (HbA1c)., DMT2, Health Literacy Brisk walking, Physical Activity}, doi = {10.5530/pj.2023.15.68}, author = {Zainuddin and Andi Zulkifli Abdullah and Nurhaedar Jafar and Suriah and Nursalam and Darmawansyah and Syahrul Syahrul and Wahiduddin and Widiantoro and Anwar Mallongi} } @article {2105, title = {Hepatitis E Inhibited by Rosmarinic Acid Extract from Clove Plant (Syzygium Aromaricum) through Computational Analysis}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {518-523}, type = {Original Article }, chapter = {518}, abstract = {

This study aims to evaluate the potential of Rosmarinic Acid as an inhibitor against Hepatitis E by interacting with the active site of the Tyrosine FYN protein. Computational approaches were employed to predict the molecular interactions between Rosmarinic Acid and Tyrosine FYN. The research methodology involved the use of software such as Pymol, Pyrex, Protein Plus, and the Lepinski Rule. Docking analysis was conducted using Pymol to obtain information about the binding energy between Rosmarinic Acid and Tyrosine FYN. The results of the analysis showed that Rosmarinic Acid exhibited a Binding Affinity of -8.3, -8, and -7.9, indicating a strong affinity towards the target protein. Additionally, Root Mean Square Deviation (RMSD) values of 0, 15.905, and 17.014 were used to assess the stability of the formed protein-ligand complex. Analysis using Protein Plus revealed interactions between Rosmarinic Acid and Tyrosine FYN. Furthermore, analysis using the Lepinski Rule to examine the physicochemical properties of Rosmarinic Acid indicated that the molecule had a mass of 360, 5 hydrogen bond donors, 8 hydrogen bond acceptors, a log P value of 1.76, and a molar reactivity of 89.8. These findings highlight the potential of Rosmarinic Acid as an inhibitor of Hepatitis E through its interaction with the Tyrosine FYN protein, providing a basis for the development of potential new therapies in the treatment of this disease.

}, keywords = {Hepatitis E, Molecular Docking., Rosmarinic acid, Syzygium aromaricum, Tyrosine FYN}, doi = {10.5530/pj.2023.15.112}, author = {Sunadi and Saddam Al Aziz and Fadhilah Fitri and Devni Prima Sari and Muhammad Raffi Ghifari and Rismi Verawati and Nita Yessirita and Oski Illiandri and Riso Sari Mandeli and Devi Purnamasari and Putri Azhari and Rahadian Zainul and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2199, title = {The Impact of Kaempferia galanga L. Extract on Nerve Growth Factor Expression in A Rat Model of Traumatic Brain Injury}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1236-1243}, type = {Research Article}, chapter = {1236}, abstract = {

Introduction: Head injuries contribute significantly to morbidity and mortality globally, and there is need of effective treatment. This study focuses on evaluating NGF (Nerve Growth Factor) expression in a rat model of traumatic brain injury, exploring the potential therapeutic effects of Kaempferia galanga L. extract. Methods: Male Wistar rats were used in the experiment, and traumatic brain injury was induced using Marmarou{\textquoteright}s weight drop model. Four groups of rats were studied: a negative control group, a group with traumatic brain injury without Kaempferia galanga L. extract, and two groups with traumatic brain injury treated with different doses of Kaempferia galanga L. extract. Rats were divided further based on the time of decapitation, either 24 or 48 hours post-injury. NGF expression was assessed using immunohistochemistry. Results: The study confirmed NGF expression variations among groups, with stronger expression observed 48 hours post-injury in rats receiving 1200 mg/kgbb of Kaempferia galanga L. extract. This suggests a potential impact of the extract on NGF expression, likely attributed to its anti-inflammatory and antioxidant properties. Discussion: Kaempferia galanga L. extract has known anti-inflammatory and antioxidant effects, which may contribute to increased NGF expression observed in this study. Conclusion: This study sheds light on the potential benefits of Kaempferia galanga L. extract in promoting NGF expression and improving outcomes in traumatic brain injury, emphasizing the need for further investigation to translate these findings into clinical practice.

}, keywords = {kaempferia galanga, Nerve Growth Factor, Traumatic Brain Injury}, doi = {10.5530/pj.2023.15.224}, author = {Muhammad Fauzan Jauhari and Lucia Yovita Hendrati and Agus Turchan and Asra Al Fauzi and Budi Utomo and Eko Agus Subagio} } @article {2104, title = {In Silico Study of Rhamnocitrin Extract from Clove Syzygium Aromaricum in Inhibiting Adenosine A1 Adenylate Cyclase Interaction}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {512-517}, type = {Original Article }, chapter = {512}, abstract = {

This study aims to analyze the potential of Rhamnocitrin, a compound found in clove extract (Syzygium aromaticum), as an inhibitor of Adenylate Cyclase through an in-silico approach. The research method involves the use of software such as Pymol, PyRx, Protein Plus, and Lipinski Rule for molecular interaction analysis and physicochemical characterization of Rhamnocitrin. The analysis results show that Rhamnocitrin has significant affinity towards Adenosine A1 with Binding Affinity values of -6.1, -5.8, and -5.7. RMSD analysis indicates good stability of the formed protein-ligand complexes, with RMSD values of 0, 3.129, and 3.696. Analysis using Protein Plus software reveals the interaction between Rhamnocitrin and Adenosine A1, while the lipinski analysis shows physicochemical characteristics of Rhamnocitrin that meet important criteria, such as a mass of 300, 3 hydrogen bond donors, 6 hydrogen bond acceptors, log P of 2.6, and molar reactivity of 77.27. These findings provide new insights into the development of potential therapies involving clove extract and Rhamnocitrin as inhibitors of Adenylate Cyclase, and further research is needed to validate their effectiveness and safety.

}, keywords = {Adenosine A1, Adenylate Cyclase inhibition, Molecular Docking., Rhamnocitrin, Syzygium aromaricum}, doi = {10.5530/pj.2023.15.111}, author = {Nita Yessirita and Rismi Verawati and Devi Purnamasari and Rollando Rollando and Riso Sari Mandeli and Muhammad Thoriq Albari and Putri Azhari and Rahadian Zainul and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @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 {2083, title = {Interaction of Cynaroside from Orthosiphon Aristatus Plant Extract on TNF Alpha as a Stimulant in Malaria and Asthma}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {581-586}, type = {Research Article}, chapter = {581}, abstract = {

This research aims to investigate the interaction between cynaroside, a natural compound found in Orthosiphon aristatus plant extract, with TNF Alpha as a stimulant in the context of malaria and asthma. The research method involved an in-silico approach using software such as Pymol, PyRx, Protein Plus, and the Lepinski Rule. The results of the study showed that cynaroside has a significant interaction with TNF Alpha, as indicated by high Binding Affinity values of -9.6, -9.3, and -9.2. Analysis using Protein Plus confirmed the interaction between cynaroside and TNF Alpha. Additionally, evaluation using the Lepinski Rule of Five revealed that cynaroside has physicochemical characteristics suitable as a potential drug compound, with a mass of 448, hydrogen bond donors of 7, hydrogen bond acceptors of 11, log p -0.401, and molar reactivity of 105.2. These findings provide a deeper understanding of the potential of cynaroside in regulating the immune response to malaria and asthma through its interaction with TNF Alpha. These results can serve as an important basis for further research in the development of more targeted and effective therapies for both of these diseases

}, keywords = {Asthma., Cynaroside, Malaria, Molecular docking, Orthosiphon aristatus, TNF Alpha}, doi = {10.5530/pj.2023.15.123}, author = {Rahadian Zainul and Rismi Verawati and Gemini Alam and Khoirun Nisyak and Trisna Kumala Sari and Muhammad Arya Ghifari and Ritbey Ruga and Putri Azhari and Romadhon and Himmatul Barroroh and Riso Sari Mandeli and Devi Purnamasari and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2135, title = {The Investigation of The Network Pharmacology and Mechanism of Action of Centella Asiatica Extract on The Atopic Dermatitis Model}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {881-890}, type = {Research Article}, chapter = {881}, abstract = {

Background: Atopic dermatitis (AD) is a chronic relapsing inflammatory skin condition which has a negative impact on children health. The well-known medicinal plant Centella asiatica extract (CE) is used in herbal skin care products to produce various pharmacological effects in dermatology. However, the molecular target of CE in suppressing inflammatory is largely unknown. Objective: the aim of this study was to examine anti-inflammatory properties and network pharmacology of CE in lipopolysaccharide (LPS)- induced AD in vitro model. Method: RAW264.7 cells were pre-treated with CE and then were stimulated with LPS and then were investigated cell viability, NO production, and the levels of pro-inflammatory mediators. In addition, the Search Tool for Retrieval of Interacting Genes (STRING), SwissTargetPrediction and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to construct the defined mechanism of action and network pharmacology. Results: CE showed the potent inhibitory effects on LPS-induced NO. In addition, CE significantly suppressed the expression of iNOS and COX-2, as well as the production of IL-2, IL-6, IL-10, and TNF- α. Furthermore, the network pharmacological analysis revealed the potential role of CE in biological processes such as regulating JAK/STATs pathway and inhibiting proinflammatory cytokines both of which were linked to AD pathogenesis. Conclusion: Our findings confirm our hypothesis that CE could be developed as a therapeutic therapy for atopic dermatitis due to its pharmacological action and signaling mechanism in the modulation of allergic skin inflammation.

}, keywords = {Atopic dermatitis, Centella asiatica, Network pharmacology, Skin inflammation.}, doi = {10.5530/pj.2023.15.168}, author = {Sucharat Tungsukruthai and Runtikan Pochairach and Aungkana Krajarng and Piracha Jumpa-ngern and Parunkul Tungsukruthai} } @article {2195, title = {The Miracle of Moringa Oleifera Leaves for the Prevention of Anemia: A Literature Review}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1258-1261}, type = {Review Article}, chapter = {1258}, abstract = {

Background: Moringa oleifera leaves contain very rich compounds that include nutrients, minerals, vitamins, amino acids, and many other compounds with numerous benefits for humans. This literature review discusses the benefits of Moringa oleifera leaves in preventing anemia. Methods: This review is a narrative review using the research of international journal sources from databased, national journals in the last ten years. The keywords anemia, hemoglobin, and Moringa oleifera/M. oleifera leaves were used. Based on the 35 journals reviewed, 12 studies were included in this review. Results: The literature results show a positive relationship between Moringa leaf extract and an increase in the value of hemoglobin levels, with a p-value \<0.05. However, this review found other benefits of Moringa oleifera leaf extract, such as improving the morphology of damaged red blood cells and antioxidants. It has become an alternative in the treatment of anemia. Conclusions: The nutrient content in Moringa leaf extract plays a significant part in increasing hemoglobin levels in the blood. Other factors that can increase the risk of anemia are micronutrient deficiency, infectious diseases (HIV/AIDS, tuberculosis, and malaria), worm infections, and genetic disorders. (25) We recommend conducting an experimental study to compare two groups given Moringa leaf extract and multi-micronutrient tablets to get more effective results in lowering the prevalence of anemia.

}, keywords = {Anemia, Moringa oleifera leaf extract}, doi = {10.5530/pj.2023.15.228}, author = {Dwi Wahyu Balebu and Ridwan Aminuddin and Veni Hadju and Arsunan Arsin and Nurhaedar Jafar and Herawati and Anwar Mallongi} } @article {2013, title = {Molecular Docking and ADME Studies of Centella Asiatica as Anti Hyperuricemia}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {384-389}, type = {Research Article}, chapter = {384}, abstract = {

Centella asiatica is a traditional natural medicine used in a number of Southeast Asian nations. (also known as Centella asiatica L., Urb., or Gotu Kola). The aim of this study is to determine the antihyperuricemia properties of Centella asiatica extract and the possibility that they will interact with the XDH enzyme. The XDH enzyme is one of three enzymes that can influence the onset of hyperuricemia with the other two are SLC22A12 and ABCG2. In this research, we employ a computational method in collaboration with a number of applications and databases. ADME analysis was carried on for some Centella asiatica constituents to determine their similarities to the drug and bioavailability components. The analysis continued on with molecular docking between the chemical compounds and several enzymes related to hyperuricemia. According to the findings, Centella asiatica contains active constituents that can be used as an alternative therapy for hyperuricemia.

}, keywords = {Centella asiatica, Hyperuricemia, Molecular Docking.}, doi = {10.5530/pj.2023.15.59}, author = {Ahmad Shobrun Jamil and Prayogi Galie Saputro} } @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 {2130, title = {Risk Factors of Stunting in Children Aged 0-23 Months in Katumbangan Health Center, Indonesia}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {851-855}, type = {Research Article}, chapter = {851}, abstract = {

The results of Indonesian nutritional status study at the regency level in 2021 showed that Polewali Mandar Regency had the highest prevalence of stunting in West Sulawesi Province at 36\% with the highest percentage of stunted toddlers being reported by Katumbangan Health Center (42.6\%). This study aims to determine the most dominant risk factors for stunting in children aged 0-23 months. This study was conducted in the working area of Katumbangan Health Center with a case-control study. The number of samples was 236 infants (0-23 months) with a ratio of cases and controls of 1:1. This study used secondary data sourced form e-PPGBM application, then analyzed by odd ratio test and logistic regression on Stata. The results showed that CED in pregnancy (OR=3.142 with 95\% CI, 1.122-10.072), LBW history (OR=5.963 with 95\% CI, 1.251-56.216) and exclusive breastfeeding (OR=2.099 with 95\% CI, 0.984-4.613). The dominant risk factor for stunting in children aged 0-23 months, namely LBW history (OR=5.092 with 95\% CI, 1.08-23.94). It is recommended for mothers to put more attention to the fulfillment of nutrition during in order to reduce the risk of LBW and also to assure that children nutritionl intake are adequate to their needs during the golden period of growth, especially infants with LBW.

}, keywords = {Infant, Risk Factors., Stunting}, doi = {10.5530/pj.2023.15.163}, author = {Nurul Iffa Safitri and Nur Nasry Noor and Wahiduddin and Ridwan Amiruddin and Nurhaedar Jafar and Balqis and Anwar Mallongi} } @article {2084, title = {Stimulation of Emodin from Aloe Vera on Protein Kinase PIM1 in the Central Nervous System Through In Silico Analysis}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {587-592}, type = {Research Article}, chapter = {587}, abstract = {

This study aims to investigate the potential of Emodin, a compound found in Aloe vera, as a stimulator of Protein Kinase PIM1 in the central nervous system using an in-silico approach. The research method involves the use of software such as Pymol, Pyrex, Protein Plus, and Lepinski Rule. Firstly, the protein structure of the target Protein Kinase PIM1 was obtained from a protein database and prepared using Pymol. Next, the molecular structure of Emodin was imported into Pyrex and subjected to geometry optimization. Docking analysis using Pymol was performed to predict the molecular interactions between Emodin and Protein Kinase PIM1. Additionally, RMSD analysis was conducted to evaluate the stability of the protein-ligand complex formed. The docking analysis results showed that Emodin exhibited significant Binding Affinity, with values of -8.4, -8.3, and -8.2, indicating a strong affinity between Emodin and Protein Kinase PIM1. The RMSD analysis indicated the stability of the protein-ligand complex, with RMSD values of 0, 1.101, and 1.122. Furthermore, analysis using Protein Plus revealed the presence of interactions between Emodin and Protein Kinase PIM1 through hydrogen bonding and hydrophobic contacts. The results of the Lepinski Rule analysis demonstrated that Emodin fulfilled several important criteria in drug design, including a molecular weight of 270, 3 hydrogen bond donors, 5 hydrogen bond acceptors, a log p value of 1.887220, and a molar reactivity of 64.480385. These findings indicate the potential of Emodin as a stimulator of Protein Kinase PIM1 in the central nervous system and provide an important foundation for the development of potential therapies for central nervous system-related disorders.

}, keywords = {Central Nervous System, Emodin, Molecular Docking., PIM1 Kinase, Stimulation}, doi = {10.5530/pj.2023.15.124}, author = {Rahadian Zainul and Rismi Verawati and Ritbey Ruga and Muhammad Arya Ghifari and Devi Purnamasari and Putri Azhari and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2069, title = {Study on the Inhibition of Sinensetin Extract from Cat{\textquoteright}s Whiskers Plant (Orthosiphon aristatus) on ATP Binding Cassette Sub-Family G Member 2 in Uric Acid}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {506-511}, type = {Original Article }, chapter = {506}, abstract = {

This study aims to investigate the potential of sinensetin, a compound found in the Cat{\textquoteright}s Whiskers plant (Orthosiphon aristatus), as an inhibitor in inhibiting uric acid through its interaction with ATP Binding Cassette Sub-Family G Member 2 (ABCG2). The in-silico approach was employed using software tools such as Pymol, PyRx, Protein Plus, and Lepinski Rule. The results of molecular docking analysis using PyRx demonstrated significant interactions between sinensetin and ABCG2, with Binding Affinity values of -6.8, -6.6, and -6.6, and RMSD values of 0, 0.785, and 1.379. The analysis using Protein Plus confirmed the interaction between sinensetin and ABCG2, supporting the previous docking findings. Furthermore, the evaluation of pharmacokinetic parameters using the Lepinski Rule of Five revealed that sinensetin meets the criteria as a potential drug compound, with a molecular weight of 372, no hydrogen bond donors, seven hydrogen bond acceptors, a log P value of 3.345, and a molar reactivity of 98.5. This research provides new insights into the development of uric acid therapy through an in-silico approach, and these findings can serve as a basis for further research involving in vitro and in vivo validation.

}, keywords = {ATP Binding Cassette, Molecular docking, Orthosiphon aristatus, Sinensetin, Uric Acid.}, doi = {10.5530/pj.2023.15.110}, author = {Anni Faridah and Rismi Verawati and Budhi Oktavia and Musa Ghufron and Devi Purnamasari and Muhammad Raffi Ghifari and Linda Rosalina and Putri Azhari and Rahadian Zainul and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2053, title = {Tanacetum Parthenium (L.) Sch Bip From Peru: Antioxidant Profile and The Antinociceptive Effect in An Experimental Model}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {435-437}, type = {Research Article}, chapter = {435}, abstract = {

Background: Tanacetum parthenium (L.) Sch Bip known as {\textquotedblleft}santa mar{\'\i}a{\textquotedblright} (Asteraceae family) is used in Peru for inflammatory diseases and also in colic, stomachache, headaches, diarrhea, among other. Objective: The aim was to determine the antioxidant profile, and analgesic effect of ethanolic extract of flowers and leaves of T. parthenium Material and Methods: Leaves and flowers of T. parthenium were soaked in 96\% ethanol and the obtained extract was analyzed using chemical reactions for identifying each secondary metabolite, 2,2-Diphenyl-1-picrylhydrazyl (DPPH) was used to determine the antioxidant capacity, and the antinociceptive effect was determined by using tail flick method. Results: Qualitative phytochemical study indicates the presence phenolic compounds, alkaloids, flavonoids, saponins and steroids in both extracts. In DPPH assay IC50 showed in leaves and flowers extract 452.10 {\textpm} 10.2 μg/mL and 270.70 {\textpm} 20.6 μg/mL respectively. The antinociceptive effect was better in leaves at doses 300 mg/ Kg than flower extract. Conclusions: The ethanolic extract of flowers of T. parthenium showed a high antioxidant activity and antinociceptive effect in mice.

}, keywords = {Analgesic, Antioxidant, Medicinal Plants., Polyphenols, Tanacetum parthenium}, doi = {10.5530/pj.2023.15.97}, author = {Oscar Herrera-Calderon and Wilfredo Bulege-Guti{\'e}rrez and Luz Alexandra Javier-Silva and Melva Iparraguirre- Meza and Victor Guillermo Sanchez-Araujo and Elizabeth Julia Melgar-Merino and Johnny Aldo Tinco-Jayo and Jos{\'e} Santiago Almeida-Galindo and Josefa Bertha Pari-Olarte} } @article {1961, title = {Uterocervical Angle Anterior, Posterior, and Cervical Length Ultrasound as a Predictors for Successful Delay in Labor of Pregnant Women with Threatened Preterm Birth (PTB)}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {52-56}, type = {Original Article }, chapter = {52}, abstract = {

Introduction: To determine whether the examination of the uterocervical angle anterior, posterior, cervical length, and combination can be used as a predictor of successful delay in labor in patients with threatened preterm birth (PTB). Methods: This is a prospective cohort analytical observational study of 44 women admitted to our hospital gestational age 28-36 weeks diagnosed with threatened preterm birth. Cervical length, anterior uterocervical angle, and posterior uterocervical angle examinations were performed. Patient then observed for 2x24 hours whether there was a delay in labor or not. If there is a delay, the patient followed until delivery. Results: CL cut off value \> 2.66 cm delaying labor for 2x24 hours and \> 2.81 cm delaying labor until term. UCA posterior cut off value \< 113.2o delaying labor for 2x24 hours and \< 107.8o delaying labor until term. Anterior UCA cut off values \< 103.2o delaying labor for 2x24 hours and \< 93.1o delaying labor until term. Statistical Analysis showed that CL was significant as a single tool for predictor of delayed labor either 2x24 hours or up to term, while posterior and anterior UCA was not. But if this 3 single tools combinate, CL, anterior UCA, and posterior UCA was statistically significant as a predictor of delay in labor either 2x24 hours or until term, with the best predictive value is a combination of CL and posterior UCA of 25.2\% for predicting delay of labor 2x24 hours and the combination of CL, posterior, and anterior UCA was 24.6\% for predicting delay labor until term. Conclusion: Cervical length ultrasound examination and the combination of CL, anterior UCA, and posterior UCA can be predictors of delayed labor in patients with threatened preterm birth but not for anterior and posterior uterocervical angle as a single tool.

}, keywords = {Cervical Length, Preterm Delivery, Threatened Preterm Birth (PTB), Uterocervical Angle Anterior, Uterocervical Angle Posterior.}, doi = {10.5530/pj.2023.15.8}, author = {Qurrata Akyuni and Agus Sulistiyono and Hermanto Tri Joewono and Lilik Djuari} } @article {2197, title = {Why Preconception Treatment is Important? A Literature Reviews}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1262-1267}, type = {Review Article}, chapter = {1262}, abstract = {

Objective: Conceptional care is a concept that has been proposed to address maternal health problems and environmental risk factors during pregnancy to improve the health of both mother and fetus during pregnancy. This article provides an overview of several studies relating to preconception care that are useful for preparing for a healthy pregnancy and fetus. Methods: This narrative review uses several sources from the Elsevier database. Key search terms such as preconception, iron status, pregnancy and fetus were used in this review. Of the 50 studies identified, 20 were eligible for inclusion in this review. Results: Preconception care is getting an increased focus as an effective way to prevent complications during pregnancy, childbirth, and postpartum as well as preventing fetal abnormalities by estimating nutritional status in the preconception period. Preconception care is aimed at supporting the health of women before pregnancy, which is useful for improving the health of a pregnancy and preventing stunted fetal growth due to poor nutritional status in the mother. Low preconception iron status will have an impact on preconception gynecological morbidity, which will cause complications in pregnancy and cause low birth weight. Conclusion: Preconception care when given regularly will affect the health of a pregnancy and the baby when born. Preconception care teaches women of reproductive age to minimize potential health risks from an early age so that if they have a baby, the baby is born in better health. Considering that a healthy baby is very late if it is prepared during pregnancy but must be prepared from the preconception period, that is why preconception is so important.

}, keywords = {Fetus, Iron status, Preconception, Pregnancy}, doi = {10.5530/pj.2023.15.229}, author = {Darmin Dina and Nurhaedar Jafar and Veny Hadju and Hasnawati Amqam and Wahiduddin and Ridwan Amiruddin and Anwar Mallongi and Yulianah Sulaiman} } @article {1783, title = {Anxiolytic and Antidepressant-like Effects of Foeniculum vulgare Essential Oil}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {425-431}, type = {Research Article }, chapter = {425}, abstract = {

Introduction: The aim of this research was to determine the anxiolytic and antidepressant-like effects of the essential oils from Foeniculum vulgare aerial parts and seeds. Methods: The oils were extracted by hydro-distillation using a modified Clevenger-type apparatus and chemical composition was performed by Gas chromatography with flame-ionization detection (GC-FID) and Gas chromatography-mass spectrometry (GC{\textendash}MS). Furthermore, an experimental trial was conducted, where 117 participants were divided into three groups, comprising a waiting list control group and two experimental groups treated with essential oils. The anxiety and depression indexes were evaluated by Zung Self-Rating Anxiety Scale (SAS) and Zung Self-Rating Depression Scale (SDS). Results: chemical analysis showed that trans- Anethole was the main component, both in the essential oil from aerial parts (35.5\%) and seeds (79.2\%). Anxiety and depression scores showed a decrease in posttest study phase in comparison with pretest in all experimental groups (p\<0.05), except for depression scores in the group treated with essential oil from aerial parts (p\>0.05). Small changes were found in the case of anxiety for group treated with essential oils from aerial parts (d = 0.41; Δ= 0.40) while moderate (d = 0.86; Δ = 0.85) and small (d = 0.38; Δ = 0.39) changes were found for anxiety and depression respectively, in the group treated with essential oil from seeds. Conclusion: The essential oil from Foeniculum vulgare seeds is more effective to relief anxiety than depression while the essential oil from Foeniculum vulgare aerial parts only exhibit small changes for anxiety.

}, keywords = {Anxiety, Depression, Essential oils, Foeniculum vulgare}, doi = {10.5530/pj.2022.14.54}, author = {Paul Alan Arkin Alvarado-Garc{\'\i}a and Maril{\'u} Roxana Soto-V{\'a}squez and Luis Enrique Rosales-Cerquin and Elda Maritza Rodrigo-Villanueva and Demetrio Rafael Jara-Aguilar and Lurdes Tuesta-Collantes} } @article {1870, title = {Artificial Sweeteners Perturbed Liver Enzymes in Rat Model}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {553-557}, type = {Research Article}, chapter = {553}, abstract = {

In the recent time there has been an increased demand of low-fat or low calorie diet universally. In the mean while the availability of low calorie products has also increased like sugar free drinks, beverages, biscuits, jams and jellies. On contrary to this, some studies suggest that the prolong use of non-nutritive sweeteners alters the homeostasis of glucose and insulin. It results in fluctuation of glucose level in blood and increase in bodyweight. This study intends to evaluate the effect of non-nutritive sweeteners on the liver function test and record the alteration in the levels of ALP, AST and ALT. Seventy rats were divided into seven equal groups, controlled group received distilled water and the rest six were given NNS Sucrose, Stevia, Sucralose, Saccharine Aspartame and Acesulfame-k, respectively. On the evaluation of Alanine aminotransferase ALT, saccharine and aspartame markedly increased the level of ALT from 40U/L to 80 U/L. Both of these NNS have shown the most raised level of Alanine aminotransferase. This represents the stress on the liver associated with the use of NNS and suggests the use to be controlled in humans.

}, keywords = {Albumin, Artificial Sweeteners, Bilirubin, Liver Enzyme}, doi = {10.5530/pj.2022.14.135}, author = {Muthear N Dawood and Shaymaa AH. Jassim and Maab Azmi Fadel and Imad A. Thanoon} } @article {1841, title = {Bioactive Compounds from Purslane (Portulaca oleracea L.) and Star Anise (Illicium verum Hook) as SARS-CoV-2 Antiviral Agent via Dual Inhibitor Mechanism: In Silico Approach}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {352-357}, type = {Original Article }, chapter = {352}, abstract = {

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes the COVID-19 pandemic that infects humans and attacks the body{\textquoteright}s immune system. The purpose of the study was to identify the potential of bioactive compounds in purslane (Portulaca oleracea L.) and star anise (Illicium verum Hook) via a dual inhibitor mechanism against SARS-CoV-2 proteases with an in silico approach. The samples were obtained from PubChem and RSCB PDB. Antivirus probability prediction was performed on PASS Online. Virtual screening was performed with PyRx via molecular docking. Visualization was used by PyMol and Discovery Studio. Compounds with the best antiviral potential are indicated by the low binding affinity value to the target proteins, namely SARS-CoV-2 TMPRSS2 and PLpro. The results showed that purslane luteolin has the best antiviral potential. However, further studies are required to validate this computational prediction.

}, keywords = {Antiviral agent, Illicium verum Hook, in silico, Portulaca oleracea L., SARS-CoV-2}, doi = {10.5530/pj.2022.14.106}, 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 Dony Novaliendry and Riso Sari Mandeli and Budhi Oktavia and Muhammad Thoriq Albari and Saddam Al Aziz and Muhammad Raffi Ghifari and Okta Suryani and Putri Azhari and Muhammad Arya Ghifari and Devi Purnamasari and Agariadne Dwinggo Samala and Mirella Fonda Maahury and ANM Ansori and Rahadian Zainul} } @article {1947, title = {Bio-Evaluation, In-Vitro and In-Vivo Anti-Inflammatory Activity, Therapeutic Efficacy, and Genotoxicity of the Potentials of the Green Seaweed Valoniopsis Pachynema using Zebra Fish Larvae (Danio Rerio) as an Animal Model}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {1037-1053}, type = {Research Article }, chapter = {1037}, abstract = {

Advancement in the medical sectors to treat regular diseases are increasing day-by-day. Yet, there is a considerable growth in the demand for the natural/herbal products as well due to their low level of side effects, cost efficiency and their multiple inhibition properties. Based on this, the present research works with an objective to examine the bioactive components, in vitro anti-inflammatory and in vivo antiinflammatory behaviour of the green marine macro algae Valoniopsis pachynema using zebra fish (Danio rerio) larvae as a skin inflammation model. In this study, the secondary metabolites are extracted using methanol solvent from the marine green seaweed, V. pachynema using the Gas Chromatography-Mass Spectrometry (GC-MS) analysis and these are further evaluated for their anti-inflammatory effects. Further screening process is accomplished for the in vitro anti-inflammatory activity by the albumin-denaturation inhibition. Results from concentration-dependent analysis is documented. The efficacy, therapeutic efficacy, and genotoxicity of the compound Valp at various concentrations are determined by recapitulating the pathophysiology of Skin inflammation in Zebrafish larvae. In evaluating the efficiency of the study, Valp at 1 pg, 10 pg, 100 pg are observed and progressed for the evaluation of therapeutic efficacy and genotoxicity. In the assessment of genotoxicity, the gene expression of mgmt gene is observed to be in control level at Valp 100 pg treated group confirming no genotoxicity. According to the results obtained, the green seaweed V. pachynema can be potentially explored as an effectual anti-inflammatory agent for its bio-functionalities

}, keywords = {Anti-inflammatory, Bioactive compounds, GC-MS, Marine algae, V. pachynema, Zebra fish larvae drug toxicity.}, doi = {10.5530/pj.2022.14.208}, author = {Bhuvaneshwari. J and Thirumalai Vasan. P} } @article {1913, title = {Correlation of the Presence of Non Structural-1 (NS1) Antigen Dengue Virus with Severity of Dengue Infection}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {813-816}, type = {Research Article }, chapter = {813}, abstract = {

Dengue is a major public health threat worldwide, affecting approximately 3 billion people. More than 100 countries in the world located in tropical and subtropical areas, there are at least 100 to 400 million people infected with the dengue virus which causes dengue hemorrhagic fever (DHF). Soluble Non Structural Protein (sNS1) DENV is a soluble NS1 protein that is secreted and found in the serum of patients during acute infection. Because of its presence early in infection, sNS1 is used as a diagnostic indicator of acute dengue infection. NS1 can directly activate platelets through TLR4 and can further increase platelet aggregation, endothelial cell adhesion, and phagocytosis by macrophages that can cause thrombocytopenia so that high sNS1 levels are associated with disease severity. From the results of the study showed p \<0.05. This indicates that there is a correlation between the presence of NS1 and the severity of dengue infection.

}, keywords = {Dengue virus, NS1 antigen, Thrombocytopenia}, doi = {10.5530/pj.2022.14.172}, author = {Ichwan Baihaki and Beti Ernawati Dewi and Viol Dhea Kharisma and Ahmad Affan Ali Murtadlo and Muhammad Badrut Tamam and Devi Purnamasari and Nunuk Hariani Soekamto and ANM Ansori and Kuswati and Riso Sari Mandeli and Kawther Ameen Muhammed Saeed Aledresi and Nur Farhana Mohd Yusof and Vikash Jakhmola and Maksim Rebezov and Pavel Burkov and Marina Derkho and Pavel Scherbakov and Rahadian Zainul and Muhammad Raffi Ghifari and Asmi Citra Malina AR Tasakka and Tengku Siti Hajar Haryuna} } @article {1771, title = {Evaluation of Antibacterial and Antioxidant Activity of Endophytic Fungi Isolated from CAPSICUM ANNUUM L. and ALLIUM CEPA L.}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {329-334}, type = {Research Article }, chapter = {329}, abstract = {

Objective: The aims of this study were to identify the endophytic fungi from Capsicum annuum L. and Allium cepa L., to determine antioxidant and antimicrobial activity of ethyl acetate extract of endophytic fungi isolated from C. annuum and A. cepa. Methods: Endophytic fungi was isolated with potato dextrose agar (PDA) from fruits of C. annuumand bulbs of A. cepa. Isolate of endophytic fungi was molecular identified to know the species or genus. Cultivation was carried out on rice media, 4 weeks on room temperature and the extraction by maceration using ethyl acetate. Antioxidant activity were tested by DPPH method. While antibacterial activity was tested by disk diffusion methods and microdilution methods. Results: Five isolates of endophytic fungi from red and green fruits of C. annuum and bulb of A. cepa have been isolated and the species or the genus have been confirmed. KCM 1 and KCM 2 isolates endophytic fungi from the red fruits of C. annuum were confirmed as Diaporthe sp and Chaetomium globosum. The KCH 1 isolate from green fruits of the C. annuum was confirmed as Trametes hirsuta. The KBM 1 and KBM 2 isolates from A. cepa were confirmed as Schizophyllum commune and Phlebia sp. The highest antioxidant and antibacterial activity was exposed by ethyl acetate extract of S. commune. Conclusion: Five isolates endophytic fungi from C. annuum and A. cepa were Diaporthe sp, C. globosum, T. hirsuta, S. commune and Phlebia sp. Ethyl acetate extract of S.commune gave highest antioxidant and antibacterial activity.

}, keywords = {Antimicrobial, Chaetomium globosum, Endophytic fungus, Onion, Red chili, Schizophyllum commune}, doi = {10.5530/pj.2022.14.42}, author = {SYLVIA RIZKY PRIMA and ELFAHMI and ELIN JULIANTI and Irda Fidrianny} } @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 {1832, title = {In Silico Screening of Bioactive Compounds from Syzygium cumini L. and Moringa oleifera L. Against SARS-CoV-2 via Tetra Inhibitors}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {267-272}, type = {Original Article }, chapter = {267}, abstract = {

The global pandemic of COVID-19 has caused disastrous consequences for both humans and the economy. The purpose of this study was to determine the potential of juwet (Syzygium cumini L.) and moringa (Moringa oleifera L.) as inhibitors of RBD spike, helicase, Mpro, and RdRp activity of SARS-CoV-2 with an in-silico approach. Samples were obtained from PubChem and RSCB PDB databases. The drug similarity analysis was determined using Swiss ADME and the Lipinski rule of five. Prediction of antivirus probabilities is carried out with PASS Online. Molecular screening is performed by molecular docking using PyRx. Visualization was used using PyMol and Discovery Studio. The bioactive compounds with the best antiviral potential had the lowest affinity bonds to the target proteins against RBD spike, helicase, Mpro, and RdRp of SARS-CoV-2. Results show that ellagic acid from java plum and myricetin from moringa have the best potential as potential antivirals. However, more research is required to validate the results of these computational predictions.

}, keywords = {Antiviral agent, in silico, Moringa Oleifera L, SARS-CoV-2, Syzygium cumini L.}, doi = {10.5530/pj.2022.14.95}, 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 Devni Prima Sari and Muhammad Thoriq Albari and Devi Pernamasari and Muhammad Arya Ghifari and Muhammad Raffi Ghifari and Riso Sari Mandeli and Muhardi and Budhi Oktavia and Trisna Kumala Sari and Titi Sriwahyuni and Putri Azhari and Mirella Fonda Maahury and ANM Ansori and Rahadian Zainul} } @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 {1912, title = {In Silico Study of the Potential of Endemic Sumatra Wild Turmeric Rhizomes (Curcuma Sumatrana: Zingiberaceae) As Anti-Cancer}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {806-812}, type = {Research Article }, chapter = {806}, abstract = {

Cancer is one of the diseases that is the highest cause of death in humans. Most human cancer cells are formed as a result of over-expression of anti-apoptotic proteins. Thus, the activation of these proteins can inhibit pro-apoptotic proteins, then apoptosis will be inhibited so that other apoptotic pathways need to be activated to prevent cancer cells from developing. Current cancer treatments, such as chemotherapy using synthetic compounds, have various side effects, so research on natural based therapies can be used as an alternative in cancer treatment. Curcuma sumatrana is one of the plants of the Zingiberaceae family which is an endemic plant from Sumatra which is found along the Bukit Barisan. The research was carried out in silico by analyzing the potential bioactivity of the compounds, testing the bioavailability, toxicity, and molecular docking of the bioactive compounds from the ethanol extract of the rhizome of C. sumatrana which had been previously identified through gas chromatography-mass spectroscopy (GCMS) analysis. The results obtained that the compound 9-Acetyl-S-octahydrophenanthrene and 3-Oxoandrosta- 1,4-dien-17.beta.-spiro-2{\textquoteright}-3{\textquoteright}-oxo-oxetanecontained in C. sumatrana has the potential to be developed as an anticancer where the compound has good bioavailability value and is not toxic and potentially can trigger apoptosis. However, the results of this study need to be analyzed further with an in vitro or in vivo approach.

}, keywords = {Anticancer, C. sumatrana, in silico}, doi = {10.5530/pj.2022.14.171}, author = {Aldi Tamara Rahman and Rafia and Aiken Jethro and Putra Santoso and Viol Dhea Kharisma and Ahmad Affan Ali Murtadlo and Devi Purnamasari and Nunuk Hariani Soekamto and ANM Ansori and Kuswati and Riso Sari Mandeli and Kawther Ameen Muhammed Saeed Aledresi and Nur Farhana Mohd Yusof and Vikash Jakhmola and Maksim Rebezov and Maksim Rebezov and Rahadian Zainul and Kiran Dobhal and Tarun Parashar and Muhammad Arya Ghifari and Deffi Ayu Puspito Sari} } @article {1914, title = {An In Silico Study to Explore the Role of EGFR in Ovarian Cancer}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {817-821}, type = {Research Article }, chapter = {817}, abstract = {

EGFR is a tyrosine kinase receptor that has a role in the tumorigenesis of many types of solid tumors. Aberrantly phosphorylated or overexpressed EGFR is associated with cellular proliferation, prevention of apoptosis, activation of invasion and metastasis, and stimulation of tumor-induced neovascularization. EGFR{\textquoteright}s hyperactivity has been observed in ovarian cancer. Although conventional chemotherapy and surgery for advanced ovarian cancer have improved over the years, still there is a critical need for the development of molecular targeted therapies. The major challenge for this approach is the complete understanding of the protein structure of this mega receptor. In this study, we explored this receptor using in silico tools. The protein structure of the EGFR kinase domain (PDB ID: 1M17) and co-crystal containing EGFR and PTP1B kinase domain fragment (PDB ID: 3I7Z) were obtained from the RCSB Protein Data Bank. We performed protein-protein docking using BioLuminate. It was found in this study that the DADEYL segment of EGFR (position 988-993) which includes autophosphorylated tyrosine at position 992, is the segment that is responsible for the overexpression of this receptor in ovarian cancer. There are currently two main classes of clinically-approved drugs which downregulate EGFR activity; tyrosine kinase inhibitors (TKIs) and monoclonal antibodies (Mabs). However, treatment with both type of therapies has been met with shortcomings. Therefore, there is a need for further studies to explore the suitable ligands that can downregulate its activity.

}, keywords = {EGFR, In silico study, Protein-protein docking, Tyrosine kinases}, doi = {10.5530/pj.2022.14.173}, author = {Vikash Jakhmola and Tarun Parashar and Pallavi Ghildiyal and ANM Ansori and Rajeev Kumar Sharma and N. G. Raghavendra Rao and Kapil Kalra and Nishan Singh and Nidhi Nainwal and Rajeev Kumar Singh and M. P Singh and Vishwadeepak Kimothi and Alok Bhatt and Ashish Dimri and Ravi Kumar and Amit Semwal and Nur Sofiatul Aini and Maksim Rebezov} } @article {1908, title = {Increased Risk of Tumor Necrosis Factor-Alpha Levels in Adult Patients with Malignancy Receiving Non-Leucodepleted Packed Red Cells Transfusion}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {778-781}, type = {Original Article }, chapter = {778}, abstract = {

Background and Objectives: Blood transfusion in patients with malignancy may evoke transfusion reactions. Leukocyte, as a major producer of cytokines, including Tumor Necrosis Factor-alpha (TNF-alpha), is considered to correlate to transfusion reactions. This study aims to determine the risk of increased TNFalpha in adult patients with malignancy who received non-leucodepleted (nLD) erythrocyte transfusion compared to those receiving leucodepleted (LD) Packed Red Cells (PRC) transfusion. Materials and Methods: This quasi-experimental study was conducted on adult patients with malignancy who required PRC transfusion and underwent outpatient treatment. The patients were divided without randomization into nLD and LD groups, and then their pre-transfusion TNF-alpha levels and the post-transfusion changes were examined. Results: This study included thirty-one patients fulfilling the inclusion criteria. The TNFalpha levels in nLD and LD groups after transfusion increased significantly (p \< 0.05), i.e., from 0.81 (0.2 - 4.2) pg/mL and 1.7 (0.15 - 6.3) pg/mL to 10.1 (1.4 - 28.9) and 5.9 (0.95 - 12.9) pg/mL. There was no significant difference in the pre-transfusion median TNF-alpha levels between the nLD and LD groups (p = 0.122). However, the post-transfusion median TNF-alpha levels of the nLD group were significantly higher (p = 0.024). It indicated that the increase in TNF-alpha levels is associated with nLD blood products transfused. The Relative Risk of the increased TNF-alpha levels in nLD-PRC transfusion was 2.01 (95\% Confidence Interval: 1,153-3,502). Conclusion: nLD-PRC transfusion poses a 2.01 times risk for increased TNF-alpha levels compared to LD-PRC transfusion.

}, keywords = {Malignancy, Non-leucodepleted, PRC transfusion, Relative risk, TNF-Alpha}, doi = {10.5530/pj.2022.14.167}, author = {Teguh Triyono and Bambang Hendriawan Prasaja Jati and Usi Sukorini} } @article {1862, title = {Isolation and Characterization of Neuroglobin and The Reducing Enzyme Metneuroglobin (Neuroglobin Fe3+) From Bovine Brain Tissue}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {504-510}, type = {Original Article}, chapter = {504}, abstract = {

Background/Aim: The brain uses 20\% of the O2 consumed by the body for energy metabolism. In 2000, found a protein that is thought to be a binding O2 in the brain, namely neuroglobin (Ngb). Ngb is a member of the hemoprotein which has a heme group. The iron ion in the haem group can be oxidized, so a reducing enzyme is needed. In this study, the isolation, purification, and characterization of Ngb protein and the reducing enzyme from oxidized neuroglobin (neuroglobin Fe3+) were carried out. Materials and methods: Ngb protein was isolated by fractionation technique using ammonium sulfate 90\% saturation, purified by anion exchange chromatography (DEAE Cellulose) and immunoaffinity chromatography, confirmed by SDS-PAGE and Western blot. The metneuroglobin-reducing enzyme was isolated by RIPA lysis buffer, purified by Affi gel blue chromatography, and confirmed by SDS-PAGE. Results: The isolated Ngb obtained has a molecular weight of 17.26 kDa. Spectrum analysis in the wavelength range of 350- 500nm, showed the afternoon peaks of deoxyNgb, oxyNgb, carboxyNgb and metNgb were 415 nm, 405 nm, 405 nm, and 420 nm, respectively. The results of the isolation of the reducing enzymes obtained consisted of 2 parts, namely the matrix-bound eluate (eluate-1) and matrix-bound eluate (eluate-2). SDSPAGE results of eluate-1, eluate-2 and Ngb-free fraction (byproduct of Ngb purification) showed the same 3 bands at a molecular weight of 72.45; 26.84 and 16.33 kDa were suspected as reducing enzymes. Conclusion: The reduction kinetics was tested by reacting the fraction and metNgb and measuring the deoxyNgb uptake formed per unit time. The results of the measurement of the ratio of NgbFe3+ to NgbFe2+ from the free fractions Ngb, eluate-1 and eluate-2, which has the best reducing activity is eluate-1 because it has the best regression value of 0.8769.

}, keywords = {Bovine brain tissue, Neuroglobin, Neuroglobin absorption spectrum, Reductase enzyme}, doi = {10.5530/pj.2022.14.127}, author = {Ninik Mudjihartini and Dewi Pratiwi Purba and Fadilah Fadilah and Mohammad Sadikin and Sri Widia A. Jusman} } @article {1849, title = {Leaf Effect of C. Trifolia L. as Nf-B and Tnf-Α Inhibitor Compounds with In Silico Method}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {407-415}, type = {Research Article }, chapter = {407}, abstract = {

Introduction: Infection H. pylori causes inflammation through various pathways to induce proinflammatory cytokines such as IL-1, IL-6, IL-8, and TNF-α. The transcription factor NF-kB is a crucial regulator of the immune response and inflammation and regulates many cellular processes that are important in carcinogenesis, including transformation, proliferation, angiogenesis, and metastasis. Antiinflammatory plant C. trifolia L was shown to inhibit the activity of NF-B and several pro-inflammatory cytokine mediators. This study proved that the active compound from the plant{\textquoteright}s leaves, C. trifolia L has potential as an inhibitor of NF-B and TNF-α. Method: This study used a docking method with a grid box mimicking the bond between the receptor and the inhibitor control complex. Results: The bioactivity of Cayratria trifolia compounds as anti-inflammatory was shown in the inflammation parameters used, namely Interleukin 10 agonist, Interleukin agonist, Interleukin antagonist, Interleukin 6 antagonist, Interleukin 4 antagonist, Interleukin 2 agonist, Interleukin 1 antagonist, Interleukin 1b antagonist, Interleukin 10 antagonist, Interleukin 12 agonist, and Interleukin 1a antagonist. Interleukin 2 agonists showed the highest activity of all compounds. Piceid compounds showed high anti-inflammatory activity with interleukin 10 agonists, interleukin agonists, interleukin 6 antagonists, and interleukin 2 agonists. The compounds stilbenes, piceid, resveratrol, cyclopentadecane, and hentriacontane showed potency higher interleukin-6 inhibition than the other 22 compounds. These five compounds were continued for molecular docking analysis. The low bond energy is correlated with the number of bonds and the variety of interactions. The higher the number of bonds and the type of interaction, the lower the bond energy. The lower the bond energy, the stronger the interaction between the ligand and protein. Conclusion: Based on the prediction of anti-inflammatory bioactivity, five potential compounds were identified, namely cyclopentadecane, resveratrol, stilbenes, piceid, and hentriacontane. The five compounds bind to NFkB on the active site of the binding site with DNA, and this inhibition causes DNA to be unable to restrain NFkB transcription factors, and transcription does not occur. This proves that the active compound from the leaves of the plant C. trifolia L has potential as an inhibitor of NF-κB compounds. Inhibition of 6 compounds on TNF at the TNF receptor proves that the active compound from the leaves of the plant C. trifolia L has potential as a TNF-α inhibitor compound. The active ingredient Piceid exhibits predominant anti-inflammatory potential with lower binding energy and stronger interactions than other complexes.

}, keywords = {C. trifolia L, H. Pylori, in silico, NFkB, TNF-α}, doi = {10.5530/pj.2022.14.115}, author = {Judya Sukmana and Widjiati and Siswandono and I Ketut Sudiana and Hari Basuki Notobroto and Iswinarno Doso Saputro and Yoes Prijatna Dachlan and Endang Joewarini} } @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 {1892, title = {Parathyroid Carcinoma Mimicking Multiple Myeloma: A Tale of Refractory Hypercalcemia}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {863-866}, type = {Research Article }, chapter = {863}, abstract = {

Primary hyperparathyroidism yields various symptoms, including hypercalcemia, pathological fracture, and renal impairment. Parathyroid carcinoma is the rarest cause of primary hyperparathyroidism, accounting for \<1\% of the cases. We reported a case of a 46-year-old male with closed fractures at the humerus and femur. Further findings revealed severe refractory hypercalcemia, renal impairment, anemia, and bone lytic lesion (CRAB). No palpable cervical mass was identified. Surprisingly, the serum protein electrophoresis was normal, and urinary Bence-Jones protein was negative along with normal bone marrow aspiration. Hence, multiple myeloma was unlikely. The intact parathyroid hormone level was very high, along with a suspicious nodule on the left thyroid lobe (TIRADS 4). Total thyroidectomy and total parathyroidectomy were performed. The post-surgical pathological examination confirmed the diagnosis of parathyroid carcinoma. After the surgery, the patient was in stable condition with normal intact parathyroid hormone and serum calcium levels. In this case, primary hyperparathyroidism was caused by parathyroid carcinoma with {\textquotedblleft}CRAB{\textquotedblright} symptoms, mimicking multiple myeloma. Primary hyperparathyroidism should be considered in the patient with refractory hypercalcemia.

}, keywords = {Case report, Hypercalcemia, Multiple myeloma, Parathyroid tumor, Primary hyperparathyroidism}, doi = {10.5530/pj.2022.14.180}, author = {Christian Jonatan and Sony Wibisono} } @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 {1791, title = {Phytochemical Evaluation and Antioxidant Activity of Virginia tobacco Leaves (Nicotiana tabacum L. var virginia) Fractions with DPPH and FTC Methods}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {544-548}, type = {Original Article}, chapter = {544}, abstract = {

Introduction: Virginia tobacco (Nicotiana tabacum var. Virginia) is one of the most extensive varieties of tobacco plants. Nicotiana tabacum var. Virginia leaves known to contain alkaloids, saponins, tannins, phenol, flavonoids, triterpenoids and glycosides. In addition to cigarette raw materials, tobacco is also able to be efficacious as an antibacterial, antifungal and bioinsecticide. Objective: The aim of this study to determine the total phenol and total flavonoids and also antioxidant activity of Virginia tobacco leaves fractions. The fraction with the largest compound content was evaluated further for its antioxidant activity. Methods: Virginia tobacco leaves was fractioned into dichloromethane (DCM), ethyl acetate, butanol and water fractions. Phenol levels were determined with Follin-Ciocalteu reagent using the UV-Vis spectrophotometer method measured at 743.50 nm and gallic acid as a reference compound. Total flavonoid levels were determined with AlCl3 reagent using the UV-Vis spectrophotometer method measured at 434.50 nm and quercetin as a reference compound. Antioxidant activity was evaluated with DPPH and Ferric Thiocyanate (FTC) method and the standard used was quercetin. Results: Total phenol levels in Virginia tobacco leaves of DCM, ethyl acetate, butanol and water fractions respectively were 191.2386 mgGAE/g, 201.2913 mgGAE/g, 180.5714 mgGAE/g, 212.8692 mgGAE/g. Total Flavonoid levels respectively were 6.0927 mgQE/g, 6.9659 mgQE/g, 5.1112 mgQE/g, 8.3346 mgQE/g. Antioxidant of water fraction was evaluated further using DPPH and FTC method with IC50 respectively were 75.9148μg/ml and 67.8972 μg/ml. Conclusion: Overview of total phenol and flavonoid levels fractions and antioxidant can be used as an additional initial reference for Virginia tobacco leaves development as source of medicinal substances.

}, keywords = {Atherosclerosis, Hylocereus polyrhizus, LDL cholesterol levels, Red dragon fruit peel}, doi = {10.5530/pj.2022.14.69}, author = {Kori Yati and Misri Gozan and Mardiastuti and Vivi Anggia and Rini Prastiwi and Mahdi Jufri} } @article {1812, title = {Potential Roles of Purslane (Portulaca oleracea L.) as Antimetabolic Syndrome: A Review}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {710-714}, type = {Review Article}, chapter = {710}, abstract = {

The number of cases of obesity and type 2 diabetes mellitus (T2DM) is part of the metabolic syndrome case. Purslane (Portulaca oleracea L.) is a plant that has been clinically tested and has the potential to prevent and treat metabolic syndrome as well as pathogenic and pathophysiological activities that cause disease. The aim of this study is to discuss and conclude information regarding the activity and use of purslane (P. oleracea) as an antimetabolic. This review article is based on scientific publications found on Google Scholar and PubMed databases using the keywords of {\textquotedblleft}Portulaca obesity{\textquotedblright}, {\textquotedblleft}Portulaca overweight{\textquotedblright}, {\textquotedblleft}Portulaca dyslipidemia{\textquotedblright}, and {\textquotedblleft}Portulaca metabolic syndrome{\textquotedblright}. This plant acts on numerous pathways in the metabolic syndrome such as reduction of lipids, blood sugar, body weight and total cholesterol. Purslane (P. oleracea) can be used as a candidate for a new herbal plant as an anti-metabolic syndrome.

}, keywords = {Body weight, Insulin resistance, Metabolic syndrome, Obesity., Portulaca oleracea}, doi = {10.5530/pj.2022.14.90}, author = {Nur Sofiatul Aini and Arif Nur Muhammad Ansori and Viol Dhea Kharisma and Muhammad Farraz Syadzha and Muhammad Hermawan Widyananda and Ahmad Affan Ali Murtadlo and Rasyadan Taufiq Probojati and Md. Emdad Ullah and Sin War Naw and Vikash Jakhmola and Rahadian Zainul} } @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 {1767, title = {Screening of Secondary Metabolites and Antioxidant Activity of Wild Edible Termite Mushroom}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {301-307}, type = {Original Article}, chapter = {301}, abstract = {

Wild edible mushrooms produce a variety of bioactive compounds that are known to have antioxidant properties. Natural antioxidants can protect against oxidative induced free radicals without any side effects. Thus, they are consumed by people for food and nutraceutical values. The purpose of this study was to evaluate the phytochemicals and antioxidant activity of three wild edible termite mushrooms (Termitomyces albuminosus, T. eurhizus and T. robustus). Different phytochemicals were screened in the 50\% ethanol, methanol and water extracts of three termite mushrooms. Total phenolic and flavonoid contents were determined by Folin-Ciocalteau and aluminium chloride method respectively. The antioxidant activity of three termite mushrooms was evaluated by DPPH assay. Qualitative screening of phytochemicals has revealed that alkaloid, steroid, fatty acid, flavonoid, saponin, tannin, carbohydrate and protein are found in the 50\% ethanol, methanol and water extracts of three species of termite mushroom. A high amount of total phenolic and flavonoid content was found in the 50\% ethanol extract of T. albuminosus, T. eurhizus and T. robustus (TPC: 50.28, 54.56 and 57.63 mg GAE/g extract; TFC: 16.30, 18.43 and 18.80 mg QE/g extract respectively). Due to high phenolic and flavonoid content, 50\% ethanol extract of three termite mushrooms has shown high antioxidant activity (i.e., lowest IC50: 710.00 - 714.05 μg/ml). These termite mushrooms have antioxidant properties due to the presence of bioactive secondary metabolites that can potentially be used as a source of natural antioxidants in the form of food and nutraceutical.

}, keywords = {DPPH assay, Flavonoid, phenolic, Phytochemical, Termite mushroom}, doi = {10.5530/pj.2022.14.38}, author = {Anita Kumari Tharu and Mukti Ram Paudel and Ananda Prakash Joshi and Laxman Bhandari and Hari Prasad Aryal} } @article {1800, title = {Utilization of Secondary Metabolites in Algae Kappaphycus alvarezii as a Breast Cancer Drug with a Computational Method}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {536-543}, type = {Original Article}, chapter = {536}, abstract = {

Breast cancer is one of the worst diseases that affect female people. Long-term treatment with therapy or surgery has a detrimental impact on the patient. The algae Kappaphycus alvarezii has gotten a lot of interest as a breast cancer medication because it contains chemicals that are expected to be anti-cancer. The objectives of this paper were to see how secondary metabolites in algae interact with the Nuclear Factor- kappaB protein kinase in breast cancer. The ligands and proteins were obtained from the PubChem and PDB websites, respectively. Swiss ADME was then used to assess the Pharmacokinetics and Drug likeness Properties. The last stage involved using molecular docking with PyRx and molecular dynamics to identify the interaction and visualization between the ligand and the target protein. The findings of the test revealed that the maraniol chemical had a superior binding capacity with NF kB protein kinase because it has a chromone group that controls transport efficiently in preventing breast cancer proliferation.

}, keywords = {Breast cancer, K. alvarezii, Molecular Docking., NF kB protein kinase}, doi = {10.5530/pj.2022.14.68}, author = {AF Dibha and S Wahyuningsih and ANM Ansori and VD Kharisma and MH Widyananda and AA Parikesit and MT Sibero and RT Probojati and AAA Murtadlo and JP Trinugroho and TH Sucipto and DDR Turista and I Rosadi and ME Ullah and V Jakhmola and R Zainul} } @article {1334, title = {Antidepressant-Like Behavioral and Spatial Memory Effects in Peruvian Red Maca (Lepidium meyenii)-Treated Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {81-88}, type = {Original Article}, chapter = {81}, abstract = {

Introduction: Lepidium meyenii, known with the vernacular name of {\textquotedblleft}Maca{\textquotedblright}, is a Brassicaceae family that has been widely used by Peruvian traditional medicine in cases of sexual dysfunction, memory loss, and several other diseases and pathologies. Objetive: The aim of the study was to test the potential effects of aqueous extract of Red Maca (AQ-RM) on antidepressant-like behavioral in male rats and spatial memory in ovariectomized (OVX) rats. Methods: Forced swimming test was used to examine the potential antidepressant AQ-RM activity in male rats. Fluoxetine and amitryptiline were included as reference drugs. Morris Water Maze test was employed to examine the effect of AQ-RM on spatial memory in ovariectomized (OVX) rats. Such effects were compared to exogenous estradiol administration. The potential role of oxidative stress on spatial memory loss was assessed by measuring malondialdehyde (MDA) levels in rats brain homogenates. Results: AQ-RM enhances swimming and climbing activities while reducing the time of immobility in male rats. Meanwhile, it prevents the decrease in the time spent in the target quadrant and displays higher values in the number of crossings in OVX-rats as compared to OVX-control rats. MDA levels in brain homogenates were decreased in OVX-rats receiving AQ-RM. Conclusion: Oral administration of AQ-RM has anti-depressive application in male rats; and increases the ability of learning and memory in OVX rats.

}, keywords = {Antidepressant activity, Forced swimming test, Lepidium meyenii, Morris water maze test, Red Maca, Spatial memory}, doi = {10.5530/pj.2021.13.12}, author = {Roberto O Yba{\~n}ez-Julca and Ivan M Quispe-D{\'\i}az and Daniel Asunci{\'o}n-Alvarez and Kelly S{\'a}nchez-Mu{\~n}oz and Albert Vargas-Go{\~n}as and Jazminy Morote-Guzman and Ronald Yaro-Marcelo and Edmundo A Venegas-Casanova and Rafael Jara-Aguilar and Pedro Buc Calderon and Julio Benites} } @article {1354, title = {Antimicrobial Effect of Different Types of Honey on Selected ATCC Bacterial Strains}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {217-225}, type = {Research Article}, chapter = {217}, abstract = {

Honey is a complex sweet highly viscous liquid and is composed of various ingredients such as sugar, proteins, minerals, and polyphenolic compounds. Honey is used in traditional medicine systems for centuries because of its ability to inhibit the pathogenesis of various diseases through modulating various biological activities. In this study, antimicrobial potential of different types of honey was tested against selected pathogenic bacterial strains through agar well diffusion method. Four types of honey were used in the present investigation, and the potential antimicrobial activities of these varieties were further compared with that of antibiotics commonly used against targeted microbial strains. Among all of the four tested honey, three types were classified as blossom honey, being Talha (Acacia sp) honey (TH), Zahoor (mixed flower) honey (ZH), and Manuka (Leptospermum based honey) honey (MH). Both gram positive and gram negative bacterial species were used for this investigation. The pathogenic gram-positive bacterial strains includedEscherichia coli ATCC 29213, Enterococcus faecalis ATCC 29212 and methicillin-resistant Staphylococcus (MRSA) ATCC 43300. Three gram negative bacteria like Escherichia coli ATCC 25922, Klebsiella pneumonia ATCC 700603 and Pseudomonas aeruginosa ATCC 27853 were also used to confirm the antimicrobial activities. As reflected from our study, we found that three varieties of honey including TH, ZH, and MH (with different UMF +20, +16, +5) displayed a broad spectrum antibacterial activity against all tested microbial strains. However, all strains showed a high frequency of resistance to BF honey. Gram-positive (G+) bacteria were found to be more sensitive to all tested honey types except (BF) as indicated by significantly higher zone of inhibition (ZOI) values than those of gram-negative (G-) bacteria. As a conclusion, this study suggests that antimicrobial potential of honey types might be helpful in order to treat the pathogenic microorganisms threatening the public health and changing antibiotics into last-resort drugs.

}, keywords = {Enterococcus faecalis, Staphylococcus aureus, Talha honey, Zahoor honey and Manuka honey}, doi = {10.5530/pj.2021.13.31}, author = {Aseel Aljaghwani and Khaled S Allemailem and Lujain F Aljaghwani and Faris Alrumaihi and Rejo Jacob Joseph and Amjad Ali Khan and Mohammad aljaghwani and Arshad H Rahmani and Ahmad Almatroudi} } @article {1389, title = {Antioxidant Capacity and Protective Effect of Aqueous and Hydroalcoholic Extracts of Senecio rhizomatus Rusby "Llancahuasi" on Erythrocytes Subjected to Oxidative Stress}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {516-527}, type = {Research Article}, chapter = {516}, abstract = {

Objective. To evaluate the antioxidant capacity and protective effect of aqueous and hydroalcoholic extracts of Senecio rhizomatus Rusby in rat erythrocytes subjected to oxidative stress with hydrogen peroxide (H2O2). Methodology. This study used an experimental design. The extracts were obtained through maceration with 96{\textdegree} ethanol (SeR96), 70{\textdegree} ethanol (SeR70), 50{\textdegree} ethanol (SeR50) and through infused water (SeRAc). Secondary metabolites were identified through colorimetric reactions and precipitation. In each extract, we could determine the capacity to eliminate 2,2-diphenyl-1-picrylhydrazyl radical (DPPH), the reduction of ferric ion and the total polyphenol content. In addition, the activity on the plasma membrane redox system (PMRS) was evaluated in each extract. The protection against oxidative stress in erythrocytes was evaluated by determining the content of reduced glutathione (GSH) and malondialdehyde (MDA). Results. Alkaloids, flavonoids, phenolic compounds, sesquiterpene lactones and sugars were identified in all the extracts. The total polyphenols content showed a correlation with the reduction of ferric ion (r=0.885) and with DPPH radicals elimination (r = -0.899), where the one with the highest antioxidant capacity was SeR50. Thus, the SeR50 (all concentrations) and SeR70 (100 μg/mL concentration) significantly increased the PMRS activity compared to the control group. After inducing oxidative stress in erythrocytes, all the extracts maintained the GSH level and inhibited MDA formation significantly compared to the H2O2 group. Conclusion. The antioxidant capacity of hydroalcoholic extracts (96{\textdegree}, 70{\textdegree}, 50{\textdegree}) and aqueous infusion of Senecio rhizomatus Rusby is related to the content of polyphenols. They increase the plasma membrane redox system activity in rat erythrocytes and protect them from oxidative stress induced with H2O2, showing an increase in the concentration of reduced glutathione and a decrease in malondialdehyde.

}, keywords = {Antioxidant, Lipoperoxidation, Plasma membrane redox system, Reactive Oxygen Species, Reduced glutathione}, doi = {10.5530/pj.2021.13.65}, author = {Justil-Guerrero Hugo Jes{\'u}s and Ch{\'a}vez-Flores Juana Elvira and C{\'a}rdenas-Orihuela Robert Armando and Ramos- Jaco Antonio Guillermo and {\~N}a{\~n}ez-del-Pino Daniel and V{\'a}squez-Quispe {\'A}ngel David and Rojas-Cardenas Nathalie Felicita and Fern{\'a}ndez-Flores N{\'e}lber} } @article {1660, title = {Antioxidant Capacity of Chuquiraga Spinosa Less. "Huamanpinta" and Prevention of Carrageenan-Induced Inflammation in Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1287-1296}, type = {Research Article}, chapter = {1287}, abstract = {

Objective: To evaluate the antioxidant capacity of Chuquiraga spinosa extracts and prevention of carrageenan-induced inflammation in mice. Methodology: Experimental design: plant species, erythrocytes and male BALB C53 mice, were considered as biological material. Antioxidant capacity was evaluated in 50\%, 70\%, 96\% and aqueous ethanolic extracts by 2,2-Diphenyl-1-Picrylhydrazyl reduction, malondialdehyde inhibition in oxidized erythrocytes with H2O2 and correlating with polyphenol content equivalent to gallic acid/gram dry extract. Inflammation was evaluated by inoculating carrageenan 2\% in "subcutaneous air bag" of mice: 1) White, 2) carrageenan, 3) dexamethasone 2 mg/kg, 4-6) ethanolic extract 70\% doses 100, 250 and 500 mg/kg respectively; determining nitric oxide, malondialdehyde, total proteins, albumin, leukocytes in exudate and histological changes. Results: Alkaloids, flavonoids, terpenes, phenolic compounds, tannins, carbohydrates, triterpenes, steroids and sesquiterpene lactones were identified; aqueous extract presented greater reduction of 2,2-Diphenyl-1-Picrylhydrazyl (CI50 = 58.99 μg/mL), ethanolic extract 70\% presented greater inhibition of malondialdehyde in erythrocytes (CI50 = 16.44 nm/mL); It was observed that the higher the amount of polyphenols, the greater the reduction of 2,2-Diphenyl-1-Picrylhydrazyl (r=-0.909) and the greater the inhibition of malondialdehyde (r=-0.781). With 500 mg/kg of 70\% ethanolic extract there was greater anti-inflammatory effect inhibiting malondialdehyde, nitric oxide, albumin, total proteins and leukocytes in 55.55\%, 81.92\%, 41.20\%, 31.51\% and 32.45\% (p\<0.01) respectively and less infiltration of leukocytes and lymphocytes in air sac membrane. Conclusion: The extracts of aerial parts of Chuquiraga spinosa showed antioxidant capacity correlated to polyphenol content. The 70\% ethanolic extract prevented inflammation in mice in a dosedependent manner.

}, keywords = {Antioxidant, Ethanolic extract, Leukocytes, Lipoperoxidation, Nitric oxide, Oxidative stress}, doi = {10.5530/pj.2021.13.163}, author = {Hugo Jes{\'u}s Justil-Guerrero and Jorge Luis Arroyo-Acevedo and Juan Pedro Rojas-Armas and Miriam Palomino- Pacheco and Magaly Villena-Tejada and Wilmer Atilio Segura V{\'\i}lchez} } @article {1723, title = {Anxiolytic-like Effect of Luma chequen Essential Oil: A Pilot Study}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1607-1613}, type = {Original Article}, chapter = {1607}, abstract = {

Introduction: Essential oils are complex substances used widely extended in the form of aromatherapy or phytotherapy, some of them as agents to relieve anxiety and stress. In this sense this study was conducted to examine the anxiolytic-like effect of Luma chequen essential oil. Methods: The essential oil was extracted by steam distillation and the chemical composition was investigated by Gas chromatography with flame-ionization detection (GC-FID) and Gas chromatography-mass spectrometry (GC{\textendash}MS). Moreover, a randomized, double blind, placebo-controlled trial was conducted, where 48 participants were divided into two groups, comprising a control group (CG) treated with placebo, and an experimental group (EG) treated with aromatherapy based on Luma chequen essential oil. The anxiety index was evaluated by State-Trait Anxiety Inventory (STAI). Measures were taken at two times: pretest and posttest. Results: The chemical analysis showed that α-pinene was the main component (56.5\%). State and Trait anxiety scores showed a decrease in posttest study phase in comparison with pretest in experimental group compared to placebo (p\<0.005 for state anxiety and p\<0.05 for trait anxiety). Cohen{\textquoteleft}s d score was 0.84 in State anxiety, while it was 0.52 for Trait anxiety. Percentages of change showed reductions of anxiety variable ranging between 14.94\% for State anxiety and 13.60\% for Trait anxiety. Conclusions: These results suggest that aromatherapy based on essential oil of Luma chequen was moderately effective in improving anxiety.

}, keywords = {Anxiety, Essential oil, Luma chequeen.}, doi = {10.5530/pj.2021.13.207}, author = {Paul Alan Arkin Alvarado-Garc{\'\i}a and Maril{\'u} Roxana Soto-V{\'a}squez and Luis Enrique Rosales-Cerquin and Demetrio Rafael Jara-Aguilar and Santiago M. Benites} } @article {1337, title = {The Effect of Giving Red-fleshed Watermelon Juice (Citrullus lanatus (Thunb.)) on Pregnant White Mice (Mus Musculus) Exposed by Monosodium Glutamate (MSG) Orally on the Number and Morphology of Fetus}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {97-102}, type = {Original Article}, chapter = {97}, abstract = {

Introduction: Infertility can occur due to the presence of free radicals. One of the most popular of free radical is monosodium glutamate. Free radicals from monosodium glutamate can be prevented by antioxidant compounds. Red-fleshed-fleshed watermelon is a fruit that contains antioxidant compound such as lycopene. Aim: This research was conducted to see the effect of red-fleshed-fleshed watermelon juice on the fetus including number, morphology, visual abnormalities and body weight of pregnant white mice exposed to monosodium glutamate solution orally. Total of 25 female white mice aged around 2-3 months were used as test animals. Methods: Pregnant white mice were divided into 5 test groups. Group I and II served as negative controls (whithout treatment) and positive controls (exposed to monosodium glutamate solution orally at dose of 1g/kgBW). Group III was given a solution of monosodium glutamate orally at dose of 1 g/KgBW added red-fleshed-fleshed watermelon juice at dose of 1.4 g/kgBW. Group IV was given solution of monosodium glutamate orally at dose of 1 g/KgBW added red-fleshed-fleshed watermelon juice at dose of 4.2 g/kgBW. The research data were processed using the one-way ANNOVA test. Results: The result showed that mice body weight, fetal number and morphology (body weight, body length, tail length, and head diameter) did not significantly influence (p\>0.05). However, it significantly affected the weight gain of mice during pregnancy. However, it significantly affected the weight gain of mice during pregnancy day 6 to day 17 of pregnancy (p\<0.05) and found abnormalities in the fetus such as low birth weight (LBW) and haemorrhage in group II and III. Conclusion: It can be concluded that watermelon juice at dose of 2.8 g/kgBW and 4.2 g/kgBW are effective in ward offfree radicals from monosodium glutamate orally at dose of 1 g/kgBW.

}, keywords = {Fetus, Infertility, Lycopene, Monosodium glutamate, Red-fleshed watermelon}, doi = {10.5530/pj.2021.13.14}, author = {Dwisari Dillasamola and Fitri Rachmaini and Dian Ayu Juwita and Rini Haryati} } @article {1399, title = {Evaluation of Antioxidant Activity of Some Medicinal Plants and their Combination}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {596-599}, type = {Research Article}, chapter = {596}, abstract = {

Introduction: Oxidative Stress leads to several complications within the human body. It is the reason behind the generation of several diseases. Free radicals if generated in excess amount can damage the body to a great extent. Finding newer and potent medicinal plants that can fight oxidative stress can be useful in combating the harmful effects of free radicals. Methods: In the current study ethanolic extract of Ocimum kilimandscharicum, Thymus serpyllum, Spilanthes acmella and their combination in equal ratio were used for their ability to counter oxidative stress. The plants were collected from the district of Pithoragarh, Uttarakhand and extracted by soxhlet{\textquoteright}s apparataus using absolute ethanol (99.9\%). The extracts were then dried and used for the study. Result: It was seen that highest absorbance was shown by ascorbic acid at the lowest as well as the highest concentration in the reducing power assay. Also, the combination of the extracts showed the highest absorbance among all the extracts at both the lowest and highest concentration. Conclusion: A higher absorbance indicates a better antioxidant potential. The best effect was shown by the combined extract among all the extracts.

}, keywords = {Flavonoids, Oxidative stress, Phenols, Reducing power}, doi = {10.5530/pj.2021.13.75}, author = {Tanuj Joshi and Vijay Juyal} } @article {1620, title = {Evaluation of Xanthine Oxidase Inhibitory and Antioxidant Activities of Three Organs of Idat (Cratoxylum glaucum Korth.) and Correlation with Phytochemical Cont}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {971-976}, type = {Research Article}, chapter = {971}, abstract = {

Introduction: Idat (Cratoxylum glaucum Korth.), belonging to the genus Cratoxylum, is known to contain xanthone, quinone, flavonoids, and other phenolic compounds. Objectives: to analyze total phenolic, flavonoid, antioxidant activity, and inhibitory xanthine oxidase activities of leaves, stem, and cortex of idat. Methods: Extraction of leaves, stem, and cortex of idat was carried out by reflux using n-hexane, ethyl acetate, and ethanol as a solvent. Antioxidant activity was tested by the DPPH method and calculated to get the antioxidant activity index (AAI). Determination of total phenolic and flavonoid levels by ultraviolet-visible spectrophotometry. Results: Spectrophotometers measured the inhibitory activity on xanthine oxidase in 96-well plates with allopurinol as standard. Total phenolic and flavonoid content from C. glaucum extracts varied from 6.62 to 48.77 g GAE/g extract and 1.54 - 25.96 g QE/100 g extract, respectively. The ethanol extracts of leaves, stem, and cortex were very strong antioxidant activity with Antioxidant Activity Index (AAI) values 3.89; 4.55; 10.50, meanwhile AAI of ascorbic acid and quercetin 9.46 and 14.81 respectively. The n-hexane of stem extract had a strong xanthine oxidase inhibitory activity with the IC50 was 36.64 μg/ml, while allopurinol was 5.02 μg/ml. Conclusions: Total phenolic content contributed to antioxidant activity. Phenolic compounds in leaves extracts led to the xanthine oxidase inhibitory and antioxidant activities. The extract of C. glaucum was active as an antioxidant and potentially an inhibitor of xanthine oxidase agents.

}, keywords = {Antioxidant, Cratoxylum glaucum, Xanthine oxidase inhibitory}, doi = {10.5530/pj.2021.13.125}, author = {Dadang Juanda and Irda Fidrianny and Komar Ruslan Wirasutisna and Muhamad Insanu} } @article {1431, title = {Inotropes in Chronic Beta-Blocker Therapy}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {828-834}, type = {Review Article}, chapter = {828}, abstract = {

The increasing rate of cardiovascular disorders contributes to rising hospitalized patients receive chronic oral beta-blocker therapy. Beta-blockers remain one of the fundamental therapy for chronic heart failure. Still, their role in decompensated heart failure and severe sepsis during hospitalization is often debated and inconsistent in clinical practice. In recent years, evidence of the efficacy and clinical outcomes of beta-blockers in acute heart failure (AHF) have accumulated. Clinical research indicates that chronic beta-blockade withdrawals should be prevented, or as soon as hemodynamic stabilization and euvolemic condition are reached, it should be reinstituted. As a subset of AHF patients with low cardiac output required inotropes, the choice of proper agent is fundamental. Different inotropic agents such as inhibitors of the phosphodiesterase, levosimendan, and dobutamine also their associations with beta-blockers are discussed.

}, keywords = {Beta-blocker, Decompensated heart failure, Inotropes, Severe sepsis}, doi = {10.5530/pj.2021.13.105}, author = {Mochamad Yusuf Alsagaff and Melly Susanti and Mochammad Thaha and Christian Jonatan} } @article {1356, title = {Learning and Memory Enhancing Activity of Polyherbal Formulation on Streptozotocin Induced Memory Impairment in Rats via Reducing Mitochondria{\textendash}Targeted Cytochrome}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {230-240}, type = {Research Article}, chapter = {230}, abstract = {

Introduction: Neurodegenerative diseases and/or brain injury may occur due to mild to severe memory disorders in which Alzheimer{\textquoteright}s disease (AD) is defined as degradation of neurons and there is no effective therapy or cure for the disease. The intention behind this study was to determine memory enhancing effect of an Ayurvedic polyherbal formulation (PHF) in Streptozotocin-induced memory deficit experimental animal models. Methods: Polyherbal formulation (PHF) was a suspension of three plant extracts i.e. Alpinia galanga, Glycerrhiza glabra and Convolvulus pluricaulis along with other excipients. Different behavioral animal models like Social recognition test (SRT), Morris water maze (MWM) test, Pole climbing test (PCT) and Elevated plus maze (EPM) test were used to evaluate efficacy of Polyherbal formulation (PHF) in learning and memory process of animals. Gene expression was performed by RT-PCR and western blot. Results: Results indicated that time of social recognition during trial 2 (SIT2) was reduced significantly (P\<0.01) due to PHF administration. In MWM test, treatment with PHF significantly (P\<0.01) reduced [F (4, 20) = 6.9] latency to reach hidden platform from session 3. Similarly, PHF was also found effective in pole climbing test and EPM test. RT-PCR results showed p53 regulates the Bcl-2 family proteins its expression in the given experiment was appreciably reduced in PHF (200mg/kg). NR1, NR2B and GAP-43 proteins leads to reduction of brain cell damage. Conclusion: Thus, PHF may be an effective formulation for learning and memory process against STZ-induced memory impairment.

}, keywords = {Alpinia galanga, Convolvulus pluricaulis, Elevated Plus Maze, Glycerrhiza glabra, Pole climbing test, Social recognition test}, doi = {10.5530/pj.2021.13.33}, author = {Deepa Shukla and Sajal Srivastava and Talha Jawaid} } @article {1359, title = {Medicinal Value of Three Agricultural Weed Species of the Asteraceae Family: A Review}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {264-277}, type = {Review Article}, chapter = {264}, abstract = {

Ageratum conyzoides L., Tridax procumbens L. and Bidens pilosa L. are well known plant species of the Asteraceae family that are considered weeds in intensive agriculture. These weeds are traditionally known to have medicinal properties and have been used for therapeutic treatments. However, it is only the lack of proper knowledge, awareness and screening that have limited their use in pharmaceutical sectors. This review attempts to consolidate the traditional, phytochemical and pharmacological studies that have been carried out on Ageratum conyzoides L., Tridax procumbens L. and Bidens pilosa L., which we note are widely spread throughout the world. This study was conducted through a coherent search on Ageratum conyzoides L., Tridax procumbens L. and Bidens pilosa L. with respect to traditional uses, phytochemical and pharmacological studies that have been performed on these three agricultural weeds all over the world. An exploration of reported descriptions of the potential medical importance of three agricultural weed species (A. conyzoides, T. procumbens and B. pilosa) has been presented. The present review would encourage further clinical investigations into these three plants and their extracts to more closely define the range of uses of these herbs for clinical applications. This, in turn, would give a clear understanding whether these weed species might be targeted to be conserved in a sustainable manner rather than eradicated.

}, keywords = {Ageratum conyzoides, Bidens pilosa, Pharmacological, Phytochemical, Traditional use, Tridax procumbens}, doi = {10.5530/pj.2021.13.36}, author = {Mithila Jayasundera and Singarayer Florentine and Kushan U Tennakoon and Bhagirath Singh Chauhan} } @article {1727, title = {Molecular Study of Acalypha indica to Leptin, Alpha Glucosidase, and its Antihyperglycemic Effect on Alpha Glucosidase}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1639-1647}, type = {Research Article}, chapter = {1639}, abstract = {

Introduction: The purpose of this study is to find potential inhibitors of leptin as a proinflammatory adipokine and alpha glucosidase as an enzyme that mediate hyperglycaemia; to alter the chronic complications of obesity from herbal Acalypha indica (Ai). This study was conducted using in silico molecular docking to evaluate the Ai compounds interaction with leptin and alpha glucosidase. The in vitro assay to alpha glucosidase was done to explore antihyperglycemic effect of Ai, as hyperglycaemia is the key process of chronic complication of obesity. Material and Methods: Protein target were leptin and alpha glucosidase; compounds from Ai plant were repundusinic, mauritanin, hesperetin, acaindinin, and glucogalin in pdb format. Molecular docking using autodock vinna. In vitro assay of Ai antihyperglycemic activity was done to alpha glucosidase and was define as IC50 level. Result: The results from the docking analysis demonstrated that compounds from Ai roots contain antihyperglycemic-antiobesity activity which acted by inhibiting leptin and alpha glucosidase receptors. Repundusininc and mauritanin compounds contain hydrogen bond with the greatest leptin enhancer activity on Ser9, Thr35, Glu8, Ser9, Thr25, Gln111, Lys211, Leu7 for repundisinic and Glu8, Thr25, Gly112 and Leu7 for mauritanin. Hesperetin, acaindinin and glucogallin were the most identical compounds with similar affinity binding value to alpha glucosidase. Ai roots was already proven as anti-hyperglycemic-antiobesity which was further confirmed by in vitro assay to alpha glucosidase (IC50 19,429 μg/ml.). Conclusion: The results demonstrated that Ai have anti hyperglycaemic-antiobesity effects and was found to be potentially as antihyperglycemic by in vitro assay to alpha glucosidase.

}, keywords = {Acalypha indica, Alpha glucosidase., Antiobesity, Leptin}, doi = {10.5530/pj.2021.13.211}, author = {Rani Wardani Hakim and Fadilah Fadilah and Tri Juli Edi Tarigan and Sri Widia A Jusman and Erni H Purwaningsih} } @article {1418, title = {Nephro- and hepatoprotective effect of Rosmarinus officinalis against damage induced with antiTB drugs using a chronic model}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {722-729}, type = {Original Article}, chapter = {722}, abstract = {

Nephro- and hepatoprotector effect of MeOH extract from R. officinalis against the liver and kidney damage caused by the mixture of RIF:INH:PZA, using a chronic in vivo model are described. MeOH extract (EMRO) was prepared by maceration process and was administered by oral via during 91 days in male Balb/C mice with RIF:INH:PZA-induced renal/liver damage, using silymarin (SIL) as a positive control. EMRO (250 mg/kg) favoured body weight gain respect to the antiTB group, this gain was better than that shown by the SIL. The AST and ALT values of the group that received the EMRO extract and SIL were similar to that the control group and low compared to the group antiTB with liver damage. In addition, the GPx, CAT and POx values of the group treated with the EMRO were similar to that the control group. In the liver histological analysis, no significant alteration was observed; however, a severe nephritis was observed in anti-TB group (II) and this effect was less in groups III (antiTB/SIL) and IV (antiTB/EMRO). MeOH extract enhances body weight gain and primarily protects the kidney and liver from damage caused by the antiTB drug mixture when was administered for 91 days.

}, keywords = {Antitubercular drug, Hepatoprotection, Methanolic extract, Nephroprotective effect, Rosmarinus officinalis}, doi = {10.5530/pj.2021.13.92}, author = {Siordia-Reyes Georgina A and Cornejo-Garrido Jorge and Jim{\'e}nez-Arellanes M. Adelina} } @article {1641, title = {Phytochemical and Biological Characterization of Aqueous and Ethanolic Extracts of Parthenium hysterophorus}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1122-1133}, type = {Original Article}, chapter = {1122}, abstract = {

Introduction: Parthenium hysterophorus is a plant used in traditional medicine to treat health issues and which could be a source of phytochemicals with possible antioxidant activity without causing cytotoxic effects. Hence, this work was designed to evaluate its phytochemical profile, cytotoxicity, and antioxidant activity. Methods: The aqueous (AE) and ethanolic (EE) extracts of P. hysterophorus flowers were obtained by decoction and ultrasound, respectively. Their phytochemical composition was determined by colorimetric tests and RP-HPLC-MS analysis. Their cytotoxic activity was tested by a hemolysis assay. The antioxidant activity was evaluated with the Trolox equivalent antioxidant capacity (TEAC), 2,2-diphenyl-1- picrylhydrazyl (DPPH), and hydroxyl radical (-OH) scavenging assays. In addition, the effect of the extracts on the activity of the antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT) from human erythrocytes, was evaluated. Results: The phytochemical screening of the AE and EE by colorimetric test showed the presence of flavonoids, steroids, triterpenes, saponins, coumarins, sesquiterpene lactones, tannins, and carbohydrates. In addition, the RP-HPLC-MS analysis identified some phenolic compounds such as flavonols, methoxyflavonols, flavones, methoxyflavones, and hydroxycinnamic acids. The hemolysis assay showed non-cytotoxic activity by AE, but EE exhibited a hemolytic effect. Furthermore, the AE and EE showed significant antioxidant activity to inhibit radicals in the TEAC, DPPH and -OH scavenging assays. Moreover, the SOD activity only showed a significant increase by AE. However, the two crude extracts increased the CAT activity, at the highest concentrations. Conclusion: P. hysterophorus has phytochemicals with antioxidant activity to inhibit radicals and increase the activity of antioxidant enzymes in vitro.

}, keywords = {antioxidant activity, Cytotoxicity, Parthenium hysterophorus, Phytochemicals}, doi = {10.5530/pj.2021.13.145}, author = {MA Alfaro Jim{\'e}nez and A Zugasti Cruz and SY Silva Belmares and JA Ascacio Vald{\'e}s and CA Sierra Rivera} } @article {1669, title = {Phytochemical Composition and Antibacterial Activities of Syzygium polyanthum Methanolic Leaves Extract}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1355-1358}, type = {Original Article}, chapter = {1355}, abstract = {

Background: Since a long time ago, Syzygium polyanthum has become traditional herb for health, and thus many studies done to confirm the medical effectiveness. Objectives: This present study was conducted to evaluate phytochemical compounds and antibacterial activities of methanolic extract of S. polyanthum leaves. Materials and Methods: In the present study, standard methods of determination were used to determine the phytochemical compounds of S. polyanthum. The methanol extract of S. polyanthum leaves were subjected for antimicrobial activity. Antibacterial activity was evaluated against five bacterial strains by determining minimum inhibitory concentration (MIC) and zone of inhibition. Diameters of the zone of inhibition were compared with standard antibiotics. Results: Phytochemical analyses qualitatively reveal the presence of alkaloids, saponin, terpenoids and steroid. The extract was found to exert antibacterial activity against four tested bacteria which are S. aureus, S. pyogenes, MRSA and K. pneumoniae except for E. coli. The zones of inhibition shown by the disc diffusion method for S. aureus were between 8.6 to14.0 mm, S. pyogenes were between 8.4 to 12.0 mm, MRSA was between 10.0 to 13.2 mm and K. pneumoniae were between 8.0 to 10.6 mm. Meanwhile, there was no zone of inhibition was observed for E. coli. The MIC was determined ranging from 6.25 to 12.5 mg/ml against all the tested bacteria. The highest value of MIC showed by S. aureus, S. pyogenes, MRSA and K. pneumoniae which is 6.25 mg/mL. Conclusion: The tested leaves extract showed promising antibacterial activity against both Gram positive and Gram-negative bacteria. Phytochemical screening revealed the presence of alkaloids, saponin, terpenoids and steroid in methanolic leaves extract qualitatively and these compounds could be responsible for antibacterial properties of leaves extract of S. polyanthum.

}, keywords = {Syzygium polyanthum; Phytochemical; Antibacterial}, doi = {10.5530/pj.2021.13.171}, author = {Noor Zarina Abd Wahab and Nur Saidatul Aqilah Ja{\textquoteright}afar} } @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 {1631, title = {A Review on Antioxidant and Antidiabetic Activities of Nephelium Lappaceum L.}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {1053-1057}, type = {Review Article}, chapter = {1053}, abstract = {

Introduction: Diabetes mellitus is a chronic disease that occurs in the majority of people worldwide. The number of cases in many countries has been increasing year by year. In Malaysia, the statistics show that the number of diabetic case in 2019 was 3.6 million and expected to increase in 2025 by 7 million. This disease can develop as a result of oxidative stress production in the body. Nephelium lappaceum was claimed traditionally being used to treat diabetes mellitus. This research is conducted to review the available literature regarding the antioxidant and antidiabetic activities of Nephelium lappaceum extracts and constituent that contributes to this activity. Methods: The studies included in this review have been selected using several databases including Google Scholar, Wiley Online Library, Science Direct and Pubmed. The keywords used in database search were {\textquotedblleft}Nephelium lappaceum{\textquotedblright}, {\textquotedblleft}antioxidant{\textquotedblright} and {\textquotedblleft}antidiabetic{\textquotedblright} and covered the period from 2007 onwards. Results: This review revealed that Nephelium lappaceum extracts have good antioxidant and antidiabetic activities when tested using various methods. These activities are due to the presence of several phytoconstituents in the extract. Conclusions: In conclusion, Nephelium lappaceum possess antioxidant and antidiabetic activities. It has the potential to be developed as an antidiabetic and antioxidant agent which can be used to treat various oxidative stress-related diseases, including diabetes mellitus.

}, keywords = {Antidiabetic, Antioxidant, Diabetes mellitus, Nephelium lappaceum L., Phytoconstituents, Rambutan}, doi = {10.5530/pj.2021.13.136}, author = {Wan Nor Iffah Husna Wan Mustaffa and Wan Hafizah W. Jusof} } @article {1400, title = {Role of Spices in Offering Natural Immunity to Fight Various Diseases}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {600-613}, type = {Review Article}, chapter = {600}, abstract = {

Adequate nutrition intake is one of main factors to strengthen immunity. Traditional and cultural practices of food consumption involve use of several spices in limited quantities as part of food. Spices have offered versatile biological effects due to presence of valuable biochemicals. The aim of the present paper is to review published scientific evidence on potential role of spices in offering innate and adaptive immunity to human body. It has been demonstrated that, turmeric, one of the widely used spices, acts as an anti-viral agent through inhibition of viral entry into cells, suppression of viral replication and modulation of cytokines. A field study revealed that nations with higher consumption of spices have shown lesser COVID-19 cases and higher recovery rates. Further, spices also have shown to possess antioxidant activity superior or equivalent to ascorbic acid and are known to regulate inflammation processes. Evidence generated from the published literature is compelling to arrive at a conclusion that consumption of spices might improve immunity there by offering protection against various diseases including COVID-19. It is also noted that there are lesser number of human clinical trials in this area which warrants immediate attention to provide scientific evidence to immunity offered by spices.

}, keywords = {COVID-19, Diet, Immunity, Nutrition, Spices}, doi = {10.5530/pj.2021.13.76}, author = {T Sudhakar Johnson and D. B. Anantha Narayana} } @article {1133, title = {Anti-arthritic Property of Sahacharadi Kashayam Against Freund{\textquoteright}s Complete}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May2020}, pages = {459-464}, type = {Original Article}, chapter = {459}, abstract = {

Introduction: The available modern molecular drugs for the therapy of Rheumatoid arthritis are beset with several side effects and alternative drugs are urgently needed. The present investigation was performed to evaluate the anti-arthritic activity of Sahacharadi Kashayam (SK), an Ayurvedic formulation, against Freund{\textquoteright}s complete adjuvant (CFA) - induced arthritis in rats. Methods: In this experimental trial, SK was administered at doses of 0.5, 1.0 and 1.5 ml/kg body weight orally to adjuvant (CFA) induced arthritic rats. The anti-arthritic activity was evaluated by using paw volume, haematological parameters and arthritic biomarkers. The efficacy of the Kashayam was compared with the standard Leflunomide (10 mg/kg) drug. Results: Significant reduction in paw volume and thickness by SK (0.5 ml dose) has been found and there was considerably improvement in haematological parameters and arthritic markers in CFA rats till 14 days. After 14th day SK treatment with doses (1.0 and 1.5ml), however, reoccurrence of inflammation and pathological changes were observed in rats. Conclusion: The study clearly indicated the anti-arthritic role of SK. Future studies, however, are warranted to provide a new approach in relation to the therapeutic dose and treatment period of SK which may eventually lead to the development of a new category of the anti-arthritic agent.

}, keywords = {Anti-arthritic activity, Arthritis, Biomarkers, Sahacharadi Kashayam}, doi = {10.5530/pj.2020.12.71 }, author = {P Praveen Kumar and K Prabhu and Mudiganti Ram Krishna Rao and Mallika Jain and K Kalaivani and Shruthi Dinakar and Sampad Shil and N Vijayalakshmi} } @article {1312, title = {Antihypertensive, Antidiabetic, Antioxidant and Cytotoxic Activities of Indonesian Traditional Medicine}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1623-1629}, type = {Research Article}, chapter = {1623}, abstract = {

Background: Indonesian people have long used herbal medicine (jamu) to overcome various diseases, including hypertension and diabetes mellitus. Hypertension and diabetes mellitus are two diseases that are directly related and require proper and thorough management. Objectives: The present study investigated the antihypertensive, antidiabetic, and cytotoxic activities ethanol extracts of Indonesian traditional medicine (jamu). Material and Methods: Jamu was extracted by maceration using ethanol. Antihypertensive and antidiabetic activity investigated by measurement of ACE inhibitor, an alpha-glucosidase inhibitor, and antioxidant activity at a concentration ranging from 125-1000 μg/mL, respectively, by in vitro method. Cytotoxic evaluation of the extract was carried out using Brine Shrimp Lethality Test (BSLT). Results: measurements of ACE inhibitors, alpha-glucosidase inhibitor and antioxidant activity showed that herbal extracts had ACE inhibitors, alpha-glucosidase inhibitors, and antioxidant activity with IC50 values of 292.15 μg/mL, 36.13 μg/mL, and 24.43 μg/mL respectively. Ethanol extract of herbal medicine (jamu) exerts a cytotoxic effect on larvae of shrimp Artemia salina with an IC50 value of 215.04 μg/mL. Conclusion: Jamu extract has antihypertensive and antidiabetic activity in vitro and cytotoxic effects.

}, keywords = {ACE inhibitors, Alpha-glucosidase inhibitors, Antioxidant, Cytotoxic, Jamu}, doi = {10.5530/pj.2020.12.222}, author = {Aprilita Rina Yanti Eff and Hermanus Ehe Hurit and Sri Teguh Rahayu and Muhammad Unggul Januarko and Putu Gita Maya WM} } @article {1205, title = {Anti-inflammatory Activity of Nigella sativa oil Mediated Silver Nanoparticles}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1086-1092}, type = {Research Article}, chapter = {1086}, abstract = {

Aim: The aim of the study was to employ Nigella sativa oil in the synthesis of silver nanoparticles and to assess the anti-inflammatory activity of the Nigella sativa oil mediated silver nanoparticles. Background: The introduction of Nanoparticles (NPs) has transFigured many fields like medicine, nutrition and electronics. The usage of nanotechnology in medicine particularly for drug delivery is revealed to have numerous benefits. Nanoparticles are being used to decrease toxicity and side effects that drugs may impose to the patient. Nigella sativa is considered as a miracle seed. It has been reported to have anti-inflammatory, diuretic, and antihypertensive activity. Plant mediated biological synthesis of nanoparticles is simple and eco-friendly method. This work therefore was aimed to synthesize Nigella sativa oil mediated silver nanoparticles and evaluate its anti-inflammatory activity. Materials and Methods: Nigella sativa oil mediated silver nanoparticles were synthesised by short term (1 day) interaction of Nigella sativa seed extract (1 ml) with 2mM AgNO3 solution and centrifuged to obtain silver nanoparticles. The nanoparticles were characterised by UV-Visible spectrophotometer, FTIR and Scanning Electron Microscopy (SEM). Further the oil mediated AgNPs were evaluated for anti-inflammatory activity by in vitro and in vivo methods. Results: Nigella sativa oil mediated AgNPs were biofabricated with ease and exhibited good anti-inflammatory activity compared to standard. Conclusion: This study concludes that Nigella sativa seed oil mediated silver nanoparticles have the potential to be used as an effective antioxidant. Hence, it may be used in many medicinal applications to treat inflammation.

}, keywords = {Anti- Inflammatory effect, Nigella sativa, Rananculaceae, SEM analysis, Silver nanoparticles}, doi = {10.5530/pj.2020.12.153}, author = {Sheik Shehensha and M Vijaya Jyothi} } @article {1256, title = {Black Horehound (Ballota nigra Linn) Induces Apoptosis in Prostate Cancer Cells (PC-3) Through Intrinsic Signalling Cascade}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1377-1382}, type = {Research Article}, chapter = {1377}, abstract = {

Background: Prostate cancer is the most commonly diagnosed cancer among men. The disease varies widely in its clinical aggressiveness. Ballota nigra Linn (Black horehound) is a three-foot, perennial herb of the family Lamiaceae and it has been shown to have various pharmacological properties such as antioxidant, hypoglycemic, neuro-sedative, antibacterial, insecticidal and anticholinesterase activities. However, the elucidation of B.nigra for its anticancer activity in prostate cancer has not been studied so far. Methodology: Prostate cancer PC3 cells were treated with different concentrations of B.nigra (50, 100, 200 \& 400μg/ml) for the analysis of Bcl-2, Phosphorylation of Bcl2 (p-Bcl2) and tumor suppressor protein p53, Case pase-3 and caspase-9 in PC3 cells. Results: The B.nigra ethanolic leaf extract reduced the levels of anti apoptotic proteins (Bcl-2, p-Bcl2) and increased the level of tumor suppressor protein p53, caspase-3 and 9 significantly (p\<0.05). Conclusion: Results of the study show that B.nigra has potential anticancer activity by modulating intrinsic activity of apoptotic signaling in PC-3 cells. Thus, B.nigra may have a potential therapeutic option for the treatment of prostate cancer.

}, keywords = {Apoptosis, Ballota nigra, Intrinsic pathway, PC3, Prostate cancer}, doi = {10.5530/pj.2020.12.190}, author = {Selvaraj Jayaraman and Ponnulakshmi Rajagopal and Vishnupriya Veeraraghavan and Poonguzhali Sivagnanam and Divya Ravikumar and Sumetha Suga Deiva Suga and Kavin Mozhi James and Surapaneni Krishna Mohan} } @article {1097, title = {Effects of Beta-Carboline Alkaloids of Peganum Harmala on Induced Rat Ileum Contractions}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {260-265}, type = {Original Article}, chapter = {260}, abstract = {

Peganum harmala L., Zygophyllaceae popularly known as Wild Syrian rue, a well-known plant in folk medicine for many pharmacological uses including antispasmodic activity. Chemical composition of the plant showed that the most important constituents of this plant are betacarboline alkaloids such as harmalol, harmaline, and harmine. In this work, we aimed to evaluate the effects of these three major harmala alkaloids on induced rat ileum contractions, induced by acetylcholine, BaCl2 and KCl. Of these three harmala alkaloids, harmalol and harmaline produced a concentration-dependent spasmolytic activity, which was found to be reversible (i.e. disappeared after tissue wash-up. Both alkaloids inhibited acetylcholine and KCl-induced ileum contractions but BaCl2 -induced contractions were only inhibited by harmalol but not harmaline. Harmine did not show any inhibitory activity.

}, keywords = {Harmaline, Harmalol, Harmine, Ileum, Peganum Hermala L, Rat, Spasmolytic, β-Carbolines alkaloids}, doi = {10.5530/pj.2020.12.40}, author = {Amjad T Shatarat and Sawsan Abuhamdah and Eman Alefishat and Mohamed K Al-Essa and Rima Altaweel R and Faisal Mohammed and Darwish Badran and Hanan Jafar} } @article {1285, title = {Extraction of Quercetin from Nothopanax scutellarium Leaves via Ionic Liquid-based Microwave-assisted Extraction}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1512-1517}, type = {Original Article}, chapter = {1512}, abstract = {

Introduction: Nothopanax scutellarium leaves have been used in Indonesian traditional medicine to treat several diseases. Previous studies used conventional extraction methods with large volumes of organic solvents, long extraction times, and low levels of quercetin content. This study was aimed to identify the optimal solvent among different ionic liquids that has the highest quercetin content. Methods: Ionic liquids including 1-butyl-3-methylimidazolium bromide, 1-butyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium chloride, 1-butyl-3-methylimidazolium hydrogen sulfate, and 1-hexyl-3-methylimidazolium bromide, for extracting quercetin from N. scutellarium leaves using microwave-assisted extraction under the following conditions: ratio, 1:10; operation time, 10 min; and power, 10 W. Then, quercetin was fractionated using ethyl acetate and separated using 0.01 mol/L sodium bocarbonate, dipotassium phosphate or sodium cloride. The total flavonoid content was determined using a UV-Vis spectrophotometer, and quercetin content was determined using HPLC. Results: Extraction with 1-butyl-3-methylimidazolium chloride using NaCl as the separation salt was associated with the highest total flavonoid (360.57 mg/g) content among the ILs, whereas 1-butyl-3-methylimidazolium tetrafluoroborate combined with sodium chloride generated the highest quercetin content (26.13 mg/g). Conclusion: 1-butyl-3-methylimidazolium tetrafluoroborate is the optimal solvent for extracting quercetin from N. scutellarium leaves.

}, keywords = {Flavonoid, Green extraction, Green technology, Ionic liquid, Mangkokan Leaf}, doi = {10.5530/pj.2020.12.207}, author = {Ika Aulia Rahmi and Mahdi Jufri and Abdul Mun{\textquoteright}im} } @article {1239, title = {In vitro Assay and Study Interaction of Uncaria gambir (Hunter) Roxb. as Anti-fibrotic Activity Against A549 Cell Line}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1232-1240}, type = {Original Article}, chapter = {1232}, abstract = {

Aim: The aim of this study is to finding inhibitor potential from several compounds in gambir plant by using in vitro MTT assay and study interaction with molecular docking. The interaction of amino acids on the binding site with substances in the gambir plant was analyzed to determine its potential as a herbal-based therapy candidate for pulmonary fibrosis. Material and Methods: Protein target using TGFβ1 and NF-κB and compounds from gambir plant ((+)-Catechin. Epigallocatechin gallate, (+)-Epicatechin, Gambiriin A1, Gambiriin A2, Gambiriin B1, Gambiriin B2, Gambiriin C, Procyanidin B1, Procyanidin B3). Result: The results from docking analysis observed that compounds from gambir fruit contain anti-fibrotic activity which act by inhibiting DNA transcription of NF-κB and TGF-β1receptors. The compound Procyanidin B3, an essential amino acid, contains a hydrogen bond with the greatest NF-κB inhibitory activity on Gly214 and Lys337. Compounds from Uncaria gambir (Hunter) Roxb. can be an inhibitor to TGFβ1, all the compounds are on the active site of TGFβ1, and use native ligand which is an inhibitor of TGFβ1 (Naphtyridine). The positive compound catechin has the highest inhibitory activity. Gambiriin B1 and Gambiriin A2 are the most identical compounds with similar affinity binding value. Uncaria gambir (Hunter) Roxb. is already a proven antifibrotic which is further confirmed by (IC50: 19,255 {\textpm} 1.08 μg/ml, p \< 0.05) in A549 cell line. Conclusion: The results demonstrated that Gambiriin have cytotoxic effects and was found potentially as anti-fibrotic by MTT assay and in silico evaluation.

}, keywords = {Gambiriin compounds, Inhibitor of p50 NF-κB, Molecular docking, Pulmonary fibrosis, TGF-β1 receptors}, doi = {10.5530/pj.2020.12.172}, author = {Desdiani Desdiani and Iris Rengganis and Samsuridjal Djauzi and Agus Setiyono and Mohamad Sadikin and Sri Widia A Jusman and Nuryati Chairani Siregar and Suradi and Putri C Eyanoer and Fadilah Fadilah} } @article {1150, title = {In-vitro Antioxidant and In-Vivo Hepatoprotective Activity of Ethenolic Extract of Tectona grandis Bark Against CCl4 Induced Liver Injury in Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {598-602}, type = {Research Article}, chapter = {598}, abstract = {

Objectives: The systematic screening of Tectona grandis bark with the purpose of discovering new bioactive compounds as a hepatoprotective agent and to establish the scientific basis for the therapeutic actions of traditional plant medicines. Methods: Tectona grandis bark ethenolic extract was studied for the hepatoprotective activity against CCl4 induced liver injury in rats. Serum enzymes level, total bilirubin and histopathological study of liver were performed. This extract{\textquoteright}s DPPH radical scavenging potential was also studied. Results: Oral administration of ethenolic extract of Tectona grandis bark (200 mg/kg) exhibited significant reduction (p\<0.05) in CCl4-induced increased levels of SGPT, SGOT, ALP and bilirubin (Total) concentration. Treatment with Liv 52 syrup also reversed the hepatotoxicity significantly (p\<0.05). Histopathological studies also provided supportive evidence for biochemical analysis. This extract also showed better activity in quenching DPPH radical. Conclusion: Tectona grandis bark ethenolic extract shown to have hepatoprotective and antioxidant action due to presence of quinones and tannin like phytoconstituents.

}, keywords = {Antioxidant, CCL4 induced hepatopathy, Hepatotoxicity, Histopathology, Quinones, Tectona grandis}, doi = {10.5530/pj.2020.12.89 }, author = {Rajkumar S Bagali and Sunil S Jalalpure and SS Patil} } @article {1158, title = {Lathraea squamaria L. (Orobanchaceae): A Review of its Botany, Phytochemistry, Traditional Uses and Pharmacology}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {667-673 }, type = {Review Article}, chapter = {667}, abstract = {

This paper presents the results of the review pharmacognostic study of common toothwort, a perennial plant, parasitizing on the roots of trees. Currently, in Russian traditional medicine, there is considerable experience in the use of сommon toothwort (Lathraea squamaria L.) herb and roots as antitumoral, biligenic, infertility-treatment and diuretic drugs. The chemical composition of L. squamaria has not been quite well determined. Phenylethanoid glycosides (acteoside, isoacteoside), iridoid glycosides (aucubin, and aucuboside ester, 6{\textquoteright}-O-glucopyranosyl-aucubin, melampyroside, 6{\textquoteright}-O-glucopyranosyl melampyroside), simple sugars, fatty acids, organic acids, β-sitosterol were identified. Further study of L. squamaria raw materials is a very promising field including implementation in official medicine.

}, keywords = {Aucubin, Chemical compounds, Common toothwort, Iridoids, Lathraea squamaria, Orobanchaceae, Parasitic plants}, doi = {10.5530/pj.2020.12.98}, author = {Bokov DO and Barkalova VE and Suslikova MA and Sokhin DM and Kakhramanova SD and Rendyuk TD and Strelyaeva AV and Antsyshkina AM and Balobanova NP and Prostodusheva TV and Grikh VV and Krasnyuk II1 (junior) and Marakhova AI and Moiseev DV} } @article {1149, title = {Memory Enhancing Efficacy of an Ayurvedic Polyherbal Formulation on Scopolamine-Induced Memory Deficit Experimental Models}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {589-597 }, type = {Research Article}, chapter = {589 }, abstract = {

The present study was performed to determine the efficacy of an ayurvedic polyherbal formulation (PHF) in the learning and memory process of animal models. The prepared PHF was a suspension of three plant extracts i.e. Alpinia galanga (AG), Glycyrrhiza glabra (GG) and Convolvulus pluricaulis (CP) along with other excipients. Learning and memory assessment of PHF was performed using different behavioral models in scopolamine-induced memory impairment animals. Biochemical estimation was performed to determine the enzymatic level of MDA, GSH and AChE level in rats. Results indicated that the time of social investigation trial 2 (SIT2) was reduced significantly compared to SIT1 due to the treatment of PHF. In the water maze test, plant extracts significantly decreased the latency time in the 4th and 5th sessions comparing to session 1. Administration of AG, CP, GG, and PHF caused amelioration of scopolamine-induced memory impairment in the MWM test. The extracts and PHF were also effective in reducing latency time in the pole climbing test. Biochemical parameters exhibited a reduction in MDA and AChE levels with an increase in GSH level after treatment with extracts and PHF. It can be concluded from the study that PHF is an effective formulation for learning and memory processes against scopolamine-induced memory impairment. Further, the isolation of active constituents is desired from different plant extracts.

}, keywords = {Alpinia galanga, Convolvulus pluricaulis, Glycyrrhiza glabra, Latency time, Pole climbing test, Social recognition test}, doi = {10.5530/pj.2020.12.88}, author = {Deepa Shukla and Sajal Srivastava and Talha Jawaid} } @article {1315, title = {Physicochemical, Phytochemical, Heavy Metal and Microbiological Analysis of Moringa oleifera Lam. Leaves}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1541-1546}, type = {Original Article}, chapter = {1541}, abstract = {

Background: Moringa oleifera leaves is one of the highly patronized herbs on the Ghanaian market. It is used for the treatment and prevention of several diseases. It is imperative that available and effective methods can be utilized to assess the quality of samples before being consumed. Objective: A study of the leaves was conducted to ascertain its physicochemical, phytochemical, heavy metal and microbiological content to develop a simple but acceptable criteria which could be useful in ensuring the quality of this crude drug. Materials and Methods: The qualitative and quantitative morphological features, physicochemical, phytochemical, microbial load and flouresent features of the leaves of M. oleifera were evaluated. Results: M. oleifera leaves were found to be glaborous with opposite leaflet, leaflet tripinnate, with a micronate apex and possessing an entire margin. Microscopy showed vein islets, rosette calcium oxalate crystals, polygonal epidermal cells and unicellular trichomes. The 50 \% ethanol soluble extractives of M. oleifera were highest, followed by the water and petroleum ether. Tannins, alkaloids, gylcosides, phenols, flavonoids, phenols, gums, and mucilage were present. Conclusion: The documented pharmacognostic features may be used as part of daily protocols to correctly identify and determine the quality of the the crude plant. The preliminary phytochemical, heavy metal and microbiological limits can be further used to ascertain the quality of raw materials of M. oleifera before they are used.

}, keywords = {Fluorescence, Heavy metal, Microbiological, Pharmacognostic, Physicochemical}, doi = {10.5530/pj.2020.12.211}, author = {Emelia Oppong Bekoe and Yakubu Jibira and Gladys Amponsah Agyei} } @article {1241, title = {Phytotherapeutic Evidence Against Coronaviruses and Prospects for COVID-19}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1252-1267}, type = {Original Article}, chapter = {1252}, abstract = {

The emergence of the novel β-coronavirus (SARS-CoV-2) and subsequent outbreak of COVID-19, is a global health challenge with no known treatment to date and has culminated in significant morbidity and mortality. This article highlights current understanding on SARSCoV- 2 based on the available scientific evidence on human coronavirus (HCoV) infections, which could offer novel insights and therapeutic targets for SARS-CoV-2, the causative agent of COVID-19. Specifically, the paper presents available phytotherapeutic evidence against pathogenic HCoVs with a view to identifying potent plant-derived antiviral agents that could be developed to aid the fight against coronaviruses and the current COVID-19. Evidently, elucidation of CoV integral proteins such as the spike protein, angiotensin-converting enzyme 2, 3C-like cysteine protease and papain-like protease, as good targets for drug developments has lent credence to the use of medicinal plants or their metabolites as prophylaxis or treatment interventions in CoV infections and holds promising ground for SARS-CoV-2. While some promising phytocompounds are currently under clinical trials for COVID-19, increased research into plants and in-depth characterization of their metabolites could reveal more interesting results that would benefit humanity in its fight against emerging and re-emerging viral infections including the current COVID-19. Overall, given the current body of evidence on the potential development of phytotherapeutics for COVID-19, fears need to be allayed while clinical trials continue. Conclusively, the lockdown and other preventive measures which have been implemented in most parts of the world should be humanely exercised and supported to ensure compliance and safety of lives.

}, keywords = {Antivirals, Coronavirus, COVID-19, Drug target, Natural products, Plant metabolites, Plants, SARS-CoV-2}, doi = {10.5530/pj.2020.12.174}, author = {Abdullahi Temitope Jamiu and Christiana Eleojo Aruwa and Ismail Abiodun Abdulakeem and Abdulwakeel Ayokunnun Ajao and Saheed SABIU} } @article {1177, title = {Protection of Erythrocytes against Lipoperoxidation and Antiinflammatory Effects of Ethanolic Extract of Encelia canescens Lam Leaves in Mice}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {798-804}, type = {Original Article}, chapter = {798}, abstract = {

Background: Encelia canescens Lam is a plant traditionally used in Peru for medicinal purposes, and is attributed antioxidant properties, indicating that it could be used in the prevention of non-communicable diseases. Objective: This study aims to evaluate the protection of erythrocytes from lipoperoxidation and the anti-inflammatory effect of ethanolic extract of E. canescens leaves in mice. Materials and methods: Protection from lipoperoxidation was evaluated by inhibition of hemolysis and quantifying malondialdehyde (MDA) concentration against oxidative stress induced with hydrogen peroxide (H2O2) at 200, 150, 100, 50 and 25 μg/mL E. canescens concentrations. The 1\% carrageenan-induced air pouch model was used for evaluated inflammation, where albumin, total proteins, MDA, number and leukocyte differentiation were determined in the exudate, and a histopathological evaluation was performed. The concentrations evaluated were 100, 250 and 500 mg/kg of E. canescens Results: All the concentrations evaluated protected protected erythrocytes from lipoperoxidation (p\<0.05), being E.D. value 200 μg/mL. Regarding anti-inflammatory effect, the albumin, total proteins and MDA values of the treatment groups were lower than carrageenan 1\% group (p\<0.05), but, due to less leukocyte migration and presence of macrophages and the histopathological evaluation, the E.D value was 500 mg/kg. Conclusion: Ethanolic extracts of E. canescens leaves protect erythrocytes from lipoperoxidation and have dose-dependent anti-inflammatory effects maybe for presence of p-hydroxyacetophenone-derived, and these could be new safer anti-inflammatories.

}, keywords = {Antiinflammatory, Carrageenan, Encelia canescens Lam, Hemolysis, Lipoperoxidation, Malondialdehyde}, doi = {10.5530/pj.2020.12.114}, author = {Fern{\'a}ndez-Flores N and Rojas-Cardenas NF and Vásquez-Quispe AD and Chávez-Flores Juana E and Justil-Guerrero Hugo J and Parre{\~n}o-Tipian JM and Silva-Correa Carmen R and Villarreal-La Torre V{\'\i}ctor E} } @article {1320, title = {Representatives of the Genus Goryanka (Epimedium L) {\textendash} a Promising Source of Raw Materials for the Creation of Medicines for the Treatment of Erectile Dysfunction in Men}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1710-1715}, type = {Research Article}, chapter = {1710}, abstract = {

Erectile dysfunction and multiple mechanisms of its development are one of the most pressing problems of modern medicine. In the twenty-first century, millions of men around the world suffer from sexual disorders, and the number of such patients is only growing from year to year. The flavonoid icariin, contained in plants of the genus Epimedium L., is a promising pharmacologically active substance used for erectile dysfunction, due to its ability to affect type 5 phosphodiesterase, inhibiting its activity. To date, domestic and foreign pharmaceutical companies produce biologically active food additives and herbal preparations, which include Goryanka extract. But the range of standardized herbal medicines is very small.

}, keywords = {Drug, Epimedium Estrellita, Icariin, Impotence}, doi = {10.5530/pj.2020.12.231}, author = {Bukinich Darya Dmitrievna and Salova VG and Odintsova EB and Rastopchina OV and Solovyovа NL and Kozlova AM and Krasniuk II (jun) and Krasniuk II and Kozlova Zh M} } @article {1127, title = {Standardization of Indonesian Traditional Antihypertensive Medicines (Jamu) through the ACE Inhibitor Mechanism}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {422-429}, type = {Original Article}, chapter = {422}, abstract = {

Introduction: Herbal medicine (jamu) is a traditional Indonesian drug that has been used by the community in efforts to overcome health problems. One of the herbs that are frequently used by the public is antihypertensive jamu. This study aimed to determine the standardization parameters of 8 antihypertensive jamu in the form of specific and nonspecific parameters, antioxidant and angiotensin-converting enzyme inhibitor (ACEI) activity. Materials and methods: Jamu were extracted using ethanol. Nonspecific parameters that are water content, ash content, ash insoluble acid content, level of substances dissolved in alcohol and water, Coliform microbial contamination, and mold/yeast numbers. Determination of specific parameters including determining organoleptic (color and texture), chemical content, identification of infrared spectrum, in-vitro antioxidant activity, and ACE inhibitor activity. Results: nonspecific parameter such is the average water content of 5.92-8.1 v / w; total ash content of 5.85-7.2 w / w, levels of ash insoluble acid content were 0.45-0.55 w/w and the level of substances dissolved in alcohol and water were 24.22-54.21 and 24.22-54,21, respectively. The eight extracts were uncontaminated with coliform, mold, and yeast microbes. Antioxidant and ACE inhibitor activity test showed that all eight extracts had antioxidant activity in vitro with IC50 values ranging from 9.31 - 157.9 ppm and ACE inhibitor activity with the IC50 value is in the range of 18.37-740.8 ppm. Conclusion: The eight antihypertensive jamu met the standard of extract parameters both the specific and nonspecific and have potential in-vitro activities as ACE inhibitors.

}, keywords = {ACE inhibitor, Antihypertensive, Antioxidant, Herbal medicine (jamu)}, doi = {10.5530/pj.2020.12.65}, author = {Aprilita Rina Yanti Eff and Sri Teguh Rahayu and Putu Gita Mahayasih and Muhammad Unggul Januarko} } @article {1123, title = {Study of the Effect of Lampeni (Ardisia humilis Vahl.) Planting Condition toward the Alpha-glucosidase Inhibition Activity in vitro}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {377-385}, type = {Research Article}, chapter = {377}, abstract = {

Background: The quality of a medicinal plant is influenced by agronomic conditions and harvesting time. Objective: This study aimed to evaluate the effect of planting method (openair (OA) and shedding house (SH)) and harvesting time (2, 4, 6 months) of Lampeni (Ardisia humilis Vahl.) toward the inhibitory activity of alpha-glucosidase. Methods: The Lampeni seedling were placed under controlled light conditions (SH) and on direct sun exposure (OA). Harvesting of the leaves was carried out at the age of 2, 4, and 6 months after plantation (2m, 4m, and 6m). Each leaves dry powder was refluxed with methanol 70\% and followed by liquid-liquid partition using n-hexane, ethyl acetate (EtOAc), and water. All samples were evaluated toward inhibition of the alpha-glucosidase enzyme in vitro. Total phenol levels were determined using Folin-Ciocalteu reagent. Results: The results showed that EtOAc fractions of both plantation techniques exhibited the highest inhibition of alpha-glucosidase. The highest activity was demonstrated by the 4m-OA-EtOAc fraction (IC50, 93.50 ppm) and followed by the 6m-OA-EtOAc fraction (IC50, 98.13 ppm). Based on the kinetic study, the inhibition type of the two most active samples were categorized as a non-competitive type. Total phenolic contents were decreased in the following order: 6m-SH-EtOAc \> 4m-OA-EtOAc \> 6m-OAEtOAc \> 4m-SH-EtOAc fraction. It was shown that there was no positive correlation between the strength of inhibition with total phenolic content. Conclusions: This study concluded that Lampeni at open-air plantation harvested on fourth months demonstrated the highest alpha-glucosidase inhibitory activity, although there was no positive correlation between the inhibition activity and phenolic content.

}, keywords = {Alpha-glucosidase, Ardisia humilis Vahl., Lampeni, Open-air, Shedding house, total phenolic}, doi = {10.5530/pj.2020.12.59}, author = {Sri Ningsih and Fifit Juniarti and Idah Rosidah and Adam Arditya Fajriawan and Kurnia Agustini and Syofi Rosmalawati and Agung Eru Wibowo and Erliana Sasikirana and Wahono Sumaryono} } @article {1088, title = {Thin Layer Chromatography Fingerprinting and Clustering of Orthosiphon stamineus Benth. from Different Origins}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {79-87}, type = {Original Article}, chapter = {79}, abstract = {

Introduction: Orthosiphon stamineus has been widely used across Asian countries for the treatment of various diseases. The quality of herbal medicine determine its safety as well as efficacy; and geographical origin is important factor contributing on the quality of herb and its products. Materials and Methods: Thin Layer Chromatography (TLC) method combined with chemometric, Principal Component Analysis (PCA), has been employed to evaluate the quality of Orthosiphon stamineus leaves collected from eleven origins in Indonesia. Results: The results showed that mobile phase suitable for Orthosiphon stamineus was chloroform, dichloromethane, ethyl acetate (7:4:1). The method used has met the requirements of TLC system stability and precision. TLC-fingerprints analyzed with chemometrics showed an ability to discriminate Orthosiphon stamineus from various origins. PCA score plot of the first two principal components (PC) clearly distinguished 3 clusters of samples, whereas the loading plot of the first two PC showed that compounds with the Rf values of 0.0-0.1, 0.1-0.2, 0.2-0.3, and 0.9-1.0 are the most important compounds for clustering of samples. Conclusions: TLCfingerprint combined with the PCA was able to discriminate among the leaves of Orthosiphon stamineus originated from various locations. TLC-fingerprints analyzed with chemometrics can be used as an alternative of marker-oriented method to evaluate the quality of Orthosiphon stamineus.

}, keywords = {Geographical origin, Herbal medicine, Marker, Principal Component Analysis, Quality, TLC}, doi = {10.5530/pj.2020.12.13}, author = {Kartini Kartini and Ervina Rustiana Dewi and Fandi Achmad and Nikmatul Ikhrom Eka Jayani and Mochammad Arbi Hadiyat and Christina Avanti} } @article {961, title = {Aloe Vera Peel Extract Administration Increased Antioxidant Enzyme Levels of Serum and Seminal Plasma in Type 2 Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {962-967}, type = {Original Article}, chapter = {962}, abstract = {

Background: Diabetes mellitus (DM) is considered as a complex metabolic disorder characterized by hyperglycemia. Aim: The present study aimed to evaluate the effect of Aloe vera peel extract on the antioxidant levels of serum and seminal plasma of type 2 diabetic rats. Materials and Methods: Male Wistar rat was injected by 65 mg/kg streptozotocin (STZ) combined with 230 mg/kg of Nicotinamide acid (NA) intraperitoneally. The rats were declared to have diabetic with fasting blood glucose level \> 200 mg/dl 72 hours after induction. Diabetic rat samples were divided into four groups, control group (diabetes without treatment) and three groups were treated by Aloe vera peel extracts orally: 100 mg (P.1), 200 mg (P.2), and 400 mg/kg body weight (P.3), respectively. Antioxidant levels of serum and seminal plasma, including superoxide dismutase (SOD), catalase (CAT) and glutathione (GSH) were examined after 28 days of treatment. Results: The levels of SOD, CAT, and GSH in the group receiving Aloe vera peel extract were statistically significant (p \<0.05) higher than the control. There were also significant differences between the dose variations group. Conclusion: Aloe vera peel extract can significantly increase antioxidant levels in serum and seminal plasma of type 2 diabetic mice.

}, keywords = {Aloe vera peel extract, Antioxidants, Diabetes, Seminal Plasma, Serum}, doi = {10.5530/pj.2019.11.152}, author = {Wulan Christijanti and Achmad Zulfa Juniarto and Lisyani B. Suromo} } @article {787, title = {Antioxidant and Anti-inflammatory Activities of Bauhinia ungulata L. (Fabaceae) on LPS-Stimulated RAW 264.7 Cells}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {37-42}, type = {Original Article}, chapter = {37}, abstract = {

Objective: The present study aimed to investigate the antioxidant, immunomodulatory and antimicrobial activities of Bauhinia ungulata L. Method: A flavonoid-rich fraction was obtained from the Bauhinia ungulata L stem, called the ethyl acetate fraction of Bauhinia ungulata (FABU). The total antioxidant capacity of the FABU was determined through the phosphomolibdenium reduction method. For the evaluation of its antioxidant activity on a cell culture model, LPS-stimulated RAW 264.7 cells were treated with different concentrations of FABU and the reactive oxygen species (ROS), nitric oxide (NO), hydrogen peroxide (H2O2) and thiobarbituric acid reactive substances (TBARS) production levels were measured. For the analysis of its immunomodulatory capacity, TNF-α, TGF-β and IL-10 levels were determined in the culture supernatant. In order to determinate the antimicrobial activity of FABU, antifungal and antibacterial susceptibility testing was performed against Candida albicans, methicillinsensitive Staphylococcus aureus, methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa strains. Result: The FABU demonstrated neither significant antimicrobial activity nor immunodulatory capacity; on the other hand, its potential antioxidant activity was demonstrated by the phosphomolibdenium reduction assay. Also, FABU treatment inhibited the ROS, NO, H2O2 and TBARS levels in the supernatant of LPS-stimulated cells. Conclusion: A significant reduction in the amount of reactive oxygen and nitrogen species (RONS) was observed, in addition to lipid peroxidation inhibition. Our data suggest that the FABU is a natural antioxidant complex that may interfere in the cascade of cell damage caused by free radicals and a promising potential drug in chronic disease models in which immunopathogenicity involves high levels of RONS.

}, keywords = {Bauhinia ungulata; RAW 264.7 cells; Lipopolysaccharide; Free radicals; Antioxidant activity}, doi = {10.5530/pj.2019.1.7}, author = {Raphael de Oliveira Rodrigues and Juliana Navarro Ueda Yaochite and Milena Aguiar Braga and Amanda Ribeiro de and Sousa and Greyce Luri Sasahara and Said Gon{\c c}alves da Cruz Fonseca and Thiago Dias de Vasconcelos Ara{\'u}jo and Gilvandete and Maria Pinheiro Santiago and Le{\^o}ncio Mesquita de Sousa and Jarbas Lima de Carvalho and Francisca Bruna Stefany Aires and do Nascimento and H{\'e}lio Vitoriano Nobre J{\'u}nior and Aparecida Tiemi Nagao-Dias} } @article {859, title = {Antiulcer Property of Mussaenda philippica}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {603-607}, type = {Original Article}, chapter = {603}, abstract = {

Introduction: Mussaenda philippica (Rubiaceae) is a shrub distributed in all the planes of India, Philippines and South-East Asia. Its synonyms are M. grandiflora, M. acutifolia, M. frondosa etc. The plant is preferred as medication for the treatment of jaundice, dysentery, stomachache and influenza. The current study was based on the evaluation of antiulcer property of M. philippica leaves extract. Methods: The methods used were pylorus ligated, ethanol induced and 0.2(M) NaOH induced ulcer in rats. Results: In pylorus ligation model, aqueous extract (200 mg/kg) produced a substantial reduction in ulcer index followed by decrease in gastric volume, total acidity associated with a raise in pH, which, confirmed that tested extract of the plant act by altering the mucosal barrier Thus, the gastro protective effect of this extract may be due to the presence of flavonoid in the plant. In the same way, aqueous extract of the plant showed significant effect against ethanol induced gastric ulcer in rat as compared to methanol-treated group, which, may be due to leukotriene antagonistic effect or the inhibition of 5-lipooxygenase pathway. In NaOH induced ulcer model, aqueous extract of M. philippica revealed significant antiulcer effects on the basis of pH effect and ulcer index in rats. The anti-ulcerogenic and anti-secretory effect of the tested M. philippica leaves extracts point out its possible cyto-protective effect. Conclusion: In conclusion the aqueous extract of M. philippica leaves possess potential antiulcer activity in experimental rat models.

}, keywords = {Anti-secretory, Gastric volume, Methanol extracts, Mussaenda philippica, Pylorus ligation}, doi = {10.5530/pj.2019.11.96}, author = {Rasmita Jena and Durga Madhab Kar and Diptirani Rath and Kaushik Sur Roy and Goutam Ghosh} } @article {783, title = {A Comparative Antibacterial Activity of Three Common Spices Extract and their Anti-Proliferative and Apoptotic Effectiveness against Human Breast Adenocarcinoma Cells}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {88-93}, type = {Original Article}, chapter = {88}, abstract = {

Objective: The present study was performed to analyse the antibacterial potential as well as the anti-proliferative and apoptotic efficacy of three common spices viz. Cardamom (Elettaria cardamomum), Cinnamon (Cinnamomum verum) and Fennel (Foeniculum vulgare). Methods: Antibacterial activity was determined by well diffusion assay against selected bacterial strains. Anti-proliferative activity was evaluated by cell viability assay and the apoptotic effect was observed by nuclear fragmentation analysis in MCF-7 cells. Results: The antibacterial activity result revealed that Cinnamon extract (CIE) showed maximum antibacterial activity against selected test organism followed by Cardamom (CAE) and Fennel (FEE). The cell viability results revealed that FEE induces the highest cytotoxicity (IC50 73.9 μg/ml) against MCF-7 cells, while CIE showed the lowest efficacy (IC50 98.2 μg/ml) as compared to control. Conclusion: The findings revealed that CIE has the most potent antibacterial efficacy, whereas FEE was found to be a more potent anti-proliferative and apoptotic agent against human breast carcinoma MCF-7 cells.\ 

}, keywords = {Anti-proliferative, Antibacterial, Apoptotic, Cell viability, Nuclear fragmentation}, doi = {10.5530/pj.2019.1.16}, author = {Shabana Bano and Asif Jafri and Nashrah Ahmad and AK Sharma and Md Arshad} } @article {974, title = {Comparative Evaluation of Anti-Inflammatory Potential of Ethanolic Extract of Leaf, Bark and Flower of Tecoma stans with Ibuprofen- An In vitro Analysis}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1088-1092}, type = {Research Article}, chapter = {1088}, abstract = {

Background: Endodontics has always been indebted to pharmaceutical sciences to provide it with necessary analgesics and anti-inflammatory agents. More specifically, there has always been a need for anti-inflammatory phytotherapeutic agents as the commercially available synthetic anti inflammatory drugs have their own limitations due to undesirable side effects. Hence, novel potent analgesic and anti-inflammatory drugs without considerable side effects from the natural sources are under evaluation. Tecoma stans (Bignoniaceae) is an ornamental plant found throughout India. It has been shown to have variety of medicinal properties. In the present study, we have shown that potential anti inflammatory activity of different parts of Tecoma stans (T.stants) and compared with standard drug. Aim: To evaluate the in vitro anti inflammatory potential of different parts of T.stans ethanolic extract and to compare the anti inflammatory activity with standard drug ibuprofen. Methodology: The ethanolic extraction of T.stans{\textquoteright}s bark, leaves and floweres was done as per the standard method. Different concentrations (100, 200, 300, 400 and 500 μg/ml) of the extracts were used for anti-inflammatory activity by inhibition of albumin denaturation. All samples were analyzed in triplicate. The results were statistically analyzed. Results: All the three parts of the plant extract have shown to have anti inflammatory activity in a dose-dependent manner. However, the leaf and flower extracts of T.stans were found to have 100 percent anti-inflammatory pontential than standard drug ibuprofen. Conclusion: It is concluded from the present findings that T.stants possess anti-inflammatory properties which could be due to presence of active constitutents presen in the plant extracts. Hence, T.stans may serve as one of the anti inflammatory herbal durgs for Endontic infection-induced inflammation and related to dental diseases. Further studies on the identification of the active principles present in the leaf and flower extract are warranted to assertatin its potentials.

}, keywords = {Anti-inflammatory Effect, Bark, Flower, Leaf, Tecoma stans}, doi = {10.5530/pj.2019.11.170}, author = {Swarna SK and Nivedhitha MS and Vishnu Priya V and Gayathri R and Selvaraj J and Madhan K and Shyamala Devi B} } @article {793, title = {Comparative Studies Between Mauritia flexuosa and Mauritiella armata}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2018}, pages = {32-36}, type = {Original Article}, chapter = {32}, abstract = {

Mauritia flexuosa and Mauritiella armata belong to the family Arecaceae and are widely found in Brazil. Aim: In this work were evaluated: the phytochemical profile of the secretion popularly known as M. flexuosa wine, antioxidant activity of leaf, root and petiole hydroethanolic extracts of the two species, as well as the quantification of flavonoids and the chromatographic profile by means of high performance liquid chromatography. Material and Methods: The chromatographic profile was determined by high performance liquid chromatography, quantification of flavonoids and antioxidant activity, were performed by spectrophotometric method. Results: Antioxidant activity and presence of flavonoids were observed in the extracts of all the analyzed structures of the two species. The phytochemical profile of the wine evidenced the presence of secondary metabolites reported in other structures of M. flexuosa. In the chromatographic analysis, it was observed that the extracts evaluated have between three and nine compounds. Conclusion: Further studies should be performed to identify the active compounds in the two species.

}, keywords = {antioxidant activity, Arecaceae, Flavonoids, Phytochemical, Secondary metabolites}, doi = {10.5530/pj.2019.1.6}, author = {Vanessa de Andrade Royo and Juliana Almeida Rocha and Kamylla Teixeira Santos and Jeane Ferreira Leal Freitas and Clarice Avelar Almeida and Bianca Ribeiro and Elytania Veiga Menezes and Dario Alves de Oliveira and Murilo Malveira Brand{\~a}o and Afranio Farias de Melo J{\'u}nior} } @article {870, title = {Effect of Porana paniculata Whole Plant on Blood Glucose Levels and Lipid Profile of STZ Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, year = {2019}, month = {March 2019}, pages = {xx-xx}, type = {Original Article}, chapter = {xx}, abstract = {

Background: To establish the antidiabetic potential of Porana paniculata whole plant belongs to Convolvulaceae family. Methods: Extraction and preliminary phytochemical screening were conducted by standard methods. Antidiabetic activity was evaluated by streptozotocin induced diabetic rats where the hydroalcoholic extract of plant was administered orally at a dose of 250 and 500 mg/kg for 30 days. Blood glucose levels were estimated at 1st, 10th, 20th and 30th day of study. Lipid profile was studied 30th day of study and body weight of the animals was measured at day 1 and 30. Results: Plant extract significantly (p\<0.01) reduced the blood glucose levels at both the tested dose levels of 250 and 500 mg/kg. The lipid profile was estimated in which the plant extract showed significant improved in both tested dose level that is 250 and 500 mg/kg. The body weight of the animals under study was also estimated on day 1 and 30 in which a good control was observed by the plant extract. Conclusion: Antidiabetic activity of Porana paniculata whole plant extract may be due to the presence of various phytoconstituents. Present study gives a scientific evidence for the folklore claim of the plant under study for its use in diabetes.

}, keywords = {Diabetes, Folklore, lipid profile, Porana paniculata, Streptozotocin}, doi = {10.5530/pj.2019.11.xx}, author = {Sanjeeva Kumar A and Raveendra Reddy Juturu and Rama Mohan Gupta Vankadari} } @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 {857, title = {Evaluation of Anti-psoriatic Potential of the Fruit Rind of Punica granatum L.}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {466-468}, type = {Original Article}, chapter = {466}, abstract = {

Background: Pomegranate (Punica granatum L.) is universally known for its therapeutic properties due to its potential bioactive compounds. However, there is no established scientific study on antipsoriatic activity of pomegranate fruit rind. The aim of the study is to evaluate the anti-psoriatic activity of the isolated compounds and the extract from the fruit rind of P. granatum. In our previous study, the isolated compounds were evaluated for antioxidant potential. In continuation to the previous investigation, the present study is taken up to evaluate the extract and compounds for in vitro anti-psoriatic activity. Methods: Chromatographic techniques were employed to isolate the compounds from the aqueous acetone extract and in vitro anti-psoriatic activity was determined by thymidine phosphorylase inhibition assay. Results: From previous phytochemical investigation, three compounds were identified as Punicalagin, 2,3(S)-hexahydroxydiphenoyl-D-glucose and Punicalin. In the present study, the extract and the compounds were evaluated for anti-psoriatic activity. The results reveal that the isolated three compounds showed inhibitory activity of 89\% to 95\% against thymidine phosphorylase. Aqueous acetone extract also exhibited 87\% inhibition. Conclusion: Punica granatum is an ideal plant for further investigation to prove its anti-psoriatic activity.

}, keywords = {Anti-psoriatic activity, Punica granatum, Thymidine phosphorylase inhibition}, doi = {10.5530/pj.2019.11.73}, author = {Janani Jacob and Gopalan R and Lakshmanaperumalsamy P and Ramanaiah Illuri and Damaji Bhosle and Gopala Krishna Sangli and Deepak Mundkinajeddu} } @article {989, title = {GC-MS Analysis of Bioactive Phytochemicals in Methanol Extract of Aerial Part and Callus of Dipterygium glaucum Decne}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1055-1063}, type = {Original Article}, chapter = {1055}, abstract = {

Introduction: This study was designed to evaluate the phytocomponents present in aerial part and in vitro induced callus methanol extracts of Dipterygium glaucum by Gas Chromatography-Mass Spectrometry (GC-MS) technique. Methods: GC-MS analysis of aerial part sample and callus produced from leaf of D. glaucum extracted in methanol solvents was performed using GC-MS QP 2010 Plus (Shimadzu, Japan) system comprising an auto sampler (AOC-20i) and a gas chromatograph interfaced to a mass spectrometer. Results: This study was carried out to identified and comparative analysis of bioactive phytochemicals from aerial part extract and callus extract of D. glaucum. This analysis revealed that both the extracts have 69 different types of phytochemical components in varying quantities. Some of the important phytochemical compounds were Stigmasterol, β-sitosterol, γ-sitosterol, Campesterol, Squalene, n-Hexadecanoic acid, Stearic acid, Myristic acid, Quinazoline, Linalyl acetate etc. These chemical compounds have anticancer, antitumor, anti-inflammatory, antidiabetic and antioxidants properties. Conclusion: This study represents the detection and identification of different phytochemical compounds from aerial part and callus extract of D. glaucum. Thus, due to the presence of various important bioactive phytocomponents this plant is recommended as a pharmaceutically important plant.

}, keywords = {Callus, Campesterol, Capparidaceae, Fatty Acid, Stigmasterol, Terpenoids}, doi = {10.5530/pj.2019.11.165}, author = {Choudhary D and Shekhawat JK and Kataria V} } @article {975, title = {Honokiol and Magnolol Induce Apoptosis and Cell Cycle Arrest in Human Ovarian Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1114-1123}, type = {Research Article}, chapter = {1114}, abstract = {

Introduction: Ovarian cancer is a major cause of cancer-related death among women. The growth, persistence, and cancer metastasis are causes of poor prognosis and high mortality rate. Honokiol and magnolol are derivative compounds extracted from the root and stem bark of Magnolia officinalis. Many studies have reported that honokiol and magnolol have anti-tumour effects on various types of cancer. The present study investigates the anti-tumour effect of these compounds on human ovarian cancer. Methods: Ovarian cancer cell lines, SKOV3 and ES-2 cells were tested with honokiol and magnolol to determine their responses including the cytotoxicity, cell proliferation, induction of cell apoptosis and metastasis ability. Result: The results indicate that low concentrations of honokiol and magnolol suppressed the proliferation of ovarian cancer cells through induction of cell cycle arrest at G0/G1 and down-regulation of the cyclin D1 protein. These compounds also exhibited an anti-metastatic ability mediated by inhibiting migration, adhesion, and MMP activities. Additionally, high concentrations of honokiol and magnolol could activate cell death associated with the apoptosis signalling pathway, either along an intrinsic or extrinsic pathway. Conclusion: The data provides evidence that honokiol and magnolol have potential anti-tumour properties and minimal toxicity on normal cells, and could therefore be applied in the treatment of ovarian cancer.

}, keywords = {Apoptosis, Honokiol, Magnolol, Metastasis, Ovarian Cancer, Proliferation}, doi = {10.5530/pj.2019.11.174}, author = {Worawat Songjang and Arunya Jiraviriyakul} } @article {933, title = {Modification of Hexavalent Chromate Hepatotoxicity by Ethanol Extract of Moringa oleifera in Wistar Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {764-770}, type = {Original Article}, chapter = {764}, abstract = {

Background: The association of hexavalent chromate toxicity with oxidative stress necessitated the search for antidote from medicinal plants with antioxidant properties. One of such plants is Moringa oleifera. Objective: To investigate the hepatoprotective and antioxidative properties of ethanol extract of Moringa oleifera (EEMO) against potassium dichromate (K2Cr2O7) induced hepatocellular damage and oxidative stress in male Wistar rats. Materials and Methods: Thirty rats were assigned into six groups of five animals each: distilled water, 12 mg/kg bd.wt K2Cr2O7, 3.5 mg/kg bd.wt EEMO, 7.0 mg/Kg bd.wt EEMO, 3.5 mg/Kg bd.wt EEMO+K2Cr2O7, 7.0 mg/kg bd.wt EEMO+K2Cr2O7. The EEMO was administered consecutively for thirty-five days, while K2Cr2O7 was injected intraperitoneally once weekly before the animals were sacrificed. Liver function and oxidative stress markers including alanine aminotransferase (ALT), aspartate aminotransferase (AST), superoxide dismutase (SOD), glutathione -S-transferase (GST) and malondialdehyde (MDA) levels were monitored in the serum and liver. Histopathology of the liver was also carried out. In addition, proximate analysis of the powdered leaves and phytochemical composition of EEMO were also evaluated. Results: The K2Cr2O7 significantly (p \< 0.05) increased AST, ALT and MDA levels coupled with decreased SOD and GST activities as well as hepatic lesions when compared with control. However, the two doses of EEMO modified the hepatotoxicity and oxidative stress towards that of control. The EEMO is rich in phenolics and other phytochemicals including hexamethylquercetagetin and hexa-Omethylmyricitin that may account for the observed antioxidative and ameliorative effect. Conclusion: Our results suggest that ethanol extract of Moringa oleifera modify hexavalent chromate hepatotoxicity by reducing oxidative stress.

}, keywords = {Antioxidant, Hepatotoxicity, Moringa oleifera, Oxidative stress and potassium dichromate}, doi = {10.5530/pj.2019.11.121}, author = {Akinwumi Kazeem A and Osifeso Olabode O and Jubril Afusat J and David Olaitan O} } @article {994, title = {An Overview of Phytochemical and Pharmacological Potentials of Punica granatum L}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1167-1171}, type = {Review Article}, chapter = {1167}, abstract = {

Pomegranate (Punica granatum) is considered as {\textquotedblleft}A pharmacy unto itself{\textquotedblright} in Ayurvedic medicine and also used in several other systems of medicine. The plant belongs to the family Lythraceae containing pomegranate as a predominant species. Various parts of the plant exhibits significant pharmacological activities due to its wide range of potential bioactive compounds. Many biological activities proved its antioxidant, anticancer, anti-inflammatory, antimicrobial, anti- athersclerotic, antidiabetic actions and many more. This article provides a review of phytoconstituents of Punica granatum and its diverse array of biological properties.

}, keywords = {Bioactive compounds, Lythraceae, Pharmacological activities, Phytoconstituents, Punica granatum, Traditional medicine}, doi = {10.5530/pj.2019.11.181}, author = {Janani Jacob and Rajiv P and Gopalan R and Lakshmanaperumalsamy P} } @article {873, title = {Pharmacognostic Evaluation and Antimicrobial Activity of Root of Careya arborea}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {608-612}, type = {Short Communication}, chapter = {608}, abstract = {

Background: Careya arborea is known for its traditional medicinal properties and reported for potent antitumor, antioxidant, hepatoprotective and many other activities. Its stem bark, leaves and fruits were studied biologically, but so far its root has not been studied. Aim: The aim of the present study is to standardize the root of Careya arborea and its extracts pharmacognostically and also to screen its extracts for their antimicrobial activities against several bacteria and fungi using standard procedures. Materials and Methods: Loss on drying, extractive and ash values, fluorescence and phytochemical analysis of the root and its extracts were studied using standard procedures. Antimicrobial activity was carried out by determining minimum inhibitory concentration. Results: Among all the extracts, the successive ethyl acetate extract was found to be the most active with lowest MIC values against L. acidophilius, S. aureus, C. freundii, P. aeruginosa and M. luteus. The successive chloroform extract was also found to be highly active against P. aeruginosa and fungi, M. furfur and C. albicans. Conclusion: The results are helpful in standardizing the root of the plant and since several of the root extracts possess antimicrobial properties, there is a need to isolate its constituents.

}, keywords = {Antibacterial, Antifungal, Careya arborea, standardization}, doi = {10.5530/pj.2019.11.97}, author = {Bandenawaz Ramadurga and Rakesh Kumar Jat and Shrishailappa Badami} } @article {852, title = {Phytochemical, in vitro Antioxidant and in vivo Safety Evaluation of Leaf Extracts of Tragia plukenetii}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {338-345}, type = {Original Article}, chapter = {338}, abstract = {

Objective: To investigate the phytochemical properties, in vitro antioxidant and in vivo safety profile of leaf extracts of Tragia plukenetii (TP). Methods: TP leaves were obtained from the south part of India (Guntur District, Andhra Pradesh) and it was extracted with different solvents (benzene extract (BE), chloroform extract (CE) and methanolic extract (ME)). These TP extracts were analyzed for the in vitro antioxidant activity by DPPH reducing power, β-carotene-linoleic acid complex and iron chelation assays followed by in vivo acute oral and dermal toxicities using Swiss mice and Wistar rats respectively. Results: The present study results revealed ME exhibited an effective and powerful antioxidant activity when compared to a standard antioxidant, butylated hydroxytoluene (BHT). ME was found to be effective in DPPH, β-carotene-linoleic acid complex and iron chelation assays respectively. In vivo acute oral toxicity study revealed that mice treated with up to 5000 mg/kg of BE, CE and ME did not show any signs of toxicity. Furthermore, similarly, acute dermal toxicity study demonstrated that BE, CE and ME did not exhibit any signs of dermal toxicity up to 1000 mg/kg in rats. Conclusion: TP extracts possess an excellent antioxidant activity with a devoid of any signs of acute oral and dermal toxicities.

}, keywords = {Dermal toxicity, DPPH assay, Iron chelation, Oral toxicity, Tragia plukenetii., β-carotene-linoleic acid complex}, doi = {10.5530/pj.2019.11.50}, author = {Srinivasa Reddy Bonam and Sathish Kumar Manoharan and Vijayapandi Pandy and Anji Reddy Raya and Rama Rao Nadendla and Manjunathan Jagadeesan and Ankem Narendra Babu} } @article {926, title = {Phytochemical, in vitro Antioxidant and in vivo Safety Evaluation of Leaf Extracts of Tragia plukenetii}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {848}, type = {Corrigendum}, chapter = {848}, abstract = {

In principle, this figure represents non-toxic effect of TP. As all the treatment groups are non-toxic, we have optimistically represented the figure. Due to the manual error while copying the figure 4, BE image was taken from different group instead of actual one. This has been rectified in the corrected image of figure 4. In ground reality, however, the present modifications in the figure do not alter the scientific meaning of the figure or the outcome of the study conclusions. Read more...

}, keywords = {Nil}, author = {Srinivasa Reddy Bonam and Sathish Kumar Manoharan and Vijayapandi Pandy and Anji Reddy Raya and Rama Rao Nadendla and Manjunathan Jagadeesan and Ankem Narendra Babu} } @article {922, title = {Phytochemical Screening, HPTLC Fingerprinting and Invitro Antioxidant Activity of Root Extract of Asparagus racemosus}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {818-823}, type = {Original Article}, chapter = {818}, abstract = {

Background: Asparagus racemosus is a climber shrub used in Indian medicine for centuries. It has been used as galactogogue and nerve tonic in folk medicine. The recent research on A. racemosus has revealed its disease fighting properties such as anti-bacterial, immunomodulatory, cardio protective, anti-stress, etc. Phytochemicals present in the plants are associated with their therapeutic capabilities. Hence, phytochemical screening of a therapeutic plant is essential. Materials and Methods: A preliminary qualitative screening of phytoconstituents present in the ethanol and aqueous extract of the plant was done. high-performance thin layer chromatography (HPTLC) was used to create a phytochemical fingerprint of the plant extract. Further, a series of antioxidant assays, i.e., 2,2-diphenyl-1- picrylhydrazyl (DDPH) radical, Nitric oxide (NO) radical, Superoxide (SO) radical and 2,2{\textquoteright}-azinobis( 3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical scavenging assays were done. Results: The phytochemical screening and the HPTLC fingerprint showed the presence of phenolic compounds, flavonoids, glycosides, triterpenoids, saponins etc. They also showed free radical scavenging property and hence can be used as potential primary antioxidant. Conclusion: A preliminary screening created a phytochemical profile of A. racemosus extracts. These phytoconstituents may be linked to the various known therapeutic applications of the plant. This may aid in further extensive studies for identifying and isolating compounds with potential therapeutic value in A. racemosus.

}, keywords = {Antioxidants, Asparagus racemosus, Chromatography, Phytochemistry, Phytoconstituents, Therapeutics}, doi = {10.5530/pj.2019.11.131}, author = {Kalaivani Selvaraj and Girija Sivakumar and Aruthra Arumugam Pillai and Vishnu Priya Veeraraghavan and Srinivasa Rao Bolla and Geetha Royapuram Veeraraghavan and Gayathri Rengasamy and Joel P Joseph and Janardhana PB} } @article {1034, title = {Preliminary Phytochemical Investigation of Hypnea valentiae with Antigluconegenesis Activity in Goat Eye}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1406-1408}, type = {Original Article}, chapter = {1406}, abstract = {

ROS is known to the main spark off the pathogenesis of cataract. In the Red seaweed the protein content along with Carotenoids are highly having the anti-oxidant activity to nullify the Oxidative stress. Along this ward, the Selected Red Seaweed where macerated in different solvent system. From that, the phytochemical parameters, were investigated. However, it showed that the Aqueous extract of Hypnea valentiae posse the protein, Carbohydrate, tannin and cartotenoids. The indexed extract pointed with the antigluconesgenesis effect in the isolated goat eye. The results suggest that the Hypnea valentiae extract under investigation can delay the diffusion onset and/or prevent the progression of cataract. In this, anti-cataract potential may be attributed to the presence of high protein and carotenoids. Photographic evaluation, further, confirmed the observation.

}, keywords = {Anti gluconeogenesis, Aqueous extract, Goat eye, Hypnea valentiae}, doi = {10.5530/pj.2019.11.217}, author = {S Dhanalakshmi and S Jayakumari} } @article {944, title = {Protective Effect of the Ethanolic Extracts of Leaves of Chuquiraga spinosa Less and Baccharis genistelloides on Benign Prostatic Hyperplasia in Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {858-865}, type = {Original Article}, chapter = {858}, abstract = {

Introduction: Benign prostatic hyperplasia (BPH) is one of the most common conditions affecting middle-aged men, with oxidative stress postulated as an important factor in its development. Objective: To evaluate the protective effect of the association of the ethanolic extract of Chuquiraga spinosa (ChS) and Baccharis genistelloides (BaG) on benign prostatic hyperplasia in rats. Materials and Methods: Sixty-six male rats were randomized into groups: 1) Inductor Group: Testosterone enanthate (ET) 25 mg/Kg on days 8 and 14 intramuscularly. 2) Group P80: Polysorbate-80 3\% 10 mL / Kg. 3) Positive Group: ET + Dutasteride (DU) 0.5 mg / Kg, 4) ET + ChS 250, 5) ET + ChS 500, 6) ET + BaG250, 7) ET + BaG 500, 8) ET + ChS 250 + BaG 250, 9) ET + ChS 500 + BaG 500, 10) ET + ChS 250 + BaG 500, 11) ET + ChS 500 + BaG250. PSA, nitric oxide (NO) and malondialdehyde (MDA), prostate dimensions by ultrasound and histopathological findings were quantified as main markers. Results: Lower levels of NO, MDA and PSA were observed in all groups treated with extract compared to the Inductor group (p \<0.01), with the reductive capacity of the mixture ChS 250 + BaG 500 and ChS 500 + BaG 250 compared with Dutasteride (p \<0.05). The volume of the prostate was lower in the Dutasteride, P80 and ChS250 + BaG500 groups compared to the inducer (p \<0.05). Regarding the histopathological study, it was observed that the association of variable doses (ChS250 + BaG500 and ChS500 + BaG250) had a better protective effect. Conclusion: Under experimental conditions, the association of the extracts of Chuquiraga spinosa and Baccharis genistelloides has an effect in the protection of BPH induced with testosterone, which could be linked to its antioxidant capacity of the extracts.

}, keywords = {Baccharis genistelloides, Benign prostatic hyperplasia, Chuquiraga spinosa, Dutasteride, Testosterone}, doi = {10.5530/pj.2019.11.138}, author = {Robert Palomino-De-La-Gala and Hugo Justil-Guerrero and Jorge Arroyo-Acevedo and Juan Rojas-Armas and Cristian Aguilar-Carranza and Jaime Mart{\'\i}nez-Heredia and Edwin Cieza-Macedo and Carlos Garc{\'\i}a-Bustamante and Oscar Herrera-Calderon and Edwin Enciso-Roca and Roberto Ch{\'a}vez- Asmat and Lester Dominguez-Huarcaya} } @article {797, title = {Reversible Hepatotoxicity of Cassytha filiformis Extract: Experimental Study on Liver Function and Propofol-Induced Sleep in Mice}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {69-74}, type = {Original Article}, chapter = {69}, abstract = {

Objective: To study the liver toxicity of Cassytha filiformis L. extract and its reversibility in mice. Methods: A total of 108 male mice were used to investigate the hepatotoxicity of Cassytha filiformis extract (CFE) and the reversibility of its toxicity to the liver. Seventy-two mice were treated with CFE orally for 7 consecutive days. A half of these animals were used to study the sleep time on propofol-induced sleep that comprised the sleep onset time (SOT) and duration of sleep (DOS), while another half was used for the quantitation of serum alanine transaminase (ALT) activity. To investigate the reversibility of the liver toxicity, thirty-six mice were treated with daily CFE for 7 days. Activities of ALT and alkaline phosphatase (ALP) were determined and the liver weight ratio was measured on day 0, 1, 3 and 7 after the termination of the CFE treatment. Data of liver toxicity determination were analyzed by two-way ANOVA followed by Duncan{\textquoteright}s multiple range test, while data of the reversibility was analyzed by Pearson{\textquoteright}s correlation. The significance level was taken at 95\% of confidence interval. Results: CFE shortened the SOT and prolonged the DOS significantly compared with control (p\<0.05). The activity of ALT was increased due to the toxicity of CFE. However, the ALT/ALP activities decreased and liver weight ratio increased gradually after the extract treatment was discontinued. The trend of these data was correlated significantly (p\<0.05). Conclusion: Cassytha filiformis L. extract is toxic to the liver but the toxicity is reversible depending on doses.

}, keywords = {Cassytha filiformis, Liver function, Propofol, Reversible toxicity, Sleep time}, doi = {10.5530/pj.2019.1.13}, author = {Yori Yuliandra and Armenia Armenia and Rahmad Arief and Mifta Hul Jannah and Helmi Arifin} } @article {896, title = {Screening and Evaluation of Lectin and Anti-Cancer Activity from the Phloem Exudate/Sap of the Indian Dietary Ethnomedicinal Plants}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {570-578}, type = {Original Article}, chapter = {570}, abstract = {

Objective: Lectins are extremely significant biomolecules to study several biological progressions. In this present investigation, we are screening the crude phloem exudate/ sap sample from different ethnomedicinal plants were evaluated for lectin and anticancer activity. Methods: The lectin activity of crude phloem exudate/sap samples were confirmed by haemgglutination assay and anticancer activity by using trypan blue, MTT and in-ovo CAM angiogenic assay. The tumor cell nuclei resulting in Giemsa stain, AO/EtBr stain, DNA Fragmentation and Caspase- 3 inhibitor assay. Results: Our experimental data show that the phloem exudate/sap sample S2 (Musa Acuminata), sample S4 (Euphorbia Geniculate) exerting the potent lectin activity, sample S5 exerting very low lectin activity against the trypsinized rabbit erythrocytes and decreases the cell viability in EAC cells in-vitro. Sample S2, S4 and S5 exerts significant cytotoxic effect against the various human cancer cell lines and regressed the neovasculature (development of new blood vessels) in the developing CAM embryos when compared to the other crude samples. The apoptotic inducing activity of crude phloem exudate/sap samples was revealed by DNA fragmentation assay, caspase-3 inhibitor assay and cellular morphology were studied by fluorescence staining methods. Conclusion: This study reports that some of the isolated crude phloem exudate/sap samples show potent lectin activity and anti-cancer activity in different human cancer cell lines. The further additional experiment needs to purify and characterize the bioactive lectin components from the potent sample which is responsible for pro-apoptotic, anti-angiogenic activity and mechanism involved.

}, keywords = {Angiogenesis, Apoptosis, EAC, Haemagglutination, Lectin, VEGF}, doi = {10.5530/pj.2019.11.91}, author = {Balaji Kyathegowdanadoddi Srinivas and Madhu Chakkere Shivamadhu and Preethi Saligrama Devegowda and Gurukar Mathew and Theethagounder Tamizhmani and Senthilkumar Gnanavadevel Prabhakaran and Shankar Jayarama} } @article {767, title = {Ameliorative Effect of Moringa oleifera Fruit Extract on Reproductive Parameters in Diabetic-induced Male Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s54-s58}, type = {Original Article}, chapter = {s54}, abstract = {

Background: Diabetes mellitus negatively impact the male reproductive parameters. The ability of Moringa oleifera fruit to improve the reproductive parameters in diabetic-induced male has yet to be documented. Aim: To investigate the anti-hyperglycaemic potential of M. oleifera fruit aqueous extract and its effect on reproductive parameters in diabetic-induced male rats. Materials and Methods: A total of 20 male Sprague Dawley rats were divided into four groups; normal control (without diabetic induction), negative control (diabetes without treatment), positive control (diabetes with metformin) and treatment group (diabetes with 500 mg/kg M. oleifera fruit aqueous extract). Treatments were given via oral gavage for 21 consecutive days. Analysis of fasting blood glucose level, sperm quality, testicular histology and relative testis weight were performed. Results: The administration of M. oleifera fruit aqueous extract exhibited a significant reduction in fasting blood glucose level and a pronounced increase in sperm quality (sperm count, motility, viability and morphology) compared with the negative control group. M. oleifera fruit extract restored the histology of the testes as they were seen to be packed with sperms and showed an organised spermatogenesis. The relative testis weight showed no significant difference between all groups. Conclusion: The results obtained suggested that M. oleifera fruit aqueous extract possessed an antihyperglycaemic property and improved the reproductive parameters in diabetic-induced rats

}, keywords = {Diabetes mellitus, Fasting blood glucose level, Male reproductive, Moringa oleifera fruit, Sperm quality}, doi = {10.5530/pj.2018.6s.10}, author = {Amira Kamalrudin and Malina Jasamai and Mahanem Mat Noor} } @article {507, title = {Anthelmintic Activity of Fruit Extract and Fractions of Piper longum L. In vitro}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {333-340}, type = {Original Article}, chapter = {333}, abstract = {

The present study was aimed to assess the in vitro ovicidal, larvicidal and adulticidal activity of methanolic extract and its fractions from fruits of Piper longum against strongyle ova, larvae and adult amphistomes respectively. The fruits of P. longum was identified and the accession number 006 was obtained. The phytochemical analysis revealed the presence of tannins, flavonoids, glycosides, phenolics, diterpenes and triterpenes in extract and fractions of P. longum. The extract and fractions were diluted serially in 6.25 per cent tween 80 to obtain concentrations of 500, 250, 125, 62.5, 31.25, 15.63, 7.81, 3.91 and 1.95 mg/mL. Ivermectin and thiabendazole at 10 \μg/mL acted as positive controls and 6.25 per cent tween 80 as negative control. The methanolic extract was highly active against ova with IC50 of 0.026 mg/mL. The n-hexane fraction was potent in inducing larval mortality with IC50 of 1.383 mg/mL while chloroform fraction inhibited larval migration with IC50 of 1.796 mg/mL. Amphistomes were highly sensitive for methanolic extract of P. longum which possessed IC50 of 5.493 mg/mL Based on IC50 values, the methanolic extract was found to be most potent while chloroform fraction was effective against ova, larvae and also adults. GCMS analysis of potent methanolic extract revealed the presence of piperidinone, hydrocinnamic acid, ethylhexahydro azepine, methyleugenol, hexadecanoic acid and caryophyllene oxide which may have contributed for the anthelmintic activity. The acute oral toxicity study revealed mild vascular changes in liver. From the present study, it can be concluded that chloroform fraction of P. longum possessed maximum broad spectrum anthelmintic activity comparable to controls.

}, keywords = {Adulticidal, GCMS, IC50, Larvicidal, Ovicidal, Piper longum.}, doi = {10.5530/pj.2018.2.57}, url = {http://fulltxt.org/article/487}, author = {Krishnaprasad Ganapati Koorse and Sujith Samraj and Preethy John and Priya Manakkulaparambil Narayanan and Devi SS and Usha PTA and Surya Sunilkumar and Gleeja VL} } @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 {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 {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 {772, title = {Inhibitory Actions of Lagerstroemia speciosa (L.) Pers. Aqueous and Ethanolic Leaf Extracts against Carbohydrate-digesting Enzymes}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s113-s118}, type = {Original Article}, chapter = {s113}, abstract = {

Context: The leaves of Lagerstroemia speciosa (L.) Pers. (banaba) have been consumed traditionally in several Southeast Asian countries for the treatment of diabetes mellitus. The plasma glucose lowering actions of this medicinal plant were proposed to be linked with several mechanisms of action. However, its inhibitory actions against \α-amylase and \α-glucosidase, which play a major role in the regulation of postprandial plasma glucose, have not been clearly established. Aims: This study thus aimed to investigate the effects of Lagerstroemia speciosa (L.) Pers. aqueous and ethanolic leaf extracts (LSA and LSE extracts, respectively) on in vitro carbohydrate-digesting enzyme activities and enzyme kinetics. Settings and Design: In vitro carbohydrate-digesting enzyme activity assay. Materials and Methods: The activities of \α-amylase and \α-glucosidase were indicated by the amounts of maltose and p-nitrophenol generated in the reactions, respectively. Statistical analysis used: The data were analysed by using one-way ANOVA, followed by Bonferroni post-hoc test. Results: The LSA extract significantly inhibited both \α-amylase and \α-glucosidase enzymes with the IC50s of 1.21\±0.16 and 49.71\±0.86 \μg/mL, respectively. Meanwhile, the LSE extract selectively inhibited \α-amylase activity (IC50 = 22.21\±4.00 \μg/mL) with no apparent inhibition against \α-glucosidase activity. Both LSA and LSE extracts inhibited \α-amylase enzyme in a mixed inhibition manner whilst the LSA extract also acted as a mixed inhibitor against \α-glucosidase enzyme. The extracts possessed higher binding affinities toward the enzymes, indicated by the lower Ki values, when compared to acarbose (positive control). Conclusion: These results suggest the potential use of the extracts for a control of postprandial plasma glucose.

}, keywords = {Diabetes mellitus, Lagerstroemia speciosa (L.) Pers., α-amylase, α-glucosidase}, doi = {10.5530/pj.2018.6s.22}, author = {Wanwisa Khunawattanakul and Passakorn Boonma and Ronnarit Kampetch and Achida Jaruchotikamol and Benjamart Cushnie and Sakulrat Rattanakiat and Pawitra Pulbutr} } @article {514, title = {Isolation, Characterization and in vitro Pharmacological Activities of Tagetes Erectus Linn}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {384-393}, type = {Original Article}, chapter = {384}, abstract = {

Tagetes erectus (family: Asteraceae), commonly known as \‘African marigold\’, is an ornamental plant widely distributed in India. The plant has been used in traditional medicines in India and elsewhere in the treatment of cold, bronchitis, rheumatism and inflammation. The flavonoid quercetin has been isolated from the methanol extract of the plant by column chromatography and identified by co-TLC, comparison of its melting point, UV, IR and NMR spectra. Quercetin content has been estimated as 1.22 (\±0.26) \% in the methanol extract of Tageteserectus whole plant based on HPTLC method using the solvent systemchloroform: methanol (8.5:1.5). The essential oil was isolated by hydrodistillation (oil yield 0.04\% v/w) and 25 compounds comprising 93.9\% of the constituents were identified by GC-MS analysis. Monoterpenoids Predominated the oil (78.5\%), with piperitone as the major compound (40.1\%) followed by terpinolene (12.7\%) and limonene (12.0\%). The in vitro antioxidant assays of the methanol extract showed moderate activity with IC50 values 109.45 (\±1.22) g/ml for DPPH radical scavenging assay and 201.53 (\±4.48) g/ml for superoxide scavenging assay and the marker compound quercetin showed IC50 values 26.40(\±1.75) and 13.87 (\±0.54) g/ml respectively. Reducing power assay also showed moderate activity. Antibacterial activity of the methanol extract and the essential oil against gram positive and gram-negative bacteria were done using disc diffusion method. The essential oil showed remarkable activity against the tested organisms, while the extract showed only moderate activity.

}, keywords = {Antibacterial activity, Disc diffusion method, DPPH radical scavenging assay, Flavonoids, Quercetin, Terpinolene}, doi = {10.5530/pj.2018.2.64}, url = {http://fulltxt.org/article/495}, author = {Resmi S and Divya V Nair and Athulya Subhash and Rose Jose and Vishnu V and Subin Mary Zachariah} } @article {568, title = {Nephroprotective Effect of Aqueous Extract of Pimpinella anisum in Gentamicin Induced Nephrotoxicity in Wistar Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {403-407}, type = {Original Article}, chapter = {403}, abstract = {

Background: Pimpinella anisum known for its various medicinal properties is also a natural antioxidant and a free radical scavenger with no documented evidence as a nephroprotective agent. Objective: To evaluate the nephroprotective activity of aqueous extract of Pimpinella anisum seeds in a rodent model of gentamicin induced nephrotoxicity. Materials and Methods: Wistar albino rats of either sex, weighing 150\–200 g was divided into 5 groups; normal saline, gentamicin 80mg/kg, intraperitoneally for 8 days, aqueous extract of Pimpinella anisum seeds at 1, 2, and 4g/kg, per oral for 8 days, the test extract administered 3 days prior and concurrently with gentamicin for 5 days. Blood urea, serum creatinine, uric acid and blood urea nitrogen analyses and microscopic examination of kidney were performed. Results: Gentamicin treatment caused nephrotoxicity as evidenced by marked elevation in serum urea, serum uric acid, serum creatinine and blood urea nitrogen (107.5\±16.92mg/dl, 0.8\±0.09 mg/dl, 3.05\±0.29 mg/dl, 47.8\±9.07 mg/dl) respectively when compared to the saline treated groups. Co-administration of Pimpinella anisum extract with gentamicin decreased the rise in these parameters in a dose dependent manner. Histopathological analysis revealed epithelial loss with intense granular degeneration in gentamicin treated rats, whereas aqueous extract of Pimpinella anisum mitigated the severity of gentamicin-induced renal damage. Conclusion: To conclude, our data suggest that aqueous extract of Pimpinella anisum exhibits renoprotective effect in gentamicin induced renal damage and further studies on its mechanism of action are warranted.

}, keywords = {Aniseed, Drug induced nephrotoxicity, Gentamicin, Nephroprotective, Pimpinella anisum}, doi = {10.5530/pj.2018.3.66}, url = {http://fulltxt.org/article/532}, author = {Nair Aiswarya and Rao Rashmi R and Shenoy Preethi J and Vinod Chandran and S Teerthanath and Pai Sunil B and KB Rakesh} } @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 {719, title = {Phytochemical Screening and Antimicrobial Studies in Leaf Extracts of Indigofera aspalathoides (Vahl.)}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1208-1215}, type = {Original Article}, chapter = {1208}, abstract = {

Introduction: In traditional Indian herbal medicine, the plant Indigofera aspalathoides (Vahl.) has been used to treat various human ailments. Methods and Results: Various phytochemical compounds (Rf value) such as Tannin (1.14), Flavonoid (1.14), Saponin (0.87), Sterol (0.88) and Phenol (0.86) were found in the leaf extract. The antimicrobial effects of the phytoconstituents were examined for three bacterial and fungal species. The highest anti-bacterial and antifungal activities were found in flavonoid compound, where the maximum zone of inhibition was recorded in Staphylococcus aureus 18mm compared to positive control chloramphenicol (24mm). 13mm observed in A. flavus and A. ochraceous where positive control streptomycin exhibits 18mm. GC-MS analysis revealed the presence of three major compounds in 8\α (2H)-Phenanthrenol, 7-ethenyldodecahydro-1,1,4\α, 7-tetramethyl-, acetate, [4\αs(4\α\α, 4b\α, 7\α, 8\α\α, 10\α\α)], Benzoic acid, 4-methyl- , 2-oxo-2- phenylethyl ester and Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1S-(1\α,2\α,5\α)] in the crude extracts. The preparative HPLC analysis proved the presence of single peak from the crude flavonoid compounds, where the absorption maximum was between 207-290nm exhibited by the UV spectrum analysis. FTIR spectrum confirmed the presence of amide group, phenol group, carboxylic acid, alkynyl, alkene and aromatic ring. NMR studies proved the presence of phenyl group, methyl group and H2C-CH group and their molecular weight recorded as 353 through the mass spectrum analysis. Conclusion: The identified compound considered as the vital compound to design the \“green antimicrobial drugs\”.

}, keywords = {Antimicrobial activities, GC-MS, HPLC, Indigofera aspalathoides, MS, NMR}, doi = {10.5530/pj.2018.6.207}, author = {Tamilarasan Tamil Kumar and Seeni Mohamed Salique and Mohamed Hussain Muhammad Ilyas and Nooruddin Thajuddin and Annamalai Panneerselvam and Mohamed Khan Syed Ali Padusha and Hussain Syed Jahangir} } @article {489, title = {Phytochemical Screening, Antibacterial Activity, and Mode of Action on Morus nigra}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {167-171}, type = {Original Article}, chapter = {167}, abstract = {

Introduction: The Morus nigra (Moraceae) known as black mulberry is a well-grown plant in Lembang, Indonesia. Previous studies showed that black mulberry fruit has activity as antibacterial and antioxidant. The aims of this study were to evaluate the antibacterial effect of ethanol extract from stem bark, fruit, and leaves of Morus nigra, MIC and morphological changes of the most active extract against Staphylococcus epidermidis and Propionibacterium acnes. Methods: Agar diffusion and microdilution assays were used to evaluate the antibacterial effect of the extract by measuring the zone of inhibition and the minimum inhibitory concentration (MIC) of the extract against the test bacteria. Scanning electron microscopy (SEM) was performed to evaluate the morphological changes induced by the extract in cellular membrane of the bacteria. Protein and ion leakage from the bacterial cells induced by the extract were also evaluated. Results: The antibacterial activity showed the most active extract was an ethanol extract of the stem bark against S. epidermidis and P. acnes with MIC value 4 mg/ml and 2 mg/ml, respectively. The extract also induced protein and ion leakage in test bacterial cells. SEM findings revealed that the extract induced potential cellular membrane damage in 4xMIC. Conclusion: The antibacterial activity was related to the damaged of bacterial cell wall.

}, keywords = {Cellular membrane damage., Morus nigra, Propionibacterium Acnes, Staphylococcus Epidermidis}, doi = {10.5530/pj.2018.1.28}, url = {http://fulltxt.org/article/414}, author = {Diah Lia Aulifa and Sani Nurlaela Fitriansyah and Seno Aulia Ardiansyah and Diki Prayugo Wibowo and Yolanda Armiliani Julata and Desty Santi Christy} } @article {633, title = {Potential Effects of Pomegranate Juice in Attenuating LID in Mice Model of Parkinson Disease}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {700-704}, type = {Original Article}, chapter = {700}, abstract = {

Purpose: Parkinson\’s disease (PD) is one of the most important neurodegenerative diseases, known with tremor, rigidity and bradykinesia resulted from chronic degeneration and death of sub thalamic nucleus (STN). According to the treatment benefits of levodopa on Parkinson, long-term levodopa administration causes some complications called levodopa-induced dyskinesia (LID) with poorly understood pathogenesis. Literature shows that polyphenol rich compound like pomegranate protect neurons of animals that are Parkinson induced, with some controversy. Objectives: In this study, the potential effects of pomegranate in attenuating LID in parkinsonian mice induced with 4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP) were investigated. Materials: Mouse model of PD was induced by MPTP. To induce LID, valid PD mice were treated with levodopa (50 mg/kg, i.p) for 21 days. Then the effects of chronic co-administration of pomegranate juice (20 ml/kg) orally, with levodopa and continuing for another 20 days, evaluated. Behavioural tests were performed in all groups, every other day including: Abnormal involuntary movements (AIMs), cylinder and catatonia tests. Results: Levodopa in chronic administration induced dyskinesia that observed in AIMs and cylinder tests for 3 weeks when compared to untreated animals (P\<0.05 or 0.01) depending the time course). Besides, catatonia was recorded after two weeks and mounted time-dependently compared to control (P\<0.01). Chronic pomegranate co-administration improved AIMs scores for next 20 days (P\<0.01, in following days, compared to no-pomegranate treated group), attenuated cylinder scores and catatonia rates dramatically and time dependently (P\<0.01). Conclusion: Chronic pomegranate co-administration improved movements in all test results. It is then, concluded that pomegranate can be a good adjunct for attenuating LID and catatonia in mice.

}, keywords = {Levodopa-induced dyskinesia (LID), Mice, MPTP, Parkinson{\textquoteright}s disease, Pomegranate}, doi = {10.5530/pj.2018.4.116}, url = {http://fulltxt.org/article/654}, author = {Sarah Rezaee and Mahsa Hadipour Jahromy} } @article {460, title = {Aristolochia bracteolata Enhances Wound Healing in vitro through Anti-inflammatory and Proliferative Effect on Human Dermal Fibroblasts and Keratinocytes}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {November 2017}, pages = {s129-s136}, type = {Original Article}, chapter = {s129}, abstract = {

Objective: In the present study, we examined the effect of Aristolochia bracteolata extract on Human dermal fibroblast (HDF) and Human keratinocyte cell line (HaCaT) proliferation and migration during in vitro wound healing and its underlying mechanism. Method: A. bracteolata was collected and extracted using methanol. Cytotoxiciy effect of plant extract was determined by MTT assay in HDF and HaCaT. In vitro Scratch assay determined the effect of plant extracts on migration of cells and its underlying mechanism was determined by RT-PCR analysis. Result: The plant extract of A. bracteolata selectively inhibited proliferation of both the cells at higher concentration (\>100 \μg/mL) and at lower concentrations (\<25 \μg/mL), it exhibited linear and dose-dependent cell proliferation. IC50 value was 87.60\±1.67 \μg/mL for HDF and 85.50\±1.65 \μg/mL after 24 h treatment. In vitro scratch wound healing studies showed wound closure of 50.38\%\±1.39 and 69.81\%\±1.89 at a concentration of 25 \μg/mL after 24 h and 48 h, respectively. The extract was tested for anti-inflammatory activity by determination of inhibitory activity on lipopolysaccharide (LPS) induced nitric oxide (NO) production in RAW 264.7 cell lines. We found that A. bracteolata has a strong inhibitory effect on the production of NO and tumor necrosis factor-\α (TNF-\α). The plant extract of A. bracteolata inhibited inducible nitric oxide synthase (iNOS) gene expression by lipopolysaccharide (LPS). To explore the mechanism responsible for the inhibition of iNOS, gene expression was analyzed by Real- Time PCR. A. bracteolata showed a decrease in the expression of pro-inflammatory cytokine mRNA in a concentration-dependent manner. Treatment with the plant extract resulted in enhanced expression of Collagen 1 a (I) and Collagen IV in HDFs by regulating the mRNA levels of extracellular matrix (ECM) proteins and Matrix metalloproteinase-2. Conclusion: Thus, the present investigation scientifically validates the use of A. bracteolata in wound healing.

}, keywords = {A. bracteolata, Fibroblast, Keratinocytes, RAW 264.7, Scratch assay, Wound Healing}, doi = {10.5530/pj.2017.6s.169}, url = {http://fulltxt.org/article/394}, author = {Dinesh Murugan Girija and Mangathayaru Kalachaveedu and Rajasekaran Subbarayan and Preethi Jenifer and Suresh Ranga Rao} } @article {428, title = {Determination of Antipyretic and Antioxidant Activity of Cassia occidentalis Linn Methanolic Seed Extract}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {913-916}, type = {Original Article}, chapter = {913}, abstract = {

Objective: To perform the pharmacognostical screening and determination of antipyretic and antioxidant activity of Cassia occidentalis L. Methanolic seed extract by different in-vitro models. Methods: The different pharmacognostical parameters were evaluated as per standard procedure. Finally, antipyretic (Brewer\’s Yeast Pyrexia model) and antioxidant activity (DPPH and Hydrogen Pyrode Method) was evaluated by adopting different methods. Results: The extracts showed a marked antipyretic effect (Figure 1) by causing a reduction in yeast-induced fever. Methanolic extract (400 mg/kg) showed the effect to the same degree as paracetamol (20 mg/kg, i.p.). The experimentally induced laboratory model was employed in evaluating the antipyretic activities of methanolic extracts of Cassia occidentalis L. The extract caused a better hypothermal activity against yeast-induced pyrexia in rats. Free radical scavenging activity of Cassia occidentalis L. was found because polyphenolic compounds present in plant contribute significantly to the total antioxidant capacity of the seed. Flavonoids play some important pharmacological roles against diseases, such as cardiovascular diseases, cancer, inflammation and allergy. Conclusion: The results of the study indicate that the methanolic seed extract of Cassia occidentalis L. possesses strong antipyretic and antioxidant activity. This study described many pharmacognostical features and antioxidant activity of seeds of Cassia occidentalis L. which will give a new direction for the future scientific research.

}, keywords = {Antioxidant., Antipyretic, Cassia occidentalis L., Pharmacological, Phytochemical}, doi = {10.5530/pj.2017.6.143}, url = {http://fulltxt.org/article/196}, author = {Vijay Vikram Singh and Jainendra Jain and Arun Kumar Mishra} } @article {366, title = {Evaluation of Antidiabetic Activity of Hydroalcoholic Extract of Cassia fistula Linn. pod in Streptozotocin-Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {July 2017}, pages = {599-606}, type = {Original Article}, chapter = {599}, abstract = {

Background: Diabetes mellitus (DM) is a global health problem and the incidence of DM is increasing at alarming rate all over the world. Many Indian medicinal plants have been reported to possess potential antidiabetic activity and could play important role in the management diabetes. Objective: The present study aimed to evaluate antidiabetic activities of 70\% ethanolic extract of Cassia fistula pod in streptozotocin-induced diabetic rats. Materials and Methods: Diabetes was induced in male Wistar rats by single intraperitoneal injection of streptozotocin (60 mg/kg b.wt.). The diabetic rats were administered orally with C. fistula pod extract at three different doses (100, 250 and 500 mg/kg b.wt./day) for 60 days. The results were compared with standard drug glibenclamide (5 mg/kg b.wt./day) treated rats. Results: The streptozotocin treated diabetic control rats showed a significant increase in the blood glucose and glycosylated hemoglobin (HbA1c) levels with a concomitant decrease in the body weight and glycogen content in the liver as compared to normal control rats. Oral administration of C. fistula pod extract (100, 250 and 500 mg/kg b.wt./day) or glibenclamide for 60 days showed significant reduction in the blood glucose and HbA1c levels and an elevation in the body weight and hepatic glycogen content as compared to diabetic control rats. Furthermore, treatment with extract (500 mg/kg b.wt.) also showed improvement of oral glucose tolerance test (OGTT) in diabetic rats. These results were comparable to glibenclamide. Conclusion: The results of present study showed that C. fistula pod extract possess significant antihyperglycemic activity and supports the traditional use of C. fistula pod for the treatment of diabetes mellitus.

}, keywords = {Antidiabetic, Blood glucose, Cassia fistula, Glycogen, Glycosylated Hemoglobin, Streptozotocin}, doi = {10.5530/pj.2017.5.95}, url = {/files/pj-9-5/10.5530pj.2017.5.95/index.html}, author = {Ram Niwas Jangir and Gyan Chand Jain} } @article {427, title = {Evaluation of in vitro Antioxidant and Anticancer Activity of Simarouba glauca Leaf Extracts on T-24 Bladder Cancer Cell Line}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {906-912}, type = {Original Article}, chapter = {906}, abstract = {

Objective: Screening of preliminary phytochemicals, evaluation of in vitro antioxidant and in vitro anticancer activities of Simarouba glauca leaf extracts on T-24 Bladder cancer cell line. Materials and Methods: Herbal extraction was carried out by Soxhlet method using chloroform, ethylacetate, methanol, ethanol, aqueous and hydroalcohol. Phytochemical investigation was done using biochemical tests. Total phenolic content was estimated by Folin-Ciocalteu reagent (FCR) method. Antioxidant potential of leaf extracts was analyzed by Ferric ion reducing antioxidant power (FRAP) assay, Phosphomolybdenum (PM) assay and 2,2-Diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay. In vitro anticancer activity on T-24 bladder cancer cell line was assessed by MTT assay. Statistical analysis used: Statistical analysis of data was performed by analysis of variance (one-way ANOVA) and level of statistical significance between groups was carried out using GraphPad Prism version 5.0 for Windows (GraphPad Software, San Diego, CA, USA). Results: Phytochemical analysis revealed the presence of rich secondary metabolite present in all the solvent extracts. Hydroalcoholic extract showed highest presence of phenolic content (92.38\±0.29 mg/g) GAE. Ethanol and methanol extract showed highest antioxidant capacity in DPPH, FRAP and PM assay as compared to the other extracts based on the test performed. The results confirmed that ethanol extract significantly (p\<0.05) inhibited T-24 cell line with IC50 value (533.55\±25.02 \μg/mL) as compared to standard drug doxorubicin (0.16\μM/mL). Conclusions: The results of the present findings strengthen the potential property of Simarouba glauca as a resource for the discovery of novel antioxidant and anticancer agents.

}, keywords = {Antioxidant; Anticancer; Bladder Cancer; Phytochemical; Simarouba glauca.}, doi = {10.5530/pj.2017.6.142}, url = {http://fulltxt.org/article/195}, author = {Sridevi I Puranik and Shridhar C Ghagane and Rajendra B Nerli and Sunil S Jalalpure and Murigendra B. Hiremath} } @article {229, title = {GC-MS Analysis of Ethyl Acetate Extract of Whole Plant of Rostellularia diffusa}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {December 2016}, pages = {70-72}, type = {Original Article}, chapter = {70}, abstract = {

Introduction: To identify the various phyto constituents present in the unexplored plant Rostellularia diffusa (Willd.) by using gas chromatography and mass spectrometry. Methods: The whole plant of Rostellularia diffusa was extracted with ethyl acetate at room temperature for 72 h. The concentrated extract was subjected to GCMS analysis to detect the phyto constituents. Results: Totally 40 compounds were identified and the chromatograph showed 40 peaks with 40 individual compounds. The major constituents were identified in the extract were 16-Hentriacontanone (22.59\%), Hexadecanoic acid (11.23\%), Stigmast-5-en-3-ol (6.78\%), 9-Octadecenoic acid (6.30\%) and many other compounds were identified as low level. This preliminary study gives an idea to isolate the major active constituents present in the plant and also helps to develop potential pharmacologically active compounds

}, keywords = {Bioactive compounds, Gas chromatography, Mass spectrometry, phytosterol., Rostellularia diffusa}, doi = {10.5530/pj.2017.1.13}, author = {Mohamed Saleem Thattakudian Sheik Uduman and Prema Rathinam and Yogendrachari Karuru and Gangadhar Obili and Gopinath Chakka and Ashok Kumar Janakiraman} } @article {457, title = {In vitro Antioxidant and Hepatoprotective Activity of Bridelia scandens (Roxb.)Willd}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {November 2017}, pages = {s117-s121}, type = {Original Article}, chapter = {s117}, abstract = {

Natural products are emerging out as potent and alternative therapies for many diseases. Today herbs have become the part of mankind, because of its manifold ways in targeting diseased cells with minimal effects on normal cells and tissues. The present research investigated the in vitro antioxidant activity and hepatoprotective of B.scandens leaf. Preliminary phytochemical analysis exhibited the presence of most of the constituent in ethanol extract (BSE). Antioxidant capacity of various extracts of B.scandens was examined. DPPH assay revealed that ethanol extract has a good antioxidant with IC50 value of 31.68\μg/ml, whereas standard ascorbic acid with 8.78 \μg/ml. BSE revealed dose dependent response with increase in concentration for reducing power assay. ORAC assay directly measured the scavenging capacity and BSE (2485 trolox eq/gm) was found to be potent than other extracts. In vitro hepatoprotective activity was performed for BSE using MTT assay in BRL 3A cell line, which revealed nontoxic dose with CTC50 value more than 1000 \μg/ml. At the dose 200 \μg/ml, BSE and standard silymarin offered cell protection of 57\% and 76 \% respectively. Present study concludes that B.scandens leaf extract possess antioxidant potential and protect the liver cells against CCl4 damage. However in vivo studies are being carried out to validate the traditional usage of Bridelia scandens.

}, keywords = {Bridelia scandens, BRL3A, Hepatoprotective, MTT, ORAC}, doi = {10.5530/pj.2017.6s.167}, url = {http://fulltxt.org/article/392}, author = {Preetham Jinadatta and Kiran Sundera Raja Rao and Sharath Rajshekarappa and Sujan Ganapathy Pasura Subbaiah and Mruthunjaya Kenganora} } @article {426, title = {In vitro \& ex vivo Acetylcholinesterase Inhibitory Activity of Morinda citrifolia Linn (Noni) Fruit Extract}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {900-905}, type = {Original Article}, chapter = {900}, abstract = {

Background: Psychological problem is a key medical issue for numerous neuropsychiatric and neurodegenerative diseases, for example, schizophrenia, Alzheimer\’s, dementia, seizure and Parkinsonism. Morinda citrifolia (Noni) has been utilized for a considerable length of time to cure or counteract assortment of diseases by conventional therapeutic professionals in Hawaii and Polynesia. Objective: The present study is focused to identify the neuroprotective activity of Morinda citrifolia fruit extract (MCFE) on in vitro and ex vivo animal model by inhibition of acetylcholinesterase (AChE), an enzyme target used for the treatment of Alzheimer\’s disease. Methods: Acetylcholinesterase inhibition assay was performed by in vitro \& ex vivo methods as described by Ellman et al. In vitro antioxidant assay of the extract was performed by DPPH free radical scavenging activity \& nitric oxide scavenging activity. Statistical analysis used: Statistical analysis was carried out using non linear regression analysis for plotting the line of best fit for the observed values using Graph- Pad Prism software. Results: By performing in vitro antioxidant assay the IC50 value of the standard quercetin was found to be 46.22 \μg/ml as compared to the MCFE which has an IC50 value of 43.14 \μg/ml for DPPH free radical scavenging activity. Similarly the IC50 value of the standard ascorbic acid was found to be 81.85 \μg/ml as compared to the MCFE which has an IC50 value of 148.0 \μg/ml for nitric oxide scavenging activity. Acetylcholinesterase inhibition assay was performed by in vitro method and the IC50 value of MCFE and neostigmine was found to be 31.84 \μg/ml \& 19.71 \μg/ml respectively. Conclusions: The present study investigated the neuroprotective activity of MCFE and it was identified by both in vitro and ex vivo techniques that the phytoconstituents has the ability to improve the learning and memory function by inhibiting the acetylcholinesterase.

}, keywords = {Acetylcholinesterase, ex vivo., in vitro, Morinda citrifolia, Neuroprotective activity, Noni}, doi = {10.5530/pj.2017.6.141}, url = {http://fulltxt.org/article/194}, author = {Srikanth Jeyabalan and Kavimani Subramanian and Uma Maheswara Reddy Cheekala and Chitra Krishnan} } @article {340, title = {Neuropathic Pain: Literature Review and Recommendations of Potential Phytotherapies}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {May 2017}, pages = {425-434}, type = {Review Article}, chapter = {425}, abstract = {

Introduction: One of the common syndromes that affect humanity is neuropathic pain (NP), yet poorly understood with no efficient treatment till now. Consequently, it is extremely crucial to seek further evidence for accurate diagnosis and optimum treatment. The aim of this work is to summarize the findings related to neuropathic pain in terms of etiology, types, diagnosis, current and future management prospective, and identify the gaps in neuropathic pain therapy. Methods: A literature investigation was carried out by analyzing classical peer reviewed papers and textbooks, taking into consideration worldwide well established scientific databases mainly PUBMED and SCOPUS to retrieve accessible published literature. The selection of phytotherapies was based upon their potentials in relieving NP in pre-clinical or clinical models. Results: One of the most critical points in this research is that recommendations of the future plans should be focused on the engagement of phytotherapy in the treatment regimen aiming at improving patients\’ quality of life and reaching optimum efficacy and minimum toxicity. Phytotherapies offer relatively low-risk options to NP patients and have an increasing evidence to be the future of neuropathic pain management. Patients suffering from neuropathy are depending increasingly on phytotherapies; however, they need more clinical trials in order to fully understand their mechanism of actions. Conclusion: Health-care specialists should be regularly informed about neuropathic pain current therapies and promising future phytotherapies, bearing in mind the risk/benefit profile of the utilization of these therapies in the amelioration of NP.

}, keywords = {Current therapies, Diagnosis, Mechanisms, Neuropathy Pain, Phytotherapies, Recommendations}, doi = {10.5530/pj.2017.4.72}, url = {/files/PJ-9-4/10.5530pj.2017.4.72}, author = {Karim Raafat and Rawan El-Haj and Dania Shoumar and Rana Alaaeddine and Yousra Fakhro and Natalie Tawil and Farah Shaer and Amani Daher and Natalie Awada and Ali Sabra and Khouloud Atwi and Malak Khaled and Raneem Messi and Nour Abouzaher and Mohamed Houri and Samer Al Jallad} } @article {217, title = {A Review of Pharmacognostical Studies on Moringa oleifera Lam. flowers}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {December 2016}, pages = {1-7}, type = {Review Article}, chapter = {1}, abstract = {

Moringa oleifera Lam. of the family Moringaceae, popularly called \‘miracle tree\’ is a native of sub Himalayan tracts of Northern India and is widely cultivated in tropical and subtropical regions. Research on Moringa mainly pivoted around its leaves and seeds because of their immense nutraceutical potential but recently there is a greater interest in flowers too, mostly inspired by the positive outcomes of several pharmacognostical studies on flowers. Moringa flower is a rich reservoir of bioactive phytochemicals and crude flower extracts showed promising antibacterial, antifungal, anti larval, antioxidant, anti inflammatory and anticancer properties. This review concisely presents the various phytochemicals identified and isolated as well as the various bioassays employed to validate the therapeutic potential of flower. It is prepared after a detailed search on Google scholar. Reports on Moringa oleifera flower were sorted and tabulated based on the bioassays performed and solvents used for extraction. A grading pattern is adopted for comparing efficiency of different extracts in eliciting bioactivities. Many of these studies are at the preliminary stage but two of them present advanced mechanisms. First is the presence of a proteinaceous larvicidal compound \‘MoFTI\’ in the flower capable of inhibiting larval trypsin of Aedes aegypti. The second describes flower extract\’s anti inflammatory mechanism effecting via NF-KB pathway and consequent suppression of inflammatory mediators\’ activation, but short of identifying lead compound/compounds behind this effect. Thus authors suggest further studies to elucidate the detailed mechanisms, identify and isolate the active compound or compounds of synergism behind the many therapeutic potential of the Moringa flower extracts.

}, keywords = {Bioactivity, Bioassay, Extracts, Flower, GCMS, Moringa, Phytochemicals, Therapeutic}, doi = {10.5530/pj.2017.1.1}, url = {/files/PJ-9-3/10.5530pj.2017.1.1}, author = {Tom Mathew Kalappurayil and Benny Pulinilkkumthadathil Joseph} } @article {326, title = {Sub-acute Toxicity Study of The Ethyl Acetate Fraction of Asam Kandis Rinds (Garcinia cowa Roxb.) on the Liver and Renal Function in Mice}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017 }, pages = {345-349}, type = {Original Article}, chapter = {345}, abstract = {

Objective: The present study investigated the sub acute toxicity of the ethyl acetate fraction of asam kandis (Garcinia cowa Roxb) Rinds in mice. Material and Methods: Sub acute toxicity study was carried out by giving orally at dose 500, 1000 dan 2000 mg / kgBW extract to five mice at 21 days. Animals were observed individually for any clinical signs of toxicity or mortality for 14 days. Measured parameters were SGPT levels, serum creatinine levels, weight ratio of liver and kidney. Extract was given orally at dose 500, 1000 and 2000 mg/kgBW for 21 days. Observations were done on day 8th, 15th and 22th using blood serum, liver and kidneys of mice. Data were analyzed by using two-way ANOVA followed by Duncan\’s Multiple Range Test. Results: The ethyl acetate fraction of G. cowa at doses 500, 1000 and 2000 mg/kgBW gave significant effect on increasing SGPT levels and decreasing levels of serum creatinine (p \<0.05). The length of treatment gave significant effect on decreasing levels of serum creatinine, weight ratio of liver and kidney (p \<0.05). Conclusion: The dosage of the ethyl acetate fraction of asam kandis rinds provides significant effect on the SGPT and serum creatinine levels of male white mice. The duration of administration of ethyl acetate fraction of asam kandis rinds provides significant effect on serum creatinine levels, the weight ratio of liver and kidney organ of male white mice.\ 

}, keywords = {Creatinine serum, Garcinia cowa rinds, SGPT, Sub-acute toxicity, Weight ratio of liver and kidney}, doi = {10.5530/pj.2017.3.58}, url = {/files/PJ-9-3/10.5530pj.2017.3.58}, author = {Fatma Sri Wahyuni and Dessy Arisanty and Nelsi Fitri Hayaty and Dian Ayu Juwita and Almahdy} } @article {409, title = {To Evaluate the Antidiabetic and Rejuvenating Capability of Tissues on Alloxan Induced Diabetic Rats under the Effect of Ethanolic Leaf Extract of Coriandrum sativum: A Histopathological Study}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {792-798}, type = {Original Article}, chapter = {792}, abstract = {

Objective: To evaluate the antidiabetic and rejuvenating capability of tissues on alloxan induced diabetic rats under the effect of ethanolic leaf extract of Coriandrum sativum. Methods: Diabetic model was prepared by administration of alloxan monohydrate (150 mg/ kg i.p). The ethanolic leaf extracts of Coriandrum sativum at a dose of 200 and 400 mg/kg of body weight were administrated to diabetic induced groups for a period of 28 days. The effect of ethanolic leaf extract of Coriandrum sativum leaf extract on serum blood glucose, insulin, lipase, \α- amylase and LDH as well as kidney function test [urea, uric acid, albumin, protein and creatinine] were measured in the alloxan induced diabetic rats. Results: In the acute toxicity study, ethanolic leaf extract of Coriandrum sativum leaf was non-toxic at 2 000 mg/kg in rats. The increased insulin level, albumin and protein level, decreased blood glucose and other biochemical parameters level were observed in diabetic rats treated with both doses of ethanol extract of Coriandrum sativum leaf compared to diabetic control rats. In Histopathological study were revealed toward normal. Conclusion: Ethanolic extract of Coriandrum sativum leaf possesses significant antidiabetic and rejuvenating capability of tissues.

}, keywords = {Alloxan, Coriandrum sativum., Pancreas and Kidney Tissue, Wistar Rats}, doi = {10.5530/pj.2017.6.124}, url = {http://fulltxt.org/article/177}, author = {Bhaskar Sharma and Gaurav Sharma and Suresh Chand Joshi and Sunil Kumar Singh} } @article {101, title = {Antibacterial activity of Shin{\textquoteright}iseihaito (Xin Yi Qing Fei Tang) against Streptococcus pneumoniae}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {20-23}, type = {Original Article}, chapter = {20}, abstract = {

Objective: Shin\&$\#$39;iseihaito (Xin yi qing fei tang in Chinese, SSHT), a formula in traditional Japanese Kampo medicine and Chinese medicine comprising nine crude drugs, Gypsum, Ophiopogon Tuber, Scutellaria Root (SR, root of Scutellaria baicalensis), Gardenia Fruit, Anemarrhena Rhizome, Lilium Bulb, Magnolia Flower, Loquat Leaf, and Cimicifuga Rhizome, is commonly used to treat sinusitis associated with purulent nasal discharge and reddish nasal mucosa. We evaluated anti-bacterial activity of SSHT extract on Streptococcus pneumoniae, the major cause of bacterial sinusitis. Materials and Methods: Sterile paper disks impregnated with SSHT extract or each extract of its component were placed on sheep blood agar plates inoculated with Streptococcus pneumoniae (ATCC 49619). The diameter of inhibitory zone was measured after 20-24 h incubation. Results: SSHT extract and each water extract of Ophiopogon Tuber, SR, Gardenia Fruit, Anemarrhena Rhizome, Lilium Bulb, Magnolia Flower, and Cimicifuga Rhizome showed significant antibacterial activity against Streptococcus pneumoniae, and SR extract exhibited the largest inhibitory zone. SR extract was partitioned into AcOEt, BuOH, and water layer, and water layer was further separated into 80\% EtOH soluble and insoluble fraction. Among them, only 80\% EtOH soluble fraction was exhibited antibacterial activity. In this fraction, we found baicalin as the major compounds, and baicalin exhibited antibacterial activity against Streptococcus pneumoniae in concentration-dependent manner. \ Conclusion: SSHT has antibacterial activity against Streptococcus pneumoniae, and SR and its major constituent baicalin contribute to the antibacterial activity of SSHT against Streptococcus pneumoniae.

}, keywords = {Antibacterial activity, Baicalin, Scutellaria baicalensis, Shin{\textquoteright}iseihaito, Sinusitis, Streptococcus pneumoniae.}, doi = {10.5530/pj.2016.1.4}, author = {Toru Konishi and Masaaki Minami and Zhixia Jiang and Tetsuya Arai and Toshiaki Makino} } @article {126, title = {Medicinal Plants for Treatment of Cancer: A Brief Review}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {December 2015}, pages = {87-102}, type = {Review Article}, chapter = {87}, abstract = {

Cancer is actually a group of many related diseases that all have to do with cells. Cancer cells are characterized by unregulated growth, as well as insufficient and inappropriate vascular supply. Moreover, a core of cells was subjected to micro environmental stress conditions, and has decreased apoptotic potential through genetic alterations, thereby resulting in resistance to apoptosis. Cancer is one of the major causes of death worldwide where the number of cancer patients is in continuous rise. Cancer is a major public problem whose estimated worldwide new incidence is about 6 million cases per year. It is the second major cause of deaths after cardiovascular diseases. Chemotherapy remains the principal mode of treatment for various cancers. A number of synthetic anticancer drugs are available in practice, but the side effects and the drug interactions are major drawbacks in its clinical utility. Most of the currently used chemotherapy drugs for cancers are known to develop resistance, exhibit non-selective toxicity against normal cells and restrict by dose-limiting side effects. Hence, cancer treatment and development of drugs for this disease remains a major clinical challenge. On the other hand, plants are an exceptionally viable source of biologically active natural products which may serve as commercially significant entities in themselves or which may provide lead structures for the development of modified derivatives possessing enhanced activity and/or reduced toxicity in traeatment of cancer. Herbal medicines are now attracting attention as potential sources of anticancer agents and are widely used due to availability of the materials, affordability, relatively cheap and little or no side effects, wide applicability and therapeutic efficacy which in turn has accelerated the scientific research. For these reasons, World Health Organization (WHO) supports the use of traditional medicines which are efficacious and non toxic. In this review we have summarized few plants having anticancer activity.

}, keywords = {Allopathic Drugs, Breast cancer, Cancer, Cancer Cell Lines., Chemotherapy, Medicinal Plants.}, doi = {10.5530/pj.2016.2.1}, author = {Sonika Jain and Jaya Dwivedi and Pankaj Kumar Jain and Swaha Satpathy and Arjun Patra} } @article {139, title = {Pharmaco-Chemical characterization and Acaricidal Activity of Ethanolic Extract of Chassalia Curviflora (Wall ex Kurz.) Thwaites.}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {January 2016}, pages = {215-219}, type = {Original Article}, chapter = {215}, abstract = {

Introduction: C. curviflora, an important ethno-medicinal plant used by the Kurichia local people in Western Ghats region of Wayanad is yet to be explored pharmacologically. It is used as paste on the body of cattle and birds for curing skin diseases. Objectives: To characterize the pharmacochemical features and to study the acaricidal effect of ethanolic extract of C. curviflora on engorged female ticks of R. (B.) annutatus. Methods: The pharmaco-chemical features such as physico-chemical, proximate, phytochemical, fluorescence, and HPTLC profiling were carried out using standard techniques. The pulverized leaves were subjected to soxhlet extraction using ethanol. The ethanolic extract at different concentrations (10\% to 1.25\%) was tested against ticks using adult immersion test (AIT). Result: The preliminary phytochemical investigation showed high contents of saponins, alkaloids and flavonoids. The HPTLC profiling of ethanolic extract showed the presence of 14 polyvalent components. Based on AIT, the extract at 10\% revealed 43.76\% of inhibition of fecundity (IF) and 29.16\% of adult tick mortality. Conclusion: The results revealed that the extract has some active compounds that may influence in the reproductive system of female ticks.

}, keywords = {Acaricidal activity, Chassalia curviflora, Fecundity., HPTLC, Pharmaco-chemical, R. (B.) annutatus}, doi = {10.5530/pj.2016.3.6}, author = {Ajeesh Krishna Thumadath Palayullaparambil and Adarsh Krishna Thumadath Palayullaparambil and Sanis Juliet and Kumuthakalavalli Renganathan and Ramasubbu Raju and Sunil Athalathil and Reghu Ravindran and Leena Chandrashekar and Suresh Narayanan Nair and Srikanta Ghosh} } @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 {184, title = {Rasayana Herbs of Ayurveda to Treat age Related Cognitive Decline: An Update}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Oct 2016}, pages = {411-423}, type = {Review Article}, chapter = {411}, abstract = {

Introduction: Cognitive decline associated with aging could be minor or major neuro-cognitive disorder presenting with progressive intellectual deterioration interfering with day to day activities. Behaviour and personality changes may complicate the life in due course. Significant increase in global prevalence of people aged above 60 years has raised concerns on effective management of old age problems. Age related cognitive deficits and dementia raise to the level of epidemics and established management is yet underway. Principles of preventive health and rasayana (rejuvenative) herbs of Ayurveda are being extensively researched up on for their effectiveness in dementia. In this fourteen such herbs with anti dementia property are discussed with relevant research update. Methods: Herbs like amalaki (Emblica officinalis), hareetaki (Terminalia chebula), haridra (Curcuma longa), manduka parni (Centella asiatica), aindri (Bacopa monniera), yastimadhu (Glycirrhiza glabra), guduchi (Tinospora cordifolia), shankhapushpi (Convolvulus pleuricaulis), vacha (Acorus calamus), jyotishmati (Celastrus panniculata), kushmanda (Benincasa hispida), Jatamamsi (Nardostachys jatamamsi), ashvagandha (Withania somnifera) and kapikacchu (Mucuna pruriens (Linn.)) are already proven of their efficacy in experimental and preclinical levels. The contents and research evidences are collected from ayurveda database on medicinal plants used in Ayurveda and Siddha and other authentic literature, Google scholar, Science direct, online and print journals. Discussion: The herbs in discussion mostly act on reactive oxygen species and oxidative stress injury by antioxidant properties and neuroprotective activity. Acetylcholine esterase inhibition, N-Methyl-D-Aspartate antagonism, Dopaminergic activity, Anti-amyloidogenic activity, Inhibition of Tau aggregation, neuroprotection and immune modulation are activity path ways. Tridosha namely Kapha, Pitta and Vata may be viewed to be categorically predominant in initial, middle and final stage of dementia. Selected herbs thus can be specific based on the pathology and relevant dosha predominance. Conclusion: Rasayana herbs with current updates and inferences can serve as an eye-opener for further researches at molecular and clinical aspect.

}, keywords = {Ayurveda, cognitive decline, Dementia, Herbs, Medhya, Rasayana.}, doi = {10.5530/pj.2016.5.1}, author = {Reena Kulkarni and Suhas Kumar Shetty and Rajarajeshwari N M and Prasanna Narasimha Rao and Nayan J} } @article {104, title = {Seed oil chemical composition of Platychaeteaucheri (Boiss.) Boiss}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {42-43}, type = {Original Article}, chapter = {42}, abstract = {

Background: Platychaete aucheri is an endemic plant to the south of Iran and no phyochemical investigations is reported on the seeds oil. Materials and Methods: The chemical composition of Platychaete aucheri seeds oil was extracted by suxhelet apparatus, methyl esterificated and analyzed by GC and GC/MS spectroscopy method. Results: 16 compounds were determined in total and taraxasterol (19.0\%), \γ-sitosterol (14.1\%) and lupeol (11.8\%) were characterized as the most abundant components. Conclusion: Regarding the presence of high amounts of triterpenoids and sterols in the seed oil, related biological activities are expected from the studied oil.

}, keywords = {Asteraceae, gamma-Sitosterol., Platychaete aucheri, Seed oil, Taraxasterol}, doi = {10.5530/pj.2016.1.9}, author = {Jinous Asgarpanah and Narges Dakhili and Fatemeh Mirzaee and Maedeh Salehi and Maryam Janipour and Elaheh Rangriz} } @article {174, title = {Study on Inflammation and the Nervous system of Ethanol extract of Jatropha Curcas seed}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {June/2016}, pages = {335-340}, type = {Original Article}, chapter = {335}, abstract = {

Introduction: Jatropha curcas L. seeds are used in traditional medicine to treat a variety of diseases or conditions. The aim of this study is to evaluate effects on inflammation and the nervous system of ethanol extract of J. curcas seeds. Materials and methods: It was used 64 mice divided in 8 groups; respectively, 4 groups received 400, 600, 800 and 1000 mg/kg of ethanol extract of J. curcas seed; and the rest intake Diclofenac, Diazepam, Caffeine and a control group not received any substance. The effects on inflammation was evaluated by Carrageenan-Induced paw oedema test and by Paw skin temperature. Neurological symptoms of toxicity were evaluated using the Irwin test. For the analysis of quantitative variables were used the following tests: one-way ANOVA, Tukey, Shapiro-Wilk and Pearson correlation; for qualitative variables Chi square was used. Results: According to the paw oedema, it was showed a trend on an inflammatory effect of the seeds of J. curcas; this activity was statistically significant in doses of 1000 mg/kg. Also, the skin temperature measurements outcomes reveal a positive dose response manner. Regard to neurological manifestations, Straub tail was founded in doses of 400 mg/kg. Stereotypies were founded in doses of 400, 600, 800 and 1000 mg/kg throughout the evaluation. Conclusion: J. curcas seeds were showed an inflammatory effect. In addition, effects on the nervous system were founded as stereotypes and Straub tail.

}, keywords = {Carrageenan, Inflammation, Jatropha curcas, Nervous System., Seeds}, doi = {10.5530/pj.2016.4.5}, author = {Zambrano-Huailla Alexander and Zambrano-Huailla Rommel and Goicochea-Lugo Sergio and Zavala-Flores Ernesto and Garc{\'\i}a-Berrocal Jorge and Chau-Saravia Angel and Pante-Medina Carlos and Salazar-Granara Alberto} } @article {200, title = {Synthesis of Plant Mediated gold Nanoparticles using Azima Tetracantha Lam. Leaves extract and Evaluation of their Antimicrobial Activities}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Oct 2016}, pages = {507-512}, type = {Original Article}, chapter = {507}, abstract = {

Aim: The demand for nanoparticles is increasing day by day due to their wide range of applications in various areas including pharmaceutical industry. Nanoparticles are formally synthesized by chemical methods in which the toxic and flammable chemicals are used. Methods: This article reports about an effective, rapid and eco-friendly technique for the fabrication of gold nanoparticles from gold chloride solution using Azima tetracantha Lam. leaves extract. The effects of the leaves extract of Azima tetracantha, the concentration of Gold chloride solution, the time of the reaction and the effect of tem\¬perature on the rate of the reaction were investigated. The synthesized gold nanoparticles (AuNPs) were characterized by using various techniques such as Dynamic Light Spectroscopy (DLS), Scanning Electron Microscopy (SEM), UV-Vis spectra gave surface plasmon resonance (SPR) at 540 nm, Fourier Transform Infrared spectroscopy (FTIR) and X-ray diffraction (XRD). This revealed the reduction of gold ions (Au+) to gold metal (Au0) which indicated the formation of gold nanoparticles (AuNPs). Results: The antimicrobial action of biosynthesized AuNPs indicated effective activity against bacterial pathogens Aeromonas liquefaciens, Enterococcus fecalis, Micrococcus luteus, Salmonella typhimurium and fungal pathogens Candida albicans, Cryptococcus sp, Microsporum canis, Trichophyton rubrum. Conclusion: This revealed that gold nanoparticles could provide a safer alternative to conventional antimicrobial agents.

}, keywords = {Antimicrobial Activity., Azima tetracantha Leaves Extract, Biosynthesis, Characterization, Gold Nanoparticles}, doi = {10.5530/pj.2016.5.17}, author = {Abirami Hariharan and Tajuddin Nargis Begum and Mohamed Hussain Muhammad Ilyas and Hussain Syed Jahangir and Premkumar Kumpati and Shilu Mathew and Archunan Govindaraju and Ishtiaq Qadri} } @article {53, title = {Antioxidant and DNA Damage Protective Effects of Asparagus racemosus in Human Colon and Mice Muscle Cells}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {182-190}, type = {Original Article}, chapter = {182}, abstract = {

Introduction: The present study was designed to investigate the in vitro antioxidant and macromolecule damage protective effects of Asparagus racemosus water (AWE) and methanolic (AME) fractions of roots. Methods: The in vitro antioxidant activity of AWE/AME was estimated by free radical scavenging assays. The DNA damage of HT29 and C2C12 cells was analyzed by comet assay. The plasmid DNA damage and protein oxidation were carried out by agarose gel electrophoresis and SDS-PAGE analysis respectively, where as lipid peroxidation was performed by TBARS assay. Results: Both the extracts showed scavenging activity with IC50 values of 417.4 \± 19.5 / 298 \± 13.5, 381 \± 18.2 / 235 \± 11.9, 54.8 \± 2.95 / 31.6 \± 1.52, 28.9 \± 1.73 / 19.7 \± 1.55 \μg/mL for DPPH, metal chelating, ABTS and Nitric oxide scavenging activities respectively. Similarly the methanolic extract showed more potent reducing power and total antioxidant activities over water fraction. The AME showed 56.8\% and 41.2\% protection against H2O2 (Hydrogen peroxide) induced DNA damage of HT29 human colon cells and C2C12 murine myoblasts. The extract also showed protection against H2O2 induced plasmid DNA damge, AAPH induced protein oxidation of bovine serum albumin (BSA) and lipid peroxidation of rat hepatic tissue. Conclusion: Over all this study showed remarkable antioxidant and macromolecule damage protective effects of A. racemosus. The observed biological properties may be attributed to the high content phenols and flavonoids in the methanolic extract A. racemosus over water extract.

}, keywords = {AAPH, Asparagus racemosus, C2C12, HT29, Protein oxidation, Single cell gel electrophoresis.}, doi = {10.5530/pj.2015.3.7}, author = {Girindrababu Venkattappa Jayashree and Puttasiddiah Rachitha and Krishnaswamy Krupashree and Kandikattu Hemanth Kumar and Farhath Khanum} } @article {1442, title = {Antioxidant and DNA Damage Protective Effects of Asparagus racemosus in Human Colon and Mice Muscle Cells}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {9th Feb, 2015}, pages = {182-190}, type = {Original Article}, chapter = {182}, abstract = {

Introduction: The present study was designed to investigate the in vitro antioxidant and macromolecule damage protective effects of Asparagus racemosus water (AWE) and methanolic (AME) fractions of roots. Methods: The in vitro antioxidant activity of AWE/AME was estimated by free radical scavenging assays. The DNA damage of HT29 and C2C12 cells was analyzed by comet assay. The plasmid DNA damage and protein oxidation were carried out by agarose gel electrophoresis and SDS-PAGE analysis respectively, where as lipid peroxidation was performed by TBARS assay. Results: Both the extracts showed scavenging activity with IC50 values of 417.4 \± 19.5 / 298 \± 13.5, 381 \± 18.2 / 235 \± 11.9, 54.8 \± 2.95 / 31.6 \± 1.52, 28.9 \± 1.73 / 19.7 \± 1.55 \μg/mL for DPPH, metal chelating, ABTS and Nitric oxide scavenging activities respectively. Similarly the methanolic extract showed more potent reducing power and total antioxidant activities over water fraction. The AME showed 56.8\% and 41.2\% protection against H2O2 (Hydrogen peroxide) induced DNA damage of HT29 human colon cells and C2C12 murine myoblasts. The extract also showed protection against H2O2 induced plasmid DNA damge, AAPH induced protein oxidation of bovine serum albumin (BSA) and lipid peroxidation of rat hepatic tissue. Conclusion: Over all this study showed remarkable antioxidant and macromolecule damage protective effects of A.racemosus. The observed biological properties may be attributed to the high content phenols and flavonoids in the methanolic extract A. racemosus over water extract.

Key words: AAPH, Asparagus racemosus, C2C12, HT29, Protein oxidation, Single cell gel electrophoresis.

}, keywords = {AAPH, Asparagus racemosus, Protein oxidation, Single cell gel electrophoresis.}, author = {Girindrababu Venkattappa Jayashree and Puttasiddiah Rachitha and Krishnaswamy Krupashree and Kandikattu Hemanth Kumar and Farhath Khanum} } @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 {1472, title = {Comparative pharmacognostic, phytochemical and biological evaluation between five Chlorophytum species}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {16th Jan, 2015}, pages = {147-156}, type = {Original Article}, chapter = {147}, abstract = {

Five species, Chlorophytum borivilianum Santapau and Fernades, Chlorophytum comosum (Thunb.) Jacq., Chlorophytum tuberosum Br., Chlorophytum laxum R. Br. and C. arundinaceum, of very popular Ayurvedic plant Safed Musali are collected and comparatively evaluated for morphological, microscopical, physicochemical and biological parameters.

Key words: Chlorophytum, borivilianum, comosum, tuberosum, laxum, arundinaceum, DPPH, SRB, HL-60.

}, keywords = {Arundinaceum, Borivilianum, Chlorophytum, comosum, DPPH, HL-60., Laxum, SRB, tuberosum}, author = {Sharada. L. Deore and Neha B. Jajoo and Kailaspati P.A Chittam and T.A.Deshmukh} } @article {81, title = {Comparative Pharmacognostic, Phytochemical and Biological evaluation between five Chlorophytum species}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {317-325}, type = {Original Article}, chapter = {317}, abstract = {

Objective: To establish comparative pharmacognostic, phytochemical and biological evaluation parameters between five Chlorophytum species i.e. Chlorophytum borivilianum Santapau and Fernades, Chlorophytum comosum (Thunb.) Jacq., Chlorophytum tuberosum Br., Chlorophytum laxum R. Br. and Chlorophytum arundinaceum Baker, of very popular Ayurvedic plant Safed Musali. Materials and methods: Comparative evaluations of Macro and microscopical, physico-chemical parameters of tubers of all five species were investigated and preliminary phytochemical analysis, estimation of major phytochemicals and TLC profiles were also carried out for qualitative phytochemical evaluation. In-vitro antioxidant and anticancer activity was carried out for extract of tubers of all five species. Results: Macro, micro, powder microscopical parameters of tubers of five species were examined and recorded the result. Tubers of all the five species are distinct in their morphology as well as anatomical characters. Physicochemical characters (Ash values, Loss on drying (LOD), swelling index and foaming index) as well as total saponin content shows great variability among five species. Results of In-vitro antioxidant by DPPH method shows difference in antioxidant potential between tubers of all five species. Extract of tubers of all five species do not show any type of In-vitro anticancer activity by SRB method against HL 60 leukemia cell line. Conclusion: All of the evaluated parameters are very good pharmacognostic standards for future comparative identification and authentication of specific species because all five species shows morphological, anatomical, chemical differences as well as varies in antioxidant potential.

}, keywords = {Arundinaceum, Borivilianum, Chlorophytum Comosum, DPPH, HL-60, Laxum, SRB, Tuberosum.}, doi = {10.5530/pj.2015.5.12}, author = {Sharada Laxman Deore and Neha Brijmohan Jajoo and Kailaspati Prabhakar Chittam and Tushar Atmaram Deshmukh} } @article {66, title = {Comparison in vitro of Antioxidant Activity between Fifteen Campanula Species (Bellflower) from Palestinian Flora}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {276-279}, type = {Original Article}, chapter = {276}, abstract = {

Background: The natural antioxidant products in the plant kingdom play an important role in the healthy life style and reduce the risk for various chronic diseases.Objective: The objective of this study was to investigate different antioxidant pharmacological property of methanol extract for fifteen species of Campanula plant from Palestinian flora. Methods: The antioxidant activity of fifteen Campanula species growing wildly in Palestine were studied using 2,2-diphenylpicrylhydrazyl (DPPH) radical scavenging activity and their antioxidant activity was compared to Trolox antioxidant activity. Results: The results clearly demonstrate a very high antioxidant activity of the Campanula sulphurea and Campanula sidoniensis and they showed almost the same antioxidant activity of Trolox. The other twelve species extracts also exhibited excellent antioxidant activity in DPPH radical scavenging activity in comparison with trolox standard. Conclusion: Methanol extract of Campanula can be valuable for treatment of different diseases and could be used as a possible new source of natural antioxidants in the food, nutraceuticals, pharmaceuticals and cosmetic industry.

}, keywords = {Antioxidant, Bellflower, Campanula species, Campanulaceae, DPPH radical scavenging activity.}, doi = {10.5530/pj.2015.5.4}, author = {Nidal Amin Jaradat and Murad Abualhasan} } @article {1450, title = {Comparison in Vitro of Antioxidant Activity between Fifteen Campanula Species (Bellflower) from Palestinian Flora}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {29th Apr, 2015}, pages = {9-9}, type = {Original Article}, chapter = {9}, abstract = {

Background: The natural antioxidant products in the plant kingdom play an important role in the healthy life style and reduce the risk for various chronic diseases. Objective: The objective of this study was to investigate different antioxidant pharmacological property of methanol extract for fifteen species of Campanula plant from Palestinian flora. Methods: The antioxidant activity of fifteen Campanula species growing wildly in Palestine were studied using 2,2-diphenylpicrylhydrazyl (DPPH) radical scavenging activity and their antioxidant activity was compared to Trolox antioxidant activity. Results: The results clearly demonstrate a very high antioxidant activity of the Campanula sulphurea and Campanula sidoniensis and they showed almost the same antioxidant activity of Trolox. The other twelve species extracts also exhibited excellent antioxidant activity in DPPH radical scavenging activity in comparison with trolox standard. Conclusion: Methanol extract of Campanula can be valuable for treatment of different diseases and could be used as a possible new source of natural antioxidants in the food, nutraceuticals, pharmaceuticals and cosmetic industry.

Key words: Antioxidant, Bellflower, Campanula, Bellflower, Campanulaceae, DPPH radical scavenging activity

}, keywords = {Antioxidant, Bellflower, Campanula, Campanulaceae, DPPH radical scavenging activity.}, author = {Nidal Amin Jaradat and 1Murad Abualhasan} } @article {1458, title = {Evaluation of cytotoxic, DNA protecting and LPS induced MMP-9 down regulation activities of Plectranthus amboinicus (Lour) Spreng. essential oil.}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {27th Nov, 2014}, pages = {32-36}, type = {Original Article}, chapter = {32}, abstract = {

Introduction:Plectranthus amboinicus (Lour) Spreng is a known medicinal plant used in Siddha and Ayurveda medicines in India. It has enormous medicinal potential to treat various diseases. Methods: The present study focused on the use of essential oil obtained from the leaves of Plectranthus amboinicus to test cytotoxicity against breast (MCF-7) and colorectal (HT-29) cancer cell lines, to protect DNA from H2O2 induced genotoxicity through comet assay and to treat inflammation in lipopolysaccharide (LPS) induced over expression of matrix metalloproteinase-9 (MMP-9) in human peripheral blood mononuclear cells (PBMCs) by gelatin zymogram and inhibition at transcriptional level confirmed using RT-PCR (reverse transcriptase polymerase chain reaction). Results: Cytotoxicity of essential oil against MCF-7 and HT-29 cancer cell lines revealed the IC50 values of 53 \± 0.01 and 87 \± 0.01\μg/mL respectively. At 200 \μg/mL essential oil protected against 75\% of DNA damage in 3T3-L1 fibroblast cells. Essential oil showed significant reduction in production of MMP-9 in a concentration dependent manner. Conclusion: Overall, the results showed that essential oil of P. amboinicus is a potent bioactive substance and it could be used in herbal medicine preparations.
Key words: Essential oil , Cytotoxicity , Antigenotoxicity, Zymogram, RT- PCR.

}, keywords = {Antigenotoxicity, Cytotoxicity, Essential oil, RT- PCR, Zymogram}, author = {Ramaraj Thirugnanasampandan and Gunasekar Ramya and Madhusudhanan Gogulramnath and Rajarajeswaran Jayakumar and M.S. Kanthimathi} } @article {32, title = {Evaluation of cytotoxic, DNA protecting and LPS induced MMP-9 down regulation activities of Plectranthus amboinicus (Lour) Spreng. essential oil}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {32-36}, type = {Original Article}, chapter = {32}, abstract = {

Introduction: Plectranthus amboinicus (Lour) Spreng is a known medicinal plant used in Siddha and Ayurveda medicines in India. It has enormous medicinal potential to treat various diseases. Methods: The present study focused on the use of essential oil obtained from the leaves of Plectranthusamboinicusto test cytotoxicity against breast (MCF-7) and colorectal (HT-29) cancer cell lines, to protect DNA from H2O2 induced genotoxicity through comet assay and to treat inflammation in lipopolysaccharide (LPS) induced over expression of matrix metalloproteinase-9 (MMP-9) in human peripheral blood mononuclear cells (PBMCs) by gelatin zymogram and inhibition at transcriptional level confirmed using RT-PCR (reverse transcriptase polymerase chain reaction). Results: Cytotoxicity of essential oil against MCF-7 and HT-29 cancer cell lines revealed the IC50 values of 53 \± 0.01 and 87 \± 0.01 \μg/mL respectively. At 200 \μg/mL essential oil protected against 75\% of DNA damage in 3T3-L1 fibroblast cells. Essential oil showed significant reduction in production of MMP-9 in a concentration dependent manner. Conclusion: Overall, the results showed that essential oil of P. amboinicus is a potent bioactive substance and it could be used in herbal medicine preparations.

}, keywords = {Antigenotoxicity, Cytotoxicity, Essential oil, RT- PCR., Zymogram}, doi = {10.5530/pj.2015.7.3}, author = {Ramaraj Thirugnanasampandan and Gunasekar Ramya and Madhusudhanan Gogulramnath and Rajarajeswaran Jayakumar and M.S. Kanthimathi} } @article {1478, title = {Flavonoids from Eupatorium illitum and Their Antiproliferative Activities}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {09th Mar, 2015}, pages = {178-181}, type = {Original Article}, chapter = {178}, abstract = {

Objective: To isolate the chemical constituents of the aerial parts from Eupatorium illitum, elucidate their structures and evaluate their antiproliferative activity on human cancer cell lines. Materials and Methods: The ethanolic extract of Eupatorium illitum afforded five compounds, which were characterized using spectroscopic techniques and by comparison with data from the literature. Antiproliferative activities of selected isolates were evaluated. Results: The flavonoids Kumatakenin (1), Ermanin (2), 7-methoxy-aromadendrin (3) and Naringenin (4), together with 4-hydroxybenzoic acid (5) were isolated. Compounds 1, 2, 4 and 5 were evaluated for their antiproliferative activity on the human cancer cell lines A549 (lung), HBL-100 (breast), HeLa (cervix), SW1573 (lung), and T-47D (breast) presenting a wide range of bioactivities. In general, best results were observed for 5. Conclusion: Compounds 1-5 are reported for first time from Eupatorium illitum. Isolated phytochemicals show moderate to low antiproliferative activities when evaluated on the aforementioned human cancer cell lines.

Key words: Eupatorium illitum, Ermanin, 4-Hydroxybenzoic acid, Kumatakenin, 7-Methoxy-aromadendrin, Naringenin.

}, keywords = {4-Hydroxybenzoic acid, 7-Methoxy-aromadendrin, Ermanin, Eupatorium illitum, Kumatakenin, Naringenin.}, author = {Qu{\'\i}rico A Castillo and Jorge Triana and Jos{\'e} L Eiroa and Jos{\'e} M Padr{\'o}n and Gabriela B Plata and Ernesto V Abel-Santos and Luis A. B{\'a}ez and Diana C Rodr{\'\i}guez and Marco A Jim{\'e}nez and Mar{\'\i}a F P{\'e}rez-Pujols} } @article {51, title = {Flavonoids from Eupatorium illitum and Their Antiproliferative Activities}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {178-181}, type = {Original Article}, chapter = {178}, abstract = {

Objective: To isolate the chemical constituents of the aerial parts from Eupatorium illitum, elucidate their structures and evaluate their antiproliferative activity on human cancer cell lines. Materials and Methods: The ethanolic extract of Eupatorium illitum afforded five compounds, which were characterized using spectroscopic techniques and by comparison with data from the literature. Antiproliferative activities of selected isolates were evaluated. Results: The flavonoids Kumatakenin (1), Ermanin (2), 7-methoxy-aromadendrin (3) and Naringenin (4), together with 4-hydroxybenzoic acid (5) were isolated. Compounds 1, 2, 4 and 5 were evaluated for their antiproliferative activity on the human cancer cell lines A549 (lung), HBL-100 (breast), HeLa (cervix), SW1573 (lung), and T-47D (breast) presenting a wide range of bioactivities. In general, best results were observed for 5. Conclusion: Compounds 1-5 are reported for first time from Eupatorium illitum. Isolated phytochemicals show moderate to low antiproliferative activities when evaluated on the aforementioned human cancer cell lines.

}, keywords = {4-Hydroxybenzoic acid, 7-Methoxy-aromadendrin, Ermanin, Eupatorium illitum, Kumatakenin, Naringenin.}, doi = {10.5530/pj.2015.3.6}, author = {Qu{\'\i}rico A Castillo and Jorge Triana and Jos{\'e} L Eiroa and Jos{\'e} M Padr{\'o}n and Gabriela B Plata and Ernesto V Abel-Santos and Luis A. B{\'a}ez and Diana C Rodr{\'\i}guez and Marco A Jim{\'e}nez and Mar{\'\i}a F P{\'e}rez-Pujols} } @article {1459, title = {Immunomodulatory Activity of Atalantia monophylla DC. roots}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {27th Nov, 2014}, pages = {37-43}, type = {Original Article}, chapter = {37}, abstract = {

Objective: The objective of the present study was to evaluate the immunomodulatory activity of the roots of Atalantia monophylla. In the present study Pet. Ether, Chloroform and Methanolic fractions of the ethanolic extract of the roots of Atalantia monophylla, were administered orally, in the doses of 10 mg/kg and 30 mg/kg, to evaluate the immunomodulatory activity. Materials and Methods: The Methanolic fraction showed most significant effect when compared with control group, in the dose of 30 mg/kg, in the E.Coli induced abdominal sepsis and Carbon Clearence Test as models for non-specific immune response. In the models of the Specific immune response, cell mediated immune response to SRBC - delayed type of hypersensitivity (DTH) the methanolic fraction in the dose 30 mg/kg, when compared with control group, showed most significant effect on decrease in footpad edema after treatment. Results: Humoral immune response was assessed by Sheep erythrocyte agglutination test, in which the Methanolic fraction of Atalantia monophylla in the dose of 30 mg/kg showed most significant (p\<0.05) increase in antibody titer after treatment when compared with control group. Conclusion: The present investigation reports that the Methanolic fraction of the ethanolic extract of the roots of Atalantia monophylla, in the dose of 30 mg/kg showed most significant immunomodulatory activity.

Key words:Atalantia monophylla, Immunomodulatory, Phagocytosis, Cell-mediated immune response, Humoral immune response.

}, keywords = {Atalantia monophylla, Cell-mediated immune response, Humoral immune response., Immunomodulatory, Phagocytosis}, author = {V. R. Patil and V. M. Thakare and V.S. Joshi} } @article {34, title = {Immunomodulatory Activity of Atalantia monophylla DC. roots}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {37-43}, type = {Original Article}, chapter = {37}, abstract = {

Objective: The objective of the present study was to evaluate the immunomodulatory activity of the roots of Atalantia monophylla. In the present study Pet. Ether, Chloroform and Methanolic fractions of the ethanolic extract of the roots of Atalantia monophylla, were administered orally, in the doses of 10 mg/kg and 30 mg/kg, to evaluate the immunomodulatory activity. Materials and Methods: The Methanolic fraction showed most significant effect when compared with control group, in the dose of 30 mg/kg, in the E.Coli induced abdominal sepsis and Carbon Clearence Test as models for non-specific immune response. In the models of the Specific immune response, cell mediated immune response to SRBC-delayed type of hypersensitivity (DTH) the methanolic fraction in the dose 30 mg/kg, when compared with control group, showed most significant effect on decrease in footpad edema after treatment. Results: Humoral immune response was assessed by Sheep erythrocyte agglutination test, in which the Methanolic fraction of Atalantia monophylla in the dose of 30 mg/kg showed most significant (p\<0.05) increase in antibody titer after treatment when compared with control group. Conclusion: The present investigation reports that the Methanolic fraction of the ethanolic extract of the roots of Atalantia monophylla, in the dose of 30 mg/kg showed most significant immunomodulatory activity.

}, keywords = {Atalantia monophylla, Cell-mediated immune response, Humoral immune response, Immunomodulatory, Phagocytosis}, doi = {10.5530/pj.2015.7.4}, author = {VR Patil and VM Thakare and VS Joshi} } @article {40, title = {Quality Control Standardization and In-Vitro Antioxidant Activity of Aganosma dichotoma K. Schum Root}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {74-82}, type = {Original Article}, chapter = {74}, abstract = {

Introduction: Aganosma dichotoma K. Schum (AD) is a large climber with very stout stem belonging to the family Apocynaceae. The Plant has significant medicinal value as described in traditional system of medicine. The objective of the present study is to scientifically develop a standard monograph for AD on the basis of its pharmacognostical and phytochemical aspects. Methods: The study includes quality control standardization as per the standard methods provided in World Health Organization for standardization of medicinal plants. Fluorescence drug analysis, preliminary phytochemical screening of different fractions, quantification of some phytoconstituents and in-vitro antioxidant activity were also carried out. Quantification of Quercetin in the ethanolic extract of A. dichotoma was determined by HPTLC analysis. The ethanolic extract of root of A. dichotoma was subjected to in-vitro antioxidant activity. Results: The diagnostic characters of A. dichotoma root were evaluated on the basis of macroscopical and microscopical characters. Physicochemical parameters were evaluated such as 6.7\% w/w loss on drying with; ash values (in \% w/w): 13.75 total ash, 5.75 acid-insoluble ash, 3.6 water-soluble ash; Extractive values (\% w/w): 12.75 water, 11.82 ethanol, 2.26 ethyl acetate, 3.13 chloroform, and 3.16 pet ether; foaming index 181.81; swelling index 3.2 ml/g; hemolytic activity 227.89 unit/gm of powder drug and crude fiber content was 19.4\%. Total numbers of starch grain in 1 mg of root powder were 2,49,981. Quantification of quercetin in the ethanolic extract was assessed by HPTLC analysis and was found to contain 2.40\%, w/w. Conclusion: The parameters determined in the present study may provide necessary information for identification and authentication of plant material.

}, author = {Deepali Pandey and Apurva Joshi and S. Hemalatha} } @article {1505, title = {Pharmacognostical Studies of Bryophyllum pinnatum (Lam.) Kurz.}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {3rd Sept, 2014}, pages = {20-26}, type = {Original Article}, chapter = {20}, abstract = {

Context:Bryophyllum pinnatum (Lam.) Kurz. widely used in traditional as well as folk medicinal systems is locally known as Panphuti. Traditionally it is used for the treatment of kidney stones, urinary tract infection, burns and diarrhoea. Aims: In the present study, pharmacognostic studies of root, stem and leaf of Bryophyllum pinnatum (Lam.) Kurz. is carried out in order to standardize the plant for its phytochemical, phyiso-chemical and pharmacognostical. Methods and Material: For standardization of plant material morphological and anatomical characterization was carried out. Physico-chemical parameters viz. ash content, extractive values, heavy metal content was carried out as per Ayurvedic Pharmacopoeia of India. Phytochemical investigations were made to know the presence of various bioactive molecules, amino acid composition. Results: Intrastelar and extrastelar secondary growth with wood and periderm formation along with deposition of starch grains were observed in pith region of root and cortical region of stem. Calcium oxalate crystals were also present in the cortical region of the stem. Leaf lamina showed spongy parenchyma in mesophyll region and anisocytic type of stomata. Anthocyanin pigment was present below epidermal cells in petiole. Physico- chemical results can be serves as quality control data. Quantitatively carbohydrate, protein, flavonoids, phenolic compounds, saponins and pro-antocyanidins were found to be present in root, stem and leaf part of Bryophyllum pinnatum (Lam.) Kurz. Conclusion: The results of the study could be useful in setting some diagnostic indices for the identification and preparation of a monograph of the plant.

Key words:Bryophyllum pinnatum (Lam.) Kurz., Pharmacognosy, Phytochemical, Physico-chemical.

}, keywords = {Bryophyllum pinnatum (Lam.) Kurz, Pharmacognosy, Physico-chemical., Phytochemical.}, author = {Sharma Abhishek J. and Chandra Naresh} } @article {1516, title = {Protective Effects of Beetroot Extract against Phenyl Hydrazine Induced Anemia in Rats}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {2nd July 2014}, pages = {1-4}, type = {Original Article}, abstract = {

Background: Anemia can be regarded as one of the oldest blood malformation known over a century. Megaloblastic anemia arises due to curtailed formation of erythrocytes, which leads to formation of a large number of underdeveloped erythrocytes. Proper nutritional supplementation may be useful in such condition. Beta vulgaris or beetroot is one of the important vegetables consumed worldwide. The aim of the present work was to evaluate anti-anemic potential of beetroot. Methods: Beetroot was extracted with ethanol. Phytochemical and phytoanalytical studies were performed on extract. Anemia was induced by phenyl-hydrazine. Animals were treated with extract throughout the study for 24 days. The red blood cell (RBC) number and hemoglobin concentration were determined every 3 days for 24 days. Results: Extract was found to be rich in folic acid, ascorbic acid, and iron. Following the induction of anemia, the number of erythrocytes and the hemoglobin concentration decreased by 62.51\% and 69.64\%, respectively. Administration of standard hematinic preparation and extract (200 mg/kg) resulted in signifi cant increase (P\< 0.001; P\< 0.01) in the number of RBCs as well as hemoglobin concentration when compared to the untreated phenyl hydrazine-induced anemic rats. Conclusion: Extract effectively raised the level of hemoglobin and erythrocyte count at dose 200 mg/kg. Vitamin and minerals found in beetroot are most likely active ingredients responsible for its hematinic effects. Still, methodical studies are obligatory to derive its effects on humans.

Key words:Beta vulgaris, erythrocytes, hemoglobin, phenyl hydrazine.

}, keywords = {Beta vulgaris, erythrocytes, Hemoglobin, phenyl hydrazine}, author = {Anupam Jaiswal and Aditya Ganeshpurkar and Ankita Awasthi and Divya Bansal and Nazneen Dubey} }