Pharmacognosy and Phytochemical Screening of some Plant Derived Medicine to Treat Dysmenorrheal Pain by the Rajbanshi Community - Priyankar Roy; Palash Mandal; Subhasis Panda; Sonia Mitra Roy; Arunika Subba (Pharmacognosy Journal, 2018)
Introduction: Dysmenorrhea is a sort of painful menstrual disorder. Several plants like Allium sativum L., Areca catechu L., Zingiber officinale Roscoe, Crinum amoenum Ker Gawl. Ex Roxb, Cuscuta reflexa Roxb. Nymphaea rubra Roxb. Ex Andrews, Piper nigrum L., Citrus limon (L.) Osbeck were used in appropriate ratio to make herbal formulation to cure dysmenorrheal pain by the traditional healers of Rajbanshi community. Objective: By semi-structured questionnaires in the course of scheduled interviews with the local herbal practitioners, four herbal formulations (coded as DYS1, DYS2, DYS3 and DYS4) were recorded. Pharmacognostic characterization was carried out for the authentication of the powder drugs which includes powder microscopy, fluorescence analysis and physicochemical evaluation. The presence of any therapeutic potential in DYS1, DYS2, DYS3 and DYS4 was determined by qualitative evaluation of phytochemicals of various successive solvent extracts based on their polarity. Thin layer chromatography was performed for screening various phyto-active compounds like arbutin, alkaloids, coumarins, cardiac glycoside, etc. Results: Powder microscopy revealed the presence of calcium oxalate crystal, stone cells etc. Various fluorescence colors were exhibited by these herbal drugs under UV after reacting with chemical reagents. Physical analyses values were also obtained in a satisfactory way. TLC and qualitative phytochemical analysis showed the presence of active phytoconstituents like arbutin, alkaloids, coumarins, cardiac glycoside etc. Conclusion: The results support the use of plants as a traditional medicine for the prevention disorders like Dysmenorrhea. Further evaluation is required for determining the efficacy of those herbal drugs and the active phytoconstituents involved in Dysmenorrheal therapy.
Keywords: Antioxidant; Dysmenorrhea; Pharmacognostic evaluation; Successive solvent extraction; Thin layer Chromatography.; Traditional healer

Pharmacognosy, Phytochemical Study and Antioxidant Activity of Sterculia rubiginosa Zoll. Ex Miq. Leaves - Rini Prastiwi; Berna Elya; Rani Sauriasari; Muhammad Hanafi; Ema Dewanti (Pharmacognosy Journal, 2018)
Introduction: Sterculia rubiginosa Zoll ex.Miq leaves have been used as traditional medicine in Indonesia. There is no report about pharmacognosy and phytochemical study with this plant.Objective: The main aim of this research is to establish pharmacognosy, phytochemical study and antioxidant activity of Sterculia rubiginosa Zoll.ex. Miq. Leaves. The plant used to cure many diseases of Indonesia. Methods: In the present study, pharmacognosy and phytochemical study of plant material were performed as per the Indonesian Herb Pharmacopoeia. Results: Microscopy powder of Sterculia rubiginosa Zoll.ex. Miq. Leaves shows star shape trichoma as a specific fragment. Physicochemical parameters including total ash (17,152 %), acid-insoluble ash (0,922 %), water-soluble extractive (1,610 % w/w), alcohol-soluble extractive (4,524 % w/w), hexane-soluble extractive (4,005 % w/w), and ethyl acetate-soluble extractive (3,160 % w/w) were evaluated. Phytochemical screening of ethanol extracts showed the presence of tannins, flavonoids, alkaloids, steroids-terpenoids, glycosides, and phenols. And absent of saponins and Anthraquinones. Antioxidant activity with IC50 157, 4665 ppm and flavonoid total was 59,436 mg/g quercetin equivalent. Conclusion: The pharmacognosy, physiochemical, and phytochemical evaluation provides information for the safety, identification, and class of chemical constituent’s presents in this crude extract.
Keywords: Antioxidant; Pharmacognosy; Phytochemical; Sterculia rubiginosa zoll. ex Miq

Pharmacological Evaluation of Bacopa monnieri Extract against Depressive like Behavior Induced by Ethanol Withdrawal in Rats - Lalit Sharma; Aditi Sharma; Girdhari Lal Gupta; Gopal Singh Bisht (Pharmacognosy Journal, 2018)
Background: Alcohol withdrawal syndrome lead to relapse to alcohol use and depression is the most common symptom of withdrawal. Bacopa monnieri is a traditional memory enhancer and has reported antidepressant properties as well. Objective: The present study was designed to evaluate the protective effects of Bacopa monnieri extract in alcohol withdrawal depressive-like behavior in alcohol-dependent rats. Methods: Plant drug was extracted with ethanol (70% v/v) using soxhlet extraction. Ethanol 7.2%, v/v was given to the rats in a liquid diet for 21 days and then was withdrawn from the diet and animals were observed at 6th and 24th h for withdrawal signs like depressive behavior and locomotor hyperactivity. Results: The phytochemical testing of extract revealed the presence of flavonoids, alkaloids, steroids, and tannins. Bacopa monnieri extract (100, 200 and 300 mg/kg, oral) and fluoxetine (10 mg/kg i.p) treatment at the 6th and 24th h of ethanol withdrawal produced the significant (p<0.001) decrease in the immobility time as compared to the disease control rats when tested on forced swim test and tail suspension test. Bacopa monnieri extract and fluoxetine treatment produced significant (p<0.001) inhibitory effects on locomotor hyperactivity as well. Histopathological examination did not show any remarkable pathological and microscopic changes. Conclusion: Findings from the present study showed that Bacopa monnieri extract treatment has beneficial effects on ethanol withdrawal depressive-like behavior in rats.
Keywords: Bacopa monnieri; Depression; Ethanol withdrawal syndrome; Histopathology; Locomotor hyperactivity

Pharmacological Studies of Oxalis Pes-caprae L. - Syeda Naila; Muhammad Ibrar (Pharmacognosy Journal, 2018)
Background: Oxalis pes-caprae is also called as “sourgrass” or soursob. The roots, stems and leaves of Oxalis pes-caprae have high medicinal values and have the function of antiinflammatory and analgesia, clearing heat, removing toxicity. In present study Oxalis pescaprae belonging to family oxalidaceae evaluated for pharmacological activities like cytotoxicity, phtotoxicity, antibacterial and antifungal bioassays. Materials and Methods: Cytotoxic activity was performed by brine shrimp bioassay using methodology of Atta- ur- Rahman et al., 2001. The phytotoxic activity was investigated by applying Lamna minor (as test species) following Atta-ur-Rahman et al., 2001. Anti-bacterial screening was conducted following Rathan (2000). Anti-fungal screening was carried out using agar well diffusion method following Perez et al. (1990) and Atta-ur-Rahman et al. (1991). Results: Its ethanolic extract showed highly significant (100%) cytotoxicity with LD50 8.98 at 1000 ppm. Lemna minor phytotoxicity assay showed that O. pes-caprae chloroform extract showed 90% inhibition at 1000 ppm with FI50 0.1048. Antibacterial bioassays showed that all the samples of the plant were significant against Xanthomonas, Clavibacter machengnitis and Bacillus at 1000, 1500 and 2500 ppm doses. Dose dependent antifungal activities against test species (Aspergillus flavus, Penicillium and Fusarium solani) were noticed for all the extracts at 100 and 1000 ppm. Conclusion: Pharmacological potentials showed that this plant can be used in upcoming time for extracting numerous active constituents for their pharmacological preparations.
Keywords: Antibacterial activity; Antifungal activity; Cytotoxic activity; Oxalis pes-caprae; Pharmacology; Phytotoxic activity; Whole plant

Pharmacophore Modelling of Brassicaceae Members as Potent HIF (Hypoxia Inducible Factor) Inhibitors Involved in Cancer Angiogenesis - Jeyavel Renukadevi; Ganesan Nandhinidevi; Muthiah Bavanilatha; Hemanath Tharani; Rajarajan Sathiyabama; Subramani Vasumathi (Pharmacognosy Journal, 2018)
Angiogenesis is considered as an essential pathological feature of cancer due to its interplay between cancer and other diseases. Natural products found to act as antiangiogenic agents that mediate the angiogenic switch between pro and anti angiogenic factors. Among the different targets, HIF is an important and critical factor that stands as a key mediator between angiogenesis, inflammation and cancer. In our study different phytochemicals of Brassicaceae were analysed for their drug like properties and mapped for pharmacophore development. The developed pharmacophore was virtually screened and further subjected to Lipinski and ADMET filters. The molecular interaction studies of the 10 retrieved compounds were studied by binding with HIF. Among the compounds 1stdrug like molecule HTS 0115 (C15H21BrN2O3) was found to have best docked score and its interaction was further validated using dynamics simulation. The compound found to share the pharmacophoric features with progoitrin a biochemical form of glucosinolate with reported anticancer and anti thyroid activities. Thus the drug like compound HTS 0115 can be further optimised as a putative HIF inhibitor in tumor angiogenesis.
Keywords: Angiogenesis; Brassicaceae; HIF; Molecular docking; Pharmacophore; Simulation

Photoactivated chlorophyllin and acetylcholinesterase/ cytochrome oxidase activity in Fasciola gigantica cercaria larvae - Dinesh Kumar Singh; Divya jyoti Singh (Pharmacognosy Journal, 2018)
Objective: The effect of chlorophyllin (CHL), CHL + freeze dried cow urine (FCU) and FCU on acetylcholinesterase (AChE) and cytochrome oxidase activity in the nervous tissue of the host snail Lymnaea acuminata, and parasitic cercaria larvae of Fasciola gigantica were studied. Methods: Whole cercaria larvae and snail nervous tissue was homogenized and supernatant was used as an enzyme source. Enzyme activity was measured in 10-mm path length cuvette using incubation mixtures and change in optical density was recorded. Results: Sublethal 4 h LC50 40% and 80% of these formulations in sunlight and laboratory conditions caused no significant change in AChE activity in the nervous tissue of host snail. It was noted that sublethal in vivo 8 h exposure to 40% and 80% of 4 h LC50 of single and binary combination of CHL+FCU, CHL and FCU significantly altered the AChE and cytochrome oxidase activity in the cercaria larvae. Binary combinations of CHL+FCU in sunlight were more effective in inhibiting both the enzymes. Conclusion: The present study reported that enzymes AChE and cytochrome oxidase were inhibited by chlorophyllin formulations and thus causing the larval death inside the snail body without affecting the snail itself which is an important bioindicator of aquatic ecosytem.
Keywords: Acetylcholinesterase; Cercaria larva; Cytochrome oxidase; Fasciola Gigantica; Lymnaea acuminata; Nervous tissue

Physicochemical Analysis of Sumbul-al –Teeb (Nardostachys jatamansi D.C.) Rhizome along with its HPLC Profile - Mohammad Rashid; Aziz ur Rahman; Qazi Zaid Ahmad; Tajuddin; Syed Shariq Mian (Pharmacognosy Journal, 2018)
Introduction: Sumbul-al–Teeb (Nardostachys jatamansi) is a well known traditional medicinal plant used for therapeutic effect in Unani and Ayurvedic System of Medicine. It has been reported to have many therapeutic activities like antifungal, antimicrobial, antioxidant, hepatoprotective and cardioprotective properties. It is also useful in the management of insomnia and CNS disorders. The present study aims towards the evaluation of the parameters involved in the determination of the quality and purity of Nardostachys jatamansi rhizome and its standardization. Methods: Organoleptic characters, extractive values, ash values, phyto-chemical analysis, TLC, fluorescence analysis and HPLC profile etc. were the parameters used for the standardisation of the test drug. Result: Total ash values, water and alcohol soluble extractive values, moisture contents and volatile oil percentage was found to be 7.08%, 3.54%, 2.5%, 8.6% and 02% respectively. TLC profile of N. jatamansi shows 04, 08 and 10 spots in UV short and long wavelength and exposure to iodine vapours respectively. The HPLC pattern shows 34 peaks and the peak no. 01 and 08 are major peaks having area concentration and retention time as 25.974% at 2.8 min. and 29.967% at 4.399 min. respectively. Conclusion: The study will provide referential information for the good quality, purity and identification for the future batches of Nardostachys jatamansi.
Keywords: Phyto-chemical analysis; Quality; standardization; Unani

Physicochemical Standardization of Polyherbal Powder Formulation: Safoof-e-Makhana - Gazi Jahangeer Rather; Hamiduddin; Mohd Ikram, Shaista Fatima; MD Naquibuddin (Pharmacognosy Journal, 2018)
Introduction: Safoof-e-Makhana (SM) is a Unani polyherbal powder formulation used to treat Sexual disorders. Formulation consists of following herbs Orchis latifolia, Hygrophila auriculata, Asparagus racemosus and Elettaria cardamomum. The main aim of this study was to standardize Safoof-e-Makhana (SM), on the basis of organoleptic characters and physico-phytochemical analysis. Methods: The drugs were cleaned, dried in shade and powdered by passing through sieve # no. 80 as per the method described in UPI / National Formulary of Unani Medicine. This Safoof formulation was evaluated using physicochemical tests: powder characterization, extractive value, alcohol and water soluble matter, Ash value, LOD at 1050C, pH and HPTLC fingerprinting. Statistical analysis used: Mean ± SEM. Results: Organoleptic characters of the formulation are light brown colour, characteristic odour, sweet taste and moderately fine texture. Physicochemical parameters displayed water soluble extractive (21.83 ± 0.08), alcohol soluble extractive (7.87 ± 0.09), total ash (4.76 ± 0.08), acid insoluble ash (3.36 ± 0.01), water soluble ash (0.89 ± 0.25), LOD at 105oC (11.38 ± 0.34), pH of 1% and 10% solution were 6.6 ± 0.1 and 6.0 ± 0.1 respectively. Phytochemical qualitative analysis displayed presence of alkaloids, tannins, flavanoids, steroids, terpenoids, carbohydrates, volatile oil. HPTLC fingerprinting data was also set in. Conclusion: The standardization of this formulation was done and the data obtained would be used as a standard for future reference.
Keywords: Formulation; Physicochemical; Polyherbal; Powder; Safoof-e- Makhana; standardization; Unani Medicine

The Phythochemical Research of Armenian Apricot Gums (Gummi armeniacae) - Chichoyan Naira Babken; Mamyan Suren; Shaboyan Naira; Melikyan Yelena (Pharmacognosy Journal, 2018)
Aim: The plant derivative, the gum’s exudates are of great interest among polysaccharides. Nowadays, it is of crucial importance to study the structural peculiarities and the conditioned biological activity of the Gummi Armenicae of native origin as an alternative version of the Gummi Arabicae. Materials and methods: As a material for research served the gum procured from Apricot trees (Armenian Vulgaris Lam.), cultivated in different regions of Armenia annually in spring during juice motion period in 2010-2014 years. The quantity of polysaccharides in gum was determined by the method of gravimetric balance after drying. The quantitative ratio of monosaccharide in the examined polysaccharide complex was detected by the method of MRI. Results: By the methods of spectral analysis (PMR 1H and NMR 13C) the structure of Apricot gums polysaccharide fraction was detected. From the analysis of PMR 1H and NMR 13C spectra it is obvious that polysaccharide complex fraction is composed from the rest of α- L-arabionopyranose, β -L-arabionopyranose, α- D-galactopyranose, β -D-galactopyranose, α -D-glucopyranose, β -D-glucopyranose. Low molecular compounds in nonpolar fraction of apricot gum were determined by GC-MS method. The results show that in Rt1=22.5, Rt2=26.3, Rt3=31.4. Simple phenols were registered – peaks of catechols` hydroquinones, pyrogallols, amounts of which are respectively 7.58%, 4.27%, 5.69%.
Keywords: 13C NMR; Apricot gum; Chemical structure; GC-MS; Simple phenols

Phytochemical Analysis, Antioxidant Assay and Antimicrobial Activity in Leaf Extracts of Cerbera odollam Gaertn - Abinash Sahoo; Thankamani Marar (Pharmacognosy Journal, 2018)
Introduction: In the current study, methanol and aqueous extracts of leaf of Cerbera odollam Gaertn were screened for its antibacterial, antifungal, phytochemicals and antioxidant activities. Phytochemical constituents were investigated both qualitatively and quantitatively. Methods: The leaf extracts of Cerbera odollam Gaertn were prepared by drying and extracted using Soxhlet apparatus into methanol and aqueous media, which were subjected to phytochemical screening. Total phenols, tannins, flavanols, alkaloids and its antioxidant activity were determined using spectroscopic techniques. Antimicrobial activity were determined using well diffusion method. Results: Aqueous extract exhibits higher content of phenols, tannins, flavanols and alkaloids, whereas methanol extract exhibits higher content of anthocyanin and cardiac glycoside respectively. Aqueous extract exhibits higher inhibitory concentration (IC %) value for DPPH (2, 2-Diphenyl-1-picrylhydrazyl) and H2O2 radical scavenging assay and reducing power (RP) assay. The methanol extracts exhibited higher inhibitory concentration (IC %) value in SO and NO radical scavenging assay, exhibiting antioxidant properties in five antioxidant models that were investigated. The methanol extract showed some antibacterial activity against Bacillus subtilis, Staphylococcus aureus, Salmonella typhi and Escherichia coli with inhibitory zone ranging from 2 mm to 3 mm, whereas the aqueous extract showed no activity. High antifungal activity was found against Saccharomyces cerevisiae and Candida albicans for methanol extract and moderate for aqueous extract with inhibitory zone ranging from 9mm to 26 mm. Conclusion: The finding of our study have suggested that the extracts of Cerbera odollam Gaertn, possesses a significant amount of phytochemicals and exhibits antioxidant and antifungal activities.
Keywords: Antibacterial; Antifungal; Antioxidants; Cerbera odollam. G; Phytochemicals; Radical scavenging

Phytochemical Analysis of Nigella sativa L. Utilizing GC-MS Exploring its Antimicrobial Effects against Multidrug-Resistant Bacteria - Fatima A. Saleh; Nada El-Darra; Karim Raafat; Iman El Ghazzawi (Pharmacognosy Journal, 2018)
Introduction: The alarming increase in bacterial strains resistant to existing antimicrobial agents has demanded alternative strategies. Medicinal plants are now considered as an alternative treatment because of their secure choice in several diseases. Among them, Nigella sativa is a promising traditional herb having rich medical background. The aim of the study is to perform phytochemical analysis of Nigella sativa L. Utilizing Gas chromatographic–mass spectrometric (GC/MS) exploring its antioxidant and antibacterial activity against multidrug resistant (MDR) gram-positive and gram-negative bacteria. Methods: Total phenolic, tannin, and flavonoid content of N. sativa seed extracts and its commercially available oil were determined. Their radical scavenging activity using DPPH was also tested. The antibacterial activity of N. sativa seed extracts and its oil against MDR gram-positive and gram-negative bacterial strains was studied using disc diffusion test and the biofilm formation assay. GC-MS studies were also performed. Results: Among the different preparations used, N. sativa oil showed the highest antioxidant and antibacterial activity against highly resistant gram-positive bacteria with the greatest suppression of biofilm formation, which was attributed to its high bioactive contents. Conclusion: This study indicates that N. sativa extracts and its oils can be used as natural antibacterial agents to treat infections caused by multidrug resistant bacteria.
Keywords: Antibacterial; Antioxidant; GC-MS analysis; Multidrug resistant bacteria; Nigella sativa

Phytochemical Composition and Evaluation of the Antioxidant Activity of the Ethanolic Extract of Calendula suffruticosa subsp. suffruticosa Vahl - Sofiane Ismahene; Seridi Ratiba; Cortes Martinez Diego Miguel; Cabedo Nuria (Pharmacognosy Journal, 2018)
Aim: Calendula suffruticosa ssp. suffruticosa Vahl, Medicinal and Aromatic plant, spontaneous and widespread in the Mediterranean region and in the Northeast of Algeria, is widely used by the local population for its medicinal properties. Methods: The chemical composition of the ethanolic extract of Calendula suffruticosa was established for the first time using GC / MS. The antioxidant activity of the ethanolic extract was evaluated in vitro by the DPPH (2,2-diphenyl-1-picrylhydrazyl) test, the FRAP assay and β-carotene bleaching assay. Results: sixty-four compounds are identified by GC/MS analysis, six are predominant: α-linoleic acid (24.20%), linoleic acid (23.58%), Stigmasterol (8.53%), 2-Metyl-Z-4-tetradecene (6.62%) And α-Bisabolol (1.70%). The free radical scavenging by DPPH method indicated that the ethanolic extract of C. suffruticosa showed a very high antioxydant activity with an IC50 = 0.017 ± 1.00 mg / ml. This extract also showed an ability to reduce very high iron with a maximum optical density of 1.157 at a concentration of 0.5 mg / ml and an antioxidant activity compared to the β-carotene / linoleic acid test of order of 75 ± 1.02%. Conclusion: These results show for the first time the richness of phytochemicals and the strong antioxidant activity of the species Calendula suffruticosa endemic to north-east of Algeria.
Keywords: antioxidant activity; Calendula suffruticosa; DPPH; FRAP; GC / MS; Phytochemical composition

Phytochemical Constituents, Total Saponins, Alkaloids, Flavonoids and Vitamin C Contents of Ethanol Extracts of five Solanum torvum Fruits - Desmond Ato Koomson; Benjamin Danso Kwakye; Williams Kweku Darkwah; Bismark Odum; Mabel Asante; Gideon Aidoo (Pharmacognosy Journal, 2018)
Introduction: Phytochemicals are frequently used in chemotherapeutic treatment or may be used as chemo preventive agents with chemoprevention. The study report the quantification of phytochemical constituents and vitamin C contents from ethanol extracts of Solanum torvum fruits. Method: The main objective for this research was to use standard procedures to determine phytochemical and vitamin C content. Results: The estimated alkaloids found in mature fruits were 6.32 ± 0.12 mg/g and 16.94 ± 2.3 mg/g in the immature fruits. Total saponins in mature and immature fruits were 8.60 ± 2.6 mg/g and 16.90 ± 9.4 mg/g respectively. Total flavonoids in mature and immature fruits were 21.14 ± 4.4 mg/g and 14.24 ± 1.8 mg/g respectively. Also vitamin C contents were 11.79 ± 2.0 mg/g in mature fruits and 8.70 ± 0.26 mg/g in immature fruits. With the exception of alkaloids whose difference in the mature and immature was significant, other differences obtained were not significant. Conclusion: The study showed that the extracts contain diversity of phytochemicals in appreciable amount that can expertly keep the body against oxidative stress triggered by free radicals and therefore be used as a source of potent natural products.
Keywords: Alkaloids; Ethanol Extract; Flavonoids; Phytochemicals; Saponins; Solanum torvum fruits

Phytochemical Investigation and Screening for Inflammatory Bowel Disease Activity of Ethanolic Extract of Kariyat - Nilesh Balasaheb Chougule; Sachin Annasaheb Nitve; Kailasam Koumaravelou (Pharmacognosy Journal, 2018)
Objectives: The present study investigates the protective effect of Kariyat against Indomethacin and Acetic Acid induced Inflammatory Bowel Disease in male wistar rats. Material Method: HPTLC and GC-MS investigations indicated presence of steroid, phenols, terpenoid, alkaloids, saponine, flavonoids. IBD was induced by administration of Indomethacin (7.5mg/kg b.w. S.c.), Acetic Acid (4% v/v). Two different models used to induce IBD named Indomethacin induces enter colitis and Acetic Acid induces enter colitis in case of Indomethacin induces enter colitis the compromises 5 groups (n=6), normal, control, standard treated (Prednisolone 2mg/kg p.o.), KEE treated (100 mg/kg b.w.), KEE treated (200 mg/kg b.w.) in case of Acetic Acid induces colitis the compromises 5 groups (n=6), normal, control, standard treated (Prednisolone 2mg/kg p.o.), KEE treated (100mg/kg b.w.), KEE treated(200mg/kg b.w.). After treatment of 7 days animals were sacrificed and colon was isolated for macroscopic and microscopic studies. Quantification of inflammation was done by using myeloperoxidase assay (MPO), Lactate dehydrogenase (LDH), Lipid peroxidase (LPO). Result: Evaluation based on macroscopic features showed significantly lower score values for drug treated and standard drug treated groups compared to the disease control groups. Histological examination of disease control group showed massive necrosis of the mucosa and sub mucosa. Drug treated group showed mild lesions, regeneration and inflammatory reaction. The Prednisolone treated group showed suppressed inflammatory reaction. The results observed from MPO, LDH and LPO assays showed significant improvement of disease with extract treated groups compared to disease control group. Histopathological examination of Kariyat treated group revealed less damage compared to Indomethacin and Acetic Acid Induced group. Conclusion: Kariyat have shown to be effective in Indomethacin and Acetic Acid induced colitis in rats, which has protected the animals against experimentally induced disease because of its antioxidant and anti-inflammatory activity.
Keywords: Indomithacin.; Inflammatory bowel Disease; Kariyat

Phytochemical Investigation of Psoralea bituminosa L. and its Anti-Diabetic Potentials - Sara Al Ayoubi, Karim Raafat; Abdalla El-Lakany; Maha Aboul-Ela (Pharmacognosy Journal, 2018)
Introduction: Psoralea bituminosa L. (Fabaceae), is a very important medicinal plant, used in traditional medicine in Europe, Asia, and America, and in Africa for, its antiseptic, antihyperglycemic and anti-oxidative potentials. The objective of this study is to investigate the potential of Psoralea bituminosa (Pbt.) in the management of diabetes and diabetic – induced thermal hyperalgesia. Moreover, this study aimed also to investigate the volatile oil constituents of Pbt. growing in Lebanon utilizing GC-MS method. Methods: Blood glucose level (BGL) was measured using gluco-meter while diabetic-induced thermal hyperplasia of Pbt. growing in Lebanon was measured using tail flick and hot plate methods. Antioxidant was measured using DPPH free radicals method. Volatile oil of fresh and dried aerial parts of Pbt. was analyzed using GC-MS. Results: The result of study conducted on Lebanese Pbt. revealed that acute anti-diabetic activity of Pbt. in the 3 extracts subjected a decrease in BGL ranging between 34% to 38.5%. In subchronic anti-diabetic activity of Pbt. BGL dropped in range 19% to 44%. Moreover, Pbt. extract showed 1.7% to 13.6%increase in body weight at all doses with respect to 8th day. On the other hand, alloxan diabetic induced mice reported melioration by 63.8% to 86.3% on the 8th week alloxan after injection in diabetic – induced thermal hyperalgesia hotplate latency method. Nevertheless, a marked improvement in tail flick latency on the 8th week after alloxan injection by 22.7 % to 48.6 %. Pbt. extract revealed DPPH radical decreases at 82.6% at concentration of 100 mg/mL, respectively. Total flavonoid content measured of Pbt. was 135.83 mg/g while total phenolic content showed 217.48 mg/g. Conclusion: Psoralea bituminosa  showed a significant effect in the management of diabetes and neuropathic pain conditions and limiting expected side-effects, which might be used as a future antidiabetic therapy.
Keywords: Antidiabetic; Antioxidant; Diabetic neuropathy; Essential oil; Psoralea bituminosa

Phytochemical Investigation of Psoralea bituminosa L. and its Anti-Diabetic Potentials - Sara Al Ayoubi; Karim Raafat; Abdalla El-Lakany; Maha Aboul-Ela (Pharmacognosy Journal, 2018)
Introduction:Psoralea bituminosaL. (Fabaceae), is a very important medicinal plant, used in traditional medicine in Europe, Asia, and America, and in Africa for, its antiseptic, antihyperglycemic and anti-oxidative potentials. The objective of this study is to investigate the potential of Psoralea bituminosa (Pbt.) in the management of diabetes and diabetic – induced thermal hyperalgesia. Moreover, this study aimed also to investigate the volatile oil constituents of Pbt. growing in Lebanon utilizing GC-MS method. Methods:Blood glucose level (BGL) was measured using gluco-meter while diabetic-induced thermal hyperplasia of Pbt. growing in Lebanon was measured using tail flick and hot plate methods. Antioxidant was measured using DPPH free radicals method. Volatile oil of fresh and dried aerial parts of Pbt. was analyzed using GC-MS. Results: The result of study conducted on Lebanese Pbt. revealed that acute anti-diabetic activity of Pbt. in the 3 extracts subjected a decrease in BGL ranging between 34% to 38.5%. In subchronic anti-diabetic activity of Pbt. BGL dropped in range 19% to 44%. Moreover, Pbt. extract showed 1.7% to 13.6%increase in body weight at all doses with respect to 8th day. On the other hand, alloxan diabetic induced mice reported melioration by 63.8% to 86.3% on the 8th week alloxan after injection in diabetic – induced thermal hyperalgesia hotplate latency method. Nevertheless, a marked improvement in tail flick latency on the 8th week after alloxan injection by 22.7 % to 48.6 %. Pbt. extract revealed DPPH radical decreases at 82.6% at concentration of 100 mg/mL, respectively. Total flavonoid content measured of Pbt. was 135.83 mg/g while total phenolic content showed 217.48 mg/g. Conclusion:Psoralea bituminosa showed a significant effect in the management of diabetes and neuropathic pain conditions and limiting expected side-effects, which might be used as a future antidiabetic therapy. Keywords:Psoralea bituminosa,Antidiabetic,Antioxidant,Essential oil,Diabetic neuropathy.

Phytochemical Profile and Antioxidant Activity of Propolis Ethanolic Extract from Tetragonula Bee - Diah Kartika Pratami; Abdul Mun’im; Andini Sundowo; Muhamad Sahlan (Pharmacognosy Journal, 2018)
Objective: This research aimed to determine the phytochemical composition and the antioxidant properties in vitro of three types propolis collected from the region of South Sulawesi Province of Indonesia. Methods: Samples from three types of propolis: smooth, rough and mix were extracted with 96% ethanol. The propolis ethanolic extracts (PEE) was dried and studied their antioxidant properties by using FRAP (Ferric Reducing Antioxidant Power) and DPPH radical scavenging assays. Total phenolic compounds were quantified by Folin-Ciocalteu, and total flavonoid contents were also quantitatively determined by the AlCl3 colorimetric method with a microplate reader. The chemical compounds were identified by an ultraperformance liquid chromatography TOF mass spectrometer (UPLC-TOF-MS) using the MS mode. Results: The sequence of potential antioxidant activity of PEE is smooth propolis > mix propolis > rough propolis. Which showed by EC50 value with DPPH assays are 25.54; 31.66; and 69.96 μg/mL, respectively and also showed by EC50 value with FRAP assays consecutively were 26.41; 32.10; and 34.62 μg/mL.Smooth propolis has the lowest EC50 value of all the types of propolis examined, contains total flavonoid content 791.06+13.06 mg QE/g extract and total phenolics content 426.91+61.08 mg GAE.g-1 extract. Chemical component identified by UPLC-TOF-MS using the MSE mode were (-)-Sesamin C20H18O6; Curcumin C21H20O6; 8-epi- Helenalin C15H18O4; and Kushenol F C25H28O6. Conclusion: Smooth propolis which taken from inside the nest was the most potent antioxidant among of all the types of examined propolis. The antioxidant activity was influenced by the phenolic content of Propolis.
Keywords: DPPH; FRAP; Microplate method; TFC; TPC; UPLC-TOF-MS

Phytochemical Screening and Antimicrobial Studies in Leaf Extracts of Indigofera aspalathoides (Vahl.) - Tamilarasan Tamil Kumar; Seeni Mohamed Salique; Mohamed Hussain Muhammad Ilyas; Nooruddin Thajuddin; Annamalai Panneerselvam; Mohamed Khan Syed Ali Padusha; Hussain Syed Jahangir (Pharmacognosy Journal, 2018)
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 8α (2H)-Phenanthrenol, 7-ethenyldodecahydro-1,1,4α, 7-tetramethyl-, acetate, [4αs(4αα, 4bα, 7α, 8αα, 10αα)], Benzoic acid, 4-methyl- , 2-oxo-2- phenylethyl ester and Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1S-(1α,2α,5α)] 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

Phytochemical Screening, Antibacterial Activity, and Mode of Action on Morus nigra - Diah Lia Aulifa; Sani Nurlaela Fitriansyah; Seno Aulia Ardiansyah; Diki Prayugo Wibowo; Yolanda Armiliani Julata; Desty Santi Christy (Pharmacognosy Journal, 2018)
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

Phytochemical Screening, LC-MS Studies and Antidiabetic Potential of Methanol Extracts of Seed Shells of Archidendron bubalinum (Jack) I.C. Nielson (Julang Jaling) from Lampung, Indonesia - Hanafi; Candra Irawan; Henny Rochaeni; Lilis Sulistiawaty; Achmad Nandang Roziafanto; Supriyono (Pharmacognosy Journal, 2018)
Background: Some Malaysia and Indonesia people believed that root and seed shell of Archidendron bubalinum can treat diabetes. However, seed shell of Archidendron bubalinum has not yet to be scientifically proven and confirmed their ability to treat diabetes. The study of the potential of this seed shell was also scarcely available. Objective: The recent work was aimed to investigate the phytochemical screening of methanol extracts of seed shells of Archidendron bubalinum and to evaluate their chemical compositions and antidiabetic activities. Material and Methods: The methods of phytochemical screening were including alkaloids, flavonoids, tannins, polyphenols, saponins, and terpenoids. Their chemical compositions were determined by Liquid Chromatography-Mass Spectrometry (LC-MS) and antidiabetic activities were performed by α-glucosidase inhibitory method. Results: The phytochemical screening showed that methanol extracts of seed shells of Archidendron bubalinum contain flavonoids, tannins, polyphenols, and terpenoids. This extracts exhibited antidiabetic activity with IC50 7.77 μg/mL. This result was supported by LC-MS analysis which showed the presence of phlorizin and astilbin, in which these compounds had high inhibitory activity against α-glucosidase or diabetes. Conclusion: LC-MS analysis revealed the presence of polyphenol compounds namely phlorizin and astilbin in which had high α-glucosidase inhibitory activity, might largely contribute in the antidiabetic activity. Key words: Phytochemical screening, Mass spectrometry
Keywords: Anti-diabetic; Archidendron bubalinum; Mass spectrometry; Phytochemical screening

Phytochemical Screening, Total Flavonoid and Total Phenolic Content and Antioxidant Activity of Different Parts of Caesalpinia bonduc (L.) Roxb - Elin Novia Sembiring; Berna Elya; Rani Sauriasari (Pharmacognosy Journal, 2018)
Background: Caesalpinia bonduc (L.) Roxb are traditionally used in Indonesia to treat various diseases, but still limited study about different part of this plant. Objective: The aim of this study was to screen the phytochemicals, to evaluate the total flavonoid and total phenolic contents as well as antioxidant activity of ethanol extract of root, stem, leaves, and seed kernel of C. bonduc. Methods: Each part of plant were extracted by reflux using 70% ethanol as the solvent for 2 h and repeated 3 times. Total flavonoid content was determined by aluminium chloride colorimetric assay on 415 nm. Total phenolic content was determined with Folin-Ciocalteu 1:4 on 765 nm using microplate reader. Antioxidant activity was determined using 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenger methods. Results: Phytochemical screening showed that all of samples positively contain flavonoid and saponin. Total flavonoid content was the highest in leaf and the lowest in root whereas total phenols content was highest in leaf and the lowest in seed kernel. The crude extracts displayed DPPH free radical scavenging activity with highest value in leaf extract followed by root, stem, and seed kernel. Conclusion: The 70% ethanol leaf extract of C. bonduc showed the highest yield, total flavonoid content and total phenolic content among other parts investigated. Moreover, leaf extract has highest DPPH free radical scavenging activity (79.802 μg/ml) which could be related to its higher phenolic content.
Keywords: Caesalpinia bonduc; DPPH; Phytochemical screening; total flavonoid; total phenolic content

Phytochemical Test and Cytotoxic Activity of Macroalgae Eucheuma cottonii against Cervical HeLa Cells - Ade Arsianti; Yully Astika Nugrahayning Aziza; Kartika Dwi Kurniasari; Baiq Kirana Dyahningrum Mandasari; Riathul Masita; Futihati Ruhama Zulfa; Micheylla Kusumaning Dewi; Cut Raisya Zahira Zagloel; Norma Nur Azizah; Rista Putrianingsih (Pharmacognosy Journal, 2018)
Intoduction: Marine resource of macroalgae Eucheuma cottonii from East Lombok, Nusa Tenggara Barat, Indonesia, have potential as anti-cervical cancer agent. Objectives: Finding cytotoxic activity of Eucheuma cottonii hexane, ethylacetate, chloroform and ethanol extracts against cervical HeLa cells by MTT cell proliferation assay. Methods: The extracts was tested in phytochemical and cytotoxic activity test. Phytochemical test to identify composition of secondary metabolite such as flavonoid, alkaloid, saponins, tannin, triterpenoid, steroid and glycoside. The amount of substances contained in the extract sample was analyzed by Thin Layer Chromatography (TLC). Cytotoxic activity using HeLa cells. Results: Phytochemical test of E. cottonii extracts showed the positive result for metabolite of flavonoid, whereas the TLC analysis revealed that the extracts containing five chemical compounds. Ethanol, n-hexane, chloroform, and ethyl acetate extracts of E. cottonii exhibited a strong cytotoxic activity against cervical HeLa cells with IC50 of 7.54 μg/mL, 5.73 μg /mL, 4.82 μg /mL and 4.34 μg / mL, respectively. Conclusion: The results suggest that macroalgae Eucheuma cottonii could be used as a new anti-cervical cancer’s candidate.
Keywords: Anti-cervical cancer; Cytotoxicity; Eucheuma cottonii; HeLa cell lines; Phytochemical test; Seaweed

Potential Bioactive Compounds Isolated from Boesenbergia rotunda as Antioxidant and Antimicrobial Agents - Sri Atun; Sri Handayani; Anna Rakhmawati (Pharmacognosy Journal, 2018)
Objective: This study was conducted to identify some bioactive compounds of Boesenbergia rotunda rhizome and to test as antioxidant and antimicrobial agents. Methods: The milled dried rhizome of B. Rotunda (5kg) was extracted exhaustively with ethanol. The ethanol extract was partitioned three times by n-hexane, chloroform, and ethyl acetate respectively. Each fraction was fractionated by vacuum liquid chromatography (VLC) and then purified by column chromatography gravitation. Structural identification of all pure compounds were elucidated based on spectroscopic methods (UV, IR, and NMR).The antioxidant activity was tested by 2,2-diphenyl- 1-picrylhydrazyl (DPPH). Antimicrobial character was screened for activities againts pathogenic bacteria i.e. Escherichia coli ATCC-11229, Staphylococcus aureus ATCC-25923, Staphylococcus epidermidis FNCC-0048, and Streptococcus mutans by the disk-diffusion method. The assay was done in triplicate, and chloramphenicol was used as the positive control. Results and Discussion: From ethanol extract of B. rotunda three known compounds of flavanones, namely 2’,4’-dihydroxy-6-methoxychalcone (compound-1), 5-hydroxy-7- methoxyflavanone (compound-2), and 5,7-dihydroxyflavanone (compound-3) were isolated. The ethanol extract of B. rotunda and the three isolated compounds -1,-2, and -3 showed an antioxidant activity with the IC value of 92.64; 46.66; 62.84, and 62.66 μg/mL, respectively. The zone of inhibition of extract and the three isolated compounds showed moderate activity against Escherichia coli ATCC-11229, Staphylococcus aureus ATCC-25923, Staphylococcus epidermidis FNCC-0048, and Streptococcus mutans.The maximum zone of inhibition was 13.20±0.76 mm at the maximum concentration used (500 μg/mL) against Escherichia coli ATCC-11229, and the minimum inhibitory concentration(MIC) for each bacteria was found to be 0.5μg/mL. Conclusion: The result of the study suggests that B. rotunda rhizome contains potential bioactive compounds which could be suitable for antioxidant and the treatment of various infections caused by Escherichia coli ATCC-11229, Staphylococcus aureus ATCC- 25923, Staphylococcus epidermidis FNCC-0048, and Streptococcus mutans.
Keywords: Antimicrobial; Antioxidant; Bioactive compound; Boesenbergia rotunda

Potential Effects of Pomegranate Juice in Attenuating LID in Mice Model of Parkinson Disease - Sarah Rezaee; Mahsa Hadipour Jahromy (Pharmacognosy Journal, 2018)
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’s disease; Pomegranate

Preliminary of Pharmacokinetics Study of Brown Seaweed (Turbinaria decurrens Bory) Extract in Colon Cancer Model Mice Induced by AOM (Azoxymethane) and DSS (Dextran Sodium Sulphate) - Nurul Qurrota’Ayun; Astria Deviyani Zakaria; Anton Bahtiar (Pharmacognosy Journal, 2018)
Introduction: Colon Cancer is one of leading cancer that causes morbidity and mortality worldwide, causes 774,000 deaths. Fucoxanthin contained brown seaweed Bory) extracts showed cytotoxic activity by and study, including colon cancer. This study aims to examine the absorption profile of fucoxanthin in blood plasma on colon cancer model mice. Methods: Mice were induced by azoxymethane (AOM) and two cycle dextran sulfate sodium (DSS). Mice were given an extract of brown seaweed Bory that contain fucoxanthin. Fucoxanthin content in blood plasma analyzed using mobile phase methanol: acetonitrile by Reversed- Phase High-Performance Liquid Chromatography (RP-HPLC) analysis. Results: The maximum concentration of fucoxanthin in blood was at 4 hours after administration, and the plasma concentration is 2.15 nmol/L, T1/2 6.25 h, and AUC 10.75 nmol/L/h Conclusions: The method was applied successfully in a pharmacokinetic study and the resulting oral brown seaweed bioavailability calculated.
Keywords: Brown seaweed; Colon cancer; Fucoxanthin

Profile of HMGB1 mRNA Expression and TLR4 Protein in BALB/c Mice Model Sterile Injury after Systemic Lidocaine Administration - Robert Hotman Sirait; Mochammad Hatta; Syafri K.Arief; Tigor P. Simanjuntak; Bambang Suprayogi (Pharmacognosy Journal, 2018)
Background: High mobility group box 1 (HMGB1) is a cytokine proinflamation which contributes to inflammation. HMGB1 physically interacts with toll like receptor 4 (TLR4) to release macrophage cytokines. The aim of this study was to demonstrate the effectiveness of systemic lidocaine administration to inhibit the expression of HMGB1 mRNA and TLR4 protein in mice BALB/c mice with sterile injury. Material and Methods: Twenty adult male BALB/c mice were divided into lidocaine and control groups. A sterile injury is done by closed fracturing the left thigh bone of the mice. The lidocaine group was treated with 2 mg/kgBW lidocaine through tail vein injection after 4 h of sterile injury. The control group was given distilled water therapy as a substitute for lidocaine. Mice blood is extracted from the tail vein before trauma, 4 h after trauma, and 2 h after the administration of lidocaine and distilled water is complete. The HMGB1 mRNA expression was examined by quantitative real-time polymerase chain reaction (qPCR) while the TLR4 protein level was determined with enzyme-linked immunosorbent assay (ELISA) according to the manufacturer’s instructions. Result: The HMGB1 mRNA expression and TLR4 protein levels in BALB/c that sustained inflammation due to a sterile injury was significantly decreased in the lidocaine group (p < 0.00). Conclusion: Administration systemic 2 mg/kgBW of lidocaine is effectively inhibits HMGB1 mRNA and TLR4 protein in mice that sustain inflammation due to a sterile injury.
Keywords: HMGB1 mRNA; lidocaine; Sterile injury; TLR4

Protective Effect of Dietary Curcumin and Capsaicin on LPS-Induced Inflammation in Mice - Thriveni Vasanthkumar; Manjunatha Hanumanthappa; Prabhakar BT (Pharmacognosy Journal, 2018)
Objective: The current study aimed to evaluate the anti-inflammatory potency of combined curcumin and capsaicin against lipopolysaccharide (LPS) induced organ damage in mice. Methods: Adult male albino mice were distributed into five experimental groups for treatment with olive oil, LPS, curcumin, capsaicin and their combination, respectively, for 7 days prior to LPS induced inflammation. At the end of the experiment, blood samples were collected and used for the analysis of serum non-specific enzymes including serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), alkaline phosphatase (ALP), total bilirubin (TB), urea, creatinine and sugar, while the organ homogenates were subjected for the evaluation of antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutothione S transferase (GST), nitric oxide (NO); lipid peroxidation (LPO) and it was further confirmed by histopathological study of different organs. Results and Conclusion: Curcumin, capsaicin and their combination had shown significant restoration of non-specific serum enzymes, antioxidant enzymes and attenuated inflammatory cells infiltration thereby preventing tissue/organ damage in LPS-challenged mice. However, the protective effect was found to be more when the two compounds were fed in combination. This beneficial potency of combined spice treatment is may be due to the contribution of diversified active moieties of curcumin and capsaicin in combination compared to individual molecules.
Keywords: Capsaicin; Curcumin; Lipid peroxidation; LPS; Septic shock; Superoxide dismutase

Purified Anthocyanin from in vitro Culture of Bridelia retusa (L.) Spreng. Capable of Inhibiting the Growth of Human Oral Squamous Cell Carcinoma Cells - Aswathy Jayasree Madanakumar; Bosco Lawarence; Manoj GS; Murugan Kumaraswamy (Pharmacognosy Journal, 2018)
The present study aims in vitro cell suspension culture of Bridelia retusa, isolation of anthocyanin, purification, fractionation and its anti-metastatic potential against oral squamous carcinoma cells. Experimental results reveal that 2, 4-D either alone or in combination with kinetin supplemented in MS medium showed significant initiation of callus from leaf explants than stem. Growth hormones, pH, light, and carbon source influence anthocyanin synthesis. Maximum callus induction was noticed with 2.5 mg/L N6-benzyladenine (BA) + 2 mg/L 2, 4-dichlorophenoxyacetic acid (2, 4-D) (98.9%). Fresh and dry weight of the calli were i.e., 1.9 ± 0.04 and 0.45 ± 0. 03 g respectively. Optimal response was seen with light on MS medium contain 4% glucose + 2.5 mg/L BA and 2 mg/L 2, 4-D at pH 3.5 yielded 2.8 mg /g of anthocyanins. Suspension culture medium fortified with 2, 4-D (2.5 mg/L) + BA (2 mg/L) at pH 5.0 induced anthocyanin production at pH 4.4 – 4.6. HCl-ethanol extraction for 90 min yielded the maximum anthocyanin content. Fractionation of anthocyanin using HPLC coupled with mass spectrometry revealed 07 fractions such as acylated cyanidins, two peonidins, cyanidin 3-p-coumaroyl and feruloyl diglucoside-5-glucosides. In the search of novel therapeutic drugs against cancer, cytotoxicity effect of B.retusa anthocyanin extracts on human oral squamous cell carcinoma (SCC4, SCC9 and SCC25) cells using cell adhesion and cell viability assay was carried. The morphological alterations in SCCs cells after treatment with B.retusa anthocyanin includes nuclear condensation, fragmentation and apoptotic cells as revealed by Hoechst stain. Flow cytometry showed arresting of SCC25 cells mostly in the G0/G1 and S-G2/M stages with a concomitant up regulation of sub-G1 fraction, indicating cell death by apoptosis. Apoptosis was further substantiated by the activation of caspase-3 expression in the SCC25 cells treated with B.retusa anthocyanin. Thus, it is possible to suggest that B.retusa anthocyanin cause apoptosis of SCCs and warrant further investigation using animal models.
Keywords: Anthocyanin; Anti-metastatic potential; Apoptosis; Bridelia retusa; Cell suspension; in vitro culture; Purification

Purified Anthocyanin, its Elicitation from Cell Cultures of Begonia malabarica and Begonia rex-cultorum ‘Baby Rainbow’and it’s In vitro Cytotoxicity Analysis by MTT Assay - Aswathy Jayasree Madanakumar; Murugan Kumaraswamy (Pharmacognosy Journal, 2018)
Background: According to recent statistics, cancer accounts about marked percentage of total deaths in the world, although there are many therapeutic approaches. Unfortunately, the cytotoxicity properties of most chemotherapy drug are nonspecific and therefore do not distinguish between normal healthy cells and tumor cells, these events have led to inappropriate and toxic therapeutic agents with a wide range of side effects. However, several experimental and epidemiological studies have suggested that fruits and vegetables are associated with low risk of various types of cancer. Anthocyanins are natural pigments that provide intense purple to red color in plants. Anthocyanin possess the ability to inhibit oxidative stress and to induce apoptosis in malignant cells, thus may prevent carcinogenesis. Methods: Antiproliferative properties of purified anthocyanin extract from elicited cell suspension cultures of Begonia malabarica and Begonia rex-cultorum ‘Baby rainbow’ was investigated in terms of MTT assay. Anthocyanin extracts were tested for their ability to inhibit the growth of HT29 (colon cancer cells), MG63 (Osteosarcoma), HeLa (Cervical cancer cells) and L929 (Mouse Fibroblast L929) cell lines. Results: Cell viability decreased in a dose dependent manner in all the considered cell lines treated with anthocyanin extracts. The extract of Begonia rex-cultorum ‘Baby rainbow’ exhibited significant cytotoxic activity against all tumor cell lines than Begonia malabarica extract. Begonia malabarica and Begonia rex-cultorum ‘Baby rainbow’ anthocyanin extract exhibited the highest cytotoxicity towards HT29 and HeLa cell lines respectively. But, MG63 resulted in comparatively higher percentage of viability of cell lines at the same concentrations. The anthocyanin extract produced significant morphological alterations on cell lines in culture. Meanwhile, the extracts showed poor cytotoxicity against the normal cell line. Conclusion: The morphological alteration of the treated cancer cells presented clear evidence of significant cytotoxicity of anthocyanin extracts of both Begonias in all the three cell lines. Thus, anthocyanin may act as chemopreventive agents for various cancer cell lines.
Keywords: Anthocyanin; Begonia; Cancer; Cell suspension.; Cytotoxicity; MTT Assay

Qualitative and Quantitative Test of Total Flavonoid Buni Fruit (Antidesma bunius (L.) Spreng) with UV-Vis Spectrophotometry Method - La Hamidu; Aktsar Roskiana Ahmad; Ahmad Najib (Pharmacognosy Journal, 2018)
The aim of this research is to determine of total flavonoid content in the Buni fruit (Antidesma bunius L. Spreng) extract. The extract was produced by stratified maceration method with the different solvent, i.e n-Hexane, Ethyl acetate and ethanol. The analysis of chemical compound using chemical reagent and Thin Layer Chromatography (TLC) method. The method is used to determines total flavonoid contains Buni fruit (Antidesma bunius L.) extract was based on the amount of Rutin Equivalent (RE) were used. The result shows that the flavonoid content higher in the n-Hexane extract is 10.72 %, then ethyl acetate extract is 7.9 % and 3.56 % ethanol extract was counted to or as a Rutin.
Keywords: Antidesma bunius L. Spreng; Flavonoid content; Spectrophotometry UV-VIS

Quantitative and Optimization of Anthocyanin Extracted from Pomegranate (Punica Granatum) Extract by High-Performance Liquid Chromatography (HPLC) - Ridzwan Norhaslinda; Jumli Mimie Noratiqah; Baig Atif Amin; Rohin Mohd Adzim Khalili (Pharmacognosy Journal, 2018)
Objective: P. granatum is one of the oldest edible fruits of tropical and subtropical regions. This fruit had high antioxidant contained by hydrolysable tannins and anthocyanin compounds that give many health benefit properties. This study aims to quantify and optimized anthocyanin from P. granatum extract. Methods: A total of 50g of the flesh was soaked into two different polar solvents; water and 50% ethanol within a ratio of 1:10; w/v for 24-hr. Then, three different methods of extraction were done and test each with HPLC analytical, respectively. Results: The validated method proved to be linear in the range of 5 – 30 ug/mL and with LOD and LOQ determined respectively for Cy3, Cy3, 5, Pg3, and Pg3, 5. The method also shows recovery (%) close to 100 when accuracy was accessed. For samples, blender water extract had a higher composition of Cy3, Cy3, 5 and Pg3, 5 (22.77 ± 8.82 mg/100 g e.p; 25.36 ± 9.95 mg/100 g e.p; 11.16 ± 5.85 mg/100 g e.p) content as compared to other. Conclusion: As a conclusion, the present methodology proved to be capable of detecting and quantifying Cy3, Cy3, 5, Pg3, Pg3, 5 in a single run. Also, comparatively the composition of each AC detected in blender water extract is significantly higher in value than the other methods. It should regard as a valuable source of antioxidant with the potential used for health benefits properties worldwide.
Keywords: 5-diglucoside; Cyanidin 3; Cyanidin 3-glucoside; Pelargonidin 3; Pelargonidin 3-glucoside

Quantitative and Optimization of Phenolic Acid Extracted from Pomegranate by High Performance Liquid Chromatography (HPLC) - Jumli Mimie Noratiqah; Ridzwan Norhaslinda; Baig Atif Amin; Rohin Mohd Adzim Khalili (Pharmacognosy Journal, 2018)
Objective: Pomegranate is scientifically known as Punica granatum L. which is a nutrient dense fruit rich in phytochemical compounds. Phenolic content is the main compound attribute for the most of the functional properties in pomegranate. The aim of this study is to quantify and optimize the composition of phenolic acids extracted from pomegranate extract by using High-performance Liquid Chromatography (HPLC). Method: The pomegranate extracted with three different methods by using two different solvents which is 50% ethanol and water. The methods were blended (aril+ seed), Soaking (aril+ seed) and soaking + squeezed manually. HPLC-PDA was used as equipment to quantify and optimize the phenolic acids extracted from pomegranate. Result: Validation method of HPLC was analysed according to the percentage of recovery, LOD, LOQ and coefficient correlation. Result showed that GA was detected in all sample from different method of extraction applied while CA compound not detected in any of extraction method applied. FA compound was only detected in blended method by 50% ethanol and water as solvent while EA compound was detected only in water extraction of all three methods applied. Conclusion: As a conclusion, according to the standard calibration data curve showed that this method proved to detect and quantify the targeted compounds. By comparing the data obtained from this study, it showed that water blended extract method is significantly higher content of targeted compound except for the CA compound. To the best of our knowledge, this sample can be a valuable source of antioxidant for better used in health benefits.
Keywords: Caffeic acid; Ellagic acid; Ferulic acid; Gallic acid; HPLC; Pomegranate extract

Renin and Angiotensin Converting Enzyme Inhibition of Standardized Bioactive Fractions of Hyphaene thebaica L. Mart Growing in Egypt - Noha A Khalil; Amira Abdel Motaal; Khaled Meselhy; Soad M Abdel khalek (Pharmacognosy Journal, 2018)
Introduction: Hyphaene thebaica L. fruit is known in Egypt for its antihypertensive activity. However a standardized herbal extract/fraction was never prepared. Methods: A biologically guided fractionation was carried out in-vitro for the 50% and 70% ethanol extracts of Hyphaene thebaica L. fruit using the angiotensin converting enzyme (ACE) inhibition and renin inhibition assays. A validated reversed phase HPLC method was developed for the standardization of the active fractions. Results: The ethyl acetate fraction of the 70% extract contained higher percentages of the three bioactive markers chlorogenic acid, quercetin and apigenin (1.940 ± 0.140%, 2.994 ± 0.349% and 0.612 ± 0.0354%, respectively) relative to the ethyl acetate fraction of the 50% extract (1.384 ± 0.157%, 0.342 ± 0.0834% and 0.070 ± 0.00225%, respectively). The butanol fraction of the 70% extract was found to possess the highest antihypertensive activity (93.69 ± 5.695 % renin inhibition activity at 0.5 mg/mL and IC50 of 0.001436 +0.00044 mg/mL for ACE inhibition activity). A standard calibration curve for the three compounds was established at a concentration range of 0.1-50 μg/Ml, they showed good linearity with a correlation coefficient (R2) of (1.00, 1.00 and 0.999; respectively). A high degree of precision (relative standard deviation values <5%) was achieved. The limits of detection for the three compounds were 0.428, 0.368 and 0.849; respectively, while the limits of quantitation were 1.29, 1.11 and 2.57, respectively. Conclusions: Current results showed that the butanol fraction of the 70% extract revealed the highest antihypertensive activity through ACE and renin inhibition mechanisms. In addition, recorded observations concerning linearity of the used bioactive markers offer a support for the possible utility of the tested fractions as potent standardized antihypertensive drugs.
Keywords: Antihypertensive; Doum; HPLC; Phenolics; standardization; Validation

Repairing Effects of Aqueous Extract of Kalanchoe pinnata (Lmk) Pers. on Lupus Nephritis Mice - Niken Indriyanti; Afrillia Nuryanti Garmana; Finna Setiawan (Pharmacognosy Journal, 2018)
Kalanchoe pinnata (Lmk) Pers (KP) has an immunosuppressive effect on delayed-type hypersensitivity test. Based on it, this research aimed to determine the repairing effects of aqueous extract of KP on lupus nephritis mice and identified its active compound. The KP extract profile was determined using UPLC-QTOF-MS/MS instrument. We examined six mice groups consisting of three curative treatment groups, one standard group receiving prednisone, one preventive group receiving KP extract, and one healthy (healthy and untreated) group. At the end of the experiment, we measured the proteinuria and renal histology parameters. To recognize the active compound in the KP profile, we performed in silico assays for the flavonoid compounds to bind to the glucocorticoid receptor. We played in silico tests for the flavonoid compounds to identify the active compound in the KP profile. We found the repairing effect of KP was detected in the kidney, demonstrated by its low proteinuria level and its better tissue structure. In the curative group, the urine protein level and its glomerular inflammation decreased. In the preventive group, the aqueous extract of KP could prevent lupus nephritis manifestations in the kidney. Bryophyllin A is the most active compound of the KP. However, further research is needed to understand the mechanism involved. We conclude, the aqueous extract, especially its bryophyllin A, have beneficial effects in repairing the function and tissue structure of lupus manifestations in mice kidney.
Keywords: Docking; Glomerulonephritis; Inflammation; Lupus; Proteinuria

Review on Ethnomedical Uses, Pharmacological Activity and Phytochemical Constituents of Samanea Saman(jacq.) Merr. Rain Tree - Shanmugam Vinodhini; Devi Rajeswari V (Pharmacognosy Journal, 2018)
Medicinal plants have been used as therapeutic drug throughout the world. But, a very few of them have been scientifically validated. Samanea Saman belongs to the Leguminosae family commonly known as rain tree and is native to tropical America. S.saman tree has different parts like a leaf, fruits, pods, seeds, and wood. S.saman is currently studied for the production of biogas which is easily obtained in the urban and rural areas. S.saman has been used in traditional medicine as a remedy for the treatment of different diseases. The phytochemical screening of the plant revealed the presence of alkaloids–C8H17ON and C17H36ON3 pithecolobine and saponin (samarin). Natural products are mainly derived from medicinal plants, which are tested in vitro and in vivo models and used to investigate the mechanism of action of drugs with potential biological properties. Additionally, S.saman were recommended as the suitable tree for planting in the urban environment as this species can reduce the outdoor temperature for all types of ground covers. This review is mainly focused on antioxidant, antibacterial, anti-diabetic potential, insecticidal, antifungal, analgesic, anti-ulcer and cytotoxic activities. However, this study helps to develop new strategies for the designing of novel drugs to treat various diseases related to human race.
Keywords: Chemical constituents; Gas production; Nanoparticles; Pharmacological activities; Samanea saman

A Review on Himalayan Pine Species: Ethnopharmacological, Phytochemical and Pharmacological Aspects - Aditi Sharma; Lalit Sharma; Rohit Goyal (Pharmacognosy Journal, 2018)
Introduction: Ever since ancient times, medicinal plants recognized as major source of therapeutics, as rescue for human diseases and maintain health. There is an exponential increase in usage of green medicines due to less cost and fewer side effects. The family Pinaceae, is largest conifer in species diversity. Pinus is the largest genus of monoecious, resiniferous, evergreen trees commonly known as Pines. Three species of pines occur wild in Indian Himalayas Pinus roxburghii, Pinus wallichiana , Pinus gerardiana. In addition, the constituents present in these plants are beneficial for the purpose of treatment of various ailments. Methods: Information was collected from scientific journals, books, and reports via electronic search tools( Medline, Pubmed etc.) Results: This review summarizes the existing information on three species of Pinus in relation to their pharmacognostic properties, phytochemistry, ethanopharmacology and pharmacological activities.
Keywords: Ethanopharmacology; Himalayas; Pharmacology; Phytochemistry; Pinus; Pinus gerardiana; Pinus roxburghii; Pinus wallichina

A Review on Phytochemical and Pharmacological Potential of Alpinia galanga - Anirban Chouni; Santanu Paul (Pharmacognosy Journal, 2018)
Introduction: From the ancient Vedic era, green plants are being used for their medicinal properties to treat several diseases. Green plants represent a big source of bioactive compounds. Alpinia galanga (Linn.) of Zingiberaceae family is one amongst those medicinally important plants. Different parts of the plant are used in the treatment of many diseases for its anti-fungal, anti-tumour, antimicrobial, anti-inflammatory, anti-diabetic, antioxidant, antiulcer and many other properties. Several active compounds such as 1’S-1’-acetoxychavicol acetate, 1’S-1’-acetoxyeuginol acetate, 1, 8-cineol, α-fenchyl acetate, β-farnesene, β-bisabolene, α-bergamotene, β-pinene, β-Sitosteroldiglucoside (AG-7), β-sitsterylArabinoside (AG-8), 1’-acetoxychavicol acetate (galangal acetate), p-hydroxycinnamaldehyde has been extracted from the plant. Methods: Relevant information was collected from scientific journals, books, and reports via electronic search using Medline, PubMed, Science Direct and Scopus. Results: This review provides a comprehensive report on Alpinia galanga having anti-proliferative, apoptotic, anti angiogenic as well as cytotoxic efficacy and their mode of action in vitro as well as in vivo condition. Conclusion: Considering the ability of the golden treasure present in Alpinia galanga, this review is aimed to summarize the information of the chemical constituents, pharmacological and therapeutic effects of the plant.
Keywords: 1’s’-1’- Acetoxychavicolacetate; Alpinia galanga; Anticancer; Antimicrobial; Bioactivity

A Review on Phytopharmacopial Potential of Epilobium angustifolium - Prasad Kadam; Manohar Patil; Kavita Yadav (Pharmacognosy Journal, 2018)
Nature has been a source of medicinal agents for thousands of years, and an impressive number of modern drugs have been isolated from natural sources which are based on their use in traditional medicine. Epilobium angustifolium L is a perennial herbaceous plant that belongs to the Onagraceae family. It exhibits various therapeutic properties like anticancer, antibacterial, anti-inflammatory, antioxidant, and anti-aging properties. Epilobium angustifolium L. contains polyphenols and secondary metabolites like oenothein B. Information was collected via Medline, PubMed, and Science Direct. Also some data have been collected from scientific journals, books, and reports. This review gives the current information on the chemical composition, traditional uses, and documented biological activities of Epilobium angustifolium L. These studies reveal that Epilobium angustifolium L is a source of medicinally active compounds and have various pharmacological effects. These studies will be helpful to create interest toward Epilobium angustifolium L and may be useful in developing a new direction for further research.Epilobium angustifolium L.is a medicinally important plant belongs to Onagraceae family. Extract from the plant is used in the treatment of many diseases for its anti-tumor, antimicrobial, anti-inflammatory, antioxidant, anti-ulcer and many other properties. The medicinal properties of fireweed have been attributed to its high content in polyphenols and more particularly to the most abundant of its secondary metabolites: Oenothein B.
Keywords: Biological activities; Epilobium angustifolium L; Herbaceous; Oenothein B; Pharmacological Effects

Role of Catecholamine Pathways in Action of Orexin B Induced Open Field Activity by Nucleus Accumbens in Wistar Rats - Rashmi Kaup Shiva; Ganaraja Bolumbu; Santosh Mayannavar (Pharmacognosy Journal, 2018)
Aims: To elucidate whether exploratory behaviour changes following Orexin B infusion in NAc is mediated through catecholamines in male Wistar rats. Methods: Inbred male Wistar rats (n= 24) were divided into three groups. Control, Treated 1 (Orexin B) and Treated 2 (Orexin B antagonist) groups. Using stereotaxic method, guide cannula was set in place bilaterally to reach Nucleus Accumbens. Orexin B and its antagonist, TCS-OX2-29 were infused in separate groups of overnight fasted rats. Following open field activity, catecholamines (Dopamine, Adrenaline, and Noradrenaline) were estimated in brain tissue homogenate by ELISA. Data were expressed as mean±SEM (ANOVA; Student-Newman Keuls test,).p<0.05 were considered as statistically significant. Results: Orexin B infusion significantly increased noradrenaline levels in Nucleus accumbens when compared to controls. TCS-OX2-29 significantly decreased noradrenaline in Nucleus accumbens during open field exploration activity. Adrenaline was not altered significantly during open field activity. Conclusion: These results suggest that Orexin B, which plays a role in the regulation of motor and exploratory behaviour when infused in NAc mediates these actions through noradrenergic neurotransmission in Nucleus Accumbens.
Keywords: Dopamine; Noradrenaline; Nucleus Accumbens; Orexin B; TCSOX2- 29

The Role of Pomelo Peel Extract for Experimentally Induced Wound in Diabetic Rats - Asser Ashraf Ahmad; Ihab Ibrahim Al Khalifa; Zead Helmi Abudayeh (Pharmacognosy Journal, 2018)
Introduction: Delayed wound healing is a chronic complication in diabetic patients than in healthy individuals. Pomelo belongs to the genus Citrus of the family Rutaceae, an important fruit with great benefits for humans in the world. Previous studies showed that pomelo peels contain an abundant bioactive compound, which may promote wound healing in experimental animals. Aim: The current study was carried to prepare optimized extraction of pomelo peels using different experimental conditions and investigate the possible healing effect of oral treatment with pomelo peel extract (PPE) on induced excision skin wound in diabetic rats. Materials and Methods: This study was done on rats divided into five groups each of 8 rats (two treatment groups given PPE (400 and 600) mg/kg by oral gavage compared to two control groups and standard plant for wound healing). Diabetes was induced by intraperitoneal injection of a single dose of Streptozotocin (STZ) 65 mg\kg body weight. After diabetes induction, full thickness excision wound was made in rats, and the study continued for 3 weeks. Results: This study showed significant reduction in blood glucose and both percentage and time to wound closure in the treated groups, also a significant increase in hydroxyproline and total protein content of the healed wound tissue in the treated groups compared with control groups and comparable to standard plant extract treated groups. Conclusion: Experimental data proposed that oral administration of pomelo peel extract rich in vitamins and flavonoids has a good therapeutic potential in the treatment of complicated wounds in diabetes.
Keywords: Flavonoids; Peel; Pomelo; Vitamin C; Wound

Simultaneous Quantification of Bioactive Triterpene acids (Ursolic acid and Oleanolic acid) in Different Extracts of Eucalyptus globulus (L) by HPTLC Method - Arti Gupta; Pooja Maheta; Renu Chauhan; Sonia Pandey; Jitendra Singh Yadav; Shailesh Shah (Pharmacognosy Journal, 2018)
Objective: To develop a novel analytical method for simultaneous determination of two triterpenic acids by high-performance thin layer chromatography in methanol and dichloromethane extracts of Eucalyptus globulus leaf. Ursolic acid was also isolated from Eucalyptus globulus leaf. Materials and Methods: Two triterpenic acids (ursolic and oleanolic acid) were extracted using methanol and dichloromethane as the extraction solvents. Study for total triterpenoids present in Eucalyptus globulus leaves was carried out which shows considerable amount of terpenoids present. Because of the similarity of chemical structure, the prechromatographic derivatization was necessary to separate these triterpenic acids. The samples were treated by 1% iodine solution in chloroform directly on the chromatographic plate and developed with the mobile phase consisting of petroleum ether, ethyl acetate and acetone (7.8:2.2:0.1, v/v/v). After drying, the plates were sprayed with 10% (v/v) ethanol solution of sulfuric acid and heated to 120 °C for 3 min. Quantification was performed in absorbance/transmittance mode at a wavelength of 345 nm. The developed HPTLC method was validated for linearity, precision and accuracy. Results: Correlation coefficient (r2 > 0.99), R.S.D. values, detection limits as well as recovery values were found to be satisfactory. Ursolic acid was isolated from E. globulus leaves. The identification of isolated ursolic acid was done on the basis of Rf value (0.26) for HPTLC and peak interpretation for FT-IR. Conclusion: The method has been successfully applied in the analysis of both triterpenic acids in medicinal herbs.
Keywords: HPTLC; Iodine derivatization; Oleanolic acid; Triterpenes; Ursolic acid

Sterols from Lentinus tigrinus - Consolacion Y. Ragasa; Maria Carmen S. Tan; Ma. Ellenita De Castro; Mariquit M. De Los Reyes; Glenn G. Oyong; Chien-Chang Shen (Pharmacognosy Journal, 2018)
Aim: To investigate the chemical constituents of the dichloromethane extract of the fruiting bodies of the mushroom Lentinus tigrinus. Materials and Methods: The chemical constituents of L. tigrinus were isolated by silica gel chromatography, while the chemical structures of the isolated compounds were identified by NMR spectroscopy. Results: The dichloromethane extract of the fruiting bodies of L. tigrinus afforded cerevisterol (1), and a mixture of stellasterol (2) and ergosterol (3) in about 4:5 ratio. Conclusion: To the best of our knowledge, this is the first report on the isolation of 1-3 from the fruiting bodies of L. tigrinus.
Keywords: Cerevisterol; Ergosterol; Lentinus tigrinus; Polyporaceae; Stellasterol

Structural Elucidation of Peanut, Sunflower and Gingelly Oils by Using FTIR and 1H NMR Spectroscopy - Veeraprakash Bathini; Suresh Kumar Kalakandan; Muthukumaran Pakkirisamy; Karthikeyen Ravichandran (Pharmacognosy Journal, 2018)
Aims: The present study focused on FTIR and 1H-NMR spectroscopic methods to assign structural connectivity and purity of the oils. Methods: Non-destructive Fourier Transform Infrared (FTIR) and 1H nuclear magnetic resonance (1H-NMR) spectroscopy techniques are used to assign the structural confirmation of the triacylglyceride (TAG) functional component in three different oils namely Sunflower, Peanut, and Gingelly oils respectively. Results: FTIR spectrum shows a very high intense band at 1744 cm-1 associated with the existence of the ester carbonyl functional group (O-C=O) and very weak shoulder peak of cis double-bond (C=C) stretching was noticed at ∼1655 cm-1. In 1H-NMR spectrum shows well resolved chemical shift values in the range 5.3-0.8 ppm corresponding to characteristic group in aliphatic region. Conclusion: Each distinct peak was determined based on chemical shift as well as splitting pattern values. For olefin signal as triplet, tertiary methine protons as singlet, well separated oxymethylene seen as triplet at ~4.2 ppm owing to presence of high electronegative oxygen atom connected to methylene chain gives more deshielding effect. As for bis-allylic, α-carbonyl methylene, β-carbonyl methylene, allylic, saturated methylene along with terminal methyl proton signals are noticed in the span of 2.3-0.8 ppm. A remarkable feature of the spectra is well resolved chemical shift values is clearly support presence of longer hydrocarbon chains. Absence of multiplet coupling peaks and disappearance of signals in down shield region > 5.4 ppm confirms the absence of trans stereoisomer (E-conformation), aromatic and heterocyclic epoxide compounds.
Keywords: 1H-NMR; FTIR; TAG; Unsaturation; WHO; Z-Conformation

Studies on Positive and Negative ionization mode of ESI-LC-MS/ MS for screening of Phytochemicals on Cassia auriculata (Aavaram Poo) - Paranthaman Ramakrishnan; Sureshkumar Kalakandan; Muthukumaran Pakkirisamy (Pharmacognosy Journal, 2018)
Background: Cassia auriculata (Avaram) is an important medicinal plant in India Improved awareness in medicinal flowers has led to an increased need for efficient extraction methods and screening of flavonoid derivatives. Objective: To standardization of extraction solvent system and Characterization of flavonoids through positive and negative electrospray ionization mode using LC-MS/MS from Cassia auriculata extract. Materials and Methods: The different solvents like Methanol, Water, Acetonitrile, Ethyl Acetate, Ethanol, Chloroform, Hexane, Acetone Diethyl ether used frot he identification of flavonoids (Gallic acid, Theanine, Theobromine, Theophylline, Caffeic acid, Caffeine, Ferulic acid, Theacrine, Catechin, Quercetin, EpiGallo Catachin, catechin gallate, Epicatachin gallate and Quercetin hexoside. Results: Based on the peak area percentage the extraction solvent was standardized. The percentage of relative & absolute intensity of screened flavonoids was observed using LC-MS in positive and negative electrospray ionization. The results show that the methanol extract has more percentage of peak area, relative intensity and absolute intensity. The MS results showed that the negative ionoization has more intensity values of flavonoids and the signal-to-noise ratio was high in negative ionization mode compare to positive mode. Conclusion: Based on the results the methanol is the suitable extraction solvetnt and negative ionization mode of ESI-LC-MS/MS was appropriate for the screening of flavonoids on Cassia auriculata flower extracts.
Keywords: Caucalis platycarpos L.; Methanol; Eelectrospray ionization; Flavonoids; UHPLCESI- MS

Systematic Review and Meta-analysis of Andrographis serpyllifolia (Rottler ex Vahl) Wight: An Ethno-pharmaco- botanical Perspective - Suma Krishnaswamy; Bopaiah A Kushalappa (Pharmacognosy Journal, 2018)
Andrographis serpyllifolia (Rottler ex Vahl) Wight, belonging to Acanthaceae, has been recorded in ethnobotanical archives as a plant possessing potent anti- snake and scorpion venom activity. Its leaf extract has been proven a highly effective drug to combat bovine mastitis. The present review compiles most of the available experimental data emphasising phytochemical profiles and the pharmacological actitvty of this medicinal geophyte. This kind of systematic review encompassing all experimentally proven aspects of the plant, gaps in research and potential areas for future investigation is not available in literature published with regard to this plant so far.
Keywords: Andrographis serpyllifolia; Botanical aspects; Ethnobotany; Pharmacological screening; Phytochemical screening

Therapeutic Index of Methanolic Extracts of Three Malaysian Phyllanthus Species on MCF-7 and MCF-10A Cell Lines - Wan Adnan Wan Omar; Siti Nur Dalila Mohd Zain (Pharmacognosy Journal, 2018)
Introduction: Phyllanthus species such as P. urinaria, P. niruri and P. debilis are common herbs found in Malaysia that are traditionally used for treatment of chronic diseases such as liver diseases, kidney stones and cancer. Phyllanthus species were shown in vitro to have many biological functions such as anti-cancer, anti-inflammatory, hepatoprotective and anti-diabetic. Aims: The goal of this in vitro study was to assess the cytotoxic effect of the methanolic extract of P. urinaria, P. niruri and P. debilis on MCF-10A and MCF-7 cells (i.e., normal and cancerous breast cell lines) and to determine the therapeutic index of each Phyllanthus species. Materials and Methods: We determined the therapeutic index for each Phyllanthus sp. and its selective toxicity towards these cells. The toxicity of sample toward the cells are measured by trypan blue cell counting method. Results: Our results showed that P. debilis had the lowest IC50 concentration in MCF-7 cells and the highest IC50 concentration in MCF-10A cells and its therapeutic index was higher than that found in P. niruri and P. urinaria. The high therapeutic index of P. debilis suggests that this species has greater selective cytotoxicity in MCF-7 cancer cells than in MCF-10A normal cells. Thus, the methanolic extract of P. debilis should be further characterised and developed for future use as an anti-cancer agent.
Keywords: Cytotoxicity; MCF-10A; MCF-7; Phyllanthus; Therapeutic index

Total Phenolic Content and Tyrosinase Inhibitory Potential of Extracts from Cajanus cajan (L.) Millsp. - Prasob-on Rinthong; Suthira Maneechai (Pharmacognosy Journal, 2018)
Background: Cajanus cajan (L.) Millsp. (Fabaceae) is a legume plant which used for human food and animal feed. Objective: The present study was aimed to investigate total phenolic content and tyrosinase inhibitory potential of the root, stem and seed parts of C. cajan. Method: Crude extracts were prepared by reflux extraction using methanol, dichloromethane and water as solvents. Total phenolic contents of the obtained extracts were analyzed by Folin- Ciocalteu colorimetric method and the inhibitory effect on tyrosinase activity was determined spectrophotometrically. Results: The results revealed that dichloromethane seed extract had more total phenolic content than those of methanol and water seed extracts, respectively. Dichloromethane seed extract had the highest total phenolic content of 92.00 ± 1.24 mg GAE/ g extracts. However, the highest tyrosinase inhibitory activity was found in the root methanol extract with IC50 of 3.55 ± 0.35 mg/ml. Conclusion: Type of extraction solvent was an important factor on phenolic contents of C. cajan extracts. The extracts of C. cajan inhibit slightly tyrosinase inhibitory.
Keywords: Cajanus cajan; Dichloromethane seed extract; Root methanol extract; total phenolic content; Tyrosinase inhibitor

Total Phenolic, Total Flavonoid, Quercetin Content and Antioxidant Activity of Standardized Extract of Moringa oleifera Leaf from Regions with Different Elevation - Evi Sulastri; Muhammad Sulaiman Zubair; Nurafni Israyanti Anas; Syakila Abidin; Ririen Hardani; Risfah Yulianti; Aliyah (Pharmacognosy Journal, 2018)
Context: Moringa oleifera is the famous plant that has been used as medicinal plant for diverse pharmacological activity. Aims: To evaluate the total phenolic, total flavonoid, quercetin content as well as the antioxidant activity of standardized extract of Moringa oleifera (Lamk) leaf, collected from three regions with different elevation. Materials and Methods: The leaves were extracted by maceration method using ethanol 96% and evaporated by rotary evaporator to obtain the viscous extract. The determination of total phenolic and total flavonoid were performed by spectroscopic method, while the quercetin concentration were determined by high performance liquid chromatography (HPLC). The antioxidant activity was evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) method. Results: Ethanolic extracts of Moringa oleifera leaf from region with medium altitude (Sigi regency) showed higher total phenolic, total flavonoid, quercetin concentration and antioxidant activity than regions with low and high altitude (Parigi and Palu cities). Conclusion: This study reveals the potency of standardized extracts of Moringa oleifera growing in medium altitude (Sigi regency) to be developed as antioxidant herbal medicine.
Keywords: Antioxidant; Kelor; Moringa oleifera; total flavonoid; total phenolic

A Triterpene and a Depside from Parmotrema austrocetratum Elix and J. Johnst. - Consolacion Y. Ragasa; Maria Carmen S. Tan; Virgilio C. Linis; Chien-Chang Shen (Pharmacognosy Journal, 2018)
Introduction: Parmotrema austrocetratum Elix and J. Johnst. (syn. Rimelia austrocetrata Elix and J. Johnst.) which belongs to a large genus of lichenized fungi, Parmotrema Massalongo under family Parmeliaceae was investigated for its chemical constituents. Methods: The compounds were isolated by silica gel chromatography and their chemical structures were elucidated by NMR spectroscopy. Results: Chemical investigation of the dichloromethane extract of Parmotrema austrocetratum Elix and J. Johnst. has led to the isolation of zeorin (1) and atranorin (2). Conclusion: P. austrocetratum shares similar chemical characteristic with other Parmotrema species which afforded atranorin. This work highlights the first reported isolation of 1 from P. austrocetratum and the genus Parmotrema.
Keywords: Atranorin; Parmeliaceae; Parmotrema austrocetratum; Rimelia austrocetrata; Zeorin

Virtual Screening of Indonesian Herbal Database as Murine Double Minute-2 (MDM2) Inhibitor - Alexander Victory; Rezi Riadhi Syahdi; Arry Yanuar (Pharmacognosy Journal, 2018)
Background: Murine Double Minute-2 (MDM2) overexpression causes the p53 deficiency, so the role p53 as a cell regulator does not work in the case of cancer. Methods: In this study, virtual screening of Indonesian herbal database to discover MDM2 inhibitors was carried out. Autodock and Autodock Vina validated with Directory of Useful Decoy-Enhanced (DUD-E). Validation parameters were performed with Enrichment Factor, Receiver Operating Characteristics, and Area Under Curve. Results: The validation with the grid box 70x70x70 on Autodock resulting AUC value 0.72, while in Autodock Vina 0.43. Autodock Vina did not fulfilll the standard value but still used for comparison. Based on the virtual screening result, top ten compounds from Autodock are Nimolicinol, Jacoumaric acid, Isoarborinol, Lantic acid, Diosgenin, Theasaponin E1, Taraxasterol, Leucadenone C, Simiarenol, and Alpha-Amyrin were found to have strong interaction with MDM2, with binding energy (ΔG) ranging from -8.83 to -9.65 kcal/mol. The Autodock Vina screening resulted in the identification of Yuehchukene, Morusin, Cyanidin, Leucadenone C, Roxburghine-B, Ocidentoside, Beta-sitosterol, Curine, Withangulatin, and Jacoumaric acid as potential inhibitors with binding energy (ΔG) ranging from -8.7 to -9.4 kcal/mol. Conclusion: Jacoumaric acid and Leucadenone C were shown to interact with the active site in MDM2 at residues Leu54, Ile61, Met62, and Ile99.
Keywords: Cancer; Docking; Indonesian Herbal; Inhibitor; MDM2; Virtual Screening

Volatile Compound Analysis using GC-MS, Phytochemical Screening and Antioxidant Activities of the Husk of “Julang-Jaling” (Archidendron bubalinum (Jack) I.C Nielsen) from Lampung, Indonesia - Candra Irawan; Foliatini; Hanafi; Lilis Sulistiawaty; Maman Sukiman (Pharmacognosy Journal, 2018)
Background: “Julang-jaling” (Archidendron bubalinum (Jack) I.C Nielsen) fruits are commonly used as traditional food and in the treatment of blood sugar and heart disease. However, the research about the phytochemicals of the parts of this plants and their bioactivity was rare. Objective: The recent study was aimed to analyze volatile compounds in the extract of “julang-jaling” husks and evaluate their antioxidant and antimicrobial activities. Material and methods: The extraction was conducted using n-hexane, ethyl acetate, and methanol as extracting agent. The phytochemical assay was performed for all extracts, and followed by volatile compound analysis using GC-MS. The antioxidant assay was performed using DPPH method, and the antimicrobial activity was conducted using agar disc diffusion method. Results: The phytochemical assay showed that all extracts of “julang-jaling” husks contain various phytoconstituents having potential bioactivity. All extracts exhibit antioxidant activity with different level of activity depend on the type of extract. The IC50 value were 273.57 ppm, 324.913 ppm, 735 ppm, for ethyl acetate, methanol and n-hexane, respectively. All extracts were able to inhibit the growth of Bacillus cereus, with the highest antimicrobial activity was gained for ethyl acetate extract. Both ethyl acetate and methanolic extract have antimicrobial activity toward E. coli, but no extracts yield positive results for Aspergillus flavus and Aspergillus niger. Conclusion: GC-MS analysis revealed the presence of hexadecanoic acids and their ester form in all extract, which might largely contribute in the antioxidant and antimicrobial activity.
Keywords: Antimicrobial activity; Antioxidant; Archidendron bubalinum (Jack) I.C Nielsen; GC-MS; Phytochemicals

Withaferin A attenuates Alcohol Abstinence Signs in Rats - Nandkishor Ramdas Kotagale; Ankit Kedia; Rupali Gite; Shubham Nilkanth Rahmatkar; Dinesh Yugraj Gawande; Milind Janraoji Umekar; Brijesh Gulabrao Taksande (Pharmacognosy Journal, 2018)
Background: Withania somnifera (WS) have been reported to inhibit acquisition and expression conditioned place preference, self-administration and withdrawal anxiety of psychostimulants. In the present work, we have assessed the effect of withaferin A on somatic and affective symptoms of ethanol withdrawal syndrome in rats. Methods: Animals had given free access to ethanol uninterrupted for 21 days through liquid diet. Withaferin A (5, 10 and 20 mg/kg) was injected (ip) either during the development of ethanol dependence phase (days 15 – 21 or 30 min before ethanol withdrawal assessment. Withdrawal signs characterized by changes in somatic signs were measured in the open field followed by evaluation of anxiety parameters, locomotion, and depressive behavior. Results: Withaferin A treatment 30 min before 24 h postethanol withdrawal assessment did not alter the scores of somatic behavioral signs in ethanol abstinence animals. However, withaferin A (10 and 20 mg/kg, ip) from day 15-21 prevented the ethanol withdrawal-induced elevated scores of somatic behaviors, hyperlocomotion, depressive behavior, and anxiety. Withaferin A treatment did not influence the blood ethanol levels in dependent and withdrawn animals. However, withaferin A administration attenuated the elevated plasma corticosterone and ACTH levels in ethanol-withdrawn rats, suggesting withaferin A induced anti-stress effect and stabilization of HPA axis activity could have facilitated the inhibitory effect of withaferin A on ethanol withdrawal syndrome. Conclusion: The finding supports further investigation of withaferin A and other bioactive components of WS in alcohol addiction.
Keywords: Anxiety; Corticosterone; Ethanol withdrawal; HPA axis; Withaferin A.

Yoga Research a Scientometric Assessment of Global Publications Output during 2007-16 - BM Gupta; KK Mueen Ahmed; SM Dhawan; Ritu Gupta (Pharmacognosy Journal, 2018)
The paper examines 3966 global publications on yoga research, as covered in Scopus database during 2007-16. The global output on yoga research output registered 7.79% growth, and citation impact averaging to 10.44 citations per paper. The top 10 most productive countries in yoga research individually contributed global share from 1.31% to 38.35%, with largest global publication share coming from USA (38.35%), followed by India (19.29%), U.K. (6.61%), Canada (5.09%), etc. Together, the 10 most productive countries accounted for 83.74% and 96.67% global publication and global citation share during 2007-16. Five of top 10 countries scored relative citation index above the world average i.e. more than 1: Canada (1.81), USA (1.37), Germany (1.34), U.K. (1.31) and Italy (1.12) during 2007-16. The international collaborative publications share of top 10 most productive countries in yoga research varied from 12.68% to 42.59% during 2007-16. Medicine, among subjects, contributed the largest publication share (78.67%), followed by 9 other subjects with global share between 5.09% and 9.56%. The top 25 most productive organizations and authors together contributed 21.63% and 16.84% respectively as their global publication share and 35.37% and 25.10% respectively as their global citation share during 2007-16. Among the total journal output of 3719 papers, the top 15 journals contributed 21.22% share to the global journal output during 2007-16. Of the global yoga research output, the top 44 publications registered high citations from 101 to 1092 and they together cumulated 8304 citations, averaging to 188.72 citations per paper. These 44 highly cited papers were published in 35 journals, 5 papers were published in Cochrane database of systematic reviews (Online), 2 papers each in Annals of Internal Medicine, Integrative Cancer Therapies, Journal of Alternative and Complementary Medicine and Pain and 1 paper each in other journals.
Keywords: Bibliometrics; Global publications; Medical diseases; Scientometrics; Yoga research

ACE Inhibitory Activity, Total Phenolic and Flavonoid Content of Watercress (Nasturtium officinale R. Br.) Extract - Catty Amalia Yaricsha; Rissyelly; Katrin (Pharmacognosy Journal, 2017)
Introduction: Hypertension is the main risk factor for cardiovascular disease. There are many developed antihypertension drugs, one of them is focusing in ACE (Angiotensin Converting Enzyme) inhibition activity. ACE inhibition activity known can decrease vasoconstriction effect and also can decrease bradykinin degradation (vasodilator) by creating NO (nitric oxide). Methods: In this study, we conducted an in vitro ACE inhibition activity test which was obtained from watercress on 70% ethanolic extract and each fraction (n-hexane, ethyl acetate, and n-butanol). Results: Results of the study showed that ethanolic extract of watercress had ACE activity with IC50 value was 19.05 μg/mL and the highest IC50 of each fraction is ethyl acetate with IC50 value was 2,303 μg/ mL. n-butanol fraction had the highest total phenolic content with 15.798 mg GAE/g of the extract, while the highest total flavonoid content was obtained on ethyl acetate fraction with 82.847 mg QE/g of the extract. Conclusion: The results suggest that Watercress (Nasturtium officinale R. Br.) possess ACE inhibitory activity.
Keywords: ACE inhibitor; Flavonoid; phenolic; Watercress (Nasturtium officinale R. Br.)

ACE Inhibitory Activity, Total Phenolic and Flavonoid Content of Pereskia saccharose Griseb. Leaves Extract - Sarlina Jihan Lusiyanti; Katrin; Rissyelly; Nuraini Puspitasari; Putu Gita Maya Widyaswari Mahayasih (Pharmacognosy Journal, 2017)
Introduction: Angiotensin-converting enzyme inhibitors (ACEi) are drugs that can control hypertension. Pereskia saccharose Griseb. leaves have been used traditionally as antihypertensive. Objective: The objective of this study was to determine the antihypertensive activity through inhibition of ACE activity, the total phenolic content and total flavonoid content of the ethanolic extract of Pereskia saccharose Griseb. leaves and its fractions. Methods: Extraction was done by maceration with 80% ethanol and fractionation performed by liquid-liquid partition. Results: In vitro ACE inhibitory activity assay of the ethanolic extract using ACE Kit-WST Dojindo had IC50 value of 3.448 μg/mL and ethyl acetate fraction had IC50 value of 1.714 x 10-3 μg/mL. Ethyl acetate contained the highest amounts of both TPC (72.991 ± 0.932 mg GAE/g sample) and TFC (61.337 ± 1.612 mg QE/g sample). Conclusion: The results suggest that Pereskia saccharose Griseb. possess ACE inhibitory activity.
Keywords: ACE inhibitor; Flavonoid; Pereskia saccharose Griseb; phenolic

Active Constituents of Pomegranates (Punica granatum) as Potential Candidates in the Management of Health through Modulation of Biological Activities - Arshad Husain Rahmani; Mohamed Ali Alsahli; Saleh Abdulrahman Almatroodi (Pharmacognosy Journal, 2017)
Pomegranates fruits have innumerable health benefits and its implication in diseases cure have been widely recognized since ancient time. Moreover, pomegranate fruits, seeds and peels are intensively used in traditional medicine as a natural therapy. It contains numerous valuable ingredients such as flavonoids, ellagitannin, punicalagin, ellagic acid, vitamins and minerals. The principal constituents including punicalagins and ellagitannin are responsible for immeasurable health benefits due to its strong antioxidant activity. Additionally, constituents of pomegranate show health promoting effect through the modulation of physiological and biochemical pathways. Recent evidences suggested that pomegranates fruits, peels and seeds illustrate therapeutics implications in health management via inhibition of free radical effect and modulation of enzymes activity linked with diseases development and progression. In this review, we summarize the therapeutic role of pomegranate fruits, seeds and peels in the health managements based on in vitro and in vivo studies.
Keywords: Anti-inflammatory Effect; Anti-oxidant; Heptoprotective Effect; Neuroprotective Effect and Anti-microbial Effects; Pomegranates

Acute and Sub-acute Toxicities of Thai Silkworm Powder (Bombyx mori Linn.) From Three Races in Male Wistar Rats and In vitro Antioxidant Activities - Surapong Rattana; Teeraporn Katisart; Bunleu Sungthong; Chirapha Butiman (Pharmacognosy Journal, 2017)
Background: The silkworm powder from Japanese and Korean races has a high biological activity. However, there was less scientific evidence regarding bioactivities in Thai silkworm races. Objective: This research was interested in toxicity and antioxidant activities of Thai silkworm races. Material and methods: The 5th instar, 3rd day of growth stage of Thai traditional silkworm (Nanglai, Nangnoi and Samrong races) were lyophilized by freeze dryer and ground as silkworm powder. The acute and sub-acute toxicities studies were carried out in male Wistar rats. The antioxidant capacities of silkworm powder were investigated with DPPH, ABTS and FRAP methods. Results: The acute toxicity in rats by single dose oral administration show that the high dose at a concentration of 2,000 mg/kg b.w. did not have toxicity in rats. The sub-acute toxicity in rats by oral administration showed that the high dose concentration at 2,000 mg/kg body weight for 6 weeks had no toxicity in all group either. In addition, the hematological parameters and lipid profiles of treated group and control groups were not significantly different. The antioxidant study showed that silkworm powders were not significant difference in all groups of samples in three assays (DPPH, ABTS and FRAP). However, significant difference had been found in comparison to ascorbic acid (p < 0.05). Conclusion: Silkworm powder from three races of Thai silkworm did not produce any toxicity in male rats. In addition, the silkworm powder also exhibited antioxidant activities.
Keywords: antioxidant activities.; hematological parameters; lipid profile; Silkworm; toxicities

Alkaloid from Phoebe declinata Nees Leaves - Berna Elya; Basah Katrin; Roshamur Cahyan Forestrania; Rosmalena Sofyan; Ryan Adi Chandra (Pharmacognosy Journal, 2017)
Introduction: Genus Phoebe have been reported to produce isoquinoline alkaloids as aporphines, noraporphines, and benzylisoquinolines. Many of these isolates exhibit diversified biological activities, including cytotoxic activity. Objective: The objective of this study is to determine cytotoxic activity of compound isolated from Phoebe declinata againts MCF-7 (breast cancer cell line). Methods: Extraction was done by reflux using n-hexane, antioxidant activity measured by DPPH method and reducing power method, cytotoxic activity measured by MTT assay using MCF-7 cell line, struture eucidation was confirmed by NMR. Results: The antioxidant activity measured using DPPH method for 1 and 2 showed IC50 value of 6.42 and 11.80 μg/mL respectively and using reducing power method for 1 and 2 showed IC50 value of 7.02 and 13.74 μg/mL respectively. Compound (1) and (2) exhibited cytotoxic activity against MCF-7 cells with an IC50 value of 82.978 and 93.179 μg/mL. Conclusion: Compound (1) and (2) exhibited antioxidant activity and cytotoxic activity against MCF-7.
Keywords: Alkaloid; antioxidant activity; Cytotoxic activity; DPPH; MCF-7 cell line.; Phoebe declinata nees

Alpha-Glucosidase Inhibitory Activity and Fractionation of Bioactive Compounds from bark Extracts of Sibucao (Caesalpinia sappan L.) In the Philippines - Ea Kristine Clarisse B. Tulin; Ma Theresa P. Loreto; Edgardo E. Tulin (Pharmacognosy Journal, 2017)
Diabetes is a chronic disease that affects millions of people around the world. Although conventional medicine is available, it is usually accompanied by serious side effects such as gastrointestinal problem. Thus, the search for alternative medicine from natural sources is of primary importance. Context: The study is concerned with Caesalpinia sappan L. found in the vicinity of Baybay City, Leyte Philippines. Furthermore, it deals with ethanolic and aqueous extracts of the bark only. It was conducted to determine the alpha-glucosidase inhibitory activity of C. sappan to provide evidence to support its efficacy as a folkloric medicinal plant. Aims: This work aimed to evaluate the alpha-glucosidase inhibitory activity of aqueous and ethanolic bark extracts of Sibucao (Caesalpinia sappan L.) and to partially fractionate its bioactive compounds. Settings and Design: Extracts were prepared in increasing concentration to get IC50 values. Samples were analysed in triplicate both for extracts and fractions collected from chromatography. Methods and Material: Caesalpinia sappan L. bark samples were collected from the vicinity of Visayas State University. Plant materials were dried, weighed and stored. Aqueous and ethanolic bark extracts were prepared using water and 20% ethanol. The total phenolic content of the extracts were determined and the α-glucosidase inhibitory activity of crude bark and aqueous extracts were measured using the method of Kim et al., 2011. Partial fractionation of bioactive compounds was done successively using gradient elution. The α-glucosidase inhibitory activity of fractions were then determined and Rf values of active compounds were measured using thin layer chromatography (TLC). Results: Results revealed that aqueous extract (2000 ppm) and ethanolic extract (2000 ppm) show high α-glucosidase inhibitory activity of 100% and 59% respectively. IC50 values of aqueous and ethanolic extract were found to be 300.52 ± 1.467 ppm and 1560.81 ± 2.582 ppm, respectively. TLC of fractions show 7 peaks for aqueous extract and 6 peaks for ethanolic extract in which compound with Rf value 0.70 had the highest inhibitory activity of 65%. Conclusions: Taken together, the high α-glucosidase inhibitory activity of aqueous extracts support the effectiveness of C. sappan L. bark decoctions. In addition, results from bioassay-guided fractionation can be used as an effective tool for further isolation and characterization of α-glucosidase inhibitors from Caesalpinia sappan L. in the Philippines.
Keywords: Caesalpinia sappan; Flavonoids; Fractionation; Type II diabetes; α-glucosidase

Antibacterial Activity of Endophytic Fungi Isolated from the Bark of Cinnamomum mercadoi - Jia P. Marcellano; Alyssa S. Collanto; Rolly G. Fuentes (Pharmacognosy Journal, 2017)
Introduction: Cinnamomum mercadoi is a medicinal tree endemic to the Philippines. Cinnamomum species have been extensively studied for their endophytic fungi with pharmacological importance. This study aims to isolate and evaluate the antibacterial activity of endophytic fungi associated with the bark of C. mercadoi. Materials and Methods: Endophytic fungi were isolated from surface sterilized bark samples aseptically. The pure isolates were identified through their morphological characteristics. Agar plug diffusion assay was employed in the primary screening of their antibacterial activity against Staphylococcus aureus, Bacillus cereus, Escherichia coli and Pseudomonas aeruginosa. Four active endophytes were fermented and extracted with ethyl acetate (EtOAc). The antibacterial activity of the EtOAc extracts was screened using the disk diffusion assay. The minimum inhibitory activity (MIC) was evaluated using the microdilution method. Results: Twelve (12) endophytes were isolated from the bark of C. mercadoi. All endophytes exhibited antibacterial activity on at least one of the test pathogens. However, only two of the four endophytes subjected to the secondary screening showed wide-spectrum activity and inhibited the growth of all test bacteria. Fusarium sp. 2 was identified to have the most promising activity with MIC values ranging from 2.1 - 4.2 mg/mL. Conclusion: C. mercadoi harbors endophytes, particularly Fusarium sp. 2, which possess antibacterial activity and thus a potential source of antibacterial compounds.
Keywords: Cinnamon; Escherichia; Fusarium

Antibacterial Activity Of Shin’iseihaito (Xinyiqingfeitang) And its Components Against Methicillin-Resistant Staphylococcus aureus - Toru Konishi; Masaaki Minami; Toshiaki Makino (Pharmacognosy Journal, 2017)
Objective: Shin’iseihaito (xinyiqingfeitang 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 (CR, rhizome of Cimicifuga heracleifolia), is commonly used to treat sinusitis associated with purulent nasal discharge and reddish nasal mucosa. We evaluated anti-bacterial activity of SSHT extract on methicillin-resistant Staphylococcus aureus (MRSA), one cause of bacterial sinusitis. Materials and Methods: Sterile paper disks impregnated with SSHT extract, the combination of crude drugs composing SSHT according to the traditional pharmacological theory, or each component were placed on Mueller-Hinton agar plates inoculated with several strains of MRSA isolated from the patients. The diameter of inhibitory zone was measured after 18–24 h incubation. Results: SSHT extract showed antibacterial activity against 128/190 (66.8%) MRSA clinical isolates. The effect of the extract of SSHT without heat-clearing drugs (SSHT–HC) or without exterior-releasing drugs (SSHT–ER) were significantly lower than that of SSHT extract. Each water extract of SR, Loquat Leaf, Magnolia Flower and CR showed significant anti-MRSA activity, and SR extract exhibited the largest inhibitory zone. Conclusions: SSHT has antibacterial activity against MRSA clinical isolates, and SR mainly contributes to the antibacterial activity of SSHT against MRSA clinical isolates.
Keywords: Antibacterial activity; Methicillin-resistant Staphylococcus aureus (MRSA); Scutellaria baicalensis; Shin’iseihaito; Sinusitis

Antibacterial and Antioxidant Activity of Black Mulberry (Morus nigra L.) Extract for Acne Treatment - Arif Budiman; Diah Lia Aulifa; Arif Satria Wira Kusuma; Astri Sulastri (Pharmacognosy Journal, 2017)
Introduction: Black mulberry is rich in phenols and is hence usable in the treatment of acne. It also contains anthocyanin, a well-known antioxidant. This study aimed to examine the antibacterial and antioxidant properties of black mulberry (Morus nigra L.) extract as a potential raw material for use in beauty care products. Method: Fruit extract was obtained using maceration method with 96% ethanol. The antibacterial activity of the extract was determined by disc diffusion method, while the minimal inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined by microdilution method. Furthermore, the antioxidant activity of the extract was tested by DPPH method. Result: The results showed a 2.5% MIC against S. epidermidis and P. acnes, confirming the antibacterial activity of black mulberry extract. The MBC values for the respective bacterium were 2.5% and 5%. Regarding antioxidant activity, the IC50 value of black mulberry extract was 146.731 mg/mL, suggesting its medium potential. Conclusion: Morus nigra extract has antibacterial activity against S. epidermidis and P. acnes, and has medium potential as antioxidant.
Keywords: Anti acne; Antioxidant; Morus Nigra Extract; Propionibacterium Acnes; Staphylococcus Epidermidis

Antibrucellosis Activity of Medicinal Plants from Western Ghats and Characterization of Bioactive Metabolites - Sri Raghava; Sharanaiah Umesha (Pharmacognosy Journal, 2017)
Background: Brucellosis is one of the most prevalent bacterial zoonosis which is transmitted to humans from animals. As an alternative to conventional antibiotics, medicinal plants are valuable resources for new agents against antibiotic-resistant strains. Objective: To evaluate the antibrucellosis activity of different medicinal plants collected from the Western Ghats against Brucella abortus, Brucella melitensis, Brucella suis. Identification and characterization of the bioactive metabolites of the potent antibrucellosis agent by Thin Layer Chromatography and Gas chromatography mass spectroscopy. Methods: Antibacterial assay was carried for the ethanolic extract of different medicinal plants, the potential and effective medicinal plants extract was subjected for purification by TLC and the bioactive metabolites were characterized by the GC MS analysis. Results: Acacia nelotica, Terminalia arjuna, Eugenia jambolana and Callistemon citrinus showed the antibrucellosis activity comparatively Callistemon citrinus had the strong antibrucellosis activity. Further the crude sample was purified by TLC profiling, compounds with different retention factor were screened for antibrucellosis activity, and the bioactive metabolites were identified by GC-MS analysis. Conclusion: For the first time the different medicinal plants from Western Ghats were screened for the antibrucellosis activity. The crude and TLC purified Callistemon citrinus ethanolic extract exhibited strong antibrucellosis activity. The bioactive compounds identified were reported for the first time and the bioactive metabolites identified exhibited as potential antibacterial agents against brucellosis and other Human pathogens.
Keywords: Antibrucellosis; Bioactive compounds; GC-MS; Medicinal plant; TLC

Anti-HIV Activity of Phytosterol Isolated from Aerva lanata Roots - Rajendra Prasad Gujjeti; Estari Mamidala (Pharmacognosy Journal, 2017)
Background: AIDS in humans, which is caused by the HIV remains among the leading causes of death worldwide. Objective: The study was undertaken to investigate the HIV-RT inhibitory activity of Phytotesrols extracted from roots of Aerva lanata. Methodology: Sequential maceration method was performed for preparation of extracts using hexane, chloroform, ethyl acetate, acetone and methanol solvents. RetroSys HIV-1 RT (Innovagen, Sweden) kit was used to determine the HIV-RT inhibitory activity of all solvents extracts. Results & Discussion: All extracts showed significant inhibitory activity. Chloroform extracts shows highest inhibition of recombinant HIV-RT (89.0%) at 2 and mg/ml concentration. Phytosterols isolated from chloroform extracts. These results were remarkable and can be used to develop a new drug for HIV treatment or other infectious diseases caused by the pathogenic micro-organisms, for which plant sterols may play a distinctive role. Conclusion: Further work is in progress to evaluate the advanced spectroscopic studies are required for the structural elucidation, identification and characterization of the active compound from this plant.
Keywords: Aerva lanata; Characterization; HIV-1; Phytosterols; Reverse transcriptase; Structural elucidation

Anti-hyperglycemic and Anti-hyperlipidemic Effects of Extract from Houttuynia cordata Thumb. in Streptozotocin-Induced Diabetic Rats - Patcharee Poolsil; Wilawan Promprom; Chusri Talubmook (Pharmacognosy Journal, 2017)
Aim: Various properties of Houttuynia cordata Thumb. has been reported. However, few studies on its pharmacological effects have been documented. To elucidate whether there are more pharmacological effects of this plant, this study was therefore, carried out to determine the anti-hyperglycemic and anti-hyperlipidemic effects of 80% ethanol extract of H. cordata (HCE). Their antioxidant activity and acute toxicity were also conducted. Methods: HCE at a dose of 250 mg/kg was oral given to Streptozotocin-induced diabetic rats daily for 8 weeks. DPPH assay and HCE at the doses of 1,000, 2,000 and 3,000 mg/kg were employed in antioxidant and acute toxicity studies. Results: HCE lowered FBG in the diabetic, but not in the normal treated rats. HCE did not affect the body weight of all rats, but recovered TP, Alb, Glob, BUN, CREA, UA, TB, AST, ALT, ALP, and reduced the elevated CHO, TG and LDL in the diabetic rats. HCE possessed relatively low antioxidant activity with IC50 of 115.98± 0.82 μg/mL compared to Vitamin C (42.54+1.37 μg/ml), but did not produce any symptoms of acute toxicity. Conclusions: The extract of H. cordata may have beneficial properties and is a new agent for diabetic treatment and improve renal and hepatic functions.
Keywords: Acute toxicity; Anti-Hyperglycemic; Anti-Hyperlipidemic; Antioxidant; Houttuynia cordata Thumb

Antihyperglycemic Effect of Silkworm Powder, Fibroin and Sericin from Three Thai Silkworm (Bombyx mori Linn.) in Streptozotocin-Induced Diabetic Rats - Surapong Rattana; Teeraporn Katisart; Chirapha Butiman; Bunleu Sungthong (Pharmacognosy Journal, 2017)
Objective: The present study was aimed to investigate the antihyperglycemic activities of Thai silkworm (Bombyx mori Linn.) powder, fibroin and sericin from three races of Thai silkworm including Nangnoi, Nanglai, and Samrong in streptozotocin-induced diabetic rats. Materials and Methods: All rats were daily and orally administered with silkworm powder (5th-instar, 3rd-day), fibroin, and sericin at a dose of 250 mg/kg for 6 weeks. After that, various parameters including body weight, blood glucose, hematological and biochemical parameters were determined. Results: The results revealed that fasting plasma glucose level in 6th week of Nanglai fibroin, Nangnoi fibroin and Nangnoi sericin expressed a better reduction of FPG in diabetic rats compared with diabetic control groups (p<0.05). All hematological parameters of each group were not different within those values (p>0.05). In case of blood urea nitrogen, creatinine and alkaline phosphatase value showed that some of treated groups was different from diabetic control (p<0.05), while all of treated groups showed different in cholesterol and high density lipoprotein value (p<0.05). Conclusion: Silkworm powders, fibroin and sericin of three races exhibited a therapeutic potential for the reduction plasma glucose level. Treatments of silkworm powder, fibroin and sericin did not have any effect on hematological parameters. Improvement of blood urea nitrogen, creatinine, alkaline phosphatase values and lipid profiles also were also observed in the treatment groups.
Keywords: Antihyperglycemic effect; Diabetic rats; Fibroin.; Sericin; Silkworm

Anti-inflammatory activity of isolated compounds from the stem bark of Garcinia cowa Roxb - Fatma Sri Wahyuni; Daud Ahmad Israf Ali; Nordin Hj. Lajis; Dachriyanus (Pharmacognosy Journal, 2017)
Objective: To find the anti inflammatory active compounds from methanol extract of Garcinia cowa. Methods: To evaluate the inhibitory activity of isolated compounds on nitric oxide (NO) production, culture media was assayed using Griess reaction. An equal volume of Griess reagent (1% sulphanilamide and 0.1% N-(L-naphthyl)-ethylene diamine dihydrochloride, dissolved in 2.5% H3PO4) was mixed with culture supernatant and color development was measured at 550 nm using a micro plate reader. The amount of nitrite in the culture supernatant was calculated from a standard curve (0–100 μM) of sodium nitrite freshly prepared in deionized water. Percentage of the NO inhibition was calculated by using nitrate level of IFN-γ/LPS-induced group as the control. Results: Isolated compounds, tetraprenyltoluquinone, rubraxanthone and α-mangostin from stem bark of Garcinia cowa Roxb were evaluated for their anti-inflammatory activity. Only α-mangostin exhibited strong anti-inflammatory activity with 83.42 % inhibition of NO and without inducing severe cytotoxicity at 50 μM. Rubraxanthone showed weak inhibition of NO with 23.86 % inhibition of NO while maintained 77.32 % of cell viability. TPTQ also showed the strong inhibition of NO with 80.98 % inhibition but unfortunately this compound also induced severe cytotoxicity with 39.62% viability. Conclusion: α-Mangostin exhibited strong anti-inflammatory activity without inducing severe cytotoxicity at 50 μM. Rubraxanthone showed weak inhibition of NO while Tetraprenyltoluquinone also showed the strong inhibition of NO however this compound also induced severe cytotoxicity.
Keywords: Anti-inflammatory; Garcinia cowa; Nitric oxide; rubraxanthone; tetrapreniltoluquinone; α-mangostin

Antimalarial and Antioxidant Potentials of Extract and Fractions of Aerial part of Borreria ocymoides DC (Rubiaceae). - Sunday Adeleke Adesegun; Celestina Ifeoma Orabueze; Herbert Alexander Babatunde Coker (Pharmacognosy Journal, 2017)
Introduction: Borreria ocymoides (Burm F) DC is a weak, erect and decumbent herb that has several folkloric, ethno medicinal uses and is included in antimalarial preparations by some traditional healers. It is also used in treatment of ring worm, eczema and microbial infections. Objectives: To evaluate antimalarial activity of extract and fractions of Borreria ocymoides in Plasmodium berghei infected mice and to investigate their antioxidant activity using 1, 1-diphenyl-2-picryl-hydrazile (DPPH). Methods: The methanol extract of aerial part of B. ocymoides and the solvent fractions obtained from partition between organic solvents were assessed for antimalarial activity against chloroquine sensitive Plasmodium berghei NK65 infected mice using the suppressive and curative test procedures. Chloroquine (10 mg/ml) was used as positive control. The antioxidant activity was evaluated using DPPH radical scavenging ability and determination of total phenolic content. Results: The crude extract (250 and 500 mg kg-1) produced a dose dependent anti-plasmodial activity in the suppressive and curative tests. The chemo suppression activity was best in the ethyl acetate fraction (87.31%) and in the order ethyl acetate >dichloromethane > hexane > aqueous fraction. The DPPH radical scavenging activity of the extract increased with concentration. The antioxidant activity was less than ascorbic acid used as positive control. Oral administration up to 5 g/kg produced no noticeable deleterious effect 24 hours after dosing and up to 7 days afterwards. Conclusion: The results indicated that the extract has a potent anti-plasmodial activity against Plasmodium berghei and the activity seems to reside in the mid-polar fractions. Thus, the plant is a potential source of new antimalarial agents.
Keywords: Antimalarial; Antioxidant; Borreria ocymoides; Plasmodium berghei; Solvent fractions

Antimicrobial, Analgesic and Anti - Inflammatory Activity Reported on Tamarindus indica Linn Root Extract - Sangeeta Gupta; Amit Singh (Pharmacognosy Journal, 2017)
Objective: Tamarindus indica (Family- Fabaceae) show various folkloric uses in treatment of various ailments such as rheumatisum, dysentery, jaundice etc. Aim: The research was conducted to investigate its phytoconstituients and various activity such as antimicrobial, analgesic & anti-inflammatary of AETIRE. Method: The antimicrobial activity was performed on 4 bacterial stains containing (B.subtilis, S.aureus, P. aeruginosa & E.coli) on AETIRE using Disc diffusion method. The Analgesic activity was tested by thermal and chemical induced pain through Hot plate and AAIWT. And carrageenan induced rat paw oedema model is used to evaluate antiinflammatory activity. Result: Phytoconstituients such as tannins, alkaloids, saponins, flavonoids and carbohydrates present in both the extract. The maximum zone of inhibition of about 21mm & 22mm was shown on B.subtilis strain by both the extract when compared with standard drug (Tetracycline & Gentamycin). In AAIWT and hot plate test the AETIRE of concentration (100, 200 mg/kg) produce significant dose-dependent inhibition of pain response with maximum 54.33% protection against acetic acid induced pain and about 74.83% inhibition against thermally induced pain by the aqueous extract 200mg. & the anti- inflammatory activity shown by AETIRE (100 & 200mg/kg) caused significant dose dependent inhibition of oedema with maximum 45.94% inhibition in the Carrageenan induced rat paw oedema by the AE. Conclusion: Therefore the AE of Tamarindus indica root was more effective in showing analgesic and anti-inflammatory activity when compared to the standard drug in each model while ethanol extract show effective antimicrobial activity.
Keywords: Analgesic; Anti- inflammatory activity; Antimicrobial; Fabaceae; Tamarindus indica

Antioxidant Activity and Isolation of Xanthine Oxidase Inhibitor from Ruellia tuberosa L. Leaves - Aktsar Roskiana Ahmad; Berna Elya; Abdul Mun’im (Pharmacognosy Journal, 2017)
Introduction: The leaves of Ruellia tuberosa L. have been known to demonstrate strong antioxidant and xanthine oxidase (XOD) inhibitory activities. The aim of this study was to isolate antioxidant and XOD inhibitor from the leaves of the plants. Methods: Isolation of antioxidant and XOD inhibitor were conducted using chromatography techniques. The structure of the isolated compound was elucidated by spectroscopic methods. Results: In this study, a flavonoid was isolated and characterized as methoxylated flavonoid based on the spectral data including UV, IR, GC-MS, and NMR. The compound demonstrated DPPH free radical scavenging activity with IC50 of 28.79 μg/ml, and XOD inhibitory with IC50 of 0.67 μg/mL. Conclusion: The isolated compound was determined as 5-hydroxy-3,7-dimethoxy-2-(4-((3S,4S,5S,6R)-4,5, 6-trihydroxy-2(hydroxymethoxy)-tetrahydro-2H-pyrane-3-iloxy) phenyl)-4H-chromen-4-on or camarosids. The isolated compound demonstrated strong DPPH free radical scavenging and XOD inhibitory activity.
Keywords: Antioxidant; DPPH; Flavonoid.; Ruellia Tuberosa; Xanthine Oxidase

Antioxidant Activity and Lipoxygenase Enzyme Inhibition Assay with Total Flavonoid Content from Garcinia hombroniana Pierre Leaves - Shinta Marlin; Berna Elya; Katrin (Pharmacognosy Journal, 2017)
Objective: Garcinia hombroniana Pierre leaves extract have been known to contain flavonoid, but it has not been known yet for its antioxidant activity and inhibition of lipoxygenase activity. This study aims to determine antioxidant activity and inhibition of lipoxygenase activity of G. hombroniana leaves extract. Method: Antioxidant activity tested by using FRAP (Ferric Reducing Antioxidant Power) method and inhibition of lipoxygenase activity using baicalein as the positive control. Total flavonoid assay is also quantitatively done by AlCl3 colorimetric method on the most active extract using quercetin as the positive control. Results: The test result showed that the n-hexane, ethyl acetate and methanol extract of G. hombroniana Pierre leaves have antioxidant activity which showed by EC50 value consecutively are 36.260; 2.969; and 7.416 μg/mL, and also can inhibit lipoxygenase activity which showed by IC50 value consecutively are 2.052; 0.134; and 1.314 μg/mL. Ethyl acetate extract of G. hombroniana Pierre leaves has the most active antioxidant activity and inhibition of lipoxygenase activity. Total flavonoid content of ethyl acetate extract of G. hombroniana Pierre leaves is 42.004 mg QE/g sample. Conclusion: Garcinia hombroniana Pierre leaves extract has antioxidant activity and can inhibit lipoxygenase activity.
Keywords: Antiinflammation; Antioxidant; Flavonoid; FRAP; Garcinia hombroniana Pierre; Lipoxygenase

Antioxidant Activity and Lipoxygenase Enzyme Inhibition Assay with Total Flavonoid Assay of Garcinia porrecta Laness. Stem Bark Extracts - Amalia Cipta Sari; Berna Elya; Katrin (Pharmacognosy Journal, 2017)
Introduction: The genus Garcinia which is rich of secondary metabolites, mainly flavonoids, have known to have antioxidant and anti-inflammatory activity through the inhibition of lipoxygenase. There isn’t found literature indicating research on inhibition of lipoxygenase activity been done in this plant. The purpose of this study is to obtain the data and determine the potential antioxidant activity, and inhibition of lipoxygenase activity of Garcinia porrecta Laness. stem bark extracts. Methods: This research is included FRAP (Ferric Reducing Antioxidant Power) method antioxidant assay, in vitro lipoxygenase inhibition assay, flavonoids qualitative analysis by thin layer chromatography, and total flavonoids assay in the most active extract. Results: The results showed the methanol, ethyl acetate and n-hexane extracts of G. porrecta Laness. stem bark using FRAP method, has antioxidant activity with EC50 values respectively 1.33; 4.97; and 19.96 μg/mL and lipoxygenase inhibition activity with IC50 values 0.23; 0.52; and 4.87 μg/mL. The most active extract in the both assay is methanol extract which has total flavonoids of 5.66 mg QE/g (quercetin equivalent). Conclusion: The results from the study show extracts of the stem bark of G. porrecta Laness. has antioxidant activity and potential for lipoxygenase inhibition.
Keywords: Antioxidant; Flavonoid; FRAP; Garcinia porrecta Laness; Lipoxygenase

Antioxidant Activity and Lipoxygenase Enzyme Inhibitory Assay with Total Flavonoids Content from Garcinia hombroniana Pierre Stem Bark Extract - Amanda Listiyani; Berna Elya; Nuraini Puspitasari (Pharmacognosy Journal, 2017)
Introduction: Garcinia has been known as a rich source of xanthones, flavonoids, and phenols. The aim of this research is to obtain data of antioxidant activity and to observe potential inhibition of lipoxygenase activity that most active from methanolic, ethyl acetate and n-hexane extracts with total flavonoids content from most active extracts from the bark of Garcinia hombroniana Pierre. Methods: The antioxidant activity was measured using the ferric reducing antioxidant power (FRAP), the anti-inflammatory assay was measured using inhibition of lipoxygenase activity test, qualitative analysis of flavonoids using thin layer chromatography, and total flavonoids content was measured using AlCl3 colorimetric method. Results: The results showed that the ethyl acetate extract from G. hombroniana Pierre stem bark as the most active extract for antioxidant and lipoxygenase inhibition activity with EC50 and IC50 value consecutively 15.34 μg /ml; 0.26 μg /ml. Total flavonoids content of ethyl acetate is 7.430 mg QE/g extract. The results of this study showed bark extract Garcinia hombroniana Pierre has antioxidant activity and potent to inhibit lipoxygenase activity. Conclusion: Based on the research for methanolic, ethyl acetate and n-hexane extract, it can be concluded that the ethyl acetate extract of G. hombroniana Pierre as the most active extract for antioxidant and lipoxygenase inhibition activity.
Keywords: Antioxidant; Garcinia hombroniana Pierre; Inflammation; Lipoxygenase; Total flavonoids content

Antioxidant Activity and Lipoxygenase Inhibition Test with Total Flavonoid Content from Garcinia kydia Roxburgh Leaves Extract - Nur Laily Putri; Berna Elya; Nuraini Puspitasari (Pharmacognosy Journal, 2017)
Introduction: Antioxidant is one of the therapeutic strategies to overcome oxidative stress and inhibit synthesis of inflammatory mediators through lipoxygenase pathway. Garcinia is the largest of Clusiaceae family which has been proven to provide antioxidant and anti-inflammatory activity. Garcinia kydia Roxburgh is one of the plants of this genus which is known to have antioxidant activity but lipoxygenase inhibition activity from this plant was unknown. Methods: This study aimed to test antioxidant activity of the methanol, ethyl acetate and n-hexane extract from Garcinia kydia Roxburgh leaves by FRAP (Ferric Reducing Antioxidant Power) method, anti-inflammatory activity was tested by inhibiting lipoxygenase and total flavonoid content by colorimetric methods AlCl3. Results: The results showed an antioxidant activity of methanol extract, ethyl acetate and n-hexane leaves of Garcinia kydia Roxburgh have EC50 value, respectively 18,448; 12,389 and 31,260 μg/mL, and the lipoxygenase inhibition activity have IC50 value, respectively 0,556; 0,212 and 3,575 μg/mL. Ethyl acetate extract of Garcinia kydia Roxburgh leaves was the most active extract in this study which has total flavonoid content, 30,650 mgQE/ gram extract. Conclusion: The conclusion, Garcinia kydia Roxburgh has antioxidant and lipoxygenase inhibition activity, with ethyl acetate extract as the most active extract which contains total flavonoids.
Keywords: Antioxidant; Flavonoid content; FRAP; Garcinia kydia Roxburgh; Lipoxygenase

Antioxidant Activity, Biochemical Components and Sub-Chronic Toxicity of Different Brown Rice Kefir Powders - Supaporn Chunchom; Chusri Talubmook; Sirirat Deeseenthum (Pharmacognosy Journal, 2017)
Aims: This study aimed to investigate and compare antioxidant activity, biochemical components and subchronic toxicity of brown rice kefir powder from three different coloured rice varieties; Khao Dawk Mali 105 (KDMLKP, white), Red Hawm (RHKP, red), and Hawm Nil (HNKP, dark purple), with cow milk kefir powder (CMKP). Medthods: Antioxidant activity performed by using ferric reducing antioxidant power (FRAP) assay and 2, 2´-diphenyl-1-picrylhydrazyl (DPPH) assay. Biochemical components values including gamma-aminobutyric acid and alpha-tocopherol were determined using high performance liquid chromatography, but total phenolic compounds was detemined using the Folin-Ciocalteu reagent. Sub-chronic toxicity test, KDMLKP, RHKP and HNKP at the doses of 150 mg/kg were given orally to the rats every day for 90 days. Results: Antioxidant activity showed that brown rice kefir powders were significantly (p≤0.05) higher than cow milk kefir powder. Interestingly, HNKP provided the highest FRAB value and the lowest IC50 of DPPH assay. HNKP had also the highest biochemical component values. Repeat administration of KDMLKP, RHKP and HNKP did not produce any symptoms of sub-chronic toxicity; mortality, hematological values, and blood biochemistry in the rats. Moreover, RHKP produced HDL increasing without CHO, TG and LDL changing in rats. Conclusions: These data indicate that brown rice kefir powders show no sub-chronic toxicity and exhibit more antioxidant activity and biochemical component values than cow milk kefir powder. Surprisingly, RHKP showed HDL increasing while HNKP had the highest potent antioxidant activity and biochemical components. Thus, both rice kefir powders are safe and probably a new biochemical resource for health. `
Keywords: antioxidant activity; Biochemical Components; Brown Rice Kefir Powder; Rice; Sub-Chronic Toxicity

Antioxidant and Anti-hypercholesterolemic potential of Vitis vinifera leaves - Sushma Devi; Randhir Singh (Pharmacognosy Journal, 2017)
Background: Grapes (Vitis vinifera) are universally appreciated fruit for their delicacy, nutrition and accepted as functional food. The objective of the present study is to evaluate antioxidant and anti-hypercholesterolemic potential of Vitis vinifera leaves extract. Methods: Qualitative and quantitative phytochemical screening of methanolic (VVME) and aqueous (VVAE) extract was carried out to identify the phytoconstituents. Antioxidant potential was evaluated by employing in-vitro and in vivo assays. The anti-hypercholesterolemic activity was evaluated by inducing hypercholesterolemia with high cholesterol diet for 21 days in experimental animals. Results: In VVME, total tannins, total flavonoids and total phenolic contents were found to be present in major amount. Both extract has significant in-vitro and in-vivo antioxidant efficacy. Different doses i.e. 100, 200 and 400 mg/kg of VVME and VVAE significantly attenuated the lipid levels. Moreover, VVME was found to be more effective as compared to VVAE and also, effectiveness was confirmed with histological results. Conclusion: It can be concluded that antioxidant and anti-hypercholesterolemic efficacy of Vitis vinifera might be due to presence of antioxidant property and active phytoconstituents.
Keywords: Antioxidant; Cholesterol Diet; Hypercholesterolemia; Total Phenolic Content Etc.; Vitis vinifera

Apoptosis Induction of Cervical Carcinoma HeLa Cells Line by Dichloromethane Fraction of the Rinds of Garcinia cowa Roxb - Fatma Sri Wahyuni; Siska Febria; Dessy Arisanty (Pharmacognosy Journal, 2017)
Objective: This study aims to determine the apoptosis induction of HeLa cervical carcinoma cells death by dichloromethane fraction of the rinds of Garcinia cowa Roxb. Methods: Apoptosis induction of HeLa cell line was observed using a double staining method. Results: The result of double staining observation showed that an apoptosis occurs which marked with yellowish green fluorescence and cell fragmentation. The average percentage of apoptotic cells was higher in the treated variables (70.38%) compared to the control variables (12.26% ). Statistical analysis by Independent Sample T-Test showed apoptosis Sig. (2-tailed) = 0.000 (<0.025). Conclusion: The dichloromethane fraction of G. cowa rind induces apoptosis in HeLa cervical cancer cells.
Keywords: Apoptosis induction; Carcinoma cells; Double stanining; Garcinia cowa Roxb.; HeLa cell line

Application of Ionic Liquid based Microwave-Assisted Extraction of the Secondary Metabolite from Peperomia pellucida (L) Kunth - Islamudin Ahmad; Arry Yanuar; Kamarza Mulia; Abdul Mun’im (Pharmacognosy Journal, 2017)
Introduction: An ionic liquid (ILs) is a new alternative solvent (containing cations and anions) has the physical and specific solutions properties, and also had proven to be a promising substituent of conventional organic solvents are flammable, volatile and toxic in various processes. The ILS application in separating the secondary metabolites compound from Peperomia pellucida (L) Kunth herbaceous can be carried out using microwaveassisted extraction method (MAE). Objective: The aim of this study was to investigate the effect of ionic liquid based microwave-assisted extraction method for attracting the secondary metabolites compound from P. pellucida compared with a conventional solvent for the enrichment of secondary metabolites (especially polyphenols group) and their HPTLC fingerprinting profile. Methods: The herb dried powder extracted by microwave-assisted extraction using an ionic liquid such us 1-Butyl-3-methylimidazolium chloride ([BMIM]Cl), 1-Butyl-3-methylimidazolium Bromide ([BMIM]Br). The obtained extract solution was partitioned using an organic solvent; the extract was evaporated to obtain a dry extract and determination the HPTLC fingerprinting profile. Results: Based on the research results was obtained from the various types of solvents there are differences in the extraction of secondary metabolite.
Keywords: HPTLC profile; Ionic liquid; Microwave-assisted extraction; Peperomia pellucida (L) Kunth; Secondary metabolite.

Aristolochia bracteolata Enhances Wound Healing in vitro through Anti-inflammatory and Proliferative Effect on Human Dermal Fibroblasts and Keratinocytes - Dinesh Murugan Girija; Mangathayaru Kalachaveedu; Rajasekaran Subbarayan; Preethi Jenifer; Suresh Ranga Rao (Pharmacognosy Journal, 2017)
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

Ashwagandha Root Extract Inhibits Acetylcholine Esterase, Protein Modification and Ameliorates H2O2-Induced Oxidative Stress in Rat Lymphocytes - Ajay Pal; Kandikattu Hemanth Kumar; Bharat Bhushan; Vinod Saharan (Pharmacognosy Journal, 2017)
Background: Herbs have long been the basis of medical treatment but the practice of herbalism is not strictly based on evidences gathered using scientific methods. Ashwagandha (Withania somnifera L.) is a traditional medicinal herb used in the treatment of various ailments. Objective: In current study we have evaluated the acetylcholine esterase (AChE) inhibitory and antioxidant potential of Ashwagandha root extract (ARE) in in-vitro and ex-vivo models to give a scientific base to its use in herbal medicine. Methodology: Simplest extraction e.g. maceration method was performed for preparation of extracts using methanol as solvent. Both in vitro and in vivo experimental trial were executed to evaluate the efficacy of root extract. Result and Discussion: ARE substantially scavenged free radicals and effectively prevented protein degradation as well as modification as studied by SDS-PAGE and Western blotting. Pre-treatment with ARE protected rat lymphocytes against H2O2-induced oxidative damage. H2O2 treatment resulted in DNA fragmentation and significantly decreased the activities of key antioxidant enzymes namely superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, glucose-6-phosphate dehydrogenase while decreased and increased the content of glutathione and malondialdehyde, respectively. ARE pre-treatment almost reversed these changes indicating its efficiency to suppress hydrogen peroxide-induced oxidative stress. Conclusion: The study provides the scientific basis of pleiotropic functions of Ashwagandha.
Keywords: Acetylcholine esterase; Antioxidants; Ashwagandha; DNA damage; Protein carbonylation; Rat lymphocytes

Assessment of Biological Activity and Comparison of UPLC and RP-HPLC Chromatographic Profiles of Clausena excavata Burm.F. - Guntupalli Chakravarthi; Alavala Rajasekhar Reddy; Maddi Ramaiah (Pharmacognosy Journal, 2017)
Clausena excavata Burm. F. (Rutaceae) has long been associated with medicinal benefits in folk medicine, particularly in the treatment of cancer and its related disorders in the eastern region of Thailand. In the the present study Ultra Pressure Liquid Chromatography (UPLC) analysis of methanolic leaf extracts of Clausena excavata were carried out using short (5 cm × 2.1 mm I.D.) columns, containing 2 μm particles at very high pressures (up to 16000 psi) to obtain high efficiency separations in very short run times. The results indicate that UPLC provided better resolution compared to routine RP-HPLC. The analysis time was drastically reduced (4 min.) which is proved to be a faster and more economical analytical tool than RP-HPLC. In addition to that, the present study also evaluates anti-fungal activity against dermatophytes Trichophyton rubrum and Trichophyton mentographytes by using an agar incorporation technique. The anti-fungal activity may be due to the presence of Angelecin and gallic acid in the plant extract.
Keywords: Angelecin; Clausena; HPLC; Rutaceae; UPLC

Bioactive Propensity of Macroalgae from the Andaman & Nicobar Islands - Sivadasan Deepa; Pitchiah Venkateshwaran; Nambali Valsalan Vinithkumar; Ramalingam Kirubagaran (Pharmacognosy Journal, 2017)
Aims: Marine macroalgae are the rich source of biologically active metabolites and potential source for development of novel biotechnological products. The present study was made to explore the metabolically active compounds from the macroalgae of the Andaman & Nicobar Islands. Methods and Material: Different solvents such as methanol (MeOH), ethyl acetate (EtoAc), butanol (BuOH) and aqueous (H2O) extracts of nine macroalgae were tested for antimicrobial, antibiofilm and cytotoxicity (brine shrimp larvae). Results: Out of the 36 extracts 27 extracts showed antimicrobial activity against the human pathogens and 14 extracts revealed antibiofilm activities. The three EtoAc extracts of Sargassum ilicifolium, MeOH extract of Sargassum sp. and MeOH extract of Padina tetrastromatica showed inhibition against 8 pathogenic bacteria. Also, aqueous extract of Padina tetrastromatica (71.82 %) and BuOH extract of Dictyosphaeria cavernosa (71.58 %) exhibited higher antibiofilm nature. The highest cytotoxic effect was exhibited by species Actinotrichia fragilis and all its four extracts significantly (P<0.01) inhibited the brine shrimp larvae, among this aqueous extract showed the lowest LC50 value, 31.7 μg/ml, followed by EtoAc extract, 89.33 μg/ml. Conclusion: It was observed that different species have different kind of bioactive nature.
Keywords: Antibiofilm; Antifouling; Antimicrobial; Bioactivity; Cytotoxic Effect; Marine Macro Algae.

Botanical Features for Taxonomic Evidence of Erythroxylum monogynum Dried Leaf - Sabeena Hussain Syed; Ajay Gajanan Namdeo (Pharmacognosy Journal, 2017)
Introduction: Erythroxylum monogynum belonging to family Erythroxylaceae is commonly found in southern parts of India. Traditionally, leaves of the plant possess high medicinal value and known for the treatment of diabetes, jaundice and to kill intestinal worms, which are scientifically reported. However, no elaborative pharmacognostic study of leaves has been performed yet. Objective: To pharmacognostically standardize the leaves by studying anatomical characters of transversal section and powdered leaves. Material and methods: Leaf samples were studied by macroscopy, microscopy, physicochemical and preliminary phytochemical analysis as recommended by WHO. Results: Externally the leaves are elliptic - lanceolate, alternate, base attenuate, apex obtuse and entire margin. Internally it shows the presence of paracytic stomata confined to lower epidermis, conjoint, collateral arc shaped vascular bundles encircled by sclerenchyma, lignified fibers and xylem vessels with spiral thickening. Powder microscopy revealed the presence of epidermis with papillae, phytochemical and physicochemical of powdered drug proved useful to differentiate the powdered drug material. Conclusion: The establishment of botanical features of leaf material will be useful in identification and standardization of Erythroxylum monogyum in obtaining quality formulations.
Keywords: microscopy; Paracytic stomata; Physicochemical; Phytochemical; standardization; Vascular

Botanical Pharmacognosy of Centella asiatica (Linn.)Urban - Madathilparambil Vasu Sudhakaran (Pharmacognosy Journal, 2017)
Introduction: Centella asiatica (Linn.) Urban is an important medicinal plant with rejuvenate properties, used in Ayurveda for promoting vitality and life. The plant is often considered as a ‘panacea’ for several human ailments and the biological actions often has been ascribed to its pentacyclic triterpene compounds, mainly asiatic acid, madecassic acid and triterpene saponin-asiaticoside, madecassoside. The plant is also highly specialized for the richness of several micronutrients, iron, phosphorus, sodium, vitamin C, vitamin A, carotene and dietary fibers. Objectives: The present study was performed with the objectives of elaborating the macroscopic and histo-morpho diagnostic profile of Centella asiatica and to analyze the quantitative, and powder microscopic peculiarities to support its pharmacognostic characterization. Materials and Methods: Microscopic evaluation, quantitative standards and powder microscopy were carried out using the root, stolon, petiole and leaves. Results: Distribution of slightly lobed leaf margin with actinodromous major venation pattern, amphistomatic epidermis with animocytic stomata, distinctive contour of the midrib and petiole, occurrence of crystals in the idioblasts of the cortical parenchyma of root, stem, stolon, palisade and mesophyll. Vascular system with several free collateral bundles in the stem were features characteristic of the species. These findings in conjunction with reduction in lignified elements, arenchyma lacunae, sclerenchymatous netting in root, periphloematic sclereids in petiole, and stolon could be remarkable features diagnostic of the taxon. Conclusion: The present macroscopic and histo-anatomical observations of stem, root, stolon, petiole and leaves of Centella asiatica and powder microscopic, quantitative standards put forth could provide useful information for the regulatory aspects of the quality control measures of the crude drugs.
Keywords: Animocytic stomata; arenchyma; calcium oxalate; crystal idioblasts.; periphloematic sclereids

Botanical Pharmacognosy of Holostemma ada-kodien Schult - Sudhakaran Madathilparambil Vasu (Pharmacognosy Journal, 2017)
Background: Holostemma ada-kodien Schult. is a perennial, twinning, laticiferous climbing herb belongs to the family Asclepiadaceae. It is an important medicinal plant with rejuvenate properties, used in Ayurveda for promoting vitality and life. The roots are sweet, ophthalmic, emollient, aphrodisiac, expectorant and galactagogue. It is highly specialized for the richness of a diverse array of aminoacids such as alanine, aspartic acid, glycine, serine, thereonine, valine, and terpenoid sugars. Aim: The present study was performed with the objectives of elaborating the macroscopic and histo-morpho diagnostic profile of Holostemma ada-kodien and analyse the quantitative, and powder microscopic peculiarities to support its pharmacognostic characterization. Materials and Methods: microscopic evaluation, quantitative standards and powder microscopy were carried out using the stem, root tuber, root and leaves. Results: Distribution of uniseriate, tricellular clothing trichomes in the epidermal tissues of the midrib, entire leaf margin with campylodromous major venation pattern, amphistomatic epidermis with anisocytic stomata, dorsiventral differentiation of mesophyll, small palisade ratio, small stomatal index, and the vascular system with several free collateral bundles in the petiole were features characteristic of the species. Gelatinous fibers distributed as concentric ‘white rings’ in the cortical tissues of the stem as distinct groups, deposition of druses crystals of calcium oxalate in the epidermal tissues of the lamina, ground tissues of petiole, cortical tissues of stem, root, root tubers and parenchymatous pith of the stem. Secondary xylem appeared fissured as radial and tangential strips, like the spokes of a wheel in cross section of the root tuber. Xylem core seemed irregular and wedge shaped in the mature root, with more axial and radial parenchyma and less xylem fibers also features characteristic of the taxon.
Keywords: Anisocytic stomata; compound starch grains; druses crystals; gelatinous fibres; stone cells

Characterization and Distribution of Flavonoids from Flowers in Different Horticultural Types of Begonia. - Saffidine Karima; Chirol Nadine; Benayache Fadila; Jay Maurice (Pharmacognosy Journal, 2017)
Background: The begonias are ornamental plants known by the varied forms and colors of their flowers, as well as their decorative foliage. Objective: This study attempts to characterize the flavonoids isolated from flower extracts of different horticultural cultivars of the genus Begonia. Material and methods: The compounds of the ethyl acetate and aqueous extracts were separated by chromatographic methods and identified by UV spectra and chemical techniques. Results: The analysis allowed the characterization of flavonoids belonging to flavonol types in the free aglycones and glycoside forms of kaempferol and quercetin. On the other hand, fingerprinting analysis and quantification of major flavonoids of 184 cultivars were performed by high-performance liquid chromatography (HPLC). Among twenty five (25) components which were detected and separated: ten were corresponding to quercetin 3-Oglucosyl- rhamnoside (Rt=23.5), quercetin 3-O-glucoside (Rt=25), kaempferol 3-O-glucosylrhamnoside and its acylated derivative (Rt=32), kaempferol 3-O-glucoside (Rt=33), quercetin 3-O-p.coumaroyl-diglucoside (Rt=37), quercetin 3-O-P.coumaroyl-glucoside (Rt=40.5), quercetin (Rt=41.5), kaempferol and its acylated derivative (Rt=47). Only non-acylated glycosides of quercetin and kaempferol contributed to chemical variations among different cultivars based on the results of PCA. Conclusion: The genus Begonia is very heterogeneous and it is possible to distinguish several chemotypes whose differences rely on the complementarities between the metabolic pathways involved in the biosynthesis of glycosides of quercetin and kaempferol.
Keywords: Begonia; Chemotype; Distribution; Flavonoids; HPLC.

Chemical Constituents of Dracontomelon Dao (Blanco) Merr. et Rolfe - Consolacion Y. Ragasa; Tyson C. Batarra; Julius Leonard A. Vivar; Mariquit M. De Los Reyes; Chien-Chang Shen (Pharmacognosy Journal, 2017)
Introduction: The leaves, twigs and flowers of Dracontomelon dao (Blanco) Merr. et Rolfe, an indigenous Philippine tree were investigated for their chemical constituents. Methods: The compounds were isolated by silica gel chromatography and their structures were identified by NMR spectroscopy. Results: Chemical investigation of D. dao led to the isolation of cardol (1), β-sitosteryl-3β-glucopyranoside-6, O-fatty acid esters (2), β-sitosteryl fatty acid esters (3), and a mixture of β-sitosterol (4a) and stigmasterol (4b) from the petiole; 1, a mixture of 4a and 4b, anacardic acid (5), triacylglycerols (6), monoacylglycerol (7), long-chain fatty acid esters (8), and linoleic acid (9) from the twigs; and a mixture of 4a and 4b, 5, 6, 8, long-chain fatty alcohols (10), and long- chain hydrocatbons (11) from the flowers of D. dao.The structures of 1 and 5 were elucidated by extensive 1D and 2D NMR spectroscopy, while those of 2-4 and 6-11 were identified by NMR spectroscopy. Conclusion: This is the first report on the isolation of 1, 4b and 6-9 from D. dao.
Keywords: 3-Alkylphenols; Anacardaceae; Anacardic Acid; B-Sitosteryl Fatty Acid Esters; B-Sitosteryl-3β-Glucopyranoside-6’-O-Fatty Acid Esters; Cardol; Dracontomelon dao (Blanco) merr. Et Rolfe

Chemical Profile and Antioxidant Properties of Mundulea sericea - Mahendra Shivshankar Khyade; Mohan Baban Waman (Pharmacognosy Journal, 2017)
Objectives: To evaluate the phytochemical composition and the antioxidant activity of aqueous-methanolic (20:80) leaves extract of Mundulea sericea Willd. Methods: The extract of leaves was tested for antioxidant activity using various in vitro models viz., 2,2-diphenyl-1-picrylhydrazyl (DPPH), nitric oxide, ABTS, ferric reducing antioxidant power (FRAP), total antioxidant activity and reducing power. The phytochemical composition (GC-MS and HPLC) along with total phenolic and flavonoid content of the extract at different concentrations were also determined. Results: Total phenolic and flavonoid contents were found to be equivalents to 107.86 ± 0.53 μg of gallic acid and 44.53 ± 0.156 μg of rutin /mg of dried hydro-methanolic methanolic extract, respectively. Among various antioxidant assays performed, maximum inhibition was observed for ABTS (IC50 13.26 ± 0.396 μg) followed by DPPH (IC50 79.83 ± 0.306 μg) and NO (IC50 6.35 ± 0.23 μg/mL) assay. The GC-MS analysis revealed over 38 compounds; the prevailing compounds were Sec- Butyl ethyl sulfoxide and Di-methyl sulfoxonium formyl methylide. The RP-HPLC analysis further confirmed the presence of rutin, cinnamic acid and salicylic acid. Conclusion: The results of the present study demonstrated that Mundulea sericea leaves possess high phenolic with flavonoid contents and also revealed potential antioxidant activity so these leaves could be used as a viable source of natural antioxidants for industrial and pharmaceutical preparations.
Keywords: Antioxidant; Flavonoids; GC-MS; Leaf extract; Mundulea sericea; Phenolics; RP-HPLC

Chemical Profile and Biological Activities of Essential oil of Aerial parts of Artemisia monosperma Del. Growing in Libya - Soheir Mohamed El Zalabani; Soad Hanna Tadros; Abeer Mohamed El Sayed; Areej Almaktouf Daboub; Amany Amen Sleem (Pharmacognosy Journal, 2017)
Background: From the bioactivity stand point Artemisia monosperma Del. is reputed to have antispasmodic and anthelmintic properties. Various types of secondary metabolites were reported in A. monosperma plants from different localities. Objective: The current study was planned aiming to investigate the influence of stage of development on the composition, antimicrobial, antiinflammatory and antioxidant activities of the essential oil derived from the aerial parts of the Libyan plants. Material and Methods: A. monosperma volatiles were hydro-distilled from aerial parts of Libyan plants, collected at different stages of growth: before flowering (A1), and at beginning (A2) and by the end (A3) of flowering stage. Yields ranged from 0.16-0.26 ml/100g fresh material (A3, highest). GC/FID and GC/MS analyses were performed. Results: Among 16-20 identified components (97.63-99.00% of total composition), 11 were common in all samples. A1 and A2 showed close amounts of hydrocarbons (63.56 and 66.55%), but lesser than A3 (88.36%); monoterpenoids were mainly represented by sabinene (13.15-22.85%), β-pinene (9.00-24.03%) and β-cis-ocimene (3.73-12.92%); while sesquiterpenoids appeared absent. Among oxygenated components (11.29, 31.08 and 35.44 % in A3, A2 and A1), bornyl acetate was the major monoterpenoid (8.00-31.00%, highest in A1); and the sesquiterpenoid, β-eudesmol (8.01%) was detected in A2 only. Moreover, A2 demonstrated significant antifungal effect against Aspergillus fumigatus and Geotricum candidum (MIC 0.98 and 0.24 μg/ml). Conclusion: A3 exerted the highest anti-inflammatory activity as compared to the other volatiles. A1 restored the reduced blood GHS level in diabetic animals almost as efficiently as Vitamin E. The antioxidant activity of the volatiles is decreased during the flowering stage, being the highest before flowering (A1); this could be associated to the decreasing bornyl acetate content of the samples.
Keywords: Anti-oxidant; Antiinflammatory; Antimicrobial; Artemisia monosperma; Essential oil composition; GC-MS; Libya.

Chemo-profiling, Antioxidant Potential and Ionomic Analysis of Cichorium intybus L. - Bisma Malik; Tanveer Bilal Pirzadah; Inayatullah Tahir; Reiaz Ul Rehman (Pharmacognosy Journal, 2017)
Background: Cichorium intybus commonly called as chicory or coffee weed was traditionally used for the treatment of various ailments associated with liver, kidney and heart. The aim of the present study was phytochemical screening, in-vitro evaluation of antioxidant potential, element analysis of wild and cultivated chicory and GC-MS analysis of methanolic leaf extract of wild chicory grown in Kashmir Himalaya. Method: To achieve this goal, the qualitative and quantitative analysis was done to determine the antioxidant potential. Element analysis was done using AAS and metabolite fingerprinting was done using GC-MS to ascertain the presence of active phytoconstituents in chicory leaves. Results: The qualitative screening of leaf extracts from wild and cultivated chicory indicates the presence of important bioactive constituents. The leaf extract of wild chicory constituted the higher amount of total phenol and flavonoid contents and also showed strong radical scavenging activities of DPPH, SOD and hydrogen peroxide radical as indicated by lower values of IC50 compared to cultivated chicory. Furthermore, both extracts of wild chicory showed the highest total antioxidant potential for the reduction of Fe3+ to Fe2+ when compared with cultivated chicory. The results from the elemental analysis shows that leaf extract of wild chicory exhibits higher concentration of elements as compared to cultivated one, thus can be used as a potential bio-fortified crop. The GC-MS analysis determines the presence of 78 different compounds in the methanolic leaf extract of wild chicory. The major phytochemical constituents were phytol (7.96%) and stigmat-5-en-3-ol (6.45%). Conclusion: The findings of the present study suggested the therapeutic potential of chicory leaves; particularly wild chicory proves to be a potent source of natural antioxidant against free radical associated damages. Metabolite profiling study revealed important metabolites having potent pharmacological actions.
Keywords: Aas; Antioxidant Activities; Cichorium Intybus; GC-MS.; Phytochemical analysis

Chlorophyllin Treatment Against the Snail Lymnaea acuminata: A new tool in Fasciolosis Control - Kavita Singh; D.K. Singh; Vinay Kumar Singh (Pharmacognosy Journal, 2017)
Objective: To observe the toxicity of chlorophyllin against Lymnaea acuminata to control fasciolosis caused by liver fluke fasciola gigantica, very prominent in eastern region of Uttar Pradesh. Materials and Methods: Ten snails Lymnaea acuminata were placed in a glass aquarium containing 3 L of dechlorinated tap water. These snails were treated with different concentrations of chlorophyllin. Chlorophyll was extracted from spinach with the help of macerated leaves and kept for 2 h in 100% ethanol at 55ºC. Results: The results of the experiment showed that the photodynamically active chlorophyllin, at low concentration was able to kill the snails under exposure of solar radiation in summer season instead of winter season. In winter, extracted chlorophyllin toxicity against L. acuminata in sunlight (96 h LC50 91.82 mg L-1) /laboratory condition (96 h LC50 921.93 mg L-1) was less than pure chlorophyllin in sunlight (96 h LC50 12.05 mg L-1) /laboratory condition (96 h LC5019.22 mg L-1), respectively. In summer, pure chlorophyllin was more toxic in sunlight (96 h LC50 3.90 mg L-1) than laboratory condition (96 h LC50 7.18 mg L-1). Pure chlorophyllin is more than five times toxic than synthetic molluscicides. Treatment of chlorophyllin caused no toxic effect against the fish (Colisa fasciatus). The result presented in this paper is found very beneficial and ecologically safe, as a photodynamic substance chlorophyllin, which found in every green plant. Conclusion: Phytotherapy of snails by photodynamic water soluble chlorophyllin to control fasciolosis can be used as potent molluscicides with low cost and easily biodegradable.
Keywords: Chlorophyllin; Fasciola Gigantica; Fasciolosis; Lymnaea acuminata; Photodynamic Reaction.; Plant Molluscicide

Chronic Toxicity of Leaf Extract from Sphagneticola trilobata (L.) Pruski - Areeya Suchantabud; Teeraporn Katisart; Chusri Talubmook (Pharmacognosy Journal, 2017)
Context: Sphagneticola trilobata (L.) Pruski. is a member of the family Asteraceae and has used traditionally in the prevention and treatment of various diseases. Aim: The research was aimed to determine chronic toxicity of 80% ethanolic leaf extract from S.trilobata (STLE). Materials and Methods: STLE at the doses of 200 or 400 mg/kg b. w. was oral given to the healthy Wistar rats daily for 90 days. Statistical analysis used: Statistical analysis was carried out using F-test (One-Way ANOVA) followed by Duncan’s New Multiple Range Test. Results: STLE did not produce any signs or symptoms of chronic toxicity. And also, the mortal rat was not observed during a period of an observation. Furthermore, STLE did not alter the body weight, relative organ (liver, pancreas, kidney and heart) weight, hemoglobin (Hb), hematocrit (Hct), red blood cell (RBC), white blood cell (WBC), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), neutrophil, lymphocyte, monocyte, platelet, alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), blood urea nitrogen (BUN), creatinine, blood cell characteristics, ultrastructure of RBC, and histological features of hepatic, pancreatic and renal tissues in the STLE treated rats comparing to control rats. Conclusions: These findings indicate that the leaf extract from S. trilobata exerts non chronic toxicity in rats and can be used safely as a traditional medicine or diet complement without any effect on hepatic and renal functions.
Keywords: Blood biochemistry; Chronic toxicity; Hematological values; Histological feature; S. trilobata

Comparative Antimicrobial Study of Ethanolic Extract of Leaf and Rhizome of Curcuma longa Linn - Nikhil Singh; Sangeeta Gupta; Vaibhav Rathore (Pharmacognosy Journal, 2017)
Introduction: Curcuma longa L., botanically related to ginger belongs to the Zingiberaceae family. It is extensively used in Ayurveda, Unani and Siddha medicine as a home remedy for various diseases. Aim: The present study is to compare the antimicrobial activity of the ethanolic extracts from rhizome and leaf of Curcuma longa Linn. Method: In vitro disc diffusion method and serial dilution method has been used to determine the antimicrobial potency against various bacterial pathogens such as Klebsiella pneumoniae, Pseudomonas aeruginosa, Staphylococcus aureus and Bacillus subtilis by comparing the zone of inhibition shown by both the test extracts at different concentration (25 mg/ml, 50 mg/ml, 100 mg/ml, 150 mg/ml, 200 mg/ml, 250 mg/ml, 300 mg/ml) and there MIC value has been evaluated. Ethanol and Ampicillin were used as negative and positive control for the study. Result: The leaf and rhizome extract showed maximum zone of inhibition at 300 mg/ml concentration, which was about 7.6 mm and 8 mm on the bacterial strain Pseudomonas aeruginosa and least effectiveness for other bacterial strain such as Staphylococcus aureus and Bacillus subtilis. The recorded MIC value was at 6.25 mg/ml which showed 3.991% inhibition for rhizome extract and 3.129% inhibition for leaf extract. Conclusion: The rhizome extract was found to be more potent antimicrobial agent than the leaf extract and can be used in future studies.
Keywords: Antibacterial activity; antimicrobial agent; Bacterial stain; Curcuma longa L; Minimum inhibitory concentration; Turmeric

Comparative in vitro Antidiabetic and Immunomodulatory Evaluation of Standardized Five Select Medicinal Herbs and Spectral Analysis of Boerhavia erecta L. (Nyctaginaceae) - Suresh Kumar Karri; Angappan Sheela (Pharmacognosy Journal, 2017)
Aim: The present work compares standardized hydro-alcoholic extracts of root and stem parts of Boerhavia erecta L. (Nyctaginaceae), leaves of Plumeria acuminate R. Br. (Apocyanaceae), rhizomes of Alpinia galanga Sw. (Zingiberaceae), whole plant of Picrorhiza kurroa Royle ex Benth. (Plantaginaceae), fruits of Trapa natans L. (Trapaceae) for their in vitro antidiabetic and immunomodulatory activities, commonly used by the Trichigadi tribes (Kotas) of south India for various inflammatory disorders. Materials and Methods: Antidiabetic activity of these herbal extracts was assessed through inhibition of glycosylation of hemoglobin and glucose uptake in yeast cells methods at 50, 100 and 200 μg/mL for 72 h. Their respective immunomodulatory activities were evaluated through preservation of heat and hypotonic induced hemolysis, nitroblue terazolium assay and by inhibition of TNF-α and nitric oxide (NO) production in RAW cell lines. Results: B. erecta has shown least cytotoxicity (CTC50 15.7%) and highest % inhibition of TNF-α (58.1) and NO (45.6), statistically significant (p<0.01) to that of normal control. Also, B. erecta (BE), and P. acuminate (PA) exhibited relatively better IC50 values for TNF-α and NO at a concentration less than their respective CTC50 values. Conclusions: Spectral analysis of chloroform fraction of BE hydro-alcoholic extract established the presence of biologically active molecule in it. Root and stem parts of BE extract not only proved to be safe but also demonstrated relatively better efficacy than other established medicinal herbs in selected immune models, may be due to flavonoids or phenolic groups. Further in vivo studies on active molecule of BE towards antidiabetic and immunomodulatory activity are warranted.
Keywords: Cytotoxicity; NBT assay; Nitric oxide; Pharmacognostic; Phytochemical; Quality control; TNF -α

Comparison of Fatty Acid Profiling and RBC Membrane Stabilization Activity of Seabuckthorn (Hippophae rhamnoides and Hippophae salicifolia) Seed Oil - Suchita Dubey; M.V. Ramana; Anuradha Mishra (Pharmacognosy Journal, 2017)
Background: Seabuckthorn (SBT) is one of the most important plants of higher altitude in India and China. SBT seed oil is rich in Poly Unsaturated Fatty Acid (PUFA) which is present in a peculiar ratio capable of combating inflammation. Objective: To compare the physicochemical characteristics, fatty acid profiling and Red Blood Cell (RBC) membrane stabilization activity between two species of SBT seed oil; Hippophae rhamnoides (HR) and Hippophae salicifolia (HS) collected from Ladakh and Sikkim, India, respectively. Materials and Methods: GC-MS analysis was performed and effect of SBT seed oil was evaluated against heat and hypotonicity induced haemolysis of RBC. Protein denaturation assay was also conducted to check its probable role in chronic inflammation. Results: GC-MS analysis confirmed the presence of PUFA viz. Alpha linolenic acid (ALA) and Linoleic acid (LA) in SBT seed oil. Both significantly (p<0.05) inhibited heat and hypotonicity induced membrane destabilization in a concentration dependant manner. Maximum percentage inhibition of protein denaturation was observed at 3.6 μg/ml after incubation period of 4 hours. Conclusion: HR and HS have been proved to inhibit membrane destabilization with almost equal efficacy. Their efficacy against heat induced protein denaturation indicates that they may be useful in prevention and/or treatment of chronic inflammation as well. These findings may be attributed to the presence of PUFA. This study has contributed in establishing some preliminary evidence about PUFAs being the mainstay of their anti-inflammatory efficacy. However, in vivo studies are required to further validate the results of this study.
Keywords: GC-MS; in vitro; Protein Denaturation; RBC Membrane Stabilization; Sea buckthorn Seed Oil

A Complete Pharmacognostical Profile of Rungia repens - Karuna Modi; Mamta Shah (Pharmacognosy Journal, 2017)
Background: Rungia repens is one of the plants cited as ‘Parpata’ in Ayurvedic literature and indicated as febrifuge, antitussive and vermifuge. Aim: To generate and ensemble data of physical parameters for ascertaining the identification and develop validated HPTLC method for quantification of kaempferol in R. repens. Materials and Methods: R. repens was studied for establishing pharmacognostic standards including macro and microscopical characters, physico-chemical analysis and quantification of kaempferol by HPTLC method. Results: It is a small, much branched, prostrate or sub-erect herb with lanceolate leaf and violet flowers. Microscopically root can be characterized by collenchymatous phloem associated with wide lignified xylem; stem by epidermis with simple and glandular trichomes and collenchymatous hypodermis; and leaf by epidermis embedded with cystoliths and bearing covering and glandular trichomes. Powdered drug can be typified by cystoliths, trichomes of aforementioned type, pollen grains and fragments of cork. Further studies revealed that brunt of heavy metal and microbial load in plant material was within permissible limits. Flavonoids and phenolics were found be major components. HPTLC method was developed for quantification of kaempferol using precoated silica gel plates as a stationary phase, and toluene: ethyl acetate: dichloromethane: formic acid: methyl ethyl ketone (5: 1: 1.5: 0.5: 0.8) as a mobile phase and scanning the plate at 254 nm. Conclusion: The distinctive quality profile data and validated HPTLC method tailored for Rungia repens using kaempferol as a marker, would aid as expedient measures for its evaluation.
Keywords: Ghati pitpapada; HPTLC; Kaempferol; Pharmacognostic study; Rungia repens

Comprehensive Evaluation of Antioxidant Potential of Selected Osbeckia species and their in vitro Culture, Purification and Fractionation - Bosco Lawarence; Murugan K (Pharmacognosy Journal, 2017)
Background: Health-benefit properties of natural pigments have been intensely studied, especially the anthocyanins. In the last few decades, research on anthocyanins has attracted biologists by the increasing evidence of their health beneficial effects. Osbeckia, belongs to Melastomataceae and is well-known for colouring pigments and other bioactive compounds. In the present study, total anthocyanin and antioxidant capacity indicators were evaluated from 8 Osbeckia spp. and anthocyanin was extracted from in vitro cultures of O. aspera and O. reticulata. Materials and Methods: The antioxidant effect was studied using ABTS (2, 2’-azino-bis-3-ethyl benzthiazoline-6-sulphonic acid) radical cation decolourisation assay, the FRAP, the scavenging ability of hydroxyl radicals and the superoxide anion scavenging activity. Anthocyanin extracted from in vitro cultures were purified and fractionated using column chromatography and LC-MS MS analysis. Results: In vitro cultures of O. aspera was obtained in MS medium fortified with various combinations of Benzyl Adenine (BA), Naphthalene acetic acid (NAA) and 2, 4-D. The chromatograms of O. aspera revealed the presence of malvidin-3 -diglucoside, peonidin, delphinidin and cyanindin whereas O. reticulata cultures accumulated large amounts of malvidin, cyanindin and cyanidin aglycone. The purified anthocyanins of these species were evaluated for their antioxidant potential and was found more remarkable than the crude extracts. Conclusion: Osbeckia species are rich in anthocyanin and therefore display potential AOX power. O. aspera and O. reticulata callus was induced in vitro production of anthocyanins. The pool of anthocyanins was purified and fractionated by LCMS/ MS and AOX assays were performed with the purified anthocyanin which showed higher level activities.
Keywords: Anthocyanins; Antioxidant Capacity; Free Radicals; Osbeckia Spp.; Reactive Oxygen Species

A Comprehensive Review on Food and Medicinal Prospects of Astraeus hygrometricus - Gunjan Biswas; Sudeshna Nandi; Debashis Kuila; Krishnendu Acharya (Pharmacognosy Journal, 2017)
Edible mushrooms contain unique flavours and textures. They have high nutritional and medicinal values and have been consumed worldwide. Astraeus hygrometricus (Pers.) Morg. a wild ectomycorrhizal mushroom recognized as a food by the local people in South-East Asia as well as in Bihar, Jharkhand, South west India and South-Western region of West Bengal. However, it is considerably unknown to the communities in other parts of the world and it remains underutilized so far. Recent investigations from our laboratory have manifested the potential role of this mushroom in human health. Basidiocarps of A. hygrometricus are rich in proteins, carbohydrates, minerals, crude fibre and essential amino acids with lower concentration of fat. Experiments on animal models reveal the hepatoprotective, cardioprotective, anti-inflammatory, anticancer and hypoglycaemic efficacy of the mushroom. Additionally, researchers have found this taxon to contain many bioactive compounds shown to be responsible for antitumor, anti-leishmanial, anticandidal, antioxidant and immunomodulatory activity. The present review, summarized the scattered literature on A. hygrometricus with an emphasis on its nutritional and health promoting aspects.
Keywords: Antioxidant; Astrakurkurone; Immunomodulation; Medicinal Mushroom; Nutritive Value.

Contemporary Use of Phytocosmetics in Three Districts from North-Eastern Algeria - Amel Bouzabata (Pharmacognosy Journal, 2017)
Background: In Algeria, the cosmetic market is competitive, with an annual growth of 12%. Because of the toxicity of synthetics cosmetics, the industry is currently more concentrated on herbal cosmetics. Phytocosmetic is an important aspect of traditional medicine in Algerian culture, whose information is scanty. Objective: The present study has been conducted to assess quantitatively the use of herbs in phytocosmetics application. Method: Data was collected from 300 users via face to face interviews using semi-structured questionnaire in three districts from North-eastern Algeria: Annaba, El Tarf and Skikda. Five parameters were evaluated including the demographic characteristics, the form of cosmetic preparation and, medicinal stories used in cosmetic applications. Results: The soap (67%) and a fixed oil (56%) were the preparation forms most used in phytocosmetics applications. Although, five medicinal plants were recorded: Aloe vera (L.) Burm.F., Matricaria recutita L., Lavandula angustifolia Mill., Citrus limon (L.) Osbeck and Ricinus communis L. The highest relative citation frequency (RFC) was attributed to A. vera in the three district Skikda (0.68), Annaba (0.57), and El Tarf (0.43). Eleven traditional recipes have been described. Conclusion: This study is able to record the available information the importance of phytocosmetic in traditional medicine. However, further research should be conducted in Algeria, to explore the toxicity of these products.
Keywords: Algeria; Medicine; Phytocosmetic; Scanty.; Toxicity; Traditional

Cytotoxic Activity of Antioxidant-Riched Dendrobium longicornu - Mukti R Paudel; Mukesh B Chand; Basant Pant; Bijaya Pant (Pharmacognosy Journal, 2017)
Context: Dendrobium longicornu is a traditional medicinal plant widely used in Asia. It has many bioactive compounds like bibenzyl, phenanthrenes, phenolic compounds. There has been little research in the cytotoxic and antioxidant effects of D. longicornu. Aims: The aim of this study was to investigate the cytotoxic and antioxidant activities of this plant. Settings and Design: Antioxidant and cytotoxic activity of Dendrobium longicornu extracts. Methods and Material: The plant extracts were prepared by soxhlet’s extractor in organic solvents, acetone and ethanol. The total polyphenol content (TPC) in the extracts was determined spectrophotometrically by the Folin-Ciocalteu method and the total flavonoid content (TFC) by aluminium chloride method. The antioxidant activity was determined using DPPH (2,2-diphenyl-1-picrylhydrazyl) method. The cytotoxic activity was evaluated against human brain tumor cells (U251) and cervical cancer cells (HeLa) using MTT assay. Statistical analysis used: Regression analysis was done for calculation of IC50. Duncan multiple range test and Dunnett test were done to compare the data. Results: The Dendrobium longicornu acetonic extract (DLA) showed significantly highest TPC and TFC than Dendrobium longicornu ethanolic extract (DLE). The antioxidant activity was also significantly higher in DLA followed by DLE. Highest cytotoxicity (i.e., lowest IC50 value) was found for the DLA on U251 cells and DLE on HeLa cells. Conclusions: This result concluded that D. longicornu is a potential source of antioxidant and cytotoxic agents.
Keywords: Dendrobium longicornu; DPPH; Flavonoid; MTT; Polyphenol

Cytotoxic and Antioxidant Effects in Various Tissue Extracts of Plumbago zeylanica: Implications for Anticancer Potential - Balachandran Karpaga Raja Sundari; Srivani Telapolu; Bilikere S; Dwarakanath; Sadras. P. Thyagarajan (Pharmacognosy Journal, 2017)
Introduction: Complex natural products are emerging as a potent alternate and complement in anticancer therapies due to its multiple mechanisms of action and minimal effects on nontarget cells/tissues. Some of the traditional herbal formulations contain Plumbago zeylanica L, (commonly known as Chitraka or Chitramoolam) to treat various disorders for centuries in Africa and Asia. Methods: The quantity of Plumbagin was detected in different tissues of P. zeylanica through HPTLC analysis. We evaluated and compared the alcoholic tissue extracts of leaf, stem and root of P. zeylanica with standard pure Plumbagin for its in vitro cytotoxic effects (metabolic viability; MTT assay) in A549 Lung cancer cells and antioxidant potential (DPPH free radical scavenging and total phenol content). RNA sequencing and transcriptome analysis was performed in the most potent tissues of P. zeylanica demonstrating efficient pharmacological activity. Results: The root extract containing 1.3% of plumbagin exhibited strongest scavenging potential with 50% radical scavenging (IC50 value of 3.99 μg) in comparison with 35.85 μg in stem (0.2% Plumbagin) and 18.06 μg in leaf with 0.00007% Plumbagin. The in vitro cytotoxicity in A549 cells also showed that the root extract was most potent with an IC50 value of 164.5 μg as compared to extracts from stem (IC50= 379.5μg) and leaf (IC50= 274.9 μg). Conclusion: The strong antioxidant potential shown by the P. zeylanica extract demonstrates its ability to protect the non-target (normal) cells against oxidative stress, while the cytotoxic effects suggest that it could inhibit the growth of cancerous cells. Further, transcriptome analysis predicted the expression of potent gene transcripts coding for quinone biosynthesis in the root tissues of P. zeylanica.
Keywords: A549 Cell Line; Alcoholic Root Extract; DPPH assay; HPTLC Quantification; Plumbagin; Transcriptome Analysis

Cytotoxic Compounds from Kibatalia gitingensis (Elm.) Woodson - Mariquit M. De Los Reyes; Glenn G. Oyong; Vincent Antonio S. Ng; Chien-Chang Shen; Consolacion Y. Ragasa (Pharmacognosy Journal, 2017)
Ursolic acid (1), squalene (2), a mixture of α-amyrin acetate (3a) and lupeol acetate (3b), and isoscopoletin (4), isolated from the dichloromethane extracts of the leaves and twigs of Kibatalia gitingensis, were evaluated for their cytotoxic activities against three human cancer cell lines, breast (MCF-7) and colon (HT-29 and HCT-116), and a normal cell line, human dermal fibroblast-neonatal (HDFn), using the in vitro PrestoBlue® cell viability assay. Compounds 1-4 exhibited strong cytotoxic activities against HT-29 cells with IC50 values ranging from 0.6931 to 1.083 μg/mL. Furthermore, 1-4 were moderately cytotoxic against HCT-116 cells with IC50 values ranging from 4.065 to 11.09 μg/mL. These compounds were least cytotoxic against MCF-7 cells with IC50 values ranging from 8.642 to 25.87 μg/mL. The most cytotoxic against HT-29 cells, HCT-116 cells and MCF-7 cells are 2, 4 and 1, respectively.
Keywords: Apocynaceae; Cytotoxicity; HCT-116; HDFn; HT-29; Isoscopoletin; Kibatalia gitingensis; Lupeol acetate; MCF-7; PrestoBlue® cell viability assay.; Squalene; Ursolic acid; α-amyrin acetate

Cytotoxic Effect of Caralluma fimbriata Against Human Colon Cancer Cells - Shenai Ashwini; Devaraj Ezhilarasan; Roy Anitha (Pharmacognosy Journal, 2017)
Aim: The present study was designed to examine the cytotoxic effects of ethanolic leaf extract of Caralluma fimbriata in the COLO 320 cell line. Materials and Method: The anti-proliferative effects were evaluated using the MTT assay. The COLO 320 cells were treated with different concentrations of the leaf extract of Caralluma (100 – 300 μg/ml) for 24 h. The cell viability and IC50 was calculated from the cytotoxicity. The morphology of the Caralluma treated cells, control, and positive control were observed under reverse phase inverted microscope. Result: The C. fimbriata ethanolic leaf extract showed dose dependant increase in cytotoxicity in COLO 320 human colon cancer cells. The maximum cytotoxic effect was noticed with maximum dose used in this study i.e., 300 μg with an IC50 value of 233.87 μg. Conclusion: The present study shows that the ethanolic leaf extract of Caralluma fimbriata is capable of reducing cell proliferation by inducing cytotoxicity of COLO 320 cells.
Keywords: Caralluma fimbriata; COLO 320 cell line; Colonic cancer; Cytotoxicity; MTT Assay

Cytotoxicity and Oral Acute Toxicity Studies of Litsea glutinosa C. B (ROB) Stem Bark Ethanol Extract - Arunodaya Hosahalli Sumithregowda; Krishna Venkatarangaiah; Kumaraswamy Malleshappa Honnenahally; Vinaykumar Nagenahalli Manjunath (Pharmacognosy Journal, 2017)
Background: Litsea glutinosa (Lauraceae) stem bark is widely used in folk medicine as a hepatoprotective, anti-diarrheal and anti-dysenteric drug but there is a lack of information about its toxicity. Objective: To evaluate cytotoxicity and acute toxicity of the stem bark ethanol extract (BEE). Materials and Methods: In vitro cytotoxicity of BEE was measured against breast adenocarcinoma, prostate, and colon carcinoma cell lines. In the acute toxicity tests, rats received oral doses of BEE as 1000, 2000, and 3000 mg/kg body weight. Mortality, signs of toxicity, body weight, food consumption, and gross findings were observed for 14 days. Blood samples were collected from anesthetized animals and used for hematological and biochemical parameters. Histopathological study was performed using liver and kidney samples. Results: The BEE does not show significant cytotoxic effect against the tested cell lines up to the range from 5 to 320 μg/ml. In acute toxicity study, also lethality was not observed up to 3000 mg/kg b.w. No significant differences were noticed in body and organ weights and histopathology examinations between the control and treated groups. Conclusion: This study authenticates stem BEE may contain bioactive compounds of potential therapeutic significance which are relatively safe from toxic effects, and evidences the medicinal use of this plant in folk medicine.
Keywords: Acute toxicity; Breast adenocarcinoma cell line; Haematology.; Litsea glutinosa; MTT Assay

Cytotoxicity Effect and Morphological Study of Different Duku(Lansium domesticum corr.) Extract towards Human Colorectal Adenocarcinoma Cells Line (HT-29) - Rohin Mohd Adzim Khalili; Jumli Mimie Noratiqah; Ridzwan Norhaslinda; Abd Hadi Norhayati; Baig Atif Amin; Arshad Roslan; A. Latif Ahmad Zubaidi (Pharmacognosy Journal, 2017)
Context: Lansium domesticum corr. is a member of the family Meliaceae, and known locally as duku and has been used traditionally in the prevention and treatment of various illness. Aim: To study the cytotoxic effect and morphological changes of human colorectal adenocarcinoma cells (HT-29) treated with different duku (Lansium domesticum corr.) extracts. Methods: The L.domesticum corr. fruit extracts were processed involving three different solvents; methanol, ethanol and ethyl acetate. HT-29 cell lines were treated with different concentrations of L. domesticum corr. (0-100 μg/ml) extracts for a total of 24, 48 and 72 hours. Cytotoxicity of cells line was determined by using MTT assay as per IC50 values. Results: Methanol extract of L. domesticum corr. showed IC50 value at 6.79 ± 0.00 μg/ml and 50.0 ± 0.00 μg/ml respective, while ethyl acetate extract of L. domesticum corr. reached IC50 value at 86.00 ± 0.08 μg/ml, and 96.0 ± 0.12 μg/ml. There was no IC50 value of ethanol extract from L.domesticum corr. Only methanol extract showed toxicity towards HT-29 cells line. Conclusion: To the best of our knowledge, this is the first repeat the exploring the effect of duku (L. domesticum corr.) extract on HT-29 cells line.
Keywords: Anti-proliferative effect; colorectal cancer; IC50 value.; MTT Assay; polarity extracts

Cytotoxicity of Fucoidan from Three Tropical Brown Algae Against Breast and Colon Cancer Cell Lines - Alim Isnansetyo; Fadilah Nor Laili Lutfia; Muhammad Nursid; Trijoko; Ratna Asmah Susidarti (Pharmacognosy Journal, 2017)
Introduction: Fucoidan is a sulfated polysaccharide that has a wide range of bioactivities including anti-cancer. This polysaccharide commonly is extracted from marine brown seaweed. There is lack of information on the fucoidan extracted from tropical brown algae and its anti-cancer activity. Objectives: The objectives of this study were to purify fucoidan from Sargassum sp., Turbinaria sp. and Padina sp., and to evaluate their cytotoxicity against breast cancer (MCF-7) and colon cancer cells (WiDr). Materials and Methods: Fucoidan extraction was conducted by using acid extraction method. Purified fucoidans were obtained by DEAE cellulose column chromatography and confirmed by HPLC and FT-IR spectrometry. The cytotoxicity was evaluated by using the MTT (3-[4,5-dimethylthiazol-2-yl] -2,5- diphenyltetrazolium bromide) assay. Results: Fucoidan from Sargassum sp. and Turbinaria sp. showed low cytotoxicity with IC50 ranging between 461-663 μg/mL. Higher cytotoxicity against MCF-7 and WiDr was showed by fucoidan from Padina sp. with IC50 of 144 and 118 μg/mL, respectively. While its IC50 against Vero cells was 501 μg/mL.Standard fucoidan from Fucus vesiculosus exhibited IC50 of 60, 63 and 211 μg/mL against MCF-7, WiDr and Vero Cells, respectively. Although the IC50 was higher than that of standard fucoidan, Padina sp. fucoidan showed cytotoxicity comparable with standard fucoidan at concentrations below 100 μg/mL. Conclusion: These results indicated that Padina sp.fucoidan showed potential selective cytotoxicity, and promising for the development of an anti-cancer compound.
Keywords: Breast cancer; Colon cancer; Cytotoxicity.; Fucoidan; Phaeophyta

Designing monographs for Rosmarinus officinalis L. and Lavandula angustifolia L.: Two Lebanese species with significant medicinal potentials - Mariam Koleilat; Karim Raafat; Abdalla El-Lakany; Maha Aboul-Ela (Pharmacognosy Journal, 2017)
Introduction: The world health organization recommends validating medicinal plants to ensure safety and efficacy. Lavandula is valued for the production of essential oil used in aromatherapy. Rosmarinus is known for its folk use as anti-oxidant and antidiabetic. This study aims to design monographs for Rosmarinus officinalis (Linn.) and Lavandula angustifolia (Linn.) cultivated, in conditions similar to their natural habitat, at Beirut Arab University botanical garden. Also screening the antioxidant activity of both plants, and assessing the antidiabetic effect of R. officinalis (Linn.). Methods: macroscopic and microscopic examination, hydrodistillation to obtain essential oils (EOs), thin layer chromatography, Gas chromatography-Mass spectrometry, and physiochemical properties of the EOs were determined. The antioxidant effect of the EOs is determined by DPPH assay. The antidiabetic effect of Rosemary EO is investigated using alloxan-induced diabetic mice. Results: the qualities of studied species are in agreement with the standards described in WHO monographs and in the British pharmacopeia. Composition of the EO produced from either Rosemary (REO) or Lavender (LEO) collected at different months showed differences. The EO of both showed significant antioxidant effects in DPPH assay (p<0.05). In vivo investigation of the antidiabetic effect of REO showed a significant antidiabetic effect in diabetic mouse model (p<0.05). Conclusion: both plant species and their EOs fulfilled most of standards specified by the British Pharmacopeia 2013. Rosemary collected in April (Spring) showed the best antioxidant activity. Lavender collected in September (Early Fall) showed the best antioxidant activity. REO revealed significant lowering in blood glucose level at the dose of 110 mg/kg.
Keywords: Glandular trichome; Optical rotation; Prismatic crystals of Calcium oxalate; Refractive index; Rosmarinic acid

Determination of Antipyretic and Antioxidant Activity of Cassia occidentalis Linn Methanolic Seed Extract - Vijay Vikram Singh; Jainendra Jain; Arun Kumar Mishra (Pharmacognosy Journal, 2017)
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

Determination of Rubraxanthone in the Latex of Asam Kandis (Garcinia cowa Roxb) by Reverse Phase High Performance Liquid Chromatography. - Dachriyanus; Nova Susanti Asjar; Meri Susanti (Pharmacognosy Journal, 2017)
Context: Rubraxanthone is a major compound found in Garcinia cowa Roxb which has various biological activities. This compound is likely to be responsible for the pharmacological activities of this plant. The latex of this plant was one of the source of this compound. To prevent counterfeiting, it is essential to develop a method of analysis to determine the levels of these compounds in the latex of G. cowa. Aims: To develop and validated a reverse phase-high performance liquid chromatography (RP-HPLC) technique for determination of rubraxanthone in the latex of G. cowa. Settings and Design: RP-HPLC analysis. Methods and Material: The sample was powdered and dissolve in methanol and then subjected to Reverse Phase High Performace Liquid Chromatoraphy (RP-HPLC). Separation was carried out in a reversed-phase column Shimadzu Shimp-pack VP–ODS (4.6 x 250 mm). The elution was performed with isocratic solvent using formic acid 0.4 % v/v in methanol (15:85) with a flow rate 1 ml/minute. The solvents used for the mobile phase were filtered through membrane filter (0.45 mm pore size) and degassed before use. Total running time was 20 minutes and the sample injection volume of injection was 20 ml. While the wavelength of the UV-VIS detector was set at 243.2 nm. Results: The detection and the quantitation limits of rubraxanthone were 1.119 mg/mL and 3.731 μg/mL, respectively. A regression analysis was performed, with the observation of good linearity (r = 0.998). The values obtained for precision and accuracy determination are in agreement with ICH guidelines. It was found that rubraxanthone in dichloromethane extract of latex G. cowa was 56.56%. Conclusions: The results demonstrated that the developed method is a reliable HPLC technique for determination of rubraxanthone in the latex of G. cowa.
Keywords: Counterfeiting; Isocratic method; Latex of Garcinia cowa Roxb; RP-HPLC; rubraxanthone; Standarization

Development and Evaluation of Herbal Sunscreen - Mukund Manikrao Donglikar; Sharada Laxman Deore (Pharmacognosy Journal, 2017)
Thus present research work deals with the development and evaluation of topical photo protective formulation, containing antioxidant, wound healing, anti-inflammatory and rather photo protective poly phenols like curcumin, quercetin, resveratrol and safranal. The present research work provides stable natural photo protective formulation with antioxidant potential, high SPF and more important uniform UVA/UVB protection.
Keywords: Curcumin; Quercetin; Resveratrol; safranal; SPF.; Sunscreen

Differentiation of Five Commercially Available Triphala churnas of an Ayurvedic Formulation by Elemental Fingerprint - Venkata Siva Satyanarayana Kantamreddi; V. Thirumala Veni; Murali Krishna Malasani; Boddana Simhachalam (Pharmacognosy Journal, 2017)
Introduction:Triphala churna (TPC) is one of the well known Ayurvedic powdered preparations of Indian System of Medicine and is used in the treatment of various diseases. Elemental pattern of TPC was developed in order to investigate the identity and quality of commercial TPC drugs. Method: Inductively coupled plasma mass spectrometry (ICP-MS) was used for the quantitative determination of ten essential and trace elements in five marketed samples of Triphala churna. The concentration patterns of these elements were deciphered by multivariate statistical analysis such as hierarchical cluster analysis (HCA), fuzzy c-means (FCM) and k-means (KM) cluster analysis. Results: The elemental concentrations ranged from 1.3 mg/kg (Cr, TPC3) to 14220 mg/kg (K, TPC4). The elemental fingerprint of Triphala churna was established based on three churnas viz. TPC1, TPC3 and TPC5, which were found in one cluster with a very high degree of similarity by KM, FCM and HCA techniques. Conclusion: Based on the results, the graphical pattern of elements detected in these samples can be considered as elemental fingerprint of Triphala churna and can be used for authentication and/or to determine the quality of commercial TPC drugs.
Keywords: Ayurvedic Drugs; Elemental Fingerprint; Fuzzy c-Means; Hierarchical Cluster Analysis; Inductively Coupled Plasma Mass Spectrometry; k-Means; Triphala churna

Distribution, Ethnobotany, Pharmacognosy and Phytoconstituents of Coptis teeta Wall.: A Highly Valued and Threatened Medicinal Plant of Eastern Himalayas - Temin Payum (Pharmacognosy Journal, 2017)
Objectives: To study the distribution, traditional knowledge, dose and preparations, phytoconstituents, pharmacognostic characters and to correlate phytoconstituents and the claimed health benefits among the tribal people of Arunachal Pradesh if any, the present study was carried out. Methods: Field survey and interview were used for ethnobotany and protocol given in Shah and Seth (2010), Kakote et. al.,(2012) and Wallis (2011) was followed to study pharmacognostic studies while GC-MS was used in the studies of phytoconstituents. Results: This study reports numbers of volatile and non-volatile compounds from the rhizome of Coptis teeta with high percentage of berberine alkaloids. The study also reports alkaloid deposition at parenchymatous tissues and vascular tissues of rhizome. Phytoconstituents presents in the ethanolic extract of C.teeta cold be related to health problems and phytoconstituents as claimed by tribal people of Arunachal Pradesh. Conclusion: Locally called Mishmi teeta in Arunachal Pradesh, Coptis teeta Wall. is a well-known medicinal plant used among Mishmi and other tribes of Arunachal Pradesh for health problems like loose motion, stomach pain, diarrhoea and malaria. This endemic and threatened medicinal plant contains numbers of biologically active compounds and need in-situ as well as ex-situ conservation.
Keywords: Berberine; Eastern Himalayas; Medicinal plant; Mishmi tribe; Phytoconstituents; Threatened

DNA Fingerprinting Profile and Quality Control Standardization of Folklore Medicinal Plant Exacum lawii - Sonam Sharma; Siva Hemalatha (Pharmacognosy Journal, 2017)
Context and Aim: Exacum lawii (Gentianaceae) is bitter folk medicinal herb. The study deals with molecular investigation by DNA fingerprinting profile of Exacum lawii, quality control and phytochemical standardization of Exacum lawii. Methods: The DNA fingerprinting profile was performed by RAPD technique using 3 pairs of primers. The quality control standardization was done as per the WHO guidelines and official methods of AOAC. Phytochemical standardization employed quantitative estimations of phytoconstituents by spectrophotometric and identification using GCMS technique. The quantification of Swertiamerin and Ursolic acid in Exacum lawii was carried by HPLC. Results: Macroscopical and microscopical examination confirmed the diagnostic morphological and histological features. The content of vitamins, minerals and fatty acids were estimated. Physicochemical parameters obtained within the provided limits as per WHO. The phytochemical screening of ethanolic extract and its fraction revealed the presence of alkaloids, flavonoids, phenols, tannins, terpenoids, glycosides and steroids Total phenolics (57.4mg/g tannic acid equivalent), total tannins (15.3 mg/gm), total flavonoids (51.4 mg/gm rutin equivalent), total flavonols (5.4 mg/gm) and carbohydrates (12.6 mg/gm D-fructose equivalent) content were estimated using spectroscopic techniques. The GC-MS data revealed 20 compounds. Swertiamerin and Ursolic acid content was 119.59 mg/gm and 5.34 mg/gm respectively. Conclusion: Present study provides the referential information to develop a monograph for quality control standardization of Exacum lawii. Key words: Exacum lawii, DNA fingerprinting, Swertiamerin, Ursolic acid, GC-MS.
Keywords: DNA fingerprinting; Exacum lawii; GC-MS.; Swertiamerin; Ursolic acid

Effect of Gamma Irradiation on Angiotensin Converting Enzyme Inhibition, Antioxidant Activity, Total Phenolic Compound and Total Flavonoid of Peperomia pellucida Herbs Extract - Anies Monica Adhitia; Alisa Nur Octaviani; Rissyelly; Katrin Basah; Abdul Mun’im (Pharmacognosy Journal, 2017)
Introduction: Peperomia pellucida L. Kunth has been reported to have some biological activities such as antihypertensive and antioxidants. Herbal materials susceptible to contamination during processing and storage which can shortens their shelf life. Gamma-irradiation has been used as a method for preservation. Methods: This research aimed to analyze the effect of gamma-irradiation on inhibition activity of angiotensin converting enzyme (ACE), antioxidant activity, total phenol content, total flavonoid, and thin layer chromatography profiles of P. pellucida L. Herbs extract. The extract was irradiated with 60Co gamma rays at 2.5; 5; 7.5; dan 10 kGy. Results: Irradiation up to 10 kGy did not change ACE inhibitory activity and TLC profile. No significant differences were noted in the inhibition activity of ACE and the type of chromatogram profiles between non-irradiated extract and irradiated extracts up to a dose of 10 kGy while total flavonoids showed a significant decrease. In addition, total phenolic content and antioxidant activity showed a significant increase of extracts were irradiated up to 5 kGy and decrease at dose 7,5 kGy and 10 kGy. Gamma-irradiation up to 10 kGy didn’t affect the activity of ACEinhibitor in-vitro while significant difference (P <0.05) of antioxidant activity, total flavonoids and phenolic content of the extract P. Pellucida. Conclusion: In conclusion, gamma - irradiation can be used as a preservation method for ethanol extract P. Pellucida L. Kunth herbs.
Keywords: ACE; Antioxidant; Extract; Gamma-irradiation; Peperomia pellucida; Total flavonoids; total phenolic

Effect of Gamma Irradiation on Suruhan (Peperomia pellucida (L.) Kunth) Herb Powder - Mubarika Sekarsari Yusuf; Intan Wulandari; Lili Amelia; Katrin; Arikadia Noviani; Rissyelly; Abdul Mun’im (Pharmacognosy Journal, 2017)
Introduction: Peperomia pellucida (L.) Kunth is known as a raw material for herbal medicine; Preservation of herbs powder by gamma irradiation is reported to be able to keep products free from contamination. Methods: This study aims to evaluate the effect of gamma irradiation (0; 2.5; 5; 7.5; and 10 kGy) on the ACE inhibitory activity (ACE Kit – WST test kit method), antioxidant activity (DPPH radical scavenging method), total phenolic content (colorimetric method using Folin-Ciocalteu reagent), total flavonoid content (colorimetric method using AlCl3 and sodium acetate), and TLC profiling (silica gel F254 as the stationary phase and dichlormethane:methanol [92:8] as the mobile phase) of suruhan herb powder. Results: Results showed that the 2.5 kGy irradiation dose gave the smallest alteration in ACE inhibitory activity compared to others irradiated doses. Furthermore, the 5 and 7.5 kGy dose didn’t cause significant change (p>0.05) on antioxidant activity, total phenolic content, and total flavonoid content. Antioxidant activity was found to correlate with the total phenolic content but not with the total flavonoid content. Conclusion: Based on these finding, it is concluded that gamma irradiation can be used as a preservation method for P. pellucida herb powder.
Keywords: Angiotensin converting enzyme; antioxidant activity; Peperomia pellucida; total flavonoid; total phenolic

Effects of Rainfall on the Antimicrobial Activity and Secondary Metabolites Contents of Leaves and Fruits of Anadenanthera colubrina from Caatinga Area. - Daniel Rodrigo Cavalcante de Araújo; Luís Cláudio Nascimento da Silva; Wolfgang Harand; Júlia Morais Fernandes; Thaciane da Cunha Soares; Silvana Maria Zucolotto Langassner; Raquel Brandt Giordani; Rafael Matos Ximenes; Alexandre Gomes da Silva; Márcia Vanusa da Silva; Maria Tereza dos Santos Correia (Pharmacognosy Journal, 2017)
Background: Anadenanthera colubrina (Vell.) Brenan var. cebil (Griseb) is a plant widely used for medicinal proposes in Brazilian Northeast. Objective: This study aimed to analyze the influence of rainfall indexes (RI) in antimicrobial activity and phytochemical constituents of extracts from leaves and fruits of A. colubrina. Material and Methods: Samples were collected in Catimbau National Park (Buíque, Pernambuco, Brazil) at September 2010 (RI: 75 mm) and January (RI: 65 mm), April (RI: 162 mm) and June 2011 (RI: 73 mm). The extracts were prepared by Soxhlet extraction using cyclohexane, chloroform, ethyl acetate and methanol. The antimicrobial activity was determined by MIC and MBC values. Results: All extracts showed antimicrobial activity, but ethyl acetate extracts (from all periods) were more active. Strong correlations were found between the RI and the average MIC of MLE (ρ: -0.99), EALE (ρ: -0.81), CHFE (ρ: -0.81), EAFE (ρ: -0.80); while moderate and weak correlations were found for other extracts. Through a HPLC analysis was possible to reveal that the samples collected from dry periods had more chemical diversity (as they presented more peaks). Gallic acid and quercetin (and derivative compounds) were identified. The levels of quercetin were enhanced in extracts from dry months. Conclusion: Our results showed that the rainfall has a positive effect on the antimicrobial activity of leaves and fruits of A. colubrina, however these extracts showed more chemical diversity during dry months.
Keywords: Antimicrobial agents; Medicinal plants; Natural products; Semi arid area

The Efficacy Study of Snake Fruit (Salacca edulis Reinw Var. Bongkok) Extract as Skin Lightening Agent - Astrid Tilaar; Anna Ranti; Abdul Mun’im (Pharmacognosy Journal, 2017)
Introduction: The whitening skin product market has been growing significantly in Asia Pacific. Indonesia is one of those countries that mainly think that having a white color skin is simply beautiful. Therefore, it motivates Indonesian women to buy more whitening product for their beauty needs. Objective: The purpose of this research is to find raw material for whitening product from Indonesian plants that can be useful as skin lightening agents. This study investigated the potential of snake fruit (Salacca edulis Reinw var. Bongkok) ethanolic extract as skin lightening agent. Fruits of Salacca edulis Reinw contains flavonoids which have been reported to play a part in skin depigmentation. Methods: A randomized double-blind study on 17 human volunteers showed marked skin lightening effects using cream containing 3% extract as there was a significant reduction in skin melanin index which compared favorably with the base cream (p <0,05). Results: The result strongly suggested that snake fruit ethanolic extract can be used as raw material for skin lightening agents and therefore Indonesia dependency on imported raw materials could be reduced.
Keywords: Antioxidant; Melanin index; Salacca edulis Reinw; Snake fruit extract; Tyrosinase

Evaluation of Anti Arthritic Potential of Gloriosa superba (L.) Elite Germplasm Collected from Eastern Himalayas, India - Ankita Misra; Akanksha Srivastava; Mohammad Khalid; Poonam Kushwaha; Sharad Srivastava (Pharmacognosy Journal, 2017)
Introduction: Gloriosa superba (L.) is a traditionally known medicinal plant for its potential antigout property. The species is rich source of colchicine alkaloid and is commercially exploit in the international market for the same. Method: In the present study, elite chemotype of G. superba was identified from natural population in Eastern Himalayas based on their colchicine content through HPTLC calibrated method. The selected elite chemotypes were further evaluated for in vitro anti-arthritic potential via inhibition of protein denaturation along with hydroxyl radical scavenging potential. Result: The HPTLC quantification data reveals that the content of colchicine varies from 0.044 to 0.184% having maximum content in NBG-128 from Jorhat, Assam. The results of bioassay reflect a potentiating anti-arthritic and hydroxyl radical scavenging with statistically insignificant difference within the elite germplasms. Conclusion: The presence of bioactive polyphenolics with significant hydroxyl radical scavenging will further suggest that inhibition of inflammatory mediator cells by extract is superimposed action of colchicine and other chemical inhibitors like polyphenolics. The study will aid in site specific exploration of high metabolite yielding chemotype(s) with validated pharmacological action for commercial cultivation to meet out the industrial demand of colchicine and herbal product development.
Keywords: Anti arthritic; Colchicine; Elite chemotype; G. superba; HPTLC

Evaluation of Anti-Anxiety Effect of Brassica oleracea L. Extracts in Experimental Animals - Divneet Kaur; Richa Shri; Anjoo Kamboj (Pharmacognosy Journal, 2017)
Introduction: Oxidative stress in the brain causes nervous system impairment. Hence the use of antioxidants could be an effective approach to prevent disorders such as anxiety. Plants containing phenolic constituents are reported to be potent antioxidants. Brassica oleracea L. commonly known as broccoli, is rich in phenolics mainly flavonoids and possesses excellent antioxidant property, however its anxiolytic potential has not been investigated. Thus in the present study antianxiety activity of extracts of broccoli was evaluated in experimental animals. Materials and Methods: Various pharmacognostic parameters of the plant material were studied following standard procedures. Groups of six mice each were taken as different treatment groups. Control group received vehicle (1% Carboxy Methyl Cellulose), positive control received Diazepam (2mg/kg) as standard drug while test groups received petroleum ether and hydroalcoholic extracts (50, 100 and 200 mg/kg body weight, p.o.). The effects were evaluated on Elevated Plus Maze (EPM), hole board and mirror chamber tests. Statistical analysis was performed using ANOVA, followed by Turkey’s post-hoc test. Results: Hydroalcoholic extract shows dose dependent increase in the average time spent and frequency of entries in the open arms of the EPM; decreased latency, increased time spent and frequency of entries in the mirror chamber; increased number of head dips in hole board test as compared to control was observed. These effects were comparable to the effect produced by diazepam. Phytochemical screening of the bioactive extract revealed the presence of alkaloids, phenols, flavonoids and tannins. Conclusion: From our study, it can be concluded that hydroalcoholic extract of Brassica oleracea at the dose of 200 mg/kg possesses marked anxiolytic activity.
Keywords: Antianxiety; Brassica oleracea; Elevated Plus Maze; Hole Board; Mirror Chamber Test

Evaluation of Antidiabetic Activity of Hydroalcoholic Extract of Cassia fistula Linn. pod in Streptozotocin-Induced Diabetic Rats - Ram Niwas Jangir; Gyan Chand Jain (Pharmacognosy Journal, 2017)
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

Evaluation of in vitro Antioxidant and Anticancer Activity of Simarouba glauca Leaf Extracts on T-24 Bladder Cancer Cell Line - Sridevi I Puranik; Shridhar C Ghagane; Rajendra B Nerli; Sunil S Jalalpure; Murigendra B. Hiremath (Pharmacognosy Journal, 2017)
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 (0.16μM/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.

Evaluation of in-vitro Anthelmintic Activity of Ximenia americana, Hopea ponga and Vitex leucoxylon - Arun Kashivishwanath Shettar; Ankala Basappa Vedamurthy (Pharmacognosy Journal, 2017)
Objective: Evaluating Anthelmintic activity of Ximenia americana, Hopea ponga and Vitex leucoxylon extracts by using in vitro assay. Methods: The serial exhaustive extraction was carried out with a series of solvents: chloroform, ethyl acetate, methanol, ethanol and water with increasing polarity using Soxhlet apparatus. The concentrated and dried extracts were evaluated for anthelmintic activity by employing standard in vitro method (Pheretima Posthuma model). Results: In vitro anthelmintic study shows that in case of Ximenia americana chloroform extract showed higher anthelmintic activity where as incase of Hopea ponga and Vitex leucoxylon methanol extract exhibited significant activity when compared to other solvent extracts. Conclusion: Results confirm that methanol extract of Hopea ponga exhibited highest anthelmintic activity among all tested extracts. This study provides scientific evidence that the leaves of Ximenia americana, Hopea ponga and Vitex leucoxylon have anthelmintic efficacy. However further comprehensive chemical and pharmacological investigation should be carried out to isolate the active compounds and appropriate elucidation of its mechanism of action and it helps in the development of new pharmaceuticals to treat Helminthiasis.
Keywords: Hopea ponga; in vitro anthelmintic activity; Pheretima Posthuma model; Vitex leucoxylon; Ximenia americana

Evaluation of Lens Aldose Reductase Inhibitory and Free Radical Scavenging Potential of Fractions of Lonchocarpus cyanescens: Potential for Cataract Remediation - Emmanuel Oladipo AJANI; Saheed SABIU; Kuburat Temitope ODUFUWA; Taiwo Bashir Ibrahim; Bamidele Adewale Salau (Pharmacognosy Journal, 2017)
Introduction: Current research effort at discovering effective anticataract agent is focus on evaluating Aldose reductase inhibition (ARI) capacities of medicinal plants and plant extracts. The present study was aimed at investigating the in vitro ARI activity of fractions of Lonchocarpus cyanescens leaves on partially purified AR from goat lens. Methods: Phytochemical constituents of the leaves were screened for using aqueous and methanolic extract while in vitro free radical scavenging and ARI activities of the fractions were evaluated using partially purified aldose reductase. Kinetics of the enzyme in the presence of fractions of the leaves was then compared using Lineweaver-Burk plot. Results: Phenol, flavonoid, tannins and phlobatannins were detected in both extracts. All the fractions inhibited AR significantly but this was strongest with aqueous (IC50, 0.06 ± 0.02 mM-1 and chloroform fractions (IC50, 0.09 ± 0.01 mM-1). Ethyl acetate, hexane and methanol fraction showed competitive inhibition whereas the aqueous and chloroform fractions showed mixed inhibition with a different Vmax and Km when compared with DL-glyceraldehyde. All the fractions also showed antioxidant capacities but this was also strongest with aqueous fraction. Conclusion: The study confirms the ARI and antioxidant capacity of Lonchocarpus cyanescens which may be attributed to its phenolic constituents and whose extraction is solvent dependent. The plant may therefore serve as a base for the development of anticataract agent.
Keywords: Aldose reductase; Cataract; Free radical; Medicinal plant; Phytochemical constituents.

An examination of the Antimicrobial and Anticancer Properties of Khaya senegalensis (Desr.) A. Juss. Bark Extracts - Camille Rabadeaux; Lou Vallette; Joseph Sirdaarta; Craig Davis; Ian Edwin Cock (Pharmacognosy Journal, 2017)
Background: Khaya senegalensis (Desr.) A. Juss. is a common component of the pharmacopeia’s of multiple African groupings which inhabit the areas in which it grows. Amongst these groups there is a myriad of medicinal uses in the treatment of a wide variety of bacterial, fungal and protozoal infections, as well as in the treatment of cancers. This study was undertaken to test K. senegalensis bark extracts for the ability to inhibit microbial and cancer cell growth, and thus to validate traditional African medicinal usage of this plant in treating a variety of diseases. Materials and Methods: K. senegalensis bark powder was extracted by both solvent maceration and subcritical fluid extraction (SFE). The extracts were tested for the ability to inhibit bacterial and G. duodenalis growth. Inhibition of Caco-2 and HeLa cancer cells was evaluated using MTS-based colorimetric cell proliferation assays. Toxicity was evaluated using an Artemia franciscana nauplii bioassay and GC-MS headspace analysis was used to identify phytochemical components. Results: K. senegalensis bark extracts displayed strong inhibitory activity against bacterial triggers of several autoimmune inflammatory diseases. The growth inhibitory activity of the methanolic and subcritical extracts was particularly noteworthy against P. mirabilis (MIC values of 185 and 211μg/mL, respectively against the reference strains). These extracts were similarly potent growth inhibitors of K. pneumoniae and A. baylyi and were moderate inhibitors (MIC >1000μg/mL) of P. aeruginosa and S. pyogenes growth. The methanolic and subcritical K. senegalensis extracts were also potent inhibitors of G. duodenalis (187 and 328μg/mL, respectively), as well as Caco-2 (268 and 470μg/mL, respectively) and HeLa carcinomas (155 and 174μg/mL, respectively). GC-MS analysis of the SFE extract revealed relative abundances of a variety of mono- and sesquiterpenoids. Furthermore, all K. senegalensis bark extracts were non-toxic in the Artemia franciscana toxicity assay, indicating their safety for therapeutic use. Conclusion: These studies validate traditional African therapeutic usage of K. senegalensis in the treatment of microbial infections, autoimmune inflammatory diseases and some cancers.
Keywords: African mahogany; Anti bacterial activity; Anti-cancer activity; Anti-proliferative activity; Giardia duodenalis; Meliaceae; Sub-critical fluid extraction; Terpenoid.

Exploring a novel edible mushroom Ramaria subalpina: Chemical characterization and Antioxidant activity - Krishnendu Acharya; Kanad Das; Soumitra Paloi; Arun Kumar Dutta; Manoj Emanuel Hembrom; Somanjana Khatua; Arvind Parihar (Pharmacognosy Journal, 2017)
Background: During macrofungal inventorisation from an unexplored subalpine forest of Sikkim Himalayas, a new edible mushroom, Ramaria subalpina was found and documented in consultation with the forest dwellers. Objective: The aim of the present study was to understand the antioxidative potentiality and bioactive constituents of a novel taxon, Ramaria subalpina, that is highly prized by the ethnic people of subalpine Sikkim Himalayas, India, for its flavor, texture and gastronomic delicacy since time immemorial. Methods: Chemical composition and antioxidant properties of methanolic extract of dried basidiocarps were assessed using HPLC and several in vitro assay systems. Results: Methanolic extract had phenolics in highest amount, among which pyrrogallol was identified. It also showed potent antioxidant activity. Conclusion: The present study suggests that Ramaria subalpina has strong medicinal prospects. This novel mushroom can safely be added to the world’s edible mushrooms list.
Keywords: antioxidant activity; DPPH; Ferrous ion chelating; HPLC; India.

Extracellular L-Asparaginase from Streptomyces labedae VSM-6: Isolation, Production and Optimization of Culture Conditions Using RSM - Ushakiranamayi Mangamuri; Muvva Vijayalakshmi; Venkat Siva Rama Krishna Ganduri; Satish Babu Rajulapati; Sudhakar Poda (Pharmacognosy Journal, 2017)
Objective: The present study was intended to isolate actinomycetes VSM-6 from deep sea sediment samples of Bay of Bengal that is potent to produce L - asparaginase. Materials and Methods: The identification of the isolate was executed by polyphasic taxonomy. Optimization was carried out one factor at a time (O-F-A-T) for the production of the L - asparaginase. RSM was pledged to optimize the L - asparaginase production by S.labedae VSM-6. Central composite design was applied to study the influence of the variables and their interactive effects on the production of L - asparaginase. Unstructured Kinetic modelling for L - asparaginase production was adopted using Leudeking-Piret (LILP) and Logistic Incorporated Modified Leudeking-Piret (LIMLP) models. Results: Optimization using One-Factor-At-A-time registered a turnout of 8.92 IU/ml of L - asparaginase production. But results obtained from the statistical design are in agreement with the experimental results. The model followed the second order polynomial equation and the model adequacy was determined by the P value (<0.0001), Coefficient determination (R2) with a value of 0.9942 and the adjusted R2 = 0.9087 which determines that the model was significant. The experimental values are in compliance with the model anticipated values and catalogued an escalation in yield of L - asparaginase (10.17 IU/ml) by RSM. Unstructured Kinetic modelling for L - asparaginase production adopting Leudeking-Piret (LILP) and Logistic Incorporated Modified Leudeking-Piret (LIMLP) models showed L - asparaginase production of (10.17 IU/ml), closer to model anticipated value (10.23 IU/ml) so unstructured models provided a better approximation for L - asparaginase production by S.labedae VSM-6. Conclusion: From our study we have reported for the first time the production of L - asparaginase from S.labedae VSM-6 using central composite design and kinetic modelling.
Keywords: Central Composite Design; Kinetic Modelling; L - asparaginase; Optimization; Response Surface Methodology; Statistical Analysis.; Streptomyces labedae

Extracellular-Signal Regulated Kinase Signalling Pathway Mediates the Increased Proliferation of EPCs Treated with Garlic (Allium sativum) Extract, Purple Sweet Potato (Ipomoea batatas) Extract and Vitamin C - Yudi Her Oktaviono; Alisia Yuana Putri; Makhyan Jibril Al-Farabi; Yesita Rizky Firmansyah; Ferry Sandra (Pharmacognosy Journal, 2017)
The endothelial progenitor cell (EPCs) proliferation capability is reduced in the patient with stable coronary artery disease (SCAD). Garlic (Allium sativum), purple sweet potato (Ipomoea batatas), and vitamin C are proven antioxidant which potentially improve EPCs proliferation ability. Objective: To investigate the effect of garlic (Allium sativum), purple sweet potato (Ipomoea batatas), and vitamin C in EPCs proliferation from CAD patients and identify the involvement of Extracellular-Signal Regulated Kinase (ERK) Signalling Pathway. Material and Method: Mononuclear cells were isolated from SCAD patients and cultivated with colony-forming unit (CFU)-Hill medium and divided into untreated (control), garlic extract (10 mcg/ml and 100 mcg/ml), purple sweet potato extract (1 mcg/ml and 25 μg/ml), and vitamin C (10 μg/ml and 250 μg/ml). EPCs proliferation was measured using the MTT Assay. Results: This research shows that EPCs proliferation was increased in the treatment with garlic extract at 10 mcg/ml and 100 mcg/ml dose (0.267 ± 0,003 and 0.391 ± 0.008 ; p < 0.05), purple sweet potato extract at 1 mcg/ml and 25 μg/ml dose (0.250 ± 0.005 and 0.3562 ± 0.023 ; p < 0.001), and vitamin C at 10 μg/ml and 250 μg/ml dose (0.259 ± 0.016 and 0.306 ± 0.022 ; p < 0.001). Increased ERK expression was found in the treatment with garlic extract, purple sweet potato extract and vitamin C. Conclusion: Garlic extract, purple sweet potato extract, and vitamin C can increase EPC proliferation through the ERK signaling pathway.
Keywords: Antioxidant; Endothelial Progenitor; ERK; Proliferation

Fasting Blood Glucose Levels and Hematological Values in Normal and Streptozotocin-Induced Diabetic Rats of Mimosa pudica L. Extracts - Ampa Konsue; Chayan Picheansoonthon; Chusri Talubmook (Pharmacognosy Journal, 2017)
Context: M. pudica is a common plant found in moist waste ground, lawns, open plantations and weedy thickets. Aims: The fasting blood glucose levels (FBG) and hematological values of M. pudica aqueous(MPA) and hydro-ethanolic (MPHE) extract were evaluated in normal and streptozotocin (STZ)-induced diabetic rats. Materials and Methods: MPA and MPHE 125, 250 and 500 mg/kg body weight (b.w.) were administered orally and daily to the rats for 8 weeks. The FBG were determined weekly. Red blood cells (RBC), hemoglobin (HM. pudicab), hematocrit (Hct), platelet, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), white blood cells (WBC), lymphocytes, monocytes, neutrophils and eosinophil were evaluated. Results: MPA and MPHE had no effect on blood glucose levels in normal rats. All doses of all extracts showed significantly (p<0.05) decreasing FBG in diabetic rats. Especially MPA at the dose of 250 mg/kg b.w. showed more potent significantly (p<0.05) decreasing blood glucose levels than anti-diabetic drug glibenclamide at the end of experiment. All extracts had no effect on RBC, Hb, Hct, platelet, MCH, MCHC, lymphocytes, monocytes neutrophils and eosinophils. Surprisingly, the extracts were decreased WBC and MCV in diabetic rats. In addition, all of the extracts did not produce the alteration of blood cells structure in all rats. Conclusion: This study indicated that the extracts were hypoglycemic effect and improve hematological values in diabetes which confirms the traditional use of the plant.
Keywords: Blood glucose level; Hematological values; Mimosa pudica; Red blood cell; White blood cell

Formulation Development and Evaluation of Anti-inflammatory Potential of Cordia obliqua Topical Gel on Animal Model - Richa Gupta; Ghanshyam Das Gupta (Pharmacognosy Journal, 2017)
Background: The plants of genus Cordia has been used in traditional medicine for many diseases from history. Cordia obliqua Willd. is also a medicinally important plant and it has been proved by modern scientific research. Objective: This study is aimed to formulate and characterize a topical gel from Cordia obliqua leaf methanol extract and evaluate its effect on carrageenan induced rat paw edema. Materials and Methods: The methanol extract was prepared by successive solvent extraction using soxhlet apparatus. Topical gel was designed to prepare by Dispersion method using Carbopol 940 as polymer. The various gel characteristics was studied by standard procedures like Homogeneity, grittiness, extrudability, drug content, spread ability and in-vitro diffusion study. The anti-inflammatory potential of gel was evaluated by Carrageenan induced rat paw edema method in comparison with standard Diclofenac Sodium gel 1% on Albino rats. Results: The herbal gel was found homogeneous with good extrudability, no grittiness, pH 6.79 and drug content 93.167%. The anti-inflammatory activity of herbal gel was found comparable with standard Diclofenac Sodium gel and has shown 82.71% edema inhibition after 4 h of treatment. Conclusion: Cordia obliqua gel was found suitable as a standard topical gel formulation and it can be used safely for treatment of edema.
Keywords: Carbopol 940; Carrageenan induced edema; Cordia; in-vitro diffusion; Topical gel

Fractionation and α-glucosidase Inhibitory Activity of Fractions from Garcinia hombroniana Pierre Leaves Extracts - Nita Triadisti; Rani Sauriasari; Berna Elya (Pharmacognosy Journal, 2017)
Background: Diabetes mellitus become one of the biggest global health problems of the 21st century. Type 2 diabetes play role for the majority of cases of diabetes worldwide which is characterized by the increase of postprandial blood glucose level. Maintaining postprandial glucose level through inhibition of α-glucosidase is one of the essential strategies in the treatment of diabetes. Inhibitory effect of α-glucosidase was commonly used to identify active compounds potentially to treat diabetes. Natural resources have potency as antidiabetic that can be used in diabetes treatment. Objective: The objective of the study is to separate active fraction in the crude extract of Garcinia hombroniana leaves to facilitate obtaining a pure biologically active compound as the α-glucosidase inhibitor. Methods: Fractionation to separate active fraction was performed using column and thin layer chromatography methods while α-glucosidase inhibitory activity assay was performed in vitro using spectrophotometric methods at λ 400 nm. Results: Ethyl acetate and methanol extract of G. hombroniana yielded 14 and 12 fractions, respectively. Two fractions with the higher percent inhibition compared to other factions are fraction 8 from ethyl acetate extract (FEA8) and fraction 3 from methanol extract (FM3). The IC50 values of FEA8, FM3 and acarbose are 16.370 μg/mL, 59.042 μg/mL, and 39.534 μg/mL respectively. Conclusion: Fraction 8 from ethyl acetate extract of G. hombroniana leaves (FEA8) was separated and known in this study as the most bioactive α-glucosidase inhibitor agent compared with another extract, fractions, and acarbose.
Keywords: Column chromatography; Diabetes mellitus; Fractionation; Thin layer Chromatography; α-glucosidase

GC-MS Analysis and Antioxidant Activity of Bauhinia nakhonphanomensis Leaf Ethanolic Extract - Wilawan Promprom; Wannachai Chatan (Pharmacognosy Journal, 2017)
Context: Bauhinia nakhonphanomensis Chatan. A new species that is endemic to Thailand. Aims: Leaves of B. nakhonphanomensis were extracted and the extract was used in gas chromatography-mass spectrometry (GC-MS) analysis to evaluate the total phenols, total flavonoids and antioxidant activity. Methods: The extract of B. nakhonphanomensis was analyzed by GC-MS. Quantitative analysis for total phenols was done by the Folin-Ciocatteu method and for total flavonoids by the aluminium chloride method. The antioxidant activity of the ethanolic extract was evaluated by the DPPH method. Results: GC-MS analysis revealed the presence of 19 phytochemical constituents. These compounds were identified by comparing their retention times and peak areas with those from the literature and by interpretation of the mass spectra. The major chemical constituents were inositol (48.55 %), alpha-tocopherol (12.21 %) and phenol (6.61 %). Total phenolic content was 48.69±0.56 mg/100 of Gallic acid equivalent (GE). The total flavonoid contentwas 10539± 6.14 mg/100 of quercetin equivalent (QE). Antioxidant activity was 17.07±0.24 μg/100 of ascorbic acid equivalent antioxidant capacity (AEAC).Conclusion: These findings are the first report and suggest that the rich phytochemical content of B. nakhonphanomensis has good antioxidant activity.
Keywords: antioxidant activity; Bauhinia Nakhonphanomensis; GC-MS; total flavonoid content; total phenolic content

GC-MS Analysis of Ethyl Acetate Extract of Whole Plant of Rostellularia diffusa - Mohamed Saleem Thattakudian Sheik Uduman; Prema Rathinam; Yogendrachari Karuru; Gangadhar Obili; Gopinath Chakka; Ashok Kumar Janakiraman (Pharmacognosy Journal, 2017)
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

GC-MS Analysis of Indrakeeladri Native Medicine used in the Treatment of Stroke - Sundarachary Nagarjunakonda; Sridhar Amalakanti; Sristi Ram Dhishana; Maddi Ramaiah; Lalitha Rajanala (Pharmacognosy Journal, 2017)
Context: A stroke or cerebrovascular disease is an abrupt onset of neurological deficit that is attributable to a focal vascular cause. Antiplatelet drugs, anticoagulants and thrombolytics are used in ischemic stroke. Indrakeeladri, is a village in Andhra Pradesh in India where traditional local practitioners prescription has long been practiced for treatment of stroke by using unknown and undisclosed formulation (gulikalu) without any name and labeling. Patients who have taken treatment at Indrakeeladri have noticed improvement in their symptoms particularly in speech. Aims: We endeavoured to analyze the formulation to know its composition as this analysis might help us in preparation of newer drugs for stroke. Settings and Design: GC MS analysis. Methods and Material: The sample was powdered and tested for its solubility in different solvents of increased polarity strength and then subjected to Gas Chromatography Mass Spectrometry (GCMS) analysis in order to know its chemical components. Results: The sample was soluble only in water. The GC-MS analysis of the test sample revealed the presence of methyl tetradecanoate, dodecanoic acid methyl ester and methyl 10-methyl undecanoate as the major constituents. These substances are known to have inhibitory effect on blood coagulation. Conclusions: Further studies need to be carried out to find out whether these components of native medicine have a role in the treatment of stroke or not.
Keywords: Dodecanoic acid methyl ester; Methyl 10-methyl undecanoate; Methyl tetradecanoate; Native medicine; Stroke

GC-MS analysis of n-Hexane Extract of Fruits of Trichopus zeylanicus ssp. travancoricus Burkill ex K. Narayanan - Sasi Kala Nambi; Ramasubbu Raju (Pharmacognosy Journal, 2017)
Aim: The present study focused to analyse the bioactive compounds present in the fruits of Trichopus zeylanicus ssp. travancoricus Burkill ex K. Narayanan by using GC-MS. Methods: The dried and pulverized fruit materials were extracted with n-hexane for 6-8 h. The phytochemical constituents were analysed by GC-MS. Results: Totally 23 bioactive compounds were identified with RI and SI factors. Of the twenty-three compounds detected from n-hexane extract, Tetradecane (27.87%), Hexadecane (27.26%), Nonadecane (22.25%) and Pentacosane (8.13%) were detected as major compounds. Conclusion: The obtained bioactive compounds were reported as potentially active in various medicinal treatments and can be used for the treatment of various diseases.
Keywords: Agasthyamalai; Hexadecane; Kani tribe; Nonadecane; Tetradecane

GC-MS analysis of Tasmannia lanceolata Extracts which Inhibit the Growth of the Pathogenic Bacterium Clostridium perfringens - Mitchell Henry Wright; Cameron Jay Lee; Megan Sarah Jean Arnold; Joseph Shalom; Alan White; Anthony Carlson Greene; Ian Edwin Cock (Pharmacognosy Journal, 2017)
Introduction: Clostridium perfringens is the etiological agent of clostridial myonecrosis and enteritis necroticans. Infections result in exotoxin production, tissue necrosis and unless promptly treated, often result in death. Methods: Tasmannia lanceolata extracts were investigated for C. perfringens growth inhibitory activity by disc diffusion analysis and MIC determination. Toxicity was evaluated by Artemia nauplii bioassay and the most potent extracts were phytochemically evaluated by GC-MS headspace analysis. Results: All T. lanceolata berry and leaf extracts displayed potent C. perfringens growth inhibition. The berry extracts were more potent growth inhibitors than the corresponding leaf extracts, although the leaf extracts were also potent growth inhibitors. The berry aqueous, methanolic and ethyl acetate extracts were particularly potent growth inhibitors, with MIC values of 654, 65 and 329 μg/mL respectively. T. lanceolata leaf also displayed good efficacy, with an MIC of 839, 1255 and 625 μg/mL for the aqueous, methanolic and ethyl acetate extracts respectively. All extracts were nontoxic in the Artemia franciscana bioassay, with LC50 values substantially > 1000 μg/mL. Non-biased GC-MS analysis of the aqueous, methanolic and ethyl acetate berry extracts revealed the presence of high relative levels of a diversity of terpenoids. Conclusions: The lack of toxicity of the T. lanceolata extracts and their potent growth inhibitory bioactivity against C. perfringens indicates their potential as medicinal agents in the treatment and prevention of clostridial myonecrosis and enteritis necroticans. GC-MS metabolomic profiling studies indicate that these extracts contained a diversity of terpenoids, with monoterpenoids being particularly abundant.
Keywords: Enteritis necroticans; Gas gangrene; Myonecrosis; Tasmannia Lanceolata; Winteraceae

GC-MS headspace analysis of Terminalia ferdinandiana fruit and leaf extracts which inhibit Bacillus anthracis growth - Mitchell Henry Wright; Joseph Sirdaarta; Alan White; Anthony Carlson Greene; Ian Edwin Cock (Pharmacognosy Journal, 2017)
Background: Terminalia ferdinandiana (Kakadu plum) is an endemic Australian plant with an extremely high antioxidant capacity. The fruit has long been used by the first Australians as a nutritional food and as a medicine and recent studies have reported its potent growth inhibitory activity against a broad panel of bacteria. Despite this, T. ferdinandiana extracts are yet to be tested for the ability to inhibit the growth of Bacillus anthracis. Materials and Methods: Solvent extracts were prepared using both the fruit and leaf of Kakadu plum. The ability to inhibit the growth of B. anthracis was investigated using a disc diffusion assay. Their MIC values were determined to quantify and compare their efficacies. Toxicity was determined using the Artemia franciscana nauplii bioassay. The most potent extracts were investigated using non-targeted GC-MS head space analysis (with screening against a compound database) for the identification and characterisation of individual components in the crude plant extracts. Results: Solvent extractions of T. ferdinandiana fruit and leaf displayed good growth inhibitory activity in the disc diffusion assay against B. anthracis. Fruit ethyl acetate and methanolic leaf extracts were particularly potent growth inhibitors, with MIC values of 451 and 377μg/mL respectively. The fruit methanolic and chloroform extracts, as well as the aqueous leaf extracts also were good inhibitors of B. anthracis growth, albeit with lower efficacy (MIC values of 1800 and 1414 μg/mL respectively).The aqueous fruit extract and leaf chloroform extracts had only low inhibitory activity. All other extracts were completely devoid of growth inhibitory activity. Furthermore, all of the extracts with growth inhibitory activity were nontoxic in the Artemia fransiscana bioassay, with LC50 values >1000 μg/mL. Non-biased GC-MS phytochemical analysis of the most active extracts (fruit ethyl acetate and methanolic leaf) putatively identified and highlighted several compounds that may contribute to the ability of these extracts to inhibit the growth of B. anthracis. Conclusions: The low toxicity of the T. ferdinandiana fruit ethyl acetate and methanolic leaf extracts, as well as their potent growth inhibitory bioactivity against B. anthracis, indicates their potential as medicinal agents in the treatment and prevention of anthrax.
Keywords: Anthrax; Bacillus anthracis; Combretastatin; Kakadu plum; Metabolomics.; stilbene; Tannin; Zoonotic

Genetic variability and relationship studies of Ber Ziziphus nummularia (Burm. F.) using morphological and molecular markers - Yashmin Akhtar; Ravish Choudhary; Kailash Chandra Sharma; Manju Sharma (Pharmacognosy Journal, 2017)
Introduction: Ber (Ziziphus nummularia (Burm. F.) is the most commonly occurring branched thorny shrub species in the Indian desert. A total of 10 Zadber accessions collected from different agroclimatic regions of India, were evaluated for phenotypic and genotypic variations using morphological and inter-simple sequence repeats (ISSR) markers. Materials And Methods: Morphological characterization was done using descriptors and Molecular characterization studies was done with fifty primers of University of British Columbia (UBC) procured from Geno Biosciences Pvt. Ltd., were used for ISSR-PCR optimisation trials. Eleven primers, which gave the best amplification results with the sample DNA, were selected for final ISSR-PCR analysis. Results: Significant variability was observed in the selected Zadber accessions by the analysis of five quantitative and 25 qualitative morphological characters of leaves, fruits and seeds. ISSR markers also showed polymorphism (86.58%). Jaccard’s genetic similarity value of ISSR was found in the range of 0.45-0.77 (average 0.61) suggesting moderate level of genetic diversity within the Zadber group. Two of the eleven ISSR primers were also able to generate cultivar specific amplicons, which may be used for identification of accessions Zadber-5 and Zadber-8. Conclusion: The present study revealed that morphological and molecular markers can be successfully utilized for determining genetic diversity and genetic relationship of Zadber cultivars and used in breeding programmes.
Keywords: Genetic variability; ISSR; Morphology; UPGMA; Zadber

Hepatoprotective Effect of Curcumin and Capsaicin against Lipopolysaccharide Induced Liver Damage in Mice - Thriveni Vasanthkumar; Manjunatha Hanumanthappa; Prabhakar BT; Santhosh Kondajji Hanumanthappa (Pharmacognosy Journal, 2017)
Objective: The present study was undertaken to evaluate the possible ameliorative role of curcumin, capsaicin and their combination against lipopolysaccharide (LPS) induced hepatic toxicity in mice. Methods: Animals were distributed into five experimental groups: Normal control, vehicle control, curcumin, capsaicin and combined curcumin and capsaicin treatment groups respectively, for 7 days prior to LPS induced liver toxicity (3 mg/kg b.w. in saline). Hepatoprotective effect of individual and combined spice principles were evidenced by the measurement of serum marker enzyme activities such as, SGPT, ALP and TB and it was further confirmed by histopathological observation of liver tissue section. Results: The administration of LPS increased serum nonspecific enzymes (SGOT; 174.2±3.79 IU/L, SGPT; 124.0±3.14 IU/L, ALP; 320.15±3.88 IU/L and total bilirubin level; 2.32±1.23 mg/dL), however dietary curcumin and capsaicin decreased the activities of these non–specific serum enzymes including total bilirubin indicating amelioration of the severe LPS induced hepatotoxicity, while the combined spice principles were more significant as shown by the levels of enzymes activities SGOT; 89.9±1.39 IU/L, SGPT; 85.9±1.83 IU/L, ALP; 138.4±2.05 IU/L including total bilirubin level; 0.86±0.03 mg/dL. Conclusion: Dietary curcumin and capsaicin individually are protective to LPS induced hepatotoxicity, the beneficial effect was found to be more when the two compounds were fed in combination.
Keywords: ALP.; Capsaicin; Curcumin; Hepatoprotective activity; Lipopolysaccharide; SGOT; SGPT

Hindering Effect of Resveratrol on Oxidative Changes and Na+K+-ATPase activity in Rat Hepatocytes Exposed to Prenatal stress - Gayathri Megashyam Rao; Sudhanshu Sekhar Sahu; Beena Vichithra Shetty (Pharmacognosy Journal, 2017)
Introduction: The fetal programming hypothesis states that conditions during pregnancy, including stress, will have long-term effects on adult health, probably via epigenetic mechanisms. Methodology: Pregnant rats were subjected to restrain stress either during early or late pregnancy with and without resveratrol. Blood and liver tissues were collected from 40 days old offsprings of the above rats to study the prenatal effect on corticosterone, and stress development. Results: It was found that levels of corticosterone advanced protein and lipid oxidation products, GSHRx, increase significantly in offsprings of stressed rats and decreased on intervention with resveratrol, whereas total antioxidants, vitamin C, GSH, SOD and Na+K+- ATPase decreased with stress and increase on resveratrol intervention as compared to controls. Conclusion: The alterations may be due to the effect of stress on HPA axis. Results also support the prevention/protective effect of resveratrol on oxidative stress and may be used as a measure to prevent the metabolic changes in adult life due to prenatal stress.
Keywords: Cortisol; Na+K+-ATPa; Oxidative Changes; Prenatal Stress; Resveratrol

Histo-Chromatographic Finger Printing Profiles of the Root of Plumbago zeylanica Linn and Quantification of Marker Compound, Plumbagin - Madathilparambil Vasu Sudhakaran (Pharmacognosy Journal, 2017)
Background: Plumbagin, a plant-derived naphthoquinone is known to be biosynthesized by polyacetate-malonate pathway. The ayurvedic drug Chitraka is obtained from the medicinal plant Plumbago zeylanica Linn, which belongs to the family Plumbaginaceae. The Chitraka is found used in the traditional forms of medicine for the treatment of various illnesses, since ancient times. Aim: The present study concerns the microscopic, powder and quantitative microscopic characteristics of the root of Plumbago zeylanica Linn. Materials and Methods: Delimiting the morpho-histological profile of the root using digital, stereo and polarized microscopic techniques and to develop the chromatogram of the extract of the root of Plumbago zeylanica Linn using High performance thin-layer chromatographic (HPTLC) method. Results: The presence of cortical deposition of plumbagin pigment as yellowish tints in the surface view of the sections of root, arrangement of starch grains as bunches of grapes in cortical tissues and ray parenchyma, crystal idioblasts containing calcium oxalate embedded in the intervening walls of the cortical cells, distinct band or patch of sclreids at the pericyclic region of the phloem, wood with non-storied cambium, distinct growth ring boundaries, paratracheal axial parenchyma, chains of vessels in radial multiplies of three to four, uniseriate to biseriate medullary rays with homogeneous cells, crowding of vessels at the central portion of secondary xylem, wood plugged with tylosis and low mesomorphy ratio for wood were the anatomical features characteristics of the taxon. The HPTLC profile of the methanol extract of root developed using the mobile phase, n-hexane:ethyl acetate (8:2 v/v) had revealed four phytoconstituents. The Rf value for plumbagin (C11H8O3) was found to be 0.86. Densitometric scanning had shown λmax of plumbagin at 270 nm. Spectral matching by overlaying the spectra of both standards and extract of root sample were confirmed the specificity of λmax at 270 nm for the marker compound. The calibration curve was found to be linear in the concentration range of 2.00 to 10.00 μg/ band with the polynomial calibration equation Y=178.8+91.61*X+-4.825*X2 and estimated that 5 μL of methanol extract of roots contained 1.326 μg of plumbagin. Thus the content of marker constituent (plumbagin) present in shade-dried roots of Plumbago zeylanica Linn (a Kerala habitant) was estimated as 0.179%. Conclusion: The present study suggests that the delineated characteristics of the roots of Plumbago zeylanica Linn could tag as the identifying parameters to substantiate and authenticate the raw drugs from the spurious/adulterants materials and developed HPTLC method could be effectively used for the regulatory perspectives and quality assessment of plumbagin in the polyherbal formulation/finished products of traditional medicine.
Keywords: Axial Parenchyma; Calibration Curve; Mesomorphy Ratio; Plumbagin; Tylosis

HPLC Determination of Quercetin in Three Plant Drugs from Genus Sedum and Conjecture of the Best Harvest Time - Ma Yue-ling; Chen Yu-jie; Wan Ding-rong; Chen ping; Xu Ran (Pharmacognosy Journal, 2017)
To establish a method for quercetin content determination of the three plant drugs from genus Sedum and to decide their best harvesting time. Dried herbs of Sedum sarmentosum Bunge., S. lineare Thunb. and S. erythrostictum Migo. are all traditional medicines from Genus Sedum. They all have long been used to cure hepatitis, dysentery, swelling poison and so on. It has been reported that flavonoids contained in S. sarmentosum Bunge. were one type of the active components to protect liver and reduce serum alanine aminotransferase level. Through the qualitative analysis and TLC assay, we have verified that both S. lineare Thunb. and S. sarmentosum Bunge. contain flavonoid glycosides whose aglycones include quercetin. In this study, a HPLC methodology was established to determine quercetin which was a common hydrolyzate of the flalvonoid glycosides in the three plant medicines. The determination method developed showed good linearity in the range of 41.2-412.0 μg/mL, and had a nice accuracy and repeatability. It indicated that the content of quercetine in Sedum sarmentosum, Sedum lineare and Sedum emarginatum can achieve the quality standard required by Chinese Pharmacopoeia.( No less than 0.01%), The results also revealed preliminarily a relation between collected season and medicine quality. Thus it could be used to control some flavonoids content in the three plant drugs indirectly. By determining the samples of the 3 drugs collected in different seasons, the optimal harvest periods could be preliminarily ascertained.
Keywords: best harvest time.; Genus Sedum; HPLC determination; Plant medicines; Quercetin

HPLC Fingerprint Analysis and Content Determination of Extract with Anticancer Activities of Sedi Linearis Herba - Diangang Liu; Qing Mei; Weifang Long; Xiangluan Wan; Dingrong Wan; Luyao Wang (Pharmacognosy Journal, 2017)
Aims: The purpose of this paper was to develop a HPLC fingerprint analysis method, compare the chromatographic fingerprints characteristics of the ethyl acetate extract with anticancer activity from Sedi Linearis Herba (Sedum lineare Thumb.) collected in different seasons and environments, determine the contents of active ingredients hyperoside, isoquercetin and astragalin of each sample by HPLC, provide believable scientific foundations for quality control and evaluation of Sedi Linearis Herba. Methods: The analyte was analyzed using BDS Hypersil C18 as chromatographic column, acetonitrile -0.1% acetic acid solution as the mobile phase (gradient elution). Results: The results showed that the major active ingredient contents of the samples collected in different seasons but at the same environment all had obvious differences. These ingredient contents of the samples collected in the end of April were much more than those in mid-August in general. Moreover, the major active ingredient contents of the samples picked in the same season but different environments were different too. For instance, the major ingredient contents of the sample in damp environment in August were more than those in sunny environment. Conclusion: All of these indicated that the HPLC fingerprint analysis and contents determination method established were very useful for quality analysis and control of Sedi Linearis Herba.
Keywords: Anticancer Activity Ingredients; Content Determination; HPLC Fingerprint; Sedum lineare Thunb.

HPTLC Analysis and Antiproliferative Effect of Various Extracts of Swertia alata on Growth of Leishmania donovani Promastigotes in vitro - Sakshi Bajaj; Sharad Wakode; Washim Khan (Pharmacognosy Journal, 2017)
The present study was carried out to evaluate the quality control analysis and antiproliferative effects of petroleum ether, chloroform, ethanol and aqueous extracts of Swertia alata (family Gentianaceae) on Leishmania donovani. A basic, exact, quick and reproducible high performance thin layer chromatography (HPTLC) has been created for synchronous analysis of Oleanolic acid and Swertiamarin from S. alata. Read more...
Keywords: Antiproliferative; HPTLC; Oleanolic acid; Quality control; Swertiamarin

Hypoglycemic Activity of Leaf Extracts from Tiliacora triandra in Normal and Streptozotocin-Induced Diabetic Rats - Teeraporn Katisart; Surapong Rattana (Pharmacognosy Journal, 2017)
Background: Tiliacora triandra is a common plant found in southeast Asian countries. It is traditionally used as anti-pyrogenic agent. Objective: The present study was aimed to investigate the hypoglycemic activities leaf extracts from Tiliacora triandra (TTE) in normal and streptozotocin- induced diabetic rats. Methods: TTE was prepared and daily and orally administered at dose of 300 mg/kg b.w. to the rats for 8 weeks. The body weight and blood glucose level were measured weekly. At the end of the experiments, blood samples were collected from cardiac puncture and analyzed for serum insulin levels. The pancreatic tissues were stained by hematoxylin-eosin for histo-pathological investigations. Results: Normal and diabetic rats treated with TTE and glibenclamide tended to have an increased body weight. TTE significantly decreased the blood glucose level by 25.01 ± 19.77% in week 3 in diabetic rats and similar to that of glibenclamide group (27.01 ± 11.89%). However, the extracts slightly decreased the blood glucose level in normal rats by 9.48 ± 2.14% in week 2. TTE significantly increased serum insulin level by 21.63 ± 1.39 IU/mL in diabetic rats compared to the controls (10.63 ± 0.37 IU/mL) but not in normal rats. In additions, TTE activated the regeneration of pancreatic Islets of Langerhans in diabetic rats which in turn stimulated insulin secretion. Conclusion: TTE exhibits the hypoglycemic potential by stimulating insulin secretion from the pancreas.
Keywords: Hypoglycemic Effect; Streptozotocin-Induced Diabetic Rats.; Tiliacora triandra

Hypoglycemic and Hypolipidemic Activities of Ethanolic Extract from Mimosa pudica L. in Normal and Streptozotocin-Induced Diabetic Rats - Piyapong Yupparach; Ampa Konsue (Pharmacognosy Journal, 2017)
Context: Mimosa pudica L. its unique property to collapse when touched and opens up. Aims: To evaluate hypoglycemic and hypolipidemic activities of 80% ethanolic extract from whole plant of Mimosa pudica L. (MPE) by measuring fasting blood glucose in normal and streptozotocin (STZ)-induced diabetic rats treated with MPE. Materials and Methods: An eight-week study using MPE was performed in normal and streptozotocin (STZ)-induced diabetic rats. Hypoglycemic activities in normal and STZ-induced diabetic rats and oral glucose tolerance test (OGTT) and biochemical data include total cholesterol (TC), triglycerides (TG), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) of MPE were compared with glibenclamide, a standard anti-diabetic drug. Results: OGTT showed that MPE did not decrease blood glucose both in normal and STZ-induced diabetic rats comparable to controls and glibenclamide treated rats. Moreover, MPE did not affect FBG in the normal rats. However, it significantly (p<0.05) decreased FBG in the diabetic rats while MPE increased HDL and decreased TC, TG and LDL in the diabetic rats. Conclusions: The results from this study confirmed the traditional use of Mimosa pudica L. for the treatment of diabetes mellitus.
Keywords: Hypoglycemic; Hypolipidemic; Mimosa pudica; Oral glucose tolerance test.

Cuminum cyminum – A Popular Spice: An Updated Review - Rudra Pratap Singh; Gangadharappa H.V.; Mruthunjaya K (Pharmacognosy Journal, 2017)
Spices are bio-nutrient supplements that enhance the taste, flavor and aroma of food and also treat several diseases. Cumin (Cuminum cyminum) is one such most popular spice that is used as a culinary spice for their special aromatic effect. Cumin is a traditional and much used spice from Middle Ages because it was an icon of love and fidelity. Cumin is available in different appearances such as anise, fennel and black cumin and the difference between them is their characteristics. The proximate analysis of the cumin seeds reveals that they contain fixed oil, volatile oils, acids, essential oils, protein and other elements. In cumin, contains an important component such as pinene, cymene, terpinene, cuminaldehyde, oleoresin, thymol and others that have shown their uses according to the disease. Cumin has proved several benefits with the help of availability of nutrients. It is an important element of iron for energy, immunity systems, lactation and skin diseases. Cumin also shown various pharmacological effects but has some side effects. So, volatile plants generally come out as a complex mixture of less molecular weight lipophilic compounds that derived from different biosynthetic pathways and also contribute to a variety of physiological functions.
Keywords: Cumin; Cuminaldehyde; Cymene; Spice; Thymol

Identification and Characterization of Berberine in Tinospora cordifolia by Liquid Chromatography Quadrupole Time of Flight Mass Spectrometry (LC MS/MS Q-tof) and Evaluation of its anti Inflammatory Potential - Mohind C. Mohan; Anu P. Abhimannue; Prakash Kumar B (Pharmacognosy Journal, 2017)
Introduction: Tinospora cordifolia (Willd.) Miers ex Hook F and Thomas commonly called as gudduchi or amrita is a widely used plant in traditional medicinal system of Ayurveda. A UPLC MS/MS Q-tof method for the identification and characterization of berberine in Tinospora cordifolia (Willd.) Miers. ex HooK.F. and Thomas. and to evaluate the anti inflammatory potential of bioactive fraction. Materials and Methods: The presence of berberine in Tinospora cordifolia was determined by HPLC and was subsequently isolated by HPTLC. The anti inflammatory property of the fraction containing berberine was demonstrated to have an inhibitory activity on 5 lipoxygenase, an enzyme involved in inflammatory pathway and its IC50 value was obtained. The binding interactions between berberine and 5-LOX were demonstrated by docking studies. Result: The presence of berberine in Tinospora cordifolia methanolic extract was identified by HPLC and HPTLC analysis and confirmed by UPLC MS/ MS Q-tof. The fraction containing berberine inhibited 5-LOX with an IC50 of 0.041± 0.0003μg/mL as compared to that of NDGA (positive control) which showed an IC50 of 2.75 ± 0.05 μg/mL. Molecular docking of berberine with 5-LOX showed a binding energy of -8.942 ± 0.039665 kcal/mol and Ki of 273.16 ± 3.026 nM as compared to the NDGA which has a binding energy of -7.186 ± 0.170503 kcal/mol and Ki 5.604± 1.618 μM. Conclusion: Tinospora cordifolia can be used as a source of berberine and possible anti inflammatory activity of Tinospora cordifolia may be attributed to the presence of berberine.
Keywords: 5 Lipoxygenase; Berberine; Mass spectrometry; Molecular Docking.; Tinospora cordifolia

Immunomodulatory Activity of Bioactive Fraction (PBC) from Phyllostachys bambusoides - Sunil Kumar; Gaurav Sharma; Amit Kumar (Pharmacognosy Journal, 2017)
Background: The lack of vaccines and limitations of currently available strategies demand a need to develop safe and efficacious immunomodulators. Phyllostachys bambusoides is traditionally used for various autoimmune and infectious disorders, a property possibly attributable to presence of flavonoids like orientin and iso-orientin. Objective: the objective of this study was, to search a potent immunomodulator which elicit both Th1 and Th2 immune response. Methods: The animals were (Balb/c) treated with the bioactive fraction (PBC) from P. bambusoides (100 and 200 mg/kg body weight) for 14 days with SRBC (Sheep Red Blood Cells) as an antigen. Haemagglutination antibody (HA) titre, delayed type hypersensitivity (DTH) reaction, phagocytic index, NO production, analysis of cytokines in serum and CD80/ CD86 population in spleen. Results: PBC significantly enhanced the expression of IgM and IgG titre and DTH response in a dose dependant manner after 24 and 48 h in BALB/c mice with a maximum response at 200 mg/Kg. Besides humoral and cell mediated immunity, it also enhanced phagocytic index, nitric oxide production, which further leads to protection against Candida albicans infection. It also, enhanced the expression of CD80 and CD86 in splenic cells. Conclusion: Taken together these in vitro and in vivo data, our results suggest that PBC acts as an effective immunostimulator which specially enhances macrophage function during infection. This further supports the role of PBC in immunopharmacologic applications.
Keywords: Cytokine.; Ha Titre; Immunostimulation; Macrophages; Phyllostachys Bambusoides

In vitro Antibacterial Activity of Alkaloids Isolated from Leaves of Eclipta alba Against Human Pathogenic Bacteria - Swapna Gurrapu; Estari Mamidala (Pharmacognosy Journal, 2017)
The susceptibility of five human pathogenic bacterial species to an alkaloids isolated from the leaves of this plant was screened using the agar well diffusion and broth micro-dilution assay. The purity of isolated alkaloids was checked by TLC and qualitative phytochemical analysis and total alkaloids were quantified. In the present study, the inhibitory action of the alkaloid was found to increase with an increase in concentration against all bacterial strains. The maximum zone of inhibition was observed at the concentration of 500 μg/ml against all the bacteria. In this study, the S. aureus and E. coli are the more susceptible than the other selected human pathogenic bacteria. Based on the observations, E. alba appears to be a valuable source for antimicrobial properties and helps to produce antimicrobial agents to treat human pathogenic infections. Context: Different parts of Eclipta alba crude extracts are used traditionally for the treatment of several diseases of liver, skin and stomach. Aims: To study the in vitro antimicrobial activity of alkaloids isolated from E. alba against human pathogenic bacteria. Settings and Design: The susceptibility of five human pathogenic bacterial species to an alkaloids isolated from the leaves of this plant was screened using the agar well diffusion and broth micro-dilution assay. Methods and Material: The purity of isolated alkaloids was checked by TLC and qualitative phytochemical analysis and total alkaloids were quantified. Agar-well diffusion and Broth micro-dilution methods were selected to assess the antimicrobial activity. Statistical analysis used: One-way analysis of variance (ANOVA) was used to determine statistical significance. Results: In the present study, the inhibitory action of the alkaloid was found to increase with an increase in concentration against all bacterial strains. The maximum zone of inhibition was observed at the concentration of 500 μg/ml against all the bacteria. In this study, the S. aureus and E. coli are the more susceptible than the other selected human pathogenic bacteria. Conclusion: Based on the observations, E. alba appears to be a valuable source for antimicrobial properties and helps to produce antimicrobial agents to treat human pathogenic infections.
Keywords: Agarwell diffusion; Alkaloid; Antimicrobial activity; Broth micro-dilution assay.; Eclipta alba; Human pathogenic bacteria

In vitro Antioxidant and Hepatoprotective Activity of Bridelia scandens (Roxb.)Willd - Preetham Jinadatta; Kiran Sundera Raja Rao; Sharath Rajshekarappa; Sujan Ganapathy Pasura Subbaiah; Mruthunjaya Kenganora (Pharmacognosy Journal, 2017)
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 31.68μg/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

In vitro & ex vivo Acetylcholinesterase Inhibitory Activity of Morinda citrifolia Linn (Noni) Fruit Extract - Srikanth Jeyabalan; Kavimani Subramanian; Uma Maheswara Reddy Cheekala; Chitra Krishnan (Pharmacognosy Journal, 2017)
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

In vitro Studies on Basella rubra Different Extracts as Inhibitors of Key Enzymes Linked to Diabetes Mellitus - B. Samuel Thavamani; Vanitha Subburaj (Pharmacognosy Journal, 2017)
Enzyme, inhibiting carbohydrate metabolism and thereby decreasing glucose level is a class of drugs helpful in the management of type 2 Diabetes mellitus. Naturally existing α-amylase and α-glucosidase inhibitors from medicinally significant plants are shown to be effective in the management of postprandial hyperglycemia. In this investigation, leaf extract (BRLE), stem extract (BRSE), fruit extract (BRFRE) and flower extract (BRFLE) of Basella rubra were subjected to evaluate their antioxidant potential and their possible inhibitory effects on α-amylase and α-glucosidase. BRLE, BRSE, BRFRE, BRFLE (at concentration 100μg/ml) exhibited 65.78, 56.84, 63.1, 61.03% of α-amylase inhibitory activity respectively with IC50 values of 71.66, 89.69, 73.68, 80.37 μg/ml respectively. In the same way BRLE, BRSE, BRFRE, BRFLE (at concentration 100 μg/ml) exhibited 97.63, 92.79, 82.17, 92.71 % of α-glucosidase inhibition with an IC50 value of 26.97, 28.53, 41.30, 38.80 μg/ml respectively. Among the samples, the leaf extract of B. rubra registered higher content of total phenolics and flavonoids and also higher antioxidant activity in DPPH, nitric oxide and NBT radical scavenging assays. Though all the parts had shown potent inhibitory effects on α-amylase and α-glucosidase, the highest inhibitory potency was observed in the leaf extract of Basella rubra (p<0.001).
Keywords: Basella rubra; Diabetes mellitus; Postprandial hyperglycemia; α-Amylase inhibitory activity

In vitro Study of Xanthine Oxidase Inhibitory of Gambir (Uncaria gambir) Hunter Roxb Extracts - Eriawan Rismana; Sri Ningsih; Fachry Fachrudin (Pharmacognosy Journal, 2017)
Introduction: Hyperuricemia was a metabolic disorder characterized by high levels of uric acid due to the action of the enzyme xanthine oxidase (XO). Some natural substances with antioxidant activity proved capable of inhibiting the activity of the enzyme XO. Pharmacological benefit of polyphenol compounds had been proved. Gambir (Uncaria gambir) Hunter Roxb, a native plant, had been proved antioxidant activity, so that it had potential to be developed as an inhibitor of the XO. This study aimed to evaluate the activity of Gambir as XO inhibitor. Methods: These extracts of Gambir were preparation from Gambir and Gambir leaf using ethanol 50% and ethanol 96%, respectively. The polyphenol content and Xanthine oxidase inhibitory activity was evaluated by spectrophotometry, meanwhile analysis of (+)catechin was determined by high pressure liquid chromatography (HPLC). Results: Screening XO inhibitory activity in vitro showed that ethanolic 96% extract of Gambir leaf showed the highest activity, i.e. 50% relative to standard allopurinol at the final concentration of 100 ppm. Conclusion: There was no positive correlation between XO inhibitory activity and polyphenol or (+)catechin content.
Keywords: (+) Catechin.; Gambir (Uncaria gambir) Hunter Roxb; Inhibitory; Polyphenol; Xanthine Oxidase

Indonesian Mirabilis jalapa Linn. : A Pharmacognostical and Preliminary Phytochemical Investigations - Endang Hanani; Rini Prastiwi; Lina Karlina (Pharmacognosy Journal, 2017)
Introduction: Mirabilis jalapa Linn. is an important medicinal plant and used extensively by the people from different countries for the treatment of several disorders. The plant was the raw material for the herb-drug product, so some parameters identified were needed to ensure the safety, quality and efficacy of the product. Objective: The aim of this study was to undertake pharmacognostical studies to fulfill the work required for the identification the M. jalapa plant, which is collected from the Bogor area, Indonesia. Methods: Macroscopic and microscopic evaluation, fluorescence standards, phytochemical screening and physicochemical parameters were carried out on the above plant. Results: The parameters values of total ash, water soluble and acid insoluble ash were obtained 11.81, 5.06 and 0.41%, respectively. Moisture content, alcohol, water and ether soluble extractive were found to be 12.41, 11.02, 18.63 and 7.17% respectively. The results of preliminary phytochemical analysis of aqueous ethanolic extract of this drug were positive for alkaloids, tannins, flavonoids, steroid, triterpenoids, saponin, phenols, glycosides and carbohydrate. Thin layer chromatography (TLC) of alcoholic, chloroform and aqueous extracts showed 9, 7 and 4 spots respectively. Conclusion: The present study on botanical pharmacognosy and TLC profile of this plant above thus provides useful information for correct identification and quality control parameters for the crude drugs, and also will be useful in making monograph of the plant.
Keywords: Chromatography Profile; Flourescence Character; Microscopic; Nyctaginaceae; Physicochemical

Influence of Extraction Parameters on the Yield, Phytochemical, TLC-Densitometric Quantification of Quercetin, and LC-MS Profile, and how to Standardize Different Batches for Long Term from Ageratum conyoides L. Leaves - Anita Paulina Tambunan; Anton Bahtiar; Raymond Rubianto Tjandrawinata (Pharmacognosy Journal, 2017)
Introduction: Ageratum conyzoides Linn is one of the Indonesian herbs are used as folk medicine. There are many studies to the therapeutic activity. However, the study of the influence in extraction parameters and how to standardize different batches of plant is still limited. Objective: The present study was designed to investigate the influence of extraction parameters on the variables matter, yield, phytochemical profile, and total quercetin from A. conyzoides L. leaves extract. The study also evaluates Liquid Chromatography-Mass Spectroscopy (LC-MS) and TLC fingerprint profiles of the extract to determine the proper quality of plant material of A. conyzoides L. leaves. Methods: Different temperatures (from 0°C to 60°C), solvent types (water and 70% ethanol (%v/v), and extraction time (192 h VS 2 h) were used to investigate the influence of extraction parameters. The profiles of extract were performed by TLC and LC-MS method. Results: The extract yield was influenced by temperature, solvent types, and time extraction. Our results suggest that the digestion technique at 60°C with 70% ethanol for 2h was recommended for the extraction method to obtained high yield and quercetin content as bioactive compound in A. conyzoides L. leaves extract. The range of quercetin content (40–52 ppm) combined with TLC and LC-MS profile can be used to determine the proper quality of plant material. Conclusion: All parameter of extraction have an affect on the yield extract and total quercetin on the final extract. Thus, there is a need an optimized method to obtain the suitable method.
Keywords: Ageratum conyzoides; Lc-Ms; Quercetin; Standardization.; Tlc-Densitometric

Inhibition Activity of Angiotensin Converting Enzyme (ACE) and Determination of Total Phenolic and Flavonoid Compound from Bitter Melon Leaves (Momordica charantia L.) - Putri Lestari; Katrin; Rissyelly; Putu Gita Maya Widyaswari Mahayasih (Pharmacognosy Journal, 2017)
Introduction: Hypertension is a leading problem in Indonesia, because of the high prevalence and the long term effect. Bitter melon leaves (Momordica charantia L.) has been traditionally utilized to treat hypertension, yet not many studies explained the antihypertension effect of this plant. Methods: This study was conducted to test the benefit of bitter melon leaves as antihypertension using angiotensin converting enzyme inhibition activity in 80% ethanolic extract and its fractions (n-hexane, ethyl acetate, and n-butanol) using ACE kit-WST (Dojindo, Japan). Then the antihypertension activity was associated with the phenolic content which was expressed in gallic acid equivalent (GAE) and total flavonoid in quercetin equivalent (QE). Results: Result of the study showed that the IC50 value obtained from the ethanolic extract to inhibit ACE activity was 7.52 μg/mL and the highest inhibition obtained in ethyl acetate fraction with IC50 value was 4,29 μg/mL. Phenolic total and flavonoid total determination also showed that the highest content obtained in ethyl acetate fraction with 18.752 mg GAE/gr extract and 8.310 mg QE/gr extract, respectively. Conclusion: According to the study, it could be concluded that bitter melon (Momordica charantia L.) leaves provide inhibition activity against Angiotensin Converting Enzyme (ACE) and chemical compounds that were expected to play an active role in inhibiting ACE were flavonoid and tannin.
Keywords: Angiotensin converting enzyme; antihypertension; Momordica charantia L.; total flavonoid.; total phenolic

Inhibition Kinetics of Acetylcholinesterase and Phosphatases by the Active Constituents of Terminalia arjuna and Tamarindus indica in the Cerebral Ganglion of Lymnaea acuminata - Neelam Soni; Dinesh Kumar Singh; Vinay Kumar Singh (Pharmacognosy Journal, 2017)
Introduction: Paper demonstrates effect of the active molluscicidal components arjunolic acid (Terminalia arjuna bark) and procynadine (Tamarindus indica seed) on the activity of acetylcholinesterase (AChE) and phosphatases (ACP/ALP) in the cerebral ganglion of snail Lymnaea acuminata. Materials and Methods: Kinetics of AChE/ACP/ ALP inhibition in the cerebral ganglion of snail Lymnaea acuminata was studied via in vivo (40% and 80% of 96 h LC50) and in vitro treatments (0.3 μg to 7.0 μg) of the column purified fractions, arjunolic acid and procynadine. Results: In vivo exposure of procynadine and arjunolic acid significantly inhibit acetylcholinesterase (AChE), acid phosphatase (ACP) and alkaline phosphatase (ALP) activities in the cerebral ganglion of L. acuminata exposed to 80% of 96h LC50. In in vitro treatment maximum inhibition in AChE/ACP/ALP activities in the cerebral ganglion of snail were noted when exposed to 7.0 μg of arjunolic acid and 0.9 μg of procynadine. Column purified fraction of T. arjuna bark and T. indica seed caused non-competitive and uncompetitive inhibition of AChE activity, respectively. Column purified fraction and arjunolic acid of T. arjuna bark caused uncompetitive inhibition of ACP while column purified fraction and procynadine of T. indica seed caused competitive inhibition. Competitivenon- competitive inhibition of ALP activity in the cerebral ganglion of L. acuminata was observed after treatment of column purified active components of both plants. Conclusions: The molluscicidal activity of T. arjuna bark (arjunolic acid) and T. indica seed (procynadine) against snail L. acuminata is due to the inhibition of AChE/ACP/ ALP. Their inhibition kinetics against AChE/ACP/ALP, were different in cerebral ganglion of snail.
Keywords: Arjunolic acid; Enzymes; Lymnaea acuminata; Procynadine; Tamarindus indica; Terminalia arjuna

Inhibition of Alpha-Glucosidase and Antioxidant Test of Stem Bark Extracts of Garcinia fruticosa Lauterb - Nusaibah Zahratunnisa; Berna Elya; Arikadia Noviani (Pharmacognosy Journal, 2017)
Introduction: Diabetes mellitus (DM) is one of the global health emergencies that characterized by high blood glucose levels (hyperglycemia). Type 2 DM is the most common type in diabetic populations. Inhibition of alphaglucosidase can ameliorate postprandial hyperglycemia that occurs in patients with type 2 DM. Adding antioxidants to the therapy of DM is intended to reduce complications caused by oxidative stress. Some species of Garcinia have been proven to inhibit alpha-glucosidase and have antioxidant activity, but there is no research on Garcinia fruticosa Lauterb. Therefore, the aims of this research were to determine the activity of Garcinia fruticosa Lauterb. stem bark in inhibiting alpha-glucosidase and as an antioxidant. Methods: In this research, the Garcinia fruticosa Lauterb. stem bark was dried, grinded, and extracted by multistage maceration using n-hexane, ethyl acetate, and methanol. Inhibition of alpha-glucosidase test has been done in vitro on concentrated extracts and measured by microplate reader at 400 nm. The antioxidant test has been done using DPPH scavenging method and was measured by microplate reader at 519 nm. Results: Ethyl acetate extract is the most active extract for both test. IC50 values for inhibition of alpha-glucosidase test are 20.18 μg/mL that is more active than standard (acarbose) which has IC50 value 141.55 μg/mL. Meanwhile, IC50 value from an antioxidant test is 8.93 μg/mL that is not more active than standard (quercetin) which has IC50 value 2.51 μg/mL. Conclusion: Phytochemical screening shows that the ethyl acetate extract contains alkaloids, flavonoids, glycosides, saponins, and tannins.
Keywords: Alpha-glucosidase; Antioxidant; DPPH; Garcinia fruticosa Lauterb. Stem bark; Phytochemical screening

Inhibition of Caco-2 and HeLa proliferation by Terminalia carpentariae C. T. White and Terminalia grandiflora Benth. extracts: Identification of triterpenoid components - Reece Courtney; J. Sirdaarta; A. White; I. E. Cock (Pharmacognosy Journal, 2017)
Background: Terminalia spp. are characterised by their high antioxidant capacities and many have anticancer activity. This study examines the anti-proliferative activity of T. carpentariae leaf and T. grandiflora leaf, fruit and nut extracts against Caco-2 and HeLa carcinoma proliferation. Materials and Methods: Powdered T. carpentariae leaf and T. grandiflora leaf, fruit and nut were extracted and tested for anti-proliferative activity against Caco-2 and HeLa cancer cell lines using colorimetric cell proliferation assays. Toxicity was evaluated using an Artemia franciscana nauplii bioassay. The extract with the most potent anti-proliferative activity was examined using GCMS analysis and triterpenoid compounds were identified by comparison with a compound database. Results: T. carpentariae leaf and T. grandiflora leaf, fruit and nut extracts displayed potent anti-proliferative activity against Caco-2 and HeLa carcinoma cells. The methanolic T. grandiflora leaf extract was particularly effective at blocking the proliferation of the colorectal carcinoma Caco-2 (IC50 = 372 μg/mL). The methanol T. carpentariae and T. grandiflora leaf extracts were similarly potent inhibitors of HeLa cervical cancer cell proliferation with IC50 values of 864 and 833 μg/mL respectively. The methanolic T. grandiflora fruit and nut extracts, as well as all aqueous and ethyl acetate extracts, were moderate to good inhibitors of carcinoma proliferation. In contrast, chloroform and hexane extracts were generally devoid of anti-proliferative activity. The methanolic T. grandiflora extracts displayed low toxicity in the Artemia nauplii bioassay. All other extracts were non-toxic. GC-MS analysis of the methanolic T. grandiflora leaf extract identified 3 lanostane and 2 pentacyclic triterpenoids. Conclusion: The low toxicity and anti-proliferative activity observed with the T. carpentariae and T. grandiflora extracts against Caco-2 and HeLa indicate their potential for the prevention and treatment of some cancers.
Keywords: Anticancer activity; Australian plants; Caco-2; Chemotherapy; Combretaceae; HeLa; Native almond; Wild peach

Investigation of cytotoxicity induced by Nigella sativa and Azadirachta indica using MDA-MB-231, HCT 116 and SHSY5Y cell lines - Sayani Banerjee; Shefali Pandey; Purbasha Mukherjee; Afia Sayeed; Apoorva Vasant Pandurangi; Shinomol George; Sahabudeen Sheik Mohideen (Pharmacognosy Journal, 2017)
Background: Indian herbal plants are widely used as medicine in the ancient ayurvedic and culinary purposes. Nigella sativa that also called as in black cumin is a flowering plant in the family ranunculiceae that is native to Southeast Asia. More recently Nigella sativa is also been used as anti cancer drug and protective agent against gamma radiation induced adverse effects in cell lines. Azadirachta indica commonly called as neem, is a tree belonging to mahogany family meliaceae. Azadirachta indica is also a traditional medicinal plant that used from a very long time in Indian ayurvedic and it is also been reported to have many beneficial effects including but not limited to anti-cancer and anti-diabetic effects. Objective: Find the IC50 values of Nigella sativa and Azadirachta indica ethanolic extracts in MDA-MB-231, HCT 116 and SHSY5Y cell lines. Methods: In this study we selected two cancerous cell lines (MDA-MB-231, HCT 116) and one neuronal cell line (SHSY5Y) and studied the effect of the two plant extracts namely Nigella sativa and Azadirachta indica on the cell metabolic activity. Results: This study revealed that cancerous cell lines are more prone to the plant extracts than the neuronal cell lines. These results suggest positive clues on how such medicinal plant extracts act against cancerous cells alone while affecting the normal cells to a limited extent. However, further studies are required to find if this effect is due to cytotoxicity, cytostaticity, or anti-adhesive property.
Keywords: Ayurvedic medicine; Cancer cells; Herbal plants; Neuronal cells

In-vivo Hepatoprotective Activity of Methanolic Extracts of Sphaeranthus amaranthoides and Oldenlandia umbellate - Somnath De; Ramalingam Suresh; Akula Murali Sri Sudhakar Babu; Siddabathuni Aneela (Pharmacognosy Journal, 2017)
Objective: The present study was carried out to evaluate the in vitro hepatoprotective activity of unexploited plants, Sphaeranthus amaranthoides and Oldenlandia umbellate on CCl4 induced liver injury, which are indigenous to South India. Methods: in the present study the methanolic extracts from Sphaeranthus amaranthoides and Oldenlandia umbellata were studied against the carbon tetrachloride hepatotoxicity. Results: significant hepatoprotective effect was obtained against carbon tetrachloride induced liver damage as judged from serum marker enzyme activities (SGOT, SGPT, ALT, and TB) and a normal architecture of liver compare to toxic control. Conclusion: the result revealed that methanolic extracts of Sphaeranthus amaranthoides and Oldenlandia umbellata could be useful in preventing CCl4 induced liver injury.
Keywords: ALP; CCl4; Hepatoprotective activity; Oldenlandia umbellata; SGOT; SGPT; Sphaeranthus amaranthoides; TB.

Isolation and Identification of Compounds from the Leaf Extract of Melaleuca alternifolia - Gagan Shah; Dhandeep Singh; Uttam Singh Baghel (Pharmacognosy Journal, 2017)
Introduction: Melaleuca alternifolia also known as Tea tree oil belonging to family Myrtaceae. This plant has diverse and therapeutic uses in traditional herbal medicine for treating Skin care, First Aid, Household Cleaning, Hair care, Aromatherapy, Feminine care, Chronic illness, and Dental care in Australia. Method: The methanolic extract of Melaleuca alternifolia family Myrtaceae was subjected for Soxhlet extraction in round bottomed flask with petroleum ether. The petroleum ether extracted leaf powder was dried and once again subjected to Soxhlet extraction successively with different solvents viz, chloroform, ethyl acetate and methanol. Result: The IR spectra showed characteristic absorption bands at 3421 cm-1 indicating the presence of a OH group, at 1691cm-1 for C=O group, 2848 cm-1. The 1HNMR spectra showed a triplet signal at δ 10.44, 9.48, 13.21 showing the presence of OH group and Carboxylic acid. The 13C NMR spectra showed signals at δ 16.28 for a methyl carbon, δ 29.89 for a methylene carbon, The ESI-negative mode mass spectrum showed pseudo molecular ions at m/z 515 for [M+] ion. Conclusion: Based on spectral analysis and comparison of the spectral data with literature values, the compounds were identified as 3,3’dimethylellagic acid and its aglycone portion with some little impurity.
Keywords: 3; 3’dimethylellagic acid; Aromatherapy; Chloroform; Melaleuca alternifolia; Methalonic; Myrtaceae

Isolation, Purification of Quercetin from in vitro Cell Suspension Culture of Caesalpinia pulcherrima and its Analysis by HPLC-DAD and NMR - Aswathy Jayasree Madanakumar; Greeshma Murukan; Bosco Lawarence; Murugan Kumaraswamy (Pharmacognosy Journal, 2017)
Background: Caesalpinia pulcherrima, belongs to Caesapiniaceae, is a known medicinal plant widely distributed in India and is used in traditional medicine for the treatment of various ailments. Many phytochemicals are reported from the plant as potential source of crude drug. Materials and Methods: An efficient and simple reproducible protocol was developed for callus production using leaf explants of C. pulcherrima. The combination of 2, 4-D, kin and BA, was used for the callus induction. Subsequently, cell suspension culture and quercetin synthesis from in vitro callus was attempted. Role of effect of elicitors (Sucrose, ABA and salicylic acid) in cell suspension culture was carried in MS medium containing 2,4-D + BA + kinetin. Flavonoids was purified, fractionated by HPLC-DAD and NMR. Results: 2, 4-D (2.5 mg/L), BA (2.5 mg/L) + kin (1 mg/mL) was effective for maximum callus induction from leaf explants. Significant cell suspension culture was noticed with liquid MS medium containing 2,4-D (2 mg/L)+ BA (1mg/L)+ kinetin (1.5 mg/L). Sucrose, ABA and salicylic acid (SA) at different concentrations influenced cell biomass and quercetin accumulation. The addition of ABA/SA along with sucrose was found to have no remarkable effect on cell biomass and also quercetin synthesis. However, cells cultured in the medium fortified with 45 g/L sucrose without ABA/ SA showed the highest quercetin content (16.5 mg/g). Flavonoids was purified, fractionated by HPLC-DAD and NMR revealed the presence of 9 components such as quercetin, isoquercetin, quercetrin, rutin, quercetin 3-O-β-D-xyloside, quercetin 3-Oarabinopyranoside, quercetin 3-O- α-arabinopyranosyl (1→2) β-galactopyranoside, isorhamnetin 3-O-rutinoside and an unknown compound. Conclusion: C. pulcherima reveals significant synthesis of quercetin. Quercetin content recorded in cell suspension culture was significantly higher compared with in vivo plants grown in fields and the compounds were identified by NMR.
Keywords: Caesalpinia pulcherrima; Callus; Cell suspension culture; Elicitors; growth hormones; Quercetin

Laetiporus sulphureus (Bull.: Fr.) Murr. as Food as Medicine - Somanjana Khatua; Sandipta Ghosh; Krishnendu Acharya (Pharmacognosy Journal, 2017)
Laetiporus sulphureus is a sulphur yellow coloured polyporous mushroom and popularly known as “chicken of the woods”. Over the generations, this cosmopolitan macrofungus has become an integral part of tribal cuisines particularly for its taste. Besides, it has equal importance in folk medicine being widely used for treatment of pyretic diseases, coughs, gastric cancer and rheumatism. Thus, the species is considered as a natural reservoir of both nourishment as well as drug therapy and consequently it has become increasingly popular in scientific world. Nutritional sciences recently have witnessed it as a sustainable food supply to growing population due to enrichment of carbohydrate (trehalose> mannitol> fructose), protein (histidine, isoleucine, leucine, lysine, methionine, threonine), minerals (calcium, phosphorus, magnesium, sodium, potassium, iron, zinc, manganese, copper), vitamins (B, D, E), polyunsaturated fatty acids (linoleic acid, oleic acid, palmitic acid) and fibre. Conversely, the mushroom has also been regarded as an abundant source of chemical compounds including phenolics, triterpenes, polysaccharides with wide range of biological activities such as antiinflammatory, antimicrobial, antioxidant, antihyperglycemic, antitumor and immunomodulation effects. Therefore, a complete summary of the research progress on this fungus is necessary for further studies and commercial exploitation. In this context, the present review attempts to congregate current knowledge on nutritional value, myco-chemistry and therapeutic potential of this culturally important species. However, investigation on bioavailability, quality control, toxicology data and clinical assessment are highly recommended for future research.
Keywords: Bioactive components; Commercial Importance; Ethnic Relevance; Nutritious Food; Pharmacological Effects; “Chicken of the Woods”

Lipid Peroxidation Inhibitory Activity In vitro of Mezzetia parviflora Becc. Wood Bark Polar extract - Mufidah Murdifin; Ermina Pakki; Gemini Alam; Marianti A. Manggau; Lukman Muslimin; M. Rusdi; Elly Wahyudin (Pharmacognosy Journal, 2017)
Introduction: The wood bark of Mezzetia parviflora Becc, has long served as one of the most important traditional herbal medicine sources in Buton Regency, Southeast Sulawesi. M. parviflora extracts were rich in polyphenols. This study was aimed to explore the lipid peroxidation inhibitory activity of polar extract of M. parviflora. Methods: The polar extract is the result of ethanol extract partition solved in acetone. The extract will keep polar components which are insoluble in acetone. Assayed methods applied are ß-carotene bleaching inhibition, thiobarbituric acid reactive substance (TBARS) measurement, and continuous monitoring of conjugated dienes formation in LDL. Results: M. parviflora extract inhibit ß-carotene/ linoleic acid oxidation, showed by IC50 value of 15.83 μg/ml in 30th minute; but the potency will be reduced to IC50 value of 111.19 μg/ml and 225.07 μg/ml after the 60th and 120th minute of incubation. M. parviflora extract inhibit MDA formation as for linoleic acid peroxidation product until the third day; at 20, 40, 60, 80 and 100 μg/ml inhibit MDA formation as many as 29.16 ± 2.41%, 4.24% ± 43.27, 54.08 ± 2.87%, 59.88 ± 1.90%, and 69.75 ± 2.32%, respectively. M. parviflora extract at 50 μg/ml can inhibit LDL-oxidation induced by CuSO4, performed by LDL-oxidation lag-time elongation until 70 minutes, similar ability was performed by epigallocathecin gallate at 5 μg/ml. Conclusions: M. parviflora extract expressed relatively strong protection against lipid and LDL oxidation which can serve as the scientific basis of its development as a remedy for various diseases caused by lipid peroxidation.
Keywords: Conjugated diene; Low-density lipoprotein; Malondilaldehyde; Mezzetia parviflora Becc; Polyphenol

Micro-morphoanatomical approach for comparative analysis of Tinospora cordifolia (Willd.) Miers and its adulterant plant using SEM and Cryostat - Vidya Shivram Patil; Nutan Padmnabh Malpathak (Pharmacognosy Journal, 2017)
Background: Tinospora cordifolia (Willd.) Miers, belongs to Menispermaceae, commonly known as “Guduchi”or “Amrita” and has immense importance in Ayurvedic medicine. Several studies have been carried out on pharmacology, pharmaceutical, anticancer activity and clinical trials of T. cordifolia, however not much information is available on the adulterants that are added with the genuine plant. Considerable work has been done on pharmacognosy but very few studies have been performed on the anatomy of T. cordifolia. Objectives: Comparative micro-morphoanatomical analysis of T. cordifolia and P. daemia, is important for quality control of fresh and dried samples of the root, stem and leaves. Material and Methods: The plant materials of T. cordifolia and P. daemia were collected, and identified. Fixed sample subjected to cryostat microtomy and sections were observed under light microscope. Micromorphology were studied by light as well as scanning electron microscope. Results: Anatomical studies are cheap and important tool for identification of the correct medicinal plant. Adulterant plant does not contain active principles like Berberine and Tinosporin nor have similar morpho-anatomical characters. Because of the similar appearance and resemblance of dried adulterant plant samples, medicinally important T. cordifolia often get adulterated with other plants. SEM study revealed morpho-anatomical differences like the abundance of starch in cortical and ray parenchyma, different types of trichomes, etc. Cryostat techniques were used for sectioning and showed the presence of xylem plates with wide multicelluar rays. Conclusion: Morphological and anatomical differences were observed in T. cordifolia and P. daemia. The given results showed significant differences therefore this study aims to help in accurate identification and avoid adulteration of a medicinally important plant.
Keywords: Berberine; Morpho-anatomy; Pergularia daemia; SEM study.; Tinospora cordifolia; Tinosporin

Microscopic and Physicochemical Evaluation of Leaves of Sphaeranthus indicus Linn - Sonia Singh; Bhupesh Chander Semwal; Gurulingappa S Neeli (Pharmacognosy Journal, 2017)
Objective: To study the pharmacognostic characters of a medicinally important crude drug, Sphaeranthus indicus Linn. Methods: Various pharmacognostic parameters involved in organoleptic, microscopic, physicochemical, phytochemical and fluorescence evaluation were carried out. Results: The macroscopy study showed that the leaves was observed as sessile, obovate-oblong apex, tapered base, dentate margin, simple, serrate lamina, surface glabrous. The leaf microscopy showed the presence of diacytic stomata, unicellular covering trichomes, arc shaped vascular bundle which contain lignified xylem and non lignified phloem, cortical parenchyma and a thin strip of collenchyma, micro rosette calcium oxalate crystals. The powder characteristics of leaf showed the presence of lignified fibers, medullary rays, bordered pitted xylem vessels, calcium oxalate crystals, stomata, epidermal cells and covering trichomes. Physicochemical parameters like total ash value was 9.21%, water soluble ash 1.56%, acid insoluble ash 1.35%, swelling index 4 mL, loss on drying 1.09% and foreign matter was 0.20%w/w respectively where as stomatal indexes of upper and lower surfaces were 33.2 and 23, respectively. The phytochemical screening revealed the presence of carbohydrates, flavonoids, alkaloids, volatile oil, fats and oils, tannins and phenolic compounds. Conclusion: The present study provides the scientific data for the proper authentification and establishment of quality control standards for the therapeutic use of Sphaeranthus indicus.
Keywords: Histochemical evaluation; Organoleptic evaluation; Phytochemcial screening; Sphaeranthus indiucs.

Microscopic Characterization of Croton cordiifolius Baill. (Euphorbiaceae) - Iasmine Andreza Basilio dos Santos Alves; Rafaela Damasceno Sá; Marília Barbosa Cadena; Rafael Matos Ximenes; Karina Perrelli Randau (Pharmacognosy Journal, 2017)
Background: Croton cordiifolius Baill. is popularly known as “quebra-faca” in the Brazilian Northeast and is used to treat general inflammation, pain, and gastrointestinal disturbances. Objective: This paper aims to study the anatomical characteristics of C. cordiifolius. Materials and Methods: Cross-sections and paradermic sections of root, stem, petiole and leaf blade were obtained by hand and submitted to double staining with astra blue and safranin process for the anatomical study. Maceration was performed according to the method of Jeffrey. Results: The secondary root has peridermis, parenchymatic cortex, collateral vascular system surrounded by sclerenchyma. The secondary stem has peridermis, cortical region with lignified cells, isolated groups of fibers, laticifers, prismatic crystals, druses and starch. The vascular system of the stem is bicollateral. The petiole and the leaf blade have stellate, simple and glandular trichomes. The leaf blade is hypostomatic, with paracytic stomata. The mesophyll is isobilateral and the midrib shows a concave-convex contour. Laticifers occur in stem, petiole and leaf blade. Prismatic crystals and druses are found in all organs analysed. Through the maceration it was possible to identify the type of vessel elements. Conclusion: The anatomical features are useful for differentiation of other species of Croton and provide support to their quality control.
Keywords: Croton cordiifolius; Euphorbiaceae; Pharmacobotany; Plant anatomy; Quebra-faca

Microscopical Evaluation, Phytochemical Analysis and HPTLC Fingerprinting of Tuber of Actinoscirpus grossus (L.f.) Goetgh. & D.A.Simpson - Savin Chanthala Ganapathi; Rajendra Holla; Shivaraja Shankara; Sunil Kumar Koppala Narayana; Ravi Mundugaru (Pharmacognosy Journal, 2017)
Actinoscirpus grossus (L.f.) Goetgh. & D.A.Simpson (Cyperaceae), is a Perennial with long stolons and rhizomes ending in small tubers. It is popularly known as Kasheruk in Sanskrit. The plant is traditionally used as anti-diarrheal, anti-emetic, and tonic to the liver. In order to do the detail standardization of plant macro-microscopical observation, phytochemical analysis and HPTLC Finger printing of tuber was performed according to pharmacopoeia procedure. Microscopic analysis has showed thick-walled polygonal epidermal cells of young root stalk in surface view, elongated phloem parenchyma filled with starch grains, spiral to annular vessel fragments and simple starch grains scattered all over the powder. Phytochemical analysis showed presence of carbohydrate, coumarins, flavanoids, steroid, tannin, and terpenoid. Ethanol extract of plant were fingerprinted in toluene: ethyl acetate (7:3). The developed plates were visualized in UV 254, 366, and then derivatised with vanillin sulphuric acid and scanned under UV 254 and 366 nm. These specific identities will be useful in identification and authentication of the raw drug.
Keywords: Ethanol Extract; HPTLC; Pharmacognosy; Phytochemical analysis; Quality control; standardization

Molecular Docking, ADMET Analysis and Dynamics Approach to Potent Natural Inhibitors against Sex Hormone Binding Globulin in Male Infertility - Morvin Yabesh Jobu Esther; Vijayakumar Subramaniyan; Arulmozhi Praveen Kumar; Mahadevan Subramanian; Manogar Palani (Pharmacognosy Journal, 2017)
Objectives: The Sex Hormone Binding Globulin (SHBG) plays an important role in male infertility. Methods: The present research computationally emphases to SHBG protein with 47 natural phytocompounds using docking studies. Results: From the results showed the interactions between 1KDM protein with 47 phytocompounds, a natural compound chlorogenic acid showed the best glide docking XP score -7.255 kcal/mol and the binding energy value of -47.869 kcal/ mol. Based on the result, the chlorogenic acid and target were run on MD simulations stable at 10 ns. Conclusion: Finally, this study concludes the chlorogenic acid is a suitable drug candidate for infertility.
Keywords: ADMET property; Male infertility; MD simulations; Molecular docking; Phytocompounds; SHBG

Morphological and Anatomical Study of the leaves of Laurus nobilis L. (Lauraceae), growing in the Introduction of the Northern Caucasus region (Russia) - Fatima Kazbekovna Serebrynaya; Naida Mahmudovna Nasuhova; Dmitryi Alexeevich Konovalov (Pharmacognosy Journal, 2017)
In this article results of morphological and anatomical research Laurus nobilis L. are resulted. These plants are growing in the conditions of culture in the Botanical garden of Pyatigorsk medical and pharmaceutical institute (Northern Caucasus region). Introduction: Laurus nobilis L. is grown up as a decorative species in Europe, RUSSIA, the USA and other countries. Chemical composition of the leaves is characterized by essential oil components, sesquiterpene lactones, phenolic and other compounds. Material And Methods: Micro morphological research of vegetative bodies was carried out with the help of a well-known technique. We carry out morphological and anatomical research of a leaf blade and a petiole of a leaf of a plant, which is grown up in a Botanical garden in the Pyatigorsk medical and pharmaceutical institute. Results: The diagnostic characteristics of a leaf blade necessary for an establishment of authenticity of raw materials are revealed. The leaf is hypostomal, dorsoventral, stomatal apparatus of paracytic type. The idioblasts with the essential oil are obtained between mesophyll cells. Idioblasts thin-walled, large enough. In the field of the main vein under an epidermis the collenchyma of lamellar type in 4-7 layers settles down. The leaf petiole on cross-section section has the saddle-like form, without a ledge on the abaxial side of leaf. Under an epidermis the parenchyma settles down, is presented by live cells of the roundish or oval form. Between parenchyma cells it is possible to observe numerous cells-idioblasts with contents of yellow colour. Conclusions: As diagnostic signs of leaf (a leaf blade and a petiole) it is possible to consider numerous cells - idioblasts with an essential oil, the leaf is hypostomatical, dorsoventral, stomatal apparatus of paracytic type. The idioblasts with the essential oil are obtained between mesophyll cells.
Keywords: Anatomical Structure of Leaf; Essential Oil.; Laurus Nobilis; Morphological and Anatomical Study

Mosquito Larvicidal and Pupicidal Activity of Tephrosia purpurea Linn. (Family: Fabaceae) and Bacillus sphaericus against, Dengue Vector, Aedes aegypti - Ramesh Venkadachalam; Vijayakumar Subramaniyan; Manogar Palani; Mahadevan Subramaniyan; Prabhu Srinivasan; Murugan Raji (Pharmacognosy Journal, 2017)
Objective: The bio-efficacy of Tephrosia purpurea leaf extract and bacterial insecticide, Bacillus sphaericus larvicidal activity was assessed against the first to fourth instars larvae of Aedes aegypti, under the laboratory conditions. Methods: The plant material was shade dried at room temperature and powdered coarsely. T. purpurea and B. sphaericus show the various concentrations of larvicidal and pupicidal activity against various instars larvae of A. aegypti. Results: The LC50 of T. purpurea against the first to fourth instars larvae were 139.24, 176.24, 219.28, 256.27, and 326.29 ppm and the 480.72, 541.21, 580.34, 672.20, and 762.80 ppm, respectively. B. sphaericus against the first to fourth instars larvae the LC50 values were 46.16, 56.23, 69.82, 80.81 and 96.12 ppm and the LC90 values 141.68, 172.46, 184.21, 193.31 and 218.16 ppm, respectively. However, the combined treatment of T. purpurea + B. sphaericus (1:2) material shows highest larvicidal activity of the LC50 values 80.08, 82.21, 88.00, 92.21 and 98.16 ppm; The LC90 values of 108.39, 118.71, 136.75, 149.02 and 153.24 ppm, against A. aegypti in all the tested concentrations than the individuals and clearly established that there is a substantial amount of synergist act. Conclusion: The present study reported that both T. purpurea and B. sphaericus materials could serve as a potential larvicidal agent. Since, A. aegypti is a container breeder vector mosquito this user and eco-friendly and low-cost vector control strategy could be a viable solution to the existing dengue disease burden. Therefore, this study provides first report on the mosquito larvicidal activity the combined effect of T. purpurea leaf extract and B. sphaericus against as target species of A. aegypti.
Keywords: Aedes aegypti; Bacillus sphaericus; Dengue vector; Larvicidal activity.; Tephrosia purpurea

Neuropathic Pain: Literature Review and Recommendations of Potential Phytotherapies - Karim Raafat; Rawan El-Haj; Dania Shoumar; Rana Alaaeddine; Yousra Fakhro; Natalie Tawil; Farah Shaer; Amani Daher; Natalie Awada; Ali Sabra; Khouloud Atwi; Malak Khaled; et al. (Pharmacognosy Journal, 2017)
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

Neuroprotective Effect of Pedalium murex Linn. Leaf against Lipopolysaccharide Induced Behavioural Disorders in Rats - Swaminathan Gomathi; Rajagopal Shanmuga Sundaram; Vellaichamy Muthupandi Annapandian; Manickam Vijayabaskaran (Pharmacognosy Journal, 2017)
Introduction: Effective treatment is necessary to minimize the neuronal damage and oxidative stress. Traditional medicines offer potent pharmacological activity with minimal side effects compared to synthetic drugs to treat such chronic disorders. There is no renowned remedy for arrest or rescuing infection or inflammation-induced brain damage. The present study was aimed to evaluate the neuroprotective effect of ethanol extract of Pedalium murex Linn. (EEPM) leaves against lipopolysaccharide (LPS)-induced endotoxemia. Methods: Neurodegeneration was induced in rats with a single intraperitoneal injection of LPS (1 mg/kg). The induced endotoxemia constantly linked with battery of behavioural tests viz., choice reaction time task (CRT), 8-arm radial maze (RAM) and water maze test (WMT). At the end of the study, rats were sacrificed, brain hippocampal region was removed and biochemical parameters were measured. Results: In WMT swimming length (cm) was increased in LPS-treated rats when compared to control animals, the swimming length (EEPM; 400 mg/kg) was found to be significant; in RAM, different doses of EEPM at 100, 200 and 400 mg/kg decreased the number of errors in entry 4.00±0.36, 4.16±0.16and 3.33±2.79 respectively when compared with control animals (2.66± 0.21). EEPM at 400 mg/kg showed significant activity, in CRT apparatus increased incorrect lever pressing was observed in LPS-treated rats when compared to control animals. Incorrect lever pressing was minimized by EEPM at 400 mg/kg (43.5±2.40). Conclusions: Our results showed that EEPM is a hopeful aspirant for hindrance of infection and inflammation induced brain damage by LPS.
Keywords: Behavioural studies; Learning; Memory; Neuroprotective; Oxidative stress; Pedalium murex.

A Novel Approach towards Green Extraction for Glycyrrhitinic Acid by Ionic Liquid Based Microwave Assisted Extraction and Optimization through Response Surface Methodology - Meenu Bhan; Saurabh Satija; Chanchal Garg; Harish Dureja; Munish Garg (Pharmacognosy Journal, 2017)
Background: Extraction process plays an important role in extraction of herbal bioactive components. Ionic liquid based microwave assisted extraction (IL-MAE) has the potential to yield maximum analytes from the crude drugs in shorter time period with less solvent consumption and greater efficiency. Objective: The present study aimed to develop new protocol of Ionic Liquids based Microwave-assisted Extraction (ILs-MAE) of glycyrrhetinic acid from licorice; optimization of the protocol through RSM and comparison of IL-MAE with conventional extraction techniques like maceration and soxhlation by HPTLC. Materials and Methods: A novel ionic liquid-based microwave assisted extraction (IL-MAE) method was carried out for glycyrrhitinic acid from Glycyrrhiza glabra using ionic liquid, 1-butyl-3-methyl-imidazolium chloride ([bmim]Cl) and optimized by response surface methodology. The variable microwaveassisted extraction parameters selected were concentration of [bmim]Cl, extraction time and microwave power while solid-liquid ratio and extraction temperature were kept constant. Response surface methodology was applied for developing, improving and optimizing the whole process and comparison of IL-MAE with maceration and soxhlation by HPTLC. Results: The yield of glycyrrhitinic acid was found to be 0.48 % w/w in maceration in 7 days, 0.76 % in soxhlation in 3 h and 2.54 % w/w in IL-MAE in 4 min. Conclusion: IL- MAE of glycyrrhitinic acid from Glycyrrhiza glabra was proved to be better in respect of extraction efficiency, time and quantity of solvent used. Meanwhile, there was great reduction in the environmental pollution by using the green solvents/ ionic liquids (ILs), which is a great benefit to all.
Keywords: Glycyrrhitinic acid; Glycyrrhiza glabra; Microwave assisted extraction; Novel; Response surface methodology.; [bmim]Cl

Pharmacognostic and Antimicrobial Studies of Garcinia latissima Miq. Leaves (Clusiaceae) - Neneng Siti Silfi Ambarwati; Islamudin Ahmad; Berna Elya; Amarila Malik; Muhamad Hanafi (Pharmacognosy Journal, 2017)
Introduction: Garcinia latissima Miq known as Dolo magota (Maluku), is a medicinal plant belonging to the family Clusiaceae. The purpose of the research was to explore the phytoconstituents present, pharmacognostic details, and their antimicrobial efficacy. Methods: The preliminary phytochemical components were qualitatively examined using the standard method systems. The antimicrobial screening was carried out using the good diffusion method and the minimum inhibitory concentration (MIC) using dilution method. Results: The phytochemical screening of different extract of G. latissima Miq leaves revealed the presence of tannins, saponins, and alkaloids and the results were tabulated. The ethyl acetate and methanolic extracts from its leaves showed antimicrobial activity especially for Bacillus subtilis, a positive bacteria; the hexane extract did not show any activity against the selected microba. Conclusion: The results of the phytochemical and bio-efficacy study revealed most valuable information and also support the continued sustainable use of this leaves in the traditional system of medicine.
Keywords: Antimicrobial; Garcinia Latissima; Pharmacognostical; Phytoconstituent

Pharmacognostic and Cytotoxicity Evaluation of Indonesia Native Plant of Piper acre Blume Leaves (Piperaceae) - Islamudin Ahmad; Neneng Silfi Siti Ambarwati; Muhammad Arifuddin; Laode Rijai; Abdul Mun’im (Pharmacognosy Journal, 2017)
Piper acre Blume (Piperaceae) is an Indonesia native plant that is used as a traditional medicine and commonly known as ‘Sirih Hitam’ or ‘Sirih Hutan’. The scientific data from the plant is still very limited. The aims of the present study was to know a pharmacognostic, and cytotoxicity of P. acre Blume leaf. The macroscopic characters showed that the leaves have a characteristic odor, heart-shaped, margin was finely flat, venation was curved, the upper surface was dark green and slippery while the lower surface was pale green and soft. The microscopic characters revealed upper and lower epidermis cells, glandular trichomes, concentric vascular bundle, paracytic stomata. The fluorescence characteristics showed a variety of chemical constituents present in the plant materials. The preliminary phytochemical investigation of various extracts showed the presence of alkaloid, flavonoid, saponin, terpenoid, tannin, carotenoid, and steroid. The physicochemical properties (yield, color, consistency) of the n-hexane, ethyl acetate, and ethanol extract were 31.57% w/w (green concentrated solid), 13,59% w/w (green concentrated solid), and 16.35% w/w (brownish green liquid). Based on the cytotoxicity using brine shrimp lethality assay of the n-hexane extract (2.46 μg/ml), ethyl acetate extract (0.925 μg/ml), and ethanol extract (5.741 μg/ml) showed that the extract had the cytotoxic activity.
Keywords: Cytotoxicity; Pharmacognostic; Physicochemical; Piper acre Blume; preliminary phytochemical

Pharmacognostic and Phytochemical Characteristics of Ailanthus altissima (Mill.) Swingle Stem and Root Bark: A Comparative Study - Weekar Younus Raja; Zulfiqar Ali Bhat; Ishtiyaq Ahmad Chashoo (Pharmacognosy Journal, 2017)
Introduction: Ailanthus altissima (Simaroubaceae) is a large tree indigenous to China. It is known as the “Tree of Heaven”, used in traditional medicine in many parts of Asia, including China to treat cold, gastric diseases, diarrhea and endoparasites. It is also used as a bitter aromatic drug and as an antitumoral. Objective: The present study deals with comparative pharmacognostical parameters for the bark of stem and root of Ailanthus altissima, Mill. Swingle. Materials and Methods: The stem and root bark were collected, shade dried and powdered plant material was studied for its proximate values by standard methods. The extracts were subjected to a preliminary phytochemical screening for the detection of various phytoconstituents. Results: Proximate analysis revealed that the dry plant powder of stem bark has 6.48 % total ash, 0.42% acid insoluble ash, 4.60 % water soluble ash and for root bark 7.22 % total ash, 0.74% acid insoluble ash, 5.98 % water soluble ash. The Loss on drying for stem and root bark were found out to be 6.62 % and 10.46 % respectively. The stem and root bark of plant powder were found to possess phytoconstituents. Fluorescence analysis revealed the behaviour of the plant powder when treated with different chemical reagents. Conclusion: The present study reveals the preliminary phytochemical and proximate analysis of stem and root bark of Ailanthus altissima. Information obtained from these studies can be used as markers in the identification and standardization of this plant as a herbal remedy and also towards monograph development on the plant.
Keywords: Alkaloids; Fluorescence analysis; Proximate Analysis; Simaroubaceae; Tree of Heaven

Pharmacognostic and Phytochemical Standardization of White Tea Leaf (Camellia sinensis L. Kuntze) Ethanolic Extracts - Meiliza Ekayanti; Lia Ardiana; Sarah Zielda Najib; Rani Sauriasari; Berna Elya (Pharmacognosy Journal, 2017)
Background: Tea or also known as Camellia sinensis (Theaceae family) is the most popular plant and beverage in the world because of the sensory properties, prices are relatively cheap, stimulant effects, and their potential health benefits but white tea is not widely known. White tea is made from unfermented tea leaves young shoots protected from sunlight to avoid polyphenols degradation which inhibits of the chlorophyll formation and causing the white color on the leaf buds. Objective: The objective of research and development of herbal medicine is to improve the quality and safety of natural products. Materials and Methods: Macroscopical and microscopical features of the leaf have been analysis using an optical microscope and fragment analysis under scanning electron microscopy (SEM). Phytochemical and physico-chemical analysis were evaluated. The observation of the FTIR spectrum profiles is done by interpreting the typical peak that appears. Results: The leaf has actinocytic stomata, unicellular trichomes, heterogenous mesophyll which is characterized by the presence of calcium oxalate crystals and sclereid cells. Phytochemical analysis indicated resources the presence of tannins, flavonoids, glycosides and saponins.The content of polyphenol from white tea leaves ethanolic extract is 35.73% with the largest concentration of catechins is 18.84% and 17.43% tannins. The derivative content of catechins is EGCG with 7.37%. FTIR analysis showed functional groups of O-H, C-H, N-H, C=O, C=C, and C-O. Conclusion: Pharmacognostic and phytochemicals features established in this study may be used as part of the pharmacopoeial standard which can play an important role in its standardization.
Keywords: Characteristic; Macroscopic; Microscopic; Physico-chemicals; Phytochemicals; Theaceae.

Pharmacognostic Evaluation and Analgesic Efficacy of Ethanolic Extract of Euphorbia dracunculoides L. - Umbreen Khattak; Rehman Ullah; Shafqat Ali Khan; Barkatullah; Sami Ullah; Saima (Pharmacognosy Journal, 2017)
Background: Euphorbia dracunculoides L is available in market in raw form. It is used by people for the treatment of warts, snake bite and epilepsy. Present study is about Euphorbia dracunculoides L. belonging to the family Euphorbiaceae, comprises pharmacognostic study, physiochemical analysis and their pharmacological efficacy. Materials and Methods: The macroscopic study was carried out through sensory organs like size, shape, texture etc. Physiochemical analysis was carried out through proper procedure from relevant literature, and analgesic activity was done through proper method by following literature. Results: Macroscopic study showed that the plant is an annual herb, stem is branched from the base, yellow green at the bottom and light green at the top, glabrous, smooth, contains white latex, its leaves are sessile, alternate, dark green, simple, stipulated, sub-acute or acute at the apex and entire margin. Root is yellowish in colour, conical in shape, smooth texture, downward in position. Powder drug study which was performed revealed various structures. Phytochemical screening includes both qualitative and quantitative analysis which was carried out indicated the presence of carbohydrates, proteins, saponins, sterols, alkaloids, phenolic compounds, glycosides, flavonoids and tannins. Proximate analysis showed proteins, crude fat, crude fibre, carbohydrates, moisture contents and ash. Elemental analysis revealed the presence of macro and micronutrients i-e Na, Zn, Mg and Fe, Cu, Ag and Au. Analgesic effect was dose dependent. Plant extract showed maximum inhibition of writhing 1.66±0.32 (96.61%) at 300 μg/ml. Conclusion: The pharmacognostic study, physiochemical analysis and their pharmacological efficacy is helpful in the standardization of drug.
Keywords: Analgesic activity.; Euphorbia Dracunculoides L. Macroscopic Study; Pharmacognostic evaluation; Physio chemical Analysis; Powder Drug Study; Whole plant

Pharmacognostic Evaluation and Determination of Secondary Plant Metabolites by HPTLC and its Antioxidant Activity in Myrica esculenta - Prashant Kumar; Abhishek Gupta; Anita Singh (Pharmacognosy Journal, 2017)
Introduction: Myrica esculenta Buch.-Ham. (Myricaceae) is commonly known as Box Berry, Kaiphal, and Katphala in Ayurveda. As per the Ayurvedic literature the palnt is used for variety of diseases and disorders. Method: The present study deals with the pharmacognostical standardization, HPTLC analysis and antioxidant activity of methanolict extracts of the leaves of M. esculenta. The plant showed high phenolic and flavonoid content. In-vitro antioxidant study of dried leaves of Myrica esculanta was performed using methanolic extract. Results: Antioxidant activity of M. esculenta methanolic extract showed the least IC50 value of 60 ± 1.15 μg/ml. Standard ascorbic acid showed an IC50 value of 2.03 ± 0.06 μg/ml. The calibration curve of Gallic acid showed r2 of 0.949 and Rf of gallic acid was found to be 0.44 ± 0.006. Quantification of gallic acid in the samples of leaves of M. esculenta has been performed and the gallic acid was found to be 0.056%. Conclusion: The presence of gallic acid has not yet been reported and quantified in this species which may be utilized for the proper standardization of the drug. The present study showed new natural antioxidant that can replace the synthetic ones to be used in foods and cosmetics.
Keywords: Antioxidant; DPPH; Gallic acid; HPTLC; Myrica Esculenta

Pharmacognostic Evaluation & Antimicrobial Activity of Endangered Ethnomedicinal Plant Crepidium acuminatum (D. Don) Szlach - Mamta Arora; Gurjinder Kaur; Parvinderdeep S Kahlon; Anupama Mahajan; Jaspreet K Sembi (Pharmacognosy Journal, 2017)
Background: Crepidium acuminatum (D. Don) Szlach (family Orchidaceae) is an ethnomedicinal plant. It is used in breathing disorders, burning sensation, Cough, decrease in bone tissue, blood disorders, tuberculosis, as refrigerant, aphrodisiac, in insect bites, rheumatism, as tonic and in general debility. It is vital component of Ayurvedic formulation “Astavarga” with trade name “Jeevak means vitality of life. Despite the common utilization of this plant, no conclusive study has been reported so far regarding the pharmacognostic evaluation and antimicrobial activity. Aim: The present study was carried to evaluate pharmacognostic evaluation and the potential of C. acuminatum as antimicrobial. Materials and Methods: Organoleptic, histochemical, microscopic, physicochemical, extractive yield were studied to standardise pharmacognostic characters and well diffusion method were carried out for antimicrobial activity. Five extracts viz. Hexane, Chloroform, Ethanol, Ethyl acetate and aqueous were evaluated against 4 bacterial strains viz. E. coli (MTCC 40), S. aureus (MTCC 87), P. aeruginosa (MTCC 424), B. subtilis (MTCC 121). Results: The diagnostic characters were evaluated and documented. All the extracts showed good antimicrobial activity. Conclusion: Obtained standards will provide referential information for correct identification, purity, standardization and preparation of monograph. The work confirms that the studied plant has potent antimicrobial activity and has potential for antimicrobial drug. These results may constitute a basis for promising future applied research that could investigate the use of this plant as antimicrobial drug.
Keywords: Antimicrobial; Crepidium acuminatum (D. Don) Szlach; Histochemical; Pharmacognostic evaluation; Physicochemical; Zone of Inhibition

Pharmacognostic Evaluation of Leaf and Stem Wood Extracts of Artocarpus hirsutus Lam. - Mahadeva Nayak; Ananthanarayanan Nagarajan; Muhammed Majeed (Pharmacognosy Journal, 2017)
Introduction: Artocarpus hirsutus Lam., a plant known for its fruits, used as a traditional medicine to treat skin diseases including hydrocele, pimple, heal sores, cracks in the skin. Pharmacological studies on the bark, root, leaf and fruit extracts of this species support their significance as antioxidants, as well as their efficacy on diuretic, antibacterial, anti-fungal and antiulcer activity. Methods: The present study focused on microscopic study, phytochemical analysis, HPLC and HPTLC finger print evaluation of leaf and stem wood extracts. Results: Microscopic analysis demonstrates its characteristic parameters namely hairy trichomes, pearl glands, vascular bundles, epidermis and is expected to assist easy identification of the genus. Conclusion: The solvent system, chloroform:methanol (8:2) was found to be the best as TLC eluent to visualize all major components of this species. HPLC and HPTLC finger prints not only confirm the presence of two major components, oxyresveratrol and artocarpin in stem wood extract, but also prove their absence in the leaf extract.
Keywords: Artocarpus hirsutus Lam.; HPLC.; HPTLC finger prints; microscopy; Phytochemical analysis

Pharmacognostic, Phytochemical and Physicochemical Investigations of Hypericum hookerianum Wight & Arn. (Hypericaceae) of Palni Hills, India - Mahendrakumar M; Nirmalraj S; Ravikumar M; Bharath B; Seeni S; Perinbam K (Pharmacognosy Journal, 2017)
Introduction: Hypericum hookerianum Wight and Arn. (Hooker’s wort) is a lesser known unfamiliar yet critically endangered native therapeutically active native medicinal plant. It is being characterized by the presence of various secretory glands. Methodology: In this present study, characterization of the plant in terms of morphology, anatomy and histochemistry of tissues and phytochemicals and antimicrobial potentials were made. Results: The epidermal layer contains oil cells while histochemistry showed the presence of the secondary metabolites. Qualitative analysis indicated presence of maximum phytocompounds in the high polar ethanolic extract; flavonoids, anthocyanin and phenol are prominently present and quantified. Conclusion: The results suggest that the less studied herb, H. hookerianum is a multifaceted high value species having a wide range of phytochemicals with abundant medicinal properties.
Keywords: Hypericum hookerianum; Palni Hills.; Pharmacognosy; Physiochemistry

Pharmacognostic Specification and Mangiferin Content of Aquilaria crassna Leaves. - Worathat Thitikornpong; Boonsri Ongpipattanakul; Chanida Palanuvej; Nijsiri Ruangrungsi (Pharmacog Journal, 2017)
Background: Aquilaria crassna Pierre ex Lecomte (Thymelaeaceae) has been used as a medicinal plant in many aspects. Previous research has revealed that A. crassna leaves contain mangiferin as an active compound. Although the active component has been investigated, the pharmacognostic specification and quantification of mangiferin from A. crassna leaves have never been established. Objective: The current study aimed to conduct and develop a pharmacognostic standard according to WHO guidance as well as the validated method for quantifying mangiferin content. Materials and Methods: Dried A. crassna leaves from 15 separated locations throughout Thailand were investigated for pharmacognostic specification. Their mangiferin contents were quantitatively analysed by TLC densitometry with win CATS software. Results: Macroscopic-, microscopic- characteristics and TLC fingerprinting combined with physicochemical parameters were reported in this study. The loss on drying, moisture content, and total ash content as well as acid-insoluble ash content were determined to be 8.62 ± 0.13, 8.16 ± 0.14, 6.82 ± 0.09 and 1.49 ± 0.03%, respectively. Ethanol- and waterextractive values were found to be 9.05 ± 0.39 and 16.94 ± 0.22 %, respectively. In addition, the validation method for quantifying the mangiferin content was developed. The contents of mangiferin in A. crassna leaf extract determined by TLC-densitometry and TLC-image analysis were found to be 1.2992 ± 0.5980 and 1.3036 ± 0.5874 % by dried weight, respectively. The results between these two analytical methods were shown to have an insignificant difference. Conclusion: This study provides the necessary information for authentication and standardisation of A. crassna leaves.
Keywords: Aquilaria crassna leaves; Mangiferin; Pharmacognostic specification; TLC image analysis; TLC-densitometry

Pharmacognostic Standardization and Chromatographic Fingerprint Analysis on Triterpenoids Constituents of the Medicinally Important Plant Plumeria rubra f. rubra by HPTLC technique - Gunja Srivastava; Abhishek Gupta; Manjul Pratap Singh; Anurag Mishra (Pharmacognosy Journal, 2017)
Introduction: Plumeria rubra f. rubra commonly known as Lal Gulachin has wide horizon of medicinal possessions. Plant is found in India and in its tropical regions. Though the plant and its extracts have been indigenously valued as folklore medicine diversely in India, yet literature lacks somewhere in reverse pharmacognostical approach of this plant which reflects that plant have not been evidently explored therapeutically. There are several forms of Plumeria rubra among which P. rubra f. rubra is much appraised in India than its other forms. Method: In Present study the anticipated potential of this plant has been validated by laying down its pharmacognostical standards along with measurement of its active therapeutic constituent Ursolic acid and Lupeol via. HPTLC, information from organized search of published literature remarks that Ursolic acid and lupeol is ubiquitous to this plant. Results: Microscopic features revealed the presence of paracytic type of stomata, crescent bicollateral vascular bundle, calcium oxalate crystal and clothing trichomes in leaves whereas bark showed the presence of distinct periderm with cork and phellogen, sclereids, bast tissue with parenchymatous cells. Methanolic extract of both parts of plant was subjected to HPTLC. In HPTLC studies the Ursolic acid content in leaves was found to be 0.96% whereas in bark was detected as 0.051%, lupeol content in leaves and stem was found to be 0.014% and 0.018%. Conclusion: The data generated could be significantly used as reference for the standardization and quality control of Plumeria. rubra f. rubra, as no such work has been reported yet.
Keywords: HPTLC; Lupeol; Pharmacognosy; Plumeria rubra f. rubra; standardization; Ursolic acid

Pharmacognostic Studies and HPLC Analysis of Roots of Helicteres isora (L.) - Pinal A. Harde; Mamta B. Shah (Pharmacognosy Journal,, 2017)
Background: The juice of roots of Helicteres isora Linn. has been widely used as an antidiabetic in traditional medicine. Objective: The present study deals with pharmacognostical studies and determination of oleanolic acid from the roots of H. isora by new HPLC method. Materials and methods: Detailed study of morphological, microscopical characteristics, physicochemical parameters and phytochemical screening of roots were carried out. The sapogenins were isolated from the roots of H. isora. RP-HPLC method was developed and validated for estimation of oleanolic acid from the sapogenins of roots of H. isora. Results: Detailed quality control parameters of roots of H. isora were reported. Total content of oleanolic acid was 0.075%w/w from roots of H. isora determined by HPLC. Conclusion: The present study is useful for accurate identification and authentication of roots of H. isora. The HPLC method for determination of oleanolic acid from the roots of H. isora is efficient, precise, reliable and sensitive and can be adopted for routine analysis.
Keywords: Helicteres isora; HPLC; Oleanolic acid; Sapogenins

Pharmacognostic Studies and Nephroprotective Potential of Hydroalcoholic Extract of Trichosanthes cucumerina in Acute Renal Failure - Doppalapudi Prasanthi; Sreedevi Adikay (Pharmacognosy Journal, 2017)
Objective: The present research work unearthed not only pharmacognostic features of the seeds of Trichosanthes cucumerina but also the nephroprotective activity of 60% hydro alcoholic extract against Cisplatin-induced Wistar rat model. Materials and methods: Present study dealt with the detailed pharmacognostic study of the seeds of Trichosanthes cucumerina. 60% hydro alcoholic extract was prepared by hot extraction method. Preliminary phytochemical screening was carried out. Based on acute toxicity studies nephroprotective effect of the extract was screened at 200 and 400 mg/kg, b. w. in curative and prophylactic regimen. Nephrotoxicity was induced in male Wistar rats by administration of Cisplatin (5mg/kg, b.w. i.p. as a single dose). Nephroprotective activity was assessed by estimating serum markers and urinary functional parameters supported by anti-oxidant studies and histopathological aspects. Results: Microscopic studies showed that the seed coat had outer aerenchymatous tissue, inner parenchymatous tissue and innermost compact lines of sclereids. Physicochemical evaluation yielded alcohol and water soluble extractive values of 20.8 and 8.05%w/w. Total ash, acid insoluble and water soluble ash values were 7.15, 6.45 and 0.5 respectively. Fluorescence analysis imparted characteristic colours to the seed powder when observed under visible and UV light. Cisplatin-induced nephrotoxicity was indicated by increased levels of serum markers and urinary functional parameters which were reversed by the extract in dose dependent manner. The results were substantiated by anti-oxidant studies and histopathological studies. Conclusion: Various pharmacognostic parameters evaluated assisted in identification and standardization of seeds of Trichosanthes cucumerina in crude form. Present study revealed that hydroalcoholic extract attenuated the nephrotoxicity and provided the strengthened scientific evidence for the use of seeds of Trichosanthes cucumerina in nephrotoxicity.
Keywords: Anti-oxidants; Cisplatin; Histopathological studies; Pharmacognostic studies; Trichosanthes cucumerina

Pharmacognostical and Physicochemical Analysis of Cleome viscosa L. Seeds - Harpreet Singh; Amrita Mishra; Arun Kumar Mishra (Pharmacognosy Journal, 2017)
Aim: The seeds of Cleome viscosa L. are used to treat tumor, emesis, diarrhea, epilepsy and hyperthermia. Seeds are used to heal wound also. In order to ensure the use of only genuine and uniform material in treatment of ailments by herbs and herbal formulations, pharmacognostical standardization and physiochemical parameters evaluation is needed. Methods: Morphological and powder microscopic characters of seed powder were studied. The physiochemical parameters studied were LOD, total ash, acid insoluble, water soluble, sulphated ash, extractives, volatile oil content and crude fibre content etc. Further, florescence analysis and element analysis of seed powder was performed by undergoing chemical reaction +UV method and EDAX method respectively. Results: Brown colored seeds with rough seed surface with seed size 0.1 cm were recorded. The pods were brown coloured when air dried. They were 4-5 cm long containing 8-12 small seeds. Powder microscopic study revealed the presence of fragment of epidermis of testa, groups of cells resembling like stone cells and irregularly shaped protein bodies were observed. Florescence Analysis revealed the presence of chromophores. EDAX analysis showed the presence of Mg, Al, Si, S, Cl, K, Ca and Cu etc in different amount. Conclusion: Pharmacognostical and physiochemical parameters were established which would facilitate quick identification and selection of the herbal drugs from various adulterants.
Keywords: Cleome viscosa L.; Crude fibre; Macroscopic; Microscopic; Physicochemical

Pharmacognostical and Physico-chemical Standardization of Euphorbia neriifolia Leaves. - Prashant Y. Mali; Shital S. Panchal (Pharmacognosy Journal, 2017)
Objective: To investigate pharmacognostical and physico-chemical standardization of Euphorbia neriifolia leaves. Materials and Methods: Fresh and dried leaves with powder samples of E. neriifolia were examined macroscopically and microscopically. As per Ayurvedic Pharmacopeia of India and World Health Organization guidelines on quality control methods for medicinal plants materials suggested parameters were determined for standardization of E. neriifolia leaves. Physico-chemical, primary phytochemical, fluorescence and quantitative screenings along with primary HPTLC fingerprinting assessment were performed. Results: Macroscopic examination demonstrated that fresh leaf of E. neriifolia has dark green in colour, herbaceous odour with characteristic taste. Dried leafs are grey brownish in colour, characteristic odour with broken crumpled and papery fracture. Microscopy of leaf showed the single layered thick rectangular or tubular adaxial epidermal cells. Mesophyll tissue was differentiated into two or three layered adaxial zones of radially elongated palisade cells and wider abaxial spongy mesophyll cells revealed the differentiated dorsiventral lamina. Mid-rib composed of epidermis, collenchymas and spongy parenchyma cells. Physico-chemical parameters like, foreign matter was found to be 0.46%. Total ash, acid insoluble ash and water soluble ash was found 6.33%, 1.23% and 6% respectively. Loss on drying was found to be 4.69%. Swelling and foaming index was found 11.7 ml and 333 ml respectively. Quantitative screening suggested that the leaf powder has indicated alkaloid and saponin estimation as 0.26% and 3.67% respectively. The HPTLC fingerprinting of EN6 extract fraction was showed the Rf values at 254 nm with their respective UV-visible spectrum wavelengths scanned in between 200-400 nm. They are 0.01 (265 nm), 0.05 (369 nm), 0.09 (263 nm, 264 nm), 0.18 (400 nm), 0.20 (279 nm), 0.31 (400 nm), 0.44 (378 nm), 0.45 (382 nm), 0.54 (377 nm), 0.55 (383 nm), 0.62 (400 nm), etc. at different concentrations of sample application. The HPTLC plate was also scanned at 366 nm and 540 nm. Conclusion: The present investigation is an additional standardization research in support with previous reports and will be helpful for qualitative and quantitative standardization of herbal formulations containing E. neriifolia. Further investigations are going on this extract fraction in reference to identification, quantification and validation of HPTLC methods using various standard marker compounds along with exploration of its pharmacological activities.
Keywords: Euphorbia Neriifolia; HPTLC.; Macroscopic; Pharmacognostical; Physico-Chemical

Pharmacognostical Standardization & Phytochemical Evaluation of Alphonsea sclerocarpa Thwaites Bark & Leaves - Venkata Naga Anantha Sandhya Rani Nandyala; Kothapalli Bonnoth Chandrasekhar (Pharmacognosy Journal, 2017)
Introduction: The genus Alphonsea sclerocarpa Thwaites (Annonaceae) includes species distributed widely in the tropical areas. Whole plant of Alphonsea sclerocarpa is traditionally believed for its eminent therapeutic benefits. Despite its medicinal properties the plant seems to be less explored and hence this research aims at exploring the Pharmacognostical parameters for standardization. Physicochemical and Phytochemical analysis was also carried out to establish quality control parameters for the drug. Methods: Morphoanatomical (Transverse Section of Leaf Lamina & Margin, Radial Longitudinal Section & Tangential Longitudinal Section of phloem in bark) and Powder microscopic analysis were carried out by employing Formalin fixed as well Macerated specimens. Physicochemical Parameters like Loss on drying, Ash Value, Extractive values etc were carried out as per WHO guidelines. Phytochemical Analysis was also carried out and the phytochemical profile was established. Results: Transverse section of Leaf revealed the presence of Plano convex vascular bundles. Ensheathed by a bundle of sclerenchyma. Transverse section of bark has shown the presence of highly compressed, heavily suberised phellem cells. Tangential longitudinal section (TLS) revealed the presence of Spindle shaped bi or Multi seriate medullary rays. In Radial longitudinal section (RLS) the phloem cells appear rectangular and thin walled. Powder microscopy revealed the presence of Fibres, fibre-tracheids and Calcium oxalate crystals. Total ash value of Bark & Leaf was found to be 8.75 & 7 % respectively. Conclusion: The established Pharmacognostical, Physico-chemical & Phytochemical parameters will suffice for establishing Monographs for the plant drug.
Keywords: Monograph; Radial Longitudinal Section; standardization; Tangential Longitudinal Section

Phenolic Constituents, Anti-Inflammatory and Antidiabetic Activities of Cyperus laevigatus L. - Abdelsamed Ibrahim Elshamy; Mohamed El-Shazly; Yomna Mahmoud Yassine; Mona Anwar El-Bana; Abdel- Razik Farrag; Mahmoud Ibrahim Nassar; Abdel Nasser Singab; Masaaki Noji; Akemi Umeyama (Pharmacognosy Journal, 2017)
Background: Cyperus species are well known traditional plants and used for several diseases around the world. Aim of the Study: Our study aimed to identification of the phenolic constituents in addition to evaluation of different extracts of Cyperus laevigatus L as antioxidant, antiinflammatory and antidiabetic agents. Materials and Methods: The phenolic constituents were identified using spectroscopic techniques. The antioxidant activity was evaluated using in vitro DPPH assay. Total extract, methanol and EtOAc fractions were evaluated for their antiinflammatory activity using RAW 264.7 macrophages assay. Antidiabetic activity of the total extract was examined biochemically and histopathologically using streptozotocin-induced diabetic rats. Results: A new flavone, chrysoeriol 7-O-β-(6‴-O-acetyl-β-D-glucopyranosyl)-(1→4) glucopyranoside (1), along with seven knowns (2-8) were isolated from Cyperus laevigatus L. The structures of isolated compounds were established depending upon 1D, 2D-NMR and HR-ESI-MS. The MeOH and EtOAc fractions exhibited significant antioxidant activity while the isolated flavonoids exhibited from moderate to weak antioxidant activity. The total extract, MeOH and EtOAc fractions exhibited significant anti-inflammatory activity using LPS-stimulated RAW 264.7 macrophages model by decreasing of NO accumulation by 76 – 66% and 84 – 67%, of the original accumulation values with increasing concentrations in comparison with the reference drug, dexamethasone. The total extract exhibited antidiabetic activity in streptozotocin-induced diabetic rats and this effect was manifested by decreasing serum levels of glucose, glucagon and NO. It also increased level of insulin and promoted paraoxonase activity. Conclusion: These results proved that this plant may be multiple sources for medicinal natural drugs especially for anti-inflammatory and antidiabetic.
Keywords: Anti-inflammatory; Antidiabetic.; Antioxidant; Cyperus Laevigatus; New Flavone

Photodynamic Toxicity of Chlorophyllin against Fasciola gigantica Carrier Snail Indoplanorbis exustus in Visible Spectral Band - Divya Chaturvedi; Dinesh Kumar Singh; Vinay Kumar Singh (Pharmacognosy Journal, 2017)
Background: Fasciolosis is one of the most debilitating diseases caused by liver flukes Fasciola hepatica and F. gigantica. Snail Lymnaeidae and Planorbidae is the intermediate host of these flukes. Snail population management is a good tool to control fasciolosis because gastropods represent the weakest link in the life-cycle of trematode. Aim of the present study is to explore the molluscicidal activity of chlorophyllin in visible spectral band against Fasciola gigantica carrier snail Indoplanorbis exustus. Methods: Chlorophyll was transformed into water-soluble chlorophyllin in 100% ethanol by using different types of chemicals. Ten snails Indoplanorbis exustus were placed in a glass aquarium containing 3 L of dechlorinated tap water. These snails were treated with different concentrations of chlorophyllin in sunlight as well as exposed to different visible spectral band of light. Results: Pure chlorophyllin (96 h LC50 6.54 mg/l) in sunlight was more toxic than extracted chlorophyllin (96 h LC50 939.65 mg/l). There was a significant variation in the toxicity of chlorophyllin with snails, exposed to visible spectral band of light. The highest and lowest toxicity of chlorophyllin against I. exustus was noted in yellow light (96 h LC50 2016.79 mg/l) and green light (96 h LC50 2433.16 mg/l). High performance liquid chromatography (HPLC) study reveals that the active molluscicidal component extracted in spinach leaves is chlorophyllin. Conclusion: Due to the photodynamic nature of chlorophyllin, it has the potential to control the population of vector snails and ultimately fasciolosis in developing countries.
Keywords: Chlorophyllin; Fasciolosis; Indoplanorbis exustus; Photodynamic Product; Visible light band.

Phytochemical and Quality Assessment of Acacia nilotica Linn and Acacia leucophloea willd Flowers - Raju Ilavarasan; Leela Vadivelu (Pharmacognosy Journal, 2017)
Objective: The quality criteria for herbal drugs are based on a clear scientific definition of the raw material. Even though global herbal resources have a great potential as natural drugs and are of great commercial importance, they are very often procured and processed without any scientific evaluation, and launched onto the market without any mandatory safety and toxicology studies. On that basis, an attempt was made on a well-known herbal drug A.nilotica flower and A.leucophloea flower by evaluation of phytochemical and toxicological parameters like heavy metals, aflatoxins, total microbial load and pesticide residues. Method: The procedures recommended in AOAC, ASTA were followed to determine analysis of heavy metals, aflatoxins, microbial load and pesticide residues. Thin layer chromatographic technique was used to separate the chemical compounds present in the drug. Result and Conclusion: Results obtained during this experiment revealed that heavy metals, aflatoxins, total microbial load and pesticidal residues were variable but found within the prescribed limits. Phytochemical evaluation revealed that the catechin phytoconstituents is absent in A.leucophloea flowers when compared with A.nilotica flowers. Hence, there is an urgent need for mandatory evaluation of these parameters in every crude drug before further processing to ensure safety and efficacy of Indian medicinal plants for better acceptance at International platform. The study revealed specific identities for the particular crude drug which will be useful in identification and control to adulterations of the raw drug.
Keywords: A. leucophloea; A. nilotica flowers; Phytochemical; TLC and Catechin

Phytochemical Evaluation and Chromatographic Fingerprint Analysis on Flavonoids Compounds in Leucas aspera (Willd.) Link Leaf by HPTLC - Vellaichamy Muthupandi Annapandian; Rajagopal Shanmuga Sundaram; Swaminathan Gomathi (Pharmacognosy Journal, 2017)
Introduction: Leucas aspera is one of the important medicinal plants in Indian medical system and it belongs to Lamiaceae family. Leucas aspera (Willd) Link (L. aspera) belongs to Leucas genus, widely distributed throughout India. L. aspera has many vernacular names and is commonly known as Thumbai. Flavonoid is a phenolic compound which is widely distributed in the plants and responsible for many biological activities. Preliminary phytochemical analysis gives a broad idea to the researchers for their further research. Methods: In this present study, we did a preliminary phytochemical screening, quantitative estimation of total flavonoids and fingerprinting profile of flavonoids compounds using five different solvent extracts obtained from leaves of L. aspera. Results: Preliminary phytochemical screening confirmed the presence of flavonoid compounds in L. aspera. Higher concentration of total flavonoid compounds was noted in ethanol extract compared to petroleum ether, chloroform, isopropyl alcohol and ethyl acetate extracts. A densitometric high performance thin layer chromatography (HPTLC) study showed more number of flavonoid compounds are present in ethanol extract compared to other solvents. Conclusions: Results of this study revealed, L. aspera leaf is a rich source of flavonoid content and it can be used to alleviate many chronic illness and various diseases. This study results warrants for further isolation, identification and characterization of active principle which is responsible for the biological activity.
Keywords: Chromatographic; Fingerprinting; Flavonoids; HPTLC; Leucas aspera.

Phytochemical, Free Radical Scavenging Activity and Thin Layer Chromatography Analysis of Methanolic Extracts of Six Wild Mushroom Species Collected From the Shai Hills Reserve of Ghana - Ebenezer Owusu; Gladys Schwinger; Matilda Dzomeku; Mary Obodai; Isaac Asante (Pharmacognosy Journal, 2017)
Objective: Six different mushroom species (Termitomyces, Ganoderma, Amauroderma, Mycena, Marasmus and an unknown) were studied to ascertain their phytochemical and antioxidant properties and determine their TLC analysis of methanolic extracts. Materials and Methods: The DPPH (1,1-diphenyl-2-picrylhydrazyl) model was employed to determine free radical scavenging activity of the methanolic extracts of the mushrooms, aluminum chloride calorimetric method for flavonoid, Thin layer chromatography (TLC) for retention factor and atomic absorption spectrophotometric (AAS) for macro and micronutrients. Results: Phytochemical analyses of the methanolic extract revealed the presence of antioxidants, phenols and flavonoids. The antioxidant values (IC50 (μg/ml)) ranged from 1.56 x 10-4 to 21.07 x10-4.Total phenol content ranged between 2.54 and 17.53 mg/g GAE with a mean of about 11.27 mg/g GAE. Total flavonoid content also ranged from 5.46 to 23.75 mg/g RUE with a mean of 13.41 mg/g RUE. Micronutrients such as cadmium, iron, lead, manganese and zinc were determined. Also macronutrients determined included, calcium, potassium, magnesium and sodium. Sodium ranged the highest with values ranging 6966.67 mg/L to 9600.00 mg/L followed by iron ranging from 1613.67 to 3040.00 mg/L. Percentage crude protein ranged between 11.09 % and 28.24 %. Alkaloid was present in only Mycena sp and Ganoderma sp with a band each of Rf value of 0.49. A total of 18 different bands were recorded for flavonoid with Rf values that ranged between 0.20 and 0.97, respectively. Conclusion: The antioxidant potential of the methanolic extracts of the mushroom samples in this study recorded higher values. This indicates that mushrooms have high antioxidant properties and rationalizes further investigation in the potential discovery of new natural bioactive principles from these mushrooms.
Keywords: Antioxidant; Extracts; Flavonoids; Mushrooms; Phytochemical

Phytochemical Investigation and Pharmacognostic Standardization of Polycarpaea corymbosa Lam - Karuna Modi; Mamta Shah (Pharmacognosy Journal, 2017)
Background: Polycarpaea corymbosa is one of the plants cited as ‘Parpata’ in Ayurvedic literature and indicated for boils, inflammatory swellings, and ulcers. Aim: The present study is an attempt to generate and encompass the data of physical parameters for ascertaining the identification and develop a validated HPTLC method for quantification of lupeol in P. corymbosa. Materials and Methods: The whole plant was studied for establishing pharmacognostic standards including macro and microscopical characters, physico-chemical analysis and quantification lupeol by HPTLC method. Results: It is a small, much branched, erect or spreading herb with linear leaf and silvery-white cymes. Microscopically root can be connoted by continuous or discontinuous concentric rings of xylem and phloem; stem by papillose epidermis with multicellular branched collapsed and glandular trichomes, sclerenchymatous pericycle and hollow pith; and leaf by numerous collateral meristele enclosed within parenchymatous bundle sheath. Further studies evinced that brunt of heavy metal and microbial load in plant material was within permissible limits. Flavonoids, phenolics and saponins were found be major components. HPTLC method was developed for quantification of lupeol using precoated silica gel plates as a stationary phase, and toluene: methanol (9.4: 0.6) as a mobile phase and scanning the plate at 545 nm. Conclusion: The information demonstrated on pharmacognostic parameters and validated HPTLC method for estimation of lupeol for Polycarpaea corymbosa, would aid as coherent measures for its assessment.
Keywords: HPTLC; Lupeol; Parpata; Pharmacognostic study; Polycarpaea corymbosa.

Phytochemical Screening and Antimicrobial Activity of Rhizomes of Hedychium spicatum - Ritu Arora; Avijit Mazumder (Pharmacognosy Journal, 2017)
Background: The use of and search for drugs and dietary supplements derived from plants have accelerated in recent years. Objective: In this study the rhizomes of Hedychium spicatum (Zingiberaceae) were evaluated for phytochemical parameters & antimicrobial activity by determining its MIC (by checker board method) and zone of inhibition (by cup plate method). Phytochemical parameters were studied with the aim of drawing the pharmacopoeial standards for this species. This study was also designed to evaluate the antimicrobial efficacy of the methanolic extract of the rhizomes of H. spicatum against various diarrhea and dysentery causing drug resistant microorganisms isolated from patients admitted in hospitals. Methods and Material: The raw materials of H. spicatum were procured from the local supplier. Various Microbial strains included various drug resistant hospital isolates collected and characterized in the Dept. of Pharmaceutical Technology, Jadavpur University, India. Results: It was evident from the results that the extract was highly active against Shigella boydii, Shigella. soneii, Shigella flexneri, B. cereus, Vibrio cholera, E. coli, S. aureus, Ps. aeruginosa and K. pneumoniae. The result of determination of zone of inhibition was compared with that of standard drug (Ciprofloxacin). This study has pointed to the potential application of H. spicatum as a bactericide and fungicide. Conclusions: The findings of this study further reinforces the importance of H. spicatum rhizomes in traditional healthcare practice and its use in culinary. Further investigation is however needed to isolate and purify the bioactive antimicrobial principles for potential development into generic antimicrobials.
Keywords: Bactericide; Diarrhea. H. spicatum; Fungicide; MIC

Phytochemical Screening and Content Determination of Different Species of Genus Caesalpinia belonging to Different Origin with Antidiabetic Activity - Amna Parveen; Zahra; Muhammad Qudratullah Farooqi; Whang Wan Kyunn; Muhammad Arshad (Pharmacognosy Journal, 2017)
Aim: The main aim of the study is to investigate the phytochemical screening of C. decapetala along with the content determination of different species of genus Caesalpinia with respect to their antidiabetic activity and identification of most bioactive species belonging to different origins. Methods: To achieve our goal different species of genus Caesalpinia collected from China and Pakistan were subjected to open column chromatography, High Pressure Liquid Chromatography (HPLC), antioxidant, and antidiabetic assays for evaluation. Results: From η-BuOH fraction of C. decapetala extract, eight compounds were isolated using open column chromatography and identified as apigenin-7-rhamnoside (1), 4-O-methylepisappanol (2), caesalpinol (3), daucosterol (4), astragalin (5), kaempferol (6), quercitrin (7), and naringin (8) using Nuclear Magnetic Resonance (NMR) spectroscopy. HPLC analysis of different species of genus Caesalpinia showed that the most active antidiabetic compound ‘quercitrin’ was present more in C. pulcherrima followed by decreasing order in C. sappan, C.decapetala, and C. bonduc. Conclusion: The results indicated that quercitrin is the most bioactive content and C. pulcherrima is most bioactive specie of China origin from genus Caesalpinia.
Keywords: Antidiabetic; Antioxidants; Caesalpinia; Flavonoids; HPLC Fingerprint; Phytochemical content.

Phytochemical Screening, GC-MS, FT-IR Analysis of Methanolic Extract of Curcuma caesia Roxb (Black Turmeric) - Muthukumaran Pakkirisamy; Suresh Kumar Kalakandan; Karthikeyen Ravichandran (Pharmacognosy Journal, 2017)
Aims: The purpose of the current study is to monitor the phytochemical constituents in the Curcuma caesia Roxb.by GC MS and FT-IR analysis. Methods: The Rhizomes of Curcuma caesia Roxb was extracted with Methanol at room temperature for 8 h. The bioactive compounds of Curcuma caesia Roxb have been evaluated using GC-MS and FT-IR. Results: Preliminary phytochemical analysis revealed the presence of tannins, terpenoids, flavonoid, alkaloid, phenol, phytosterol Quinones and saponins. Totally 15 compounds were identified and the chromatograph showed peaks with individual compounds. The major constituents were identified in the Methanolic extract were α-Santalol (46.90%), Retinal (10.72%), Ar-tumerone(10.38%), Alloaromadendrene (5.93%), Megastigma-3,7(E),9-triene (4.80%), Benzene, 1-(1,5-dimethyl- 4-hexenyl)-4-methyl(4.38%) , 5,8,11,14,17-Eicosapentaenoic acid, methyl ester, (all-Z)-(4.26%) Tricyclo[8.6.0.0(2,9)]hexadeca-3,15-diene, trans-2,9-anti-9,10-trans-1,10 (3.26%) and many other compounds were identified as low level. The FTIR analysis confirmed the presence of N-H , O-H , C=C , C-H, C-O and CH3 functional groups. Conclusion: The result of this study offer a platform of using Curcuma caesia Roxb as herbal alternative for various diseases and it can be used as functional and pharmaceutical food.
Keywords: Curcuma caesia Roxb; FT-IR; GC MS; Phyto chemical; α-Santalol and Retinal.