Phyto-Pharmacognostical Studies and HPTLC Fingerprinting Profile of Uvaria narum (Dunal) Wall. Ex Wight - Kalpana Sabanna Patil; Raju Ratan Wadekar (Pharmacognosy Journal, 2017)
Objective: To study the pharmacognostic characters and phytochemical investigation of medicinally important crude drug, Uvaria narum (Dunal) Wall. Ex Wight (Annonaceae) Methods: Organoleptic characters, microscopic evaluation, leaf constants, quantitative physico-chemical evaluations (Ash value, extractive value, moisture content), preliminary phytochemical screening, quantitative estimation of total phenolic and flavonoid content in alcoholic and aqueous extract of Uvaria narum and HPTLC fingerprinting profile were studies on leaves of Uvaria narum by employing standard methods of analysis. Results: Leaf is dorsiventral, having distinct upper and lower surface. Stomata are of paracytic type and present only on lower epidermis. Upper epidermal cells are polygonal with cuticle and contain simple starch grains. A single layer of palisade cells is present below upper epidermis. Leaf do not bears any trichomes. Mid rib region shows collenchymatous cells on both surfaces. Xylem bundles are arranged in an arc. The space between collenchymas and vascular bundle is occupied by parenchymatous cells, some of which are filled with calcium oxalate crystals of prism as well as of rosette type (30-40 m in diameter). HPTLC fingerprint study of alcoholic and aqueous extracts confirmed the presence of quercitin as biomarker polyphenolic compound. Conclusion: These findings will be useful in establishing pharmacognostic and phytochemical standards for correct identification, as well as assessment of purity, quality of this plant, which definitely gaining the relevance in plant drug research and establishment of plant monograph.
Keywords: Histochemical evaluation; HPTLC fingerprinting; Morpho-Anatomical; Physicochemical; Uvaria Narum

Pre and Post-Treatment Effects: Estimation of Serum Testosterone and Lipid Peroxidation Levels on Moringa olifera Extract Induced Cadmium Exposed Rats - Pratik Kumar Chatterjee; Vinodini Nithyananda Madom Anantharaya; Rashmi Kaup Shiva; Nayanatara Arun Kumar; Sneha Bhoja Shetty; Suman Veerappa Budihal; Mangalore Ramesh Bhat; Kunal (Pharmacognosy Journal, 2017)
Background: Cadmium (Cd), is a toxic metal which affects various organs including testis. It produces oxidative stress leading to male infertility. Moringa tree, is a natural plant with a great therapeutic value and hence it is found to be effective both in prevention and treatment of various conditions including reducing toxicity of hazardous materials. The aim of the present study was to examine the effects of Pre-and Post-treatment with Moringa oliefera leaf extract (MoE) on testis in cadmium exposed rats. Materials and Methods: The present study was conducted at the Department of Physiology, Kasturba Medical College (KMC), Mangalore, Manipal University (MU), Karnataka, India, between (2011-2013). This prospective study consisted a total of 30 rats. These were divided into 5 groups with group I being the control. Data were presented as mean ±SD. student’s t test was used as statistical tool, p<0.05 considered statistically significant. Group IV and V were pre-and post-MoE treated groups respectively. Serum testosterone and tissue lipid peroxidation levels were estimated. Results: Treatment with MoE prior and after administration of cadmium, respectively showed an increase significantly in the testosterone levels and a decrease in the tissue lipid peroxidation as compared to the group treated with cadmium. However, the pre-treatment showed better results in combatting the toxic effects of cadmium. Conclusion: This study shows that Moringa olifera leaf extract altered the testosterone and tissue lipid peroxidation levels. Also, pre-treatment showed better outcome. <div class="ephox-sloth-bin ephox-sloth-bin_22207819311505710213931" style="position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;" contenteditable="true" aria-hidden="true"> Background: Cadmium (Cd), is a toxic metal which affects various organs including testis. It produces oxidative stress leading to male infertility. Moringa tree, is a natural plant with a great therapeutic value and hence it is found to be effective both in prevention and treatment of various conditions including reducing toxicity of hazardous materials. The aim of the present study was to examine the effects of Pre-and Post-treatment with Moringa oliefera leaf extract (MoE) on testis in cadmium exposed rats. Materials and Methods: The present study was conducted at the Department of Physiology, Kasturba Medical College (KMC), Mangalore, Manipal University (MU), Karnataka, India, between (2011-2013). This prospective study consisted a total of 30 rats. These were divided into 5 groups with group I being the control. Data were presented as mean ±SD. student’s t test was used as statistical tool, p<0.05 considered statistically significant. Group IV and V were pre-and post-MoE treated groups respectively. Serum testosterone and tissue lipid peroxidation levels were estimated. Results: Treatment with MoE prior and after administration of cadmium, respectively showed an increase significantly in the testosterone levels and a decrease in the tissue lipid peroxidation as compared to the group treated with cadmium. However, the pre-treatment showed better results in combatting the toxic effects of cadmium. Conclusion: This study shows that Moringa olifera leaf extract altered the testosterone and tissue lipid peroxidation levels. Also, pre-treatment showed better outcome.
Keywords: Cadmium; MDA; Morniga olifera extract.; Oxidative stress; Testosterone

Preliminary Acute Oral Toxicity Study of White Tea Leaf (Camellia sinensis (L.) Kuntze) Ethanolic Extracts - Lia Ardiana; Meiliza Ekayanti; Sarah Zielda Najib; Rani Sauriasari; Berna Elya (Pharmacognosy Journal, 2017)
Background: White tea is a kind of tea which manufactured with minimal processing only drying without fermentation process. White tea prepared from very young tea leaves or buds of Camellia sinensis (L.) Kuntze, Theaceae, covered with tiny, silvery hairs, and dried immediately after picking to prevent oxidation and commonly used as a beverage and herbal medicine. Objective: The present study was aimed to evaluate the safety of the white tea leaf ethanolic extract (WTE) with acute toxicity tests. Methods: The acute oral toxicity of WTE performed at dose 1250, 2500, and 5000 mg/Kg BW of Deutschland, Denken, and Yoken (DDY) mice. The animals observation for any mortality, behavioral, body weight and feed-water consumption pattern during the 14- day study. The liver, kidney, and heart isolation performed on day-15 to observe macroscopic and relative organ weight (ROW). Results: No treatment-related toxic symptom or mortality observed for the first 4 hours and 24 hours after oral administration of WTE at a dose of 1250, 2500, and 5000 mg/kg BW. All the groups of mice did not show the significant changes in behavior, breathing, and motoric activity. Conclusions: This studies showed that the oral LD50 of WTE was greater than 5000 mg/kg BW and suggests that the WTE is practically non-toxic in a single dose of level 5000 mg/kg BW.
Keywords: Acute toxicity; Camellia Sinensis (L.) Kuntze; Safety; Teh Putih; Theaceae

Quantification of Ethanol Content in Traditional Herbal Cough Syrups - Ming Shin Neo; Shraddha Manish Gupta; Tahir Mehmood Khan; Manish Gupta (Pharmacognosy Journal, 2017)
Introduction: The use of alcohol as an excipient in pharmaceutical preparations raises safety concerns, especially when used in high concentration. This study aims to scrutinize the ethanol concentration in traditional herbal cough syrups available over-the-counter (OTC) in Malaysia. Method: Enzymatic analysis was adopted to estimate the alcohol contents of five selected syrups. The principle reaction involved ethanol oxidation by nicotinamide-adenine dinucleotide (NAD) in the presence of the enzyme alcohol dehydrogenase (ADH), forming acetaldehyde, reduced NAD (NADH) and a proton. The ethanol concentration of each syrup was quantitatively determined by detecting NADH using UV spectrophotometry at detection wavelength of 340 nm. Results: The ethanol percentage by volume (% v/v) in the tested syrups ranges from 0.102% to 2.576%. All five syrups studied comply with the FDA requirement for drugs for adults and children >6 years since they do not contain more than 5% ethanol. However, three syrups do not fulfil the requirement for use in children <6 years as they contain higher than 0.5% ethanol, yet they are inappropriately indicated on their packaging for use in children >3 years. In terms of safety, all studied syrups fulfil European Medicine Agency’s (EMA) recommendation as they will not induce a blood alcohol concentration (BAC) higher than 0.125g/L after a single dose. Nevertheless, none of these syrups comply with Malaysian Drug Registration Guidance on labelling requirements as they do not disclose their alcohol contents on the packaging. Conclusion: More rigorous regulation on alcohol content in herbal preparations, and disclosure of alcohol content in product packagings should be enforced.
Keywords: Alcohol content; Enzymatic analysis; Ethanol concentration; Herbal cough medicine; Herbal preparation; Quantitative analysis.

Quantitative Analysis of Irigenin in the Different Species of Iris Plant by RP- HPLC and its Efficacy Against Different Plant Pathogens - Sajad Hassan Wani; Hilal Ahmad Bhat; Javid Iqbal Mir; Shahid Ali Akbar; Sajad Un Nabi; Desh Beer Singh; Nazeer Ahmad (Pharmacognosy Journal, 2017)
Irigenin belongs to family of isoflavonoids, isolated from Iris Plant of Kashmir Himalaya. A rapid and specific reverse phase high pressure chromatography (RP HPLC) method for quantitative analysis of irigenin in the different species of Iris Plant was developed. The samples were analyzed on RP-C18 e column (chromolith, 5μm, 4.6×100 mm). The HPLC system was operated at ambient temperature (±30c). The mobile phase consisted of methanol: water. The detecting wavelength at 260 nm and flow rate of 0.6 ml/min. The standard irigenin was diluted using the mobile phase at a known concentration of 1mg/ml; the sample was filtered through sample filter of 0.45 μ pore size. The filtrate was introduced on to a reverse phase analytical column. The content of irigenin in the different species of Iris Plant was determined. The HPLC showed an excellent performance in separating the irigenin in different species of Iris Plant. Furthermore, the antipathogenic activity. The test compound at each respective concentration was found to be statistically superior against scab. Furthermore, the test compound @ 5000 ppm proved significantly most effective by providing (82.49%) inhibition in the mycelia growth of apple scab. It was followed by fusarium (77.27%) at 5000 ppm. Lowest reduction in mycelia growth (65.78%) was recorded in marssonina and did not differ significantly from Alternaria (67.47%) at 5000 ppm. Furthermore, lowest inhibition of mycelia growth was recorded at 1000 ppm. Similar trend was recorded for rest of the pathogens i.e. highest reduction at 5000 ppm, lowest at 1000 ppm and at 2000, 3000 and 4000 ppm it ranges between the first two but increases with increase in concentration. From this study irigenin is potent compound which can be used for controlling the growth of respective pathogens.
Keywords: Bio efficacy; Irigenin; Iris Plant; RP-HPLC

A Quantitative Approach to Estimate both Essential and Non-essential Elements in Some Commercial Samples of Triphala churna by using WD-XRF Spectrometry - Venkata Siva Satyanarayana Kantamreddi; V. Thirumala Veni; G. Y. S. K. Swamy (Pharmacognosy Journal, 2017)
Introduction: The need for quality control of herbal drugs is in demand in order to ensure the purity, safety and efficacy of herbal products. A total of 19 elements including essential and non-essential elements were characterized in five commercial samples of Triphala churna using WD-XRF spectrometry. Method: The WD-XRF method was validated for each element by a pre-calibrated program using five Chinese certified reference materials of vegetable standards (NCS ZC73012, NCS ZC73013, NCS ZC73017, NCS ZC85006 and NCS DC73348). Results: The following elements were detected in all the samples out of 19 elements tested with increasing order of concentrations (mg/kg): Cr (3) < Cu (7) < Ba (24) < Zn (31) < Pb (46) < Mn (57) < S (700) < Na (1064) < Mg (1250) < Fe (1329) < P (1400) < Cl (2960) < Ca (3110) < Si (4350) < K (15130). Lead (41-46 mg/kg), a nonessential element was found above its PDE limit (≤ 10 mg/kg). Conclusion: WD-XRF method was found simple, rapid, reliable and non-destructive technique to investigate the elemental concentrations in herbal drugs.
Keywords: Ayurveda; Elemental analysis; ICP-MS; ISM; Triphala churna; WD-XRF

RETRACTED: 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

A Review of Pharmacognostical Studies on Moringa oleifera Lam. flowers - Tom Mathew Kalappurayil; Benny Pulinilkkumthadathil Joseph (Pharmacognosy Journal, 2017)
Moringa oleifera Lam. of the family Moringaceae, popularly called ‘miracle tree’ is a native of sub Himalayan tracts of Northern India and is widely cultivated in tropical and subtropical regions. Research on Moringa mainly pivoted around its leaves and seeds because of their immense nutraceutical potential but recently there is a greater interest in flowers too, mostly inspired by the positive outcomes of several pharmacognostical studies on flowers. Moringa flower is a rich reservoir of bioactive phytochemicals and crude flower extracts showed promising antibacterial, antifungal, anti larval, antioxidant, anti inflammatory and anticancer properties. This review concisely presents the various phytochemicals identified and isolated as well as the various bioassays employed to validate the therapeutic potential of flower. It is prepared after a detailed search on Google scholar. Reports on Moringa oleifera flower were sorted and tabulated based on the bioassays performed and solvents used for extraction. A grading pattern is adopted for comparing efficiency of different extracts in eliciting bioactivities. Many of these studies are at the preliminary stage but two of them present advanced mechanisms. First is the presence of a proteinaceous larvicidal compound ‘MoFTI’ in the flower capable of inhibiting larval trypsin of Aedes aegypti. The second describes flower extract’s anti inflammatory mechanism effecting via NF-KB pathway and consequent suppression of inflammatory mediators’ activation, but short of identifying lead compound/compounds behind this effect. Thus authors suggest further studies to elucidate the detailed mechanisms, identify and isolate the active compound or compounds of synergism behind the many therapeutic potential of the Moringa flower extracts.
Keywords: Bioactivity; Bioassay; Extracts; Flower; GCMS; Moringa; Phytochemicals; Therapeutic

Saffron (Crocus sativus) and its Active Ingredients: Role in the Prevention and Treatment of Disease - Arshad Husain Rahmani; Amjad Ali Khan; Yousef Homood Aldebasi (Pharmacognosy Journal, 2017)
Introduction: Crocus sativus is a member of iridaceae family and its use in health management is in practice since ancient time. Additionally, research based on clinical trials and animal models have advocates its role in disease cure without any severe adverse complications. The aim of this study is to summarize the study of saffron and its ingredients based on in vivo and in vitro and role in disease cure and prevention. Materials: This study was designed through the search engines such as Pub Med, Scopus and Google Scholar. The keywords used for the search were mainly focused on Saffron with health benefit and its therapeutics role in different diseases. Result: Saffron stigma is mixture of various components and recent studies have proven that saffron and its active ingredients play a key role in disease management. Moreover, clinical trials based study on the use of saffron and its individual components have confirmed the health promising effects. Conclusion: Although Saffron has potential role in the disease cure and prevention via modulation of anti-oxidant, anti-inflammatory, anti-tumour, anti-microbial and anti-diabetic activity. Furthermore, advanced research is needed to elaborate the role of saffron in health management and its mechanism of action in the modulation of biological activities.
Keywords: Anti-inflammatory; Anti-tumour activity; Antioxidant; Crocus sativus; Toxicity level.

Screening Indigenous Medicinal Plants of Northeast India for Their Anti-Alzheimer’s Properties - Roohollah Sobhani; Amarta Kumar Pal; Atanu Bhattacharjee; Sivaprasad Mitra; Kripamoy Aguan (Pharmacognosy Journal, 2017)
Introduction: Alzheimer’s disease (AD) is a progressive neurologic disease of the brain that affects intellectual abilities, reasoning and memory. Acetylcholine (ACh) is involved in the maintenance of cognitive process. Pathologically, ACh production is compromised in the brains of AD affected people. Presence of acetylcholinesterase (AChE) in the synaptic cleft, which hydrolyzes ACh, further decreases the ACh-levels, and thereby, additionally compromises cognition. The tribal people of North East India have been using indigenous plants as traditional medicine for brain disorders. We assayed whether the plants used in the traditional tribal knowledge for the treatment of brain disorders might contain better AChE-inhibitors. Methods: We collected 10 traditional medicinal plants from Northeast India. A total of 39 plant extracts were prepared using three solvent systems. The Acetylcholinesterase (AChE) activity was measured with Ellman method. The experiment was done in triplicate for each level of inhibitor. The activity was measured at 412 nm wavelength using Plate Reader. The standard student t-test was used to show significant difference in IC50 values between extracts. Results: The result are reported based on Km, Vmax, IC50 (μg/μl), percentage inhibition and inhibition pattern. Two extracts had competitive inhibition, 11 extracts had mixed inhibition, 2 extracts had non-competitive inhibition, 11 extracts had uncompetitive inhibition and 4 extracts did not provide any proper pattern. The IC50 for these plant extracts were at the range of 0.51-12.4 μg/μl. Notably, Cinnamomum camphora (leaf: chloroform), Litsea glutinosa (stem; chloroform), and Litsea glutinosa (stem; methanol) showed IC50 values of 0.51, 0.53 & 0.81 μg/μl, respectively.
Keywords: AChE-inhibition; Alzheimer’s; Ellman assay; Kinetics; Medicinal plants

Screening of Antidepressant Activity of Punica granatum in Mice - Rajeshwari Shastry; Aadhya Sharma; Vinay Sayeli; Ullal Sheetal Dinkar (Pharmacognosy Journal, 2017)
Introduction: India is a rich source of medicinal plants used therapeutically to treat various disorders including depression. This study was undertaken to evaluate the antidepressant effect of acute and chronic administration of Punica granatum (pomegranate) whole fruit in mice. Methods: We used the aqueous extract of Punica granatum (250 and 500 mg/kg per day), standard drug used was Imipramine (10 mg/kg) and vehicle was gum acacia (10 ml/kg), orally. Four groups of animals were used and each group had six animals. In the acute study drugs/vehicles were administered 60 min prior to the experiments. In the chronic study drugs/vehicles were administered for 14 days and the last dose was given on the 14th day, 60 minutes prior to experiment. Forced Swim Test and Tail Suspension Test were used for testing antidepressant activity. Data was analyzed using one-way ANOVA with drug treatment as the independent factor. Post-hoc comparisons were performed using Dunnett’s test. Results: In acute and chronic forced swim test as well as acute tail suspension test, duration of immobility was significantly reduced in the PG 500 mg/kg, but not in the 250 mg/kg treated group. In chronic tail suspension test, duration of immobility was significantly decreased in PG 250 mg/kg and 500 mg/kg treated groups. The antidepressant activity of 500 mg/kg was comparable to that of Imipramine 10 mg/kg. Conclusion: The present study suggests that aqueous extract of whole fruit of P. granatum has antidepressant activity at 500 mg/kg. It would be advisable to encourage consumption of pomegranate extract in patients with depression because of its nutritional and functional properties.
Keywords: Depression; Forced swim test; Pomegranate.; Tail suspension test

Screening of Ethanolic Extracts of Medicinal Herbal Drugs Against Oral Microbes - Harsha L; Lakshmi Thangavelu (Pharmacognosy Journal, 2017)
Aim: The aim of the present study is to screen the ethanolic extracts of medicinal herbal drugs against oral microbes. Objective: In this study, 3 medicinal herbs were evaluated for antimicrobial activity against five common oral bacteria as a screen for potential candidates for the development of natural antibiotics. Methods: Ethanolic extracts of medicinal herbs were tested for activity against Enterococcus faecalis, Lactobacillus acidophilus, Streptococcus mutans, and Streptococcus sanguis grown in brain heart infusion (BHI) broth. A broth microdilutionassay was used to determine the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). A disk diffusion assay was performed by inoculating bacterial cultures on BHI agar plates with paper disks soaked in each of the medicinal herb extracts. Results: The ethanolic extracts of many of the 3 medicinal herbs showed antimicrobial activity against the five types of pathogenic oral bacteria. The extracts of Caralluma fimbriata, Hemidesmus indicus, and Grape seed effectively inhibited the growth of oral bacteria and showed distinct bactericidal activity. Conclusion: These results suggest that alternative medicines with proven antimicrobial effects, such as Caralluma fimbriata, Hemidesmus indicus, and Grape seed may be useful for the treatment of dental diseases.
Keywords: Anti cariogenic; Dental caries; Natural products Pathogenic; Oral bacteria

The Serum Protein Fractions in Streptozotocin (STZ) Administrated Rat Models - Cennet Ragbetli; Semiha Dede; Feride Koc; Veysel Yuksek; Murat Cetin Ragbetli (Pharmacognosy Journal, 2017)
Background: Experimental diabetes can be induced using chemical agents such as streptozotocin. Objective: This study aimed to investigate the effect of streptozotocin (STZ) which is most important agent to produce experimental diabetic model at two different doses on serum protein fractions in rat models. Materials and Methods: Twenty-four male rats that weighed an average of 250 g and were 3–4 months old were used as the experimental models. They were sorted into three groups composed of eight rats each of STZ 55 mg/kg, STZ 65 mg/kg and control. Diabetes was induced by administering STZ 55 mg/kg and 65 mg/kg intraperitoneally. The serum protein fractions were analyzed by cellulose acetate electrophoresis. Results: No significant difference was observed between the groups for all fractions except alpha-2 and beta globulins. The alpha-2 and beta globulin levels were significantly higher in the 55 mg/kg group than in the 65 mg/kg STZ and control groups (p<0.05). Conclusion: This increase may be due to the involvement of different proteins in the alpha-2 and beta globulin protein fractions.
Keywords: electrophoresis; experimental diabetes; Rat; serum proteins; STZ

Simultaneous-HPLC Quantification of Phenolic Acids in Traditionally used Ayurvedic Herb Diplocyclos palmatus (L.) Jeffry - Ankita Misra; Pushpendra Kumar Shukla; Bhanu Kumar; Abhishek Niranjan; AKS Rawat; Sharad Srivastava (Pharmacognosy Journal, 2017)
Introduction:The present study deals with the simultaneous HPLC-quantification of phenolic acid(s) in the aerial parts of Diplocyclos palmatus (Cucurbitaceae) and evaluation of their bioactivity potential through in vitro antioxidant assay’s. Method: The HPLC elution was done using C18 column using gradient (binary phases) solvent system at a flow rate of 0.6 ml/min. Total phenolic and, flavonoid contents were determined and the antioxidant potential was estimated by four assay’s viz. DPPH radical scavenging assay, ferric reducing power assay, total antioxidant capacity and 2-deoxy ribose assay. Results: The species is rich in three phenolic acids, among which gallic acid (1708 ug/g) is in maximum concentration followed by caeffic acid (437 ug/g) and protocateuchic acid (337.7 ug/g). Total phenolic content was higher (10.5 mg/g) than flavonoid content (3.78 mg/g) and TAC was found at 0.137 mg/g ASE (ascorbic acid equivalent). IC50 of D. palmatus extract for scavenging of hydroxyl radical by 2-deoxy ribose and DPPH was at concentration of 125.61 ± 0.834 (μg/ml) and 353.71 ± 0.663 (μg/ml) respectively. In vitro antidiabetiv potential, via inhibition of alpha amylase enzyme through starch iodine and 3,5- DNS assay reveals the IC50 of extract at 146.31 ± 0.415 ug/ml and 286.23 ± 0.671 ug/ ml respectively. Conclusion: The species (aerial part) was rich in phenolic acid with potential bioactivity, identified leads will be useful in further chemical characterization and pharmacological validation.
Keywords: Anti diabetic; Anti oxidant; Diplocyclos palmatus; HPLC; Phenolic acid

Standardization and Chemical Analysis of Rasam: A South Indian Traditional Functional Food - Agilandeswari Devarajan; Muthu Kumaradoss Mohan Maruga Raja (Pharmacognosy Journal, 2017)
Objective: The traditional Indian food is “functional” as it contains high amounts of dietary fiber, antioxidants, and probiotics. Rasam is a South Indian traditional spice soup. Spices are reputed to possess several pharmacological properties. Due to geographical, ethnical, and traditional differences, rasam recipe and the preparation process have a wide difference. Hence, the objective was to standardize rasam and then to perform a chemical analysis so that its pharmaceutical potential beyond nutritive effect can be explored. Materials and Methods: The quantity of ingredients and the process followed for preparing rasam by the 17 volunteers selected from in and around Vellore, Tamil Nadu was standardized. The proximate, nutritive, elemental, and phytochemical analysis were determined for the standardized rasam. Results: The total ash, acid insoluble ash, water soluble ash, and sulfated ash were found to be 1.7%, 0.04%, 0.12%, and 1.86%, respectively. The extractive values such as water soluble, ethanol soluble, and ether soluble were found to be 4.5%, 3.93%, and 0.61%, respectively. The standardized rasam showed very low-energy content of 15.13 kcal/100 g. Rasam contained alkaloids, tannins, saponins, flavonoids, terpenoids, steroids, glycosides. and volatile oil. Conclusion: The ingredients used in the preparation of rasam are medicinally claimed for various ailments, which makes it a traditional functional food. The standardized procedure provided tremendous opportunity to study the pharmaceutical potential in a systematic scientific way beyond its culinary and nutritive effect.
Keywords: Chaaru; Elemental analysis; Nutritional Value; Proximate Analysis; Saaru; Spices

Standardization of Agrotechniques and Biochemical Assessment of Crataegus oxyacantha in Western Himalaya - Gopichand; RL Meena; P Kaur; RD Singh (Pharmacognosy Journal, 2017)
C. oxyacantha is a high valued medicinal plant of Rosacea family. It is used to cure cardiac disorder in ayurvedic medicines. A field experiment was laid out in 2004 in CSIR-IHBT farm, by using different quantity of FYM and various spacing. Low growth in plant height was observed in first five years with higher dose of FYM, but in 2015 the significant height growth was recorded. From 2008 to 2015 all types of FYM applications produced statistically significant yield of seed production except in 2012 and 2014. The 22.50t/ha was the most statistically significant dose of FYM in relation to seed yield. The spacing did not produce any significant results for seed production. A vegetative propagation trial of C. oxyacantha was also laid out using semi hard stem cuttings and some selected hormones (IAA, IBA, GA3 and Abscisic acid) with different concentrations. Statistically significant shoot sprouting (78.35%) was recorded when IBA of 1000 mg/L was used followed by 67.74% in case of 1500 mg/L of the same hormone. While lowest shoot sprouting (27.85%) was observed using 2000 mg/L of Abscisic acid. A statistically significant 5.67 cm and 5.33 cm shoot lengths were observed using 2000 mg/L of IAA and 1000 mg/L of IBA, respectively. In the case of shoot tillers 3.33 was recorded in 1500 mg/l. of IAA. Two new compounds and 9 known compounds were isolated from fruit extract.
Keywords: Bioactive compounds; Crataegus oxyacantha; FYM; Hormones; Spacing

Sub-acute Toxicity Study of The Ethyl Acetate Fraction of Asam Kandis Rinds (Garcinia cowa Roxb.) on the Liver and Renal Function in Mice - Fatma Sri Wahyuni; Dessy Arisanty; Nelsi Fitri Hayaty; Dian Ayu Juwita; Almahdy (Pharmacognosy Journal, 2017)
Objective: The present study investigated the sub acute toxicity of the ethyl acetate fraction of asam kandis (Garcinia cowa Roxb) Rinds in mice. Material and Methods: Sub acute toxicity study was carried out by giving orally at dose 500, 1000 dan 2000 mg / kgBW extract to five mice at 21 days. Animals were observed individually for any clinical signs of toxicity or mortality for 14 days. Measured parameters were SGPT levels, serum creatinine levels, weight ratio of liver and kidney. Extract was given orally at dose 500, 1000 and 2000 mg/kgBW for 21 days. Observations were done on day 8th, 15th and 22th using blood serum, liver and kidneys of mice. Data were analyzed by using two-way ANOVA followed by Duncan’s Multiple Range Test. Results: The ethyl acetate fraction of G. cowa at doses 500, 1000 and 2000 mg/kgBW gave significant effect on increasing SGPT levels and decreasing levels of serum creatinine (p <0.05). The length of treatment gave significant effect on decreasing levels of serum creatinine, weight ratio of liver and kidney (p <0.05). Conclusion: The dosage of the ethyl acetate fraction of asam kandis rinds provides significant effect on the SGPT and serum creatinine levels of male white mice. The duration of administration of ethyl acetate fraction of asam kandis rinds provides significant effect on serum creatinine levels, the weight ratio of liver and kidney organ of male white mice.
Keywords: Creatinine serum; Garcinia cowa rinds; SGPT; Sub-acute toxicity; Weight ratio of liver and kidney

Synthesis of Nanoparticles Produced by Ethanol Extract of Boesenbergia rotunda Rhizome Loaded with Chitosan and Alginic Acid and its Biological Activity test - Sri Atun; Sri Handayani (Pharmacognosy Journal, 2017)
Introduction: B. rotunda used as a traditional medicine to treat illnesses such as rheumatism, muscle pain, febrifuge, gout, gastrointestinal disorders, flatulence, carminative, stomach ache, dyspepsia, and peptic ulcer. To enhance the stability, solubility and activity of the extract B. rotunda, should be developed into a product nanoparticles. Objective: This work reports the synthesis of nanoparticles produced by ethanol extract of Boesenbergia rotunda rhizome loaded with chitosan and alginic acid, and its biological activity test as antioxidant. Method: The synthesis of nanoparticles used an ionic gelation. Activity of the nanoparticle products as antioxidant was tested by the DPPH (2,2-diphenyl-1-picrylhydrazyl) method. Results: This work showed that nanoparticles chitosan produced by ethanol extract B. rotunda can be synthesized at a concentration (% w/v) of chitosan/ Na-TPP (sodium tripolyphosphate) and ratio of 8: 1, the size range of the nanoparticles were 389 to 877 nm, with a zeta potential of + 41.87 mV, and precentage nanoparticle 98.1%. The corresponding nanoparticles alginic acid can be synthesized at a concentration (% w/v) of alginic acid/ Ca2+ and ratio of 5: 1, the size range of the nanoparticles were 197 to 877 nm, with a zeta potential of -82.1 mV, and precentage nanoparticle 90.2%. Furthermore, nanoparticles result of the combination of alginic acid –chitosan can be synthesized at a concentration (% w/v) alginic acid/chitosan/ca2+ and ratio of 6.7: 2: 1, the size range of the nanoparticle were 226 to 877 nm, and precentage nanoparticle 29.7%. The morphology of each nanoparticle products was spherical and a smooth surface. The chitosan-alginic acid nanoparticles show higher activity than the starting material ethanol extract of B. rotunda.
Keywords: alginic acid; Antioxidant; B. rotunda; chitosan-alginic acid combination; Nanoparticles chitosan

To Evaluate the Antidiabetic and Rejuvenating Capability of Tissues on Alloxan Induced Diabetic Rats under the Effect of Ethanolic Leaf Extract of Coriandrum sativum: A Histopathological Study - Bhaskar Sharma; Gaurav Sharma; Suresh Chand Joshi; Sunil Kumar Singh (Pharmacognosy Journal, 2017)
Objective: To evaluate the antidiabetic and rejuvenating capability of tissues on alloxan induced diabetic rats under the effect of ethanolic leaf extract of Coriandrum sativum. Methods: Diabetic model was prepared by administration of alloxan monohydrate (150 mg/ kg i.p). The ethanolic leaf extracts of Coriandrum sativum at a dose of 200 and 400 mg/kg of body weight were administrated to diabetic induced groups for a period of 28 days. The effect of ethanolic leaf extract of Coriandrum sativum leaf extract on serum blood glucose, insulin, lipase, α- amylase and LDH as well as kidney function test [urea, uric acid, albumin, protein and creatinine] were measured in the alloxan induced diabetic rats. Results: In the acute toxicity study, ethanolic leaf extract of Coriandrum sativum leaf was non-toxic at 2 000 mg/kg in rats. The increased insulin level, albumin and protein level, decreased blood glucose and other biochemical parameters level were observed in diabetic rats treated with both doses of ethanol extract of Coriandrum sativum leaf compared to diabetic control rats. In Histopathological study were revealed toward normal. Conclusion: Ethanolic extract of Coriandrum sativum leaf possesses significant antidiabetic and rejuvenating capability of tissues.
Keywords: Alloxan; Coriandrum sativum.; Pancreas and Kidney Tissue; Wistar Rats

Total Phenolic Contents and Free Radical Scavenging Activity of Guaiacum officinale L. Extracts - Suthira Maneechai; Vachiraporn Pikulthong (Pharmacognosy Journal, 2017)
Backgound: Guaiacum officinale L. is an alien species to Thailand. It is used as anti-arthritis and anti-rheumatoid agents in Indian folklore medicine. Objective: The present study was aimed to investigate total phenolic contents and free radical scavenging activity of the extracts from Guaiacum officinale L. (Zygophyllaceae). Methods: The plant parts including bark, twig and leaf were extracted using different solvents (ethyl acetate, water and ethanol). Total phenolic contents were determined by Folin-Ciocalteu Colorimetry method while free radical scavenging activity of the extracts was investigated by 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity assay. Results: The results show that the highest total phenolic content is found in the ethyl acetate twig extracts (20.3±0.0031 μg GAE/1 μg extracts). The ethanolic twig extracts had the highest free radical scavenging activity with IC50 of 0.45±0.0188 mg/ml. Conclusion: The extracts from Guaiacum officinale L. exhibit good anti-oxidant activity and may be suitable for development as drugs and supplementary food.
Keywords: Ethanolic twig extracts; Ethyl acetate twig extracts.; Free Radical Scavenging Activity; Guaiacum Officinale L; Total Phenolic Contents

Toxicity Assessment and Evaluation of Analgesic, Antipyretic and Anti-Inflammatory Activities on Cordia obliqua Leaf Methanol Extract - Richa Gupta; Ghanshyam Das Gupta (Pharmacognosy Journal, 2017)
Background: Cordia obliqua Willd. Plant belongs to genus Cordia and family Boraginaceae. Commonly it is known as Clammy Cherry and in Hindi Lasora. Earlier very few researches were carried out to explore its medicinal importance as compared with other Cordia species. Objective: To determine maximum safe dose and explore analgesic, anti-inflammatory and antipyretic activities of Cordia obliqua leaf methanol extract. Materials and Methods: As per our previous study report, the leaf methanol extract is rich in phyto-constituents and has good antioxidant effect; so only methanol extract was studied here. The maximum safe dose of methanol extract was found by acute oral toxicity study according to OECD guidelines 423. For analgesic effect, hot plate and tail flick method, for anti-inflammatory, Carageenan induced rat paw edema and for antipyretic study, yeast induced pyrexia method were used. Results: The extract dose up to 2000mg/Kg was found safe with no any side effects. Three dose levels were tested for all activities. The medium (250 mg/Kg) and high (500 mg/Kg) dose of methanol extract was found effective in all activities when compared with standard. The result for antipyretic activity was found better than other activities. Conclusion: It can be concluded that Cordia obliqua leaf is safe and effective drug for relief of pain, fever and inflammation.
Keywords: Carageenan induced edema; Clammy Cherry; Hot plate; Tail flick; Yeast induced pyrexia.

Toxicology and Oral glucose Tolerance Test (OGTT) of Thai Medicinal Plant Used for Diabetes controls, Phyllanthus acidus L. (EUPHORBIACEAE) - Napapach Chaimum-aom; Sanong Chomko; Chusri Talubmook (Pharmacognosy Journal, 2017)
Aim: The present study aimed to investigate toxicity and oral glucose tolerance test (OGTT) of Phyllanthus acidus leaf extract (PAE) on Wistar rat. Methods: PAE was prepared and administered orally to experimental animals used. The extract was tested for toxicity in rats at a dose of 0, 1,000, 1,500 and 2,000 mg/kg body weight p.o once daily for 14 days. The hypoglycemic effects of PAE on normal rats and orally glucose-induced hyperglycemic rats were compared with distilled water and glibenclamide. A single dose (250 mg/kg body weight) of PAE was administered and blood glucose level was obtained by pricking the tail vain using glucometer at time -30, 0, 30, 60, 120 and 240 minutes. Results: All doses of the extract did not exert any sign or symptom of toxicity and the dead rat was not found. The body weight, white blood cell (WBC), mean corpuscular volume (MCV), platelet (PLT), plateletcrit (PCT), mean platelet volume (MPV), platelet distribution width (PDW), blood chemistry, blood urea nitrogen (BUN), creatinine, alkaling phosphatase (ALP) and organ weight of liver were not significantly different between control and treated rats. However, red blood cell (RBC), hematocrit (HCT), lymphocyte (LYM), and hemoglobin (Hb) at a dose 1,500 mg./kg body weight were significantly lower than those in the control group. The blood glucose levels of PAE treated groups were not different with control and Glybenclamide treated. Conclusion: The findings of the present study can be concluded that the PAE are practically non-toxic at a lower dose.
Keywords: Blood glucose; Diabetes; Medicinal plant; Phyllanthus acidus; Toxicity

Triptolide Mediated Amelioration of Breast Cancer via Modulation of Molecular Pathways - Swadesh Sarkar; Santanu Paul (Pharmacognosy Journal, 2017)
Triptolide is the main bioactive molecule isolated from a root extract of Tripterigium wilfordii Hook F. of Celastraceae family. Chemically, it is a diterpenoid triepoxide molecule and its chemical formula is C20H24O6. Its five-membered unsaturated lactone ring (D-ring) is crucial for anti-tumor potential and carbonyl group at C-18 position is essential to exert important influence on the interaction between triptolide and the targeted protein(s). It is bio-synthesized from deoxy-D-xylullose-5-phosphate (DOXP) pathway in the cell. Triptolide can induce apoptosis in a number of breast cancer cells by up-regulating different pro-apoptotic and down-regulating different anti-apoptotic molecules. In vitro experiments indicate that it can down regulate several cell cycle related genes and induces S-phase cell cycle arrest. Triptolide treatment can also modulate the expression of different cell signaling molecules, e.g. ERK, NF-κB, FAK, VEGF, β-catenin, AKT etc. In vivo experiments indicate that triptolide can effectively reduce breast tumor growth in the mouse model. Apart from the single drug treatment, triptolide can effectively be applied in combination therapy. Application of Triptolide with other chemotherapeutic drugs, very efficiently check the proliferation of tumor cells which reduces the effective concentration of the commercially available drugs thus reducing their toxic sideeffects. Although triptolide is very effective against a number of diseases, its higher degree of multi-organ toxicity limits its use of further clinical trial. Therefore, to reduce the toxic effects, a number of strategies have been developed which increase its water solubility and at the same time decrease the toxic effect. In this review article, we have addressed how triptolide participates in the antitumor processes in breast cancer cells.
Keywords: Apoptosis; Breast cancer; Cytotoxicity; Molecular pathway.; Tripterigium wilfordii; Triptolide

Vibrational Analysis and Thermal Behavior of Salvia hispanica, Nigella sativa and Papaver somniferum Seeds - Paula Carrión-Prieto; Pablo Martín-Ramos; Salvador Hernández-Navarro; Iosody Silva-Castro; Manuela Ramos-Silva; Jesús Martín-Gil (Pharmacognosy Journal, 2017)
Introduction: Salvia hispanica L., Nigella sativa L. and Papaver somniferum L. are involved in opiate-dependent behavior. It is known that the seeds of these three herbs contain high amounts of antioxidants, which are helpful in disease prevention, but further research is needed on some of their other phytochemical components (terpene alkaloids, benzoquinones and others), which are claimed to affect human opioid receptors. Methods: Seeds from the three afore mentioned plants have been studied by ATR-FTIR vibrational spectroscopy and thermo analytical techniques (TG/DTG, DTA and DSC). Results: The infrared spectrum has confirmed the presence of the ester carbonyl of terpenoid alkaloids (such as nigellamine) and the fully conjugated cyclic dione structure of quinones (e.g., thymoquinone). As regards the thermal stability of these seeds, small differences have been observed in their thermal profiles (endothermic effects at around 333ºC for chia, 268ºC for black cumin and 319ºC for poppy seeds), which can be ascribed to their different content in carbohydrates. Conclusions: The functional groups of the main active constituents and the thermal behavior of these three seeds have been elucidated.
Keywords: ATR-FTIR; Black cumin; Chia; Poppy; Thermal analysis

Acetaminophen Induced Oxidative and Histopathological Alterations in Hepatic Tissue: Protective Effects of Alstonia Scholaris Leaf Extracts - Pawan Kumar Verma; Rajinder Raina; Mudasir Sultana; Maninder Singh; Pawan Kumar (Pharmacognosy Journal, 2016)
Introduction: Alstonia scholaris Linn. is the common ingredients of various herbal formulation. Objectives: Present study was aimed to evaluate the oxidative and histopathological alterations in acetaminophen (APAP) induced hepatotoxicity and protective mechanisms of different leaf extracts of A. scholaris. Methods: Forty two wistar rats were randomly divided into seven groups with six rats in each and subjected to different treatments. Alterations in total oxidant status (TOS), total antioxidant status (TAS), oxidative stress index (OSI), total thiols (TTH), catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione-s-transferase (GST), malondialdehyde (MDA) levels and histopathological alterations in hepatic tissue were analyzed to assess the extent of hepatic damage induced by APAP and the protection imparted against it by aqueous or ethanolic leaf extract of A. scholaris. Results: Single high oral dose of APAP administration increased (p<0.05) hepatic levels of TOS, OSI and MDA and reduced TAS, TTH, SOD, CAT, GPx and GST activities indicating alteration in antioxidant system of hepatic tissue. The histopathological studies showed severe hepatic degeneration, vacuolization and granulation in cytoplasm, fragmentation of nuclei and membranes and infiltration of mononuclear cells on APAP treatment. Pre and post-treatments of aqueous or ethanolic extract following APAP administration restored TTH, reduced MDA and TOS and increased TAS compared to APAP treatment alone. Conclusions: Observations of histopathological and antioxidant parameters indicates that restoration of TAS and TTH levels by leaf extracts may be the primary protective mechanism in APAP induced hepatotoxicity. Further treatments with ethanolic extract showed more hepatoprotective potential than the aqueous extract of A. scholaris.
Keywords: Acetaminophen; Alstonia scholaris; Malondialdehyde.; Super oxide dismutase; Total antioxidant status; Total thiols

Acute and sub-acute Toxicity study of Aqueous extracts of Canscora heteroclita (L) Gilg in Rodents - Rajasekaran Aiyalu; Arivukkarasu Ramasamy (Pharmacognosy Journal, 2016)
Background: Canscora heteroclita (C. heteroclita) being used in the Ayurvedic system of medicine in India for treatment of various diseases. No systematic toxicity study for this plant was described. Objective: The present study was undertaken to assess the safety use of this plant in traditional practice. Materials and Methods: The acute oral toxicity study of aqueous extract of Canscora heteroclita (AECH) was carried out as per the OECD guidelines 423 in mice and the sub-acute toxicity was carried out at a dose of 200 mg/kg and 400 mg/kg as per OECD 407 guidelines in male and female rats. Results: Mice administered upto 2000 mg/kg as a single dose orally not caused any signs of toxicity or mortality in mice. In sub-acute toxicity study in rats, AECH at two different daily doses of 200 and 400 mg/kg for 28 days did not cause any significant change including the hematological and biochemical parameters. Histopathological examinations showed normal architecture suggesting no morphological disturbances. Conclusion: No deaths or any signs of toxicity was observed after oral administration in acute toxicity study upto a dose of 2000 mg/kg of AECH in mice and upto a dose of 400 mg/kg of AECH in sub acute toxicity study in rats.
Keywords: Acute toxicity; Biochemical; Canscora heteroclita; Histology.; Sub-acute toxicity

Acute and Sub-acute Toxicity Study of Aqueous Extracts of Enicostemma axillare (Lam.) Raynal in Animal models - Aiyalu Rajasekaran; Ramasamy Arivukkarasu (Pharmacognosy Journal, 2016)
Background: Enicostemma axillare (Lam.) Raynal is used in traditional practice for the treatment of diabetes, malaria and liver disorders. No systematic toxicity study was described for this plant and hence the present was undertaken to evaluate acute and sub-acute toxicity of aqueous extract of Enicostemma axillare (AEEA). Objective: The acute oral toxicity study of AEEA was carried out as per the OECD guidelines 423 in mice and the sub-acute toxicity was carried out as per the guidelines set by OECD 407 in male and female rats. Materials and Methods: Body weight, food and water consumption, hematological parameters, biochemical parameters, organ weight and histopathological analysis were carried out. Results: No gross toxicity and mortality was observed upto a dose of 2000 mg/kg. For sub-acute toxicity test, 200 mg/kg and 400 mg/kg daily dose of AEEA administered orally for 28 days in male and female group of rats not exhibited any signs of toxicity and mortality. Conclusion: In acute oral toxicity study, the oral administration of AEEA in mice was found to be safe up to a dose of 2000 mg/kg. Both male and female treated rats showed no change in hematological, biochemical and histological investigations and no signs of toxicity were observed upto the dose of 400 mg/kg in rats.
Keywords: Acute toxicity; Enicostemma axillare; Histology; OECD guidelines; Sub-acute toxicity.

Acute toxicity study of Phyllanthus niruri and its effect on the cyto-architectural structure of nephrocytes in Swiss albino mice Mus-musculus - Tanuja Singh; Ruchi; Anjali singh; Ravish Kumar; Jitendra Kumar Singh (Pharmacognosy Journal, 2016)
Background: In the era of herbal renaissance, world is moving towards the medicinal plant that repairs and strengthening the body system without any toxic side effects. Popular medicinal plant Phyllanthus niruri contains various bioactive molecules, the present study aimed to observe the biochemical and cyto-architectural alterations in kidney associated with acute oral toxicity (LD50) of aqueous extract of P.niruri in Swiss albino mice. However, limited data is available about the toxicity of herbal remedies used for medication, which is a critical constrain. Materials and Methods: For the acute oral toxicity study, the animals were divided into six groups of 6 mice each. Group–I was named control group and the treatment groups were administered aqueous leaf extract of P.niruri orally at different doses of 500 mg/Kg bw (Group-II), 1000 mg/Kg bw (Group-III), 2000 mg/Kg bw (Group-IV), 2500 mg/Kg bw (Group-V) and 3000 mg/Kg bw (Group-VI) for 15 consecutive days. The mice were sacrificed on and serum was collected for the biochemical analysis. The kidney was dissected and processed for histological analysis. Results: The LD50 dose of P.niruri was found to be 2590.984 mg/Kg bw in Swiss albino mice model in laboratory condition. The result showed the elevated serum level of urea in treated group of mice at higher doses which was found to be statistically significant as compared to the control (Group–I). There were no any significant increase in serum creatinine has been observed. Histological alteration were observed at higher dose more than 2500 mg/Kg bw (Group-VI). Conclusion: It is evident from our study that P. niruri may have toxic effect at high doses. Therefore, it should be ingested with precautions.
Keywords: Biochemical; Histological analysis; Kidney; LD50; P. niruri.

Analytical Quantifiation, immunomodulatory and Sulforhodamine B assay studies on Albizia lebbeck Leaves Extracts - Gaurav Mahesh Doshi; Manjushree kundalik Pawar; Kajal Haribhai Chavda (Pharmacognosy Journal, 2016)
Background: Albiza lebbeck leaves have been well known for its ethnopharmacological prospects. Objective: The present study aims three extracts (aqueous, methanolic and hydromethanolic) at two dose levels by oral administration by using immunomodulatory models and in vitro cell lines in correlation to analytical studies. Methods: The extracts were subjected to Haemagglutination Antibody Titre and DTH Delayed-Type Hypersensitivity reaction based on acute toxicity results. Chromatographic studies were undertaken comprising of Fourier Transform Infrared Spectroscopy and High performance Thin layer Chromatography and screened for in-vitro cell lines such as MCF-7 and HCT 15 by Sulforhodamine B Assay Method. Results: No response was shown at 100 mg/kg. Significant immunomodulatory effect was noticed at 200 mg/kg with Haemagglutination Antibody Titre (554.66 ± 102.78, 597.33 ± 85.35, 426.66 ± 53.98) and DTH Delayed- Type Hypersensitivity reaction (0.225±0.01, 0.21 ± 0.01, 0.23 ± 0.01) which showed decrease in paw volume (after 48 h) in case of Sheep Red Blood Cells, (0.5×109) used as antigens. Total flavonoids content in the extracts were revealed by methods described by Singleton and Quettier. Flavonols such as rutin and quercetin were detected by Fourier Transform Infrared Spectroscopy based on determination of the functional groups and High Performance Thin layer Chromatography showed well resolved spots. The extracts were screened on in-vitro cell lines (MCF 7 and HCT 15) by using Sulforhodamine B Assay method were unsatisfactory results were obtained at final concentrations of 10 μg/ml, 20 μg/ml, 40 μg/ml, 80 μg/ml. Conclusion: Thus, present paper suggests that extracts has served as a promising immunomodulator for immune system disorders.
Keywords: Delayed-Type Hypersensitivity response; Fourier Transform Infrared Spectroscopy; Haemagglutination Antibody Titre; High performance Thin layer Chromatography; MCF-7.; Quercetin; Rutin

Anti-anemia Effect of Chlorophyll from Katuk (Sauropus androgynus) Leaves on Female Mice Induced Sodium Nitrite - Suparmi Suparmi; Sampurna Sampurna; Nur Anna C.S; Alvenia Meilina Ednisari; Galuh Dea Urfani; Iqrommatul Laila; Heavin Rakhmat Saintika (Pharmacognosy Journal, 2016)
Context: Sodium nitrite (NaNO2) in blood is highly reactive with haemoglobin (Hb), thus affecting hematopoiesis and induction of methemoglobinemia. Aim: This study was conducted to determine the effect of chlorophyll from katuk (Sauropus androgynus) leaves on the level of Hb, Malondialdehyde (MDA), ferritin, and schistocytes percentage in female mice induced NaNO2. Settings and Design: Experimental research was conducted using 24 female mice strain Balb-c. Methods and Material: NaNO2 0.3 ml/head/day given during 18 days, while the chlorophyll or Cu-chlorophyllin as much as 0.7 ml/head/day given the following day for 14 days. Statistical analysis used: Results are reported as mean values ± SD and statistically analyzed by One Way Anova test with 95% significance level. Results: The Hb levels of blood plasma in the control group, NaNO2 induction, induction NaNO2 and chlorophyll of katuk leaves (NaNO2+katuk), induction of NaNO2 and Cu-chlorophyllin from K-LiquidTM (NaNO2+Cu-chlorophyllin) in sequence is 13.29 g/dl; 11.83 g/dl; 14.54 g/dl; 13.99 g/dl, whilst the MDA levels in each group is 2.10 ± 0.11 mol/L, 3.44 ± 0.38 mol/L, 2.31 ± 0.18 mol/L, 2.31 ± 0.13 mol/L, and the ferritin levels is 62.71 ± 6.42 ng/ml; 63.22 ± 7.59 ng/ml; 67.45 ± 8.03 ng/ml, and 64.74 ± 7.80 ng/ml, respectively. The fragment schistocytes ocyte percentage’s in each group is 0%, 0.11%, 0.01%, 0.03%. The ferritin levels tend to increase in NaNO2+katuk. Mann Whitney test results obtained no significant difference in Hb, MDA level and schistocytes percentage between the groups of mice that received NaNO2+katuk NaNO2+Cu-chlorophyllin (p>0.05). This indicates that chlorophyll from S. androgynus leaves as effective as Cu-chlorophyllin in decrease the MDA levels after NaNO2 treatment, and although not significant, it can increase ferritin levels. Conclusion: The antioxidant activity of chlorophyll from katuk leaves are able to decrease schistocytes percentage’s and MDA level. The increasing of Hb and ferritin level indicates its potential in the treatment of haemolityc anaemia. Further studies aimed at the mechanisms of action of this chlorophyll are needed.
Keywords: Anemia; Chlorophyll; Ferritin; Schistocytes.; Sodium nitrite

Anti-Anemia Effect of Standardized Extract of Moringa Oleifera Lamk. Leaves on Aniline Induced Rats - Abdul Mun’im; Meidi Utami Puteri; Santi Purna Sari; Azizahwati (Pharmacognosy Journal, 2016)
Background: The leaves of Moringa (Moringa oleifera Lamk.) have been empirically used as anti-anemia for pregnant woman. Objectives: In the present study, the effect of ethanolic extract of moringa leaves was evaluated on the hematology parameters (hemoglobin, red blood cell count, hematocrit), on aniline induced white female rats. Materials and Methods: Thirty female rats strain Sprague-Dawley were divided into six groups: normal, anemia and ferrous fumarate group, and three groups of Moringa leaves extract. All groups, except normal group, induced by aniline at dose 0.005 ml/ g bw intraperitonially. On fifth day, normal and anemia groups were given 0.5% CMC, ferrous fumarate group was given ferrous fumarate orally and three other groups were given Moringa leaves extract at doses 198 mg, 396 mg, and 792 mg/200 g bw until the eleventh day. Results: The results showed that as Moringa leaves extracts increased the level of hemoglobin, red blood cell count, hematocrit, and total iron content in blood. Moreover, Moringa leaves extract at dose 792 mg/200 g bw can improve red blood cell’s morphology and increased the level of hemoglobin and red blood cell count significantly (p<0.05). Conclusion: The ethanolic extract of Moringa leaves showed anti-anemia on aniline-induced rats.
Keywords: Anemia; Aniline; Erythrocyte; Moringa Oleifera L; Total Iron.

Antibacterial activity of Shin'iseihaito (Xin Yi Qing Fei Tang) against Streptococcus pneumoniae - Toru Konishi; Masaaki Minami; Zhixia Jiang; Tetsuya Arai; Toshiaki Makino (Pharmacognosy Journal, 2016)
Objective: Shin'iseihaito (Xin yi qing fei tang in Chinese, SSHT), a formula in traditional Japanese Kampo medicine and Chinese medicine comprising nine crude drugs, Gypsum, Ophiopogon Tuber, Scutellaria Root (SR, root of Scutellaria baicalensis), Gardenia Fruit, Anemarrhena Rhizome, Lilium Bulb, Magnolia Flower, Loquat Leaf, and Cimicifuga Rhizome, is commonly used to treat sinusitis associated with purulent nasal discharge and reddish nasal mucosa. We evaluated anti-bacterial activity of SSHT extract on Streptococcus pneumoniae, the major cause of bacterial sinusitis. Materials and Methods: Sterile paper disks impregnated with SSHT extract or each extract of its component were placed on sheep blood agar plates inoculated with Streptococcus pneumoniae (ATCC 49619). The diameter of inhibitory zone was measured after 20-24 h incubation. Results: SSHT extract and each water extract of Ophiopogon Tuber, SR, Gardenia Fruit, Anemarrhena Rhizome, Lilium Bulb, Magnolia Flower, and Cimicifuga Rhizome showed significant antibacterial activity against Streptococcus pneumoniae, and SR extract exhibited the largest inhibitory zone. SR extract was partitioned into AcOEt, BuOH, and water layer, and water layer was further separated into 80% EtOH soluble and insoluble fraction. Among them, only 80% EtOH soluble fraction was exhibited antibacterial activity. In this fraction, we found baicalin as the major compounds, and baicalin exhibited antibacterial activity against Streptococcus pneumoniae in concentration-dependent manner.  Conclusion: SSHT has antibacterial activity against Streptococcus pneumoniae, and SR and its major constituent baicalin contribute to the antibacterial activity of SSHT against Streptococcus pneumoniae.
Keywords: Antibacterial activity; Baicalin; Scutellaria baicalensis; Shin'iseihaito; Sinusitis; Streptococcus pneumoniae.

The Anticancer Potential of Pavonia odorata extract on Human Breast (MD-MB-231), Prostate (PC-3) and Lung (Calu-6) Cancer cell lines - Girish H V; Vinod A B; Dhananjaya B L; Satish Kumar D; Senthil Duraisamy (Pharmacognosy Journal, 2016)
Introduction: A huge reservoir of bioactive compounds exists in many species of plants, only a small percentage of which have been examined and continued to be an important source of anticancer agents. Worldwide effects are ongoing to identify new anticancer compounds from plants. With the current decline in the number of new molecular entities from the pharmaceutical industry, novel anticancer agents are being sought from traditional medicines. Objective: In the present study we investigated the efficacy of methanol extracts of Pavonia odorata, for its clonogenic inhibition on Human Breast cancer (MD-MB-231), Prostate cancer (PC-3) and Lung cancer (Calu-6) cell lines. Materials and Methods: The cytotoxic effect was evaluated by MTT assay. Results: The methanol extract of P. odorata showed significant cytotoxicity against MD-MB-231 and Calu-6, when compared to PC-3cells. Conclusion: The methanol extracts of P. odorata, showed effective cytotoxic activities in a dose dependent manner. Future work will be interesting to know the chemical composition and also better understanding the mechanism of action will help in developing it as drug for therapeutic application.
Keywords: Alternative medicine; Anti-cancer; Drugs; Indian Medicinal plants; Inhibition.

Anti-inflammatory activity of BCM-95 (bio-enhanced formulation of turmeric with increased bioavailabilty) compared to Curcumin in Wistar rats - Sayeli Vinaykumar; Urval Pundarik Rathnakar; Ullal Sheetal Dinkar; Kamath Priyanka; Tiwary Gaurav; Shenoy Ashok Kudgi; Revappala Sekhar Nishith (Pharmacognosy Journal, 2016)
Objective: To evaluate anti-inflammatory activity of bioenhanced turmeric formulation (BCM-95) compared to commercial Curcumin formulation (Curcuminoids 95%) in Carrageenan-induced acute inflammatory model. Materials and Methods: Thirty six Wistar rats were divided into six groups-Normal control (2 ml of vehicle), Standard control (Indomethacin 10 mg/kg), 2 doses of BCM 95 (10 and 20 mg/kg) and Curcuminoids 95% (10 and 20 mg/kg). Paw volume was measured using a digital plethysmometer. Vehicle or test drugs were given to rats 30 min before carrageenan administration. Baseline paw volume reading (V0) was noted just prior to administration of 0.1 ml of 1% carrageenan to right hind paw of the rat. Test paw volume readings (Vt) were measured at 30, 60, 120, 180, 240, 300 and 360 min, after carrageenan injection. Oedema expressed as increased paw volume (vt-v0) was noted and percentage inhibition of oedema was calculated for all treatment groups. Statistical analysis: Difference between groups were analyzed with ANOVA followed by Tukey test. Results: All treatment groups demonstrated significant (p<0.05) anti-inflammatory activity (oedema suppression) compared to normal control. Anti-inflammatory activity of BCM 95 treated groups were comparable to standard control group except at certain time points, whereas the same activity at all-time points with Curcuminoid 95% treated groups were significantly less than standard control group. Percentage inhibition of paw oedema was maximum with standard control group followed by BCM 95 treated groups followed by Curcuminoid 95% treated groups. Conclusion: BCM 95 treated groups showed significant anti-inflammatory activity compared to Curcuminoid 95% treated groups.
Keywords: Anti-Inflammatory agents; Bioavailability; Curcumin; Inflammation; Wistar rats.

Antiobesity activity of Zingiber officinale - Iram Nazish; S H Ansari; Poonam Arora; Adil Ahmad (Pharmacognosy Journal, 2016)
Context: Zingiber officinale Roscoe (Zingiberaceae) rhizome, known commonly as ginger is extensively used in Indian traditional system of medicine for treatment of various disorders. The ethanolic Z. officinale extract is reported to have various activity such as antidiabetic, antihyperlipidemic and antioxidant activity in experimental animals. Objective: To evaluate anti-obesity effect of aqueous Z. officinale extract in murine model of high fat diet (HFD)- induced obesity. Materials and Methods: Male Wistar rats fed with HFD (20 g/day/rat, p.o) for a period of 42 days were used to induce obesity. Aqueous Z. officinale extract (20 mg/kg b.w.) administered orally to HFD fed rats from day 8 to 50 days for a period of 42 days. Body weight gain, serum lipids, insulin and leptin parameters were measured. Results: Oral feeding of the aqueous Z. officinale extract (20 mg/kg) to HFD-induced obese rats for a period of 42 days resulted in significant reduction in body weight gain, insulin, leptin, lipids as compared to rats fed HFD alone. Further, the extract also showed significant increase in high density lipoprotein (HDL-C) levels. Discussion and Conclusion: These results show that aqueous Z. officinale extract possess significant anti-obesity potential.
Keywords: High-fat diet; Insulin.; Leptin; Rat; Zingiber officinale

Antioxidant Activity of Leaf Extract of Aegle marmelos Correa ex Roxb. - Sachin Kumar; Ramesh B. Bodla; Himangini Bansal (Pharmacognosy Journal, 2016)
Introduction: Leaf extracts of Aegle marmelos are reported to have hypoglycemic and anticancer effects. While a lot of information is available about the antioxidant activity of fruit of A. marmelos not much information is available about the antioxidant activity of the leaf of A. marmelos. Objective: The primary objective if this study was to ascertain the antioxidant activity of leaf extract of A. marmelos (AME). Methods: AME was evaluated for total phenolic content (TPC) and total flavonoid content (TFC) by Folin-Ciocalteau reagent method and by aluminium chloride method, respectively. Antioxidant activity of AME was assessed by FRAP assay, DPPH assay, ABTS cation scavenging activity and by reducing power determination. Results: High levels of TPC and TFC were found in AME which showed antioxidant activity comparable to vitamin C. Significant correlation between TPC, TFC and antioxidant activity of AME was found when Pearson’s correlation is applied. Conclusion: This study proved that the leaves of A. marmelos have high antioxidant component.
Keywords: Aegle marmelos; Cation scavenging; Free radical scavenging; Reducing power.

Antioxidant and Hypoglycemic Activities of Clausena anisata (Willd.) Hook F. Ex Benth. Root Mediated Synthesized Silver Nanoparticles - Arsia Tarnam Yakoob; Nargis Begum Tajuddin; Muhammad Ilyas Mohammed Hussain; Shilu Mathew; Archunan Govindaraju; Ishtiaq Qadri (Pharmacognosy Journal, 2016)
The present study was carried out to examine the hypoglycemic effect of Silver Nanoparticles (SNPs) using ethanolic root extract of Clausena anisata (Willd.) Hook. f. ex Benth. A cost effective and eco friendly technique for green synthesis of SNPs from 1mM AgNO3 solution through the root extract was carried out. The biosynthesized SNPs were characterized using UV spectrophotometry, Field Emission Scanning Electron Microscopy (FESEM), X-ray Diffraction analysis (XRD), Energy Dispersive Spectroscopy (EDS) and Fourier transform infra-red (FTIR) spectrometry. DPPH assay was done to determine the antioxidant activity and for in vitro hypoglycemic activity glucose uptake by yeast cells, alpha amylase inhibition assay, adsorption capacity and glucose diffusion assay was performed. The SNPs of ethanolic root extract were found to be spherical in shape and up to 32.75 nm average in size. They showed alpha amylase inhibitory activity of 83.60% at 500 μg/ml. The glucose uptake by yeast cells was found to increase with an increase in concentration. The maximum glucose uptake was found to be 69.51% at 10mM concentration. The molar concentration of glucose was directly proportional to the glucose binding capacity of extracts.The rate of glucose diffusion across the membrane was found to increase from 30 to 180 minutes. The DPPH scavenging activity was found to be potent (74.07%) at 500 μg/ml. The hypoglycemic effect exhibited by the SNPs was revealed by simple in vitro model of yeast cells, mediated by glucose adsorption, increasing glucose diffusion and glucose transport across the cell membrane.
Keywords: antioxidant activity; C. anisata; Diabetes; Glucose and Silver nitrate; Silvernanoparticles

Assessment of Total Phenolic, Flavonoid, Tannin Content and Phytochemical Screening of Leaf and Flower Extracts from Peltophorum pterocarpum (DC.) Backer ex K.Heyne: a comparative study - Peraman Muthukumaran; Nachimuthu Saraswathy; Vijayasekar Aswitha; Ramesh Balan; Venkatesh Babu Gokhul; Palanikumar Indumathi; Sivasubramani Yuvapriya (Pharmacognosy Journal, 2016)
Introduction: Total phenolic, flavonoid and tannin content of leaf and flower extract of Peltophorum pterocarpum (DC.) Backer ex K.Heyne was compared. Objective: To explore total phenolic, flavonoid and tannin content of both leaf and flower extracts of Peltophorum pterocarpum (DC) K Heyne. Method: Initially, collected fresh leaves and flower samples were shade dried and extracted with various solvents such as aqueous methanol (1:1), ethyl acetate, ethanol and aqueous. Qualitative analysis was performed for various phytochemical. Then the total phenolic content, total flavonoid content and total tannin content was estimated. Results: In preliminary phyto-chemical examination of various solvent extracts of both leaf and flowers of P. pterocarpum revealed that the presence of various phytochemicals such as phlobatannins, terpenoids, alkaloids, saponins, tannin, reducing sugars, phenols and steroids. In phtyochemical evaluation, when compare with all other solvents, Ethanolic extracts shows maximum extractive value. In case of ethyl acetate, it shows very low extractive value in all three phyto-chemicals. In phytochemical evaluation studies, total phenolic content of leaves shows highest in ethanolic extract (33.17 ± 4.72 mg/g) and lowest in ethyl acetate extract from flower (4.71 ± 0.07 mg/g), Similarly, flavonoid content of leaves shows highest in ethanolic extract (1.43 ± 0.01 mg/g) and lowest in aqueous extract of flower (0.23 ± 0.09 mg/g) but in case of tannin content, flower extracts shows higher tannin content in ethanolic extract (844.59 ± 10.38 mg/g) whereas lowest tannin content in leaf ethyl acetate extract (9.54 ± 6.98 mg/g). Conclusion: This is first report of comparative studies on total phenolic, flavonoid and tannin content of various solvent extracts both leaves and flowers from Peltophorum pterocarpum (DC) K Heyne.
Keywords: Flavonoid; Peltophorum pterocarpum; Phenolic content; Phytochemicals; Solvent extraction.; Tannin

Awareness of Complimentary and Alternative Medicine- A Cross Sectional Survey Among Pharmacists - Reshmi B; Thangavelu Lakshmi (Pharmacognosy Journal, 2016)
Aim: To determine the prevalence of complementary and alternative medicine among pharmacists. Materials and method: This survey was a cross sectional study. A set of 30 questionnaires containing 15 questions where given to various pharmacists of different colleges. Datas were collected and statistics was done using SPSS software and represented in graph form. Background: Use of complementary and alternative medicine (CAM) by the U.S. population increased significantly in the past 2 decades. The purpose of this study was to determine, among the Indian community, the prevalence and utilisation patterns of complementary and alternative medicine (CAM), attitudes associated with CAM use and communication patterns of CAM users. Conclusion: The knowledge about and use of CAM is wide among pharmacists . In- depth studies on the knowledge and use of CAM among other health care professionals and among ethnic minorities are urgently needed and may help to better manage the treatment of minor disorders as well as chronic diseases.
Keywords: awareness; Complementary and alternative medicine; knowledge; pharmacist

Bacillus anthracis growth Inhibitory Properties of Australian Terminalia spp.: Putative Identification of low Polarity Volatile Components by GC-MS Headspace Analysis - Mitchell Henry Wright; Joseph Sirdaarta; Alan White; Anthony Carlson Greene; Ian Edwin Cock (Pharmacognosy Journal, 2016)
Introduction: Anthrax is a severe acute disease caused by Bacillus anthracis infections. If untreated, it often results in mortality. Many Terminalia spp. have documented therapeutic properties as general antiseptics, inhibiting the growth of a wide variety of bacterial species. This study examines the ability of selected Australian Terminalia spp. extracts to inhibit B. anthracis growth. Methods: Solvent extracts were prepared from Terminalia carpentariae and Terminalia grandiflora plant material and investigated by disc diffusion assay for the ability to inhibit the growth of an environmental strain of B. anthracis. 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 analysed by GC-MS headspace analysis. Results: T. carpentariae and T. grandiflora leaf, fruit and nut solvent extractions displayed good growth inhibitory activity against B. anthracis. Methanolic T. Carpentariae leaf and T. grandiflora nut extracts were particularly potent growth inhibitors, with MIC values of 74 and 155 µg/mL respectively. The T. carpentariae leaf ethyl acetate extract was also a good inhibitor of B. anthracis growth (MIC 340 µg/mL). All other extracts were substantially less potent growth inhibitors. Interestingly, the T. Carpentariae leaf extracts with growth inhibitory activity were nontoxic in the Artemia fransiscana bioassay, with LC50 values >1000 µg/mL. In contrast, the LC50 value 740 µg/mL reported for the methanolic T. grandiflora nut extract indicates low-moderate toxicity. Non-biased GC-MS phytochemical analysis of the most active extracts (methanolic T. carpentariae leaf and T. grandiflora nut) putatively identified and highlighted several compounds that may contribute to the ability of these extracts to inhibit the growth of B. anthracis. Conclusions: The growth inhibitory activity of the methanolic T. Carpentariae leaf and T. grandiflora nutextracts against B. anthracis indicates their potential for the treatment and prevention of anthrax. Furthermore, thelack toxicity of the T. Carpentariae leaf and the low-moderate toxicity of the T. grandiflora nut extract, indicates that their use may extend to all forms of the disease (cutaneous, inhalation or gastrointestinal).
Keywords: Anthrax; Combretaceae; Metabolomic profiling.; Native almond; Terminalia carpentariae; Terminalia grandiflora; Wild peach

Bioactive Compounds and Cytotoxicity of Ethyl Acetate Extract From Broussonetia luzonica (Moraceae) Blanco Leaves against Hepatocellular Carcinoma (Hepg2) Cell Lines - Franelyne P. Casuga; Agnes L. Castillo; Mary Jho-Anne T. Corpuz (Pharmacognosy Journal, 2016)
Introduction: Broussonetia luzonica (Moraceae) Blanco is an edible and endemic plant in the Philippines. Other species of the plant are used traditionally in Chinese medicine to treat impotency and eye disorders and was proven to have anticancer potential. To date, there are no published scientific evidences yet to prove the cytotoxicity against hepatocellular carcinoma cell lines (HepG2) of B. luzonica. Furthermore, the bioactive compounds of the ethyl acetate leaf extract were determined. Methods: Bioactive compounds were determined using Gas Chromatography-Mass Spectrometry (GC-MS). To determine the IC50, the percentage Hepg2 Cell inhibition of the extract at 200 μg/mL, 100 μg/mL, 50 μg/Ml, 25 μg/mL And 12.5 μg/ mL concentrations against (HepG2) was evaluated using 3-(4,5-Dimethylthiazol- 2yl)-2,5-Diphenyltetrazolium Bromide (MTT) Assay. Results: GC-MS revealed the top three major bioactive compounds of ethyl acetate leaf extract based on quantity (%). These are 1,2,3-propanetriol, monoacetate (21.21%), phytol (20.28%) and squalene (6.85%). MTT assay showed that ethyl acetate extract at different concentrations exhibited marked inhibition of the HepG2. The concentration of the extracts that will inhibit 50% of the cancer cell lines (IC50) was also determined. The assay revealed that compared to positive control (doxorubicin) with IC50 5.068 μg/mL, Ethyl Acetate Extract statistically exhibited greater cytotoxic effect against HepG2 Cell Lines With IC50 1.118 μg/mL (P=0.001). Conclusion: The presence of several bioactive compounds in ethyl acetate extract from the leaves of B. luzonica confirms the importance of the plant in treatment of diseases. Furthermore, the extract manifested more potent cytotoxic activity than the positive control, indicating promising chemotherapeutic potential of the plant.
Keywords: Endemic; GC-MS; Liver cancer; MTT Assay.

Bioactive Constituents of Pulicaria jaubertii: A promising Antihypertensive Activity - El-Sayed M. El-Ghaly; Usama Shaheen; Ehab Ragab; Atef Ahmed El-hila; Mohamed Raafat Abd-Allah (Pharmacognosy Journal, 2016)
Objective: Phytochemical investigation and evaluation of antihypertensive activity of the alcoholic extract of Pulicaria jaubertii aerial parts. Material and Methods: The chloroform and ethyl acetate fractions were chromatographed on silica gel and sephadex LH 20 to afford six compounds. Their structures were elucidated on the bases of extensive NMR (1H, 13C, DEPT, COSY, HSQC, HMBC, NOESY) and MS analysis. The antihypertensive activity of the alcoholic extract was evaluated against L-NAME–induced hypertensive rats. Results: One new monoterpene glucoside; (2R, 4S)-p-menth-1-ene- 2-O-b-D-glucopyranoside [1] along with five known compounds; thymoquinol 2-O-b-D-glucopyranoside (zataroside-B) [2], quercetin 7, 3`-di-Omethylether (rhamnazin) [3], quercetin 7-O-methylether (rhamnetin) [4], quercetin 3`-O-methylether (isorhamnetin) [5] and stigmasterol 3-Ob- D-glucopyranoside [6] were isolated. The alcoholic extract significantly reduced the elevated SBP and partially restored the diminished nitric oxide metabolites. Conclusion: Compound [1] is a new and compounds [2-6] are reported for first time from Pulicaria jaubertii. The possible antihypertensive activity of the alcoholic extract may be due to its flavonoids and phenolic contents.
Keywords: Antihypertensive activity; Flavonoids; Monoterpene glucoside; Nitric oxide.; Pulicaria jaubertii

Bioactive Fraction from Datura stramonium Linn. Promotes Human immune Cells Mediated Cytotoxicity towards Lung and Breast Cancer Cells - Aditi Gupta; Sunil Kumar; Neeraj Mahindroo; Reena Vohra Saini (Pharmacognosy Journal, 2016)
Aim: The aim of the present study was to evaluate immune modulatory effect of fractions of D. stramonium L. leaves on human peripheral blood mononuclear cells (PBMC) followed by assessment of cytotoxic abilities of immunomodulated PBMC toward cancer cells. Material and methods: Bioassay (PBMC proliferation) guided fractionation of methanolic leaf extract of D. stramonium was performed to get active fraction and LC-MS was performed to identify the phytocompounds present in the bioactive fraction. The immunomodulatory potential of D. stramonium active fraction was assessed by i) MTT microcytotoxicity assay using A549 (lung carcinomas) and MCF-7 (breast cancer) cell lines and ii) analyzing the production of IL-2 and IFN-γ by human PBMC in the presence of active fraction. Results: Chromatographic fractionation guided by PBMC proliferation assay of D. stramonium extract resulted in bioactive fraction (fraction-10) exhibiting significant immunostimulatory activity [EC50=19.1±1.5 (μg/ml)] on human blood lymphocytes. Fraction-10 pretreated PBMC displayed enhanced cytotoxicity towards A549 and MCF-7 (59%±2.1% and 62%±2.3% at 1:20 effector:target ratio respectively). Moreover, fraction-10 also enhanced the secretion of IL-2 (8 fold) and IFN-γ (10 fold) by human PBMC. The preliminary phytochemical analysis of fraction-10 from D. stramonium showed the presence of terpenoids and steroids. LC-MS analysis depicted presence of four major phytoconstituents in fraction-10 as daturaolone, daturadiol, stigmasterol and sitosterol with corresponding mass spectrum (m/z) of 440, 442, 412 and 414 respectively. Conclusion: The present report concluded that active fraction-10 of D. stramonium possesses potential immunostimulators that are capable of enhancing anticancer responses of human blood lymphocytes.
Keywords: Anticancer; Cytokine; Cytotoxic; Datura stramonium.; Immunomodulation; PBMC

Bioactivity Guided Fractionation of Ethanol Extract of Caesalpinia digyna Rottler Roots - Jitender Singh; Ashwani Kumar; Anupam Sharma (Pharmacognosy Journal, 2016)
Background: Authors have reported earlier that ethanol extract of Caesalpinia digyna Rottler roots exhibits significant antianxiety activity at 400 mg/kg, po, in mice using elevated plus-maze (EPM). Objective: Aim of the study was to isolate antianxiety principle(s) from ethanol extract of C. digyna roots following bioactivity guided fractionation approach. Materials and Methods: Bioactive ethanol extract was partitioned with ethyl acetate to get ethyl acetate soluble (EASF) and ethyl acetate insoluble (EAIF) fractions. A compound (CD1) precipitated from EASF. The two fractions and CD1 were evaluated for antianxiety activity in mice. Column chromatography of EASF yielded 5 fractions (F1-F5), all of which were evaluated for antianxiety activity using EPM. Results: Present study revealed that EASF (80 mg/kg) and CD1 (40 mg/kg) exhibited significant antianxiety activity, while EAIF does not. Among the five fractions, only F4 (40 mg/kg, po), exhibited significant antianxiety activity, which was statistically comparable to that of diazepam (2 mg/kg). Conclusion: Present investigation reveals that EASF obtained by partitioning of ethanol extract of C. digyna roots with ethyl acetate, and a compound CD1, isolated from EASF, exhibit significant antianxiety activity. Among 5 fractions (F1-F5) obtained from column chromatography of EASF, only F4 exhibited significant antianxiety activity. F4 is being processed further to isolate the anxiolytic constituent(s), and CD1 is being characterized.
Keywords: Antianxiety; Bioactivity-guided fractionation; Caesalpinia digyna; Elevated plus-maze.

Bio-Flavonoids and Garcinoic Acid from Garcinia kola Heckel Seeds with Promising Antioxidant Potentials - Tchimene Kenne Michel; Anaga Arua Ottoh; Ugwoke Christopher Emeka Chukwunonye; Ezugwu Christopher Obodoike; Okunji Christopher; Iwu Maurice Mmaduakolam (Pharmacognosy Journal, 2016)
Objective: The research was carried out to investigate the anti-inflammatory effect of ethanol extract, fraction (kolaviron) and compounds (garcinoic acid, GB1 and GB2) of Garcinia kola seeds. Materials and Method: To evaluate the acute anti-inflammatory effect of extract, fraction and compounds of G. kola carrageenan-induced edema model in wistar albino rats was used. Results: Kolaviron (50 mg/kg), garcinoic acid (50 mg/kg) and the crude extract (50 mg/kg) caused 100, 83 and 74% inhibition of carrageenan-induced paw edema respectively at 6 h post administration. Indomethacin (10 mg/ kg), the reference drug induced 100% inhibition of carrageenan-induced paw oedema. While GB1 (50 mg/kg) and GB2 (50 mg/kg) was prominent at 4, 5 and 6 h post administration. Conclusion: Results showed that the extract possessed anti-inflammatory activity, which have justified their use in Nigeria traditional medicine to treat inflammation.
Keywords: Anti-inflammatory; Carrageenan; Garcinia kola; Paw edema; Wistar rats.

Bioprospecting of some medicinal plants explored for antifungal activity - Kumara Shanthamma Kavitha; Sreedharamurthy Satish (Pharmacognosy Journal, 2016)
In the present study, evaluation of different plant parts of fifteen medicinal plants belongs to different families have been screened for in vitro efficacy of antifungal activity against phyto pathogenic (Aspergillus and Fusarium species) as well as human pathogenic fungi (Candida albicans and Microsporum species) using agar well diffusion assay. The results showed that among fifteen medicinal plants, crude extracts of different solvents viz., petroleum ether, chloroform, ethyl acetate and methanol tested for antifungal activity, twelve plants were found to be effective against one or the other test fungi, among these plants, solvent extracts of Callistemon lanceolatus showed significant activity against C. albicans, Microsporum gypseum, Cordia dichrotoma leaves extracts exhibited significant activity against A. niger, A. flavus and C. albicans. Sphaeranthus indicus L. whole plant extracts exhibited significant activity against Aspergillus spp., C. albicans and Microsporum canis. Leaves extracts of Vitex negundo exhibited significant activity against A. niger, A. flavus, F. verticillioides, C. albicans and moderate activity against F. crookwellense. Extracts of Butea monosperma exhibited significant to moderate activity against all test pathogens except C. albicans. The obtained results imparts a preliminary piece of significant information regarding the antifungal potentiality of screened medicinal plants and thus our present investigation depicted an outline interpretation of significant activity with crude solvent extracts, which could be exploit for further isolation and investigation of antifungal agents for crop diseases management and human health. Keywords: Nill

Cakile maritima Scop. extracts inhibit the growth of some bacterial triggers of autoimmune diseases: GC-MS analysis of an inhibitory extract - Elsayed Omer; Abdelsamed Elshamy; Abdel Nasser El Gendy; Xin Cai; Joseph Sirdaarta; Alan White; Ian Edwin Cock (Pharmacognosy Journal, 2016)
Introduction: High antioxidant capacities have been linked to the treatment of rheumatic diseases and also in the inhibition of microbial growth. Although Cakile maritima has a high antioxidant capacity, it is yet to be tested for the ability to inhibit the growth of the bacterial triggers of autoimmune inflammatory diseases. Methods: C. maritima solvent extracts were analysed for antioxidant capacity by the DPPH free radical scavenging assay. Growth inhibitory activities against bacterial species associated with initiating rheumatoid arthritis, ankylosing spondylitis and multiple sclerosis were determined by disc diffusion assay and quantified by MIC determination. Toxicity was determined by Artemia franciscana bioassay. Results: All C. maritima solvent extracts displayed good DPPH radical scavenging activity, although the ethyl acetate extract was particularly potent with an IC50 values of 3.4 μg/mL. The other extracts also had significant radical scavenging activity, with IC50 between 4.7 and 13.6 μg/mL. The bacterial growth inhibitory activity of the extracts correlated with their free radical scavenging activity. The ethyl acetate extract displayed the most potent growth inhibitory activity against most bacterial species. This extract was particularly potent against Proteus mirabilis, Proteus vulgaris and Pseudomonas aeruginosa (MIC values of 431, 559 and 777 μg/mL, respectively). The hexane extract was also a potent inhibitor of the Proteus spp., (MIC of approximately 500-800 μg/mL). The ethyl acetate extract also inhibited Klebsiella pneumoniae growth, albeit with higher MIC’s (approximately 1500 μg/mL). All other C. maritima extract-bacteria combinations generally resulted in mid-low potency inhibition. All of the extracts were determined to be nontoxicin with the Artemia franciscana bioassay, with LC50 values substantially >1000 μg/mL. A total of 97 unique mass signals were detected in the C. maritima ethyl acetate extract by nonbiased GC-MS headspace analysis. A number of terpenoids which may contribute to the therapeutic bioactivities of the extract were putatively identified. Conclusion: The lack of toxicity and the inhibitory activity against microbial triggers of rheumatoid arthritis, ankylosing spondylitis and multiple sclerosis by the C. maritima ethyl acetate extract indicates its potential in the treatment and prevention of these diseases.
Keywords: Acinitobacter baylyi; ankylosing spondylitis; Klebsiella pneumoniae; multiple sclerosis; Proteus mirabilis; Proteus vulgaris; Pseudomonas areuginosa.; rheumatoid arthritis

Callus Induction and Elicitation of Total Phenolics in Callus Cell Suspension Culture of Celastrus paniculatus – willd, an Endangered Medicinal Plant in India - Anusha T S; Joseph M V; Elyas K K (Pharmacognosy Journal, 2016)
Celastrus paniculatus - Willd belonging to the family Celastraceae is a vulnerable medicinal plant in India. It has been employed as a stimulant, nervine tonic, rejuvenant, sedative, tranquilizer and diuretic. It is also used in the treatment of leprosy, leucoderma, rheumatism, gout, paralysis and asthma. Because of its high pharmaceutical application, this plant species were over exploited and now considered under threatened species. So the highlight of the present investigation is the induction of callus by using different concentration of various phytohormones such as 2, 4-D (0.5 - 3.0 mg/l) and NAA (0.5 - 2.5 mg/l). In order to ensure the presence of the bioactive compounds preliminary phytochemical screening of the various extracts of callus were performed. Finally elicitation of total phenolics were done in callus cell suspension cultures by using elicitors such as jasmonic acid, salicylic acid and copper sulphate. Among the applied elicitors jasmonic acid showed superiority. To our knowledge, this is the first report of the elicitation of secondary metabolites especially total phenolics from callus cell suspension cultures of Celastrus Paniculatus.
Keywords: Bioactive constituents; Callogenesis; Celastrus paniculatus; Elicitors; Total phenolics.

Chemical Composition and Antimicrobial Activity of Fresh Rhizome Essential Oil of Zingiber Officinale Roscoe - Pradeep Kumar Sharma; Vijender Singh; Mohammed Ali (Pharmacognosy Journal,, 2016)
Background: Zingiber officinale Roscoe (Zingiberaceae) is a rhizomatous perennial herb found in tropical Asia. It is extensively used worldwide as a spice, flavoring agent and herbal remedy for cold, throat and chest infections and cough. The present study was carried out to analyse an essential oil from the fresh rhizomes of Z. officinale of Ghaziabad region and to evaluate its antimicrobial activity. Materials and Methods: The fresh rhizomes were hydrodistilled to get the essential oil which was analysed by GC and GC-MS techniques. The oil was evaluated for antimicrobial activity by disc diffusion method. Results and Discussion: The essential oil was characterized by high percentage of sesquiterpenes (66.66%), monoterpenes (17.28%) and aliphatic compounds (13.58%). The predominant sesquiterpene was zingiberene (46.71%) followed by valencene (7.61%), β-funebrene (3.09%) and selina-4(14),7(11)-diene (1.03%). The major monoterpenes were characterized as citronellyl n-butyrate (19.34%), β-phellandrene (3.70%), camphene (2.59%) and α-pinene (1.09%). The essential oil exhibited significant antimicrobial activity against Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Candida albicans and Aspergillus niger. Conclusion: The essential oil mainly contained a large number of sesquiterpenes and monoterpenes and exhibited significant antimicrobial activity against pathogenic microorganisms.
Keywords: Antimicrobial activity; Chemical composition; Essential oil; GC-MS analysis; Zingiber officinale.

Chemical Constituents and in vitro anticancer activity of Tiliacora triandra leaves - Surapong Rattana; Benjamart Cushnie; Ladachart Taepongsorat; Methin Phadungkit (Pharmacognosy Journal, 2016)
Introduction:  Tiliacora triandra (F. Menispermaceae) is edible and is also known for medicinal values. The leaves are a popular flavoring in Southeast Asia, especially in the northeast of Thailand.  The objectives of this study were to determine the major constituents of the leaves of T. triandra, and assess their anticancer activities against human cancer cell lines. Methods: The leaves were extracted by a soxhlet apparatus with petroleum ether, dichloromethane, ethyl acetate and water. Major constituents were then purified and identified using chromatographic procedures and various spectroscopic techniques.  In vitro anticancer activity tests of T. triandra extracts were performed by resazurinmicroplate assay (REMA), and tested with 3 cell lines: oral cavity cancer (KB), lung cancer (NCI-H187) and breast cancer (MCF-7) cell lines. Results: The result indicated that the main compound of T. triandra leaves was oxoanolobine. The methanol extract showed the highest cytotoxic activity against lung cancer (NCI-H187) cell line whereas the water extract exhibited the highest activity against oral cavity cancer (KB) cell line. The IC50 of oxoanolobine against the NCI-H187 cell line was 27.60 ± 4.30 µg/mL. Conclusion:  T. triandra leaves contain oxoanolobine as the major constituent and have the potential of anticancer activity but are required to be investigated further.
Keywords: In vitro anticancer activity; Oxoanolobine; Phytochemistry; Tiliacora triandra; Yanang.

Chemical Profile of Essential oil of Ocimum gratissimum L. and Evaluation of Antibacterial and Drug Resistance-modifying Activity by Gaseous Contact Method - Maria Karollyna do Nascimento Silva; Victória Regina De Alencar Carvalho; Edinardo Fagner Ferreira Matias (Pharmacognosy Journal, 2016)
Introduction: Plant products with antimicrobial potential and ability to modulate the action of drugs have become the target of several studies. Many studies of the species Ocimum gratissimum Lamiaceae have reported biological activities in the essential oil and extracts of various parts of the plant. Objective: Evaluate the antibacterial and resistance-modifying activity of the essential oil of O. gratissimum (OEOg) and its major compound eugenol. Materials and Methods: OEOg was extracted by hydrodistillation, and eugenol was obtained commercially. Multiresistant strains of Escherichia coli and Staphylococos aureus were used to test for drug activity. Antibacterial and resistance-modifying activity of OEOg and eugenol was evaluated by gaseous contact. Results: Chemical analysis of OEOg demonstrated the presence of eugenol and other compounds such as 1,8-cineole and β-selinene as well. In the evaluation of the antibacterial activity, both OEOg and eugenol were unable to form a bacterial growth inhibition zone at any of the concentrations tested. However, the modulation tests with amikacin and erythromycin identified synergism with OEOg and eugenol against E.  coli and S. aureus. Gentamicin combined with OEOg showed antagonism against S. aureus but synergism against E.coli. When gentamicin was combined with eugenol, there was also synergism against S. aureus, whereas no effect was seen against E. coli. Conclusion: Given the results obtained in this study, it is concluded that OEOg and eugenol may eventually represent a new therapeutic tool against antibiotic-resistant bacteria.
Keywords: Eugenol; Gaseous contact; Modifying; Ocimum gratissimum; Resistance.

Comparative Biochemical Studies on Indian Sedges Cyperus scariosus R.Br and Cyperus rotundus L. - Lavanya Kakarla; Rajath Othayoth; Mahendran Botlagunta (Pharmacognosy Journal, 2016)
Background: Cyperus scariosus R.Br and Cyperus rotundus L are well known Indian medicinal plants in ayurveda and herbal industry. These two species are often treated as synonymous to each other, although they grow in different agro climatic conditions. Objective: In the present study, we made an attempt on comparative biochemical studies among these two species by using various spectroscopic, analytical and in silico molecular docking studies. Materials and Methods: Rhizome methanolic extracts of both the species were subjected to GC-MS and elemental analysis to identify the presence of phytochemical constituents and trace elements respectively. Following confirmation, the identified compounds were subjected to molecular docking analysis using anti-inflammatory protein COX-2 as the target receptor. Further these extracts were encapsulated into biodegradable chitosan nanoparticles and they were characterised using SEM and FT-IR analysis. Finally, the antioxidant and anti-inflammatory activity of these extract loaded nanoparticles were evaluated using in vitro assays. Results: Compounds present in both plant extracts form strong hydrogen bond interactions with COX-2. SEM analysis of C. scariosus showed chitosan nanoparticles are spherical in shape. Whereas C. rotundus forms aggregates, although they are well-dispersed in water following lyophilisation. FT-IR analysis showed that both plant extracts have different compounds, which is evident from the wavelength difference and their shift pattern as compared to blank nanoparticles. In spite of the differences, both of the drug encapsulated plant extracts showed good antioxidant and anti-inflammatory properties. Conclusion: C. scariosus and C. rotundus are different, but similar with some of the phytochemical constituents and pharmaceutical values.
Keywords: EDAX (Energy Dispersive X-ray Analysis) and COX-2 (Cyclooxygenase- 2).; GC-MS (Gas chromatography and Mass Spectroscopy); SEM (Scanning Electron Microscopy)

Comparative Powder Microscopic and HPTLC Studies on Stem barks of Symplocos racemosa Roxb. and Symplocos crataegoides Ham - Nartunai Govindarajan; Uma Maheswara Reddy Cheekala; Shantha Arcot; Susikumar Sundaramoorthy; Murugammal Shanmugam; Ramasamy Duraisamy; Venkata Narasimhaji Cheemalapati; Ilavarasan Raju (Pharmacognosy Journal, 2016)
Introduction: Comparative powder microscopic and HPTLC studies were carried out on stem barks of Symplocos racemosa Roxb. and Symplocos crataegoides Ham. to differentiate its identity in Ayurvedic formulations. Method: Powder microscopic and HPTLC studies of these barks were undertaken on a comparative basis and results are reported in this paper. The authentic samples are cleaned, powdered and passed through sieve No. 80. A few mg of powder was stained with saffranin, Toluidine blue and Iodine and photographed under different magnifications with the help of NICKON Labphot -2. HPTLC studies were followed by Sethi and Wagner et al method. Results: The colour, taste, cork cells, fibres, sclereids, starch grains, calcium oxalate crystals, number of spots and Rf values of HPTLC are found to be differentiating diagnostic characters in powdered form of S. racemosa and S. crataegoides. Conclusion: The findings of the present study is believed to be helpful in standardization of Ayurvedic formulation containing stem bark of S. racemosa and S. crataegoides as ingredients in powder form. The study sets the specific microscopic protocol and HPTLC finger print of the two drugs and may lead to global acceptance and reputation of the Ayurvedic system.
Keywords: Authentication; Curna; Dasamularistam; Lodhra; Lodhrasavam; Pharmacognosy.

Comparative Study of Antioxidant Activity of Ethanol and Aqueous Extracts of Different Parts of Nyctanthes Arbor-tristis Linn. - Saraswati Patel; Mamta Gokhale (Pharmacognosy Journal, 2016)
Background: Antioxidants play a major role in curing degenerative disease. In present time many synthetic antioxidants are commonly used but due to their toxic and carcinogenic effects, their use has been restricted. So the search for natural antioxidants is important. Studies on natural compounds is of interest due to their satisfactory health benefits with low toxicity. Objective: The antioxidant activity of ethanol and aqueous extract of shoot, seed and leaf of an important medicinal tree Nyctanthes arbor-trist is (Harsingar) were evaluated by DPPH scavenging antioxidant assays. Materials and Methods: Different concentrations 25, 50, 75, 100% of the aqueous and ethanol extracts were prepared with standard solutions (ascorbic acid 0.01, 0.03, 0.05, 0.07, 0.09, 0.1 mg/ml). To 1.5 ml solution of DPPH (0.1 mM), 0.5 ml of various concentrations of the extract and standard were added. Results: In the present study a comparative evaluation of antioxidant activity of seed, shoot and leaf of Nyctanthes arbor-tristis Linn was performed for their aqueous and ethanol extracts. Ethanol and aqueous extracts of shoot revealed more antioxidant activity then seed and leaf. Conclusion: All aerial parts of Nyctanthes arbor-tristis Linn possess antioxidant activity. The plant may be functioned out for its anticancerous properties in future.
Keywords: antioxidant activity; Aqueous extract; DPPH assay; Ethanol extracts; Nyctanthes arbor-tristis Linn.

Duboisia leichhardtii (F.Muell.) Extracts Inhibit The Growth of Bacterial Triggers of Selected Autoimmune Inflammatory Diseases - Ian Edwin Cock (Pharmacognosy Journal, 2016)
Introduction: Duboisia leichhardtii F.Muell. is a medium to large tree which is native to subtropical regions of eastern Australia. Duboisia spp. contain a number of psychoactive tropane and pyrrolidine alkaloids with reported antibacterial activity. Despite this, D. leichhardtii leaf extracts have not been rigorously examined for growth inhibitory properties against many bacteria, including the bacterial triggers of autoimmune inflammatory diseases. Methods: The antimicrobial activity of D. leichhardtii leaf solvent extracts was investigated by disc diffusion and growth time course assays against a panel of bacterial triggers of autoimmune diseases. The growth inhibitory activity was further quantified by MIC determination and growth time course assays. Toxicity was determined using the Artemia franciscana nauplii bioassay. Results: Methanolic and aqueous D. leichhardtii leaf solvent extracts were potent inhibitors of the bacterial triggers of rheumatoid arthritis and ankylosing spondylitis. The methanolic extract displayed the most potent bacterial growth inhibitory activity. It was particularly potent against P. mirabilis (MICs of 85 and 116 μg/mL against reference and clinical strains respectively) and P. vulgaris (MIC of 187 μg/mL). The methanolic extract was also a good inhibitor of K. pneumoniae growth (MICs of 143 and 118 μg/mL against reference and clinical strains respectively). The aqueous and ethyl acetate extracts were also potent bacterial growth inhibitors, albeit with higher MIC values. The antibacterial activity of the methanolic and aqueous D. leichhardtii leaf extracts were further investigated by growth time course assays which showed significant growth inhibition in cultures of P. mirabilis and K. pneumoniae within 1 h of exposure. All extracts were determined to be nontoxic in the Artemia franciscana nauplii bioassay, indicating their safety for use in preventing these autoimmune inflammatory diseases. Conclusions: The lack of toxicity of the D. leichhardtii leaf extracts and their growth inhibitory bioactivity against the bacterial triggers of rheumatoid arthritis and ankylosing spondylitis indicate their potential in the development of new therapies targeting the onset of these diseases.
Keywords: ankylosing spondylitis; Corkwood; Hyoscyamine.; multiple sclerosis; Rheumatic Heart Disease; rheumatoid arthritis; Scopolamine; Solanaceae

Estrogenic Potential of Flemingia vestita Benth Tubers in Ovariectomized Rat Model - Sunita Shailajan; Suman Kumaria; Suhas Pednekar; Sasikumar Menon; Hiranjit Choudhury; Archana Matani (Pharmacognosy Journal, 2016)
Objective: This study investigates the potential estrogenic activity of the ethanolic extract of Flemingia vestita Benth tubers using ovariectomized rat model. Materials and Methods: The ethanolic extract of F. vestita tubers has been standardized using validated HPLC method in terms of its genistein content (8.43 ± 0.05 mg/g of extract). Three to four week old young albino Wistar female rats were ovariectomized and treated for 14 days post ovariectomy with the standardized ethanolic extract at three different dose levels (100, 250, 500 mg/kg body weight) with a positive control of Estradiol valerate (1 mg/kg/day). The parameters evaluated were uterine weight, uterine glycogen, G6PDH, LDH, 17β-estradiol, progesterone, total cholesterol, triglycerides, HDL and histo architecture of uterus. Results: Treatment with the ethanolic extract of F. vestita tubers showed dose dependent increase in uterine weight, glycogen levels, G6PDH levels, estrogen and progesterone levels when compared with the ovariectomized control. Amongst three dose levels, high dose of plant extract showed significant increase in the uterine weight (p < 0.001), uterine glycogen content (p < 0.001), 17-β estradiol and progesterone levels (p < 0.001), G6PDH and LDH levels (p < 0.001) as well as significant decrease in HDL and triglycerides levels (p < 0.001) compared to ovariectomized control. Histopathological evaluation of uteri sections revealed that the high dose of the plant show increase in the endometrial response as indicated by proliferation of endometrial glands and luminal epithelium of the ovariectomized rats. Conclusion: Thus, these data suggests that ethanolic extract (500 mg/kg body weight) of F. vestita tubers may exhibit good estrogenic activity in ovariectomized rat model. Key words: Estrogenic activity, Flemingia vestita, genistein, HPLC, ovariectomized rats.
Keywords: Estrogenic activity; Flemingia vestita; genistein; HPLC; ovariectomized rats.

Evaluation of Antihyperglycemic and Antihyperlipidemic Activity of Leaf Extracts of Breynia vitis-idaea in Alloxan Induced Diabetic Rats - Jagdish Chandra Nagar; Lalit Singh Chauhan (Pharmacognosy Journals, 2016)
Aim: The present study was carried out to evaluate the hypoglycemic and hypolipidemic activity of alcohol and aqueous leaf extracts of Breynia vitis-idaea (Burm. F.) Fischer in alloxan induced diabetic rats. Methods: Diabetes was induced into albino Wistar rats by intraperitonial administration of alloxan (120 mg/kg). Normal and diabetic rats divided into different groups of six each. Alcohol and aqueous leaf extracts (300 mg/kg and 600 mg/kg) and standard drug (Glibenclamide 500 μg/kg) was administered orally for 21 days. Blood samples were collected from overnight fasted normal and diabetic rats on 0th, 7th, 14th and 21st days of treatment. Hypoglycemic activity was evaluated by measuring serum glucose level and glycosylated haemoglobin level after dosing with aqueous and alcohol extracts. Hypolipidemic activity was evaluated by measuring various biochemical parameters like total cholesterol, triglycerides, low density lipoprotein, very low density lipoprotein, high density lipoprotein and phospholipids. Results: Both the extracts significantly (P<0.001, p<0.01) reduced fasting blood glucose of alloxan diabetic rats in a dose-related manner, when compared to control and standard. They also have a significant recovery in the levels of parameters measured in lipid profile, when compared to control and standard group. Conclusion: The present investigation established pharmacological evidence to support the folklore claim that it is used as hypoglycemic and hypolipidemic agent.
Keywords: Alloxan; Breynia vitis-idaea; Glibenclamide; Hypoglycemic; Hypolipidemic.

Evaluation of Antimicrobial Potential of Some Indian Ayurvedic Medicinal Plants - Mrinmoy Nag; Pulok k Mukherjee; Rajarshi Biswas; Joydeb Chanda; Amit Kar (Pharmacognosy Journal, 2016)
Introduction: Stereospermum suaveolens Roxb., Viscum articulatum Burm., Annona squamosa, Capsicum annuum cayenne, Ananas comosus Merrill. are used for the management of microbial infection in Ayurveda. The present study was designed to standardize the extract of S. suaveolens bark (SSB), V. articulatum aerial part (VAAP), A. squamosa leaf (ASL), C. annuum fruit (CACF), A. comosus fruit (ACF) and performed antibacterial activity. Methods: The antibacterial activity of the five extracts were evaluated against certain bacteria such as B. subtilis, B. cereus, S. aureus (gram positive); E. coli, S. typhi, and P. aureugenosa (gram negative) by disc diffusion method, time course assay, pH sensitivity assay and minimum inhibitory concentration (MICs) through broth micro-dilution method. Results: The plants extracts VAAP, ASL, and CACF showed potent inhibitory activity against S. aureus with MIC 728, 742, and 698 μg ml-1, respectively, while CACF showed inhibitory activity against B. subtilis with MIC 690 μg ml-1. The results further demonstrated that the inhibitory activity of CACF against E. coli with MIC 760 μg ml-1. P. aeruginosa was inhibited by ASL and CACF with MIC 1100 and 1120 μg ml-1, respectively. The ASL showed notable MBC against the tested microorganism. Moreover, all extracts were completely inactivated bacterial strains (except B. cereus, S. typhi) within 2-10 h of exposure, determined by time course assay. Conclusion: The outcomes of our study elucidate that standardized extracts of A. comosus, A. squamosa, C. annuum, S. suaveolens, and V. articulatum may be used as natural antimicrobial agents.
Keywords: Ananas comosus Merrill; Annona squamosa; Antibacterial; Capsicum annuum cayenne; Stereospermum suaveolens Roxb; Viscum articulatum Burm.

Evaluation of antioxidant effect and anticancer activity against human glioblastoma (U373MG) cell lines of Murraya Koenigii - Mrinal Sanaye; Nimisha Pagare (Pharmacognosy Journal, 2016)
Aim: The main aim of the study was to screen the ethanolic (EEMK) and methanolic (MEMK) extracts of Murraya koenigii (MK) leaves and their alkaloid fractions (EFMK and MFMK) for their in vitro anti-oxidant and anticancer activity against U373MG cell lines. Methods: In vitro antioxidant activity of extracts and fractions was determined by DPPH Radical assay, Reducing power assay, Inhibition of lipid peroxidation, Superoxide radical scavenging assay and Hydroxyl radical scavenging assay. Cytotoxic effect of MK extracts and fractions was evaluated by performing Sulphorhodamine B (SRB) assay and Flow cytometry analysis on U373MG cell lines. Results: Extracts and fractions of MK were found to possess significant antioxidant activity. In SRB colorimetric assay, the efficacy of MK against U373MG cell line was observed due to reduced viability of U373MG cells. Dose dependent significant increase in the percentage of dead cells was also observed. MEMK exhibited significant cytotoxicity than EEMK whereas EFMK and MFMK were not found to be significantly cytotoxic against U373MG cell lines. Flow cytometry analysis revealed that the effective extract MEMK induces cell death in human glioblastoma cells through apoptotic mode of action. Conclusion: The observed anticancer activity of Murraya koenigii may be due to its antioxidant potential.
Keywords: Anticancer; Antioxidant; Flow cytometry..; Glioblastoma; Murraya Koenigii; SRB assay

Evaluation of Costus speciosus in Experimental Models of Depression in Albino Mice - Zahoor Ahmad Rather; Nateshprabhu M; Sushma DS; Rakesh Kb; Sunil Pai; Ullal sheetal D (Pharmacognosy Journal, 2016)
Introduction: Despite theavailability of numerous antidepressant drugs the therapy of depression is far from satisfactory. Two of the many reasons for this are the delay in onset of effect and the adverse effects associated with most of the antidepressants. Costus speciosus rhizome has shown adaptogenic activity. Objective: To evaluate the antidepressant activity of50% aqueous-ethanol extract of Costus speciosus (CS) leaves in experimental models of depression. Materials and Methods: Male albino mice were randomly assigned to five groups of six each. We studied three doses of the leaf extract (100, 200 and 400 mg/kg) on two models of depression – forced swim test and tail suspension test. Imipramine was used as the standard control. Both acute and chronic effects were studied. Drugs (test drug, standard control and vehicle) were administeredorally, one hour before the experiment in the acute study and daily for 14 days for the chronic study. Results: Imipramine showed significant antidepressant activity as demonstrated by a reduction in duration of immobility in both acute and chronic studies of forced swim test and tail suspension test. CS showed a dose dependent antidepressant activity. CS_100 demonstrated an antidepressant effect only in the acute forced swim test. CS_200 demonstrated an antidepressant activity in both acute and chronic forced swim test but not in tail suspension test. CS_400 showed maximum antidepressant activity in both acute and chronic studies, which was comparable to that of the standard drug imipramine. Conclusion: CS showed dose dependent antidepressant activity with CS_400 mg/kg showing maximum effect.
Keywords: Antidepressant; Costus speciosus; Forced swim test; Tail suspension; Test.

Evaluation of Healing Potential of Achyranthes aspera L. (Amaranthaceae) seeds in excision, incision, dead space and burn wound model-An in-vivo Study - Sumanta Mondal; Debjit Ghosh; Seru Ganapaty; Motati Sushrutha Reddy; Karipeddi Ramakrishna (Pharmacognosy Journal, 2016)
Objective: The present study deals with the in vivo investigation of healing properties of Achyranthes aspera L. seeds in excision, incision, dead space and burn wound model. Methods: Preliminary phytochemical tests were performed to find out different phytoconstituents in the test extract. Acute toxicity test were performed to find any abnormalities in mice. Wound healing activities were performed on Wistar rats using excision, incision, dead space and burn wound model. The percentage of wound closure and period of epithelization were recorded for excision and thermal burn wound model, whereas the breaking strength was recorded in incision wound model. In dead space wound model, hydroxyproline content and granulation tissue antioxidant enzymes like SOD and CAT were estimated. Results: The phytochemical investigation showed the presence of alkaloids, carbohydrates, tannins, flavonoids, saponins, lipids and triterpenoids. There were no abnormalities observed in the acute toxicity test. The results of wound healing activity revealed that EEAAS treated group showed an enhanced wound contraction and epithelization period in both excision and burn wound models, whereas in incision wound model the wound breaking strength was significantly increased in extract treated group compared to control. The histology of the skin of healed excised wound showed restoration to almost the normal architecture of the skin in extract treated group compared to the control. In dead space wound model, enhanced antioxidant enzymes and connective tissue markers were observed in the extract treated group. Conclusion: Thus the results conclude that EEAAS possesses potent wound healing properties with a reasonable safety profile.
Keywords: Achyranthes aspera L.; Antioxidant enzymes; Hydroxyproline; Povidone iodine; Silver sulfadiazine; Thermal burn.

Evaluation of Phytochemicals, Antioxidant, Antibacterial and Antidiabetic Potential of Alpinia galanga and Eryngium foetidum Plants of Manipur (India) - Tabarak Malik; Devendra Kumar Pandey; Priyanka Roy; Annie Okram (Pharmacognosy Journal, 2016)
Background: Alpinia galanga and Eryngium foetidum are two commonly used traditional aromatic plants of Manipur which is traditionally used in Aroma therapy. Rationale of pharmacological potentials of these plants are still unclear, even if few preliminary studies are available in literature for individual plants. Objective: This study was conducted for comparative assessment of antioxidant, antibacterial, and antidiabetic potential of A. galanga and E. foetidum. Materials and Methods: The rhizome of A. galanga and leaf of E. foetidum were extracted in methanol, ethanol and water. Phytochemicals of each extracts of Alpinia galanga and Eryngium foetidum were analyzed. The antioxidant potential of all the extracts was assessed by measuring total phenolic content, total flavonoid content and free radical scavenging potential was assessed by 1,1-diphenyl-2-picrilhydrazyl (DPPH) assay, antibacterial activity was assessed against various pathogenic and nonpathogenic bacteria in vitro by Kirby-Bauer agar well diffusion method and antidiabetic activity was assessed by α-amylase inhibition. Results: Both the plant showed presence of all the tested phytochemicals. It was observed that methanolic extracts of both the plants have higher phenolic content than ethanolic and aqueous extracts, however ethanolic extracts E. foetidum shows higher flavonoid contents. Both the plant shows similar DPPH scavenging and metal chelating activity. It was also observed that the antidiabetic potential of A. galanga is greater than E. foetidum. The methanolic and ethanolic extracts of the plants shows quite similar and good antibacterial potential than the aqueous extracts. Conclusion: The present study suggests that both Alpinia galanga and Eryngium foetidum plants of Manipur could be used as herbal remedies for the treatment of diabetes mellitus as well as managing oxidative stress and oxidative stress related disorders.
Keywords: A. galangal; Antibacterial; Antidiabetic; Antioxidant; E. foetidum.; Manipur; Phytochemicals

Finger Printing of the Anatomical Markers, HPTLC Profile and Heavy Metals Content in the Leaves of Aristolochia indica Linn. - Madathilparambil Vasu Sudhakaran (Pharmacognosy Journal, 2016)
Background: Aristolochia indica Linn is now an endangered medicinal plant belonging to the family Aristolochiaceae. Many ethono-botanically important species of Aristolochia were found used in the traditional forms of medicine for the treatment of various illnesses. Aim: The present study concerns the microscopic, fluorescent, powder, quantitative microscopic characteristics of the leaves of Aristolichia indica Linn and its physico-chemical standards. Materials and Methods: Morpho-histological profile, Highperformance thin-layer chromatographic (HPTLC) finger print profile, and heavy metals content of the leaves of Aristolichia indica Linn. Results: The presence of camptodromous pinnate venation with pentagonal shaped areoles with linear veinlet endings, non-glandular hooked trichomes, amphistomatic and anomocytic stomata, small palisade ratio, small stomatal index were the anatomical features characteristics of the taxon. Physico-chemical evaluation of the leaves gave moisture content of 10.5%, total ash 12.7%, acid insoluble ash 1.9%, acid soluble ash 10.8%. Highperformance thin-layer chromatographic (HPTLC) identification of marker compound (Aristolochic acid I or (AAI)) in methanol extract of leaves was carried out. The developed HPTLC Chromatogram had revealed nine phytoconstutents in extract of leaf sample. The Rf value for Aristolochic acid I (C17H11NO7) was found to be 0.41 and densitometric scanning had shown λmax at 318 nm for the marker compound. The content of marker constituent (AA I) present in shade-dried leaves of Aristochia indica Linn was estimated as 0.049%. The Flame atomic absorption spectrometric determination of elements had shown appreciable amounts of the elements such as Fe (0.5442 mg/g), Zn (0.026.82 mg/g), Ni (0.008 mg/g,) and Cu (0.002 mg/g) by dry weight of the leaves of Aristolichia indica. Conclusion: The present study suggests that the delineated characteristics of the leaves of A. indica, could tag as the identifying parameters to substantiate and authenticate the raw drugs from the spurious/adulterants materials and could also be effectively used for the regulatory perspectives and quality assessment of Aristololic acid Ι in the medicinal formulation/finished products. The presence of important mineral elements inside this plant showed that it could be a nutritious plant and important to the human health.
Keywords: Areoles; Aristolic acid; Heavy metals.; HPTLC finger print; Physico-chemical parameters; Stomatal index

Fingerprint Of Tiger Balm® By Thermal Desorption Gas Chromatography Mass Spectroscopy - Omar A. Aldulaimi; Wen W. Li (Pharmacognosy Journal, 2016)
Introduction: Tiger Balm® is a blend of volatile oils used for many years in control of muscle cramps and headache. Objectives: To establish a quick and accurate method of analysis for Tiger Balm®. Materials and Methods: GC-MS and TD GC-MS were used in parallel to define the metabolites available in Tiger Balm® blend, high quality standards were help in confirmation of the metabolites identities. Results: TD GC-MS was more efficient in showing the 1:1 relative abundance of camphor and menthol which can be taken as a chemical marker of this herbal medicine. Conclusion: In this work we applied efficiently the use of TD GC-MS in quality analysis of semisolid herbal medicine with volatile scents without the need of tedious pre-treatment with organic solvents, which is required by using GC-MS.
Keywords: Camphor; GC-MS; Menthol.; TD GC-MS; Tiger Balm®

Gas Chromatography - Mass Spectrometry Analysis and In vitro Antioxidant Activity of the Ethanolic Extract of the Leaves of Tabernaemontana divaricata - Muniyandi Anbukkarasi; Philip A Thomas; Mahalingam Sundararajan; Pitchairaj Geraldine (Pharmacognosy Journal, 2016)
Objective: To identify phytoconstituents present in an ethanolic extract of the leaves of Tabernaemontana divaricata and to evaluate its in-vitro antioxidant potential. Methods: The extract was subjected to gas chromatography- mass spectrometry analysis to identify phytoconstituents, and screened for hydroxyl, superoxide and 1, 1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity, reducing power and metal-chelating activity as a measure of potential antioxidant activity. Results: GC-MS analysis of the extract revealed the presence of 96 phytoconstituents, of which 17 are reported to be bioactive and 11 of these to possess antioxidant potential. When tested in-vitro, the extract exhibited the most potent radical-scavenging activity at a maximum concentration of 10 mg/ml, scavenging effects of 64%, 67% and 69% and corresponding half maximal inhibitory concentration (IC50) values of 6.7 mg/ml, 6.8 mg/ml and 6.2 mg/ml on hydroxyl, superoxide and DPPH radicals, respectively. Ascorbic acid used as a standard (10 mg/ml) showed scavenging effects of 73%, 73% and 75% and corresponding IC50 values of 5.3 mg/ml, 5.8 mg/ml and 5.2 mg/ml, respectively, on hydroxyl, superoxide and DPPH radicals. At 10 mg/ml, the extract and an ethylenediaminetetraacetic acid standard exhibited 68% and 78%, respectively, chelation of ferrous ions; at the same concentration, the reducing power of the extract and that of a butylated hydroxytoluene standard was found to be 3.855 and 4.308, respectively. Conclusion: These observations strongly suggest that the ethanolic extract of T. divaricata leaves has potent in-vitro antioxidant activity and thereby could act as a possible therapeutic agent for oxidative stressinduced pathological states.
Keywords: antioxidant activity; GC-MS analysis; Metal chelating activity.; Phytoconstituents; Reducing power; Tabernaemontana divaricata

GC- MS Analysis of Mussaenda roxburghii Hk.f.: A Folk Food Plant Used Among Tribes Of Arunachal Pradesh, India. - Temin Payum (Pharmacognosy Journal, 2016)
Introduction: Mussaenda roxhburgii Hk.f. shoot is widely used as folk food among the tribal people of Arunachal Pradesh. This study was carried out to establish the phytoconstituents of Mussaenda roxburghii shoot. Methods: Fresh shoot were collected from Mone forest of East Siang district of Arunachal Pradesh and identified by the corresponding author himself. The samples were shade dried and pulverized to powder using a mechanical grinder. 500 g powder of the sample was soaked in ethanol for 72 hours with intermittent shaking then filtered through Whatmann No. 41 filter paper and concentrated under reduced pressure at 40°C by using rotary evaporator to obtain a viscous semi solid extract. Gas-Chromatography Mass Specrometry (GC-MS) analysis of the ethanol extracts was carried out in Shimadzu GCMS-QP-2010 plus system. The identification of compounds was performed by comparing their mass spectra with data from NIST 11 (National Institute of Standards and Technology, US) and WILEY 8. Results: The GCMS chromatogram of Mussaenda roxburghii shoot ethanolic extract gave forty nine phytochemical compounds. The most prevailing compounds were hydrocoumarin with 13.6%, hexadeconoic acid, 2-hexadecen-1-ol, 3, 7, 11, 15 tetramethyl [R-[R-) with 17.52%, ethyl ester with 6.24% and Vitamin E with 2.8%. The study gave some compounds with biological interest like gamma tocopherol, Vitamin E, Neophytadiene, Squalene etc. which have been reported to be Antitumur, Antiinflammatory, Antiaging, antidiabetic, anti-inflammatory, Antipyretic, perfume, pesticide and sunscreen.
Keywords: Folk Food; GC-MS; Hydrocoumarin.; Mussaenda species; Nutraceuticals; Tribal people

GC/MS Analysis and Potential Cytotoxic Activity of Haplophyllum tuberculatum Essential Oils Against Lung and Liver Cancer Cells - Omar Mohamed Mohamed Sabry; Abeer Mohamed El Sayed; Salmin Khalid Alshalmani (Pharmacognosy Journal, 2016)
Background: Haplophyllum tuberculatum is a plant belongs to family rutacee. It is rich in volatile oils, fixed oils, alkaloids, and furanocoumarins. It is well known for the huge number of folkloric uses in middle east.  Objective: The aim of this study is to establish the chemical composition of the essential oils of Libyan H. tuberculatum and to investigate their cytotoxic potentialities. Materials and Methods: The essential oils of the aerial parts and flowers of H. tuberculatum growing in Libya were prepared by hydrodistillation. GC/MS analyses were performed on a Shimaduz capillary gas chromatograph (GC 17A ver.3) instrument directly coupled to mass spectrometer-MS QP5050A. Oil A and F of H. tuberculatum at different concentrations (0-50 µg/ml) in DMSO were tested for cytotoxicity against human tumor cell lines. Results: Oil yield was found 0.4 and 1.5 (v/w %) on dry weight basis respectively. GC/MS analysis resulted in identification of total 35 compounds. 15 compounds  were common to both oils. oil A of H. tuberculatum exhibited antitumor activities against. liver carcinoma cell line (HEPG2) and lung carcinoma cell line (H1299) 4.7 µg/ml and 4.1 µg/ml. Conclusion: Essential oil of the aerial parts of H. tuberculatum is potentially active against lung (H-1299), and liver (HEPG2) carcinoma cell lines. The observed cytotoxic, activities can be attributed to the dominance of α and γ-terpinene in this oil.
Keywords: Cytotoxicity; Essential oils; Haplophyllum tuberculatum; Liver cancer; Lung cancer.

GC-MS Analysis of Commiphora molmol Oleo-Resin Extracts which Inhibit the growth of Bacterial Triggers of Selected Autoimmune Diseases. - Isaac Biggs; Joseph Sirdaarta; Alan White; Ian Edwin Cock (Pharmacognosy Journal, 2016)
Introduction: Myrrh has been used traditionally for the inhibition of microbial growth and for the treatment of rheumatic diseases. Despite this, myrrh extracts are yet to be tested for the ability to inhibit the growth of the bacterial triggers of autoimmune inflammatory diseases. Methods: Solvent extracts prepared from commercially obtained myrrh resin were analysed for the ability to inhibit the growth of bacterial species associated with initiating rheumatoid arthritis (P. mirabilis), ankylosing spondylitis (K. pneumoniae) and multiple sclerosis (A. baylyi, P. aeruginosa) by disc diffusion assay, and quantified by MIC determination. Toxicity was determined by Artemia franciscana bioassay. The most potent inhibitory extract was investigated using non-targeted GC-MS head space analysis (with screening against a compound database) for the identification and characterization of individual components in the crude plant extracts. Results: Methanolic myrrh extract inhibited the growth of all bacterial species tested. The growth inhibition of this extract was particularly notable against P. mirabilis and K. pneumoniae, with MIC values substantially < 1000 μg/mL for both reference and clinical bacterial strains. Indeed, the MIC values of the methanolic extract against P. mirabilis reference and clinical strains were 572 and 463 μg/mL respectively. The methanolic extract also inhibited the growth of A. baylyi (MIC approximately 3000 μg/mL) and P. aeruginosa (MIC approximately 1800 μg/mL). However, the MICs against these bacteria was indicative of only moderate inhibitory activity. The aqueous, ethyl acetate, chloroform and hexane extracts also inhibited the growth of all bacterial species, albeit with moderate (MIC values 1000-5000 μg/mL) to low efficacy (MIC values >5000 μg/mL) against all bacterial species. All myrrh extracts were non-toxicin the Artemia franciscana bioassay, with LC50 values substantially above 1000 μg/mL. Non-biased GC-MS headspace analysis of the methanolic extracti dentified a high diversity of monoterpenoids and sesquiterpenoid. Conclusion: The lack of toxicity and the inhibitory activity of the methanolic myrrh extract against microbial triggers of rheumatoid arthritis, ankylosing spondylitis and multiple sclerosis indicates its potential in the treatment and prevention of these diseases.
Keywords: ankylosing spondylitis; Commiphora molmol; Monoterpenoid; Multiple sclerosis.; Myrrh; rheumatoid arthritis; Sesquiterpenoid; Terpenoid

Gc-Ms Analysis of Ethanolic Stem Extract of Clausena anisata (Willd.) Hook F Ex Benth - Arsia Tarnam Yakoob; Nargis Begum Tajuddin; Shilu Mathew; Muhammad Ilyas Mohammed Hussain; Ishtiaq Qadri (Pharmacognosy Journal, 2016)
Objective: In the present study, the bioactive components present in the ethanol stem extract of Clausena anisata was analyzed by using Gas Chromatography Mass Spectrometry analysis technique (GC-MS). Clausena anisata, a medicinal plant belonging to the family Rutaceae, is represented by 20 species available in India and used traditionally for the treatment of several ailments but there is a requirement to identify its phytoconstituents, its target, mode of action and treatment using plant products either alone or in combination with synthetic drugs. Methods: Clausena anisata stem was procured from Manamettupatti, a village of Pudukottai District, Tamil Nadu. The shade dried stem was powdered and extracted using ethanol by maceration method. One microlitre of the extract was subjected to GC-MS analysis to detect the presence of bioactive compounds present in the stem of C. anisata. Results:The results showed that the ethanol stem extract of C. anisata contained nine bioactive compounds, of which the major one is n-hexadecanoic acid (78.54%), followed by 8-octadecenoic acid, methyl ester, [E]- (6.638%). The total number of compounds obtained was compared with National Institutes of Standard and Technology (NIST) library that contains more than 62,000 known compounds based on retention time and molecular mass. Conclusion: In this study, nearly nine compounds have been identified from the ethanolic stem extract of C. anisata using GC-MS analysis which was mainly composed of fatty acids and sterols. The GC-MS analysis is used to understand the nature of active principles present in this plant revealed that the plant can be used as a potential source of new useful drugs.
Keywords: C. anisata; Ethanol; GC-MS analysis; maceration and phytoconstituents

GC-MS Analysis of n-hexane Extract of Stem Bark of Symplocos crataegoides Buch.-Ham. ex D. Don - Nartunai Govindarajan; Uma Maheswara Reddy Cheekala; Shantha Arcot; Susikumar Sundaramoorthy; Ramasamy Duraisamy; Ilavarasan Raju (Pharmacognosy Journal, 2016)
Context: The stem barks of the plant Symplocos crataegoides Buch.-Ham. ex D. Don (syn. Symplocos paniculata (Thunb.) Miq.), Fam. Symplocaceae is extensively used in Indian medicine under the names of Lodhra/Patikalodhra. Mainly it is used to cure uterine complaints, vaginal and menstrual disorders. Aim: To investigate the phytochemicals from the n-hexane extract of the stem bark of Symplocos crataegoides Buch.-Ham. ex D. Don., using GC-MS analysis. Materials and Methods: Stem bark of S.crataegoides was extracted by Soxhlet extraction method using n-hexane. The extract was injected by splitless injection mode into the GC MS 5975 C Agilent equipped with a QP- 5000 (quadrupole) Gas Chromatography - Mass Spectrometer. Results: Identification of 57 compounds from n-hexane extract. Those compounds were identified by close matches with standard MS spectra and compared with NIST - 11 and WILEY library data. Undecane (7.51%) was found as major compound followed by Isopropyl myristate, Dodecane, 1,2,4-trimethyl-benzene, Octacosane, 2-methyl-decane, 2-ethyl-1,2-dimethyl-benzene, 1,2,3,5- tetramethyl-benzene etc., other constituents were found to be in traceable quantities. Conclusion: GC-MS analysis of S. crataegoides revealed certain interesting facts of presentation of various phytoconstituents in the stem bark. The presence of various phytoconstituents contributes to the medicinal activity of the plant.
Keywords: GC-MS analysis; n-hexane extract; Patikalodhra; Symplocos Crataegoides

Green synthesis, Antioxidant Potential and Hypoglycemic Effect of Silver Nanoparticles using Ethanolic Leaf Extract of Clausena anisata (Willd.) Hook. F. Ex Benth. of Rutaceae - Arsia Tarnam Y; Nargis Begum T; Muhammad Ilyas MH; Shilu Mathew; Archunan Govindaraju; Ishtiaq Qadri (Pharmacognosy Journal, 2016)
The current study was conducted to examine the hypoglycemic effect of Silver Nano particles (SNPs) using ethanolic leaf extract of Clausena anisata (Willd.) Hook f. ex Benth. A cost effective and eco-friendly technique for the green synthesis of SNPs from 1mM AgNO3 solution through the leaf extract was carried out. The biosynthesized SNPs were characterized using UV spectro photometry, Field Emission Scanning Electron Microscopy (FESEM), X-ray Diffraction analysis (XRD), Energy Dispersive Spectroscopy (EDS) and Fourier transform infra-red (FTIR) spectrometry. DPPH assay was done to determine the antioxidant activity and for in vitro hypoglycemic activity glucose uptake by yeast cells, alpha-amylase inhibition assay, adsorption capacity and glucose diffusion assay was carried out. The SNPs of ethanol leaf extract were found to be spherical in shape and up to 60.67 nm average in size. They showed alpha-amylase inhibitory activity of 80.32% at 500 μg/ml and IC50 100 μg/ml. The glucose uptake by yeast cells was found to increase with an increase in concentration. The maximum glucose uptake was found to be 68.29% at 10mM concentration. The molar concentration of glucose was directly proportional to the glucose binding capacity of extracts. The rate of glucose diffusion across the membrane was found to increase from 30 to 180 minutes. The DPPH scavenging activity was found to be potent (71.60%) at 500 μg/ml. The hypoglycemic effect exhibited by the SNPs was revealed by simple in vitro model of yeast cells, mediated by glucose absorption, increasing glucose diffusion and glucose transport across the cell membrane.
Keywords: Nil

Growth Inhibitory Activity of Kakadu Plum Extracts Against the Opportunistic Pathogenclostridium Perfringens: New Leads in the Prevention and Treatment of Clostridial Myonecrosis - Mitchell Henry Wright; Joseph Sirdaarta; Ben Matthews; Anthony Carlson Greene; Ian Edwin Cock (Pharmacognosy Journal, 2016)
Introduction: Clostridium perfringens is the etiological agent of clostridial myonecrosis and enteritis necroticans. Infections result in exotoxin production, tissue necrosis and unless promptly treated, may result in death. Terminalia ferdinandiana (Kakadu plum) fruit has documented therapeutic properties as a general antiseptic agent. Fruit extracts have been reported to inhibit the growth of an extensive panel of pathogenic bacteria. Leaf extracts have also been shown to block the growth of several bacterial species associated with autoimmune inflammatory diseases. Methods: T. ferdinandiana fruit and leaf solvent extracts were investigated for growth inhibitory activity by disc diffusion assay against a clinical strain of Clostridium perfringens. Their MIC values were determined to quantify and compare their efficacies. Toxicity was determined using the Artemia franciscana nauplii bioassay. Active extracts were analysed by non-targeted HPLC-QTOF mass spectroscopy (with screening against 3 compound databases) for the identification and characterisation of individual components in the crude plant extracts. Results: Methanolic and aqueous T. ferdinandiana fruit and leaf extracts, as well as the leaf ethyl acetate extract, displayed growth inhibitory activity in the disc diffusion assay against C. perfringens. The leaf extracts were generally more potent growth inhibitors than the corresponding fruit extracts, although the aqueous fruit extract had substantially greater efficacy than the aqueous leaf extract. The methanolic and ethyl acetate leaf extracts were particularly potent growth inhibitors, with MIC values of 206 and 117 μg/ml respectively. The fruit methanolic extract also displayed good efficacy, with an MIC of 716 μg/ml. In contrast, the chloroform and hexane extracts of both fruit and leaf were completely devoid of growth inhibitory activity. All T. ferdinandiana extracts were either nontoxic or of low toxicity in the Artemia fransiscana bioassay. Non-biased phytochemical analysis of the methanolic and ethyl acetate leaf extracts revealed the presence of high relative levels of a diversity of galloand ellagi- tannins. Conclusion: The low toxicity of the T. ferdinandiana extracts and the potent growth inhibitory bioactivity of the leaf methanolic and ethyl acetate extracts against C. perfringens indicates their potential as medicinal agents in the treatment and prevention of clostridial myonecrosis and enteritis necroticans. Metabolomic profiling studies indicate that these extracts contained a diversity of tannins.
Keywords: Antibacterial extracts; Antioxidant; Australian medicinal plants; Enteritis necroticans; Gas gangrene.; Kakadu plum; Myonecrosis; Terminalia ferdinandiana

Health Benefits of Morinda citrifolia (Noni): A Review - Mohammad Ali; Mruthunjaya Kenganora; Santhepete Nanjundaiah Manjula (Pharmacognosy Journal, 2016)
Background: Morinda citrifolia (Noni) has been used widely as a complementary and alternative therapy in many countries owing to its potent antioxidant activity and proven health benefits. Traditionally, it finds used as a therapeutic remedy to various diseases as an antibacterial, antitumor, anthelminthic, analgesic, anti-inflammatory, immunostimulant. Also it has proved beneficial in conditions like gastritis, skin diseases, respiratory infections, menstrual and urinary tract disorders, fever, diabetes and venereal diseases. Objective: This review emphasizes on the phytochemical and mineral profile of the different parts of Noni plant. In addition, this review corroborates the pharmacological basis for the various health benefits, traditional and medicinal applications of Noni. Materials and Methods: All the available information of Noni were collected from electronic databases such as Academic Journals, Ethnobotany, Ethnopharmacology, Springer, PubMed, Google Scholar, Science Direct and other primary and secondary sources. Results: According to our search results pertaining to scientific literature, Morinda citrifolia is used for more than 40 types of ailments worldwide. Crude extract of various parts of plant and fruit juice are reported to contain amino acids, anthraquinones, fatty acids, flavonoids, iridoids, lignans, polysaccharides, sterols, sugars, terpenoids etc. which are therapeutically useful for a broad range of pathological conditions. Fourteen human clinical trials have validated the remarkable health benefits of Noni. Conclusion: Literatures prove that Noni is pharmacologically active and is used in different forms of cancer, viz. colon, esophageal, breast, colorectal cancers; cardiovascular diseases, diabetes, arthritis, hypertension. These properties are substantiated by the preclinical or/and clinical investigations.
Keywords: Anticancer.; Antioxidant; Morinda citrifolia; Neutraceutical; Phyto-constituents

Hepatoprotective effect of Prunus armeniaca L. (Apricot) leaf extracts on Paracetamol induced liver damage in Wistar rats - Varsha Raj; Arun Kumar Mishra; Amrita Mishra; Najam Ali Khan (Pharmacognosy Journal, 2016)
Objective: To evaluate the hepatoprotective effect of Prunus armeniaca L. (Apricot) leaf on paracetamol induced liver toxicity in rats. Method: Phytochemical investigation was performed to find active constituents of the plant extracts by the different phytochemical tests. After induction of liver toxicity, the biochemical parameters such as serum glutamic pyruvic transaminase (sGPT), serum glutamic oxaloacetic transaminase (sGOT), serum alkaline phosphatase (sALP), serum bilirubin (SB), thiobarbituric acid reactive substances (TBARS), γ-glutamyl transferase (GGT), lactate dehydrogenase (LDH), total protein (TP), albumin. The physical parameters including liver weight, body weight and histopathological changes in the liver were studied with Ursodeoxycholic acid as standard hepatoprotective agents. Results: The phytochemical investigation of the extracts showed the presence of Alkaloids, volatile oil, saponin glycosides, condensed tanins, terpenoids, steroids and flavonoids. Methanol and aqueous extract before the paracetamol administration caused a significant reduction in the values of sGOT, sGPT, sALP, TBARS, GGT, LDH TP, Albumin and sB (P<0.01) almost comparable to the Ursodeoxycholic acid. The hepatoprotective activity was confirmed by histopathological examination of the liver tissue of control and treated animals. Conclusions: The result concludes that Prunus armeniaca L. possesses the hepatoprotective effect against paracetamol induced liver toxicity in rats.
Keywords: Apricot; Hepatotoxicity; Liver toxicity.; Paracetamol

Identification of Indian Sida through mericarp - Kumar Avinash Bharati (Pharmacognosy Journal, 2016)
Background: some of the species of Sida are being used as medicine in traditional therapies and available in the market as broken plant parts. Therefore, adulteration is very common. A study was conducted to identify the Indian Sida L. through morphological features of mericarp found in the market samples. Methodology: the fruits of Sida are collected from field in flowering and fruiting stage. The identity of the species were determined and dried mature fruit (schizocarp) of specimens were dissected and studied under compound microscope. The market samples were purchased from various parts of the India and fruits were investigated to match the key characters have been found during the study. Results: mericarp of Sida possess huge diversity and it is a reliable character for identification. Each species of Sida has unique mericarp structure. However, some of the species like, Sida alba have four different types of mericarp but they different from mericarps of other species. I have come across with 27 different types of mericarps in Indian Sida. Conclusion: mericarp morphology is a key character to determine the identity of the species. Based on mericarp features a bracketed dichotomous key has been prepared for identification. The species of Indian Sida may be identified the help of mericarp morphology.
Keywords: India; Mericarp; Sida; Sida cordifolia.

In vitro Cytotoxicity Studies of Zn (Zinc) Nanoparticles Synthesized from Abutilon indicum L. against Human Cervical Cancer (HeLa) Cell Lines. - Badarinath Druvarao Kulkarni; Samim Sultana; Mayuri Bora; Ishita Dutta; Padmaa Milaap Paarakh; Vedamurthy Ankala Basappa. (Pharmacognosy Journal, 2016)
Background: The Zn nanoparticles synthesized from the plant sources are ecofriendly and are potent anticancer agents. Objective: The objective of the present work was to evaluate In vitro cytotoxic activity of Zn nanoparticles green synthezised from Abutilon indicum extract against HeLa cell lines (cervical cancer). Methods: The aqueous extract is prepared by cold extraction (maceration) using water as a solvent. Phytochemical analysis was done by using the standard procedures. Aqueous extract of A. indicum was used for synthesis of Zn nanoparticles. The nanoparticles were characterized by UV-Visible spectrometry and Scanning electron microscopy (SEM) techniques. In vitro cytotoxicity studies of Zn nanoparticles were done by MTT assay using HeLa cell lines. Results: The preliminary phytochemical results revealed that the aqueous extract of A. indicum contains broad spectrum of secondary metabolites like Tannins, Saponins, Glycosides, Flavonoids, Anthroquinones, Terpenoids and Steroids. The U.V spectrophotometeric analysis of Zn nanoparticles displayed maximum absorption at 270 nm and scanning electron microscopic studies showed that the nanoparticles size ranges from 50-500 nm. The MTT assay results revealed that the of Zn nanoparticles exhibits potent cytotoxicity against HeLa cell lines with IC50 value of 45.82 μg/ml. Conclusion: Thus the present study concludes that Zn nanoparticles can be used as a potent drug in alternative therapy for treating the cervical cancer patients.
Keywords: Abutilon indicum; Cervical cancer; Cytotoxicity; MTT Assay; Zn nanoparticles

Induction of hairy roots and plant regeneration from the medicinal plant Pogostemon Cablin - Han-jing Yan; Meng-ling He; Wei-Jian Huang; Dong-mei Li; Xiao-fang Yu (Pharmacognosy Journal, 2016)
An efficient transformation system for the medicinal and aromatic plant, Pogostemon cablin Benth was developed by using Agrobacterium rhizogenes ATCC15834 and C58C1. Hairy roots formed directly from the cut edges of leaf explants after infection for 2 days. The highest frequency of leaf explant transformation by A. rhizogenes ATCC15834 and C58C1 were 83.3% and 80.5% after pre culture about 2 days and infection by the bacterium containing 15 mg l-1 acetosyringone about 25 min. The PCR ampliﬁcation showed that rolB genes of Ri plasmid of A. rhizogenes were integrated and expressed into the genome of transformed hairy roots. The optimum medium for callus induction of hairy roots consisted of 2.0 mg l-1 benzyladenine (BA) and 0.1 mg l-1 a-naphthaleneacetic acid (NAA); while optimum medium for adventitious shoot regeneration from these cultures consisted of 0.1 mg l-1 BA and 0.1 mg l-1 NAA. Adventitious shoots could be rooted on 1/2MS. PCR analysis conﬁrmed that rol genes of TL-DNA of Ri plasmid was integrated with at least three copies into the genome of hairy roots-regenerated P. cablin plants. The results presented provide a possibility for breeding of a new cultivar of P. cablin.
Keywords: Agrobacterium rhizogenes; ATCC15834.; C58C1; Plant regeneration; Pogostemon cablin.

Inhibition of MDR1 in mammary cell carcinoma reverses Multidrug Resistance by SOCS1 - Debasish Pradhan; Gitanjali Tripathy; Rakesh Kumar Pradhan; Shaktiprasad Pradhan; Soumyashree Rupambika Moharana (Pharmacognosy Journal, 2016)
Introduction: Suppressors of cytokine signalling (SOCS1), a newly indentified antiapoptotic molecule is a downstream effector of the receptor tyrosine kinase-Ras signalling pathway. Current study has uncovered that SOCS1 may have wide and imperative capacities, particularly because of its close correlation with malignant tumors. Methods: To investigate the impact of SOCS1 on MDR, we analyzed the expression of P-gp and SOCS1 by immunohistochemistry and found there was positive correlation between them. At that point we effectively interfered with RNA translation by the contamination of siRNA of SOCS1 into MCF7/ ADM breast cancer cell lines through a lentivirus, and the expression of the target gene was significantly inhibited. Results: After RNAi the drug resistance was reduced altogether and the expression of MDR1 mRNA and P-gp in MCF7/ADM cell lines demonstrated a significant decrease. Likewise the expression of P53 protein increased in a statistically significant manner (p≤0.01) after RNAi exposure. Moreover, flow cytometry analysis uncovers that cell cycle and anti-apoptotic enhancing capacity of cells changed after RNAi treatment. Conclusion: These outcomes proposed SOCS1 may take part in breast cancer MDR by managing MDR1 and P53 expression, changing cell cycle and enhancing the anti-apoptotic ability of cells.
Keywords: Breast cancer; MDR1gene; Multidrug resistance; RNA interference.; SOCS1 gene

Isolation of flavonoid from Abies webbiana leaves and its activity - Dinesh Kumar Yadav; Mohammed Ali; Ashoke Kumar Ghosh; Babita Kumar (Pharmacognosy Journal, 2016)
Background: Abies webbiana commonly known as Talispatra in Bengali and Hindi, Talispatram in Sanskrit and Indian Silver Fir in English. This is a large, tall, evergreen tree occurring in the Himalayan region from Kashmir to Assam in India. It comes under the Family: Pinaceae. The present study was designed for isolation of flavonoid from ethyl acetate extract of A. webbiana leaves and assessed their toxic effect on liver and kidney. Materials and Methods: The isolation of flavonoid using different chromatographic methods (thin layer and column chromatography). The isolated flavonoid was identified; Structures and chemical bonds were analyzed by using MP, FTIR, 1-H NMR and MS spectral analysis. Effect of flavonoid on liver and kidney was assessed by inducing (0.1 ml/kg) CCl4 (i.p.) and (6 mg/kg) Cisplatin (i.p.) respectively measured by biochemical marker of liver and kidney. Results and Discussion: It was identified that isolated compound was as 4’-hydroxy quercetin on the basis of FTIR, 1-H NMR and MS spectral analysis. Isolated flavonoid reduced the increased biochemical marker (BM) of liver and kidney. The BM was increased by inducing CCl4 and Cisplatin respectively. Conclusion: Isolated compound was 4’-methoxy quercetin and significantly protect the liver and kidney.
Keywords: 1-H NMR; Abies webbiana; CCl4.; Cisplatin; Quercetin

Leaf and Stem Anatomy and Histochemistry of Dalbergia ecastaphyllum - Michelline V. Marques Das Neves; Nathalia Diniz Araújo; Eduardo De Jesus Oliveira; Maria De Fátima Agra (Pharmacognosy Journal, 2016)
Dalbergia ecastaphyllum (L.) Taub. is a shrubby of Tropical America and Africa. It is recognized as the main botanical source of red-propolis, and also by its uses in folk medicine. This work was performed by light and scanning electron microscopy in order to carry out an anatomical and histochemical study of leaves and stems of this species,to find distinctive characters to support the quality control of its ethnodrugs and derivatives. The leaf epidermis is hypostomatic with straight to curved anticlinal cell walls, papillose on the abaxial surface, with thickened cuticle and coated with epiculticular waxes as rosette. The mesophyll is dorsiventral, with palisade 2-3-layered and the spongy 4-6-layered. The petiole and midrib have vascular system collateral. The stem is cylindrical, with an uniseriate epidermis coated with thickened cuticle and angular collenchyma. The vascular system is a continuous ectofloic siphonostele. Resin idioblasts are concentrated in the inner area of the vascular tissue of the midrib, petiole and stem. The leaf and stem anatomy and histochemistry of D. ecastaphyllum provided distinctive characters for this species that can be used as an additional support for its taxonomy and for the quality control of their ethnodrugs.
Keywords: Ethnobotany; Fabaceae; Genus Dalbergia; Leguminosae; Red propolis

Macro-Microscopic evaluation, Physicochemical analysis and HPTLC Finger printing of Curculigo orchioides Gaertn. Rhizome - Deepa Yadav; Mohd Salim Reshi; Sadhana Shrivastava; Nalini Srivastava; Sunil Kumar Koppala Narayana; Sangeeta Shukla (Pharmacognosy Journal, 2016)
Introduction: Curculigo orchioides Gaertn. Family Hypoxydaceae (Amaryllidaceae) is a perennial herb with finger like rhizome. Its rhizomes have been significantly used in treatment of various ailments including cancer. Methods: Macro-microscopic analyses, physico-chemical studies and HPTLC finger printing of rhizomes of C. orchioides were performed according to pharmacopoeial procedures. Results: Microscopic analysis has shown rows of rectangular and conical cells in cork, thin walled cortex, parenchymatous cells, starch grains, crystal of calcium oxalate, mucilage cell and spiral xylem vessel in the rhizomes of C. orchioides. Physicochemical studies revealed loss on drying (10.469%), total ash (8.463%), acid insoluble ash (1.10%), water-soluble ash (2.163%), alcohol soluble extractive value (3.036%), and water-soluble extractive value (22.666%) of the raw drug. Ethanol extract of the plant were fingerprinted in petroleum ether and ethyl acetate (7.0:3.0) solvent system and scanned densitometrically after dipping in anisaldehyde-sulphuric acid reagent followed by heating at 105°C. Conclusion: These specific identities will be useful in identification and authentication of the raw drug in dried form.
Keywords: Curculigo orchioides; HPTLC fingerprinting; Pharmacognostic; Quality control.; Standaridisation

Medicinal Plants for Treatment of Cancer: A Brief Review - Sonika Jain; Jaya Dwivedi; Pankaj Kumar Jain; Swaha Satpathy; Arjun Patra (Pharmacognosy Journal, 2016)
Cancer is actually a group of many related diseases that all have to do with cells. Cancer cells are characterized by unregulated growth, as well as insufficient and inappropriate vascular supply. Moreover, a core of cells was subjected to micro environmental stress conditions, and has decreased apoptotic potential through genetic alterations, thereby resulting in resistance to apoptosis. Cancer is one of the major causes of death worldwide where the number of cancer patients is in continuous rise. Cancer is a major public problem whose estimated worldwide new incidence is about 6 million cases per year. It is the second major cause of deaths after cardiovascular diseases. Chemotherapy remains the principal mode of treatment for various cancers. A number of synthetic anticancer drugs are available in practice, but the side effects and the drug interactions are major drawbacks in its clinical utility. Most of the currently used chemotherapy drugs for cancers are known to develop resistance, exhibit non-selective toxicity against normal cells and restrict by dose-limiting side effects. Hence, cancer treatment and development of drugs for this disease remains a major clinical challenge. On the other hand, plants are an exceptionally viable source of biologically active natural products which may serve as commercially significant entities in themselves or which may provide lead structures for the development of modified derivatives possessing enhanced activity and/or reduced toxicity in traeatment of cancer. Herbal medicines are now attracting attention as potential sources of anticancer agents and are widely used due to availability of the materials, affordability, relatively cheap and little or no side effects, wide applicability and therapeutic efficacy which in turn has accelerated the scientific research. For these reasons, World Health Organization (WHO) supports the use of traditional medicines which are efficacious and non toxic. In this review we have summarized few plants having anticancer activity.
Keywords: Allopathic Drugs; Breast cancer; Cancer; Cancer Cell Lines.; Chemotherapy; Medicinal Plants.

Nutritional Evaluation of Fruits of Gynochthodes umbellata (L.) Razafim. & B. Bremer – An Underutilized Edible Fruit Plant - Anjusha Sudhakaran; Gangaprasad Appukuttan Nair (Pharmacognosy Journal, 2016)
Objective: The present investigation aimed to assess the nutritional, mineral profiling and anti-nutritional analysis of Gynochthodes umbellata (Syn. Morinda umbellata), an underutilized edible plant belongs to the family Rubiaceae. Literature perusal reveals that, there are no previous reports on nutritional studies for this valuable fruit. Methods: Nutritional, mineral profiling and anti-nutritional analysis of fruits were carried out. Results: In nutritional analysis, carbohydrates (6.98 g/100g fw), protein (2.68 g/100 g fw), crude fat (0.13 mg/g dw) and crude fibre (32.58%) content were detected. The fruits of G. umbellata, Vitamin C (25 mg/100g fw) was higher when compared to other three vitamin evaluated, Four macro elements and 6 micro elements were also quantified. Conclusion: Nutritional and Anti-nutritional analysis reveals that, the G. umbellata fruits could be used as a source of protein, vitamin and minerals and highly recommended for consumption as they contain low amount of the anti–nutrients analysed. This is the first report on nutritional analysis of G. umbellata fruit.
Keywords: Anti-nutritional analysis; Morinda umbellata; Nutritional analysis; Underutilized edible fruit.

Pharmaco-Chemical characterization and Acaricidal Activity of Ethanolic Extract of Chassalia Curviflora (Wall ex Kurz.) Thwaites. - Ajeesh Krishna Thumadath Palayullaparambil; Adarsh Krishna Thumadath Palayullaparambil; Sanis Juliet; Kumuthakalavalli Renganathan; Ramasubbu Raju; Sunil Athalathil; Reghu Ravindran; Leena Chandrashekar; Suresh Narayanan Nair; Srikanta Ghosh (Pharmacognosy Journal, 2016)
Introduction: C. curviflora, an important ethno-medicinal plant used by the Kurichia local people in Western Ghats region of Wayanad is yet to be explored pharmacologically. It is used as paste on the body of cattle and birds for curing skin diseases. Objectives: To characterize the pharmacochemical features and to study the acaricidal effect of ethanolic extract of C. curviflora on engorged female ticks of R. (B.) annutatus. Methods: The pharmaco-chemical features such as physico-chemical, proximate, phytochemical, fluorescence, and HPTLC profiling were carried out using standard techniques. The pulverized leaves were subjected to soxhlet extraction using ethanol. The ethanolic extract at different concentrations (10% to 1.25%) was tested against ticks using adult immersion test (AIT). Result: The preliminary phytochemical investigation showed high contents of saponins, alkaloids and flavonoids. The HPTLC profiling of ethanolic extract showed the presence of 14 polyvalent components. Based on AIT, the extract at 10% revealed 43.76% of inhibition of fecundity (IF) and 29.16% of adult tick mortality. Conclusion: The results revealed that the extract has some active compounds that may influence in the reproductive system of female ticks.
Keywords: Acaricidal activity; Chassalia curviflora; Fecundity.; HPTLC; Pharmaco-chemical; R. (B.) annutatus

Pharmacognostic and Preliminary Phytochemical Investigation of Leaves of Aralia Racemosa L. - D S N B K Prasanth; Atla Srinivasa Rao; Rajendra Prasad Yejella (Pharmacognosy Journal, 2016)
Objective: Ethnomedicinally, the entire plant and its parts are generally utilized by local people for the treatment of different aliment conditions without standardization. The standardization of crude drug is a crucial part of establishing its correct identity. Prior to any crude drug can be included in an herbal pharmacopeia, pharmacognostic and physicochemical parameters and standards to be established. Aralia racemosa L. perennial herb belongs to family Araliaceae. It is commonly known as American Spikenard. It is traditionally used in the treatment of Rheumatism, Whooping cough, skin diseases, pleurisy, diaphoretic, diuretic, pulmonary diseases, asthma, rheumatism, diarrhea, stimulant, expectorant, syphilis, Inflammation and Hay fever. In the view of lack of pharmacognostic study of leaf of Aralia racemosa L. Methods: The macroscopical, microscopical and physicochemical parameters were assessed according to WHO Quality Control Methods for herbal materials. The leaves of Aralia racemosa. L was subjected for successive solvent extraction and preliminary phytochemical screening was carried out, along with florescence analysis of leaf Powder with different reagents were evaluated. Results: Macroscopy of the leaves showed oval to rounded shape with tooted margin, cordate base and pointed tip. Microscopic studies revealed the presence of anisocytic stomata, bicolateral vascular bundles, lignified fibers, spiral vessels and rosette shaped calcium oxalate crystals. Physicochemical parameters such as moisture content, extractive values, ash content and fluorescent behavior of leaf powder were also determined. Preliminary Phytochemical analysis revealed the presence of various phytochemical constituents viz., glycosides, tannins, flavonoids, saponins and steroids. Conclusion: The results of current study could be served as a diagnostic tool for the standardization of this medicinal plant and will helpful in characterization of the crude drug.
Keywords: Anisocytic stomata; Aralia racemosa; Bicolateral vascular bundles; Lignified fibers.; Pharmacognostic; Rosette shaped calcium oxalate crystals

Pharmacognostic Characterization of Spondias mombin L. (Anacardiaceae) - Alex Lucena de Vasconcelos; Alan Lucena de Vasconcelos; Karina Perrelli Randau (Pharmacognosy Journal, 2016)
Background: Spondias mombin L. is fruit specie found in Tropical America and the coast of Africa, popularly known as cajazeira. Several researches with extract of leaflets show a diversity of promising pharmacological activities such as antibacterial activity, antiviral against dengue virus type 2, anti diabetic, among others. Objective: This paper aims to study the anatomical characteristics, phytochemical and histochemical from leaves of this species. Materials and Methods: Cross and paradermic sections from leaves were submitted to double staining with astra blue and safranin process for the anatomical study. Anatomical analysis of the structures was performed using an optical microscope. For ultra structure analysis, the leaf fragments, after processing and gold coating, were observed under scanning electron microscopy (SEM). The phytochemical analyses were performed using thin layer chromatography and the histochemical analyses using specific reagents for each metabolite group. Results: The leaf has anomocytic and tetracytic stomata distributed on abaxial surface. The midrib has convex symmetry with collateral vascular bundles in a closed arc disposition. The phytochemical showed the presence of mono and sesquiterpenes, triterpenes and steroids, hydrolysable tannins, phenylpropanoid glycosides, cinnamic derivatives and flavonoids. The histochemical tests allow us to state that phenolic compounds are found in the palisade parenchyma cells. Lignins can be found in woody vascular bundles and in perivascular sclerenchyma fibres. The volatile oils were evidenced in the schizogenous cavity, present in the parenchyma of the midrib. Conclusion: The results allowed characterizing anatomically the leaves of this species, outlining a profile of its phytochemical constituents and, in addition, determining which anatomical structures of storage of these metabolites by the plant.
Keywords: Anacardiaceae; Cajá; Histochemistry; Leaf anatomy

Pharmacognostic Evaluation of Epilobium hirsutum Linn. - N. A. Sheikh; T. R. Desai; R. D. Patel (Pharmacognosy Journal, 2016)
Background: Epilobium hirsutum Linn. (Onagraceae) is used widely as traditional medicine for its various medicinal values. Despite the popular utilization of this plant, still no conclusive study has been reported so far regarding the pharmacognostical standardization. Aim: Thus, the present study was aimed to scientifically establish a standard monograph of E. hirsutum on the basis of pharmacognostical aspects. Material and methods: Macroscopic, qualitative and quantitative microscopic characters of E. hirsutum were analyzed. Results: The diagnostic characters of the E. hirsutum were evaluated based on the macroscopical and microscopical characters. Conclusion: The obtained qualitative and quantitative standards will provide referential information for correct identification, purity, standardization and preparation of monograph of E. hirsutum.
Keywords: Epilobium hirsutum Linn; Great hairy willowherb.; Great willowherb; Hairy willowherb; Onagraceae

Pharmacognostic Evaluation of Melilotus officinalis Linn. - N. A. Sheikh; T. R. Desai; R. D. Patel (Pharmacognosy Journal, 2016)
Background: Melilotus officinalis Linn. (Fabaceae) historically has been used for a variety of medicinal purposes. Despite the popular medicinal utilization, still no conclusive study has been reported so far regarding the pharmacognostical standardization. Aim: Thus, the present study was focused to scientifically establish a standard monograph of M. officinalis on the basis of pharmacognostical parameters. Material and methods: The detailed macroscopic and qualitative as well as quantitative microscopic characters of M. officinalis were analyzed. Results: The morphological characters of M. officinalis were established. The transverse section of leaf shows lamina with single layered epidermis, anomocytic stomata, mesophyll, midrib with single layered epidermis and vascular strands were present in lamina. Stem contains single layered epidermis, cortex with several layers, phloem, xylem and starch grains. Root shows the presence of cork, phloem, xylem and starch grains. The powder characteristics of M. officinalis revels the presence of Epidermis, stomata, cork, parenchyma, mesophyll, fibers, spiral and pitted xylem vessels. The quantitative microscopy of leaf of M. officinalis reveals Stomatal number Upper surface (28.75 ± 2.5), Lower surface (38.37 ± 2.5); Stomatal index Upper surface (13.10 ± 1.50) Lower surface (12.58 ± 1.10); Vein islet number (96.25 ± 4.79), Vein termination number (27.50 ± 2.87) and Palisade ratio 6.5 ± 0.58. Conclusion: The obtained qualitative and quantitative standards would serve as a useful guide for correct identification, purity, standardization and preparation of monograph of M. officinalis.
Keywords: Aspurk.; Fabaceae; Melilot; Melilotus officinalis Linn; Yellow Sweet clover

Pharmacognostic Evaluation on Seeds of Madhuca longifolia (Koen.) Macbr. Var. latifolia (Roxb.) A. Cheval - Bindu Gopalkrishnan; CL. Ringmichon (Pharmacognosy Journal, 2016)
Introduction: Mahuwa i.e., Madhuca longifolia (Koen.) Macbr. Var. latifolia (Roxb) A. Cheval  belongs to family Sapotaceae. The local people and aboriginals use the oil extracted from the seeds for cooking purposes. The powdered seed has several therapeutic uses too. Recently seed oil is used as biodiesel. Although seeds and oil are in use; deliberate attempt to study them has lacked. Methods: Pharmacognosy can be the first step in deciding the status of a plant organ as a crude medicine. Hence comprehensive Pharmacognosy of Mahuwa seed was carried out by macroscopy, microscopy, histochemistry, powder study, proximate analysis and preliminary phytochemical studies. Results: The present study provides the microscopic diagnostic characters such as presence of sclerides, oil ducts, crystals etc in seed. Physicochemical studies revealed total ash (0.65%), acid insoluble ash (0.5%), water soluble ash (5.95%), alcohol soluble extractive (23.04%) water soluble extractive (17.76%) and chloroform extractive (12.3%). Histochemistry and Preliminary phytochemical screening revealed the presence of saponnins, terpenoids, anthraquinone glycoside, cardiac glycoside etc. Conclusion: These studies will help in establishing the  pharmacopeial standards for the said drug.
Keywords: Histochemistry; Mahuwa; Pharmacognosy; Phytochemistry.; Sapotaceae; Seeds

Pharmacognostic Standardisation and Phytochemical Evaluation on the Seeds of Two Vitis Vinefera L. Varieties Grown in Kashmir Valley, India - Javaid Ashraf Nowshehri; Zulfiqar Ali Bhat; Mohammad Yaseen Shah (Pharmacognosy Journal, 2016)
Introduction: Grape (Vitis vinifera L.) is one of the largest fruit crop widely grown throughout the world and their seeds are considered a relevant source of polyphenol compounds. Objective: To carry out phytochemical and pharmacognostic evaluation of the seeds of Vitis vinifera L. Var sahibi and hussaini, family vitiaceae as per WHO guidelines. Materials and Methods: In present investigation, the detailed pharmacognostic studies were carried out in terms of organoleptic properties, macroscopical, microscopical characters, physicochemical parameters, preliminary phytochemical screening for major groups of compounds and other WHO recommended parameters for standardization of the seeds of Vitis vinifera L. Var. sahibi and hussaini. Results: Macro and microscopic characters of Vitis vinifera L. seeds Var. sahibi and hussaini were analyzed. Physicochemical parameters such as foreign matter, extractive values, ash content, pH and fluorescent behaviour of seed powder were done by using WHO recommended parameters. A preliminary phytochemical screening was done and revealed the presence of different phytoconstituents like carbohydrates, flavonoids, glycosides, tannins, sterols and fixed oil. Conclusion: This is the first report of its kind on the pharmacognostic studies of Vitis vinifera L. seeds Var. sahibi and hussaini and will serve as valuable source of information towards establishing pharmacognostic standards on identification, purity, quality and classification.
Keywords: Grapes; Hussaini; Macroscopy; microscopy; Physicochemical; Sahibi.

Pharmacognostical Investigation and Preliminary Phytochemical Screening of Leaves of Myxopyrum Smilacifolium B. - Raveesha Peeriga; Chandrasekhar Kothapalli Bonnth (Pharmacognosy Journal, 2016)
Objective: The current study deals with detailed pharmacognostical study and preliminary phytochemical screening of leaf of Myxopyrum smilacifolium Blume. Myxopyrum smilacifolium Blume is a twining shrub belongs to the family Oleaceae. It is used traditionally in the treatment of cough, rheumatism, cephalalgia, notalagia and otopathy. Scrutinization of literature revealed that there is a lack of pharmacognostical and Phytochemical investigations of Myxopyrum smilacifolium Blume. Methods: The macroscopical and microscopical features were evaluated. The leaves of Myxopyrum smilacifolium Blume was subjected for successive solvent extraction and further preliminary phytochemical screening was carried out and also the behaviour of powder with different reagents were evaluated by fluorescence analysis. Results: The detailed study of pharmacognostical evaluation showed the presence of thick walled epidermal cells covered with thick cuticle, xylem and phloem elements, Glandular trichome and slightly concave collateral vascular bundles. Preliminary Phytochemical examination revealed the presence of various phytoconstituents viz., alkaloids, glycosides, tannins, saponins, terpenoids, carbohydrates and fixed oils. The fluorescence analysis manifested the behavioral variation of the powdered drug. Conclusion: The findings of the present study will be a referential information for identification and also useful for standardization of the plant material.
Keywords: microscopy; Myxopyrum.; Oleaceae; Phytochemical screening; standardization

Pharmacognostical, Phytochemical and Nutritional Evaluation of Glinus oppositifolius (L.) Aug. DC - Shantha Thirumalai Ramaseshan; Patchaimal Pitchaiah; Vandana Bharti; Kishore Kumar Ramakrishna; Venkateshwarlu Gaddam; Devesh Tewari; Chinmay Rath; Anupam Mangal; Padhi Madan Mohan; Dhiman Kartar Singh (Pharmacognosy Journal, 2016)
Objective: The primary aim of the study was to establish the pharmacognostic standards along with nutritional values on the important medicinal herb Glinus oppositifolius (L.) Aug. DC., commonly known as Parpata in South India. Material and Methods: Pharmacognostical, physicochemical, nutritional evaluation along with the TLC profiling and preliminary phytochemical screening was carried out. Results: Histological study of different parts of the plant revealed the presence of different cellular structures viz. stem showed the presence of multi cellular to unicellular trichomes, collateral vascular bundles, starch grains etc. Mesophyll of the leaves was embedded with starch grains with clustered calcium oxalate and prism shaped crystals. Anomocytic stomata were present on both the epidermis of the leaf. Powder microscopy exhibited multi cellular trichomes, clustered calcium oxalate, fibres etc. Physicochemical and histochemical studies revealed the presence of various secondary metabolites and different minerals within the acceptable limits. Thin layer chromatographic profiling showed different spots suggesting the presence of specific phytoconstituents in different extracts. The plant also revealed good nutritional value with calorific value of about 245 kcal/100g; Vitamin C 112 mg/100 g and higher amount of calcium etc. Conclusion: The results are beneficial to establish the quality control parameters of the plant species and may be served as future reference for the identification and authentication of the genuine crude drug and also provide sufficient data to recognize the use of the plant as dietary suppliment.
Keywords: Antidiabetic; Histochemical studies.; Pharmacognosy; Powder microscopy; standardization; Thin layer Chromatography.

Pharmacognostical Standardization of Goraksha pods: an important Nutritive and antidiabetic Plant - Shantha Thirumalai Ramasheshan; Patchaimal Pitchaiah; Prathapa Reddy Maramreddy; Vandana Bharti; Kishore Kumar Ramakrishana; Venkateshwarlu Gaddam; Devesh Tewari; Anupam Kumar Mangal; Madan Mohan Padhi; Kartar Singh Dhiman (Pharmacognosy Journal, 2016)
Objective: Goraksha or cluster beans are an annual legume found throughout India. It is also extensively cultivated for its pods used as vegetable for its high nutritive value, antidiabetic properties and for the source of guargum. Methods: Macroscopy, microscopy, powder microscopy, histochemical studies and preliminary phytochemical studies on the pods of Goraksha has been carried out highlighting its importance along with important diagnostic characters, which will help in the identification of pods both in fresh form as well as in dry form. Results: Study revealed presence of distantly arranged elongated uniseriate warty trichomes in the outer most layer of epidermis, presence of stone cells, simple starch grains and very small calcium oxalate crystals in the hypodermal region. Presence of unevenly thickened row of palisade layer of macro sclereids in the outer most layer of cotyledon region. Phytochemical studies revealed the presence of alkaloids carbohydrates, phenols, proteins, saponins, starch, steroids, and tannins. Conclusion: The pharmacognostical standardization revealed the presence of various specific characters which are important for the identification of the genuine pods of Cyamopsis tetragonoloba (L.) Taub.
Keywords: Cluster beans; Goraksha; Pharmacognosy; Pods. Histochemical studies.

Physicochemical and Phytochemical Analysis of Different Parts of Indian Kesar Mango–A unique variety from Saurashtra Region of Gujarat - Kalpna Rakholiya; Mital Kaneria; Sumitra Chanda (Pharmacognosy Journal, 2016)
The aim of the present study was to evaluate physicochemical and phytochemical analysis of different parts (ripe seed, unripe seed, ripe peel, unripe peel and stem) of Indian mango (var. ‘Kesar’) collected from Saurashtra region of Gujarat. The physiochemical properties such as loss on drying, total ash value, acid insoluble ash value, water soluble ash value and extractive values were carried out. The phytochemical properties such as alkaloids, flavonoids, tannins, phlobatanins, triterpenes, steroids, saponins and cardiac glycosides were also carried out. In phytochemical analysis, tannins showed maximum amounts in all five parts. The present study provides the details physicochemical and phytochemical properties of different parts of kesar mango which are useful in laying down standardization and pharmacopeia parameters.
Keywords: Kesar Mango; Physicochemical parameters; Phytochemical analysis; Ripe and Unripe Peel; Ripe and Unripe Seeds; Stem.

Physicochemical Evaluation and Pharmacognostical Standardization of Pellionia heyneana Wedd. Leaf - Vilash V; Suja SR; Latha PG; Aneesh Kumar AL; Ragesh R Nair; S Rajasekharan (Pharmacognosy Journal, 2016)
Introduction: Pellionia heyneana Wedd. Leaves have long been employed as a traditional remedy by the Cholanaikan tribe of South India to treat various ailments. Methods: Pharmacological and physicochemical evaluation of P. heyneana leaf has been carried out to determine its macro and microscopic characters, and also some of its quantitative characters as per standard procedures. Results: The pharmacognostical evaluation of P. heyneana leaves revealed the presence of characteristic microscopic features of the crude drug like cystoliths in upper epidermis, helicocytic stomata in lower epidermis, large number of peculiar shaped, huge (200-400 μm) foliar sclereids, absence of palisade tissue in the lamina etc. Powder microscopy showed the presence of calcium oxalate crystals, stone cells, multicellular trichomes, resinous blocks, spiral vessels, xylem fibre, starch grains, simple fibre etc. Conclusions: All the parameters evaluated in the study will aid to identify the authenticity of P. heyneana leaf even from the crushed or powdered form.
Keywords: Cholanaikan tribe; Fluorescence analysis; Helicocytic stomata; Pharmacognosy; Powder microscopy.

Phytochemical Analysis of Tasmannia lanceolata Extracts and Inhibition of Giardia duodenalis Proliferation - Paran Rayan; Ben Matthews; Pauline Mc Donnell; Ian Edwin Cock (Pharmacognosy Journal, 2016)
Background: Giardiasis is a debilitating disease caused by gastrointestinal parasites of the genus Giardia. Tasmannia lanceolata (Tasmanian pepper berry) has a high anti-oxidant capacity and has documented therapeutic properties for a variety of pathogenic diseases. Materials and methods: Solvent extracts of T. lanceolata berry and leaf were investigated for the ability to block G. duodenalis growth. The IC50 values of the extracts which displayed inhibitory activity were determined to quantify and compare their efficacies. Toxicity was determined using the Artemia franciscana nauplii bioassay. Active extracts were analysed by non-targeted HPLC-QTOF mass spectroscopy (with screening against 3 compound databases) for the identification and characterisation of individual components in crude plant extracts. Results: Methanolic, aqueous and ethyl acetate T. lanceolata berry and leaf extracts displayed potent G. duodenalis growth inhibitory activity. The methanolic extracts were the most potent growth inhibitors with IC50 values of approximately 180 µg/ml and 420 µg/ml for the berry and leaf methanolic extracts respectively. The aqueous, ethyl acetate, chloroform and hexane extracts also inhibited G. duodenalis growth, albeit with lower potency. HPLC-QTOF mass spectroscopy analysis of the extracts identified 45 compounds which were present in all T. lanceolata berry extracts. Forty of these were putatively identified by screening against 3 compound databases. All T. lanceolata berry and leafextracts were nontoxic in the Artemia fransiscana bioassay. Conclusion: The low toxicity of the T. lanceolata extracts and their potent G. duodenalis growth inhibitory bioactivity indicates their potential as medicinal agents in the treatment and prevention of this disease.
Keywords: Alternative therapies; Anti-Giardial activity; Anti-oxidant; Complementary; Gastrointestinal parasite; Giardisis; Tasmanian pepper.

Phytochemical and Antidiabetic Evaluation of the Methanolic Stem Bark Extract of Spathodea campanulata (P. Beauv.) Bignoniaceae - Tanayen Julius Kihdze; Ajayi Abayomi Mayowa; Oloro Joseph; Ezeonwumelu Joseph OC; Tanayen Grace Ghaife; Adzu Bulus; Arthur van Aerschot; Gert Laekeman; Agaba Amon Ganafa (Pharmacognosy Journal, 2016)
Background: Spathodea campanulata (P. Beauv.) Bignoniaceae extract (SCE) is one of many herbal medicines used widely in Ugandan traditional medicine for various ailments. Generally most of these herbal medicines are yet to be standardized or have their phytochemical content characterized. Method: This study identified the secondary metabolites in the stem bark methanolic extract and quantified them. The same extract was subjected to serial solvent fractionation, TLC characterization and antidiabetic testing. Results: The secondary metabolites were found to comprise of 7.5% alkaloids, 10% flavonoids, 13% tannins and 17% saponins per gram of plant material. The TLC characteristics of the fractions (hexane (HX), ethylacetate (EA) and methanol (ME)) viewed under UV light revealed spots with the following Rf values; the hexane partition gave HX7EA3 (0.96 and 0.68) HX9EA1 (0.68 and 0.3), EA1ME9 (0.86 and 0.58), EA3ME7 (0.87), EA7ME3 (0.85) and EA9ME1 (0.85). The ethylacetate partition gave the following HX1EA9 (0.53, 0.34 and 0.18), HX3EA7 (0.59, 0.40 and 0.26). Discussion: All the fractions produced nominal reduction of hyperglycemia. Except hexane fraction at 50 mg/kg and ethylacetate fraction at 200 mg/kg all the fractions had percentage reductions of glucose greater than that of the control at the experimental doses. Although the values of percentage reductions of hyperglycemia by the hexane fraction were apparently dose-dependent, the greatest margin of reduction of hyperglycemia was observed in the residual aqueous fraction. Conclusion: It was found that SCE contains valuable phytochemicals in appreciable quantities which are antidiabetic. The residual aqueous fraction is the most potent antihyperglycemic of the solvent fractions.
Keywords: Flavonoids; Saponins; Spathodea campanulata (P. Beauv.) Bignoniaceae; TLC Tannins; Uganda.

Phytochemical and In vitro Antidiabetic Activity of Psidium Guajava Leaves - Ramasamy Manikandan; Arumugam Vijaya Anand; Sampath Kumar; Pushpa (Pharmacognosy Journal, 2016)
Objective: The present investigation includes the preliminary screening of phytochemicals and evaluation of in vitro antidiabetic activity of Psidium guajava leaves extracts. Materials and Methods: Plant material was subjected to the extraction preparation by soxhlet apparatus by using various solvents such as aqueous, ethanol, chloroform, petroleum ether and hexane. The various kinds of phytochemicals were detected and then in vitro antidiabetic activity of P. guajava were detected by using alpha amylase and alpha glucosidase enzyme in an in vitro model. Results: The study reveals the presence of phytochemicals such as carbohydrate, tannin, flavonoids, phenols etc., Among the various extracts the aqueous and ethanolic extracts which contains the large number of phytoconstituents. The P. guajava leaves has been successfully inhibited both the enzymes in an in vitro model. The aqueous extracts of P. guajava leaves inhibited the alpha amylase and alpha glucosidase enzymes as 72.1% and 74.8% respectively. The ethanolic extract of P. guajava leaves inhibited the alpha amylase and alpha glucosidase enzymes as 97.5% and 91.8% respectively. Conclusion: From the results obtained in the current studies, the P. guajava leaves have a prominent antidiabetic property in an in vitro model and further studies can be carried out in an in vivo model and the isolation of activie compound from P. guajava leaves extract is needed.
Keywords: Alpha amylase; Alpha glucosidase; P. guajava; Phytochemical.

Phytochemical Evaluation of Polyherbal Formulation of Clinacanthus nutans and Elephantopus scaber to Identify Flavonoids - Muhammad Shahzad Aslam; Muhammad Syarhabil Ahmad; Awang Soh Mamat (Pharmacognosy Journal, 2016)
Background: Modern healthcare system recognizes herbal medicine as a form of alternative medicine and also identify as holistic approach. Everyone in life experiences different kind of wound.Clinacanthus nutans and Elephantopus scaber are well known traditional wound healing herbs. Objective: To develop a new polyherbal formulation in the treatment of wound and identify flavonoid by means of chromatography, chemical method and spectroscopic method. Preliminary phytochemical and fluorescent evaluation of Clinacanthus nutans,Elephantopus scaber and herb-herb combination. Methods and Material: Preliminary phytochemical and fluorescent evaluation of Clinacanthus nutans, Elephantopus and polyherbal formulation of both herb by chemical method. Identification of flavonoids by thin layer chromatography and fourier transform infrared spectroscopy. Results: Flavonoids have found inside polyherbal formulation by comparing the colour change after chemical analysis, Fluorescence analysis, retention time by thin layer chromatography and functional groups by fourier transform infrared spectroscopy. Conclusions: Flavonoids may responsible for its activity as wound healing. It may work with other bioactive compounds as synergistic effect.
Keywords: Clinacanthus nutans; Elephantopus scaber; Flavonoids; Herb-Herb combination; Polyherbal formulation; Wound healing.

Phytopharmacological overview of Psidium guajava Linn. - Vijaya Anand; Manikandan; Vijaya Kumar; Sampath Kumar; Pushpa; Agaath Hedina (Pharmacognosy Journal, 2016)
Psidium guajava Linn. possesses useful medicinal benefits. It has been recognized as the medicinally essential phytoconstituents, such as phenolic, flavonoid and carotenoid. Numerous pharmacological investigation have confirmed that the ability of this plant is to exhibit antimicrobial, antidiabetic, cardioprotective, neuroprotective, hepatoprotective, antioxidant and anticancer activities and it supports the traditional uses. This is a comprehensive of the phytoconstituents and pharmacological benefits.
Keywords: Anticancer.; Antidiabetic; Antimicrobial; Antioxidant; Hepatoprotective; Psidium guajava

Phytopharmacological overview of Terminalia chebula Retz - Agaath Hedina; Punniya Kotti; Juveriyah Kausar; Sivasamy; Vijaya Anand (Pharmacognosy Journal, 2016)
Phytotherapy is the traditional method used to cure many diseases. Various medicinal plants found in many parts of India are well known for their various medicinal values. The Terminalia chebula Retz. a native plant of Asia is found to have various properties like anti-oxidant and free radical scavenging activity, anti-carcinogenic activity, ant-imutagenic activity, anti-bacterial activity, anti-fungal activity, anti-viral activity, anti-diabetic, renoprotective activity, cardio-protective activity, anti-inflammatory and anti-arthritic activity. These properties of T. chebula discussed in this review are mainly due to the presence of various types of phytoconstituents.
Keywords: Anti-arthritic; Anti-carcinogenic; Anti-fungal; Anti-inflammatory.; Anti-oxidant; Free radical; Phytoconstituents; Renoprotective; Terminalia chebula

Quality Control standardization of Wild Himalayan Pear: Pyrus pashia - Siva Hemalatha; Priyanka Sharma; Satyendra Kuldip Prasad (Pharmacognosy Journal, 2016)
Introduction: To establish the pharmacognostical and phytochemical standardization parameters of Pyrus pashia fruits in order to ensure quality and safety of this traditionally acclaimed medicinal tree. Methods: The fresh fruits of P. pashia were collected and dried. Fruit was subjected to various pharmacognostical investigations, Extraction procedures, and preliminary phytochemical screening, according to WHO guidelines. Ethanolic extract was standardized to total phenolic and flavonoid content, followed by phytochemical quantification of P. pashia extract using lupeol as a chemical marker by HPLC method. Results: In the present study, microscopy of the fruit showed typical characteristics of berry, having thick fleshy pericarp differentiated into thin epicarp and thick mesocarp having wide radiating carpel chambers with one or two seeds attached in axile placentum. Further, physicochemical evaluation was done like, loss on drying, total ash value, acid insoluble ash value, water soluble ash value, fluorescence analysis etc. Heavy metal and pesticide residue analysis was also performed. Furthermore, ethanolic extract of Pyrus pashia (EPP) obtained from cold maceration and phytochemical screening of different fractions obtained by liquid partitioning revealed the presence of various secondary metabolites such as glycosides, steroids, triterpenoids, phenols flavonoids etc. Moreover, the total phenolic content and total analysis revealed that fruits are rich source of phenols and flavonoid. The HPLC chromatogram suggested that EPP contained 4.24% w/w of lupeol. Conclusion: Pharmacognostical and phytochemical investigation will ensure quality and safety of this medicinal plant, furthermore HPLC quantification will aid in authentication and development of monograph.
Keywords: HPLC.; Lupeol; Pyrus pashia; standardization; total flavonoid content; total phenolic content

Rasayana Herbs of Ayurveda to Treat age Related Cognitive Decline: An Update - Reena Kulkarni; Suhas Kumar Shetty; Rajarajeshwari N M; Prasanna Narasimha Rao; Nayan J (Pharmacognosy Journal, 2016)
Introduction: Cognitive decline associated with aging could be minor or major neuro-cognitive disorder presenting with progressive intellectual deterioration interfering with day to day activities. Behaviour and personality changes may complicate the life in due course. Significant increase in global prevalence of people aged above 60 years has raised concerns on effective management of old age problems. Age related cognitive deficits and dementia raise to the level of epidemics and established management is yet underway. Principles of preventive health and rasayana (rejuvenative) herbs of Ayurveda are being extensively researched up on for their effectiveness in dementia. In this fourteen such herbs with anti dementia property are discussed with relevant research update. Methods: Herbs like amalaki (Emblica officinalis), hareetaki (Terminalia chebula), haridra (Curcuma longa), manduka parni (Centella asiatica), aindri (Bacopa monniera), yastimadhu (Glycirrhiza glabra), guduchi (Tinospora cordifolia), shankhapushpi (Convolvulus pleuricaulis), vacha (Acorus calamus), jyotishmati (Celastrus panniculata), kushmanda (Benincasa hispida), Jatamamsi (Nardostachys jatamamsi), ashvagandha (Withania somnifera) and kapikacchu (Mucuna pruriens (Linn.)) are already proven of their efficacy in experimental and preclinical levels. The contents and research evidences are collected from ayurveda database on medicinal plants used in Ayurveda and Siddha and other authentic literature, Google scholar, Science direct, online and print journals. Discussion: The herbs in discussion mostly act on reactive oxygen species and oxidative stress injury by antioxidant properties and neuroprotective activity. Acetylcholine esterase inhibition, N-Methyl-D-Aspartate antagonism, Dopaminergic activity, Anti-amyloidogenic activity, Inhibition of Tau aggregation, neuroprotection and immune modulation are activity path ways. Tridosha namely Kapha, Pitta and Vata may be viewed to be categorically predominant in initial, middle and final stage of dementia. Selected herbs thus can be specific based on the pathology and relevant dosha predominance. Conclusion: Rasayana herbs with current updates and inferences can serve as an eye-opener for further researches at molecular and clinical aspect.
Keywords: Ayurveda; cognitive decline; Dementia; Herbs; Medhya; Rasayana.

Revelation of β-sitosterol from Benincasa hispida Seeds, Carissa congesta Roots and Polyalthia longifolia Leaves by High Performance Liquid Chromatography - Gaurav Mahesh Doshi; Pratip Kashinath Chaskar; Hemant Devidas Une (Pharmacognosy Journal, 2016)
Background: Fruit juice of Benincasa hispida (BH) is regarded as Vrindamadhava that is recommended for internal use in snake’s bites. The fruits have been reported to contain good amount of proteins, enzymes, Vitamin B1 and C1 flavonoid C-glycoside, terpenes, phenolic acids and free sugars such as glucose, rhamnose, mannitol, uronic acid, astilbin, catechin, naringenin, pectic polysaccharides and even some trace metals. Polyalthia longifolia (PL) has been well known for its ayurvedic preparations such as Sitaphala kula, Kaphapitashama, Anulomak and Krimighna. PL leaves has been reported to contain phytoconstituents like polylongine, Aporphine-Noxide alkaloids, allo-aromadendrene, caryophyllene oxide, β-caryophyllene, β-selinene, α-humulene, α-pinene and camphene. Carissa congesta (CC), known as Bengal currant, have yielded 2-acetyl phenol, carissone, carindone and Des-n-methylnoracronycine. β-sitosterol, an important phytoconstituent recognized from all these selected plants has been well known for its ethnopharmacological importance. In this new study, the research team members has focused on determining the percentage of the β-sitosterol present in the BH seeds, CC roots and PL leaves by subjecting the extract to High Performance Liquid Chromatography (HPLC). Materials and Methods: BH, CC and PL plants were shade-dried and extracted by suitable extraction methods. In HPLC, peaks obtained in the extracts were compared with the standard by matching their retention time. Results: The amounts of β-sitosterol present in the BH seeds, CC roots and PL leaves extracts obtained at 254 nm were found to be 36.00, 7.46 and 3.21% w/w respectively. Conclusion: Thus, BH, PL and CC extracts were said to contain β-sitosterol as a key constituent.
Keywords: Benincasa hispida; Carissa congesta; HPLC; Polyalthia longifolia; β-sitosterol.

A Review of Literature on Punarnavadi Mandura: An Ayurvedic Herbo-Mineral Preparation - Janmejaya Samal; Ranjit Kumar Dehury (Pharmacognosy Journal, 2016)
Background: Punarnavadi Mandura is an Ayurvedic herbo-mineral preparation primarily used as an anemia correcting agent while its role in other clinical conditions has also been studied. Objective: To understand the role of Punarnavadi Mandura in controlling anemia and other clinical conditions and its pharmacognostical and phytochemical properties. Methodology: A search of literature was carried out using “Punarnavadi Mandura” as the only key word and a total of 33 literatures were obtained of which 5 titles were finally selected for the review. Results and Discussion: Of the 5 studies identified 3 studies focused on the role of Punarnavadi Mandura as an anemia correcting agent, one study identified its role in other clinical condition (Diabetic Nephropathy), one study focused on the pharmacognostical and phytochemical analysis while one study focused on both the analysis of pharmacognostical and phytochemical properties and its role as an anemia correcting agent. As per these studies Punarnavadi Mandura is an effective remedy for iron deficiency anemia (IDA) of all ages. Statistically significant result has been obtained in subjective and hematological parameters. Furthermore its role in other clinical conditions has also been found effective, especially in Diabetic Nephropathy (DN), as a Naimithika Rasayana. Punarnavadi Mandura is currently a part of National health programme and is included in ASHA drugs kit for the management of IDA at community level. Conclusion: Given the efficacy of Punarnavadi Mandura in IDA, at all ages, its usage should be fostered more in Indian communities especially the rural communities where IDA is endemic.
Keywords: Anti-anemic; ASHA drugs kit.; Iron Deficiency Anemia; Naimithika Rasayana; Pharmacognostical; Phytochemical

Review of the phytochemical and pharmacological activities of Euphorbia hirta Linn. - Juveriyah Kausar; Durai Muthumani; Agaath Hedina; Sivasamy; Vijaya Anand (Pharmacognosy Journal, 2016)
The use of plant extract to cure diseases has been the traditional way used in many parts of the world. The synthetic drugs used now are more prone to cause side effects than curing the disease. Hence, the use of plant extract has now emerged due to their effective action against the disease without causing any side effects. The plants belonging to the family called Euphorbia are widely used in medicine for its wide medicinal properties. The plant Euphorbia hirta has properties like anti-bacterial, anti-diarrheal, anti-allergic, diuretic, anti-oxidant, anti-tumor, anti-diabetic, anxiolytic and sedative activity. This review contains the detailed information about all the properties of E. hirta.
Keywords: Anti-apoptotic.; Anti-bacterial; Anti-oxidant; Diuretic; Euphorbia hirta; Sedative

Role of Plant Based Lectins in Identifying Rare Bombay Blood Group - Raj Bharath Rudrappan; Krishnan Veeran (Pharmacognosy Journal, 2016)
Background: Lectins are proteins found in a diversity of plants and organisms. They possess the ability to agglutinate erythrocytes with known carbohydrate specificity. Methods: A lectin named Anti H is used in identification of a very rare and important blood group named Bombay blood group is extracted from the plant Ulex europaeus. Our study was done to calculate the prevalence of Bombay blood group in our Indian population using the plant based extract lectin anti H. Blood grouping was done using the tube technique using commercially available antisera. Results: Out of the total 11,512 blood samples collected and analysed, two samples were identified to be Bombay blood group. The prevalence of Bombay blood group in our study is .017%. The prevalence of the Bombay blood group varied slightly among different regions in parts of India. Conclusion: Anti H Lectin helped in identifying Bombay Blood Group which would otherwise have been missed in routine blood grouping. Plant based lectins will perform an important role in the field of transfusion medicine in near future.
Keywords: Blood grouping; Bombay phenotype; H antigen; Lectin; Ulex Europaeus.

Seed oil chemical composition of Platychaeteaucheri (Boiss.) Boiss - Jinous Asgarpanah; Narges Dakhili; Fatemeh Mirzaee; Maedeh Salehi; Maryam Janipour; Elaheh Rangriz (Pharmacognosy Journal, 2016)
Background: Platychaete aucheri is an endemic plant to the south of Iran and no phyochemical investigations is reported on the seeds oil. Materials and Methods: The chemical composition of Platychaete aucheri seeds oil was extracted by suxhelet apparatus, methyl esterificated and analyzed by GC and GC/MS spectroscopy method. Results: 16 compounds were determined in total and taraxasterol (19.0%), γ-sitosterol (14.1%) and lupeol (11.8%) were characterized as the most abundant components. Conclusion: Regarding the presence of high amounts of triterpenoids and sterols in the seed oil, related biological activities are expected from the studied oil.
Keywords: Asteraceae; gamma-Sitosterol.; Platychaete aucheri; Seed oil; Taraxasterol

Shelf Life Evaluation and Comparative HPTLC Profile of Hridya Yoga Churna - Vidhya Unnikrishnan; Karra Nishteswar; Bhupesh R. Patel (Pharmacognosy Journal, 2016)
Background: Quality, safety and efficacy of medicines used form the backbone of every health care system. Shelf‑life is the length of time, after which all substances start to degrade in their qualities and become unsuitable for consumption or sale. The saviryatavadhi of churna is considered to be 2 months according to ayurvedic classics. The use of modern packaging technology and preservatives have increased the shelf life period of ayurvedic medicines and the shelf life period of churna is 2 years according to Rule 161‑B, Drugs and Cosmetics Act. To ascertain the quality, hridya yoga churna was taken up to assess its shelf life period. Methods: Accelerated stability study (includes evaluation of organoleptic and physic-chemical parameters, assay of active constituents and microbial load) and Comparative HPTLC (High Performance Thin Layer Chromatography) were done to evaluate the shelf life of the Hridya yoga churna. Atomic absorption spectrophotometry was done to analyze the heavy metal content in the sample. Results and Conclusion: In the present study the shelf life period of Hridya yoga churna is found to be 3 years and 7 months. Similar Rf values obtained in HPTLC analysis of hridya yoga churna initially and after six months showed the minimum deterioration of the product. The presence of heavy metals namely arsenic, cadmium and lead were not detected and mercury was present within permissible limits.
Keywords: Accelerated stability; Churna; HPTLC.; Hridya Yoga; Shelf life

Should Seed Be an Alternative Source of Camptothecin From Nothapodytes nimmoniana and Chonemorpha fragrance? - Tasiu Isah (Pharmacognosy Journal, 2016)
The Southeast Asian forest is blessed with plant sources of anticancer molecules including camptothecin (CPT) but, the irrational harvest is among serious threat to its existence for use by the future generation. Among plant sources of CPT found in the region are Nothapodytes nimmoniana and Chonemorpha fragrance that are under heavy exploitation pressure for the alkaloid and other medicinal purposes. Under the natural conditions of forests, seeds produced by the plants show germination difficulties, and as a result lose viability few months after set. The unviable seeds can be used as an alternative source of CPT and other phytochemicals isolated from the species. In this study, evaluation of CPT yield of seeds and their parts was performed by high-performance thin layer chromatographic analysis to assess the feasible economic use of the seeds as an alternative source of the alkaloid. The results showed a manifold higher yield of CPT in seeds and their parts in N. nimmoniana over C. fragrance, suggesting seeds of the former that face more exploitation of its forest than the latter as a better alternative source of the alkaloid. The results also suggest that collection of the seed should be made before the onset of rain season. In this study, the economic implications of using seeds to isolate CPT are also discussed.
Keywords: Camptothecin; Chonemorpha fragrance.; Conservation; Forest Management; Nothapodytes nimmoniana; Seeds

Study of Protective Action of Spondias pinnata Bark extract on Rat Liver and Kidney against Etoposide Induced Chemical Stress - Beena Shetty; Gayathri Rao; Abhineetha; Niha Banu; Preethika; Sudarshan Reddy (Pharmacognosy Journal, 2016)
Introduction: System injury, manifested as metabolic dysfunction is a common side effect of chemotherapy. Chemical stress on hepatic and kidney cells can be evaluated by biochemical analysis, including serum aminotransferases, glutathione levels and extent of lipid peroxidation. Combined treatment of chemotherapy along with the natural products such as phytochemicals may be a newer approach to reduce the side effects and betterment of chemotherapy. Objective: The present study was conducted to assay kidney and liver associated parameters on animals exposed to etoposide, and the protective effect of different doses of Spondias pinnata bark extract on normal cells. In this study, total 24 male Wistar rats (either sex) aged between 60 to 90 days were considered. Each groups consisted of six rats. Levels of Alanine and Aspartate aminotransferases were estimated using semi-auto analyser and GSH, GST, TAO and LPx by spectrophotometry. Results and Conclusion: Data analyzed using Graph Pad 5.0. Variation in the analyzed parameters were found between control, chemotherapy and Spondias pinnata groups.  Results of the study show that significant increase in TBARS levels indicative of etoposide induced oxidative stress could be prevented by the treatment with S. pinnata. GST levels also support the preventive action of S. pinnata against etoposide induced stress. However, TAO and transaminases remain unaltered in the study groups.
Keywords: Etoposide; GSH; GST; LPx; Spondias pinnata.

Study of Quality Assurance For Peumus Boldus M Products By Botanic Profiling, Extraction Optimization, HPLC Quantification And Antioxidant Assay - Cristiane Cardoso Correia Teixeira; Tatiana Pereira de Freitas Cabral; João Paulo Barreto de Sousa; Simone de Pádua Teixeira; Jairo Kenupp Bastos; Luis Alexandre Pedro de Freitas (Pharmacognosy Journal, 2016)
Introduction: The boldo leaf has several traditional folk medicinal uses, such as for gallbladder, hepatic problems, digestive disorders, rheumatism and others. In the work reported herein, botanic profiling, extraction optimization by Soxhlet, quantification of boldine by an easy/simple to run HPLC method and antioxidant assay are proposed for the quality assurance of boldo dried leaves, standardized extracts, dried extracts, tablets and capsules. Materials and Methods; In this present work we are studying a systematic approach in the quality assurance study of quality assurance for Peumus boldus M products by the ascertainment of pharmacobotanic parameters for boldo identification, investigation of the extraction parameters by Soxhlet method, development and validation of an easy/simple to run HPLC method to quantify boldine in the raw drug, extracts, commercial tablets, capsules and coated tablets, and antioxidant assay. Results: The plant material was submitted to a pharmacognostic evaluation through morpho-anatomical diagnosis, showing that starlike trichomes can be used for boldo authentication. The HPLC validated analytical method is reliable, accurate and precise for boldine quantification. Furthermore, the Soxhlet extraction conditions were optimized. Conclusion: The methods proposed in this paper can be used for the quality assurance of boldo dried leaves, standardized extracts, dried extracts, tablets and capsules.
Keywords: antioxidant activity; Boldine; Peumus boldus; Pharmacognostic evaluation; Quantitation.

Study on Inflammation and the Nervous system of Ethanol extract of Jatropha Curcas seed - Zambrano-Huailla Alexander; Zambrano-Huailla Rommel; Goicochea-Lugo Sergio; Zavala-Flores Ernesto; García-Berrocal Jorge; Chau-Saravia Angel; Pante-Medina Carlos; Salazar-Granara Alberto (Pharmacognosy Journal, 2016)
Introduction: Jatropha curcas L. seeds are used in traditional medicine to treat a variety of diseases or conditions. The aim of this study is to evaluate effects on inflammation and the nervous system of ethanol extract of J. curcas seeds. Materials and methods: It was used 64 mice divided in 8 groups; respectively, 4 groups received 400, 600, 800 and 1000 mg/kg of ethanol extract of J. curcas seed; and the rest intake Diclofenac, Diazepam, Caffeine and a control group not received any substance. The effects on inflammation was evaluated by Carrageenan-Induced paw oedema test and by Paw skin temperature. Neurological symptoms of toxicity were evaluated using the Irwin test. For the analysis of quantitative variables were used the following tests: one-way ANOVA, Tukey, Shapiro-Wilk and Pearson correlation; for qualitative variables Chi square was used. Results: According to the paw oedema, it was showed a trend on an inflammatory effect of the seeds of J. curcas; this activity was statistically significant in doses of 1000 mg/kg. Also, the skin temperature measurements outcomes reveal a positive dose response manner. Regard to neurological manifestations, Straub tail was founded in doses of 400 mg/kg. Stereotypies were founded in doses of 400, 600, 800 and 1000 mg/kg throughout the evaluation. Conclusion: J. curcas seeds were showed an inflammatory effect. In addition, effects on the nervous system were founded as stereotypes and Straub tail.
Keywords: Carrageenan; Inflammation; Jatropha curcas; Nervous System.; Seeds

Study on Silybum marianum Seed through Fatty Acids Comparison, Peroxide Tests, Refractive Index and Oil Percentage - Iman Nasrollahi; Ebrahim Talebi; Zahra Nemati (Pharmacognosy Journal, 2016)
In this study, milk thistle seeds were collected from four regions of Iran (Ahvaz, Lorestan, Kazeroon and Zarghan). The oil extracted from seeds of plant using n-hexane solvent extraction soxhlet. The extracted oil was analyzed by gas chromatography and fatty acids were identified in all four samples. In all four samples, the oil refractive index of Milk thistle oil fatty acids vis. Linoleic acid, Oleic acid, Palmitic acid was evaluated. The Peroxide test and determination of oil percentage was performed in Milk thistle seed oil.
Keywords: Extraction; Fatty Acids; Milk Thistle; Oil; Peroxide

Sunscreens: A review - Mukund Manikrao Donglikar; Sharada Laxman Deore (Pharmacognosy Journals, 2016)
Sunlight despite of source of life and energy creating major health challenges like sunburn, pigmentation, wrinkles, dermatitis, urticaria, ageing, immune-suppression and number of skin cancers too. Sun protective clothes and or sunglasses provide insufficient and less convenient approach to get rid of all these health hazards. So sunscreen protection is popular mean among various regions of world. Present article have summarize types and classification, regulations, terminologies, evaluation methods, labeling, dosage and controversies of sunscreens. Natural chemical classes like phenolics (tannins, flavonoids), carotenoids, vitamins, oils are also discussed.
Keywords: Antioxidant.; COLIPA; IPD; ISO; Polyphenols; PPD; SPF; UV rays

Synthesis of Plant Mediated gold Nanoparticles using Azima Tetracantha Lam. Leaves extract and Evaluation of their Antimicrobial Activities - Abirami Hariharan; Tajuddin Nargis Begum; Mohamed Hussain Muhammad Ilyas; Hussain Syed Jahangir; Premkumar Kumpati; Shilu Mathew; Archunan Govindaraju; Ishtiaq Qadri (Pharmacognosy Journal, 2016)
Aim: The demand for nanoparticles is increasing day by day due to their wide range of applications in various areas including pharmaceutical industry. Nanoparticles are formally synthesized by chemical methods in which the toxic and flammable chemicals are used. Methods: This article reports about an effective, rapid and eco-friendly technique for the fabrication of gold nanoparticles from gold chloride solution using Azima tetracantha Lam. leaves extract. The effects of the leaves extract of Azima tetracantha, the concentration of Gold chloride solution, the time of the reaction and the effect of tem¬perature on the rate of the reaction were investigated. The synthesized gold nanoparticles (AuNPs) were characterized by using various techniques such as Dynamic Light Spectroscopy (DLS), Scanning Electron Microscopy (SEM), UV-Vis spectra gave surface plasmon resonance (SPR) at 540 nm, Fourier Transform Infrared spectroscopy (FTIR) and X-ray diffraction (XRD). This revealed the reduction of gold ions (Au+) to gold metal (Au0) which indicated the formation of gold nanoparticles (AuNPs). Results: The antimicrobial action of biosynthesized AuNPs indicated effective activity against bacterial pathogens Aeromonas liquefaciens, Enterococcus fecalis, Micrococcus luteus, Salmonella typhimurium and fungal pathogens Candida albicans, Cryptococcus sp, Microsporum canis, Trichophyton rubrum. Conclusion: This revealed that gold nanoparticles could provide a safer alternative to conventional antimicrobial agents.
Keywords: Antimicrobial Activity.; Azima tetracantha Leaves Extract; Biosynthesis; Characterization; Gold Nanoparticles

The Therapeutic Properties of Juniperus Communis L.: Antioxidant Capacity, Bacterial growth Inhibition, Anticancer Activity and Toxicity - Alejandra Fernandez; Ian Edwin Cock (Pharmacognosy Journal, 2016)
Introduction: J. Communi sberry is a high antioxidant fruit which is used in several traditional medicinal systems to treat a variety of diseases including rheumatism, arthritis and gout.This study was undertaken to examine the inhibitory activity of J. communis berry extracts on the growth of several bacteria associated with autoimmune inflammatory disease, and to test their ability to block CaCo2 and HeLa cancer cell proliferation. Methods: J. Communis solvent extracts were preparedusing solvents of varying polarity. The extracts were investigated by disc diffusion assay for the ability to inhibit the growth of a panel of pathogenic bacteria associated with autoimmune inflammatory diseases. Their MIC values were determined to quantify and compare their efficacies. Inhibitory activity against CaCo2 and HeLa human carcinoma cell lines was evaluated using an MTS colorimetric cell proliferation assay. Toxicity was determined using the Artemia franciscana nauplii bioassay. Results: The methanol, water and ethyl acetate J. communis berry extracts displayed moderate to potent growth inhibitory activity against bacterial triggers of rheumatoid arthritis, ankylosing spondylitis and multiple sclerosis. The methanol and water extracts displayed the broadest specificity, inhibiting the growth of all bacteria tested. The ethyl acetate extract also displayed antibacterial activity, inhibiting the growth of 9 of the 13 bacterial strains (69%). The ethyl acetate extract displayed the greatest potency, with MIC values substantially below 2000 µg/mL for all bacteria which it inhibited. It was most effective at inhibiting the growth of P. mirabilis, P. vulgaris and S. aureus, each with MIC’s ≤ 500 µg/mL. The methanol and water extracts also proved effective at blocking the proliferation of the colorectal cancer cell line CaCo2 and HeLa cervical cancer cell growth, with IC50 values in the 1300-2500 µg/mL range. All extracts were non-toxic in the Artemia nauplii bioassay. Conclusion: The lack of toxicity of the J. Communis berry extracts and their potent growth inhibitory bioactivity against bacteria and HeLa and CaCo2 carcinoma cells indicates their potential in the treatment and prevention of selected autoimmune inflammatory diseases and some cancers.
Keywords: Anti-bacterial activity; Antioxidant.; Artemia; Autoimmune inflammatory disease; CaCo2; HeLa; Juniper berry; Traditional medicine

Triterpenes from Hoya paziae Kloppenb. - Melissa Borlagdan; Fernando B. Aurigue; Ian A. Van Altena; Consolacion Y. Ragasa (Pharmacognosy Journal, 2016)
Chemical investigation of the dichloromethane extracts of the stems of Hoya paziae Kloppenb. led to the isolation of taraxerol (1), taraxeryl acetate (2), and a mixture α-amyrin acetate (3), and β-amyrin acetate (4) in about 2.5:1 ratio. The structures of 1–4 were identified by comparison of their NMR data with those reported in the literature.
Keywords: Apocynaceae; Hoya paziae; taraxerol; taraxeryl acetate; α-amyrin acetate; β-amyrin acetate

Updates on Traditional Medicinal Plants for Hepatocellular Carcinoma - Shilu Mathew; Muhammad Faheem; Mohd Suhail; Kaneez Fatima; Govindaraju Archunan; Nargis Begum; Muhammad Ilyas; Esam Azhar; Ghazi Abdullah Damanhouri; Ishtiaq Qadri (Pharmaceutical Journals, 2016)
Aim: Hepatocellular carcinoma (HCC) is a major worldwide problem primarily caused by hepatitis B and C virus infection. End stage liver cancer treatment options are limited thus requiring expensive liver transplantation which is not available in many countries. Methods: Several herbal compounds and herbal composite formulas have been studied through in-vitro and in vivo as an anti-HCC agent, enhancing our knowledge about their biological functions and targets. In this article, arecent update on the herbal medicine has been provided with reference to liver cancer. Results: For the sake of clarity, the effective herbal compounds, clinical studies of herbal composite formula, cell culture, and animal model studies safety are discussed. The effects of many herbal active compounds of Annona atemoya, Andrographis paniculata, Boerhaviadiffusa, Piper longum, Podophyllum hexandrum, Phyllanthus amarus, and Terminalia chebula, and herbal composite formula on autophagy, apoptosis, antioxidant, and inflammation characteristicshave been provided. Conclusion: This will enhance our understanding on the prevention and treatment of HCC by herbal active compounds and herbal composite formulas.
Keywords: Anticancer; Herbs; Liver cancer; Medicine; Treatment.

Validated analytical RP-HPLC method for quantitation of wedelolactone from Eclipta alba and marketed Ayurvedic formulations - Sunita Shailajan; Sasikumar Menon; Dipti Singh; Gauri Swar (Pharmacognosy Journal, 2016)
Introduction: Eclipta alba Linn. (Asteraceae) is an important ingredient of several Ayurvedic formulations. The monograph on different parts of plant like flowers, leaves, roots are listed in Ayurvedic pharmacopeia of India. The plant is reported to be effective for broad range maladies like inflammation, reproductive problems of females etc. It is also used as a hepatoprotectant, analgesic, antibacterial and antidiabetic agent. Wedelolactone is used as a bioactive marker to establish the quality of the crude drug and its formulations. In the present study, wedelolactone-based standardization of Eclipta alba and its quantitation from marketed herbal and Ayurvedic formulations has been documented using RP-HPLC. Methods: In the current work, an isocratic method has been developed and validated to quantitate wedelolactone from whole plant of Eclipta alba. This method is validated as per ICH guidelines and is used to quantitate the content of wedelolactone in polyherbal formulations like Liv52, Geriforte, Mahabhringaraj oil etc. Results: The LOD is found to be 0.5 μg/mL and the LOQ is 1 μg/mL. The linearity range of response is from 5 μg/mL to 100 μg/mL. Conclusion: The validated method is found to be simple, sensitive, accurate, rugged and reproducible. This developed method can be recommended for quality assurance and marker-based standardization of polyherbal formulations containing whole plant of Eclipta alba.
Keywords: Eclipta alba; Formulations; RP-HPLC; Validation; Wedelolactone.; Whole plant

Abutilon indicum L (Malvaceae)-Medicinal Potential Review - Rajagopal Ramasubramania raja; Koumara Velou Kailasam (Pharmacognosy Journal, 2015)
The plant Abutilon Indicum (Linn.) is belonging to malvaceae family; Also known as Mallow in english, Abutilon indicum is used as a medicinal plant. It has been reported that Abutilon indicum has Anti inflammatory and Antiproliferative activity, Anti-Arthritic activity, Analgesic and Sedative property, Antioxidant and Antimicrobial activity, Hepatoprotective activity, Anti diabetic, Anti cancer, Anti diarrhoeal, Anti-convulsant, Larvicidal, Wound healing, Anti asthmatic, Diuretic, Immunomodulatory, and Anti-estrogenic activity. It is proved that this plant contains carbohydrates, proteins and aminio acids, saponins, flavanoids, glycosides, phytosterols and phenolic compounds
Keywords: Abutilon indicum; Anti asthmatic; Anti-proliferative activity; Hepatoprotective activity; Phenolic compounds

Anti Hypertensive Activity of the Ethanolic Extract of Lantana camara leaves on high salt loaded wistar albino rats (Pharmacognosy Journal, 2015)
In an attempt to scientifically evaluate the antihypertensive activity of etanolic extract of Lantana camara in different experimental models. Anti hypertensive activity of EELC was evaluate by frog heart, anaesthetic chick and salt induced rat model. EELC produced negative inotropic and negative chronotropic effect, antagonised by atropine on isolated frog heart. EELC shows dose dependent (p<0.05) decreased mean arterial blood pressure (MABP) an anaesthetic chick. salt treated rats displayed significant (p<0.05) increase in blood level of SGOT,SGPT, Creatinine and sodium, decreases in pottassim levels compare than normal rats. Treatment of EELC (200 and 400 mg/kg) significantly balanced the ionic levels, such as lower the sodium and elevate the potassium levels. Creatinine levels were significantly (p<0.05) reduces by the treatment of EELC. These are no significant changes occurred in serum SGOT and SGPT with the treatment of EELC. The present study suggest that treatment of EELC on Salt hypertensive rats protects against renal injuries maintaining the normal ionic composition as well as parameters. Key words: EELC (ethanolic extract of Lantana camara leaves), Wistar albino rats, Hypertension, mean arterial blood pressure (MABP) and normotensive rats (NTR).
Keywords: EELC (Ethanolic extract of Lantana camara leaves); Hypertension; Mean arterial blood pressure (MABP) and Normotensive rats (NTR).; Wistar albino rats

Anti Hypertensive Activity of the Ethanolic Extract of Lantana camara leaves on high salt loaded wistar albino rats - Vijay Kumar Matta; Praveen Kumar Pasala; Silvia Netala; Satish Pandrinki; Prasad Konduri (Pharmacognosy Journal, 2015)
Background: Hypertension is the most common and major cardiovascular disease. There is an urgent need for treament of hypertension by exploration of several medicinal plants having potent anti hypertensive activity as the modern medicines are having many side effects. Objective: The study focus on scientific evaluation of antihypertensive activity of ethanolic extract of Lantana camara leaves (EELC) in different experimental models. Material & methods: Antihypertensive activity was conducted on wister albino rats by determining serum glutamic oxaloacetic transaminase (SGOT), serum glutamic pyruvic transaminase (SGPT), creatinine and Sodium levels by using Semi Autoanalyser and Flame photometer; chick mean arterial blood pressure by using condon’s mercury manometer and isolated frog heart for recording cardic responses using student kymograph. Results: EELC produced negative inotropic and negative chronotropic effect, antagonised by atropine on isolated frog heart. EELC shows dose dependent (p<0.05) decreased mean arterial blood pressure (MABP) in anaesthetic chick. Salt treated rats displayed significant (p<0.05) increase in blood level of SGOT, SGPT, Creatinine and sodium, decrease in pottassim levels in comparision with normal rats. Treatment with EELC (200 and 400 mg/kg) significantly balanced the ionic levels such as lower the sodium and elevate the potassium levels. Creatinine levels were signifi-cantly (p<0.05) reduced by the treatment with EELC. There are no significant changes occurred in serum SGOT and SGPT upon EELC administration. The present study suggests that treatment of salt hypertensive rats with EELC protects against renal injuries. Conclusion: It was concluded that ethanolic extract of Lantana camara leaves reduces work load of heart, maintain inotonic levels by negative chronotropic effect, relaxes the smooth muscles in chick and salt hypertensive rats against renal and vascular injuries is proved.
Keywords: EELC (Ethanolic extract of Lantana camara leaves); Hypertension; Mean arterial blood pressure (MABP) and Normotensive rats (NTR).; Wistar albino rats

Antibacterial Activity of Tinctures from Tree leaves belonging to the Bignoniaceae family and their Synergistic Effect with Antibiotics - Torres Carola Analía; Nuñez María Beatriz; Isla María Inés; Castro Marcela Paola; Gonzalez Ana María; Zampini Iris Catiana (Pharmacognosy Journal, 2015)
Context: Some species of Bignoniaceae are widely used in medicinal practice by the natives of South America. Aims: Tinctures and infusions from twelve tree species of this family were evaluated for in vitro antibacterial activity against pathogenic bacteria. The effect of interactions between the four most active extracts and conventional antibiotics was also evaluated. Methods and Material: Bioautography and disc diffusion methods were used to select the most active extracts, then agar macrodilution and broth microdilution method were used to determine the minimal inhibitory and minimal bactericidal concentration (MIC and MBC). Time-kill assay and checkerboard method were employed to determine the type of antimicrobial effect and synergism, respectively. Results: It could be determined that tinctures from Catalpa bignonioides, Handroanthus pulcherrimus, Tabebuia nodosa and Tecoma stans were able to inhibit bacterial growth. The MIC and MBC observed were between 125-1000 μg GAE/ ml and 500-1000 μg GAE/ml, respectively. The tested extracts were more effective against Gram-positive microorganisms. Time-kill experiments indicated bacteriostatic activity. Phytochemical screening showed terpenoids, phenols and flavonoids. Alkaloids were detected only in Tecoma stans. Among these combinations, the best was Tabebuia nodosa extract plus gentamicin. In most cases, MIC values were reduced 16-32 times for antibiotics, and even 8-16 times for extracts. Conclusion: These results revealed that some of the selected combinations could efficiently inhibit the growth of tested strains at lower concentrations than those required for the lonely use of the antimicrobial. These extracts would improve the efficacy of antibiotics against resistant bacteria, hence they could be used for anti-infective therapy.
Keywords: Checkerboard method; Fractional inhibitory concentration (FIC); Gentamicin; Tabebuia nodosa; Time-kill experiments.

Anti-diabetic Properties of Thymoquinone is unassociated with Glycogen Phosphorylase Inhibition - Nahid Mahmoud Hassan El-Ameen; Manal Mohamed Elhassan Taha; Siddig Ibrahim Abdelwahab; Asaad Khalid; Fatima Elfatih; Mona Awad Kamel; Bassem Yousif Sheikh (Pharmacognosy Journal, 2015)
Background: Nigella sativa L. (Black seed), is commonly used by traditional healers as a remedy for more than four thousand years. The antidiabetic property of N. sativa seeds oil is attributable to the presence of Thymoquinone (TQ). On the other hand many studies have been designed to investigate the possible effects of the TQ in Streptozotocin (STZ) and nicotinamide (NA)-induced diabetes in rats. Aim of the study: The aim of this study was to elucidate the mechanisms underlying the glucose lowering effects of thymoquinone. Methods: In vitro and in silico using glycogen phosphorylase (GPa) enzyme assay and docking tools were used. Results: Oral administration of TQ for 60 days, dose dependently improved the glycemic status in STZ-NA induced diabetic rats. GPa activity was measured in the direction of glycogen synthesis by the release of phosphate from glucose-1-phosphate. TQ at a concentration of 0.05 Mm inhibits GPa activity by only 14.9%. Conclusion: These results show that TQ at 60 mg/kg b.w is associated with potential antihyperglycemic effects. Furthermore, anti-diabetic properties of TQ are unassociated with glycogen phosphorylase inhibition.
Keywords: Diabetes; Docking; Enzyme; Glycogen phosphorylase inhibition; Streptozotocin; Thymoquinone.

Anti-hyperglycemic and anti-lipidemic activities of Diabac (a polyherbal formulation) in streptozotocin-nicotinamide induced type 2 diabetic rats (Pharmacognosy Journal, 2015)
The objective of the work was to investigate the antidiabetic activity of Diabac (a polyherbal formulation) in streptozotocin-nicotinamide induced type 2 diabetic rats. Oral glucose tolerance test (OGTT) was performed to evaluate effect of Diabac on elevated glucose level. The type 2 diabetes was induced by overnight fasted rats by a single intraperitoneal (i.p.) injection of 65 mg/kg streptozotocin, 15 min. after the i.p. administration of 110 mg/kg nicotinamide. The diabetic rats were treated with Diabac (250, 500 and 1000 mg/kg, p.o.) or glibenclamide (5 mg/kg, p.o) for four week. Various parameters were studied such as fasting blood sugar level, serum insulin levels, glycated hemoglobin (HbA1C), serum lipid levels, serum creatinine, urea, uric acid and liver glycogen. Treatment with Diabac significantly reduced the blood sugar levels in OGTT. Diabetic rats showed a significant increase in the levels of glycated hemoglobin, serum lipids, serum creatinine, urea and uric acid, whereas there was a decrease in serum insulin, liver glycogen and HDL-C levels as compared to normal control rats. The administration of Diabac or glibenclamide significantly decreased the levels of glycated hemoglobin, TG, TC, LDL-C, serum creatinine, urea and uric acid, whereas there was an increase in the levels of liver glycogen and HDL-C as compared to diabetic control rats. However, the treatment with Diabac did not show any significant change in serum insulin levels as compared to diabetic control rats. These results of present study concluded that Diabac has anti-diabetic and anti-lipidemic activities which are responsible for its use in traditional medicine. Key words: Diabac, glycated hemoglobin, liver glycogen, serum lipids, Streptozotocin.
Keywords: Diabac; Glycated hemoglobin; Liver glycogen; Serum lipids; Streptozotocin.

Anti-hyperglycemic and Anti-lipidemic activities of Diabac (a polyherbal formulation) in Streptozotocin-nicotinamide induced type 2 diabetic rats - Richa Agrawal; Rajesh Maheshwari; Ramachandran Balaraman; Avinash Seth (Pharmacognosy Journal, 2015)
Aim: The objective of the work was to investigate the antidiabetic activity of Diabac (a polyherbal formulation) in streptozotocin-nicotinamide induced type 2 diabetic rats. Methods: Oral glucose tolerance test (OGTT) was performed to evaluate effect of Diabac on elevated glucose level. The type 2 diabetes was induced by overnight fasted rats by a single intraperitoneal (i.p.) injection of 65 mg/kg streptozotocin, 15 min. after the i.p. administration of 110 mg/kg nicotinamide. The diabetic rats were treated with Diabac (250, 500 and 1000 mg/kg, p.o.) or glibenclamide (5 mg/kg, p.o) for four week. Various parameters were studied such as fasting blood sugar level, serum insulin levels, glycated hemoglobin (HbA1C), serum lipid levels, se rum creatinine, urea, uric acid and liver glycogen. Results: Treatment with Diabac significantly reduced the blood sugar levels in OGTT. Diabetic rats showed a significant increase in the levels of glycated hemoglobin, serum lipids, serum creatinine, urea and uric acid, whereas there was a decrease in serum insulin, liver glycogen and HDL-C levels as compared to normal control rats. The administration of Diabac or glibenclamide significantly decreased the levels of glycated hemoglobin, TG, TC, LDL-C, serum creatinine, urea and uric acid, whereas there was an increase in the levels of liver glycogen and HDL-C as compared to diabetic control rats. However, the treatment with Diabac did not show any significant change in serum insulin levels as compared to diabetic control rats. Conclusion: These results of present study concluded that Diabac has anti-diabetic and anti-lipidemic activities which are responsible for its use in traditional medicine.
Keywords: Diabac; Glycated hemoglobin; Liver glycogen; Serum lipids; Streptozotocin.

Antimicrobial Effects of Thymoquinone on Entamoeba histolytica and Giardia lamblia - Bassem Yousef Sheikh; Manal Mohamed Elhassan Taha; Waleed Syaed Koko; Siddig Ibrahim Abdelwahab (Pharmacognosy Journal, 2015)
Background: Parasitic infections are a major difficulty in tropical and subtropical countries. Traditionally medicinal plants have been used in folk medicine to treat parasitic infections and are a valuable source of novel anti-parasitics. Objective: In our search for therapeutic alternatives to anti- protozoal chemotherapy, thymoquinone, the active ingredient of Black cumin (Nigella sativa) was examined. Materials and Methods: Thymoquinone was tested against Entamoeba histolytica and Giardia lamblia using in vitro susceptibility assays and the mortality of the parasites were then obtained using the standard calculations. The compound was also tested for 48 and 72 hours on both parasites. Results: The current study indicate that the mortality of TQ showed 85.5%, 91.5% and 96.8% mortality on E. histolytica for 25 ppm at 24 hr, 48 and 72 hr, respectively, with IC50 2¥10-19,. On the other hand, this natural compound showed a mortality of 82.83%, 91.76% and 96.62% mortality on G. lamblia for 25 ppm at 24 hr, 48 and 72 hr, respectively, with IC50 4.8¥10-5. Metrondizole powder gave 70.9% mortality at 156 ppm at the same times. Conclusion: The current results indicate that TQ is more potent on E. histolytica compared to G. lamblia. Further pharmacological studies were needed to help in the clinical presentation of thymoquinone.
Keywords: Entamoeba histolytica; Giardia lamblia.; Nigella sativa; Prophetic Medicine; Thymoquinone

Anti-Nociceptive Synergism of Pregabalin and Xylopic acid Co-administration in Paclitaxel-induced Neuropathy: Isobolographic Analysis - Ameyaw Elvis Ofori; Boampong Johnson Nyarko (Pharmacognosy Journal, 2015)
Keywords: Isobolograms; Neuropathic pain; Paclitaxel; Toxicity; xylopic acid

Anti-Nociceptive Synergism of Pregabalin and Xylopic acid Co-administration in Paclitaxel-induced Neuropathy: Isobolographic Analysis - Ameyaw Elvis Ofori; Woode Eric; Kyei Samuel; Biny Peter Robert; Boampong Johnson Nyarko (Pharmacognosy Journal, 2015)
Background: Paclitaxel-induced neuropathy still remains a clinical problem for patients undergoing chemotherapy. Objective: The objective of the study was to determine the interaction between xylopic acid and pregabalinco-administration as well as their toxicity in paclitaxel-induced neuropathy. Materials and Methods: Neuropathic pain was induced in rats with 2 mg/kg of paclitaxel on alternative days for four days (days 0, 2, 4 and 6). Equi effective doses of xylopic acid and pregabalin that produced 50% anti-nociception (ED50) were determined from their log-dose response curves in the cold allodynia and thermal pain tests. Xylopic acid and pregabalin were again administered to rats in a fixed ratio combination (1:1) of their ED50’sin order to determine the experimental ED50 (Zexp) of the co-administered compounds. Isobolograms were constructed to compare the Zexp to a theoretical ED50 (Zadd). Blood samples from the various treatment groups of rats were collected for toxicological assessment of the co-administered compounds. Results: The Zexplay below the Zadd on the isobologram of the cold allodnia test. The co-administration exhibited additivity in the thermal pain test. The co-administration did not produce significant (p>0.05) toxicity in rats. The co-administration may be beneficial in paclitaxel-induced neuropathy. Key words: Isobolograms, Neuropathic pain, Paclitaxel, xylopic acid, Toxicity.
Keywords: Isobolograms; Neuropathic pain; Paclitaxel; Toxicity.; xylopic acid

Antioxidant and DNA Damage Protective Effects of Asparagus racemosus in Human Colon and Mice Muscle Cells - Girindrababu Venkattappa Jayashree; Puttasiddiah Rachitha; Krishnaswamy Krupashree; Kandikattu Hemanth Kumar; Farhath Khanum (Pharmacognosy Journal, 2015)
Introduction: The present study was designed to investigate the in vitro antioxidant and macromolecule damage protective effects of Asparagus racemosus water (AWE) and methanolic (AME) fractions of roots. Methods: The in vitro antioxidant activity of AWE/AME was estimated by free radical scavenging assays. The DNA damage of HT29 and C2C12 cells was analyzed by comet assay. The plasmid DNA damage and protein oxidation were carried out by agarose gel electrophoresis and SDS-PAGE analysis respectively, where as lipid peroxidation was performed by TBARS assay. Results: Both the extracts showed scavenging activity with IC50 values of 417.4 ± 19.5 / 298 ± 13.5, 381 ± 18.2 / 235 ± 11.9, 54.8 ± 2.95 / 31.6 ± 1.52, 28.9 ± 1.73 / 19.7 ± 1.55 μg/mL for DPPH, metal chelating, ABTS and Nitric oxide scavenging activities respectively. Similarly the methanolic extract showed more potent reducing power and total antioxidant activities over water fraction. The AME showed 56.8% and 41.2% protection against H2O2 (Hydrogen peroxide) induced DNA damage of HT29 human colon cells and C2C12 murine myoblasts. The extract also showed protection against H2O2 induced plasmid DNA damge, AAPH induced protein oxidation of bovine serum albumin (BSA) and lipid peroxidation of rat hepatic tissue. Conclusion: Over all this study showed remarkable antioxidant and macromolecule damage protective effects of A.racemosus. The observed biological properties may be attributed to the high content phenols and flavonoids in the methanolic extract A. racemosus over water extract. Key words: AAPH, Asparagus racemosus, C2C12, HT29, Protein oxidation, Single cell gel electrophoresis.
Keywords: AAPH; Asparagus racemosus; Protein oxidation; Single cell gel electrophoresis.

Antioxidant and DNA Damage Protective Effects of Asparagus racemosus in Human Colon and Mice Muscle Cells - Girindrababu Venkattappa Jayashree; Puttasiddiah Rachitha; Krishnaswamy Krupashree; Kandikattu Hemanth Kumar; Farhath Khanum (Pharmacognosy Journal, 2015)
Introduction: The present study was designed to investigate the in vitro antioxidant and macromolecule damage protective effects of Asparagus racemosus water (AWE) and methanolic (AME) fractions of roots. Methods: The in vitro antioxidant activity of AWE/AME was estimated by free radical scavenging assays. The DNA damage of HT29 and C2C12 cells was analyzed by comet assay. The plasmid DNA damage and protein oxidation were carried out by agarose gel electrophoresis and SDS-PAGE analysis respectively, where as lipid peroxidation was performed by TBARS assay. Results: Both the extracts showed scavenging activity with IC50 values of 417.4 ± 19.5 / 298 ± 13.5, 381 ± 18.2 / 235 ± 11.9, 54.8 ± 2.95 / 31.6 ± 1.52, 28.9 ± 1.73 / 19.7 ± 1.55 μg/mL for DPPH, metal chelating, ABTS and Nitric oxide scavenging activities respectively. Similarly the methanolic extract showed more potent reducing power and total antioxidant activities over water fraction. The AME showed 56.8% and 41.2% protection against H2O2 (Hydrogen peroxide) induced DNA damage of HT29 human colon cells and C2C12 murine myoblasts. The extract also showed protection against H2O2 induced plasmid DNA damge, AAPH induced protein oxidation of bovine serum albumin (BSA) and lipid peroxidation of rat hepatic tissue. Conclusion: Over all this study showed remarkable antioxidant and macromolecule damage protective effects of A. racemosus. The observed biological properties may be attributed to the high content phenols and flavonoids in the methanolic extract A. racemosus over water extract.
Keywords: AAPH; Asparagus racemosus; C2C12; HT29; Protein oxidation; Single cell gel electrophoresis.

Antioxidant and metal chelating activities of Lagenaria siceraria (Molina) Standl peel, pulp and aerial parts in relation to their total phenol and flavonoid content - Sumitra Chanda; Pooja Moteriya; Hemali Padaliya; Tejas Rathod; Yogesh Baravalia (Pharmacognosy Journal, 2015)
Objective: The aim of the present study was to evaluate the antioxidant activity and total phenol and flavonoid content of different parts (peel, pulp and aerial parts) of Lagenaria siceraria. Method: Successive extraction was done by cold percolation method using solvents of different polarity viz. petroleum ether, toluene, ethyl acetate, acetone, water. Total phenol content was determined by Folin-Ciocalteu’s reagent method and flavonoid was determined by aluminium chloride colorimetric method. The antioxidant assays evaluated were 2, 2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity, 2, 2’-Azino-bis-(3-ethyl) benzothiazoline-6-sulfonic acid (ABTS) radical cation scavenging activity and Ferric reducing antioxidant power. Results: L. siceraria peel possessed maximum phenol and flavonoid content in acetone and toluene extracts respectively. FRAP was maximum in acetone extract of peel. The peel extract demonstrated stronger DPPH activity with IC50 value of 111 μg/ml followed by pulp extract. The same extract was effective in scavenging ABTS radical with an IC50 value of 39 μg/ml while other parts were ineffective. Conclusion: This work demonstrated good antioxidant activity of L. siceraria vegetable cultivated in India and recommends that the peel of this vegetable may be of interest from a functional point of view as a major source of natural antioxidant.
Keywords: ABTS; antioxidant activity; DPPH; FRAP; Lagenaria siceraria; total phenol.

Antioxidant and metal chelating activities of Lagenaria siceraria (Molina) Standl peel, pulp and aerial parts in relation to their total phenol and flavonoid content - Sumitra Chanda; Pooja Moteriya; Hemali Padaliya; Tejas Rathod; Yogesh Baravalia (Pharmacognosy Journal, 2015)
Objective: The aim of the present study was to evaluate the antioxidant activity and total phenol and flavonoid content of different parts (peel, pulp and aerial parts) of Lagenaria siceraria. Method: Successive extraction was done by cold percolation method using solvents of different polarity viz. petroleum ether, toluene, ethyl acetate, acetone, water. Total phenol content was determined by Folin-Ciocalteu’s reagent method and flavonoid was determined by aluminium chloride colorimetric method. The antioxidant assays evaluated were 2, 2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity, 2, 2’-Azino-bis-(3-ethyl) benzothiazoline-6-sulfonic acid (ABTS) radical cation scavenging activity and Ferric reducing antioxidant power. Results: L. siceraria peel possessed maximum phenol and flavonoid content in acetone and toluene extracts respectively. FRAP was maximum in acetone extract of peel. The peel extract demonstrated stronger DPPH activity with IC50 value of 111 μg/ml followed by pulp extract. The same extract was effective in scavenging ABTS radical with an IC50 value of 39 μg/ml while other parts were ineffective. Conclusion: This work demonstrated good antioxidant activity of L. siceraria vegetable cultivated in India and recommends that the peel of this vegetable may be of interest from a functional point of view as a major source of natural antioxidant. Key words:Lagenaria siceraria, antioxidant activity, DPPH, ABTS, FRAP, total phenol.
Keywords: ABTS; antioxidant activity; DPPH; FRAP; Lagenaria siceraria; total phenol.

Antioxidant, anti-acetylcholinesterase and anti-glycosidase properties of three species of Swertia, their xanthones and amarogentin: A comparative study - Gargi Nag; Sukriti Das; Susmita Das; Suvra Mandal; Bratati De (Pharmacognosy Journal, 2015)
Aim: The aim of the study was to analyze the antioxidant, anti-amylase, anti-glucosidase and antiacetylcholinesterase (anti-AChE) properties of the leafy shoots of three Indian species of Swertia e.g. Swertia chirata and its substitutes Swertia bimaculata, and Swertia decussata, their xanthones and amarogentin. Methods: Antioxidant activity of the methanolic extracts of leafy shoots was measured in terms of DPPH, superoxide and nitric oxide radical scavenging activities as well as metal chelating properties. Enzyme inhibitory properties were measured using AChE, α-amylase and α-glucosidase respectively. Five xanthones bellidifolin (1), swerchirin (2), decussatin (3), mangiferin (4) and 1-hydroxy-3,5,8-trimethoxy xanthone (6) and one iridoid, amarogentin (5) were isolated from Swertia chirata. The activities of the isolated components were compared. Results: Swertia chirata exhibited best antioxidant and anti-AChE properties than the other two species. The plants also possessed α-glucosidase inhibitory properties but weak α-amylase inhibitory activity. Highest activities were observed in Swertia chirata. We report here, for the first time, the antioxidant, anti-AChE and anti-glycosidase activity of 1-hydroxy-3,5,8-trimethoxy xanthone. This xanthone had strongest DPPH radical scavenging activity and anti-AChE property. Conclusion: The results suggest the beneficial effects of the xanthones of Swertia chirata. But further study should be carried out to prove the efficacy in vivo. Key words: Swertia Sp., Xanthone, Glycosidase, Acetylcholinesterase, Antioxidant.
Keywords: Acetylcholinesterase; Antioxidant.; Glycosidase; Swertia Sp.; Xanthone

Antioxidant, anti-acetylcholinesterase and anti-glycosidase properties of three species of Swertia, their xanthones and amarogentin: A comparative study - Gargi Nag; Sukriti Das; Susmita Das; Bratati De (Pharmacognosy Journal, 2015)
Aim: The aim of the study was to analyze the antioxidant, anti-amylase, anti-glucosidase and antiacetylcholinesterase (anti-AChE) properties of the leafy shoots of three Indian species of Swertia e.g. Swertia chirata and its substitutes Swertia bimaculata, and Swertia decussata, their xanthones and amarogentin. Methods: Antioxidant activity of the methanolic extracts of leafy shoots was measured in terms of DPPH, superoxide and nitric oxide radical scavenging activities as well as metal chelating properties. Enzyme inhibitory properties were measured using AChE, α-amylase and α-glucosidase respectively. Five xanthones bellidifolin (1), swerchirin (2), decussatin (3), mangiferin (4) and 1-hydroxy-3,5,8-trimethoxy xanthone (6) and one iridoid, amarogentin (5) were isolated from Swertia chirata. The activities of the isolated components were compared. Results: Swertia chirata exhibited best antioxidant and anti-AChE properties than the other two species. The plants also possessed α-glucosidase inhibitory properties but weak α-amylase inhibitory activity. Highest activities were observed in Swertia chirata. We report here, for the first time, the antioxidant, anti-AChE and anti-glycosidase activity of 1-hydroxy-3,5,8-trimethoxy xanthone. This xanthone had strongest DPPH radical scavenging activity and anti-AChE property. Conclusion: The results suggest the beneficial effects of the xanthones of Swertia chirata. But further study should be carried out to prove the efficacy in vivo
Keywords: Acetylcholinesterase; Antioxidant.; Glycosidase; Swertia Sp.; Xanthone

Anti-Tyrosinase and DPPH Radical Scavenging Activities of Selected Thai Herbal Extracts Traditionally Used as Skin Toner - Bunleu Sungthong; Methin Phadungkit (Pharmacognosy Journal, 2015)
Introduction: Skin darkness may be cosmetically undesirable for some people. Plant-derived materials traditionally used for skin lightening may produce satisfactory results. Besides innate tyrosinase activity, oxidative stress also plays an important role in skin darkness by activating tyrosinase. Therefore, herbal extracts with strong anti-tyrosinase and antioxidant activities could be considered as efficacious skin lightening agents. The aims of the present study were to determine the anti-tyrosinase and antioxidant activities of Thai medicinal plant extracts indigenously used as skin toners. Methods: The activities of seven Thai medicinal plants; Zingiber cassumunar Roxb., Phyllanthus emblica Linn., Tagetes erecta Linn., Centella asiatica, Raphanus sativusvar. Longipinnatus Linn., Cassia fistula Linn. and Butea monosperma (Lam.) Taub. were investigated using the DOPA-chrome method to determine anti-tyrosinase activity and the DPPH free radical scavenging assay to determine antioxidant activity. Results: With respect to tyrosinase inhibitory activity, P. emblica, B. monosperma and R. sativusvar. Longipinnatus extracts at a concentration of 1.67 mg/mL showed strong activities with the percentage of tyrosinase inhibition at 48.38±4.77, 46.92±3.77 and 42.85±6.54 %, respectively. In addition, P. emblica and B. monosperma extracts also exhibited high antioxidant activities with the IC50values on 33.47±1.24 and 33.57±1.92 mg/mL, respectively. Conclusion: Based on tyrosinase inhibition activity and DPPH radical scavenging assays, the herbal extracts of P. emblica and B. monosperma show promise as potential skin lighteners in cosmetic formulations. Key words: antioxidant activity, Dopachrome method, skin lightening, traditional skin toners, anti-tyrosinase inhibitory activity, DPPH radical scavenging assay.
Keywords: anti-tyrosinase inhibitory activity; antioxidant activity; Dopachrome method; DPPH radical scavenging assay; skin lightening; traditional skin toners

Anti-Tyrosinase and DPPH Radical Scavenging Activities of Selected Thai Herbal Extracts Traditionally Used as Skin Toner - Bunleu Sungthong; Methin Phadungkit (Pharmacognosy Journal, 2015)
Introduction: Skin darkness may be cosmetically undesirable for some people. Plant-derived materials traditionally used for skin lightening may produce satisfactory results. Besides innate tyrosinase activity, oxidative stress also plays an important role in skin darkness by activating tyrosinase. Therefore, herbal extracts with strong anti-tyrosinase and antioxidant activities could be considered as efficacious skin lightening agents. The aims of the present study were to determine the anti-tyrosinase and antioxidant activities of Thai medicinal plant extracts indigenously used as skin toners. Methods: The activities of seven Thai medicinal plants; Zingiber cassumunar Roxb., Phyllanthus emblica Linn., Tagetes erecta Linn., Centella asiatica, Raphanus sativusvar. Longipinnatus Linn., Cassia fistula Linn. and Butea monosperma (Lam.) Taub. were investigated using the DOPA-chrome method to determine anti-tyrosinase activity and the DPPH free radical scavenging assay to determine antioxidant activity. Results: With respect to tyrosinase inhibitory activity, P. emblica, B. monosperma and R. sativusvar. Longipinnatus extracts at a concentration of 1.67 mg/mL showed strong activities with the percentage of tyrosinase inhibition at 48.38±4.77, 46.92±3.77 and 42.85±6.54%, respectively. In addition, P. emblica and B. monosperma extracts also exhibited high antioxidant activities with the IC50values on 33.47±1.24 and 33.57±1.92 mg/mL, respectively. Conclusion: Based on tyrosinase inhibition activity and DPPH radical scavenging assays, the herbal extracts of P. emblica and B. monosperma show promise as potential skin lighteners in cosmetic formulations.
Keywords: anti-tyrosinase inhibitory activity; antioxidant activity; Dopachrome method; DPPH radical scavenging assay; skin lightening; traditional skin toners

Anxiolytic Potential of Methanol Extract from Ageratum conyzoides Linn Leaves - Ravinder Kaur; Sarabjit Kaur (Pharmacognosy Journal, 2015)
Objective: Ageratum conyzoides Linn. (Asteraceae) has been widely used in African traditional medicine for healing mental and infectious diseases. The present study was designed to scientifically validate the traditional claim of A. conzyoides as anti-anxiety drug and to identify the compound responsible for the anxiolytic effects of A. conzyoides. Method: The methanol extract of A. conzyoides was prepared by soxhlet apparatus. The methanol extract was fractionated into ethylacetate and butanol fractions by liquid-liquid partitioning method. Methanol extract (100 and 200 mg/kg; p.o.) and its prepared fractions (25 and 50 mg/kg; p.o.) were evaluated for anxiolytic activity in mice by using elevated plus maze (EPM) model. Thin layer chromatography studies were performed to identify the possible anxiolytic component. Results: Methanol extract at both doses showed significant, when compared to vehicle control group, increase in time spent and number of entries in open arms of EPM confirming the anti-anxiety effects of A. conzyoides. Liquid-liquid partitioning of methanol extract gave two fractions (ethylacetate and butanol) which were administrated at 25 and 50 mg/kg doses to mice in EPM, respectively. Results showed that ethylacetate fraction was responsible for anxiolytic effects of methanol extract of A. conzyoides. The TLC studies were carried out for ethylacetate fraction and Quercetin was identified by comparing Rf values with the standard (Quercetin). Conclusion: The present investigation revealed that the extract has significant anxiolytic effect. The flavonoid quercetin may be responsible for the observed anxiolytic effects of A. conyzoides. Key words:Ageratum conyzoides, Anxiolytic, Methanol extract, Quercetin, TLC.
Keywords: Ageratum conyzoides; Anxiolytic; Methanol extract; Quercetin; TLC.

Anxiolytic Potential of Methanol Extract from Ageratum conyzoides Linn Leaves - Ravinder Kaur; Sarabjit Kaur (Pharmacognosy Journal, 2015)
Objective: Ageratum conyzoides Linn. (Asteraceae) has been widely used in African traditional medicine for healing mental and infectious diseases. The present study was designed to scientifically validate the traditional claim of A. conzyoides as anti-anxiety drug and to identify the compound responsible for the anxiolytic effects of A. conzyoides. Method: The methanol extract of A. conzyoides was prepared by soxhlet apparatus. The methanol extract was fractionated into ethylacetate and butanol fractions by liquid-liquid partitioning method. Methanol extract (100 and 200 mg/kg; p.o.) and its prepared fractions (25 and 50 mg/kg; p.o.) were evaluated for anxiolytic activity in mice by using elevated plus maze (EPM) model. Thin layer chromatography studies were performed to identify the possible anxiolytic component. Results: Methanol extract at both doses showed significant, when compared to vehicle control group, increase in time spent and number of entries in open arms of EPM confirming the anti-anxiety effects of A. conzyoides. Liquid-liquid partitioning of methanol extract gave two fractions (ethylacetate and butanol) which were administrated at 25 and 50 mg/kg doses to mice in EPM, respectively. Results showed that ethylacetate fraction was responsible for anxiolytic effects of methanol extract of A. conzyoides. The TLC studies were carried out for ethylacetate fraction and Quercetin was identified by comparing Rf values with the standard (Quercetin). Conclusion: The present investigation revealed that the extract has significant anxiolytic effect. The flavonoid quercetin may be responsible for the observed anxiolytic effects of A. conyzoides.
Keywords: Ageratum conyzoides; Anxiolytic; Methanol extract; Quercetin; TLC

Assessment of Acute and Subacute Toxicity of the Total Dichloromethane-Ethanol Extract of Morinda morindoides (Baker) Milne-Redh (ETDE) on Rats - Boga Gogo Lucien; Bahi Calixte; Yapi Houphouët Félix; N’Guessan Jean David (Pharmacognosy Journal, 2015)
Context: ETDE shown good antihypertensive and antioxidant activities in rats made hypertensive. This present study aims to assess its toxicity. Aims: This study was designed to study the toxicity of dichloromethaneethanol extract of Morinda morindoides. Settings and Design: Toxicological activity in vivo. Methods and Material: Alkaloids were characterized from reagents of Bouchardat, flavonoids by reacting the cyanidrine, tannins by the reagent Stiasny, polyphenols by reacting ferric chloride, quinones by the reagent Bornstraëgen, sterols and polyterpenes by the reaction of Libermann and saponins by observing the foam after agitation of the extract. Acute and subacute toxicity were studied using respectively 423 and 407 OECD guidelines for testing of chemicals. Statistical analysis used: The graphical representation of the data was performed using the Graph Pad Prism 5.0. The mean value is accompanied by the standard error of the mean (Mean ± SEM). The difference between the two values is considered significant when P<0.001. Statistical analysis of results was performed using analysis of variance (ANOVA). Results: The phytochemical screening showed the presence in the ETDE of polyphenols, alkaloids, flavonoids, sterols and polyterpenes. The toxicological study shows that ETDE has a LD50 between 2000 and 5000 mg/kg bw therefore classified in the hazard category 5. The administration of ETDE at repeated dose for 28 days did not significantly affect the weight gain, hematological and biochemical parameters of rats. Conclusion: ETDE toxicity is relatively low with LD50 between 2000 and 5000 mg/kg bw. It does not cause damage to the heart, liver and kidney. ETDE can be used without risk of intoxication.
Keywords: Acute toxicity; Damage; Morinda morindoides; Subacute toxicity; Weight gain.

Assessment of Cytotoxicity of Smokeless Tobacco (Shammah) In Hepg2 and WRL68 Cells Line - Siddig Ibrahim Abdelwahab; Rashad Bin Mohammed Alsanosy (Pharmacognosy Journal, 2015)
Shammah is a traditional form of chewing tobacco [Smokeless tobacco, (ST)] that is commonly used in the Middle east specially Saudi Arabia (KSA), Yemen and Sudan. The cytotoxicity of Sudanese and Yemenis ST hexane and methanol extracts was evaluated using MTT assay. Annexin-V assay has been used to detect the induction of apoptosis. Luminescence based assay also been conducted to check the level of caspases enzyme. The involvement of cell cycle check point arrest has been performed using flow cytometry analysis. The current study found that ST has the capacity to induce cell toxicity in human liver cells. The inhibitory capacity of ST in HepG2 and WRL 68 has been found to be 151 ± 2.5 and 305 ± 11.5 μg/ml for 24 h. An early apoptosis induction in HepG2 cells was observed by annexin V assay, which clearly exhibited significantly increased early and late apoptosis phases both at 24 and 48 h. Both the caspases-8 and-9 level was found to be increased by the introduction of ST to HepG2 cells significantly (p<0.05). Moreover the ST extract was able to arrest the cell cycle check point at G2/M phase. A significantly increasing pattern of hypodiploid phases of cells also been observed, which confirm the apoptosis induction again. Collectively, results presented in this study demonstrated that the ST, which is used as a euphoritic substance of abuse also, has significant level of toxicity in human cells. Moreover the mode of cell death was found to be though programmed cell death which is closely associated with cell cycle arrest
Keywords: Hepatotoxicity; In vitro models; Saudi Arabia; Shammah; Smokeless tobacco; Substance Absue Research Centre

Assessment of Cytotoxicity of Smokeless Tobacco (Shammah) In Hepg2 and WRL68 Cells Line - Siddig Ibrahim Abdelwahab; Syam Mohan,; Manal Moahmed Elhassan Taha; Rashad Bin Mohammed Alsanosy; Hamed Karimian (Pharmacognosy Journal, 2015)
Shammah is a traditional form of chewing tobacco [Smokeless tobacco, (ST)] that is commonly used in the Middle east specially Saudi Arabia (KSA), Yemen and Sudan. The cytotoxicity of Sudanese and Yemenis ST hexane and methanol extracts was evaluated using MTT assay. Annexin-V assay has been used to detect the induction of apoptosis. Luminescence based assay also been conducted to check the level of caspases enzyme. The involvement of cell cycle check point arrest has been performed using flow cytometry analysis. The current study found that ST has the capacity to induce cell toxicity in human liver cells. The inhibitory capacity of ST in HepG2 and WRL 68 has been found to be 151 ± 2.5 and 305 ± 11.5 μg/ml for 24 h. An early apoptosis induction in HepG2 cells was observed by annexin V assay, which clearly exhibited significantly increased early and late apoptosis phases both at 24 and 48 h. Both the caspases-8 and-9 level was found to be increased by the introduction of ST to HepG2 cells significantly (p<0.05). Moreover the ST extract was able to arrest the cell cycle check point at G2/M phase. A significantly increasing pattern of hypodiploid phases of cells also been observed, which confirm the apoptosis induction again. Collectively, results presented in this study demonstrated that the ST, which is used as a euphoritic substance of abuse also, has significant level of toxicity in human cells. Moreover the mode of cell death was found to be though programmed cell death which is closely associated with cell cycle arrest. Key words: Hepatotoxicity, In vitro models, Saudi Arabia, Smokeless tobacco, Substance Absue Research Centre, Shammah.
Keywords: Hepatotoxicity; In vitro models; Saudi Arabia; Shammah.; Smokeless tobacco; Substance Absue Research Centre

Cleome viscosa Linn (Capparaceae): A Review - Harpreet Singh; Amrita Mishra; Arun Kumar Mishra (Pharmacognosy Journal, 2015)
Cleome viscosa Linn. (Capparaceae) called as “Hurhur” is an annual, sticky herb found in plains of India, Africa, and Pakistan etc as a common weed. Plant and its parts (leaves, seeds, roots etc.) are used traditionally to cure variety of diseases. Traditionally the plant possess anthelmintic, carminative, anticonvulsant, antidiarhhoeal, antimicrobial, wound healing properties. The review shows that various phytochemical compound were isolated from whole plant and its parts (seeds, leaves, roots etc.). The review reveals the collection of important pharmacological activites like antimicrobial, analgesic, antiemetic, antidiarrhoeal, hepatoprotective, antifibrotic, antitumor, anticonvulsant and psychopharmacological. It also made emphasis on its application in biodiesel formation. The review draws attention towards the traditional, phytochemical and pharmacological knowledge accessible on Cleome viscosa Linn. which would be beneficial for researchers to discover novel chemical entities.
Keywords: Anticonvulsant; Biodiesel; Cleome viscosa Linn.; Cleomiscosin; Phytochemical; Psychopharmacological

Comparative analysis of phenolic contents and total antioxidant capacity of Moringa oleifera Lam - Swati Vyas; Sumita Kachhwaha; S. L. Kothari (Pharmacognosy Journal, 2015)
Introduction: Accumulation of reactive species higher than permissible limits in biological systems may lead to various degenerative disorders due to oxidative damage. Materials and Methods: Oxidation is a serious concern faced by the food industry causing deterioration of shelved-food quality. Antioxidant compounds like polyphenolics scavenge such free radicals and thus protect against oxidative stress. Consumption of polyphenol-rich plants as dietary component confers protection against such cellular damage. Results: Present study explores antioxidant capacity, total phenolic content (TPC) and total flavonoid content (TFC) of different extracts prepared from various parts of Moringa oleifera Lam. Higher TPC, TFC and antioxidant activity was shown by methanolic extracts followed by aqueous, petroleum benzene and chloroform extracts.The present study suggests that all the extracts might act as radical scavengers to certain extent possibly due to presence of polyphenolic compounds. Conclusion: M. oleifera exhibits strong antioxidant activity and could serve as prospective source of natural antioxidants to food and health industries.
Keywords: antioxidant activity; oxidation.; sequential extract; total flavonoid content; total phenolic content

Comparative pharmacognostic, phytochemical and biological evaluation between five Chlorophytum species - Sharada. L. Deore; Neha B. Jajoo; Kailaspati P.A Chittam; T.A.Deshmukh (Pharmacognosy Journal, 2015)
Five species, Chlorophytum borivilianum Santapau and Fernades, Chlorophytum comosum (Thunb.) Jacq., Chlorophytum tuberosum Br., Chlorophytum laxum R. Br. and C. arundinaceum, of very popular Ayurvedic plant Safed Musali are collected and comparatively evaluated for morphological, microscopical, physicochemical and biological parameters. Key words: Chlorophytum, borivilianum, comosum, tuberosum, laxum, arundinaceum, DPPH, SRB, HL-60.
Keywords: Arundinaceum; Borivilianum; Chlorophytum; comosum; DPPH; HL-60.; Laxum; SRB; tuberosum

Comparative Pharmacognostic, Phytochemical and Biological evaluation between five Chlorophytum species - Sharada Laxman Deore; Neha Brijmohan Jajoo; Kailaspati Prabhakar Chittam; Tushar Atmaram Deshmukh (Pharmacognosy Journal, 2015)
Objective: To establish comparative pharmacognostic, phytochemical and biological evaluation parameters between five Chlorophytum species i.e. Chlorophytum borivilianum Santapau and Fernades, Chlorophytum comosum (Thunb.) Jacq., Chlorophytum tuberosum Br., Chlorophytum laxum R. Br. and Chlorophytum arundinaceum Baker, of very popular Ayurvedic plant Safed Musali. Materials and methods: Comparative evaluations of Macro and microscopical, physico-chemical parameters of tubers of all five species were investigated and preliminary phytochemical analysis, estimation of major phytochemicals and TLC profiles were also carried out for qualitative phytochemical evaluation. In-vitro antioxidant and anticancer activity was carried out for extract of tubers of all five species. Results: Macro, micro, powder microscopical parameters of tubers of five species were examined and recorded the result. Tubers of all the five species are distinct in their morphology as well as anatomical characters. Physicochemical characters (Ash values, Loss on drying (LOD), swelling index and foaming index) as well as total saponin content shows great variability among five species. Results of In-vitro antioxidant by DPPH method shows difference in antioxidant potential between tubers of all five species. Extract of tubers of all five species do not show any type of In-vitro anticancer activity by SRB method against HL 60 leukemia cell line. Conclusion: All of the evaluated parameters are very good pharmacognostic standards for future comparative identification and authentication of specific species because all five species shows morphological, anatomical, chemical differences as well as varies in antioxidant potential.
Keywords: Arundinaceum; Borivilianum; Chlorophytum Comosum; DPPH; HL-60; Laxum; SRB; Tuberosum.

Comparison in vitro of Antioxidant Activity between Fifteen Campanula Species (Bellflower) from Palestinian Flora - Nidal Amin Jaradat; Murad Abualhasan (Pharmacognosy Journal, 2015)
Background: The natural antioxidant products in the plant kingdom play an important role in the healthy life style and reduce the risk for various chronic diseases.Objective: The objective of this study was to investigate different antioxidant pharmacological property of methanol extract for fifteen species of Campanula plant from Palestinian flora. Methods: The antioxidant activity of fifteen Campanula species growing wildly in Palestine were studied using 2,2-diphenylpicrylhydrazyl (DPPH) radical scavenging activity and their antioxidant activity was compared to Trolox antioxidant activity. Results: The results clearly demonstrate a very high antioxidant activity of the Campanula sulphurea and Campanula sidoniensis and they showed almost the same antioxidant activity of Trolox. The other twelve species extracts also exhibited excellent antioxidant activity in DPPH radical scavenging activity in comparison with trolox standard. Conclusion: Methanol extract of Campanula can be valuable for treatment of different diseases and could be used as a possible new source of natural antioxidants in the food, nutraceuticals, pharmaceuticals and cosmetic industry.
Keywords: Antioxidant; Bellflower; Campanula species; Campanulaceae; DPPH radical scavenging activity.

Comparison in Vitro of Antioxidant Activity between Fifteen Campanula Species (Bellflower) from Palestinian Flora - Nidal Amin Jaradat; 1Murad Abualhasan (Pharmacognosy Journal, 2015)
Background: The natural antioxidant products in the plant kingdom play an important role in the healthy life style and reduce the risk for various chronic diseases. Objective: The objective of this study was to investigate different antioxidant pharmacological property of methanol extract for fifteen species of Campanula plant from Palestinian flora. Methods: The antioxidant activity of fifteen Campanula species growing wildly in Palestine were studied using 2,2-diphenylpicrylhydrazyl (DPPH) radical scavenging activity and their antioxidant activity was compared to Trolox antioxidant activity. Results: The results clearly demonstrate a very high antioxidant activity of the Campanula sulphurea and Campanula sidoniensis and they showed almost the same antioxidant activity of Trolox. The other twelve species extracts also exhibited excellent antioxidant activity in DPPH radical scavenging activity in comparison with trolox standard. Conclusion: Methanol extract of Campanula can be valuable for treatment of different diseases and could be used as a possible new source of natural antioxidants in the food, nutraceuticals, pharmaceuticals and cosmetic industry. Key words: Antioxidant, Bellflower, Campanula, Bellflower, Campanulaceae, DPPH radical scavenging activity
Keywords: Antioxidant; Bellflower; Campanula; Campanulaceae; DPPH radical scavenging activity.

Component Authentication and Standardisation of an Anti-atherosclerotic Herbal Formulation-GSTC3 - Jeksy Jos Manalil; Indu Muraleedharan Suseela; Smitha Koyickalmadhom Ramavarma; Arunaksharan Narayanankutty; Achuthan Chathrattil Raghavamenon (Pharmacognosy Journal, 2015)
Context: Polyherbal drugs in traditional medicine have been time-tested for treatment of a wide variety of chronic ailments. Aims: To determine constituent components in an in-house designed polyherbal formulation GSTC3 and evaluation of consistency in preparation. Settings and Design: In this study, a hypolipidemic formulation was created using well known plant extracts such as Commiphora mukul (Hook. ex Stocks.) Eng. (Burseraceae), Salacia reticulata Wight (Celastraceae), Terminalia arjuna (Roxb.) Wight and Arn (Combretaceae) and Curcuma longa Linn (Zingiberaceae). Methods and Material: The authentication of individual plant powders was performed using techniques such as powder microscopy and characterised according to Ayurvedic pharmacopeia of India. Phytochemical screening, HPTLC analysis and physicochemical parameters were also determined. Results: The powder microscopic analysis of the individual components served as an authentication for source of plants used. Phytochemical screening ascertained that active classes of compounds reported in the individual extracts such as steroids, terpenoids and polyphenols came into the formulation. Finally, HPTLC analysis of three different batches of GSTC3 ensured stability and integrity in batch to batch preparations. Conclusion: Experimental studies have revealed the antioxidant, antiinflammatory, anti-lipidemic and anti-thrombotic efficacy of GSTC3. This standardisation procedure is essential for further development of GSTC3 into an efficient anti-atherosclerotic drug candidate
Keywords: HPTLC; Pharmacognosy; Phytochemical screening; Polyherbal formulation; Powder microscopy

Cytotoxicity Study of Ethanol Extract of the Leaves of Asam Kandis (Garcinia cowa Roxb.) on T47D Breast Cancer Cell line - Fatma Sri Wahyuni; Dini Hara Triastuti; Helmi Arifin (Pharmacognosy Journal, 2015)
Objective: To investigate the cytotoxic effect of ethanolic extract of the leaves of asam kandis (Garcinia cowa Roxb.) against T47D breast cancer cells. Methods: The cytotoxicity of ethanol extract was carried out by measuring the activity of mitochondrial dehydrogenase in living cells that have ability to convert dissolved MTT pale yellow to purple formazan product. The extract was added at various concentrations (0.1, 1, 10 and 100 μg/mL). The level of cytotoxicity was determined by calculating the IC50 value that was based on the percentage of the cell death after 24 hours treatment with the extract. Cell morphological changes were observed by using inverted microscope. Results: The IC50 value showed that ethanol extract of leaves of asam kandis could resist T47D breast cancer cells with IC50 6.13 ± 3.51 μg/mL. The statistic results proved that ethanol extract of the leaves of asam kandis could inhibit the growth of T47D breast cancer cells significantly at concentrations of 10 μg/mL and 100 μg/mL. Conclusion: The results suggest that ethanol extract of the leaves of asam kandis was potential source of herbal medicine for cancer-related ailments.
Keywords: Asam kandis; Beast cancer; Cytotoxicity; Garcinia cowa Roxb; MTT Assay; T47D.

Dynamic Comparison of Free Radical Scavenging Abilities of Hypericum Perforatum L., Herba Verbenae Officinalis, and Valeriana Officinalis L. Extracts - Yi-ming Li; Yan-Ru Liu; Bing-Kun Xiao; Jian-Yun Yang; Rong-Qing Huang (Pharmacognosy Journal, 2015)
Objectives: The purpose of this research was to compare the dynamic antioxidant activities and the free radical scavenging abilities of three botanical supplements, Hypericum perforatum L. (HPL), Herba Verbena Officinalis (HVO), and Valeriana officinalis L. (VO), which have been reported to effectively treat menopause symptoms. Methods: The antioxidant activities of the three supplements were determined by the ferric reducing ability of plasma (FRAP) assay. In addition, their free radical scavenging abilities were studied by ftheir interactions with the stable radicals of 2, 2’-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH). Results: The results indicated that the HPL ethanolic extract exhibited greater antioxidant activity (1.2688 ± 0.01 mmol Trolox/g) than the HVO ethanolic extract (1.1686± 0.043 mmol Trolox/g) and the VO ethanolic extract (0.2579 ± 0.0031 mmol Trolox/g) as compared to Nilestriol (0.0026±0.0012), a positive control agent in the experiment. Moreover, the HPL extract showed remarkable free radical scavenging activity against ABTS•+, and the HVO extract was the most potent against DPPH•. Conclusion: These activities may be attributed to the total flavonoid or phenolic acid contents of among these extracts.
Keywords: ABTS•+; DPPH•; Herba Verbena Officinalis; Hypericum perforatum L.; Menopause Oxidative Stress; Valeriana officinalis L.

Dynamic Comparison of Free Radical Scavenging Abilities of Hypericum Perforatum L., Herba Verbenae Officinalis, and Valeriana Officinalis L. Extracts - Yi-ming Li; Yan-Ru Liu; Bing-Kun Xiao; Jian-Yun Yang; Rong-Qing Huang (Pharmacognosy Journal, 2015)
Objectives: The purpose of this research was to compare the dynamic antioxidant activities and the free radical scavenging abilities of three botanical supplements, Hypericum perforatum L. (HPL), Herba Verbena Officinalis (HVO), and Valeriana officinalis L. (VO), which have been reported to effectively treat menopause symptoms. Methods: The antioxidant activities of the three supplements were determined by the ferric reducing ability of plasma (FRAP) assay. In addition, their free radical scavenging abilities were studied by ftheir interactions with the stable radicals of 2, 2’-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH). Results: The results indicated that the HPL ethanolic extract exhibited greater antioxidant activity (1.2688 ± 0.01 mmol Trolox/g) than the HVO ethanolic extract (1.1686± 0.043 mmol Trolox/g) and the VO ethanolic extract (0.2579 ± 0.0031 mmol Trolox/g) as compared to Nilestriol (0.0026±0.0012), a positive control agent in the experiment. Moreover, the HPL extract showed remarkable free radical scavenging activity against ABTS•+, and the HVO extract was the most potent against DPPH•. Conclusion: These activities may be attributed to the total flavonoid or phenolic acid contents of among these extracts. Key words: ABTS•+, DPPH•, Hypericum perforatum L.,Herba Verbena Officinalis, Menopause Oxidative Stress, Valeriana officinalis L.
Keywords: ABTS•+; DPPH•; Herba Verbena Officinalis; Hypericum perforatum L.; Menopause Oxidative Stress; Valeriana officinalis L.

Effect of various extracts of Ocimum sanctum and Mallotus phillipensis on Setaria digitata - Deepa Chundayil Kalarickal; Sujith Samraj; Darsana Udayan; Priya Manakkulaparambil Narayanan; Sreedevi Ramachandran; Sreeshitha Sreedharan Gouri (Pharmacognosy Journal, 2015)
Introduction: The anthelmintic activity of various extracts of leaves of Ocimum sanctum and Mallotus phillipensis was assessed in vitro against Setaria digitata. Materials and Methods: The leaves of Ocimum sanctum and Mallotus phillipensis were collected and were extracted using methanol, dried and stored under refrigeration till further use. The aqueous extract was taken as a decoction. The methanolic extract was further fractionated by taking solvents of increasing polarity viz, hexane, chloroform, n-butanol and water. The extract as well as the fractions were analysed qualitatively for various phytochemical constituents. Fresh nematodes (Setaria digitata) were recovered manually from the peritoneum of infested buffalo, were washed and transferred to the extract containing petriplates (concentrations of 50, 25, 12.5, 6.25, 3.125 and 1.56 mg/ml) immediately and the motility/death of Setaria digitata was noted. Results: The presence of flavonoids and tannins were detected in all the extracts where was phenolics as absent in the hexane fraction. The methanolic extract of Tulsi and Kamla produced death of nematodes in concentrations of 3.125 mg/ml and the extract of tulsi was found to be more potent. Similar results were also observed in the case of hydro alcoholic extract whereas the aqueous extract showed no effect. The chloroform fraction of Ocimum sanctum and n-butanol and chloroform fractions of Mallotus were equally potent in inhibiting the motility and producing death of the worms. The control drug, albendazole produced death in 30 minutes in both the concentrations. Conclusion: It could be concluded that higher doses of the extract are as potent as albendazole.
Keywords: Albendazole; Anthelmintic; Mallotus phillipensis; Ociumum sanctum; Setaria digitata

Effectiveness of Sidr Honey on the prevention of ethanol-induced gatroulcerogenesis: role of antioxidant and antiapoptotic mechanism - Manal Mohamed Elhassan Taha; Siddig Ibrahim Abdelwahab; Rashad Elsanousi; Bassem Y. Sheikh; Mahmood Ameen Abdulla; Saif Eldeen Babiker; Husham Elraih; Eldaw Mohamed (Pharmacognosy Journal, 2015)
Background: Sider (Ziziphus spina-christi (L.) Desf.) Honey has been used for the treatment of gastrointestinal disorders including peptic ulcer. Aim of the study: The mechanism of the antiulcer effect of sider honey was studied placing emphasis on its role to block oxidative damage and apoptosis during ethanol-induced gastric ulceration in rats. The mechanism of the antiulcer effect of sider honey was studied placing emphasis on its role to block oxidative damage and apoptosis during ethanol-induced gastric ulceration in rats. Materials and methods: Experimental animals were orally treated with sidr honey (100, 250 and 500 mg/kg, respectively) or omeprazole and subsequently exposed to 95%ethanol (5 mL/Kg, orally) to induce acute gastroulcerogenesis. Effectiveness of sidr honey was evaluated using ulcer index, pH of gastric juice, mucus content, morphological analyses, glutathione assay and malondialdehyde level. The anti-apoptotic role of sidr honey was studied using immunohistochemical staining of gastric tissues using monoclonal antibodies of Bax pathway. Results: Dose-response studies in ethanol-induced ulcer indicate that sidr honey significantly blocks gastric lesions at lower dose (100 mg/kg). Lipid peroxidation and glutathione depletion were significantly inhibited by sidr honey. Sidr honey modulated the immuno-expression of mitochondrial associated protein (Bax). Conclusion: Thus, sider honey plays a considerable role in gastro protection by acting as a potent antioxidant and antiapoptotic agent. Future study is required to explore its potential clinical usage. Key words: Antiapoptotic Mechanism, Antioxidant Agents, Gastro protection, Monofloral Nectar, Sidr Honey.
Keywords: Antiapoptotic Mechanism; antioxidant agents; Gastro protection; monofloral nectar; Sidr Honey.

Effectiveness of Sidr Honey on the prevention of ethanol-induced gatroulcerogenesis: role of antioxidant and antiapoptotic mechanism - Manal Mohamed Elhassan Taha; Siddig Ibrahim Abdelwahab; Rashad Elsanousi; Bassem Y. Sheikh; Mahmood Ameen Abdulla; Saif Eldeen Babiker; Husham Elraih; Eldaw Mohamed (Pharmacognosy Journal, 2015)
Background: Sider (Ziziphus spina-christi (L.) Desf.) Honey has been used for the treatment of gastrointestinal disorders including peptic ulcer. Aim of the study: The mechanism of the antiulcer effect of sider honey was studied placing emphasis on its role to block oxidative damage and apoptosis during ethanol-induced gastric ulceration in rats. The mechanism of the antiulcer effect of sider honey was studied placing emphasis on its role to block oxidative damage and apoptosis during ethanol-induced gastric ulceration in rats. Materials and methods: Experimental animals were orally treated with sidr honey (100, 250 and 500 mg/kg, respectively) or omeprazole and subsequently exposed to 95% ethanol (5 mL/Kg, orally) to induce acute gastroulcerogenesis. Effectiveness of sidr honey was evaluated using ulcer index, pH of gastric juice, mucus content, morphological analyses, glutathione assay and malondialdehyde level. The anti-apoptotic role of sidr honey was studied using immunohistochemical staining of gastric tissues using monoclonal antibodies of Bax pathway. Results: Dose-response studies in ethanol-induced ulcer indicate that sidr honey significantly blocks gastric lesions at lower dose (100 mg/kg). Lipid peroxidation and glutathione depletion were significantly inhibited by sidr honey. Sidr honey modulated the immuno-expression of mitochondrial associated protein (Bax). Conclusion: Thus, sider honey plays a considerable role in gastro protection by acting as a potent antioxidant and antiapoptotic agent. Future study is required to explore its potential clinical usage.

Effects of standardized stem bark extract of Mangifera indica L. in Wister rats with 2,4-dinitrophenylhydrazine-induced haemolytic anaemia - Hassan Lawal Sani; Ibrahim Malami; Sanusi Wara Hassan; Alhassan Muhammad Alhassan (Pharmacognosy Journal, 2015)
Background: The aqueous decoction of the stem back of Mangifera indica L. has been traditionally used for the treatment of various illnesses among them includes anaemia. Aims: The aim of this study was to investigate the anti-anaemic properties of the standardized stem bark extract of M. indica in animals with 2,4-dinitrophenylhydrazine-induced haemolytic anaemia. Methods and Material: An in vivo animal model was used in this experiment. 2,4-dinitrophenylhydrazine was used to induce haemolysis and treatment was done with three different concentrations (25, 50, and 100 mg/kg b.wt) of the plant extract. Astifer® was used as a positive control. Haematological parameters such as PCV, HGb concentration, and TLC were performed to determine the present of phytoconstituents within the crude extract. Results: PCV and HGb concentration was increased significantly (p<0.001) at a dose of 50 and 100 mg/kg b.wt respectively while no significant (p>0.05) effect was observed at a dose of 25 mg/kg b.wt. TLC was decreased significantly (p<0.001) at a dose 100 mg/kg b.wt when while no significant (p>0.05) effect was observed at a dose of 25 and 50 mg/kg b.wt respectively. GC-MS analysis revealed the presence of 15 compounds among viz: 2,2-Dimethoxybutane, N-Acetyl-Alpha-D-glucosamine, 1,2-Benzenediol, Phenol, 2,4-bis(1,1-dimethylethyl)-, Vitamin E, Pentadecanoic acid, 13-methyl-, methyl ester, 2-Ethylacridine, Benzofuran-6-ol-3-one, 2-(4ethoxycarbonyl)benzylidene-, 9-Octadecanoic acid, (E)-, 2,4,6-Cycloheptatrien-1-one, 3,5-bis-trimethylsilyl-, and Benzo[h]quinoline,2,4-dimethyl-. Conclusion: The results of our present finding suggest the significant anti-anaemic properties of standardized stem bark extract of Mangefera indica L. This finding highlights the potentials of the extract M. indica in the treatment of haemolytic anaemia. Key words: 2,4-dinitrophenylhydrazine, Anaemia, GC-MS analysis, Haemolysis Mangifera indica L.
Keywords: 2; 4-dinitrophenylhydrazine; Anaemia; GC-MS analysis; Haemolysis Mangifera indica L.

Effects of standardized stem bark extract of Mangifera indica L. in wistar rats with 2,4-dinitrophenylhydrazine-induced haemolytic anaemia - Hassan Lawal Sani; Ibrahim Malami; Sanusi Wara Hassan; Alhassan Muhammad Alhassan; Mshelia Emmanuel Halilu; Aliyu Muhammad (Pharmacognosy Journal, 2015)
Background: The aqueous decoction of the stem back of Mangifera indica L. has been traditionally used for the treatment of various illnesses among them includes anaemia. Aims: The aim of this study was to investigate the anti-anaemic properties of standardized stem bark extract of M. indica in animals with 2,4-dinitrophenylhydrazine-induced haemolytic anaemia. Methods and Material: An in vivo animal model was used in this experiment. 2,4-dinitrophenylhydrazine was used to induce haemolysis and treatment was done with three different concentrations (25, 50, and 100 mg/kg b.wt) of the plant extract. Astifer® was used as a positive control. Haematological parameters such as PCV, HGb concentration, and TLC were performed and to ascertain the level of haemolysis. GC-MS was used determine the present of phytoconstituents within the crude extract. Results: PCV and HGb concentration increased significantly (p<0.001) at a dose of 50 and 100 mg/kg b.wt respectively while no significant (p>0.05) effect was observed at a dose of 25 mg/kg b.wt. TLC was decreased significantly (p<0.001) at a dose 100 mg/kg b.wt while no significant (p>0.05) effect was observed at a dose of 25 and 50 mg/kg b.wt respectively. GC-MS analysis revealed presence of 15 compounds viz: 2,2-Dimethoxybutane, N-Acetyl-Alpha-D-glucosamine, 1,2-Benzenediol, Phenol, 2,4-bis(1,1-dimethylethyl)-, Vitamin E, Pentadecanoic acid, 13-methyl-, methyl ester, 2-Ethylacridine, Benzofuran-6-ol-3-one, 2-(4ethoxycarbonyl)benzylidene-, 9-Octadecanoic acid, (E)-, 2,4,6-Cycloheptatrien-1-one, 3,5-bis-trimethylsilyl-, and Benzo[h]quinoline,2,4-dimethyl-. Conclusion: The results of our present finding suggest the significant anti-anaemic properties of standardized stem bark extract of Mangefera indica L. This finding highlights the potentials of the extract and M. indica in the treatment of haemolytic anaemia.
Keywords: 2; 4-dinitrophenylhydrazine; Anaemia; GC-MS analysis; Haemolysis and Mangifera indica L.

Elucidation of β -sitosterol from Benincasa hispida Seeds, Carissa congesta Roots and Polyalthia longifolia Leaves by High Performance Thin Layer Chromatography - Gaurav Mahesh Doshi; Pratip Kashinath Chaskar; Hemant Devidas Une (Pharmacognosy Journal, 2015)
Background: Fruits of Benincasa hispida (BH) is regarded as Valliphala due to its vast plethora of medicinal properties, Carissa congesta (CC) is an imperative local plant particularly in rural communities and Polyalthia longifolia (PL) is an ornamentally significant traditionally relevance plant in India system. β-sitosterol, an active constituent identified from enormous plants has been reported to possess excellent amount of pharmacotherapeutic potential by number of researchers. Objective: In the recent studies, the research team focuses on determining the percentage of the β-sitosterol present in the BH seeds, CC roots petroleum ether extracts as well as PL leaves ethanolic extract by chromatographic technique in harmony with High Performance Thin Layer Chromatography. Materials and Methods: Respective parts of BH, CC and PL plants were shade-dried and extracted by appropriate extraction methods followed by identification of β-sitosterol from the extracts by High Performance Thin Layer Chromatography after preliminary phytochemical screening extracts for the constituents. Results: The amount of β-sitosterol present in the BH seeds, CC roots and PL leaves extracts was found to be 23.00, 5.94 and 1.81 % w/w respectively. Research studies elucidated a peak that coincided with standard peak of β-sitosterol suggesting the presence of constituent in the extracts. Conclusion: Thus, extracts contains important constituent of β-sitosterol in BH, CC and PL. Key words:Benincasa hispida, Carissa congesta, HPTLC, Polyalthia longifolia, β-sitosterol.
Keywords: Benincasa hispida; Carissa congesta; HPTLC; Polyalthia longifolia; β-sitosterol.

Elucidation of β-sitosterol from Benincasa hispida Seeds, Carissa congesta Roots and Polyalthia longifolia Leaves by High Performance Thin Layer Chromatography - Gaurav Mahesh Doshi; Pratip Kashinath Chaskar; Hemant Devidas Une (Pharmacognosy Journal, 2015)
Background: Fruits of Benincasa hispida (BH) is regarded as Valliphala due to its vast plethora of medicinal properties, Carissa congesta (CC) is an imperative local plant particularly in rural communities and Polyalthia longifolia (PL) is an ornamentally significant traditionally relevance plant in India system. β-sitosterol, an active constituent identified from enormous plants has been reported to possess excellent amount of pharmacotherapeutic potential by number of researchers. Objective: In the recent studies, the research team focuses on determining the percentage of the β-sitosterol present in the BH seeds, CC roots petroleum ether extracts as well as PL leaves ethanolic extract by chromatographic technique in harmony with High Performance Thin Layer Chromatography. Materials and Methods: Respective parts of BH, CC and PL plants were shade-dried and extracted by appropriate extraction methods followed by identification of β-sitosterol from the extracts by High Performance Thin Layer Chromatography after preliminary phytochemical screening extracts for the constituents. Results: The amount of β-sitosterol present in the BH seeds, CC roots and PL leaves extracts was found to be 23.00, 5.94 and 1.81 % w/w respectively. Research studies elucidated a peak that coincided with standard peak of β-sitosterol suggesting the presence of constituent in the extracts. Conclusion: Thus, extracts contains important constituent of β-sitosterol in BH, CC and PL.
Keywords: Benincasa hispida; Carissa congesta; HPTLC; Polyalthia longifolia; β-sitosterol

Evaluation of cytotoxic, DNA protecting and LPS induced MMP-9 down regulation activities of Plectranthus amboinicus (Lour) Spreng. essential oil. - Ramaraj Thirugnanasampandan; Gunasekar Ramya; Madhusudhanan Gogulramnath; Rajarajeswaran Jayakumar; M.S. Kanthimathi (Pharmacognosy Journal, 2015)
Introduction:Plectranthus amboinicus (Lour) Spreng is a known medicinal plant used in Siddha and Ayurveda medicines in India. It has enormous medicinal potential to treat various diseases. Methods: The present study focused on the use of essential oil obtained from the leaves of Plectranthus amboinicus to test cytotoxicity against breast (MCF-7) and colorectal (HT-29) cancer cell lines, to protect DNA from H2O2 induced genotoxicity through comet assay and to treat inflammation in lipopolysaccharide (LPS) induced over expression of matrix metalloproteinase-9 (MMP-9) in human peripheral blood mononuclear cells (PBMCs) by gelatin zymogram and inhibition at transcriptional level confirmed using RT-PCR (reverse transcriptase polymerase chain reaction). Results: Cytotoxicity of essential oil against MCF-7 and HT-29 cancer cell lines revealed the IC50 values of 53 ± 0.01 and 87 ± 0.01μg/mL respectively. At 200 μg/mL essential oil protected against 75% of DNA damage in 3T3-L1 fibroblast cells. Essential oil showed significant reduction in production of MMP-9 in a concentration dependent manner. Conclusion: Overall, the results showed that essential oil of P. amboinicus is a potent bioactive substance and it could be used in herbal medicine preparations. Key words: Essential oil , Cytotoxicity , Antigenotoxicity, Zymogram, RT- PCR.
Keywords: Antigenotoxicity; Cytotoxicity; Essential oil; RT- PCR; Zymogram

Evaluation of cytotoxic, DNA protecting and LPS induced MMP-9 down regulation activities of Plectranthus amboinicus (Lour) Spreng. essential oil - Ramaraj Thirugnanasampandan; Gunasekar Ramya; Madhusudhanan Gogulramnath; Rajarajeswaran Jayakumar; M.S. Kanthimathi (Pharmacognosy Journal, 2015)
Introduction: Plectranthus amboinicus (Lour) Spreng is a known medicinal plant used in Siddha and Ayurveda medicines in India. It has enormous medicinal potential to treat various diseases. Methods: The present study focused on the use of essential oil obtained from the leaves of Plectranthusamboinicusto test cytotoxicity against breast (MCF-7) and colorectal (HT-29) cancer cell lines, to protect DNA from H2O2 induced genotoxicity through comet assay and to treat inflammation in lipopolysaccharide (LPS) induced over expression of matrix metalloproteinase-9 (MMP-9) in human peripheral blood mononuclear cells (PBMCs) by gelatin zymogram and inhibition at transcriptional level confirmed using RT-PCR (reverse transcriptase polymerase chain reaction). Results: Cytotoxicity of essential oil against MCF-7 and HT-29 cancer cell lines revealed the IC50 values of 53 ± 0.01 and 87 ± 0.01 μg/mL respectively. At 200 μg/mL essential oil protected against 75% of DNA damage in 3T3-L1 fibroblast cells. Essential oil showed significant reduction in production of MMP-9 in a concentration dependent manner. Conclusion: Overall, the results showed that essential oil of P. amboinicus is a potent bioactive substance and it could be used in herbal medicine preparations.
Keywords: Antigenotoxicity; Cytotoxicity; Essential oil; RT- PCR.; Zymogram

Evaluation of Phytoconstituents of Bryonopsis laciniosa fruit by UV-Visible Spectroscopy and FTIR analysis - Ramya Bashyam; Malarvili Thekkumalai; Velavan Sivanandham (Pharmacognosy Journal, 2015)
Objectives: To Investigate the phytochemicals present in Bryonopsis laciniosa fruit. Methodology: Qualitative, Quantitative screening, Compound Identification by UV-Visible method and identification of functional group of the active chemical components were followed by standard procedures. Result: The results showed the presence of phytonutrients like reducing sugar, terpenoids, triterpenoids, aminoacids, anthroquinone, polyphenols, glycosides, anthocyanins, tannins, coumarins, emodins, saponins, total alkaloids, total flavonoids, lignin and serpentine. These substances may be responsible for the health related properties of the plant which are based on antioxidant,anticancer, antipyretic, antiaphoretic, antidiabetic, anti-inflammation, antiheamatisum, antimicrobial and antiviral activity. Conclusion: This study supports the popular use of Bryonopsis laciniosa fruit in preparation of various pharmaceutical formulations for human welfare. Key words: Bryonia laciniosa, FTIR, Phytochemical screening, Phytonutrients, UV-Vis.
Keywords: Bryonia laciniosa; FTIR; Phytochemical screening; Phytonutrients; UV-Vis.

Evaluation of Phytoconstituents of Bryonopsis laciniosa fruit by UV-Visible Spectroscopy and FTIR analysis - Ramya Bashyam; Malarvili Thekkumalai; Velavan Sivanandham (Pharmacognosy Journal, 2015)
Objectives: To Investigate the phytochemicals present in Bryonopsis laciniosa fruit. Methodology: Qualitative, Quantitative screening, Compound Identification by UV-Visible method and identification of functional group of the active chemical components were followed by standard procedures. Result: The results showed the presence of phytonutrients like reducing sugar, terpenoids, triterpenoids, aminoacids, anthroquinone, polyphenols, glycosides, anthocyanins, tannins, coumarins, emodins, saponins, total alkaloids, total flavonoids, lignin and serpentine. These substances may be responsible for the health related properties of the plant which are based on antioxidant, anticancer, antipyretic, antiaphoretic, antidiabetic, anti-inflammation, antiheamatisum, antimicrobial and antiviral activity. Conclusion: This study supports the popular use of Bryonopsis laciniosa fruit in preparation of various pharmaceutical formulations for human welfare.
Keywords: Bryonia laciniosa; FTIR; Phytochemical screening; Phytonutrients; UV-Vis

Flavonoids from Eupatorium illitum and Their Antiproliferative Activities - Quírico A Castillo; Jorge Triana; José L Eiroa; José M Padrón; Gabriela B Plata; Ernesto V Abel-Santos; Luis A. Báez; Diana C Rodríguez; Marco A Jiménez; María F Pérez-Pujols (Pharmacognosy Journal, 2015)
Objective: To isolate the chemical constituents of the aerial parts from Eupatorium illitum, elucidate their structures and evaluate their antiproliferative activity on human cancer cell lines. Materials and Methods: The ethanolic extract of Eupatorium illitum afforded five compounds, which were characterized using spectroscopic techniques and by comparison with data from the literature. Antiproliferative activities of selected isolates were evaluated. Results: The flavonoids Kumatakenin (1), Ermanin (2), 7-methoxy-aromadendrin (3) and Naringenin (4), together with 4-hydroxybenzoic acid (5) were isolated. Compounds 1, 2, 4 and 5 were evaluated for their antiproliferative activity on the human cancer cell lines A549 (lung), HBL-100 (breast), HeLa (cervix), SW1573 (lung), and T-47D (breast) presenting a wide range of bioactivities. In general, best results were observed for 5. Conclusion: Compounds 1-5 are reported for first time from Eupatorium illitum. Isolated phytochemicals show moderate to low antiproliferative activities when evaluated on the aforementioned human cancer cell lines.
Keywords: 4-Hydroxybenzoic acid; 7-Methoxy-aromadendrin; Ermanin; Eupatorium illitum; Kumatakenin; Naringenin.

Flavonoids from Eupatorium illitum and Their Antiproliferative Activities - Quírico A Castillo; Jorge Triana; José L Eiroa; José M Padrón; Gabriela B Plata; Ernesto V Abel-Santos; Luis A. Báez; Diana C Rodríguez; Marco A Jiménez; María F Pérez-Pujols (Pharmacognosy Journal, 2015)
Objective: To isolate the chemical constituents of the aerial parts from Eupatorium illitum, elucidate their structures and evaluate their antiproliferative activity on human cancer cell lines. Materials and Methods: The ethanolic extract of Eupatorium illitum afforded five compounds, which were characterized using spectroscopic techniques and by comparison with data from the literature. Antiproliferative activities of selected isolates were evaluated. Results: The flavonoids Kumatakenin (1), Ermanin (2), 7-methoxy-aromadendrin (3) and Naringenin (4), together with 4-hydroxybenzoic acid (5) were isolated. Compounds 1, 2, 4 and 5 were evaluated for their antiproliferative activity on the human cancer cell lines A549 (lung), HBL-100 (breast), HeLa (cervix), SW1573 (lung), and T-47D (breast) presenting a wide range of bioactivities. In general, best results were observed for 5. Conclusion: Compounds 1-5 are reported for first time from Eupatorium illitum. Isolated phytochemicals show moderate to low antiproliferative activities when evaluated on the aforementioned human cancer cell lines. Key words: Eupatorium illitum, Ermanin, 4-Hydroxybenzoic acid, Kumatakenin, 7-Methoxy-aromadendrin, Naringenin.
Keywords: 4-Hydroxybenzoic acid; 7-Methoxy-aromadendrin; Ermanin; Eupatorium illitum; Kumatakenin; Naringenin.

Free Radical Scavenging and Cytotoxic Potential of Celosia argentea - Rukhsana Abdul Rub; Manohar Janardhan Patil; Areej Abdul Siddiqui; Priyanka Rambhau Ghorpade; Alpana Subhod Moghe (Pharmacognosy Journal, 2015)
Introduction: Oxidative stress due to reactive oxygen species often leads to pathogenesis of chronic diseases such as cancer. Research states that a diet rich in polyphenols renders many health benefits by scavenging such harmful reactive species. Celosia argentea (Amaranthaceae), a common weed in India has been reported as a potential source of cheap, natural antioxidants due to its phenolic abundance. In this research work efforts were made to identify and screen the phenolic rich fractions of Celosia argentea for their antioxidant and anticancer potential. Materials and Methods: Various solvent fractions with increasing polarity were subjected to total phenolic content, followed by antioxidant assays-DPPH, ABTS and anti proliferative assays- Brine shrimp Bioassay, Antimitotic and MTT assays. Results: IC50 value of methanolic fraction for DPPH assay was statistically significant (26.25; ***P<0.001) when compared with ascorbic acid (12.50; ***P<0.001). Also TEAC values for methanolic fraction and BHT (standard) for ABTS assay were similar (2.1; ***P<0.001) Methanolicfraction at 400 μg/ml exhibited strong cytotoxicity (9.0 ± 0.81; ***P<0.001) against brine shrimps comparable to Methotrexate at 50 μg/ml(10; ***P<0.001) and significantly reduced mitotic index from 96.8 to 38.0 (***P<0.001) which was further confirmed by MTT assay where IC50 value of methanolic fraction for SiHa and MCF-7 cells was found to be 28 μg/ml with no cytotoxicity to normal cells proving its anticancer potential. Conclusion: This research proves antioxidant and anticancer potential of phenolic rich fraction of Celosia argentea and suggests it to be useful in cancer management as antifroliferative, chemo preventive and in cancer chemotherapy induced immune suppression and oxidative stress.
Keywords: Antioxidant; Brine shrimp; Mitotic index; MTT; Phenolics.

Free Radical Scavenging and Cytotoxic Potential of Celosia argentea - Rukhsana Abdul Rub; Manohar Janardhan Patil; Areej Abdul Siddiqui; Priyanka Rambhau Ghorpade; Alpana Subhod Moghe (Pharmacognosy Journal, 2015)
Introduction: Oxidative stress due to reactive oxygen species often leads to pathogenesis of chronic diseases such as cancer. Research states that a diet rich in polyphenols renders many health benefits by scavenging such harmful reactive species. Celosia argentea (Amaranthaceae), a common weed in India has been reported as a potential source of cheap, natural antioxidants due to its phenolic abundance. In this research work efforts were made to identify and screen the phenolic rich fractions of Celosia argentea for their antioxidant and anticancer potential. Materials and Methods: Various solvent fractions with increasing polarity were subjected to total phenolic content, followed by antioxidant assays- DPPH, ABTS and anti proliferative assays- Brine shrimp Bioassay, Antimitotic and MTT assays. Results: IC50 value of methanolic fraction for DPPH assay was statistically significant (26.25; ***P<0.001) when compared with ascorbic acid (12.50; ***P<0.001). Also TEAC values for methanolic fraction and BHT (standard) for ABTS assay were similar (2.1; ***P<0.001) Methanolicfraction at 400 μg/ml exhibited strong cytotoxicity (9.0 ± 0.81; ***P<0.001) against brine shrimps comparable to Methotrexate at 50 μg/ml(10; ***P<0.001) and significantly reduced mitotic index from 96.8 to 38.0 (***P<0.001) which was further confirmed by MTT assay where IC50 value of methanolic fraction for SiHa and MCF-7 cells was found to be 28 μg/ml with no cytotoxicity to normal cells proving its anticancer potential. Conclusion: This research proves antioxidant and anticancer potential of phenolic rich fraction of Celosia argentea and suggests it to be useful in cancer management as antifroliferative, chemo preventive and in cancer chemotherapy induced immune suppression and oxidative stress. Key words: Antioxidant, Brine shrimp, Mitotic index, MTT, Phenolics.
Keywords: Antioxidant; Brine shrimp; Mitotic index; MTT; Phenolics.

GC-MS Analysis of Bioactive Phytochemicals Present in Ethanolic Extracts of Leaves of Annona muricata: A Further Evidence for Its Medicinal Diversity (Pharmacognosy Journal, 2015)
Background: Folk medicine has taken an important place especially in developing countries where limited health services are available. However, the absence of scientific evaluation of medicinal plants may cause serious adverse effects. Objective: To analyze the phytochemical composition of the ethanolic extracts of leaves of Annona muricata using gas chromatography mass spectroscopy (GC-MS). Materials and methods: GC-MS Analysis was used. Results: TheGC-MS Analysis revealed 25 con¬stituents of which 12 of the compounds were identified. The major constituents were two unidentified compounds with percentage peak areas of 23.51% and 16.8%. Of the identified compounds, the outstanding in composition were 7-Tetradecenal, (Z) (peak area 9.39%), n-Hexadecanoic acid (peak area 7.12%), Oleyl Alcohol (peak area 6.15%), Phytol (peak area 5.61%), cis, cis, cis-7,10,13-Hexadecatrienal (peak area 4.26%), 2-Pentadecanol(peak area 3.93%), 9,12-Octadecadienoic acid, ethyl ester (peak area 3.21%), 1,2-Benzenedicarboxylic acid, butyl octyl ester (peak area 2.67%), and 1,E-11,Z-13-Octadecatriene (peak area 2.15%), while the rest had less than 2% composition by peak area. Conclusion: The current study suggests that ethanolic extracts ofleaves of Annona muricata are a potent therapeutic agent and paves the way for the development of several treatment regimens based on compounds from this extract. Key words:Annona muricata, ethanolic extracts, phytochemicals, GC-MS.
Keywords: Annona muricata; Ethanolic extracts; GC-MS.; Phytochemicals

GC-MS Analysis of Bioactive Phytochemicals Present in Ethanolic Extracts of Leaves of Annona muricata: A Further Evidence for Its Medicinal Diversity - Yahaya Gavamukulya; Faten Abou-Elella; Fred Wamunyokoli; Hany A El-Shemy (Pharmacognosy Journal, 2015)
Background: Folk medicine has taken an important place especially in developing countries where limited health services are available. However, the absence of scientific evaluation of medicinal plants may cause serious adverse effects. Objective: To analyze the phytochemical composition of the ethanolic extracts of leaves of Annona muricata using gas chromatography mass spectroscopy (GC-MS). Materials and methods: GC-MS Analysis was used. Results: The GC-MS Analysis revealed 25 constituents of which 12 of the compounds were identified. The major constituents were two unidentified compounds with percentage peak areas of 23.51% and 16.8%. Of the identified compounds, the outstanding in composition were 7-Tetradecenal, (Z) (peak area 9.39%), n-Hexadecanoic acid (peak area 7.12%), Oleyl Alcohol (peak area 6.15%), Phytol (peak area 5.61%), cis, cis, cis-7,10,13-Hexadecatrienal (peak area 4.26%), 2-Pentadecanol (peak area 3.93%), 9,12-Octadecadienoic acid, ethyl ester (peak area 3.21%), 1,2-Benzenedicarboxylic acid, butyl octyl ester (peak area 2.67%), and 1,E- 11,Z-13-Octadecatriene (peak area 2.15%), while the rest had less than 2% composition by peak area. Conclusion: The current study suggests that ethanolic extracts of leaves of Annona muricata are a potent therapeutic agent and paves the way for the development of several treatment regimens based on compounds from this extract.
Keywords: Annona muricata; Ethanolic extracts; GC-MS; Medicinal diversity; Phytochemicals.

GC-MS Analysis of Phytocomponents in, Pet Ether Fraction of Wrightia tinctoria Seed. - Rajani Srivastava; Alok Mukerjee; Amita Verma (Pharmacognosy Journal, 2015)
Introduction:Wrightia tinctoria R.Br. (Family: Apocynaceae) commonly called “Indrajau” is well known in Indian traditional system for its traditional uses. Materials and Methods: The present investigation was carried out to determine the possible bioactive components of plant seed ethanolic extract, pet ether fraction using GC-MS analysis. 22 components were identified from pet ether fraction obtained from elution of ethanolic extract packed in silica column. Results: The prevailing compounds from fraction F6to F9 were [1,1'-Bicyclopropyl]-2-octanoic acid, 2'-hexyl-, methyl ester (21.39%) , Trilinolein (7.74%), 2-Myristynoyl pantetheine (18.07%), 9-Octadecen-12-ynoic acid, methyl ester (4.46%), 1Hexadecanol,2-methyl (3.77%), Cyclopropane tetradecanoic acid, 2-octyl-, methyl ester (2.36%), 1b, 4a-Epoxy-2H-cyclopenta [3,4] cyclopropa [8,9]cycloundec [1,2-b]oxiren-5 (6H)-one, 7-(acetyloxy) decahydro-2,9,10-trihydroxy-3,6,8,8,10a-pentamethyl (38.91%), Geranyl isovalerate (23.58%), cis-13-Octadecenoic acid (5.91%), Quassin (3.82%), cis-10-Heptadecenoic acid (3.08%), 9,12,15-Octadecatrienoic acid 2-phenyl-1, 3-dioxan-5-yl ester (31.50%), 9,12,15-Octadecatrienoic acid, (Z,Z,Z)-2,3-dihydroxypropyl ester (14.35%), Cyclopropanebutanoic acid, 2-[ [2-[ [2- [(2-pentylcyclopropyl) methyl] cyclopropyl] methyl] cyclopropyl] methyl]-, methyl ester (10.13%), 6,9,12,15-Docosatetraenoic acid, methyl ester (3.39%), 9,12-Octadecadienoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, trans-( 2.73%), 9,12-Octadecadienoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, cis-(4.34%), Ursodeoxycholic acid (7.14%), Bufa-20,22-dienolide, 3-(acetyloxy)-14,15-epoxy-16-hydroxy-, (3á,5á,15á,16á)-(4.75%), 5H-Cyclopropa [3,4] benz [1,2-e]azulen-5-one, 9a (acetyloxy)-1,1a,1b,4,4a,7a,7b,8,9,9a-de cahydro-4a,7b,9-trihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-,[1aR-(1aà,1bá,4aá,7aà,7bà,8à,9á,9aà)]-(6.59%), Docosahexaenoic acid, 1,2,3-propanetriyl ester (10.86%), Olean-12-ene-3,15,16,21,22,28-hexol, (3á,15à,16à,21á,22à)-( 4.40%) found as the major components. Conclusion: It could be concluded that, Wrightia tinctoria contains various bioactive compounds. So it is recommended as a plant of phytopharmaceutical importance. Key words: Bioactive components, Ethanolic extract, GC-MS, Indrajau, Wrightia tinctoria.
Keywords: Bioactive components; Ethanolic extract; GC-MS; Indrajau; Wrightia tinctoria.

GC-MS Analysis of Phytocomponents in, Pet Ether Fraction of Wrightia tinctoria Seed - Rajani Srivastava; Amita Verma (Pharmacognosy Journal, 2015)
Introduction: Wrightia tinctoria R.Br. (Family: Apocynaceae) commonly called “Indrajau” is well known in Indian traditional system for its traditional uses. Materials and Methods: The present investigation was carried out to determine the possible bioactive components of plant seed ethanolic extract, pet ether fraction using GC-MS analysis. 22 components were identified from pet ether fraction obtained from elution of ethanolic extract packed in silica column. Results: The prevailing compounds from fraction F6to F9 were [1,1'-Bicyclopropyl]-2-octanoic acid, 2'-hexyl-, methyl ester (21.39%) , Trilinolein (7.74%), 2-Myristynoyl pantetheine (18.07%), 9-Octadecen-12-ynoic acid, methyl ester (4.46%), 1Hexadecanol,2-methyl (3.77%), Cyclopropane tetradecanoic acid, 2-octyl-, methyl ester (2.36%), 1b, 4a-Epoxy-2H-cyclopenta [3,4] cyclopropa [8,9]cycloundec [1,2-b]oxiren-5 (6H)-one, 7-(acetyloxy) decahydro-2,9,10-trihydroxy-3,6,8,8,10a-pentamethyl (38.91%), Geranyl isovalerate (23.58%), cis-13-Octadecenoic acid (5.91%), Quassin (3.82%), cis-10-Heptadecenoic acid (3.08%), 9,12,15-Octadecatrienoic acid 2-phenyl-1, 3-dioxan-5-yl ester (31.50%), 9,12,15-Octadecatrienoic acid, (Z,Z,Z)-2,3-dihydroxypropyl ester (14.35%), Cyclopropanebutanoic acid, 2-[ [2-[ [2- [(2-pentylcyclopropyl) methyl] cyclopropyl] methyl] cyclopropyl] methyl]-, methyl ester (10.13%), 6,9,12,15-Docosatetraenoic acid, methyl ester (3.39%), 9,12-Octadecadienoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, trans-( 2.73%), 9,12-Octadecadienoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, cis-(4.34%), Ursodeoxycholic acid (7.14%), Bufa-20,22-dienolide, 3-(acetyloxy)-14,15-epoxy-16-hydroxy-, (3á,5á,15á,16á)-(4.75%), 5H-Cyclopropa [3,4] benz [1,2-e]azulen-5-one, 9a (acetyloxy)-1,1a,1b,4,4a,7a,7b,8,9,9a-de cahydro-4a,7b,9-trihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-,[1aR-(1aà,1bá,4aá,7aà,7bà,8à,9á,9aà)]-(6.59%), Docosahexaenoic acid, 1,2,3-propanetriyl ester (10.86%), Olean-12-ene-3,15,16,21,22,28-hexol, (3á,15à,16à,21á,22à)-( 4.40%) found as the major components. Conclusion: It could be concluded that, Wrightia tinctoria contains various bioactive compounds. So it is recommended as a plant of phytopharmaceutical importance
Keywords: Bioactive components; Ethanolic extract; GC-MS; Indrajau; Wrightia tinctoria

Hepatoprotective Activity of Michelia nilagirica against Paracetamol Induced Hepatic Injury in Rats - Shaik Aminabee; Atmakuri Lakshmana Rao; Maram Chinna Eswaraiah (Pharmacognosy Journal, 2015)
Background:Michelia nilagirica belonging to the family Mangoliaceae is commonly used by many traditional healers in most of the herbal preparations for diabetes and kidney diseases. Objective: Different fractions isolated from ethanolic extract of whole plant of Michelia nilagirica is investigated for hepatoprotective activity in wistar albino rats against paracetamol induced hepatic injury. Materials & Methods: Rats were divided into eight groups. Each group contains six animals. Hepatic injury was achieved by injecting paracetamol at a dose of 2 mg/kg p.o. Results: The hepatoprotective action is seen with fraction A by reduction in serum marker enzymes like Aspartate transaminase (AST), Alanine transaminase (ALT). It also reduced the elevated levels of Alkaline phosphotase (ALP) & Serum bilirubin. Conclusion: Histopathological studies further confined the hepatoprotective activity of fraction A against paracetamol treated group. The results obtained were compared with silymarin (100 mg/kg, orally), a standard drug. Key words: Albino rats, Hepatoprotective, Michelia nilagirica, Paracetamol, Screening.
Keywords: Albino rats; Hepatoprotective; Michelia nilagirica; Paracetamol; Screening.

Hepatoprotective Activity of Michelia nilagirica against Paracetamol Induced Hepatic Injury in Rats - Shaik Aminabee; Atmakuri Lakshmana Rao (Pharmacognosy Journal, 2015)
Background: Michelia nilagirica belonging to the family Mangoliaceae is commonly used by many traditional healers in most of the herbal preparations for diabetes and kidney diseases. Objective: Different fractions isolated from ethanolic extract of whole plant of Michelia nilagirica is investigated for hepatoprotective activity in wistar albino rats against paracetamol induced hepatic injury. Materials & Methods: Rats were divided into eight groups. Each group contains six animals. Hepatic injury was achieved by injecting paracetamol at a dose of 2 mg/kg p.o. Results: The hepatoprotective action is seen with fraction A by reduction in serum marker enzymes like Aspartate transaminase (AST), Alanine transaminase (ALT). It also reduced the elevated levels of Alkaline phosphotase (ALP) & Serum bilirubin. Conclusion: Histopathological studies further confined the hepatoprotective activity of fraction A against paracetamol treated group. The results obtained were compared with silymarin (100 mg/kg, orally), a standard drug.
Keywords: Albino rats; Hepatoprotective; Michelia nilagirica; Paracetamol; Screening

Hepatoprotective effect of Livplus- A polyherbal formulation - Rajesh A Maheshwari,; Bhagyashree Pandya; R. Balaraman, Avinash K Seth; Yogesh Chand; Yadav; Vasa Siva Sankar (Pharmacognosy Journal, 2015)
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Keywords: Acetylcholine; Antitussive; Bronchoprotection; Citric acid; Cough; Cough variant asthma (CVA); Ethanolic extract of Woodfordia fruticosa (L.) Kurz (EEWF); Histamine.

Hepatoprotective effect of Livplus-A polyherbal formulation - Rajesh Maheshwari; Bhagyashree Pandya; Ramachandran Balaraman; Avinash Kumar Seth; Yogesh Chand Yadav; Vasa Siva Sankar (Pharmacognosy Journal, 2015)
Objective: The aim of the present study was to investigate the hepatoprotective effect of Livplus (a polyherbal formulation) against CCl4-induced hepatotoxicity in rats. Methods: Hepatotoxicity was induced in rats by i.p. injection of CCl4 once three days for 14 days. Livplus or Silymarin was administered along with CCl4 and the biochemical parameters like aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkalinephosphatase (ALP), total bilirubin (TB), direct bilirubin, total protein (TP), gamma-glutamyl transferase (GGT), total cholesterol (TC) and triglycerides (TG) were estimated. Furthermore, biomarkers of oxidative stress such as MDA levels, Glutathione contents, SOD and catalase activity in liver tissue were estimated. Results: Treatment with Livplus significantly reduced the elevated levels of ALT, AST, ALP, bilirubin (direct and total), GGT, TC, TG and increased levels of TP compared to CCl4 control rats. The treatment with Livplus also showed a significant increase in glutathione contents, SOD and catalase activity and a decrease in MDA levels compared to CCl4 control rats. Conclusion: The finding of present study indicates that Livplus showed a potential hepatoprotective activity. These results support the traditional use of Livplus in the treatment of liver disorders.
Keywords: CCl4; GGT; Hepatic enzymes.; Hepatotoxicity; Livplus

Hepatoprotective effect of Quail egg against carbon tetra chloride (CCl4) induced hepatic damage in albino rats - Dandare Shamsudeen Umar; Bawa Muhammad; Wasagu Ibrahim Zubairu; Magaji Umar Faruk (Pharmacognosy Journal, 2015)
Introduction: Quail egg has been used traditionally in the treatment of many ailments. Despite the wide speculations of its involvement in the treatment of liver diseases, very little scientific evidence exist to support this claim. This work investigated the hepatoprotective effect of quail egg against carbon tetrachloride (CCl4) induced liver damage in albino rats. Materials and Methods: The rats were divided into five groups of five rats per group. Animals of group A (positive control) were fed with vehicle (distilled water) on the first four days and with vehicle and CCl4 on the fifth, sixth and seventh day. Animals of group B (negative control) were given only vehicle for seven days. Animals of groups C, D and E were respectively administered with 100, 200 and 400 mg/kg body weight of quail egg for the first four days and with vehicle, quail egg and CCl4 for the fifth, sixth and seventh day. Animals were subsequently anaesthetized, and blood samples were taken for the estimation of albumin, alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), total protein (TP) and bilirubin. The liver was isolated for histopathological studies. Results: The levels of ALT, ALP and TP were significantly affected (p < 0.05) in CCl4 fed groups, indicating liver injury. The effects were reduced significantly (p < 0.05) after treatment of rats with quail egg. Furthermore, histopathological studies of the liver tissues also supported the hepatoprotective activity of quail egg- photomicrographs of treated groups showed mild reduction in vacuolarisation/ballooning degeneration of the hepatocytes. Conclusion: Quail egg showed some potentials of protecting the liver from damage by stabilising the levels of ALP, ALT and TP and reducing the degeneration of the hepatocytes. Thus, this finding has provided information that suggests utilising quail egg for treatment of liver dysfunction.

Hepatoprotective Effect of Quail Egg Against Carbontetrachloride (CCl4) Induced Hepatic Damage in Albino Rats - Dandare Shamsudeen Umar; Bawa Muhammad; Wasagu Ibrahim Zubairu; Magaji Umar Faruk (Pharmacognosy Journal, 2015)
Introduction: Quail egg has been used traditionally in the treatment of many ailments. Despite the wide speculations of its involvement in the treatment of liver diseases, very little scientific evidence exist to support this claim. This work investigated the hepatoprotective effect of quail egg against carbon tetrachloride (CCl4) induced liver damage in albino rats. Materials and Methods: The rats were divided into five groups of five rats per group. Animals of group A (positive control) were fed with vehicle (distilled water) on the first four days and with vehicle and CCl4 on the fifth, sixth and seventh day. Animals of group B (negative control) were given only vehicle for seven days. Animals of groups C, D and E were respectively administered with 100, 200 and 400 mg/kg body weight of quail egg for the first four days and with vehicle, quail egg and CCl4 for the fifth, sixth and seventh day. Animals were subsequently anaesthetized, and blood samples were taken for the estimation of albumin, alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), total protein (TP) and bilirubin. The liver was isolated for histopathological studies. Results: The levels of ALT, ALP and TP were significantly affected (p < 0.05) in CCl4 fed groups, indicating liver injury. The effects were reduced significantly (p < 0.05) after treatment of rats with quail egg. Furthermore, histopathological studies of the liver tissues also supported the hepatoprotective activity of quail egg- photomicrographs of treated groups showed mild reduction in vacuolarisation/ballooning degeneration of the hepatocytes. Conclusion: Quail egg showed some potentials of protecting the liver from damage by stabilising the levels of ALP, ALT and TP and reducing the degeneration of the hepatocytes. Thus, this finding has provided information that suggests utilising quail egg for treatment of liver dysfunction. Key Words: Quail egg, Carbon tetrachloride, Hepatotoxicity, Hepatoprotection, Histopathology.
Keywords: Carbon tetrachloride; Hepatoprotection; Hepatotoxicity; Histopathology.; Quail egg

Immunomodulatory Activity of Atalantia monophylla DC. roots - VR Patil; VM Thakare; VS Joshi (Pharmacognosy Journal, 2015)
Objective: The objective of the present study was to evaluate the immunomodulatory activity of the roots of Atalantia monophylla. In the present study Pet. Ether, Chloroform and Methanolic fractions of the ethanolic extract of the roots of Atalantia monophylla, were administered orally, in the doses of 10 mg/kg and 30 mg/kg, to evaluate the immunomodulatory activity. Materials and Methods: The Methanolic fraction showed most significant effect when compared with control group, in the dose of 30 mg/kg, in the E.Coli induced abdominal sepsis and Carbon Clearence Test as models for non-specific immune response. In the models of the Specific immune response, cell mediated immune response to SRBC-delayed type of hypersensitivity (DTH) the methanolic fraction in the dose 30 mg/kg, when compared with control group, showed most significant effect on decrease in footpad edema after treatment. Results: Humoral immune response was assessed by Sheep erythrocyte agglutination test, in which the Methanolic fraction of Atalantia monophylla in the dose of 30 mg/kg showed most significant (p<0.05) increase in antibody titer after treatment when compared with control group. Conclusion: The present investigation reports that the Methanolic fraction of the ethanolic extract of the roots of Atalantia monophylla, in the dose of 30 mg/kg showed most significant immunomodulatory activity.
Keywords: Atalantia monophylla; Cell-mediated immune response; Humoral immune response; Immunomodulatory; Phagocytosis

Immunomodulatory Activity of Atalantia monophylla DC. roots - V. R. Patil; V. M. Thakare; V.S. Joshi (Pharmacognosy Journal, 2015)
Objective: The objective of the present study was to evaluate the immunomodulatory activity of the roots of Atalantia monophylla. In the present study Pet. Ether, Chloroform and Methanolic fractions of the ethanolic extract of the roots of Atalantia monophylla, were administered orally, in the doses of 10 mg/kg and 30 mg/kg, to evaluate the immunomodulatory activity. Materials and Methods: The Methanolic fraction showed most significant effect when compared with control group, in the dose of 30 mg/kg, in the E.Coli induced abdominal sepsis and Carbon Clearence Test as models for non-specific immune response. In the models of the Specific immune response, cell mediated immune response to SRBC - delayed type of hypersensitivity (DTH) the methanolic fraction in the dose 30 mg/kg, when compared with control group, showed most significant effect on decrease in footpad edema after treatment. Results: Humoral immune response was assessed by Sheep erythrocyte agglutination test, in which the Methanolic fraction of Atalantia monophylla in the dose of 30 mg/kg showed most significant (p<0.05) increase in antibody titer after treatment when compared with control group. Conclusion: The present investigation reports that the Methanolic fraction of the ethanolic extract of the roots of Atalantia monophylla, in the dose of 30 mg/kg showed most significant immunomodulatory activity. Key words:Atalantia monophylla, Immunomodulatory, Phagocytosis, Cell-mediated immune response, Humoral immune response.
Keywords: Atalantia monophylla; Cell-mediated immune response; Humoral immune response.; Immunomodulatory; Phagocytosis

In vitro Acetyl cholinesterase inhibitory assay of Acacia catechu Willd ethanolic seed extract - Lakshmi.T; Rajendran.R (Pharmacognosy Journal, 2015)
Aim & objective: The aim of this study was to evaluate acetyl cholinesterase inhibitory activity of Acacia catechu ethanolic seed extract to introduce a new source for management of Alzheimer’s disease. Background: Alzheimer’s disease is a complex, multifactorial, progressive, neurodegenerative disease primarily affecting the elderly population and is estimated to account for 50–60% of dementia cases in persons over 65 years of age. It is likely that the inhibition of acetyl cholinesterase by Acacia catechu ethanolic seed extract that is rich in flavonoids and antioxidants may aid in the protection of neurodegenerative disorders and ultimately Alzheimer's disease. Methods: Anti cholinesterase activity is determined by adopting In vitro standard protocol. Results: According to the obtained results, the inhibitory activity (IC50 values, μg /ml) of extracts was 204.38 ± 2.54 µ g/ml. Conclusion: The results indicated and confirmed the traditional use of Acacia catechu ethanolic seed extract for management of central nervous system disorders. It showed the moderate activity in inhibition of acetyl cholinesterase at various concentrations. However, further investigations on identification of active components in the extracts are needed. Key words: Acacia catechu seed, Acetyl cholinesterase inhibitor, Alzheimer’s disease, spectrophotometric analysis.
Keywords: Acacia catechu seed; Acetyl cholinesterase inhibitor; Alzheimer’s disease; Spectrophotometric analysis.

In vitro Acetyl Cholinesterase Inhibitory assay of Acacia catechu Willd Ethanolic Seed Extract - Lakshmi Thangavelu; Rajendran Ramasamy (Pharmacognosy Journal, 2015)
Aim & objective: The aim of this study was to evaluate acetyl cholinesterase inhibitory activity of Acacia catechu ethanolic seed extract to introduce a new source for management of Alzheimer’s disease. Background: Alzheimer’s disease is a complex, multifactorial, progressive, neurodegenerative disease primarily affecting the elderly population and is estimated to account for 50–60% of dementia cases in persons over 65 years of age. It is likely that the inhibition of acetyl cholinesterase by Acacia catechu ethanolic seed extract that is rich in flavonoids and antioxidants may aid in the protection of neurodegenerative disorders and ultimately Alzheimer’s disease. Methods: Anti cholinesterase activity is determined by adopting In vitro standard protocol. Results: According to the obtained results, the inhibitory activity (IC50 values, μg /ml) of extracts was 204.38 ± 2.54 μg/ ml. Conclusion: The results indicated and confirmed the traditional use of Acacia catechu ethanolic seed extract for management of central nervous system disorders. It showed the moderate activity in inhibition of acetyl cholinesterase at various concentrations. However, further investigations on identification of active components in the extracts are needed.
Keywords: Acacia catechu seed; Acetyl cholinesterase inhibitor; Alzheimer’s disease; Neurodegenerative; Spectrophotometric analysis.

In vitro study of anti-glycation and radical scavenging activities of the essential oils of three plants from Morocco: Origanum compactum, Rosmarinus officinalis and Pelargonium asperum - Ramdan Btissam; Ramdan Raja; Amakran Amina; Vannier Brigitte; NHIRI Mohamed (Pharmacognosy Journal, 2015)
Introduction: We have carried out our study on the chemical composition; anti-glycation andradical scavenging activities of Origanum compactum, Rosmarinus officinalis and Pelargonium asperum essential oils (EO) that were harvested in the northeast of Morocco. These plants have been traditionally used in medicine as a chief ingredient of many polyherbal formulations for the treatment of several pathologies. Method: The phytochemical study was revealed by GC-MS. The protein glycation inhibitory activity of EO extracted from these plant tissues was evaluated in vitro using the model system of bovine serum albumin and methylglyoxal. The measure of DPPH• radical reducing power was used to evaluate the antiradical activity. To test each fraction, we used the IC50 value previously obtained for the crude oils. Results: The phytochemical study of these essential oils showed that p-Thymol, Eucalyptol and Citronellal were respectively the major components in the three investigated EO of O.compactum, R. officinal is and P. asperum. More than 90% of the total components were detected. The extracts and fractions with glycation inhibitory activity also showed antiradical activity when the DPPH• radical reducing power was measured. Conclusion: The glycation inhibitory activity was correlated with the antiradical potency of the extracts. Thus, the positive glycation inhibitory and antiradical activities of these plants might suggest a possible role in targeting aging and diabetic complications.The presence of various bioactive compounds confirms the application of these plants for various diseases by traditional practitioners. However, isolation of individual phytochemical constituents may proceed to find a novel drug. Key words: Aging, Antioxidant, Antiglycation, Diabetes, Essential oil, Radical scavenger.
Keywords: Aging; Antiglycation; Antioxidant; Diabetes; Essential oil; radical scavenger.

In vitro study of anti-glycation and radical scavenging activities of the essential oils of three plants from Morocco: Origanum compactum, Rosmarinus officinalis and Pelargonium asperum - Ramdan Btissam; Amakran Amina; NHIRI Mohamed (Pharmacognosy Journal, 2015)
Introduction: We have carried out our study on the chemical composition; anti-glycation andradical scavenging activities of Origanum compactum, Rosmarinus officinalis and Pelargonium asperum essential oils (EO) that were harvested in the northeast of Morocco. These plants have been traditionally used in medicine as a chief ingredient of many polyherbal formulations for the treatment of several pathologies. Method: The phytochemical study was revealed by GC-MS. The protein glycation inhibitory activity of EO extracted from these plant tissues was evaluated in vitro using the model system of bovine serum albumin and methylglyoxal. The measure of DPPH• radical reducing power was used to evaluate the antiradical activity. To test each fraction, we used the IC50 value previously obtained for the crude oils. Results: The phytochemical study of these essential oils showed that p-Thymol, Eucalyptol and Citronellal were respectively the major components in the three investigated EO of O.compactum, R. officinal is and P. asperum. More than 90% of the total components were detected. The extracts and fractions with glycation inhibitory activity also showed antiradical activity when the DPPH• radical reducing power was measured. Conclusion: The glycation inhibitory activity was correlated with the antiradical potency of the extracts. Thus, the positive glycation inhibitory and antiradical activities of these plants might suggest a possible role in targeting aging and diabetic complications.The presence of various bioactive compounds confirms the application of these plants for various diseases by traditional practitioners. However, isolation of individual phytochemical constituents may proceed to find a novel drug.
Keywords: Aging; Antiglycation; Antioxidant; Diabetes; Essential oil; Radical scavenger

In vivo Antimalarial Evaluation of Embelin and its Semi-Synthetic Aromatic Amine Derivatives - Kibrnesh Bezu; Daniel Bisrat; Kaleab Asres (Pharmacognosy Journal, 2015)
Background: In less developed countries like Ethiopia, malaria is traditionally treated by remedies prepared from medicinal plants. One such plant that falls in this category is Embelia schimperi Vatke whose fruits are employed for the treatment of a variety of ailments including taeniasis and malaria. Objective: In the present study, the in vivo antimalarial activity of embelin isolated from the fruits of Embelia schimperi Vatke and its semisynthetic aromatic amine derivatives was evaluated. Methods: Silica gel column chromatography was used to isolate embelin from the ethyl acetate extract of the fruits of E. schimperi. Aromatic substituted embelin derivatives were semi-synthesized by using a one-step condensation reaction of embelin with aromatic amines. The compounds were characterized based on their UV, IR, HR-ESIMS, 1H and 13C NMR and DEPT-135 spectral data. Antimalarial activity was evaluated using a modified Peter’s 4-day suppressive test against chloroquine sensitive Plasmodium berghei infection in mice. Results: Embelin and the semi-synthetic derivatives showed significant (p<0.05) in vivo antimalarial activity in a dose-dependent manner with 47.8-74.7% parasite suppression at tested doses of 100-400 mg/kg. Among the compounds semi-synthesized, 5-(p-tolylamino)-2-hydroxy-3-undecylcyclohexa- 2,5-diene-1,4-dione showed maximum antimalarial activity (74.7 % suppression) at a dose of 400 mg/kg. No major signs of toxicity were observed when either embelin or the semi-synthesized derivatives were administrated to mice at the highest tested dose (2 g/kg). Conclusion: The results underline that the antimalarial activity of embelin can be improved by preparing its aromatic semi-synthetic amine derivatives without affecting the safety of the parent molecule.
Keywords: A 4-Day suppressive test; Antimalarial; Aromatic substituted embelin; Embelia schimperi; Embelin.

In vivo Antimalarial Evaluation of Embelin and its Semi-Synthetic Aromatic Amine Derivatives - Kibrnesh Bezu; Daniel Bisrat; Kaleab Asres (Pharmacognosy Journal, 2015)
Background: In less developed countries like Ethiopia, malaria is traditionally treated by remedies prepared from medicinal plants. One such plant that falls in this category is Embelia schimperi Vatke whose fruits are employed for the treatment of a variety of ailments including taeniasis and malaria. Objective: In the present study, the in vivo antimalarial activity of embelin isolated from the fruits of Embelia schimperi Vatke and its semi-synthetic aromatic amine derivatives was evaluated. Methods: Silica gel column chromatography was used to isolate embelin from the ethyl acetate extract of the fruits of E. schimperi. Aromatic substituted embelin derivatives were semi-synthesized by using a one-step condensation reaction of embelin with aromatic amines. The compounds were characterized based on their UV, IR, HR-ESIMS, 1H and 13C NMR and DEPT-135 spectral data. Anti-malarial activity was evaluated using a modified Peter’s 4-day suppressive test against chloroquine sensitive Plasmodium berghei infection in mice. Results: Embelin and the semi-synthetic derivatives showed significant (p<0.05) in vivo anti-malarial activity in a dose-dependent manner with 47.8-74.7% parasite suppression at tested doses of 100-400 mg/kg. Among the compounds semi-synthesized, 5-(p-tolylamino)-2-hydroxy-3-undecylcyclohexa-2,5-diene-1,4-dione showed maximum anti-malarial activity (74.7% suppression) at a dose of 400 mg/kg. No major signs of toxicity were observed when either embelin or the semi-synthesized derivatives were administrated to mice at the highest tested dose (2 g/kg). Conclusion: The results underline that the antimalarial activity of embelin can be improved by preparing its aromatic semi-synthetic amine derivatives without affecting the safety of the parent molecule. Key words:Embelia schimperi, Embelin, Aromatic substituted embelin, Anti-malarial.
Keywords: Anti-malarial.; Aromatic substituted embelin; Embelia schimperi; Embelin

Inhibition of Bacillus anthracis growth by Australian native plants used traditionally as antibacterial medicines - Mitchell Henry Wright; Anthony Carlson Greene; Ian Edwin Cock (Pharmacognosy Journal, 2015)
Introduction: Anthrax is a zoonotic disease caused by the bacterium Bacillus anthracis. It is often fatal if left untreated. Many Australian plants have documented therapeutic properties as general antiseptics, inhibiting the growth of a wide variety of bacterial species. This study examines the ability of selected Australian plant extracts to inhibit B. anthracis growth. Methods: Solvent extracts were prepared using plants with documented ethnobotanical usage to treat bacterial infections, or published antibacterial activity. The extracts were investigated by disc diffusion assay for the ability to inhibit the growth of an environmental strain of B. anthracis. Their MIC values were determined to quantify and compare their efficacies. Toxicity was determined using the Artemia franciscana nauplii bioassay. Results: Methanolic and aqueous extracts of Eucalyptus baileyana and Eucalyptus major displayed potent antibacterial activity in the disc diffusion assay against B. anthracis. The methanolic extracts were particularly potent with MIC values as low as 290 μg/mL (E. major methanolic extract). Tasmannia insipidia and Tasmannia stipitata extracts also inhibited B. anthracis growth, albeit with low efficacy. The E. baileyana and E. major methanolic leaf extracts as well as the E. baileyana aqueous leaf extract induced significant mortality in the Artemia fransiscana bioassay, with LC50 values substantially <1000 μg/mL, indicating the toxicity of these extracts. Conclusion: The potent inhibitory bioactivity of the E. baileyana and E. major extracts against B. anthracis demonstrate their potential as medicinal agents in the treatment and prevention of anthrax. However, their toxicity indicates that their use may be limited to the treatment of the cutaneous form of the disease, or for sterilisation of infected sites.
Keywords: Anthrax; Antibacterial activity; Bacillus anthracis; Eucalyptus; Scaevola spinescens; Tasmannia stipitata; Traditional medicine.; Zoonotic

Inhibition on Urease and Thermal Induced Protein Denaturation of commonly used Antiulcer Herbal Products. Study based on in-vitro assays - Haroon Khan; Murad Ali Khan; Abdul Rauf; Ashhad Haleemi; Shivkanya Fuloria; Neeraj Kumar Fuloria (Pharmacognosy Journal, 2015)
Background: In-vitro urease inhibitory and thermal induced protein denaturation inhibitory activities was performed for two commonly used herbal products Endemali and Akseer ULCER in the treatment of ulcers. Objectives: To evaluate the antiulcer potential of two commonly used herbal products, Endemali, Akseer ULCER. Material and Method: In urease inhibitory assay, enzyme solution, extract, diferent regaents added and absorbance was measured at 630 nm (50 min, pH 8.2) and thiourea used as standard. In protein denaturation assay, the egg albumin was mixed with different concentration of test compounds, buffer absorbance was measured. Aspirin was used as standard. Results: The Endemali had a profound effect on the urease activity in a concentration dependent manner with EC50value of 0.468 mg/ml. The Akseer ULCER antagonized the urease activity markedly with EC50 value of 0.374 mg/ml. These tested herbal products caused marked inhibition of thermal induced protein denaturation in a concentration dependent manner. The potency in the form of EC50 for Endemali, Akseer ULCER was measured as 323, 337 μg/ml respectively. Conclusion: In short, the tested herbal drug showed strong inhibition on urease activity and inhibition on thermal induced protein denaturation thus our study validated their uses in the treatment of ulcers.
Keywords: Akseer ULCER; Antiurease activity; Endemali; in-vitro assay; Thermal induced protein denaturation.

Inhibition on Urease and Thermal Induced Protein Denaturation of commonly used Antiulcer Herbal Products. Study based on in-vitro assays - Haroon Khan; Murad Ali Khan; Abdul Rauf; Ashhad Haleemi; Shivkanya Fuloria; Neeraj Kumar Fuloria (Pharmacognosy Journal, 2015)
Background: In-vitro urease inhibitory and thermal induced protein denaturation inhibitory activitieswasperformed for two commonly used herbal productsEndemali and Akseer ULCER in the treatment of ulcers.Objectives: to evaluate the antiulcer potential of two commonly used herbal products, Endemali, Akseer ULCER. Material and Method: In urease inhibitory assay , enzyme solution, extract, diferentregaents added and absorbance was measured at 630 nm (50 min, pH 8.2) and thiourea used as standard. In protein denaturation assay the egg albumin was mixed with different concentration of test compounds, buffer absorbance was measured. Aspirin was used as standard. Results: The Endemalihad a profound effect on the urease activity in a concentration dependent manner with EC50 valueof 0.468 mg/ml. The Akseer ULCER antagonized the urease activity markedly with EC50 value of 0.374 mg/ml.These tested herbal products caused marked inhibition of thermal induced protein denaturation in a concentration dependent manner. The potency in the form of EC50 for Endemali, Akseer ULCER was measured as 323, 337 µg/mlrespectively. Conclusion: In short, the tested herbal drug showed strong inhibition on urease activity and inhibition on thermal induced protein denaturation thus our study validated their uses in the treatment of ulcers. Key words: Akseer ULCER, Endemali, Antiurease activity, Thermal induced protein denaturation.
Keywords: Akseer ULCER; Antiurease activity; Endemali; Thermal induced protein denaturation.

Iron Reducing and Radical Scavenging Activities of 13 Medicinal Plants From Côte d’Ivoire - Ehouman Evans; Koné Mamidou Witabouna; Bakayoko Adama; Tra Bi Fézan Honora (Pharmacognosy Journal, 2015)
Oxidative stress has been involved in the development of varied human diseases. The aim of this study was to evaluate the iron reducing power and the antiradical activity of 13 plants traditionally used as medicinal plants in Côte d’Ivoire. FRAP (ferric reducing antioxidant power) and ABTS (2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)) assays were used to assess the antioxidant property of 80 % methanol extracts prepared from the 13 plants. A high iron reducing activity was exhibited by extracts from leaves of Leea guineensis (42.76 ± 28.54 mg of TE/gdry extract) and Bersama abyssinica (39.77 ± 31.29 mg of TE/g dry extract). Smeathmannia pubescens (% ABTS = 92.44 ± 12.93 %), L. guineensis (%ABTS = 89.73 ± 15.10 %), Keetia venosa (% ABTS = 88.78 ± 17.36 %) and Sapium ellipticum (% ABTS = 85.86 ± 25.10 %), showed promising antiradical activity with IC50 values of 4.50, 5.00, 5.40 and 5.70 µg/mL respectively. These values are (p< 0.05) close to those of Trolox (CI50 = 4.10 µg/mL) and ascorbic acid (CI50 = 4.90 µg/mL). Our findings confirm the traditional use of the studied plants in treatment of various ailments. The results obtained provide promising baseline information for using these medicinal plants for improving the health status of the population. Key words: ABTS, Antioxidants, Côte d’Ivoire, FRAP, Medicinal plants

Iron Reducing and Radical Scavenging Activities of 13 Medicinal Plants From Côte d’Ivoire - Ehouman Evans; Koné Mamidou Witabouna; Tra Bi Fézan Honora; Bakayoko Adama (Pharmacognosy Journal, 2015)
Objective: Oxidative stress has been involved in the development of varied human diseases. The aim of this study was to evaluate the iron reducing power and the antiradical activity of 13 plants traditionally used as medicinal plants in Côte d’Ivoire. Materials and Methods: FRAP (ferric reducing antioxidant power) and ABTS (2,2’-azino-bis(3-ethylbenzothiazoline- 6-sulfonic acid)) assays were used to assess the antioxidant property of 80% methanol extracts prepared from the 13 plants. Results: A high iron reducing activity was exhibited by extracts from leaves of Leea guineensis (42.76 ± 28.54 mg of TE/gdry extract) and Bersama abyssinica (39.77 ± 31.29 mg of TE/g dry extract). Smeathmannia pubescens (% ABTS = 92.44 ± 12.93%), L. guineensis (%ABTS = 89.73 ± 15.10%), Keetia venosa (% ABTS = 88.78 ± 17.36 %) and Sapium ellipticum (%ABTS = 85.86 ± 25.10%), showed promising antiradical activity with IC50 values of 4.50, 5.00, 5.40 and 5.70 μg/mL respectively. These values are (p < 0.05) close to those of Trolox (CI50 = 4.10 μg/mL) and ascorbic acid (CI50 = 4.90 μg/mL). Conclusion: Our findings confirm the traditional use of the studied plants in treatment of various ailments. The results obtained provide promising baseline information for using these medicinal plants for improving the health status of the population.
Keywords: ABTS; Antioxidants; Côte d’Ivoire; FRAP; Iron.; Medicinal plants

Jackfruit (Artocarpus heterophyllus) seed extract exhibits fibrino(geno)lytic activity - Sowmyashree Gangaraju; Bhagyalakshmi Manjappa; Girish Kesturu Subbaiah; Kemparaju Kempaiah (Pharmacognosy Journal, 2015)
Objective: The current study assesses the fibrinogen and fibrin clot hydrolyzing activities of aqueous seed extract of Jackfruit (AqSEJ). Methods: The protein banding pattern of AqSEJ (100 μg) was analyzed on SDS-PAGE. The proteolytic activity of AqSEJ was confirmed by spectrophotometer and zymography experiments. Fibrinogen, fibrin and plasma protein hydrolyzing activities of AqSEJ were analyzed on SDS-PAGE under reduced conditions. Plasminogen activation and indirect hemolytic activities was analyzed using spectrophotometer. The non-toxic property of AqSEJ was tested by edema, hemorrhage in experimental mice. Results: AqSEJ exhibited proteolytic activity and the specific activity was found to be 1.04 units/mg/min. Furthermore, AqSEJ non-specifically hydrolyzed Aα, followed by Bβ and γ chains of human fibrinogen and specifically hydrolyzed α polymer and α chain of partially cross linked human fibrin clot without affecting β chain and γ-γ dimer even up to the tested dose of 30 µg for the incubation period of 8 hours. Importantly, AqSEJ did not hydrolyze other plasma proteins and devoid of plasminogen activation property. The proteolytic activity of AqSEJ was completely neutralized by PMSF and IAA, while EDTA, EGTA, 1,10-Phenanthroline did not, suggesting the presence of serine and cysteine family proteases. Moreover, AqSEJ did not cause edema and hemorrhage in experimental mice up to the tested dose of 200 µg and nontoxic to RBC cells. Conclusion: AqSEJ hydrolyzes fibrinogen and fibrin clot and non-toxic in nature. Hence, this work showcases the potential applications of Jack fruit seed proteases in the treatment of thrombotic disorders. Key words: Fibrino(geno)lysis, Hemostasis, Jackfruit, Moraceae, Non-hemorrhagic, Serine/cysteine protease.
Keywords: Fibrino(geno)lysis; Hemostasis; Jackfruit; Moraceae; Non-hemorrhagic; Serine/cysteine protease.

Jackfruit (Artocarpus heterophyllus) seed extract exhibits fibrino(geno)lytic activity - Sowmyashree Gangaraju; Bhagyalakshmi Manjappa; Girish Kesturu Subbaiah; Kemparaju Kempaiah; Rangaiah Shashidharamurthy; Jane Hoover Plow; Sebastin Santhosh Martin; Manohar Shinde; Devaraja Sannaningaiah (Pharmacognosy Journal, 2015)
Objective: The current study assesses the fibrinogen and fibrin clot hydrolyzing activities of aqueous seed extract of Jackfruit (AqSEJ). Methods: The protein banding pattern of AqSEJ (100 μg) was analyzed on SDS-PAGE. The proteolytic activity of AqSEJ was confirmed by spectrophotometer and zymography experiments. Fibrinogen, fibrin and plasma protein hydrolyzing activities of AqSEJ were analyzed on SDS-PAGE under reduced conditions. Plasminogen activation and indirect hemolytic activities was analyzed using spectrophotometer. The non-toxic property of AqSEJ was tested by edema, hemorrhage in experimental mice. Results: AqSEJ exhibited proteolytic activity and the specific activity was found to be 1.04 units/mg/min. Furthermore, AqSEJ non-specifically hydrolyzed Aα, followed by Bβ and γ chains of human fibrinogen and specifically hydrolyzed α polymer and α chain of partially cross linked human fibrin clot without affecting β chain and γ-γ dimer even up to the tested dose of 30 µg for the incubation period of 8 hours. Importantly, AqSEJ did not hydrolyze other plasma proteins and devoid of plasminogen activation property. The proteolytic activity of AqSEJ was completely neutralized by PMSF and IAA, while EDTA, EGTA, 1,10-Phenanthroline did not, suggesting the presence of serine and cysteine family proteases. Moreover, AqSEJ did not cause edema and hemorrhage in experimental mice up to the tested dose of 200 µg and non-toxic to RBC cells. Conclusion: AqSEJ hydrolyzes fibrinogen and fibrin clot and non-toxic in nature. Hence, this work showcases the potential applications of Jack fruit seed proteases in the treatment of thrombotic disorders.
Keywords: Fibrino(geno)lysis; Hemostasis; Jackfruit; Moraceae; Non-hemorrhagic; Serine/cysteine protease.

Morphological and anatomical investigations of Vicia truncatula Fish. ex Bieb. - Fatima Kazbekovna Serebryanaya; Oksana Michailovna Sharenko; Michail Alexandrovich Serkov (Pharmacognosy Journal, 2015)
Introduction: Micromorphological research of vegetative bodies of Vicia truncatula Fish. ex Bieb. as a source of a sum of diosmetine biozides (flavicine) with high antioxidant hepatoprotective and endothelial-protective activities. We have identified the main diagnostic signs of vegetative bodies which can be used when standard documentation on medicinal vegetable raw materials compile. Materials and Methods: The objects of the study were collected in North Caucasus (Russia) in June 2013-2014. Materials morphological study herbarium specimens were stored in the herbarium fund the Department of Botany (acronym PGFA). Materials micromorphological study were temporary slides are the root, leaf, stem and flowers. Results: The morphological results were compared with the Flora of the USSR. Anatomical characters of leaves and stems of the species were observed to be similar to the usual features of genus Vicia anatomy. All results are supported by photographs. The stomatal apparatus belongs to anomocytic and paracytic types, simple multicellular hairs. Conclusion: we would like to note that these investigations are one of the phases of Vicia truncatula Fish. ex Bieb. examination and the medicinal plant is considered to be a perspective source of flavicine. The morphological and anatomical research obtained data can be used in standard documentation for medicinal vegetable raw material compiling. Key words: Anatomy, Morphological and Anatomical investigations, Morphology, Vicia truncatula Fish. ex Bieb.
Keywords: Morphological and Anatomical investigations; Vicia truncatula Fish. ex Bieb.

Morphological and anatomical investigations of Vicia truncatula Fish. ex Bieb - Fatima Kazbekovna Serebryanaya; Oksana Michailovna Sharenko; Michail Alexandrovich Serkov (Pharmacognosy Journal, 2015)
Introduction: Micromorphological research of vegetative bodies of Vicia truncatula Fish. ex Bieb. as a source of a sum of diosmetine biozides (flavicine) with high antioxidant hepatoprotective and endothelial-protective activities. We have identified the main diagnostic signs of vegetative bodies which can be used when standard documentation on medicinal vegetable raw materials compile. Materials and Methods: The objects of the study were collected in North Caucasus (Russia) in June 2013-2014. Materials morphological study herbarium specimens were stored in the herbarium fund the Department of Botany (acronym PGFA). Materials micromorphological study were temporary slides are the root, leaf, stem and flowers. Results: The morphological results were compared with the Flora of the USSR. Anatomical characters of leaves and stems of the species were observed to be similar to the usual features of genus Vicia anatomy. All results are supported by photographs. The stomatal apparatus belongs to anomocytic and paracytic types, simple multicellular hairs. Conclusion: we would like to note that these investigations are one of the phases of Vicia truncatula Fish. ex Bieb. examination and the medicinal plant is considered to be a perspective source of flavicine. The morphological and anatomical research obtained data can be used in standard documentation for medicinal vegetable raw material compiling.
Keywords: Anatomy; Morphological and Anatomical investigations; Morphology; Vicia truncatula Fish. ex Bieb.

Pharmacognostic and free radical scavenging Evaluation of Cyathula prostata (Blume) L. - Mubo Adeola Sonibare; Oluwaseun Victoria Olatubosun (Pharmacognosy Journal, 2015)
Background: Cyathula prostrata (Blume) L. from the family Amaranthaceae has been used traditionally for rheumatism, dysentery, wounds and urethral discharges in the tropical regions of the world. Aim: The present study was undertaken to perform quality control standardization and to evaluate antioxidant activity of the leaf, stem, root and the whole plant of Cyathula prostrata. Methods: Macroscopic and microscopic evaluations were carried out on the plant using standard procedures. Powdered sample of the leaf was evaluated with various organic solvents for fluorescence. The chloroform, ethyl-acetate and methanolic extracts of the leaf, stem, root and whole plant were subjected to various pharmacognostic analyses and evaluated for in vitro antioxidant activity using DPPH assay.Further, thin layer chromatoghraphy was used to evaluate the chloroform extract. Results: Important epidermal features in the plant include: coastal cells, unbranched, uniseriate, multicellular and non-glandular trichomes. Leaves are amphistomatic showing mostly anomocytic and actinocytic stomata. Starch grains are restricted to the adaxial surface. Vascular bundles are mainly collateral and well-developed bundle sheath. The transverse section of stem is circular, hypodermis (1-3 layers). Cross section of the root is described in detail for the plant. Cortex has angular cells. Fluorescence studies showed different colours. Physico-chemical results are comparable with standards. The TLC profile showed presence of at least seven compounds in the leaf, root and the whole plant extracts, while nine components were obtained from the stem extract. The ethyl acetate extract of the root and ethanol extract of the stem gave the highest phenolic contents (30.09±3.768 mg GAE/g) and DPPH free radical scavenging activity (87.0 ± 0.208), respectively. Conclusion: The distinctive features established in this study are steps in identification, standardization and quality control of this medicinal plant.
Keywords: Cyathula prostrata; antioxidant; microscopy; Physicochemical parameters; standardization

Pharmacognostic and free radical scavenging Evaluation of Cyathula prostata l. (Blume) - Mubo Adeola Sonibare; Oluwaseun Victoria Olatubosun (Pharmacognosy Journal, 2015)
Background:Cyathula prostrata (Blume) L. from the family Amaranthaceae has been used traditionally for rheumatism, dysentery, wounds and urethral discharges in the tropical regions of the world. Aim: The present study was undertaken to perform quality control standardization and to evaluate antioxidant activity of the leaf, stem, root and the whole plant of Cyathula prostrata. Methods: Macroscopic and microscopic evaluations were carried out on the plant using standard procedures. Powdered sample of the leaf was evaluated with various organic solvents for fluorescence. The chloroform, ethyl-acetate and methanolic extracts of the leaf, stem, root and whole plant were subjected to various pharmacognostic analyses and evaluated for in vitro antioxidant activity using DPPH assay.Further, thin layer chromatoghraphy was used to evaluate the chloroform extract. Results: Important epidermal features in the plant include: coastal cells, unbranched, uniseriate, multicellular and non-glandular trichomes. Leaves are amphistomatic showing mostly anomocytic and actinocytic stomata. Starch grains are restricted to the adaxial surface. Vascular bundles are mainly collateral and well-developed bundle sheath. The transverse section of stem is circular, hypodermis (1-3 layers). Cross section of the root is described in detail for the plant. Cortex has angular cells. Fluorescence studies showed different colours. Physico-chemical results are comparable with standards. The TLC profile showed presence of at least seven compounds in the leaf, root and the whole plant extracts, while nine components were obtained from the stem extract. The ethyl acetate extract of the root and ethanol extract of the stem gave the highest phenolic contents (30.09±3.768 mg GAE/g) and DPPH free radical scavenging activity (87.0 ± 0.208), respectively. Conclusion: The distinctive features established in this study are steps in identification, standardization and quality control of this medicinal plant. Key words:Cyathula prostrata, standardization, microscopy, physicochemical parameters, antioxidant.
Keywords: Antioxidant.; Cyathula prostrata; microscopy; Physicochemical parameters; Standardization.

Pharmacognostic Evaluation of Indigenous Medicinal Plant Kedrostis foetidissima (Jacq.) Cogn - Kavitha R; Chittibabu CV; Subha TS (Pharmacognosy Journal, 2015)
Introduction: Ingeneral, members of Cucurbitaceae are well exploited for their medicinal, economic and culinary values, however few of them are less exploited. The present study deals with pharamcognostical evaluation of one such plant namely Kedrostis foetidissima (Jacq.) Cogn.called as Appakovai in Tamil. Methods: Pharmacognostic evaluations were carried out by organoleptic evaluation, anatomical studies and powder microscopy of leaves, roots and root tubers. Results: Organoleptic evaluation revealed that the characteristic white tubers, as storage organs, leaves exhibited a foetidodour when crushed. Anatomy of leaves showed lithocysts and anomocytic stomata, root showed the presence of fissured periderm and cleaved vascular bundles and that of root tubers showed 3 or 4 exarch xylem. Powder microscopy of root tubers showed narrow and wide fibers; long, narrow and drum shaped vessels and scattered sclereids. Conclusion: The present Pharmacognostic and Powder microscopic studiesreveals that, the characteristic features of this plantparts resembles, the other members of cucurbitaceae.
Keywords: Kedrostis foetidissima; Pharmacognosy; Powder microscopy.

Pharmacognostic Evaluation of Indigenous Medicinal Plant Kedrostis foetidissima (Jacq.) Cogn. - Kavitha R; Chittibabu CV; Subha TS (Pharmacognosy Journal, 2015)
Introduction: Ingeneral, members of Cucurbitaceae are well exploited for their medicinal, economic and culinary values,however few of them are less exploited.The present study deals with pharamcognostical evaluation ofone such plant namely Kedrostis foetidissima (Jacq.) Cogn.called as Appakovai in Tamil. Methods: Pharmacognostic evaluationswere carried out by organoleptic evaluation, anatomical studies and powder microscopy of leaves, roots and root tubers. Results: Organoleptic evaluation revealed that the characteristic white tubers, as storage organs, leaves exhibited a foetid odour when crushed. Anatomy of leaves showed lithocysts and anomocytic stomata,root showed the presence of fissured periderm and cleaved vascular bundlesand that of root tubers showed 3 or 4 exarch xylem. Powder microscopy of root tubers showed narrow and wide fibers; long, narrow and drum shaped vessels and scattered sclereids. Conclusion: The present Pharmacognostic and Powder microscopic studiesreveals that, the characteristic features of this plantparts resembles, the other members of cucurbitaceae. Key words:Kedrostis foetidissima, Pharmacognosy, Powder microscopy.
Keywords: Kedrostis foetidissima; Pharmacognosy; Powder microscopy.

Pharmacognostic specifications and quantification of oleanolic acid and lupeol in Mollugo oppositifolia Linn. - Karuna Modi; Mamta Shah (Pharmacognosy Journal, 2015)
Background: Mollugo oppositifolia, is one of the plants commonly used as, ‘Parpata’ by Ayurvedic practitioners. It is indicated as a bitter tonic, antiseptic and febrifuge. Aim: To generate and ensemble data of physical parameters for ascertaining the identification and to develop validated HPTLC method for quantification of oleanolic acid and lupeol in M. oppositifolia. Materials and Methods:M. oppositifolia was studied for establishing pharmacognostic standards including macro and microscopical characters, physico-chemical analysis and quantification of oleanolic acid and lupeol by HPTLC method. Results: It is an annual, prostrate herb with linear-lanceolate leaf and white coloured flower. Microscopically root can be characterized by crescent shaped phloem associated with continuous or discontinuous rings of xylem; stem by epidermis bearing multi-cellular simple and glandular trichomes, and sclerenchymatous pericycle; and leaf by continuous band of a palisade cells and rosettes and prisms of calcium oxalate throughout parenchyma. Powdered drug can be typified by multi-cellular trichomes, fragments of epidermis of leaf in surface view, epidermis of corolla and entire or broken seeds. Saponins and flavanoids were found be the major components. HPTLC method was developed for quantification of oleanolic acid and 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. The amount of oleanolic acid and lupeol were found to be 0.027-0.029% w/w and 0.015-0.016% w/w respectively. Conclusion: The quality parameters and HPTLC method developed would serve as useful gauge in standardization of Mollugo oppositifolia.   Key words: HPTLC, Lupeol, Mollugo oppositifolia, Oleanolic acid.
Keywords: HPTLC; Lupeol; Mollugo oppositifolia; Oleanolic acid.