Preclinical evaluation of antidiabetic activity of poly herbal plant extract in streptozotocin induced diabetic rats

Similar documents
ANTI-DIABETIC ACTIVITY OF HELICTERES ISORA ROOT

Murugan M. et al / Journal of Pharmaceutical Science and Technology Vol. 1 (2), 2009, 69-73

Abstract. Introduction

EVALUATION OF ANTIDIABETIC ACTIVITY OF TRIUMFETTA PILOSA ROTH IN STREPTOZOTOCIN- INDUCED DIABETIC RATS

IJBCP International Journal of Basic & Clinical Pharmacology. Antidiabetic activity of Plumeria rubra L. in normal and alloxan induced diabetic mice

Toxicity, Acute and Longterm Anti-Diabetic Profile of Methanolic Extract of Leaves of Pterocarpus Marsupium on Alloxan Induced Diabetic Albino Rats

Mango Modulates Body Fat and Plasma Glucose and Lipids in Mice Fed High Fat Diet

Antidiabetic and Hypoglycaemic Activity of the Crude Extracts of the Plant Leucas Aspera

ANTI-DIABETIC ACTIVITY OF RIBES NIGRUM FRUIT EXTRACT IN ALLOXAN INDUCED DIABETIC RATS

International Journal of Research in Pharmacology & Pharmacotherapeutics

THE EVALUATION OF THE ANTIDIABETIC EFFECT OF COCCINIA INDICA LEAVES EXTRACT IN STREPTOZOTOCIN INDUCED DIABETES IN RATS

Available online through ISSN

Pharmacologyonline 2: (2009) Pharmacodynamic Drug Interaction of Gliclazide and Mexiletine in Rats

Effect of Coriandrum sativum, a common herbal medicine, on endocrine and reproductive organ structure and function

Therapeutic effect of flavonoid rich extract of apricots on high-fat diet induced hyperlipidemia in rabbits

Antihyperglycemic Activity of Trianthema Portulacastrum Plant in Streptozotocin Induced Diabetic Rats

S. KUMAR 1 * and A. YADAV 2. Department of Pharmacology, Kalinga Institute of Medical Sciences, Bhubaneswar, Odisha, India. 2

HYPOGLYCAEMIC ACTIVITY OF THE LEAVES EXTRACTS OF BERSAMA ENGLERIANA IN RATS.

Comparative efficacy of Telakucha (Coccinia indica) leaves and Amaryl (R) Tablet (Glimepiride) in induced diabetes mellitus in rat

Journal of Chemical and Pharmaceutical Research

The Use of Sea Buckthorn (Hippophae rhamnoides) and Milk Thistle (Silybum marianum) in Alloxan Induced Diabetes Mellitus in Rats

The Pharmaceutical and Chemical Journal, 2018, 5(4): Research Article

Antidiabetic Activity of Alcoholic Extract of Neem (Azadirachta Indica) Root Bark

Effect of D-400, a Herbal Formulation, on Blood Sugar of Normal and Alloxan-induced Diabetic Rats

Antiobesity effect of Lipovedic formulation in rats fed on atherogenic diet

ANTIDIABETIC ACTIVITY OF KOVAI KIZHANGU CHOORANAM IN ALLOXAN INDUCED DIABETIC RATS ABSTRACT

Pharmacologyonline 3: (2009) I VESTIGATIO OF A TIHYPERGLYCEMIC EFFECT OF MORUS IGRA O BLOOD GLUCOSE LEVEL I STREPTOZOTOCI DIABETIC RATS

Hypoglycemic Activity of Seerankottai Thiravam (Semicarpus Anacardium. Linn) in Alloxan Induced Diabetic Rats

SCIFED. Publishers. SciFed Journal of Public Health. Comparing Modified and Relationship Study of Gymnema Sylvestre Against Diabetes

EFFECTS OF CAPSICUM FRUTESCENS SUPPLEMENTED DIET ON LIPID PROFILE OF WISTAR RAT.

The Endocrine Pancreas (Chapter 10) *

Synergic Activity of Fenugreek seeds and Neem leaf extracts against Alloxan induced diabetic rats.

ANTIHYPERGLYCEMIC ACTIVITY OF METHANOLIC EXTRACT OF MADHUCA LONGIFOLIA BARK

International Journal of Pharma and Bio Sciences

EFFECT OF DYKURE A POLYHERBAL FORMULATION ON TYPE-I AND TYPE-II DIABETES

Interaction of Momordica charantia with Metformin in Diabetic Rats

Control of Glucose Metabolism

Sakun Publishing House (SPH): IJPLS. Research Article Yadav et al., 7(12): Dec., 2016: ] CODEN (USA): IJPLCP ISSN:

HYPOGLYCAEMIC ACTION OF THE FLAVONOID FRACTION OF ARTOCARPUS HETEROPHYLLUS LEAF

Hyperlipidemia. Prepared by : Muhannad Mohammed Supervisor professor : Dr. Ahmed Yahya Dallalbashi

Antidiabetic Activity of Maesa indica (Roxb.) Stem Bark in Streptozotocin Induced Diabetic Rats

IMPACT OF APPLE CIDER VINEGAR ON DIFFERENT BIOMARKERS, FOR REDUCING TYPE 2 DIABETES MELLITUS CONDITION

EFFECT OF MULBERRY (MORUS INDICA) LEAVES AND BARK ON TYPE 2 DIABETICS

Evaluation of hypoglycemic and antihyperglycemic effects of Luffa cylindrica fruit extract in rats

Effect of herbal medicine Dia-No on clinical and biochemical parameters of metabolic syndrome

THE SIGNIFICANCE OF TRIGONELLA FOENUM-GRACEUM ON DIABETES MELLITUS: EFFECT ON LIPID CONCENTRATION IN BLOOD OF MALE SWISS ALBINO MICE

History of Investigation

Evaluation of Calotropis Gigantea (l.) and S. Indicus on Glycemia and Lipidemia in Sterptozotocin induced Diabetic Rats

Week 3 The Pancreas: Pancreatic ph buffering:

Pharmacologyonline 1: (2009) HYPOGLYCEMIC EFFECT OF PHOEBE LA CEOLATA O ALLOXA -I DUCED DIABETIC MICE

Original Article. Hepatoprotective effect of tualang honey supplementation in streptozotocin-induced diabetic rats

( Received on June 8, 2011 )

IMPACT OF NATUAL ANTIOXIDANT ON REDUCTION OF OXIDATIVE STRESS IN HYPERGLYCEMIC RAT FED GERMINATED PIGEON PEA DIET

Pharmacologyonline 3: (2009)

2017, Pharmapex USA, A Member of Apex Group of Companies

Effects of Luffa acutangula L. (Cucurbitaceae) Fruit Extract on the Blood. Lipid Profile of Albino Rats

The article can be downloaded from 1

Antihyperglycemic Activity Evaluation of Antidiabetic Herbal Formulations on Alloxan Induced Rats

Hormonal Regulations Of Glucose Metabolism & DM

. Research Article ISSN: X Antidiabetic profile of CINNAMON powder extract in experimental Diabetic animals

Dr. Ranjit Kumar. Scientist I Mahavir Cancer Institute & Research Centre, Phulwarisharif, Patna (Bihar), India

THE EFFECT OF VITAMIN-C THERAPY ON HYPERGLYCEMIA, HYPERLIPIDEMIA AND NON HIGH DENSITY LIPOPROTEIN LEVEL IN TYPE 2 DIABETES

A study on the effects of Moringa oleifera lam. pod extract on alloxan induced diabetic rats

18. PANCREATIC FUNCTION AND METABOLISM. Pancreatic secretions ISLETS OF LANGERHANS. Insulin

International Journal of Pharma and Bio Sciences V1(2)2010

INTERNATIONAL JOURNAL OF PHARMACEUTICAL AND CHEMICAL SCIENCES

CARBOHYDRATE METABOLISM Disorders

Toxicological Assessments of Piper nigrum on Alloxan Induced Diabetic Rats

Rat Diabetic Blood Glucose Level Profile with Stratified Dose Streptozotocin (SD-STZ) and Multi Low Dose Streptozotocin (MLD-STZ) Induction Methods

Effect of Urtica dioica Leaf Alcoholic and Aqueous Extracts on the Number and the Diameter of the Islets in Diabetic Rats

Prof. Patrick E. Ebong

AN EXPERIMENTAL STUDY OF SWARNA MAKSHIKA BHASMA AS ANTI DIABETIC MEDICINE

UNIVERSITY OF PNG SCHOOL OF MEDICINE AND HEALTH SCIENCES DIVISION OF BASIC MEDICAL SCIENCES DISCIPLINE OF BIOCHEMISTRY AND MOLECULAR BIOLOGY

Clinical abstracts. Diabetes

Herbal Products: A Novel Approach for Diabetic Patients

Summary and Conclusions

PHARMA SCIENCE MONITOR AN INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES COMPARATIVE ANTIDIABETIC ACTIVITY OF SOME HERBAL PLANTS EXTRACTS

Oil Palm Phenolics and Diabetes: Lessons from the Nile Rat

DEVELOPMENT OF NEW ANIMAL MODELS FOR TYPE 2 DIABETES MELLITUS AND PHARMACOLOGICAL SCREENING

Written By Charles Poliquin of Poliquin Performance

Diabetes Review. October 31, Dr. Don Eby Tracy Gaunt Dwayne Cottel

Diabetes Mellitus. Raja Nursing Instructor. Acknowledgement: Badil 09/03/2016

Combining Complex Pathophysiologic Concepts: Diabetes Mellitus

associated with serious complications, but reduce occurrences with preventive measures

Anti diabetic activity of Zizipus mauritiana Lam. In streptozotocin induced Diabetic Rats and its comparison with some standard flavonoids

RESEARCH ARTICLE. Received on: 08/02/2017 Published on:27/03/2017

Hypolipidemic effect of Terminalia arjuna (L.) in experimentally induced hypercholesteremic rats

METABOLISM CATABOLIC Carbohydrates Lipids Proteins

Assessment of antihyperglycemic and antihyperlipidemic activity of common ayurvedic formulation in alloxan- induced diabetic rabbits.

Journal of Chemical and Pharmaceutical Research

Jehan, A. El-Shourbagy 1 and I. S. Ashoush 2

The Antidiabetic Potentials of the Methanolic Seed Extract of Buchhlozia Coriacea

Modulatory effect of sweet almond extract on serum lipids, lipid peroxidation and histology of pancreas in alloxan-induced diabetic rats

What is Diabetes Mellitus?

Received: 10 March 2014, Accepted: 30 May 2014, Published Online: 19 June 2014 Abstract

Effect of D-400, an Ayurvedic Herbal Formulation on Experimentally-induced Diabetes Mellitus

Spontaneously Diabetic Torii Lepr fa (SDT Fatty) Rat: A Novel Model of Obese Type 2 Diabetes

Effect of Ethanolic Extract of Pterocarpus marsupium Root on Alloxan-Induced Diabetic Rats

Discussion & Conclusion

Transcription:

2016; 5(2): 45-49 Online at: www.phytopharmajournal.com Research Article ISSN 2230-480X JPHYTO 2016; 5(2): 45-49 March- April 2016, All rights reserved Dr. P.P. Gupta Professor, Department of Pharmacology, All India Institute of Medical Sciences (AIIMS), Patna, Bihar-801505, India Dr. J. Haider Associate Professor, Department of Pharmacology, BRD Medical College, Gorakhpur, Uttar Dr. R.P. Yadav Department of Pharmacology, BRD Medical College, Gorakhpur, Uttar Dr. U. Pal Department of Pharmacology, BRD Medical College, Gorakhpur, Uttar Preclinical evaluation of antidiabetic activity of poly herbal plant extract in streptozotocin induced diabetic rats P.P. Gupta, J. Haider*, R.P. Yadav, U. Pal ABSTRACT Objective: To study and compare the effect of Poly herbal plant extract (PHPE) with Glibenclamide (GL) on various parameters in Streptozotocin (STZ) induced diabetic rats. Methods: Diabetes was induced by combining High Fat-diet and injecting low dose Streptozotocin (35 mg/kg body wt.) to Sprague-dawley rats. Diabetic rats were treated with chloroform leaf extract of Azadirachta indica, aqueous leaf extract of Bougainvillea spectabilis and ethanolic seed extract of Trigonella foenum graecum combined in ratio of 1:2:3 respectively at dose of 600 mg/kg body weight by oral gavaging for 28 days. The results were compared with standard anti diabetic drug Glibenclamide given in dose of 500 µg/kg body weight. Results: Increase in body weight of both PHPE and GL treated diabetic rats was found to be statistically significant (p<0.05) compared to diabetic control rats. Decline in FBG levels of both PHPE and GL treated diabetic rats were found to be highly significant statistically (p<0.001) when compared to diabetic control rats at the end of study. Total Cholesterol (TC) and Triglycerides level in diabetic rats treated with PHPE were found to be highly statistically significant (p<0.001) compared to diabetic control rats. Pancreas of PHPE treated diabetic rats revealed partial restoration in size and number of islet of langerhans. Reduction in widening between acinar and islet cells noted. Glibenclamide treated diabetic rats showed much more improvement in pancreatic cell architecture by returning to its normal structure and size. Conclusion: In present study PHPE has shown to decrease elevated FBG level and improve in body weight at the end of study in diabetic rats which can be suggested due to modification in carbohydrate metabolic pathways, stimulation of insulin production by the pancreas, increased peripheral utilization of glucose in the cells and regeneration of β-cells of the pancreas. Keywords: Poly herbal plant extract, Glibenclamide, Fasting blood glucose, Total Cholesterol. INTRODUCTION Diabetes mellitus is one of the most common endocrine diseases, associated with a group of metabolic disorders characterized by chronic hyperglycemia with disturbances of carbohydrate, lipids, protein metabolism, glycosuria, ketosis and acidosis resulting from defects in insulin secretion, insulin action or both [1]. The effect of Diabetes mellitus includes long term damage, dysfunction and failure of various organs, especially the eyes, kidneys, nerves, heart and blood vessels [2]. Diabetes is a disease of global distribution affecting individuals of all ages with widely varying prevalence rates of 150 million in 2010 which is predicted to double by 2025 to 300 million [3]. Oral hypoglycemic agents are useful in the treatment of diabetes mellitus but their use is restricted by their pharmacokinetic properties, secondary failure rates, and accompanying side effects and the World Health Organization expert committee on diabetes has listed as one of its recommendations that traditional methods of treatment for diabetes should be further investigated [4]. In ancient literature, more than 800 plants are reported to have antidiabetic properties Ethanopharmacological surveys indicate that more than 1200 plants are used in traditional medicine for hypoglycemic activity [6]. Ancient Indian medicine has mentioned numerous dravyas (things which has biological functions and properties) have been reported effective in madhumeha (Diabetes) [7]. [5]. Correspondence: Dr. Jamal Haider Associate Professor, Department of Pharmacology, BRD Medical College, Gorakhpur, Uttar Email: jamalatbrd[at]gmail.com In the present scenario, the demand for herbal products is growing exponentially throughout the world and major pharmaceutical companies are currently conducting extensive research on plant materials for their potential medicinal value. In many journals, national and international, we find an increasing number of research publications based on herbal drugs. Many analysis based studies regarding pharmacological research in India [8-10] have been conducted in the past. In the traditional system of plant medicine it is usual to use plant formulation and combined extract of plant are used as a drug of choice rather than individual ones [11], to get the benefit of synergism and to find suitable antidiabetic activity. 45

The concept of polyherbalism is peculiar to Ayurveda. Sarandghar Samhita highlights the concept of synergism behind polyherbal formulations. It is evident that there are many herbal formulations of varying potency since these preparation act by different mechanism, it is theoretically possible that combination of these extract will produce better therapeutic response. So present study was designed to assess the combined effect of chloroform leaf extract of Azadirachta indica, aqueous leaf extract of Bougainvillea spectabilis and ethanolic seed extract of Trigonella foenum graecum on various parameters in streptozotocin induced diabetic rats. METHODOLOGY Authentification and Extraction of Plants Material- Leaves of Azadirachta indica (neem) and Bougainvillea spectabilis (bougainvillea) were procured from campus of B. R. D Medical College, Gorakhpur while seeds of Trigonella foenum graecum (methi) were purchased from nearby local shop. The leaves and seeds of plants were shade dried, finely powdered with the help of a grinder and stored in air- tight packets. They were identified and authenticated by Professor of Department of Botany, Deen Dayal Upadhyay Gorakhpur University, Gorakhpur, U.P. and the samples were preserved and deposited in repository. Extracts of individual plants samples were prepared separately. Chloroform extract of leaves of Azadirachta indica was prepared by subjecting 470 gram of neem leaf powder to soxhlet which yielded 42 gram of neem leaf chloroform extract. Aqueous extract of Bougainvillea spectabilis was prepared by soaking 400 gram of Bougainvillea leaf powder in 4 litres of Distilled water for 24 hours at room temperature. The material was then filtered next day and concentrated in water bath at 50-60 0 C to get a yeild of 35.2 gram of semi-solid aqueous extract of Bougainvillea leaf. Ethanolic extract of Trigonella foenum graecum seeds was obtained by soaking 700 gram of methi seed powder in 1400 ml of absolute ethanol (Emsure, Merck, 1.00983.2511, Germany) for 6 days at room temperature. The material was then filtered with Watt man s filter paper no.1 and evaporated in water bath at 40-45 0 C to get a yield of 60 grams of ethanolic extract of methi seed. The extracts so obtained were weighed Poly herbal plant extract used in the study at a dose of 600 mg/kg body weight, consisted of Azadirachta indica (neem), Bougainvillea spectabilis (bougainvillea) and Trigonella foenum graecum (methi) in ratio 1:2:3. Experimental Animal- Sprague Dawley rats weighing 150-200 gm were brought from Division of Laboratory Animals, CDRI, Lucknow for the present study. They were housed in spacious, polypropylene cages in Central Animal House of B.R.D Medical College, Gorakhpur which was well ventilated and maintained under standard experimental conditions (Temperature 23±20C and 12 hour light/dark cycle) throughout the experimental protocol. All the animals were fed with Normal Pellet Diet (NPD)- Nutrilab Rodent, obtained from Vetcare, Bangalore and water ad libitum for acclimatization to the laboratory conditions for 10 days prior to experimental use. All animal experiments were carried out after approval by the Institutional Animal Ethics Committee of B.R.D Medical College, Gorakhpur as per the rules and regulations of Committee for the Purpose of Control and Supervision of Experiments on Animals. Experimental Design - Type 2 Diabetes was induced by giving High Fat diet for 2 weeks followed by injection of low dose streptozotocin to rats. After the induction of diabetes, the rats were closely monitored for 7 days to detect appearance of diabetes. Thereafter with time when diabetes developed and got stabilized, blood sugar levels were estimated by glucometer and presence of diabetes was confirmed when blood glucose levels were above 250 mg/dl by glucometer (Accu-Chek Active, Model-GC, Roche, Germany). Rats were then divided into four groups with 6 rats in each group and were fed with High fat diet throughout the study period of 28 days. Group-I - Normal control rats administered only distilled water (vehicle) Group-II - Diabetic control rats administered only distilled water (vehicle) Group-III - Diabetic rats administered with Poly Herbal Plant Extract (PHPE) at a dose of 600 mg/kg Group-IV - Diabetic rats administered with Glibenclamide at a dose of 500µg/kg At the end of study, rats of all groups were anaesthetized and euthanized. Blood sample collected by intra cardiac puncture was centrifuged at 3000 r.p.m for 5 minutes for isolation of plasma for estimating Total cholesterol and Triglyceride levels. Pancreas were carefully dissected out for histopathological analysis. Estimation of Blood Glucose- FBG levels (mg/dl) of rats of all groups were estimated every week after overnight fasting by glucometer (Accu-Chek Active, Model-GC, Roche, Germany). Estimation of Total cholesterol and Triglyceride levels- Total cholesterol and Triglyceride values of all groups were determined according to the method of Span diagnostic, Liquid Gold estimation kit at the end of study. Histopathological Studies- For histopathological studies, pancreas were identified, isolated, weighed and sectioned at 8-10 micron thickness by Microtome Cryostat and the sections obtained were stained by Hematoxylin and Eosin (H&E) for microscopic examination by Kyow Getner microscope. Statistical Analysis- The results were expressed as Mean ± S.D. The unpaired Student s t-test test was used for analyzing the data between two groups. Values of p< 0.001 were considered highly significant. RESULT Effect on Body Weight- Table-1 shows diabetic control rats showed 8.2% loss of weight at the end of study as compared to their initial weights while diabetic rats treated with PHPE and GL showed 1.4% and 5.5% increase in body weight as compared to their initial weights respectively at the end of study. Increase in body weight of both PHPE and GL treated diabetic rats was found to be statistically significant (p<0.05) when compared to diabetic control rats at the end of study. Weight gain in rats treated with PHPE was comparable to weight gain in rats treated with GL at the end of study (p>0.05) as there was no significant difference found. Table 1: Effect of Poly herbal plant extract on body weight of STZ induced diabetic rats Groups (n = 6) Day 0 Day 28 % change in body weight diabetic control at day 0 NC (Group-1) 323.3± 16.02 340.0± 9.48 5.2 % p < 0.05 p < 0.001 DC (Group-2) 285.0± 10.95 261.6± 11.25-8.2 % - - D+PHPE (Group-3) 281.6± 11.25 285.0± 10.95* 1.4 % p > 0.05 p < 0.05 D+GL (Group-4) 281.0± 11.25 296.6± 18.88* 5.5 % p > 0.05 p < 0.05 Values are mean ± SD; * p > 0.05 between group 3 and group 4 at day 28; NC- Normal control, DC- Diabetic control, D + PHPE- Diabetic treated with Poly Herbal Plant Extract, D + GL- Diabetic treated with Glibenclamide. 46

Effect on Fasting Blood Glucose Table 2 shows rise of 7.8% in FBG levels of diabetic control rats at the end of study when compared to their initial values. PHPE treated diabetic rats showed decline of FBG levels by 7.9% while GL treated diabetic rats showed fall of 66.7% in FBG levels at the end of study when compared to their initial values. Decline in FBG levels of both PHPE and GL treated diabetic rats were found to be highly significant statistically (p<0.001) when compared to diabetic control rats at the end of study. Reduction observed in FBG levels in GL treated diabetic rats was more compared to PHPE treated diabetic rats and this difference was highly significant statistically (p<0.001). Table 2: Effect Poly herbal plant extract on blood glucose of STZ induced diabetic rats Groups (n=6) Day 0 Day 28 % change in FBG diabetic control at day 0 diabetic control at day 28 NC (Group-1) 86.0± 2.46 91.6± 3.91 6.5 % p < 0.001 P < 0.001 DC (Group-2) 326.5± 12.80 352.1± 6.68 7.8 % - - D+PHPE (Group-3) 323.8± 10.62 298.0± 7.42* - 7.9 % p > 0.05 p < 0.001 D+GL (Group-4) 325.4± 7.74 108.1± 5.50* - 66.7% p > 0.05 p < 0.001 Values are mean ± SD; *p < 0.001 between group 3 and group 4 at day 28, NC- Normal control, DC- Diabetic control, D+PHPE- Diabetic treated with Poly Herbal Plant Extract, D+GL- Diabetic treated with Glibenclamide treated with PHPE was observed as compared to diabetic control rats Effect on Total Cholesterol and Triglycerides- Table-3 shows at the end of study which was found to be highly statistically decline of 26% in Total Cholesterol (TC) values in diabetic rats significant (p<0.001). Fall of 54% was observed in TG levels of treated with PHPE as compared to diabetic control rats at the end of diabetic rats treated with GL as compared to diabetic control rats at study which was found to be highly statistically significant (p<0.001). the end of study which was also found to be highly statistically Reduction in TC values of rats treated with GL was 35% as compared significant (p<0.001). Although fall in TG levels was observed by to diabetic control rats at the end of study which was also found to be both group 3 and group 4 at the end of study, reduction by GL treated highly statistically significant (p<0.001). Although fall of TC values diabetic rats was more highly statistically significant (p<0.001) as was observed by both group 3 and group 4 at the end of study, compared to diabetic rats treated with PHPE. With continuous reduction by GL treated diabetic rats was more highly statistically administration of PHPE for 28 days, TG levels were found to be significant (p<0.001) as compared to diabetic rats treated with PHPE. decreased more than TC levels in diabetic rats. Similarly GL has also Similarly, decline of 37% of Triglyceride (TG) levels in diabetic rats shown more reduction in TG values at the end of study. Table 3: Effect Poly herbal plant extract on lipid profile of STZ induced diabetic rats Groups (n = 6) TC % reduction as compared to DC TG % reduction as compared to DC NC (Group-1) 131.5± 1.57 - p < 0.001 84.9± 2.06 - p < 0.001 DC (Group-2) 223.6± 2.22 - - 223.6± 2.17 - - D+PHPE (Group-3) 164.5± 1.76* -26 % p < 0.001 139.6± 2.05** -37 % p < 0.001 D+GL (Group-4) 144.0± 1.38* -35 % p < 0.001 102.3± 1.33** -54 % p < 0.001 Values are mean ± SD; *p < 0.001 for TC and **p < 0.001 for TG between group 3 and group 4 at day 28, NC- Normal control, DC- Diabetic control, D+PHPE- Diabetic treated with Poly Herbal Plant Extract, D+GL- Diabetic treated with Glibenclamide Histopathological studies - The histological study of normal control group rats on High fat diet revealed minimal pathological changes in acini and islets of Langerhans. Pancreatic islets of diabetic control group rats revealed significant architectural disarray which extended into surrounding exocrine tissue following streptozotocin induction. Peripheral widening between pancreatic acinar and islet cells was noted with shrunken pancreatic islet of langerhans. Pancreas of PHPE treated diabetic rats revealed partial restoration in size and number of islet of langerhans. Reduction in widening between acinar and islet cells was noted. Glibenclamide treated diabetic rats showed much more improvement in pancreatic cell architecture by returning back to its normal structure and size. DISCUSSION Diabetes mellitus (DM) is a chronic disease caused by inherited or acquired deficiency in insulin secretion and by decreased responsiveness of the organs to secreted insulin. Such a deficiency results in increased blood glucose level, which in turn can damage many of the body s systems, including blood vessels and nerves [12]. The WHO committee on diabetes mellitus recommended that further search into medicinal plants with potential antidiabetic effect should be sought. In view of this several medicinal plants or their extracts with potential therapeutic role in diabetes treatment are currently evaluated [13]. Plants have been used to treat many ailments since time immemorial. India has several plant species and thousands of them have claimed to possess medicinal properties. A number of plants have shown varying degree of hypoglycemic and antihyperglycemic activity. The active principles present in medicinal plants have been reported to be capable of pancreatic β-cell regeneration, insulin secretion and reversal of insulin resistance. The extracts of the chosen plants have been shown to exert antihyperglycemic and hypoglycemic effects by various mechanisms, some of them being uniquely present in the extract. Therefore in the present study the combined antihyperglycemic and hypoglycemic activity of these plant extracts was seen with the premise that the various components will complement each other and produce more potent effect and also become most of the herbal preparations for antidiabetic use which are polyherbal in content. The results were compared with standard oral hypoglycemic drug Glibenclamide. 47

Streptozotocin is a well known agent used to induce diabetes in animal model. The mechanism by which STZ brings about a diabetic state includes selective destruction of pancreatic beta cells, leading to hypoinsulinemia which as a result decreased glucose uptake and hyperglycemia which is the characteristic feature of diabetes mellitus [14]. In present study High fat diet (HFD) was administered for 28 days along with low dose of STZ which has been considered as one of alternative model by Srinivasan et al [15]. For pharmacological screening of drugs for Type 2 diabetes mellitus since it resembles the clinical manifestation of Type 2 diabetes in humans. STZ partially destroys the pancreatic β-cells resulting in deficiency of insulin and administration of HFD for 28 days along with it induces insulin resistance in rats. The present study evaluated the effect of Poly Herbal Plant Extract (PHPE) consisting of Azadirachta indica, Bougainvillea spectabilis and Trigonella foenum graecum at a dose of 600 mg/kg for 28 days on Body Weight Fasting Blood Glucose levels, Total Cholesterol and Triglyceride levels in STZ induced diabetic rats. Histopathological findings of pancreas were also studied. One of the symptoms of diabetes mellitus is weight loss. Induction of diabetes with STZ showed significant loss of body weight which may be due to increased muscle wasting. STZ by producing hyperglycemia and hypoinsulinemia causes decrease in body weight of diabetic rats as reported by Swanston et al [16]. Insulin being an anabolic hormone promotes lipogenesis and inhibits protein catabolism promoting weight gain or maintaining the weight preventing further loss. In present study weight loss of 8.2% in STZ induced diabetic control rats was observed. Continuous treatment with PHPE for 28 days showed 1.4% gain in body weight. Glibenclamide treated rats showed 5.5% increase in body weight at the end of the study. Glibenclamide has been known to induce weight gain as a result of its effect to increase insulin levels and cause increased utilization of glucose. Gain in body weight by PHPE could be due to appetite stimulating effect of saponins present in Trigonella foenum graecum seeds causing better utilization of nutrients in diet as reported by Blumenthal et al [17]. Quercetin in Azadirachta indica has been reported to have β-cell regenerating capacity by Aguirre et al [18] and D- pinitol in Bougainvillea spectabilis has been reported to have insulinomimetic activity by Botham et al [19]. Effect of Glibenclamide and PHPE on fasting blood glucose was evaluated after the study of 28 days study period. Both the treatments showed (P<0.001) hypoglycemic activity compared to diabetic control. PHPE treated diabetic rats showed decline of FBG levels by 7.9% while GL treated diabetic rats showed fall of 66.7% in FBG levels at the end of study when compared to their initial values which was quite similar with study performed by Srivastava et al [20] and Rafiq et al [21] 16.0 % reduction in fasting blood glucose was found with administration of polyherbal preparation at a dose of 1 ml/kg for 30 days in the study of Srivastava et al while Rafiq et al reported 8 % reduction in fasting blood glucose level in stevia-methi extract traeted diabetic rats at a dose of 500mg /kg for 28 days. In present study after administration of PHPE to diabetic rats for 28 days reduction of 26.0% for Total Cholesterol and 37.0% for Triglycerides was observed when compared to diabetic control group while Glibenclamide treated group showed reduction of 37.0% and 54.0% in TC and TG levels respectively at the end of study. Hypolipidemic effect of PHPE in our study was much similar with the study performed by Kumar et al [22] and Deep et al [23]. Under normal conditions insulin inhibits HMG-CoA reductase which produces cholesterol and activates lipoprotein lipase which hydrolyses triglycerides. In diabetes due to deficiency of insulin reverse occurs, leading to hypercholesterolemia and hypertriglyceridemia. Thus treatment with polyherbal formulation may be responsible for decrease in lipid levels by either insulin releasing or insulin sensitizing activity. In present study histological study of normal control group rats on High fat diet revealed pancreatic cells in their normal proportions and islet cells embedded within the acinar cells surrounded by fine capsule. Pancreatic cells of diabetic control rats of group 2 following Streptozotocin induction showed distortion in architecture of pancreas with peripheral widening between pancreatic acinar and islet cells. Shrunken size of pancreatic islet of Langerhans was noted. Similar findings were reported by Akbarzadeh et al [24]. On the other hand, pancreas of PHPE treated diabetic rats revealed some improvement in islet of Langerhans. There was an increase in the islet cell size and peripheral widening between acinar and islet cells were reduced as islet returned back to its normal structure. These findings are supported by studies of Oluwole et al [25] and Ahmed et al [26]. CONCLUSION Based on our present experimental data, it can be suggested that PHPE may prevent hyperglycemia and hyperlipidemia in STZ induced diabetic rats by its blood glucose lowering effect which can be due to various mechanisms like insulinomimetic property, β-cell regeneration, increased insulin secretion, increased peripheral glucose utilization and decreased intestinal glucose absorption. The actual mechanism by which the combination therapy protects and regenerates the damaged pancreatic cells is still unclear. This remains to be discovered. Therefore, our future studies will focus on blood insulin level, action on receptors as well as effect on oxidative stress. The antidiabetic activity of PHPE can further be tested in vitro and in other diabetic animal models to know the exact and detailed mechanisms of its antihyperglycemic effect. REFERENCES 1. American Diabetes Association. Diagnosis and Classification of Diabetes Mellitus Diabetes Care. 2011; 34(1):62-69. 2. Alberti KG, Zimmet PZ. Definition, diagnosis and classification of diabetes mellitus and its complications Part 1- diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med. 1998; 15(7):539-53. 3. King H, Aubert RE, Herman WH. Global burden of diabetes 1995 2025: prevalence, numerical estimates, and projection. Diabetes Care. 1998; 21:1414 1431. 4. Naggar E M, Antidiabetic effect of Cleome droserifolia Areial parts: Lipid peroxidation-induced oxidative stress in diabetic rats Acta Vet. Brno. 2004;74: 347. 5. Eddouks M, Maghrani M. Phlorizin-like effect of Fraxinus excelsior in normal and diabetic rats. J Ethnopharmacol. 2004; 9:149-54. 6. Kesari AN, Kesari S, Santosh KS, Rajesh KG, Geeta W. Studies on the glycemic and lipidemic effect of Murraya koenigii in experimental animals. J Ethnopharmacol. 2007;112(2):305-311. 7. Sabu MC, Subburaju T. Effect of Cassia auriculata Linn. On serum glucose level, glucose utilization by isolated rat hemidiaphragm. J Ethnopharmacol. 2002;80(2-3):203-206. 8. 8. Dandiya PC, Bapna JS. Pharmacological research in India. Ann Rev Pharmacol. 1974; 14:115 126. 9. Adithan C. Pharmacological research in India, 1972 1995 An analysis based on IPS conferences. Indian J Pharmacol. 1996; 28:125 128. 10. Singh H. Steady decline in clinical pharmacology research in India A decade trend analysis of IJP research publications (1990 1999). Abstracts of XXXIII annual conference of IPS 2000. Indian J Pharmacol. 2001; 33:51-70. 11. Kumar J. Herbal medicine for Type 2 diabetes. International Journal of Diabetes Developing Countries, 2010; 30: 111-112. 12. Matsui T, Tanaka T, Tamura S, Toshima A, Miyata Y, Tanaka K, et al. Alpha-glucosidase inhibitory profile of catechins and theaflavins. Journal of Agricultural and Food Chemistry. 2007;55:99-105. 13. Kuriyan R, Rajendran R, Bantwal G, Kurpad AV. Effect of supplementation of Coccinia cordifolia extract on newly detected diabetic patients. Diabetes Care. 2008; 31:216-220. 48

14. Marles, RJ, Farnsworth NR. Antidiabetic plants and their active constituents. Phytomedicine. 1995; 2: 137 189. 15. Srinivasan K. Combination of high-fat diet-fed and low-dose streptozotocin treated rat: A model for type 2 diabetes and pharmacological screening. Pharmacological Research. 2005; 52:313 320. 16. Swanston Flatt SK, Day C, Bailey CJ. Traditional plant treatments for diabetes.in normal and streptozotocin diabetic mice. Diabetologia. 1990; 33(8):462-464. 17. Blumenthal M, Busse W, Amp R. The complete commission monograph- Therapeutic guide to herbal medicines. Boston. Integrative Communications. 1988; 130 18. Leixuri A and Noemi A. Beneficial Effects of Quercetin on Obesity and Diabetes. The Open Nutraceuticals Journal. 2011; 4:189-198. 19. Botham KM, Mayes PA. Harper s illustrated Biochemistry. Edn 26. The McGraw-Hill Companies Inc. New York, 2006; 217-245. 20. Srivastava N, Tiwari G, Tiwari G.. Polyherbal preparation for antidiabetic activity. Indian Journal of Medical science. 2010;64(4):163-176. 21. Kazi R, Shamshad JS. Comparative efficacy of stevia leaf (Stevia rebaudiana bertoni), methi seeds (Trigonella foenum-graecum) and glimepiride in streptozotocin induced rats. International Journal of Phytopharmacology. 2011; 2(1):9-14. 22. Kumar HC, Kumar JN. Antidiabetic activity of a polyherbal Preparation. Pharmacologyonline. 2010; 2:780-787. 23. Prakash D, Murugananthan G. Herbal formulation and its evaluation for antidiabetic activity. Pharmacologyonline. 2011; 3:1134-1144. 24. Akbarzadeh AD, Norouzian MR, Mehrab S et al. Induction of diabetes by streptozotcin in rats. Indian J. Clin. Biochem. 2007; 22:60-64. 25. Oluwole BA, Laura Z. Ameliorative effects of ethanolic leaf extract of Azadirachta indica on renal histologic alterations in streptozotocininduced diabetic rats. Am J Chin Med. 2011; 39(5):903-16. 26. Mohammed FA, Syed MK, Syed SG, Syed SM, Shaikh RA, Shaikh MA et al. Antidiabetic activity of Vinca rosea extracts in alloxan-induced diabetic rats. Int J Endocrinol. 2010; 22 doi:10.1155/2010/841090 HOW TO CITE THIS ARTICLE Gupta PP, Haider J, Yadav RP, Pal U. Preclinical evaluation of antidiabetic activity of poly herbal plant extract in streptozotocin induced diabetic rats. The Journal of Phytopharmacology 2016;5(2):45-49. 49