Comparative Evaluation of the Antidiabetic Effects of Different Parts of <i>Cassia fistula</i> Linn, a Southeast Asian Plant

Einstein , John Wilking; Mohd Rais, Mustafa; Mohd, Mustafa Ali

doi:https://doi.org/10.1155/2013/714063

Journal of Chemistry

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Research Article | Open Access

Volume 2013 | Article ID 714063 | https://doi.org/10.1155/2013/714063

Comparative Evaluation of the Antidiabetic Effects of Different Parts of Cassia fistula Linn, a Southeast Asian Plant

John Wilking Einstein ,¹Mustafa Mohd Rais,¹and Mustafa Ali Mohd¹

Academic Editor: Patricia Valentao

Received11 May 2012

Accepted21 Jun 2012

Published11 Sept 2012

Abstract

The hypoglycemic effect of the methanolic and aqueous extracts of whole parts of Cassia fistula in both normoglycemic and streptozotocin-nictotinamide induced Type 2 diabetic rats were investigated. Acute toxicity, oral glucose tolerance test and glucose uptake in isolated rat hemidiaphragm were performed in normal rats. Diabetes was induced in Sprague Dawley rats by the administration of streptozotocin-nictotinamide (50, 110 mg/kg b.w., resp.) intraperitoneally. Different extracts of Cassia was administered to diabetic rats at 250 and 500 mg/kg doses for 21 days. Biochemical parameters like blood glucose, insulin, glycosylated hemoglobin, lipid profile, and serum marker enzymes were determined. The methanolic extract of the bark and leaves were show more effective in causing hypoglycemia in normoglycemic rats. Diabetic rats showed increased levels of glycosylated hemoglobin, reduced levels of plasma insulin, were significantly reverted to near normal after oral administration of the bark and leaf methanolic extracts. Glucose uptake studies in isolated rat hemidiaphragm have shown enhanced peripheral utilization of glucose. Chronic treatment of Cassia remarkably restored the normal status of the histopathological changes observed in the selected tissues. Dose dependent anti-diabetic effects with the cohorts receiving the methanolic extract of bark followed by leaves of Cassia was revealed.

1. Introduction

Diabetes mellitus (DM), caused by inherited and/or acquired deficiency or inadequate secretion of hormone insulin (type I or insulin-dependent diabetes mellitus (IDDM)) or due to a an inadequate response of target cells to insulin (type II or noninsulin-dependent diabetes mellitus (NIDDM)), or by a combination of these factors culminating in hyperglycemia is, a disease as old as mankind [1]. Recent reports indicate DM is today the world’s leading endocrine disorder, constituting approximately six percent of the population, of which 90 percent is type II DM [1]. The currently available therapeutic options, such as oral hypoglycemics and insulin, are not always satisfactory in maintaining euglycemia and in avoiding late stage DM complications. Additionally, the chronic nature of the disease and the associated complications require regular treatment and incur huge financial expenditure on the family and the healthcare system. Therefore, a need for alternative drugs that are effective, inexpensive, affordable, and safe to consume is being recognized.

One of the best approaches in identifying novel antidiabetic agents is to scientifically investigate the efficacy of medicinal plants recognized to be effective in the various traditional system of medicine [2]. Cassia fistula Linn commonly known as “golden shower” and belonging to Leguminosae family is one such plant reported to be effective as an antidiabetic agent in the various folk systems of medicine [3]. The plants are fast growing small tree or tall shrubs and are found growing throughout tropical countries of the world, from West Indies to South Asia (India, Thiland, Malaysia, Brunei Darussalam, Indonesia, Vietnam, and Philippines) and from South Africa to Egypt [4]. Almost all parts of the plants are of medicinal use in the various folk system of medicine in Southeast Asia, and scientific studies have validated many of the ethnomedicinal observations. Preclinical studies have shown that the extract of flowers, leaves, bark, and pods, namely the ether extract of leaves possess antibacterial activity against S. aureus and S. album [5]. Seeds of CF are reported to have antibacterial [6], antitumour [7], and antifertility effect [8] and four novel compounds has been isolated [9]. The antioxidant effect of the crude extracts of stem bark, leaves, flowers, and fruit pulp of C. fistula has been assessed [10]. Though the hypoglycemic efficacy of leaves and seeds of CF have been studied [11]. The methanol extract of the stem of CF and catechins isolated from the extract are shown to reduce the blood glucose levels in STZ-induced DM rats [3]. Recently in milieu of these observations and to validate the ethnomedical observations, for the first time the present study was undertaken to evaluate the hypoglycemic effects of the various parts of Cassia fistula (leaves, barks, flowers, and pods) and extracts (aqueous and methanolic) in both normal (nondiabetic) and type II DM rats (induced by STZ-nictotinamide).

2. Materials and Methods

2.1. Plant Material

The leaves, barks, flowers, and pods of Cassia fistula were together collected in 2007 and around Bangalore district, India, in April and authenticated by botanist, Dr. V. C. Subbanna, Gandhi Krishi Vignana Kendra, Bangalore, India.

2.2. Preparation of Plant Extracts

The plant materials were shade dried and pulverized in mechanical mill. The appropriate dried powdered plant materials (1 kg) were successively extracted with n-hexane, chloroform, and methanol (all solvents were HPLC grade) by soxhlet apparatus and with double distilled water (500 mL each) by reflux. The extracts were evaporated to dryness with a rotary evaporator, under reduced pressure at 40°C. The extracts are as follows: bark methanol extract (BME), bark aqueous extract (BAE), leaf methanol extract (LME), leaf aqueous extract (LAE), flower methanol extract (FME), flower aqueous extract (FAE), pods methanolic extract (PME), and pods aqueous extract (PAE). The extracts were stored at 4°C and used for further investigation.

2.3. Chemicals

Glucose and other biochemical parameters kits were obtained from Randox Laboratories Ltd. (Co. Antrim, UK). STZ and nicotinamide were purchased from Sigma Chemicals Co. (St. Louis, MO, USA). Standard drug glibenclamide (1.0 mg/kg. b.wt) pure samples were procured from Biocon Pvt. Ltd., Bangalore, India. The drugs and reagents were reconstituted in sterile double distilled water.

2.4. Animals

The study was conducted on Sprague Dawley (SD) rats, five to six weeks of age, weighing 200–250 g, which were housed in colony cages (three rats per cage) at an ambient temperature of 25 ± 2°C with 12 h light and 12 h dark cycle. The rats were fed standard diets and water ad libitum. The animals were allowed to acclimatize to the laboratory environment for 1 week. All procedures complied with the standards for the care and use of animal subjects as stated in the guidelines laid by Institutional Animal Ethical Committee (IAEC), University of Malaya, Kuala Lumpur (FAR/07/12/2007/MRM(R).

2.5. Acute Toxicity Study

The acute oral toxicity study was carried out in accordance to the guidelines set by the Organisation for Economic Co-operation and Development (OECD) 423 [12]. Sprague Dawley rats were fasted for overnight and administered range of concentration (50 to 5000 mgkg⁻¹) of the methanolic and aqueous extracts. The animals were observed continuously for the first two hours, followed by once every hour up to 6 h for any changes in behavioral, neurological, and autonomic profiles and after 24 and 72 h to identify lethality.

2.6. Effect of CF Extract on Serum Glucose Levels of Normal Fasted Rats

The fasting blood sugar level of each animal was determined after overnight fasting for 18 h. Normoglycemic rats were divided into eighteen experimental groups ( per group). The first group of animals was given saline through oral intubation and served as control. Group II was given glibenclamide (2.5 mgkg⁻¹), taken as standard. Group III–XVIII was given an aqueous and methanolic suspension of CF extracts (leaf, flower, bark, and pods) orally at a dose of 250 and 500 mgkg⁻¹, respectively. The blood samples were collected from the tail vein just prior to and at 1, 2, 4, and 8 h after the extract. Serum glucose was measured by GOD/POD enzymatic method [13].

2.7. Determination of the Oral Glucose Tolerance Test (OGTT) in Normal Rats

OGTT experiment was performed as explained by Bonner-Weir [14]. The normal rats were divided into 18 groups and were fasted overnight (18 h). The next day the rats were administered either drinking water or glibenclamide (2.5 mgkg⁻¹ used as the standard drug) or 250 and 500 mgkg⁻¹ of the extracts. Glucose (2 gkg⁻¹) was administered 30 min after the feeding of the extract. Blood was withdrawn from the tail vein under ether inhalation anesthesia at 240 min of glucose administration and estimated using biochemical kits in a semiautoanalyser STAT FAX 3300.

2.8. Evaluation C. fistula Extracts on Various Parameters in Type II DM Rats

2.8.1. Induction of NIDDM

The rats were fasted overnight and were administered freshly prepared STZ solution (50 mg/kg body weight dissolved in cold citrate buffer, pH 4.5) intraperitoneally (i.p.). Fifteen minutes after the i.p. administration, STZ, 110 mgkg⁻¹ body weight of nictotinamide (dissolved in saline) was given to the same rats by i.p. DM was identified by polydipsia, polyuria, and by measuring nonfasting plasma glucose levels. Animals with postprandial glycemia over 200–250 mgkg⁻¹, 7 days after STZ administration, were considered diabetic. Whole blood was collected from the tail vein of the rats. Control rats received only buffer. Animals, which did not develop more than 200 mgdL⁻¹ glucose levels, were rejected [15, 16].

2.8.2. Experimental Design and Treatment Schedule

The effect of the extracts was studied in STZ-nictotinamide induced diabetic rats or 21 days. The rats ( per group) were divided into 15 groups: group 1: normal rats treated with vehicle alone; group 2: diabetic control treated with STZ solution (50 mgkg⁻¹ body weight dissolved in cold citrate buffer, pH 4.5) intraperitoneally (i.p.) + 110 mg/kg body weight of nictotinamide, i.p. (dissolved in saline); group 3: diabetic rats treated p.o. (oral route) with glibenclamide (Biocon. Pvt. Ltd., India); group 4 and 5 diabetic rats were administered 250 mgkg⁻¹ of Bark methanolic and aqueous extracts respectively; groups 6 and 7 diabetic rats were administered 500 mgkg⁻¹ of bark methanolic and aqueous extracts, respectively; groups 8 and 9 diabetic rats were administered 250 mgkg⁻¹ of leaf methanolic and aqueous extracts, respectively; groups 10 and 11 diabetic rats were administered 500 mg/kg of leaf methanolic and aqueous extracts, respectively; groups 12 and 13 diabetic rats were administered 250 mgkg⁻¹ of flower methanolic and aqueous extracts, respectively; groups 14 and 15 diabetic rats were administered 500 mgkg⁻¹ of flower methanolic and aqueous extracts, respectively. The saline, standard drug, and extracts were administered p.o. to respective groups for 21 days.

Blood samples were collected from the tail vein at 0,7th, 14th, and 21st days and quantified for the blood glucose levels. On day 21, the fasted animals were euthanized under overdose of ketamine. The blood was collected by cardiac puncture and processed for estimating the levels of glycosylated hemoglobin (HbA1c) by ion exchange chromatography [17] and insulin by ELISA assay [18]. The serum was separated by centrifugation and analyzed for serum biochemical parameters, that is, aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), total cholesterol (TC), triglycerides (TG), high density lipoprotein (HDL), and non-HDL using biochemical kits in a semiautoanalyser-STAT FAX 3300.

2.8.3. Total Protein Content

The protein contents of 10% liver homogenates were determined by using Lowry’s method [19].

2.8.4. Lipid Peroxidation

Thiobarbituric acid reactive substances (TBARS) in homogenate were estimated by using standard method [20]. Briefly, 500 μL of sample (10% liver homogenate) was incubated with 300 μL of 15% trichloroacetic acid (TCA), 300 μL of 0.375% thiobarbituric acid (TBA), and 300 μL of 5 N hydrochloric acid (HCl) at 95°C for 15 min; the mixture was cooled and centrifuged and the absorbance of the supernatant was measured at 532 nm against appropriate blank. The amount of lipid peroxidation was determined by using l = 1.56 × 10⁵ M^-1cm⁻¹ and expressed as nM of (malonaldehyde) MDA/mg of protein [21].

2.8.5. Histopathological Studies

At the end of the experimental period, the animals were sacrificed by cervical dislocation. The pancreas samples fixed for 48 h in 10% formalin saline were dehydrated by passing successfully in different mixture of ethyl alcohol-water, cleaned in xylene, and embedded in paraffin. Sections of pancreas were prepared and, then, stained with hematoxylin and eosin dye (H&E), which mounted in neutral deparaffinated xylene (DPX) medium for microscopic observation.

2.9. Effect of Aqueous and Methanolic Bark, Leaf, and Flower Extracts of CF on Glucose Utilization in the Rat-Hemidiaphragm Assay In Vitro

Albino rats of either sex were maintained on a standard pellet diet and water ad libitum and fasted overnight. The animals were sacrificed by decapitation and diaphragms were taken out quickly avoiding trauma and divided into two halves. The hemidiaphragms were then rinsed in cold Tyrode solution (without glucose) to remove any blood clots and were placed in a small conical flasks containing 2 mL Tyrode solution with 2000 mg/L glucose and incubated for 30 min at 37°C in an atmosphere of 95% O₂ + 5% CO₂ with shaking at 140 cycles per min. Four sets of experiments were performed [22]. The animals were killed by decapitation and diaphragms were exposed to group I: tyrode solution with glucose (2000 mg/L) only and served as control. Group II: tyrode solution with glucose (2000 mgL⁻¹) + insulin (0.25 IU/mL). Group III: tyrode solution with glucose (2000 mgL⁻¹) bark methanol extract of CF (25 mg/mL). Group IV: tyrode solution with glucose (2000 mgL⁻¹) + insulin (0.25 IUmL⁻¹) + bark methanol extract of CF (25 mgmL⁻¹). Group V: tyrode solution with glucose (2000 mgL⁻¹) leaf methanol extract of CF (25 mgmL⁻¹). Group VI: tyrode solution with glucose (2000 mgL⁻¹) + insulin (0.25 IUmL⁻¹)+ leaf methanol extract of CF (25 mgmL⁻¹). Group VII: tyrode solution with glucose (2000 mgL⁻¹) flower methanol extract of CF (25 mgmL⁻¹). Group VIII: tyrode solution with glucose (2000 mgL⁻¹) + insulin (0.25 IUmL⁻¹) + flower methanol extract of CF (25 mgmL⁻¹). Following incubation, the hemidiaphragms were taken out and weighed. The glucose content of the incubated medium was measured by GOD/POD, enzymatic method. Glucose uptake was calculated as the difference between the initial and final glucose content in the incubation medium.

2.10. Statistical Analysis

Statistical analysis was performed using Graph Pad Prism software package Version 5.0. The values were analyzed by one-way analysis of variance (ANOVA) followed by Dunnett’s multiple comparison test.

3. Results

3.1. Phytochemical Evaluation of Extracts

The detailed studies of plant constituents for various extracts have been depicted in Table 1. Bark extracts show the presence of alkaloids, polyphenols, tannins, and some steroidal compounds whereas leaf extracts show the presence of high amount of glycosides and flavonoids. Similarly the flower and pods extracts show the presence of glycoside, alkaloids, flavonoids, some phenolic compounds, and along with all these constituents some resinous matters, respectively.

3.2. Acute Toxicity Study

The acute toxicity studies showed that the oral administration of the extracts did not cause death in the highest dose of 5 g kg⁻¹ bw. The behavioral, neurological, and autonomic responses of the treated rats were all normal indicating it to be safe.

3.3. Evaluation of the Hypoglycemic Effects in Normoglycemic Rats

The hypoglycemic effects of the various extracts were evaluated in the fasting normoglycemic animals by administering either 250 or 500 mgkg⁻¹ (corresponding to 1/10th and 1/20th of the maximum tested dose) and estimating the blood glucose levels at 1, 2, 4, and 8 h after treatment. The results showed that only BME 500 mgkg⁻¹ had shown significant hypoglycemic effect at 2 h (), 4 h () and 8 h () followed by LME 500 mg/kg which has shown hypoglycemic effect starting from the 4th h () to the 8th h (), as shown in Table 2. However, the hypoglycemic effects of both these extracts were not as effective as glibenclamide which has shown significant hypoglycemic effect starting from the 2nd h to the 8th h ().

3.4. OGTT in Normal Rats

Figure 1 shows that both the doses of BME (250 and 500 mgkg⁻¹) have significantly reduced glucose AUC similar to that of standard drug glibenclamide (); whereas only higher dose of LME 500 mgkg⁻¹ has significantly reduced glucose AUC ().

In both the above two experiments involving normal rats only bark and leaf methanolic extracts have shown significant hypoglycemic effect. There was also a trend towards decrease in glucose value of FME and aqueous extracts of bark and leaf whereas none of the extracts and doses of pods have shown any hypoglycemic effect therefore they are not included in further studies.

3.5. Evaluation CF Extracts on Various Parameters in Type II DM Rats

Chronic administration of different extracts of CF has revealed the fact that BME at 500 mgkg⁻¹ has started exhibiting the antihyperglycemic effect from 7th day onwards reaching the maximum beneficial effect on 21st day. LME at 500 mgkg⁻¹ has started showing antihyperglycemic effect on 14th day onwards (Table 3). Antihyperglycemic effect exhibited by these two groups is similar to that of standard drug glibenclamide (). Similarly both BME and LME have significantly reduced the glycosylated haemoglobin level and increased the serum insulin level; however higher dose has shown better significance level similar to that of standard drug () demonstrating the increased beta cell activity (Table 4). As chronic hyperglycemia is known to alter the levels of serum lipid profile by enhancing the levels of TC, non-HDL-C, and TG, with a concomitant decrease in the levels of HDL, we have observed increase in lipid profile level in DM control group whereas BME and LME 500 mgkg⁻¹ have shown improvement in lipid profile compared with DM control group (Table 5). Studies also have showed that the administration of BME and LME 500 mgkg⁻¹ caused a maximum reduction in the levels of liver damage enzymes AST, ALT, and ALP (Table 6). BME and LME 500 mgkg⁻¹ by decreasing the level of MDA have demonstrated the antioxidant potential of CF (Figure 2). The result was supported by histopathological evidence, in which, compared to DM control, BME has shown both increase in number of islets in beta cells and islets size (Figure 3). Normal control (Figure 3(a)), diabetic control (Figure 3(b)), glibenclamide (Figure 3(c)), and bark methanolic extract 500 mg/kg b.wt. (Figure 3(d)) show mild reduction in beta cells and decrease in the number of islets.

(a)

(b)

(c)

(d)

3.6. Effect of Methanolic Bark, Leaf, and Flower Extract on Glucose Uptake in the Rat-Hemidiaphragm Assay In Vitro

The effects of the methanolic extracts of bark, leaf, and flowers on the glucose uptake by isolated rat hemidiaphragm are shown in Table 7. In the absence of insulin only BME 500 mgkg⁻¹ has significantly enhanced the glucose uptake (). Furthermore all three extracts were observed to be effective in enhancing the uptake of glucose in the presence of insulin significantly () and were found to be more effective than insulin alone or the extracts alone.

4. Discussion

NIDDM is recognized to be a common and serious metabolic disorder throughout the world. Although, oral hypoglycemic agents/insulin are the mainstay of treatment of DM and are effective in controlling hyperglycemia, they have prominent side effects and fail to significantly alter the course DM complications [23]. The management efforts of hyperglycemia and the associated complications are labor intensive and challenging to both patients and the physicians. Furthermore, the economic burden associated with DM is severe to both the patient and the society [24].

Medicinal plants used in the various alternative and complementary systems of medicine are known to play an important role in the management of DM especially in developing countries where primary care facilities are compromised. In the present study, BME and LME at 500 mgkg⁻¹ have exhibited significant hypoglycemic property in normoglycemic rats. Similarly chronic administration of methanolic extracts of bark and leaf at 500 mgkg⁻¹ for 21 days significantly reduced glucose concentration in STZ + nicotinamide-induced diabetic rats. Both these groups have showed a comparable activity with glibenclamide-treated groups () which is a standard antidiabetic drug that stimulates insulin secretion from beta cells of islets of Langerhans. Therefore the present study result indicates insulin stimulating property of the extract. The result also satisfies the earlier reports revealed by the researchers [25, 26]. It is also important to note that the typical characteristic of diabetes is the increase of serum glycosylated protein such as glycosylated hemoglobin (HbA1C), which is a parameter for glycemic control where glucose or other reducing sugars react with the amino residues of proteins to form Amadori products–HbA1C. Animals treated with 500 mgkg⁻¹ of BME and LME have significantly decreased the HbA1C level which could be due to an improvement in insulin secretion from remnant pancreatic beta cells in diabetic rats [27]. Further the extract treated cohorts were observed to have shown statistically significant increase in serum insulin compared to DM controls. Histopathological observations also revealed that when compared to the DM control the cohorts receiving the extract had adequate number of islets and beta cells and less pyknotic nuclei and dark nuclei. In milieu of all these observations it can be hypothesized that the methanolic extract of both leaf and bark brings about its anti-hyperglycemic action by possibly potentiating secretion of insulin from β-cell of islets.

Insulin resistance is a major concern in the etiology of type II DM. Earlier literature revealed catechin could be developed into potential oral hypoglycemic drug because it possesses a potential agonist characteristic that is capable of activating insulin receptor and peroxisome proliferator-activated receptor gamma [28]. We can conclude that the estimation of glucose content in rat hemidiaphragm model indicated that BME 500 mgkg⁻¹ alone has increased the glucose uptake even in the absence of insulin suggesting its hypoglycemic potential. However, in the presence of insulin, the methanolic extracts of the bark, leaves, and flowers were also effective. It was reported that Cassia fistula (L) flower extract also has antioxidant defense in streptozotocin-induced diabetic rats [29] which was correlated with our study. The best effects were observed for the bark followed by leaves and flower and were better than insulin alone. The in vitro study of glucose utilization by isolated rat hemidiaphragm proposes that these extracts in combination with insulin potentiate its activity and enhance the utilization of glucose thereby being effective as an antidiabetic agent in type II DM.

In association to the chronic hyperglycemia, it has been known that hyperlipidemia and oxidative stress are pronounced in DM [30–32]. An atherogenic lipid profile characterized by elevated TGs and low levels of HDL-C are important contributors to insulin resistance and a risk factor for cardiovascular complications leading to 65% of death in patients with type II DM. Therefore an ideal anti-diabetic drug should have anti-hyperlipidemic effect in addition to antihyperglycemic activity. In the present study a marked increase in serum TC and TGs levels was observed in DM rats, and this observation was in agreement to earlier observations [33, 34]. Administration of the various extracts and glibenclamide reduced the levels of serum TC and TG and increased the levels of HDL-C. The best effects were observed with the 500 mgkg⁻¹ of the BME and LME. Similar results have been explained earlier by Nirmala et al. [35]. They have reported that effect of hexane extract of Cassia fistula barks on blood glucose and lipid profile in streptozotocin diabetic rats. Thus, it is reasonable to conclude that methanolic extracts of bark and leaf of CF could modulate blood lipid abnormalities in addition to antidiabetic activity. The similar report was revealed by Pitchai and Manikkam [28].

DM is one of the pathological processes known to be related to an unbalanced production of ROS, such as hydroxyl radicals (HO^•), superoxide anions (), and H₂O₂. Therefore, cells must be protected from this oxidative injury by antioxidant enzymes [36]. Free radicals and oxidative stress have long been implicated in eliciting complications of the DM condition. DM causes hypercholesterolemia. Hypercholesterolemia in turn is responsible for oxidative stress. It was reported that hypercholesterolaemia leads to increased production of OFR which exert their cytotoxic effect by causing LPO [37]. Its also known that LDL as such is not atherogenic it is the oxidized LDL which is atherogenic. Enhanced oxidative stress may depress the antioxidant defenses leading to exaggerated level of oxidized LDL and increased level of LPO. In the present study BME and LME 500 mgkg⁻¹ have decreased LPO more significantly thereby exhibited the antioxidant potential of CF.

DM is multifactorial in its pathogenesis and loss of insulin effect leads to glycogenolysis and ketogenesis, which then cumulatively lead to abnormalities in the liver function [38]. Elevation of transaminases three times the upper limits of ALT and AST enzymes indicates the liver damage induced by DM as also reported by Prince et al [39]. These observations were also replicated in our study in the DM cohorts. Administering the extracts especially BME 500 mgkg⁻¹ has produced significant beneficial effect in all the liver marker enzymes tested indicating their hepatoprotective effects.

The first probable anti-diabetic mechanism of action of the CF plant extract could be linked to increase in plasma insulin. Though the exact mechanism of action of the extract is not known, it could be due to increased pancreatic secretion of insulin from existing beta cells as shown in the biochemical tests, namely, glucose, HbA1C, and insulin. Second likely mechanism is increased binding of insulin to insulin receptor thereby increasing the uptake of glucose by CF extracts as demonstrated in rat hemidiaphragm experiment. Third mechanism could be antioxidant property as exerted by decreasing the lipid peroxidation in the present study. Previous studies have conclusively shown that the phytochemicals epicatechin, flavanoids, proanthocyanidins, and kaempferol possess hypoglycemic effects. It is well known that certain flavonoids exhibit hypoglycemic activity and pancreas beta cell regeneration ability. Thus the significant anti-diabetic effect of BME and LME may be due to the presence of more than one antihyperglycemic principle and their synergic properties [40, 41]. It was also observed that among the extracts tested the methanolic extract of the bark and leaves was the most effective. Our observations are in agreement to that of Daisy et al. [42], who have also observed that the methanol extract of Tinospora cordifolia stem was effective in reducing the blood glucose levels in STZ-induced type I DM in rats. Together both these observations indicate that the methanolic extract is effective in inducing hypoglycemic effects in both type I and II DM. Therefore all these observations clearly validate our experimental observations.

5. Conclusion

Data accrued from the present study clearly indicate that the methanolic extract of the bark and leaves at 500 mgkg⁻¹ dose exhibited significant antihyperglycemic and antilipidemic activity than at low dose (250 mgkg⁻¹) in the STZ-nictotinamide-induced DM rats. These extracts also showed improvement in parameters glycosylated hemoglobin and insulin profile as well as regeneration ofbetacells of pancreas and so might be of value in DM treatment. Therefore, further investigation is necessary to determine the exact phytoconstituent(s) responsible for anti-DM effect.

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Copyright © 2013 John Wilking Einstein et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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