Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/19115
Title: Antidiabetic effect of Coccinia grandis Linn. on streptozotocin induced diabetic rats and its role in regulating hepatic key enzymes
Authors: Meenatchi, P.
Maneemegalai, S.
Keywords: Coccinia grandis
glucose
glycated hemoglobin
hepatic key enzymes
streptozotocin
Issue Date: 2018
Publisher: Research Symposium on Pure and Applied Sciences, 2018 Faculty of Science, University of Kelaniya, Sri Lanka
Citation: Meenatchi, P. and Maneemegalai, S. (2018). Antidiabetic effect of Coccinia grandis Linn. on streptozotocin induced diabetic rats and its role in regulating hepatic key enzymes. Research Symposium on Pure and Applied Sciences, 2018 Faculty of Science, University of Kelaniya, Sri Lanka. p31.
Abstract: Coccinia grandis (L.) Voigt is an herb, growing throughout India widely used in traditional treatment of diabetes. The aim of present study was to evaluate the antidiabetic potential of ethanol extract of mature unripe fruits of Coccinia grandis (CGE) in streptozotocin (STZ)induced diabetic rats with reference to carbohydrate metabolizing hepatic enzymes. Male albino rats of Wistar strain with body weight, 180 ± 20 g were divided into 5 groups of 6 rats in each (normal control, normal + 250 mg CGE, diabetic control, diabetic + 250 mg CGE and Diabetic + 5 mg glibenclamide (GBE)). Diabetes was induced in overnight fasted experimental rats by a single intraperitoneal injection of STZ (40 mg/kg body weight) dissolved in freshly prepared citrate buffer (0.1 M, pH 4.5). The animals were considered as diabetic, if their blood glucose values were above 250 mg/dl on the third day after STZ injection. The treatment was started on the third day after STZ injection and continued for 30 days at 24 h intervals during the entire period of the experiment. After the experimental period, the plasma glucose was estimated by the method of Trinder using a reagent kit (1969) and the glycated hemoglobin (HbA1c) was estimated by the method of Drabkin and Austin (1932) and Sudhakar and Pattabiraman (1981). Administration of CGE at 250 mg/kg body weight showed a significant (p<0.05) reduction in the levels of plasma glucose, from 289.65 ± 22.63 to 154.36 ± 4.64 mg/dL and HbA1c from 1.26 ± 0.027 to 0.62 ± 0.039 mg/g of Hb when compared to diabetic control group. The levels of hepatic key enzymes viz. hexokinase, glucose-6-phosphate dehydrogenase, glucose 6-phosphatase, fructose 1,6bisphosphatase were assayed using methods of Brandstrup et al. (1957), Koide and Oda (1956), Gancedo and Gancedo (1971) and Bergmeyer (1984) respectively. Oral administration of CGE to diabetic group significantly (p<0.05) increased the activity of hexokinase from 87.53 ± 3.57 to 98.64 ± 4.63 nmoles of glucose-6-phosphate liberated/min/mg protein and glucose-6-phosphate dehydrogenase from 1.38 ± 0.14 to 1.72 ± 0.13 IU/L. In contrast, oral administration of CGE to diabetic group of animals significantly (p<0.05) decreased the gluconeogenic enzymes glucose 6-phosphatase from 0.31 ± 0.03 to 0.08 ± 0.04 IU/L and fructose 1,6-bisphosphatase from 8.26 ± 0.41 to 3.72 ± 0.36 IU/L. The results of this study demonstrated unequivocally the antidiabetic effect of C. grandis by modulating hepatic key enzymes and a good candidate for complementary and alternative medicine in the management of diabetes mellitus.
URI: http://repository.kln.ac.lk/handle/123456789/19115
Appears in Collections:IRSPAS 2018

Files in This Item:
File Description SizeFormat 
31.pdf293.68 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.