Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Antidiabetic Potential of Ficus Bengalensis Fruit Extract Studied in Alloxan-induced Experimental Diabetes in Rats


Affiliations
1 Department of Biochemistry, University of Madras, Guindy campus, Chennai – 600 025, Tamil Nadu, India
     

   Subscribe/Renew Journal


Ficus bengalensis (FB) (Moraceae) is commonly known as Banyan tree has been traditionally known for their beneficial pharmacological properties. In the absence of systemic studies in the literature, the present study was aimed to evaluate the antidiabetic potential of Ficus bengalensis fruit extract in alloxan-induced experimental diabetes in rats. The altered levels of biochemical parameters such as blood glucose, plasma insulin, haemoglobin, glycosylated haemoglobin, glycogen content in liver and muscle tissues, protein, urea, creatinine, uric aicd, AST, ALT and ALP in the diabetic rats were significantly reverted back to near basal values by the administration of Ficus bengalensis fruit extract for 30 days. The levels of lipid peroxides in the plasma and pancreatic tissues of diabetic rats were elevated significantly and were normalized by the administration of Ficus bengalensis fruit extract. The activities of pancreatic enzymic antioxidants and the levels of plasma non-enzymic antioxidants were markedly declined in the diabetic rats. Upon treatment with Ficus bengalensis fruit extract to diabetic rats, these decreased antioxidant levels were significantly improved. Further, the altered levels of lipid profile were significantly improved upon treatment with fruit extract. The results of the study indicate that Ficus bengalensis fruit extract possesses antidiabetic activity and the results are comparable with gliclazide, an oral standard hypoglycemic drug. The phytochemicals present in the Ficus bengalensis fruit may account for the observed pharmacological properties. Keywords: Medicinal plant; Ficus bengalensis; antidiabetic; antioxidant; alloxan.
Subscription Login to verify subscription
User
Notifications
Font Size


  • American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care. 35 (Suppl 1); 2012: S64-71.
  • Wild SG, Roglic A, Green R and King H. Global prevalence of diabetes. Estimated for the year 2000 and projection for 2030. Diabetes Care. 27; 2004: 1047-1054.
  • Grover JK, Yadav S and Vats V. Medicinal plants of India with hypoglycemic potentials. Journal of Ethnopharmacology. 81; 2002: 81-100.
  • Scartezzini P, Sproni E. Review on some plants of Indian traditional medicine with antioxidant activity. Journal of Ethnopharmacology. 71; 2000: 23–43.
  • Tilburt JC, Kaptchuk TJ. Herbal medicine research and global health: an ethical analysis. Bull World Health Organ. 86 (8); 2008: 594-599.
  • Manoj A, Urmila A, Bhagyashri W, Meenakshi V, Akshaya W and Kishore NG. Anthelmintic activity of Ficus benghalensis. International journal of green pharmacy. 2 (3); 2008: 170- 172.
  • Thakare VN, Suralkar AA, Deshpande AD and Naik SR. Stem bark extraction of Ficus bengalensis Linn for anti-inflammatory and analgesic activity in animal models. Indian Journal of Experimental Biology. 48 (1); 2010: 39-45.
  • Biswas TK and Mukherjee B. Plant medicines of Indian origin for wound healing activity: a review. The International Journal of Lower Extremity Wounds. 2 (1); 2003: 25-39.
  • Harborne JB. Phytochemical methods. A guide to modern techniques of plant analysis. Chapman and Hall Int., New York, 1998; 3rd ed.
  • Yamamoto H, Uchigata Y and Okamoto H. Streptozotocin and alloxan induce DNA strand breaks and poly(ADP-ribose) synthetase in pancreatic islets. Nature. 294 (5838); 1981: 284- 286.
  • Trinder P. Determination of glucose in blood using glucose oxidase with an alternate oxygen acceptor. Annuals of Clinical Biochemistry. 6; 1969: 24-27.
  • Lowry OH, Rosebrough NJ, Farr AL and Randall RJ, Protein measurement with the Folin phenol reagent. The Journal of Biological Chemistry. 193 (1); 1951: 265-275.
  • Natelson S, Scott Ml and Beffa C. A rapid method for the estimation of urea in biologic fluids. American Journal of Clinical Pathology. 21 (3); 1951: 275-281.
  • Drabkin DL and Austin JH. Spectrophotometric constants for common hemoglobin derivatives in human, dog and rabbit blood. The Journal of Biological Chemistry. 98; 1932: 719- 733.
  • Nayak SS and Pattabiraman TN. A new colorimetric method for the estimation of glycosylated haemoglobin. Clinica Chimica Acta. 109 (3); 1981: 267-274.
  • Brod J and Sirota JH, The renal clearance of endogenous creatinine in man. The Journal of Clinical Investigation. 27 (5); 1948: 645-654.
  • Caraway WT. Determination of uric acid in serum by a carbonate method, American Journal of Clinical Pathology. 25 (7); 1955: 840-845.
  • King J. The transaminases: alanine and aspartate transaminases. In: Practical clinical enzymology. Van Nostrand Reinhold, London, (1965a); 199-208.
  • King J. The hydrolases - acid and alakaline phosphatises. In: Practical clinical enzymology. Van Nostrand Reinhold, London, (1965b) 199-208.
  • Ohkawa H, Ohishi N and Vagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry. 95; 1979: 351-358.
  • Misra HP and Fridrovich T. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. The Journal of Biological Chemistry. 247; 1972: 3170-3175.
  • Takahara S, Hamilton HB, Neel JV, Kobara TY et al, Hypocatalasemia: a new genetic carrier state. Journal of Clinical Investigation. 39; 1960: 610-619.
  • Rotruck JT, Pope AL, Ganther HE, Swanson AB et al, Selenium: biochemical role as a component of glutathione peroxidise. Science. 179; 1973: 588-590.
  • Omaye ST, Turnbull JD and Sauberlich HE. Selected methods for the determination of ascorbic acid in animal cells, tissues, and fluids. Methods in Enzymology. 62; 1979: 3- 11.
  • Desai JD In: Parker (ed), Methods in enzymology, vol. 105, Academic Press, New York, 1984, pp.138.
  • Ravin HA. An improved colorimetric enzymatic assay of ceruloplasmin, The Journal of Laboratory and Clinical Medicine. 58; 1961: 161-168.
  • Sedlak J and Lindsay RH, Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Analytical Biochemistry. 25; 1968: 192–205.
  • Morales MA, Jabbagy AJ and Terenizi HR. Mutations affecting accumulation of Neurospora glycogen. News letter. 20; 1973: 24-25.
  • Parekh AC and Jung DH. Cholesterol determination with ferric acetate-uranium acetate and sulphuric acid ferrous sulphate reagents. Analytical Chemistry. 42; 1970: 1423- 1427.
  • Rice EW. In: Roedrick P and McDonal RP, editors, Standard methods in clinical chemistry. Academic Press, New York, 1970, pp. 215.
  • Burstein M, Scholnick HR and Morfin R. Rapid method for the isolation of lipoproteins from human serum by precipitation with polyanions, The Journal of Lipid Research. 11; 1970: 583-595.
  • Swanston-Flatt SK, Day C,Bailey CJ and Flatt PR. Traditional plant treatment for diabetes: Studies in normal and strptozotocin diabetic mice. Diabtologia. 33; 1990: 462-464.
  • Koenig RJ, Peterson CM, Jones RL, Saudek C, Lehrman M and Cerami A. Correlation of glucose regulation and hemoglobin A1c in diabetes mellitus. New England Journal of Medicine. 295(8); 1976: 417-420.
  • Larsen ML, Horder M and Mogensen EF. Effect of long-term monitoring of glycosylated haemoglobin levels in insulindependent diabetes mellitus. New England journal of Medicine. 323 (15); 1990: 1021-1025.
  • American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care. 31; 2006: 55–60.
  • Postic C Dentin R, and Girard J. Role of the liver in the control of carbohydrate and lipid homeostasis. Diabetes & Metabolism. 30 (5); 2004: 398-408.
  • Genuth M. Plasma Insulin and glucose profile in normal, Obese and diabetic person. Annals of Internal Medicine. 79; 1973: 812-822.
  • Prakasam A,Sethupathy S and Pugalendi KV (2004). Influence of Caseria esculenta ischolar_main extractioin on protin metabolism and marker nzymes in streptozotocin induced diabetic rats. Polish Journal of Pharmacology. 56; 2004: 587-593.
  • Almadal TP and Vilstrup H. Strict insulin treatment normalizes the organic nitrogen contents and the capacity of urea-nitrogen synthesis in experimental diabetes in rats. Diabetologia. 31; 1988: 114-118.
  • Alarcon-Aguilar FJ, Calzada-Bermejo F, Hernandez-Galicia E, Ruiz-Angeles C and Roman-Ramos R. Acute and chronic hypoglycemic effect of Ibervillea sonorae ischolar_main extracts-II. Journal of Ethonopharmacology. 97; 2005: 447-452.
  • Marchetti P, Lupi R, Del Guerra S, Bugliani M, Marselli L and Boggi U. The beta-cell in human type 2 diabetes. Advances in experimental medicine and biology. 654; 2010: 501-514.
  • Erejuwa OO, Sulaiman SA, Wahab MS, Sirajudeen KN, Salleh MS and Gurtu S. Antioxidant protection of Malaysian tualang honey in pancreas of normal and streptozotocin-induced diabetic rats. Ann Endocrinol (Paris). 71 (4); 2010: 291-296.
  • Browlee M. Biochemistry and molecular cell biology of diabetic complications. Nature. 414; 2001: 813-820.
  • Ha H and Kim KH. Pathogenesis of diabetic nephropathy: The role of oxidative stress and protein kinase C. Diabetes research and Clinical Practice. 45; 1999: 147-151.
  • Sugiura M, Ohshima M, Ogawa K, and Yano M. Chronic administration of Satsuma mandarian fruit (Citrus unshi MARC.). Improves oxidative stress in STZ induced diabetic rat liver. Biological & Pharmaceutical Bulletin. 29; 2006: 588- 591.
  • Yoshida K, Hirokawa J, Tagami S, Kawakami Y, Urata Y and Kondo T. Weakened cellular scavenging activity against oxidative stress in diabetes mellitus: regulation of glutathione synthesis and efflux. Diabetologia. 38; 1995: 201-210.
  • Frei B, England L, Ames BN. Ascorbate is an outstanding antioxidant in human blood plasma. Proceedings of the National Academy of Sciences of the United States of America 86; 1989: 6377-6381
  • Wefers H and Sies H. The protection by ascorbate and glutathione against microsomal lipid peroxidation is dependent on vitamin E. European Journal of Biochemistry. 174; 1988: 353-357
  • Winklhofer-Roob BM, Rock E, Ribalta J, Shmerling DH and Roob JM. Effects of vitamin E and carotenoid status on oxidative stress in health and disease. Evidence obtained from human intervention studies. Molecular Aspects of Medicine. 24 (6); 2003: 391-402.
  • Mooradian AD. Dyslipidemia in type 2 diabetes mellitus. Nature Clinical Practice. Endocrinology & Metabolism. 5 (3); 2009: 150-159.

Abstract Views: 418

PDF Views: 2




  • Antidiabetic Potential of Ficus Bengalensis Fruit Extract Studied in Alloxan-induced Experimental Diabetes in Rats

Abstract Views: 418  |  PDF Views: 2

Authors

S. Kavi Priya
Department of Biochemistry, University of Madras, Guindy campus, Chennai – 600 025, Tamil Nadu, India
V. Thamizhiniyan
Department of Biochemistry, University of Madras, Guindy campus, Chennai – 600 025, Tamil Nadu, India
S. Subramanian
Department of Biochemistry, University of Madras, Guindy campus, Chennai – 600 025, Tamil Nadu, India

Abstract


Ficus bengalensis (FB) (Moraceae) is commonly known as Banyan tree has been traditionally known for their beneficial pharmacological properties. In the absence of systemic studies in the literature, the present study was aimed to evaluate the antidiabetic potential of Ficus bengalensis fruit extract in alloxan-induced experimental diabetes in rats. The altered levels of biochemical parameters such as blood glucose, plasma insulin, haemoglobin, glycosylated haemoglobin, glycogen content in liver and muscle tissues, protein, urea, creatinine, uric aicd, AST, ALT and ALP in the diabetic rats were significantly reverted back to near basal values by the administration of Ficus bengalensis fruit extract for 30 days. The levels of lipid peroxides in the plasma and pancreatic tissues of diabetic rats were elevated significantly and were normalized by the administration of Ficus bengalensis fruit extract. The activities of pancreatic enzymic antioxidants and the levels of plasma non-enzymic antioxidants were markedly declined in the diabetic rats. Upon treatment with Ficus bengalensis fruit extract to diabetic rats, these decreased antioxidant levels were significantly improved. Further, the altered levels of lipid profile were significantly improved upon treatment with fruit extract. The results of the study indicate that Ficus bengalensis fruit extract possesses antidiabetic activity and the results are comparable with gliclazide, an oral standard hypoglycemic drug. The phytochemicals present in the Ficus bengalensis fruit may account for the observed pharmacological properties. Keywords: Medicinal plant; Ficus bengalensis; antidiabetic; antioxidant; alloxan.

References