Rutin improves the antioxidant status in streptozotocin-induced diabetic rat tissues

• Published in: Molecular and cellular biochemistry Vol. 293; no. 1-2; pp. 211 - 219
• Main Authors: Kamalakkannan, N, Stanely Mainzen Prince, P
• Format: Journal Article
• Language: English
• Published: Netherlands New York : Kluwer Academic Publishers-Plenum Publishers 01-12-2006; Springer Nature B.V
• Subjects: Animal tissues; Animals; Antioxidants; Antioxidants - metabolism; Blood Glucose - metabolism; Brain - drug effects; Brain - metabolism; Brain - pathology; diabetes mellitus; Diabetes Mellitus, Experimental - metabolism; Diabetes Mellitus, Experimental - pathology; Insulin; Insulin - metabolism; Kidney - drug effects; Kidney - metabolism; Kidney - pathology; Kidneys; lipid peroxidation; Lipid Peroxidation - drug effects; Lipids; Liver - drug effects; Liver - metabolism; Liver - pathology; Male; Rats; Rats, Wistar; Rodents; rutin; Rutin - administration & dosage; Rutin - pharmacology; streptozotocin; Thiobarbituric Acid Reactive Substances - metabolism
• ISSN: 0300-8177; 1573-4919
• DOI: 10.1007/s11010-006-9244-1

Rutin, a polyphenolic flavonoid, was investigated for its antioxidant potential in streptozotocin (STZ)-induced diabetic rats. Rats were rendered diabetic by a single intraperitoneal injection of streptozotocin (50 mg/kg). The levels of fasting plasma glucose and insulin were estimated. Lipid peroxidative products and antioxidants were estimated in liver, kidney and brain. Histopathological studies were carried out in these tissues. A significant (p < 0.05) increase in the levels of fasting plasma glucose, lipid peroxidative products (thiobarbituric acid reactive substances [TBARS] and lipid hydroperoxides [HP]) and a significant (p < 0.05) decrease in plasma insulin, enzymic antioxidants (superoxide dismutase [SOD], catalase, glutathione peroxidase [GPx] and glutathione reductase [GRx]) and nonenzymic antioxidants (reduced glutathione [GSH], vitamin C and E) in diabetic liver, kidney and brain were observed. Oral administration of rutin (100 mg/kg) for a period of 45 days significantly (p < 0.05) decreased fasting plasma glucose, increased insulin levels and improved the antioxidant status of diabetic rats by decreasing lipid peroxidative products and increasing enzymic and nonenzymic antioxidants. Normal rats treated with rutin (100 mg/kg) showed no significant (p < 0.05) effect on any of the parameters studied. Histopathological studies of the liver, kidney and brain showed the protective role of rutin. Thus, our study clearly shows that rutin has antioxidant effect in STZ-induced experimental diabetes.