Chronic resveratrol administration has beneficial effects in experimental model of type 2 diabetic rats

Endocr Regul. 2012 Apr;46(2):83-90. doi: 10.4149/endo_2012_02_83.

Abstract

Objective: The present study was designed to evaluate whether long-term resveratrol administration has beneficial effects on the metabolic control and oxidative stress in diabetic rats.

Methods: Male Wistar rats were divided into four groups: normal control, diabetic control, normal treated with resveratrol, and diabetic treated with resveratrol. Diabetes was induced by injection of streptozotocin (50 mg/kg; i.p.), fifteen minutes after the administration of nicotinamide (110 mg/kg; i.p.) in 12 h fasted rats.

Results: Four-month oral resveratrol administration (5 mg/kg/day) significantly attenuated the elevated levels of the blood glucose, glycosylated hemoglobin, total protein, albumin, urea, creatinine, and 8-isoprostane in diabetic rats. Moreover, resveratrol administration to diabetic rats improved the reduced levels of glutathione, total antioxidant capacity, and the antioxidant enzymes activities (superoxide dismutase, glutathione peroxidase, and catalase). No significant differences were observed in the activities of plasma aminotransferases (ALT and AST) and insulin levels between diabetic rats treated with resveratrol and diabetic controls.

Conclusion: The results suggest that chronic resveratrol administration is safe and effective, and may be considered as a beneficial therapeutic compound in diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antioxidants / pharmacology*
  • Aspartate Aminotransferases / blood
  • Catalase / metabolism
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / metabolism
  • Disease Models, Animal
  • Glutathione Peroxidase / metabolism
  • Glutathione Peroxidase GPX1
  • Hyperglycemia / drug therapy
  • Hyperglycemia / metabolism
  • Male
  • Oxidative Stress / drug effects
  • Rats
  • Rats, Wistar
  • Resveratrol
  • Stilbenes / pharmacology*
  • Superoxide Dismutase / metabolism

Substances

  • Antioxidants
  • Stilbenes
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Resveratrol
  • Glutathione Peroxidase GPX1
  • Gpx1 protein, rat