The association effect of insulin and clonazepam on oxidative stress in liver of an experimental animal model of diabetes and depression

Pharm Biol. 2013 May;51(5):533-8. doi: 10.3109/13880209.2012.747544. Epub 2013 Feb 1.

Abstract

Context: It is known that oxidative stress occurs in peripheral blood in an experimental animal model of diabetes and depression, and acute treatment with insulin and clonazepam (CNZ) has a protective effect on oxidative stress in this model.

Objective: This study evaluated the effect of insulin plus CNZ on oxidative stress parameters in the liver of diabetic male rats induced with streptozotocin (STZ) and subjected to forced swimming test (FST).

Materials and methods: Diabetes was induced by a single intraperitoneal (i.p.) dose of STZ 60 mg/kg in male Wistar rats. Insulin (4 IU/kg) plus CNZ acute i.p. treatment (0.25 mg/kg) was administered 24, 5 and 1 h before the FST. Nondiabetic control rats received i.p. injections of saline (1 mL/kg). Protein oxidative damage was evaluated by carbonyl formation and the antioxidant redox parameters were analyzed by the measurements of enzymatic activities of the superoxide dismutase (SOD), catalase and glyoxalase I (GLO). Glycemia levels also were determined.

Results: Our present study has shown an increase in carbonyl content from diabetic rats subjected to FST (2.04 ± 0.55), while the activity of catalase (51.83 ± 19.02) and SOD (2.30 ± 1.23) were significantly decreased in liver from these animals, which were reverted by the treatment. Also, the activity of GLO (0.15 ± 0.02) in the liver of the animals was decreased.

Discussion and conclusion: Our findings showed that insulin plus CNZ acute treatment ameliorate the antioxidant redox parameters and protect against protein oxidative damage in the liver of diabetic rats subjected to FST.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Catalase / metabolism
  • Clonazepam / administration & dosage
  • Clonazepam / pharmacology*
  • Depression / drug therapy*
  • Depression / physiopathology
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / physiopathology
  • Disease Models, Animal
  • Drug Therapy, Combination
  • Insulin / administration & dosage
  • Insulin / pharmacology*
  • Lactoylglutathione Lyase / metabolism
  • Liver / drug effects
  • Liver / pathology
  • Male
  • Oxidation-Reduction / drug effects
  • Oxidative Stress / drug effects*
  • Protein Carbonylation / drug effects
  • Rats
  • Rats, Wistar
  • Streptozocin
  • Superoxide Dismutase / metabolism
  • Time Factors

Substances

  • Insulin
  • Clonazepam
  • Streptozocin
  • Catalase
  • Superoxide Dismutase
  • Lactoylglutathione Lyase