Hepatic effects of rosiglitazone in rats with the metabolic syndrome

Basic Clin Pharmacol Toxicol. 2010 Aug;107(2):663-8. doi: 10.1111/j.1742-7843.2010.00553.x. Epub 2010 Mar 4.

Abstract

Rats given fructose-enriched diet develop many characteristics of the human metabolic syndrome and non-alcoholic fatty liver disease. In this study, we characterized the hepatic effects of rosiglitazone in fructose-enriched diet rats. Rats were randomly divided into three groups. One group was maintained on standard rat chow diet for 6 weeks, whereas the other two groups were given fructose-enriched diet for 6 weeks. Four weeks after the initiation of fructose-enriched diet, one of the fructose-enriched diet groups was also given rosiglitazone (10 mg/kg/day) for an additional 2 weeks. Rosiglitazone administration to the fructose-enriched diet rats was associated with decreases in the following parameters: blood pressure (-17%), plasma triglycerides (-62%), hepatic total lipids (-19%), hepatic triglycerides (-61%), hepatic malondialdehyde (-88%), glutathione reductase activity (-84%). An increase in adiponectin plasma levels (+329%), hepatic phospholipids (+46%), hepatic alpha-tocopherol concentrations (+24%) and hepatic paraoxonase activity (+68%) was observed. Rosiglitazone caused a decrease in hepatic macrovesicular steatosis score but no change in hepatic fibrosis. Administration of rosiglitazone, to rats with the metabolic syndrome has limited hepatic favourable effects: it improves hepatic lipid metabolism, decreases macrovesicular steatosis and improves some of the hepatic oxidative-anti-oxidative milieu but has no effect on hepatic fibrosis.

MeSH terms

  • Adiponectin / metabolism
  • Animal Feed
  • Animals
  • Aryldialkylphosphatase / metabolism
  • Blood Pressure / drug effects
  • Fatty Liver / chemically induced
  • Fatty Liver / drug therapy
  • Fatty Liver / metabolism
  • Fructose / administration & dosage
  • Glutathione Reductase / metabolism
  • Hypoglycemic Agents / pharmacology*
  • Lipid Metabolism / drug effects
  • Lipids / analysis
  • Liver / drug effects*
  • Liver / metabolism
  • Liver Cirrhosis / chemically induced
  • Liver Cirrhosis / drug therapy
  • Liver Cirrhosis / metabolism
  • Male
  • Malondialdehyde / metabolism
  • Metabolic Syndrome / chemically induced
  • Metabolic Syndrome / drug therapy*
  • Phospholipids / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Rosiglitazone
  • Thiazolidinediones / pharmacology*
  • alpha-Tocopherol / metabolism

Substances

  • Adiponectin
  • Hypoglycemic Agents
  • Lipids
  • Phospholipids
  • Thiazolidinediones
  • Rosiglitazone
  • Fructose
  • Malondialdehyde
  • Glutathione Reductase
  • Aryldialkylphosphatase
  • alpha-Tocopherol