Exercise training and clenbuterol reduce insulin resistance of obese Zucker rats

Am J Physiol. 1993 Mar;264(3 Pt 1):E373-9. doi: 10.1152/ajpendo.1993.264.3.E373.

Abstract

This study compared the effects of aerobic exercise training and chronic administration of the selective beta 2-adrenergic agonist clenbuterol on whole body and skeletal muscle insulin resistance in obese (fa/fa) Zucker rats. Obese rats were randomly assigned to training, clenbuterol, or sedentary control groups. Lean littermates served as a second control group. After 4-5 wk of treatment, an oral glucose tolerance test was performed, followed 1 wk later by hindlimb perfusion, during which time the rates of glucose uptake and 3-O-methyl-D-glucose (3-MG) transport were assessed in the presence of a submaximal (500 microU/ml) insulin concentration. Training resulted in a significant increase in citrate synthase and cytochrome oxidase activity in the recruited muscles. Clenbuterol induced a large increase in muscle mass but provoked a significant decrease in oxidative enzyme activity and beta-adrenergic receptor density. Both treatments increased glucose tolerance and reduced the postglucose insulin response, with the improvements being more pronounced in the clenbuterol group. However, only exercise training improved insulin-stimulated hindlimb muscle glucose uptake (11.37 +/- 0.65, 8.73 +/- 0.77, and 8.27 +/- 0.41 mumol.g-1.h-1 for trained, clenbuterol, and sedentary control groups, respectively) and 3-MG transport. These results suggest that aerobic exercise training attenuated the insulin-resistant condition in the obese Zucker rat by a mechanism other than or in addition to beta 2-adrenergic receptor activation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-O-Methylglucose
  • Animals
  • Biological Transport / drug effects
  • Biological Transport / physiology
  • Body Weight / drug effects
  • Body Weight / physiology
  • Citrate (si)-Synthase / analysis
  • Citrate (si)-Synthase / physiology
  • Clenbuterol / pharmacology*
  • Dose-Response Relationship, Drug
  • Electron Transport Complex IV / analysis
  • Electron Transport Complex IV / physiology
  • Female
  • Glucose / pharmacokinetics
  • Glucose / pharmacology
  • Glucose Tolerance Test
  • Insulin / pharmacology
  • Insulin Resistance / physiology*
  • Methylglucosides / pharmacokinetics
  • Muscles / enzymology
  • Muscles / physiology
  • Muscles / ultrastructure
  • Obesity / physiopathology*
  • Physical Conditioning, Animal*
  • Rats
  • Rats, Zucker
  • Receptors, Adrenergic / analysis

Substances

  • Insulin
  • Methylglucosides
  • Receptors, Adrenergic
  • 3-O-Methylglucose
  • Electron Transport Complex IV
  • Citrate (si)-Synthase
  • Glucose
  • Clenbuterol