Effects of exercise training and antioxidant R-ALA on glucose transport in insulin-sensitive rat skeletal muscle

J Appl Physiol (1985). 2002 Jan;92(1):50-8. doi: 10.1152/japplphysiol.000617.2001.

Abstract

We have recently demonstrated (Saengsirisuwan V, Kinnick TR, Schmit MB, and Henriksen EJ, J Appl Physiol 91: 145-153, 2001) that exercise training (ET) and the antioxidant R-(+)-alpha-lipoic acid (R-ALA) interact in an additive fashion to improve insulin action in insulin-resistant obese Zucker (fa/fa) rats. The purpose of the present study was to assess the interactions of ET and R-ALA on insulin action and oxidative stress in a model of normal insulin sensitivity, the lean Zucker (fa/-) rat. For 6 wk, animals either remained sedentary, received R-ALA (30 mg. kg body wt(-1). day(-1)), performed ET (treadmill running), or underwent both R-ALA treatment and ET. ET alone or in combination with R-ALA significantly increased (P < 0.05) peak oxygen consumption (28-31%) and maximum run time (52-63%). During an oral glucose tolerance test, ET alone or in combination with R-ALA resulted in a significant lowering of the glucose response (17-36%) at 15 min relative to R-ALA alone and of the insulin response (19-36%) at 15 min compared with sedentary controls. Insulin-mediated glucose transport activity was increased by ET alone in isolated epitrochlearis (30%) and soleus (50%) muscles, and this was associated with increased GLUT-4 protein levels. Insulin action was not improved by R-ALA alone, and ET-associated improvements in these variables were not further enhanced with combined ET and R-ALA. Although ET and R-ALA caused reductions in soleus protein carbonyls (an index of oxidative stress), these alterations were not significantly correlated with insulin-mediated soleus glucose transport. These results indicate that the beneficial interactive effects of ET and R-ALA on skeletal muscle insulin action observed previously in insulin-resistant obese Zucker rats are not apparent in insulin-sensitive lean Zucker rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimetabolites / metabolism
  • Antioxidants / pharmacology*
  • Blood Glucose / metabolism
  • Body Weight / drug effects
  • Body Weight / physiology
  • Deoxyglucose / metabolism
  • Female
  • Glucose / metabolism*
  • Glucose Tolerance Test
  • Glucose Transporter Type 4
  • Insulin / blood
  • Insulin / physiology*
  • Monosaccharide Transport Proteins / metabolism
  • Muscle Proteins / metabolism
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / physiology
  • Oxygen Consumption / drug effects
  • Physical Conditioning, Animal / physiology*
  • Rats
  • Rats, Zucker
  • Thioctic Acid / pharmacology*

Substances

  • Antimetabolites
  • Antioxidants
  • Blood Glucose
  • Glucose Transporter Type 4
  • Insulin
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Slc2a4 protein, rat
  • Thioctic Acid
  • Deoxyglucose
  • Glucose