Mechanisms underlying impaired GLUT-4 translocation in glycogen-supercompensated muscles of exercised rats

Am J Physiol Endocrinol Metab. 2000 Dec;279(6):E1311-8. doi: 10.1152/ajpendo.2000.279.6.E1311.

Abstract

Exercise training induces an increase in GLUT-4 in muscle. We previously found that feeding rats a high-carbohydrate diet after exercise, with muscle glycogen supercompensation, results in a decrease in insulin responsiveness so severe that it masks the effect of a training-induced twofold increase in GLUT-4 on insulin-stimulated muscle glucose transport. One purpose of this study was to determine whether insulin signaling is impaired. Maximally insulin-stimulated phosphatidylinositol (PI) 3-kinase activity was not significantly reduced, whereas protein kinase B (PKB) phosphorylation was approximately 50% lower (P < 0.01) in muscles of chow-fed, than in those of fasted, exercise-trained rats. Our second purpose was to determine whether contraction-stimulated glucose transport is also impaired. The stimulation of glucose transport and the increase in cell surface GLUT-4 induced by contractions were both decreased by approximately 65% in glycogen-supercompensated muscles of trained rats. The contraction-stimulated increase in AMP kinase activity, which has been implicated in the activation of glucose transport by contractions, was approximately 80% lower in the muscles of the fed compared with the fasted rats 18 h after exercise. These results show that both the insulin- and contraction-stimulated pathways for muscle glucose transport activation are impaired in glycogen-supercompensated muscles and provide insight regarding possible mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 3-O-Methylglucose / pharmacokinetics
  • AMP-Activated Protein Kinases
  • Affinity Labels
  • Animals
  • Azides
  • Biological Transport / physiology
  • Dietary Carbohydrates / pharmacology
  • Disaccharides
  • Glucose Transporter Type 4
  • Glycogen / metabolism*
  • Glycosides
  • Insulin / metabolism
  • Male
  • Membrane Proteins / metabolism
  • Monosaccharide Transport Proteins / metabolism*
  • Multienzyme Complexes / metabolism
  • Muscle Proteins*
  • Muscle, Skeletal / enzymology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Physical Exertion / drug effects
  • Physical Exertion / physiology*
  • Propylamines*
  • Protein Serine-Threonine Kinases / metabolism
  • Rats
  • Rats, Wistar
  • Signal Transduction / physiology
  • Tritium

Substances

  • Affinity Labels
  • Azides
  • Dietary Carbohydrates
  • Disaccharides
  • Glucose Transporter Type 4
  • Glycosides
  • Insulin
  • Membrane Proteins
  • Monosaccharide Transport Proteins
  • Multienzyme Complexes
  • Muscle Proteins
  • Propylamines
  • Slc2a4 protein, rat
  • Tritium
  • 2-N-(4-(1-azitrifluoroethyl)benzoyl)-1,3-bis-(mannos-4-yloxy)-2-propylamine
  • 3-O-Methylglucose
  • Glycogen
  • Protein Serine-Threonine Kinases
  • AMP-Activated Protein Kinases