Contraction-stimulated muscle glucose transport and GLUT-4 surface content are dependent on glycogen content

Am J Physiol. 1999 Dec;277(6):E1103-10. doi: 10.1152/ajpendo.1999.277.6.E1103.

Abstract

The influence of muscle glycogen content on basal and contraction-induced glucose transport and cell surface GLUT-4 content was studied in rat skeletal muscle. Wistar rats were preconditioned by a combination of swimming exercise and diet, resulting in 40% lower (LG) or threefold higher (HG) muscle glycogen content compared with nonexercised controls (NG). At rest and during contractions, 2-deoxy-D-glucose uptake in perfused fast-twitch muscle, but not slow-twitch muscle, was significantly lower in HG compared with LG. Cell surface GLUT-4 content in the fast-twitch plantaris was 994 +/- 180, 1,173 +/- 311, and 2,155 +/- 243 dpm/g in the basal condition and increased (P < 0.05) to 2,285 +/- 239, 3,230 +/- 464, and 4,847 +/- 654 dpm/g during contractions with HG, NG, and LG, respectively, the increase being significantly smaller in HG compared with LG. The contraction-induced increments in glucose transport and in cell surface GLUT-4 content were negatively correlated with the initial glycogen content (P <0.01). In conclusion, glucose transport and cell surface GLUT-4 content in resting and contracting fast-twitch muscle are dependent on the muscle glycogen content.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimetabolites / pharmacokinetics
  • Biological Transport / physiology
  • Body Weight
  • Deoxyglucose / pharmacokinetics
  • Glucose / metabolism*
  • Glucose Transporter Type 4
  • Glycogen / metabolism*
  • Hindlimb
  • In Vitro Techniques
  • Male
  • Membrane Proteins / analysis
  • Membrane Proteins / metabolism
  • Monosaccharide Transport Proteins / analysis
  • Monosaccharide Transport Proteins / metabolism*
  • Muscle Contraction / physiology*
  • Muscle Proteins*
  • Muscle, Skeletal / chemistry
  • Muscle, Skeletal / metabolism*
  • Oxygen Consumption / physiology
  • Perfusion
  • Physical Exertion / physiology
  • Rats
  • Rats, Wistar

Substances

  • Antimetabolites
  • Glucose Transporter Type 4
  • Membrane Proteins
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Slc2a4 protein, rat
  • Glycogen
  • Deoxyglucose
  • Glucose