Recruitment of GLUT-4 glucose transporters by insulin in diabetic rat skeletal muscle

Biochem Biophys Res Commun. 1990 Oct 30;172(2):728-36. doi: 10.1016/0006-291x(90)90735-6.

Abstract

The cause of reduced insulin-stimulated glucose transport in skeletal muscle of diabetic rats was investigated. Basal and insulin-stimulated glucose uptake into hindquarter muscles of 7-day diabetic rats were 70% and 50% lower, respectively, than in nondiabetic controls. Subcellular fractionation of hindquarter muscles yielded total crude membranes, plasma membranes and intracellular membranes. The number of GLUT-4 glucose transporters was lower in crude membranes, plasma membranes and intracellular membranes, relative to non-diabetic rat muscles. These results were paralleled by reductions in D-glucose-protectable binding of cytochalasin B. Insulin caused a redistribution of GLUT-4 transporters from intracellular membranes to plasma membranes, in both control and diabetic rat muscles. This redistribution was also recorded using binding of cytochalasin B. The insulin-dependent decrement in glucose transporters in intracellular membranes was similar for both animal groups, but the gain and final amount of transporters in the plasma membrane were 50% lower in the diabetic group. The results suggest that insulin signalling and recruitment of GLUT-4 glucose transporters occur in diabetic rat muscle, and that the diminished insulin response may be due to fewer glucose transporters operating in the muscle plasma membrane.

Publication types

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

MeSH terms

  • Animals
  • Cell Membrane / metabolism
  • Cytochalasin B / metabolism
  • Diabetes Mellitus, Experimental / metabolism*
  • Insulin / pharmacology
  • Intracellular Membranes / metabolism
  • Kinetics
  • Male
  • Monosaccharide Transport Proteins / metabolism*
  • Muscles / drug effects
  • Muscles / metabolism*
  • Rats
  • Rats, Inbred Strains
  • Reference Values

Substances

  • Insulin
  • Monosaccharide Transport Proteins
  • Cytochalasin B