Insulin-induced translocation of GLUT 4 in skeletal muscle of insulin-resistant Zucker rats

Diabetologia. 1994 Jan;37(1):3-9. doi: 10.1007/BF00428770.

Abstract

The genetically obese Zucker rat (fa/fa) is an animal model with severe insulin resistance of the skeletal muscle. We investigated whether a defect of insulin-dependent glucose transporter (GLUT 4) translocation might contribute to the pathogenesis of the insulin-resistant state. fa/fa rats, lean controls (Fa/Fa) as well as normal Wistar rats were injected intraperitoneally with insulin and were killed after 2 or 20 min, respectively. Subcellular fractions were prepared from hind-limb skeletal muscle and were characterized by determination of marker-enzyme activities and immunoblotting applying antibodies against alpha 1 Na+/K+ ATPase. The relative amounts of GLUT 1 and GLUT 4 were determined in the fractions by immunoblotting with the respective antibodies. Insulin induced an approximately two-fold increase of GLUT 4 in a plasma membrane and transverse tubule enriched fraction and a decrease in the low density enriched membrane fraction in all three groups of rats. There was a high individual variation in GLUT 4 translocation efficiency within the groups. However, no statistically significant difference was noted between the groups. No effect of insulin was detectable on the distribution of GLUT 1 or alpha 1 Na+K+ ATPase. The data suggest that skeletal muscle insulin resistance of obese Zucker rats is not associated with a lack of GLUT 4 translocation.

Publication types

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

MeSH terms

  • Animals
  • Antibodies
  • Cell Membrane / metabolism
  • Glucose Transporter Type 1
  • Glucose Transporter Type 4
  • Immunoblotting
  • Insulin / pharmacology*
  • Insulin Resistance / genetics*
  • Monosaccharide Transport Proteins / analysis
  • Monosaccharide Transport Proteins / biosynthesis*
  • Muscle Proteins*
  • Muscles / drug effects
  • Muscles / metabolism*
  • Obesity / genetics
  • Obesity / metabolism*
  • Protein Processing, Post-Translational
  • Rats
  • Rats, Wistar
  • Rats, Zucker / metabolism*
  • Sodium-Potassium-Exchanging ATPase / immunology
  • Sodium-Potassium-Exchanging ATPase / metabolism

Substances

  • Antibodies
  • Glucose Transporter Type 1
  • Glucose Transporter Type 4
  • Insulin
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Slc2a1 protein, rat
  • Slc2a4 protein, rat
  • Sodium-Potassium-Exchanging ATPase