Impaired autophosphorylation of insulin receptors from abdominal skeletal muscles in nonobese subjects with NIDDM

Diabetes. 1991 Jul;40(7):815-9. doi: 10.2337/diab.40.7.815.

Abstract

We studied both autophosphorylation and phosphotransferase activity of insulin receptors from abdominal skeletal muscles of nonobese subjects with non-insulin-dependent diabetes mellitus (NIDDM). Partially purified insulin receptors were labeled on their alpha-subunit with 125I-labeled insulin by chemical cross-linking and on their beta-subunit by autophosphorylation with 1000 microM ATP. Thereafter, phosphorylated insulin receptors were separated from total receptors with the anti-phosphotyrosine antibody. Thus, the percentage of phosphorylated receptors in total receptors revealed the autophosphorylation activity. Using this method, we studied the function of insulin receptors from muscle obtained by biopsy during surgery in 10 nonobese NIDDM and 8' control subjects. In diabetic subjects, insulin binding capacity from abdominal skeletal muscles was 69.4% of the control subjects. Furthermore, the percentage of phosphorylated insulin receptors stimulated by 8.3 nM insulin was significantly lower than the control subjects (mean +/- SD, 29.0 +/- 12.0 vs. 56.0 +/- 7.4%, P less than 0.01), and there was a significant inverse correlation between fasting plasma glucose levels and the percentage of phosphorylated receptors among diabetic subjects (r = 0.73, P less than 0.025). Moreover, the insulin-stimulated kinase activity toward a synthetic peptide (Glu80Tyr20) was also impaired in diabetic subjects (28.5% of control). In summary, this is the first demonstration that the autophosphorylation step of insulin receptors from abdominal skeletal muscles is impaired in nonobese NIDDM subjects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Blood Glucose / analysis
  • Body Weight
  • Female
  • Humans
  • Insulin / metabolism
  • Macromolecular Substances
  • Male
  • Middle Aged
  • Molecular Weight
  • Muscles / metabolism*
  • Phosphorylation
  • Protein-Tyrosine Kinases / metabolism*
  • Receptor, Insulin / isolation & purification
  • Receptor, Insulin / metabolism*
  • Reference Values

Substances

  • Blood Glucose
  • Insulin
  • Macromolecular Substances
  • Adenosine Triphosphate
  • Protein-Tyrosine Kinases
  • Receptor, Insulin