Defective insulin response of phosphorylase phosphatase in insulin-resistant humans

J Clin Invest. 1992 Feb;89(2):610-7. doi: 10.1172/JCI115627.

Abstract

Insulin-stimulated glycogen synthase activity in human muscle is reduced in insulin-resistant subjects. Insulin regulation of human muscle glycogen synthase may require activation of a type-1 protein phosphatase (PP-1). We investigated the change of phosphorylase phosphatase and glycogen synthase activities in muscle biopsies obtained during a 2-h hyperinsulinemic euglycemic clamp in 12 insulin-sensitive (group S) and 8 insulin-resistant (group R) subjects. Fasting phosphorylase phosphatase activity was lower in group R than in group S, and did not increase significantly with insulin infusion in group R until 20 min. In group S, phosphorylase phosphatase was significantly stimulated by 10 min, remaining significantly higher than in group R at all time points. The insulin-mediated changes in phosphatase activities were not decreased by 3 nM okadaic acid but were completely inhibited by 1 microM okadaic acid, thereby verifying that insulin-stimulated phosphorylase phosphatase is accounted for by a PP-1. Subcellular fractionation demonstrated reduced fasting PP-1 activities in both the glycogen and cytosolic fractions of muscle obtained from subjects in group R compared to those in group S. These results suggest that insulin activation of PP-1 could contribute to the stimulation of glycogen synthase by this hormone in human muscle. Lower fasting PP-1 activity in cytosol and glycogen fractions plus lower insulin-stimulated PP-1 activity could explain, in part, reduced insulin-stimulated glycogen synthase in skeletal muscle of insulin-resistant subjects.

MeSH terms

  • Adult
  • Ethers, Cyclic / pharmacology
  • Female
  • Glycogen Synthase / analysis
  • Humans
  • Insulin / pharmacology*
  • Insulin Resistance*
  • Male
  • Muscles / enzymology
  • Okadaic Acid
  • Phosphorylase Phosphatase / analysis*
  • Phosphorylation

Substances

  • Ethers, Cyclic
  • Insulin
  • Okadaic Acid
  • Glycogen Synthase
  • Phosphorylase Phosphatase