Inhibitor-1 is not required for the activation of glycogen synthase by insulin in skeletal muscle

J Biol Chem. 1999 Jul 23;274(30):20949-52. doi: 10.1074/jbc.274.30.20949.

Abstract

Glycogen synthase is an excellent in vitro substrate for protein phosphatase-1 (PP1), which is potently inhibited by the phosphorylated forms of DARPP-32 (dopamine- and cAMP-regulated phosphoprotein, M(r) = 32,000) and Inhibitor-1. To test the hypothesis that the activation of glycogen synthase by insulin is due to a decrease in the inhibition of PP1 by the phosphatase inhibitors, we have investigated the effects of insulin on glycogen synthesis in skeletal muscles from wild-type mice and mice lacking Inhibitor-1 and DARPP-32 as a result of targeted disruption of the genes encoding the two proteins. Insulin increased glycogen synthase activity and the synthesis of glycogen to the same extent in wild-type and knockout mice, indicating that neither Inhibitor-1 nor DARPP-32 is required for the full stimulatory effects of insulin on glycogen synthase and glycogen synthesis in skeletal muscle.

Publication types

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

MeSH terms

  • Animals
  • Dopamine and cAMP-Regulated Phosphoprotein 32
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / metabolism
  • Glycogen Synthase / metabolism*
  • Hypoglycemic Agents / pharmacology*
  • Insulin / pharmacology*
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Skeletal / metabolism*
  • Nerve Tissue Proteins / metabolism*
  • Phosphoproteins*
  • Proteins / metabolism*

Substances

  • Dopamine and cAMP-Regulated Phosphoprotein 32
  • Enzyme Inhibitors
  • Hypoglycemic Agents
  • Insulin
  • Nerve Tissue Proteins
  • Phosphoproteins
  • Proteins
  • deinhibitor protein, Canis familiaris
  • Glycogen Synthase