Starvation-increased insulin-dependent tyrosine phosphorylation of the 195-kDa protein in intact rat liver

Biosci Biotechnol Biochem. 1997 Dec;61(12):2122-4. doi: 10.1271/bbb.61.2122.

Abstract

Insulin stimulates tyrosine phosphorylation of 175-195 kDa proteins including insulin receptor substrate-1 (IRS-1) in various tissues and cell types. In intact rat livers, starvation increased the insulin-dependent tyrosine phosphorylation of the insulin receptor and IRS-1 as has been described by others. Surprisingly, starvation greatly increased the tyrosine phosphorylation of the 195-kDa protein induced by insulin, indicating that this protein may be a new substrate of the insulin receptor kinase. The marked increase in tyrosine phosphorylation of the 195-kDa protein may have a physiological role in signal transmission in response to insulin under starvation conditions.

MeSH terms

  • Animals
  • Insulin / pharmacology*
  • Insulin Receptor Substrate Proteins
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Molecular Weight
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Precipitin Tests
  • Proteins / metabolism
  • Rats
  • Rats, Wistar
  • Receptor, Insulin / drug effects*
  • Receptor, Insulin / metabolism
  • Starvation / metabolism*
  • Tyrosine / chemistry
  • Tyrosine / metabolism*

Substances

  • Insulin
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, rat
  • Phosphoproteins
  • Proteins
  • Tyrosine
  • Receptor, Insulin