Insulin receptor substrate-1 (IRS-1) expression in rat brain

Endocrinology. 1994 Apr;134(4):1952-5. doi: 10.1210/endo.134.4.7511094.

Abstract

IRS-1 is phosphorylated on tyrosine residues after insulin stimulation and participates in the early events of signal transduction in peripheral insulin-sensitive tissues. This study determined whether neuronal populations in the rat olfactory bulb and hippocampus (brain regions which have very high concentrations of insulin receptors) also express IRS-1 and contain phosphotyrosine, using in situ hybridization, receptor binding, and immunocytochemistry. IRS-1 mRNA was colocalized with insulin receptor mRNA in neuron cell bodies of hippocampus and olfactory bulb. Similarly, IRS-1 immunoreactivity in hippocampus and olfactory bulb was concentrated in layers that contain synapses of these neurons and have both high insulin binding and phosphotyrosine levels. Thus, IRS-1 and insulin receptors are coexpressed in discrete populations of neurons, suggesting a signal transduction mechanism by which insulin may influence metabolism and gene expression in the brain.

Publication types

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

MeSH terms

  • Animals
  • Brain / cytology
  • Brain / metabolism*
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • Immunohistochemistry
  • In Situ Hybridization
  • Insulin Receptor Substrate Proteins
  • Male
  • Neurons / metabolism
  • Olfactory Bulb / cytology
  • Olfactory Bulb / metabolism
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Phosphotyrosine
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Tyrosine / analogs & derivatives
  • Tyrosine / metabolism

Substances

  • Insulin Receptor Substrate Proteins
  • Irs1 protein, rat
  • Phosphoproteins
  • RNA, Messenger
  • Phosphotyrosine
  • Tyrosine