Caloric restriction and growth hormone receptor knockout: effects on expression of genes involved in insulin action in the heart

Exp Gerontol. 2006 Apr;41(4):417-29. doi: 10.1016/j.exger.2006.01.009. Epub 2006 Mar 9.

Abstract

Blockade of growth hormone (GH), decreased insulin-like growth factor-1 (IGF1) action and increased insulin sensitivity are associated with life extension and an apparent slowing of the aging process. We examined expression of genes involved in insulin action, IR, IRS1, IRS2, IGF1, IGF1R, GLUT4, PPARs and RXRs in the hearts of normal and GHR-/- (KO) mice fed ad libitum or subjected to 30% caloric restriction (CR). CR increased the cardiac expression of IR, IRS1, IGF1, IGF1R and GLUT4 in normal mice and IRS1, GLUT4, PPARalpha and PPARbeta/delta in GHR-KO animals. Expression of IR, IRS1, IRS2, IGF1, GLUT4, PPARgamma and PPARalpha did not differ between GHR-KO and normal mice. These unexpected results suggest that CR may lead to major modifications of insulin action in the heart, but high insulin sensitivity of GHR-KO mice is not associated with alterations in the levels of most of the examined molecules related to intracellular insulin signaling.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / metabolism*
  • Animals
  • Blotting, Western
  • Caloric Restriction*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Gene Expression
  • Glucose Transporter Type 4 / genetics
  • Glucose Transporter Type 4 / metabolism
  • Growth Hormone / genetics
  • Growth Hormone / metabolism
  • Insulin / metabolism*
  • Insulin Resistance
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Myocardium / metabolism*
  • PPAR alpha / genetics
  • PPAR alpha / metabolism
  • PPAR delta / genetics
  • PPAR delta / metabolism
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • PPAR-beta / genetics
  • PPAR-beta / metabolism
  • RNA, Messenger / analysis
  • Receptor, IGF Type 1 / genetics
  • Receptor, IGF Type 1 / metabolism
  • Receptor, Insulin / genetics
  • Receptor, Insulin / metabolism
  • Receptors, Somatotropin / genetics
  • Receptors, Somatotropin / metabolism*
  • Retinoid X Receptors / genetics
  • Retinoid X Receptors / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Signal Transduction / physiology*

Substances

  • Carrier Proteins
  • Glucose Transporter Type 4
  • Insulin
  • PPAR alpha
  • PPAR delta
  • PPAR gamma
  • PPAR-beta
  • RNA, Messenger
  • Receptors, Somatotropin
  • Retinoid X Receptors
  • Insulin-Like Growth Factor I
  • Growth Hormone
  • Receptor, IGF Type 1
  • Receptor, Insulin
  • somatotropin-binding protein