Poor fetal nutrition causes long-term changes in expression of insulin signaling components in adipocytes

Am J Physiol. 1997 Jul;273(1 Pt 1):E46-51. doi: 10.1152/ajpendo.1997.273.1.E46.

Abstract

Insulin action on adipocytes was studied in the offspring of mothers who had been fed either a control (20% protein) or a low (8%)-protein diet during pregnancy and lactation. Adipocytes isolated from low-protein offspring had significantly higher basal and insulin-stimulated glucose uptakes than controls. This may be related to a threefold increase in insulin receptors in low-protein adipocytes. Consistent with these observed changes in glucose transport, adipocytes from low-protein animals had significantly higher basal and insulin-stimulated insulin receptor substrate (IRS)-1-associated phosphatidylinositol 3-kinase (PI 3-kinase) activities. There was also more p85-associated PI 3-kinase activity in these adipocytes. There was no difference in expression in the p85 regulatory subunit or the p110-alpha catalytic subunit of PI 3-kinase. In contrast, there was a sixfold reduction in the p110-beta catalytic subunit of PI 3-kinase in adipocytes from low-protein animals. These results suggest that poor fetal nutrition during pregnancy and lactation can have long-term effects on glucose transport and on the expression of key components of the insulin signaling pathway in adipocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / metabolism*
  • Adipose Tissue / cytology
  • Adipose Tissue / metabolism
  • Adipose Tissue / pathology
  • Animals
  • Body Weight
  • Cells, Cultured
  • Epididymis
  • Female
  • Glucose / metabolism*
  • Insulin / pharmacology*
  • Insulin Receptor Substrate Proteins
  • Lactation
  • Male
  • Monosaccharide Transport Proteins / metabolism
  • Organ Size
  • Phosphatidylinositol 3-Kinases
  • Phosphoproteins / metabolism
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Pregnancy
  • Pregnancy Complications / physiopathology*
  • Prenatal Exposure Delayed Effects*
  • Protein-Energy Malnutrition / physiopathology*
  • Rats
  • Rats, Wistar
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*

Substances

  • Insulin
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, rat
  • Monosaccharide Transport Proteins
  • Phosphoproteins
  • Phosphatidylinositol 3-Kinases
  • Phosphotransferases (Alcohol Group Acceptor)
  • Glucose