Catch-up growth following intra-uterine growth-restriction programmes an insulin-resistant phenotype in adipose tissue

Int J Obes (Lond). 2013 Aug;37(8):1051-7. doi: 10.1038/ijo.2012.196. Epub 2012 Dec 11.

Abstract

Background: It is now widely accepted that the early-life nutritional environment is important in determining susceptibility to metabolic diseases. In particular, intra-uterine growth restriction followed by accelerated postnatal growth is associated with an increased risk of obesity, type-2 diabetes and other features of the metabolic syndrome. The mechanisms underlying these observations are not fully understood.

Aim: Using a well-established maternal protein-restriction rodent model, our aim was to determine if exposure to mismatched nutrition in early-life programmes adipose tissue structure and function, and expression of key components of the insulin-signalling pathway.

Methods: Offspring of dams fed a low-protein (8%) diet during pregnancy were suckled by control (20%)-fed dams to drive catch-up growth. This 'recuperated' group was compared with offspring of dams fed a 20% protein diet during pregnancy and lactation (control group). Epididymal adipose tissue from 22-day and 3-month-old control and recuperated male rats was studied using histological analysis. Expression and phosphorylation of insulin-signalling proteins and gene expression were assessed by western blotting and reverse-transcriptase PCR, respectively.

Results: Recuperated offspring at both ages had larger adipocytes (P<0.001). Fasting serum glucose, insulin and leptin levels were comparable between groups but increased with age. Recuperated offspring had reduced expression of IRS-1 (P<0.01) and PI3K p110β (P<0.001) in adipose tissue. In adult recuperated rats, Akt phosphorylation (P<0.01) and protein levels of Akt-2 (P<0.01) were also reduced. Messenger RNA expression levels of these proteins were not different, indicating a post-transcriptional effect.

Conclusion: Early-life nutrition programmes alterations in adipocyte cell size and impairs the protein expression of several insulin-signalling proteins through post-transcriptional mechanisms. These indices may represent early markers of insulin resistance and metabolic disease risk.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes
  • Adipose Tissue / pathology
  • Animals
  • Blotting, Western
  • Body Weight
  • Diabetes Mellitus, Type 2 / pathology*
  • Female
  • Fetal Development
  • Fetal Growth Retardation / metabolism
  • Fetal Growth Retardation / pathology*
  • Gene Expression
  • Insulin
  • Insulin Resistance*
  • Male
  • Metabolic Syndrome / metabolism
  • Metabolic Syndrome / pathology*
  • Obesity / pathology*
  • Phenotype
  • Phosphorylation
  • Pregnancy
  • Prenatal Exposure Delayed Effects
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • Insulin
  • Akt2 protein, rat
  • Proto-Oncogene Proteins c-akt