Comparison of two models of intrauterine growth restriction for early catch-up growth and later development of glucose intolerance and obesity in rats

Am J Physiol Regul Integr Comp Physiol. 2010 Jan;298(1):R141-6. doi: 10.1152/ajpregu.00128.2009. Epub 2009 Nov 4.

Abstract

Two models of intrauterine growth restriction, maternal food restriction (FR), and dexamethasone (DEX) exposure were compared for early postnatal catch-up growth and later development of glucose intolerance and obesity in Sprague-Dawley rats. Mated dams were randomly divided into three groups at 10 days gestational age. Group FR was food restricted (50% of nongestating rats) during the last 11 days of gestation; Group DEX received DEX injections during the last week of gestation, and Group CON, the control group, had no intervention. Birth weight, catch-up growth, body weight, and food intake were measured in male offspring for 22 wk. Body composition, blood glucose, and plasma insulin in response to a glucose load were assessed at 8, 16, and 22 wk. Pups from both FR and DEX dams had similarly lower birth weights than CON (22% and 25%, P < 0.0001), but catch-up growth, which occurred during the suckling period, was much more rapid in FR than DEX offspring (6 vs. 25 days, 95% CI). Postweaning, there were no significant differences between groups in food intake, body weight, body fat, and plasma insulin, but baseline plasma glucose at 22 wk and 2-h glucose area-under-the-curve at 8 and 22 wk were greater only in FR vs. CON offspring (P < 0.05), thereby contrasting with the lack of significant differences between DEX and CON. These results suggest that prenatal food restriction is a more sensitive model than DEX exposure for studies aimed at investigating the link between low birth weight, early postnatal catch-up growth, and later development of glucose intolerance.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Animals, Newborn / growth & development*
  • Animals, Newborn / physiology
  • Blood Glucose / metabolism
  • Body Weight / drug effects
  • Body Weight / physiology
  • Dexamethasone / pharmacology
  • Disease Models, Animal*
  • Eating / drug effects
  • Eating / physiology
  • Female
  • Fetal Growth Retardation / etiology
  • Fetal Growth Retardation / physiopathology*
  • Food Deprivation / physiology
  • Glucocorticoids / pharmacology
  • Glucose Intolerance / etiology
  • Glucose Intolerance / physiopathology*
  • Insulin / metabolism
  • Male
  • Obesity / etiology
  • Obesity / physiopathology*
  • Pancreas / metabolism
  • Pregnancy
  • Prenatal Exposure Delayed Effects / physiopathology
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Blood Glucose
  • Glucocorticoids
  • Insulin
  • Dexamethasone