Developmental programming: variations in early growth and adult disease

Clin Exp Pharmacol Physiol. 2013 Nov;40(11):795-802. doi: 10.1111/1440-1681.12092.

Abstract

Suboptimal conditions in utero are associated with the development of adult-onset diseases in offspring. Uteroplacental insufficiency in rats is a well-established animal model used to mimic and study the effects of developmental insults relevant to countries of abundant nutrient supply. However, wide-ranging outcomes for the offspring are apparent between the different investigators that use this model and also between cohorts generated in our laboratory. We aimed to explore the reasons for variability in rat models of uteroplacental insufficiency between different investigators and also between our own animal cohorts. We suggest differences in growth and disease development reflect uniqueness in susceptibility and highlight the complexity of interactions between genetic potential and environmental exposures. The impact of adverse exposures in utero has been described as having far-reaching effects that extend well beyond the first, directly exposed generation. However, the resulting phenotypes are not consistent between generations. This suggests that programmed effects are established de novo in each generation and challenges the prediction of disease. Characterization of growth and disease in the numerous rat models has led to our understanding of the impact of early life experiences on adult health. In order to drive the development of preventative and/or treatment strategies, future studies should focus on identifying the initial cause(s) of uteroplacental insufficiency, including genetic origins and the influence of poor diets.

Keywords: animal models; early life exposures; transgenerational effects.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adolescent Development
  • Adult
  • Aging*
  • Animals
  • Child
  • Child Development
  • Diet / adverse effects
  • Disease Models, Animal*
  • Female
  • Fetal Development*
  • Fetal Growth Retardation / etiology*
  • Fetal Growth Retardation / physiopathology
  • Humans
  • Male
  • Maternal Nutritional Physiological Phenomena
  • Placental Insufficiency / physiopathology*
  • Pregnancy
  • Rats
  • Rats, Inbred Strains
  • Reproducibility of Results