Ovarian dysfunction, obesity and pituitary tumors in female mice following neonatal exposure to low-dose diethylstilbestrol

Reprod Toxicol. 2014 Dec:50:145-51. doi: 10.1016/j.reprotox.2014.10.021. Epub 2014 Nov 5.

Abstract

In a previous study, we found that early life exposure to low-dose diethylstilbestrol (DES) induced early onset of spontaneous abnormalities in estrus cycle and shortened survival in female Sprague-Dawley rats. In order to confirm the repeatability of the previous study, neonates of C57BL/6J mice were orally administered DES at doses of 0.005, 0.05, 0.5 and 5 μg/kg/day, and the aging of their reproductive function was observed. As a result, delayed toxicity on ovarian function was found in females treated with 0.5 μg/kg/day of DES. Concomitantly, the females in the 0.05 μg/kg/day of DES, or greater, groups, had increased body weights and, in the 0.5 μg/kg/day of DES, or greater, groups, had developed pituitary tumors, which were causal factors in their accelerated mortality. Thus, we found that early life exposure to low-dose DES induced early onset of spontaneous abnormalities in estrus cycle not only in female rats but also in female mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Body Weight / drug effects
  • Diethylstilbestrol / toxicity*
  • Estrus / drug effects
  • Female
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity / chemically induced*
  • Organ Size / drug effects
  • Ovary / drug effects*
  • Ovary / physiology
  • Pituitary Neoplasms / chemically induced*
  • Pregnancy
  • Sexual Maturation / drug effects

Substances

  • Diethylstilbestrol