Effects of lactational exposure to soy isoflavones on reproductive system in neonatal female rats

Basic Clin Pharmacol Toxicol. 2008 Mar;102(3):317-24. doi: 10.1111/j.1742-7843.2007.00172.x. Epub 2007 Nov 28.

Abstract

To examine effects of lactational exposure to soy isoflavones on female reproductive system, soy isoflavones, 0 (control), 10, 50, 100, 150 or 200 mg/kg body weight, were administered to maternal rats by gavage daily during postnatal days 5-10. Ten female litters were killed on day 11. Uterine and ovary weights, serum oestradiol and progesterone concentrations, proliferating cell nuclear antigen, mRNA expressions of oestrogen receptor, androgen receptor and progesterone receptor in uterus or ovary were measured. When compared to the control group, litters in the 150 and 200 mg/kg body weight groups had significantly higher ovary and uterine weights (P < 0.05). Endometrial thickness was also significantly increased. Isoflavone-treated groups had increased proliferating cell nuclear antigen staining in comparison to the control group. Litters in the 50, 150 and 200 mg/kg body weight groups had significantly higher oestradiol concentration while lower progesterone concentrations than those in the control group (P < 0.05 or P < 0.01). All soy isoflavone-treated groups had androgen receptor mRNA expressions in ovary and uterus comparable to the control group. Progesterone receptor mRNA expression in the 150 and 200 mg/kg body weight groups was significantly lower than that in control group (P < 0.01). However, ovaries in the 150 and 200 mg/kg body weight groups had significantly higher oestrogen receptor mRNA expression while the uterus in these two treatment groups had significantly lower expressions, when compared to the control group (P < 0.05 or P < 0.01). In conclusion, lactational exposure to isoflavones could result in oestrogen-like actions on the reproductive system of neonate female rats, which mechanisms may be, at least, involved with modifications of hormone production and steroid receptor transcription in the reproductive system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Body Weight
  • Dose-Response Relationship, Drug
  • Estradiol / blood
  • Female
  • Gene Expression / drug effects
  • Glycine max / chemistry
  • Isoflavones / administration & dosage
  • Isoflavones / isolation & purification
  • Isoflavones / pharmacology*
  • Lactation*
  • Male
  • Organ Size / drug effects
  • Progesterone / blood
  • Proliferating Cell Nuclear Antigen / drug effects
  • Proliferating Cell Nuclear Antigen / metabolism
  • RNA, Messenger / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Estrogen / drug effects
  • Receptors, Estrogen / metabolism
  • Receptors, Progesterone / drug effects
  • Receptors, Progesterone / metabolism
  • Reproduction / drug effects*

Substances

  • Isoflavones
  • Proliferating Cell Nuclear Antigen
  • RNA, Messenger
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Progesterone
  • Estradiol