Effects of prenatal ethanol exposure on hypothalamic-pituitary-adrenal function across the estrous cycle

Alcohol Clin Exp Res. 2009 Jun;33(6):1075-88. doi: 10.1111/j.1530-0277.2009.00929.x. Epub 2009 Mar 23.

Abstract

Background: Rats prenatally exposed to ethanol (E) typically show increased hypothalamic-pituitary-adrenal (HPA) responses to stressors in adulthood. Importantly, prenatal ethanol may differentially alter stress responsiveness in male and female offspring, suggesting a role for the gonadal hormones in mediating the effects of ethanol on HPA activity. We investigated the role of ethanol-induced changes in hypothalamic-pituitary-gonadal (HPG) activity in the differential HPA regulation observed in E compared to control females across the estrous cycle.

Methods: Peripheral hormones and changes in central neuropeptide mRNA levels were measured across the estrous cycle in adult female offspring from E, pair-fed (PF) and ad libitum-fed control (C) dams.

Results: Ethanol females showed normal estrous cyclicity (vaginal smears) but delayed sexual maturation (vaginal opening). Both HPG and HPA activity were differentially altered in E (and in some cases, PF) compared to control females as a function of estrous cycle stage. In relation to HPG activity, E and PF females had higher basal and stress estradiol (E(2)) levels in proestrus compared to other phases of the cycle, and decreased GnRH mRNA levels compared to C females in diestrus. Further, E females had greater variation in LH than PF and C females across the cycle, and in proestrus, only E females showed a significant LH increase following stress. In relation to HPA activity, both basal and stress CORT levels and overall ACTH levels were greater in E than in C females in proestrus. Furthermore, AVP mRNA levels were increased overall in E compared to PF and C females.

Conclusions: These data demonstrate ethanol-induced changes in both HPG and HPA activity that are estrous phase-specific, and support the possibility that changes in HPA activity in E females may reflect differential sensitivity to ovarian steroids. E females appear to have an increased HPA sensitivity to E(2), and a possible shift toward AVP regulation of HPA activity. That PF were similar to E females on some measures suggests that nutritional effects of diet or food restriction played a role in mediating at least some of the changes observed.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenocorticotropic Hormone / blood
  • Animals
  • Arginine Vasopressin / blood
  • Central Nervous System Depressants / pharmacology
  • Central Nervous System Depressants / toxicity*
  • Corticosterone / blood
  • Estradiol / blood
  • Estrous Cycle / drug effects
  • Estrous Cycle / physiology*
  • Ethanol / pharmacology
  • Ethanol / toxicity*
  • Female
  • Hypothalamo-Hypophyseal System / drug effects
  • Hypothalamo-Hypophyseal System / physiology*
  • Luteinizing Hormone / blood
  • Male
  • Models, Animal
  • Ovary / drug effects
  • Ovary / physiology
  • Pituitary-Adrenal System / drug effects
  • Pituitary-Adrenal System / physiology*
  • Pregnancy
  • Prenatal Exposure Delayed Effects / chemically induced*
  • Prenatal Exposure Delayed Effects / physiopathology*
  • Progesterone / blood
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Central Nervous System Depressants
  • Arginine Vasopressin
  • Ethanol
  • Progesterone
  • Estradiol
  • Adrenocorticotropic Hormone
  • Luteinizing Hormone
  • Corticosterone