4.7 Article Proceedings Paper

Prenatal Alcohol Exposure Increases Vulnerability to Stress and Anxiety-Like Disorders in Adulthood

出版社

WILEY-BLACKWELL
DOI: 10.1196/annals.1418.016

关键词

chronic mild stress; prenatal alcohol exposure; elevated plus maze; HPA axis; HPG axis; sex differences; behavior; Sprague-Dawley; anxiety; fetal programming; early adversity

资金

  1. NFH/NIAAA [AA007789]
  2. BC Ministry of Children and Family Development (through the UBC Human Early Learning Partnership)
  3. Canadian Institute for Advanced Research
  4. Michael Smith Foundation for Health Research and IMPART (CIHR)
  5. NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM [R37AA007789, R56AA007789, R01AA007789] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Children and adults with fetal alcohol spectrum disorder (FASD) have elevated rates of depression and anxiety disorders compared to control populations. The effects of prenatal alcohol exposure (PAE) on anxiety, locomotor activity, and hormonal reactivity in male and female rats tested on the elevated plus maze (EPM), a task commonly used to assess anxiety-like behaviors in rodents, were examined. Pregnant dams were assigned to PAE, pair-fed (PF), or ad libitum-fed control (C) groups. At adulthood, half of all male (N = 60) and female (N = 60) PAE, PF, and C offspring were exposed to 10 days of chronic mild stress (CMS); the other half remained undisturbed. Animals were then tested on the EPM, and blood collected 30 min posttest for analysis of corticosterone (CORT), testosterone, estradiol, and progesterone. Overall, CMS exposure produced a significant anxiogenic profile. Moreover, CMS increased anxiety-like behavior in PAE males and females compared to controls and eliminated the locomotor hyperactivity observed in nonstressed PAE females. CMS also increased post-EPM CORT, testosterone, and progesterone levels in all groups, with CORT and progesterone levels significantly higher in PAE than in C females. By contrast, CMS selectively lowered estradiol levels in PAE and PF, but not C, females. CMS exposure reveals sexually dimorphic behavioral and endocrine alterations in PAE compared to C animals. Together, these data suggest the possibility that fetal reprogramming of hypothalamic-pituitary-adrenal (HPA) and -gonadal (HPG) systems by alcohol may underlie, at least partly, an enhanced susceptibility of fetal alcohol-exposed offspring to depression/anxiety-like disorders in adulthood.

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