Hypothalamic-pituitary-adrenal axis and behavioral dysfunction following early binge-like prenatal alcohol exposure in mice

• Published in: Alcohol (Fayetteville, N.Y.) N.Y.), 2015-05, Vol.49 (3), p.207-217
• Main Authors: Wieczorek, Lindsay, Fish, Eric W, O'Leary-Moore, Shonagh K, Parnell, Scott E, Sulik, Kathleen K
• Format: Article
• Language: English
• Subjects: Adrenocorticotropic Hormone - drug effects; Adrenocorticotropic Hormone - metabolism; Alcohol use; Alcoholism; Animals; Anxiety; Anxiety - metabolism; Anxiety - psychology; Behavior; Behavior, Animal - drug effects; Binge Drinking; Brain research; Central Nervous System Depressants - pharmacology; Corticosterone - metabolism; Depression; Depression - metabolism; Depression - psychology; Disease Models, Animal; Ethanol - pharmacology; FASD; Female; Fetal Alcohol Spectrum Disorders - metabolism; Fetal Alcohol Spectrum Disorders - psychology; Fetal alcohol syndrome; Hypothalamic-pituitary-adrenal axis; Hypothalamo-Hypophyseal System - drug effects; Hypothalamo-Hypophyseal System - metabolism; Male; Mental health; Mice; Morphology; Pituitary-Adrenal System - drug effects; Pituitary-Adrenal System - metabolism; Pregnancy; Prenatal alcohol exposure; Prenatal Exposure Delayed Effects - metabolism; Prenatal Exposure Delayed Effects - psychology; Psychiatry; Restraint, Physical; Rodents; Sex Factors; Stress; Stress, Psychological - metabolism; Stress, Psychological - psychology; Studies
• ISSN: 0741-8329; 1873-6823
• DOI: 10.1016/j.alcohol.2015.01.005

Abstract The range of defects that fall within fetal alcohol spectrum disorder (FASD) includes persistent behavioral problems, with anxiety and depression being two of the more commonly reported issues. Previous studies of rodent FASD models suggest that interference with hypothalamic-pituitary-adrenal (HPA) axis structure and/or function may be the basis for some of the prenatal alcohol (ethanol) exposure (PAE)-induced behavioral abnormalities. Included among the previous investigations are those illustrating that maternal alcohol treatment limited to very early stages of pregnancy (i.e., gestational day [GD]7 in mice; equivalent to the third week post-fertilization in humans) can cause structural abnormalities in areas such as the hypothalamus, pituitary gland, and other forebrain regions integral to controlling stress and behavioral responses. The current investigation was designed to further examine the sequelae of prenatal alcohol insult at this early time period, with particular attention to HPA axis-associated functional changes in adult mice. The results of this study reveal that GD7 PAE in mice causes HPA axis dysfunction, with males and females showing elevated corticosterone (CORT) and adrenocorticotropic hormone (ACTH) levels, respectively, following a 15-min restraint stress exposure. Males also showed elevated CORT levels following an acute alcohol injection of 2.0 g/kg, while females displayed blunted ACTH levels. Furthermore, analysis showed that anxiety-like behavior was decreased after GD7 PAE in female mice, but was increased in male mice. Collectively, the results of this study show that early gestational alcohol exposure in mice alters long-term HPA axis activity and behavior in a sexually dimorphic manner.