Oregon Health & Science University, Portland, Oregon.
Veterans Affairs Portland Health Care System, Portland, Oregon.
Alcohol Res. 2020 Jul 23;40(2):02. doi: 10.35946/arcr.v40.2.02. eCollection 2020.
Sexually dimorphic effects of alcohol exposure throughout life have been documented in clinical and preclinical studies. In the past, rates of alcohol use disorder (AUD) were higher in men than in women, but over the past 10 years, the difference between sexes in prevalence of AUD and binge drinking has narrowed. Recent evidence adds to historical data regarding the influence of sex steroids on alcohol drinking and the interaction with stress-related steroids. This review considers the contribution of the endocrine system to alcohol drinking in females, with a focus on the hypothalamic pituitary gonadal axis and the hypothalamic pituitary adrenal axis and their reciprocal interactions. Emphasis is given to preclinical studies that examined genomic and rapid membrane effects of estrogen, progesterone, glucocorticoids, and GABAergic neurosteroids for their effects on alcohol drinking and models of relapse. Pertinent comparisons to data in males highlight divergent effects of sex and stress steroids on alcohol drinking and emphasize the importance of considering sex in the development of novel pharmacotherapeutic targets for the treatment of AUD. For instance, pharmacological strategies targeting the corticotropin releasing factor and glucocorticoid receptor systems may be differentially effective in males and females, whereas strategies to enhance GABAergic neurosteroids may represent a biomarker of treatment efficacy in both sexes.
在临床和临床前研究中已经记录了终生暴露于酒精的性别二态效应。过去,男性的酒精使用障碍(AUD)发病率高于女性,但在过去 10 年中,AUD 和狂饮的性别患病率差异已经缩小。最近的证据增加了关于性激素对饮酒的影响以及与应激相关的类固醇相互作用的历史数据。这篇综述考虑了内分泌系统对女性饮酒的贡献,重点是下丘脑-垂体-性腺轴和下丘脑-垂体-肾上腺轴及其相互作用。强调了研究雌激素、孕激素、糖皮质激素和 GABA 能神经甾体对饮酒和复发模型的基因组和快速膜作用的临床前研究。与男性数据的相关比较突出了性别和应激类固醇对饮酒的不同影响,并强调了在开发治疗 AUD 的新型药物治疗靶点时考虑性别的重要性。例如,针对促肾上腺皮质激素释放因子和糖皮质激素受体系统的药理学策略在男性和女性中的效果可能不同,而增强 GABA 能神经甾体的策略可能代表两性治疗效果的生物标志物。