Bach Eva C, Morgan James W, Ewin Sarah E, Barth Samuel H, Raab-Graham Kimberly F, Weiner Jeffrey L
Department of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Department of Anesthesia, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Front Neurosci. 2021 Apr 30;15:669075. doi: 10.3389/fnins.2021.669075. eCollection 2021.
Alcohol use disorder (AUD) differentially impacts men and women and a growing body of evidence points to sex-dependent adaptations in a number of brain regions. In a prior study, we explored the effect of a chronic intermittent ethanol exposure (CIE) model of AUD on neuronal and molecular adaptations in the dorsal and ventral domains of the hippocampus (dHC and vHC, respectively) in male rats. We found the vHC to be particularly sensitive to CIE, showing an increase in neuronal excitability and synaptic proteins associated with augmented excitation. These findings were accompanied by a CIE-dependent increase in anxiety-like behaviors. To explore sex-dependent adaptations in the hippocampus, we conducted a similar study in female rats. CIE-treated female rats showed a relatively modest increase in anxiety-like behaviors along with a robust increase in depressive-like measures. Despite both sexes showing clear evidence of a negative affective state following CIE, the vHC of females showed a decrease, rather than an increase, in neuronal excitability. In line with the reduced sensitivity to neural adaptations in the dHC of male rats, we were unable to identify any functional changes in the dHC of females. The functional changes of the vHC in female rats could not be explained by altered expression levels of a number of proteins typically associated with changes in neuronal excitability. Taken together, these findings point to sex as a major factor in CIE-dependent hippocampal adaptations that should be explored further to better understand possible gender differences in the etiology and treatment of AUD.
酒精使用障碍(AUD)对男性和女性的影响存在差异,越来越多的证据表明,许多脑区存在性别依赖性适应。在先前的一项研究中,我们探讨了AUD的慢性间歇性乙醇暴露(CIE)模型对雄性大鼠海马背侧和腹侧区域(分别为dHC和vHC)神经元和分子适应的影响。我们发现vHC对CIE特别敏感,表现为神经元兴奋性增加以及与增强兴奋相关的突触蛋白增加。这些发现伴随着CIE依赖性焦虑样行为的增加。为了探究海马中的性别依赖性适应,我们在雌性大鼠中进行了类似的研究。CIE处理的雌性大鼠表现出焦虑样行为相对适度增加,同时抑郁样指标显著增加。尽管两性在CIE后均显示出明显的负面情绪状态证据,但雌性大鼠的vHC神经元兴奋性降低而非增加。与雄性大鼠dHC对神经适应的敏感性降低一致,我们未能在雌性大鼠的dHC中识别出任何功能变化。雌性大鼠vHC的功能变化无法用通常与神经元兴奋性变化相关的多种蛋白质表达水平改变来解释。综上所述,这些发现表明性别是CIE依赖性海马适应的主要因素,应进一步探索以更好地理解AUD病因和治疗中可能存在的性别差异。