Vanderbilt Center for Addiction Research, Nashville, Tennessee.
Molecular Physiology and Biophysics, Nashville, Tennessee.
Alcohol Clin Exp Res. 2019 Oct;43(10):2000-2013. doi: 10.1111/acer.14178. Epub 2019 Aug 30.
Alcohol use disorder (AUD) afflicts a large number of individuals, families, and communities globally. Affective disturbances, including stress, depression, and anxiety, are highly comorbid with AUD, contributing in some cases to initial alcohol use and continued use. Negative affect has a particularly strong influence on the withdrawal/abstinence stage of addiction as individuals with AUD frequently report stressful events, depression, and anxiety as key factors for relapse. Treatment options for negative affect associated with AUD are limited and often ineffective, highlighting the pressing need for preclinical studies examining the underlying neural circuitry driving AUD-associated negative affect. The extended amygdala (EA) is a set of brain areas collectively involved in generating and regulating affect, and extensive research has defined a critical role for the EA in all facets of substance use disorder. Here, we review the expansive historical literature examining the effects of ethanol exposure on the EA, with an emphasis on the complex EA neural circuitry driving negative affect in all phases of the alcohol addiction cycle. Specifically, this review focuses on the effects of alcohol exposure on the neural circuitry in 2 key components of the EA, the central nucleus of the amygdala and the bed nucleus of the stria terminalis. Additionally, future directions are proposed to advance our understanding of the relationship between AUD-associated negative affect and neural circuitry in the EA, with the long-term goal of developing better diagnostic tools and new pharmacological targets aimed at treating negative affect in AUD. The concepts detailed here will serve as the foundation for a companion review focusing on the potential for the endogenous cannabinoid system in the EA as a novel target for treating the stress, anxiety, and negative emotional state driving AUD.
酒精使用障碍(AUD)在全球范围内影响大量个体、家庭和社区。情感障碍,包括压力、抑郁和焦虑,与 AUD 高度共病,在某些情况下导致初始饮酒和持续饮酒。负性情绪对成瘾的戒断/禁欲阶段有特别强烈的影响,因为 AUD 患者经常报告压力事件、抑郁和焦虑是复发的关键因素。与 AUD 相关的负性情绪的治疗选择有限且通常无效,这突出表明需要进行临床前研究,以研究驱动 AUD 相关负性情绪的潜在神经回路。扩展的杏仁核(EA)是一组共同参与产生和调节情绪的大脑区域,广泛的研究已经确定了 EA 在物质使用障碍的各个方面的关键作用。在这里,我们回顾了广泛的历史文献,研究了乙醇暴露对 EA 的影响,重点是在酒精成瘾周期的所有阶段驱动负性情绪的复杂 EA 神经回路。具体来说,本综述侧重于酒精暴露对 EA 中 2 个关键组成部分的神经回路的影响,即杏仁核中央核和终纹床核。此外,还提出了未来的方向,以推进我们对 AUD 相关负性情绪和 EA 中神经回路之间关系的理解,长期目标是开发更好的诊断工具和新的药理学靶点,以治疗 AUD 中的负性情绪。这里详细介绍的概念将作为关注 EA 内源性大麻素系统作为治疗驱动 AUD 的压力、焦虑和负性情绪状态的新型靶点的潜在性的伴侣综述的基础。