Neuroscience and Behavior Program, University of Massachusetts, Amherst, Massachusetts.
Department of Psychological and Brain Sciences at the University of Massachusetts, Amherst, Massachusetts.
Alcohol Res. 2020 Oct 8;40(2):04. doi: 10.35946/arcr.v40.2.04. eCollection 2020.
Sex differences may play a critical role in modulating how chronic or heavy alcohol use impacts the brain to cause the development of alcohol use disorder (AUD). AUD is a multifaceted and complex disorder driven by changes in key neurobiological structures that regulate executive function, memory, and stress. A three-stage framework of addiction (binge/intoxication; withdrawal/negative affect; preoccupation/anticipation) has been useful for conceptualizing the complexities of AUD and other addictions. Initially, alcohol drinking causes short-term effects that involve signaling mediated by several neurotransmitter systems such as dopamine, corticotropin releasing factor, and glutamate. With continued intoxication, alcohol leads to dysfunctional behaviors that are thought to be due in part to alterations of these and other neurotransmitter systems, along with alterations in neural pathways connecting prefrontal and limbic structures. Using the three-stage framework, this review highlights examples of research examining sex differences in drinking and differential modulation of neural systems contributing to the development of AUD. New insights addressing the role of sex differences in AUD are advancing the field forward by uncovering the complex interactions that mediate vulnerability.
性别差异可能在调节慢性或大量饮酒如何影响大脑导致酒精使用障碍(AUD)的发展方面发挥关键作用。AUD 是一种多方面且复杂的障碍,由调节执行功能、记忆和应激的关键神经生物学结构的变化驱动。成瘾的三阶段框架(狂欢/陶醉;戒断/负面情绪;专注/期待)对于理解 AUD 和其他成瘾的复杂性很有用。最初,饮酒会引起短期影响,涉及多巴胺、促肾上腺皮质释放因子和谷氨酸等几种神经递质系统介导的信号。随着持续的陶醉,酒精会导致功能失调的行为,这些行为部分归因于这些和其他神经递质系统的改变,以及连接前额叶和边缘结构的神经通路的改变。利用三阶段框架,本文综述了研究饮酒中性别差异和对导致 AUD 发展的神经系统的差异调节的例子。新的研究结果探讨了 AUD 中的性别差异的作用,通过揭示介导脆弱性的复杂相互作用,推动了该领域的发展。