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皮质杏仁核回路在过度饮酒、戒酒和酒精使用障碍中的作用。

A role for circuitry of the cortical amygdala in excessive alcohol drinking, withdrawal, and alcohol use disorder.

作者信息

Xiao Tiange, Roland Alison, Chen Yueyi, Guffey Skylar, Kash Thomas, Kimbrough Adam

机构信息

Department of Basic Medical Sciences, College of Veterinary Medicine, Purdue University, West Lafayette, IN, United States.

Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, NC, United States; Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill, NC, United States.

出版信息

Alcohol. 2024 Dec;121:151-159. doi: 10.1016/j.alcohol.2024.02.008. Epub 2024 Mar 4.

DOI:10.1016/j.alcohol.2024.02.008
PMID:38447789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11371945/
Abstract

Alcohol use disorder (AUD) poses a significant public health challenge. Individuals with AUD engage in chronic and excessive alcohol consumption, leading to cycles of intoxication, withdrawal, and craving behaviors. This review explores the involvement of the cortical amygdala (CoA), a cortical brain region that has primarily been examined in relation to olfactory behavior, in the expression of alcohol dependence and excessive alcohol drinking. While extensive research has identified the involvement of numerous brain regions in AUD, the CoA has emerged as a relatively understudied yet promising candidate for future study. The CoA plays a vital role in rewarding and aversive signaling and olfactory-related behaviors and has recently been shown to be involved in alcohol-dependent drinking in mice. The CoA projects directly to brain regions that are critically important for AUD, such as the central amygdala, bed nucleus of the stria terminalis, and basolateral amygdala. These projections may convey key modulatory signaling that drives excessive alcohol drinking in alcohol-dependent subjects. This review summarizes existing knowledge on the structure and connectivity of the CoA and its potential involvement in AUD. Understanding the contribution of this region to excessive drinking behavior could offer novel insights into the etiology of AUD and potential therapeutic targets.

摘要

酒精使用障碍(AUD)对公共卫生构成了重大挑战。患有AUD的个体长期过度饮酒,导致中毒、戒断和渴望行为的循环。本综述探讨了皮质杏仁核(CoA)——一个主要在嗅觉行为方面进行过研究的皮质脑区——在酒精依赖和过度饮酒表现中的作用。虽然广泛的研究已经确定了许多脑区参与AUD,但CoA已成为一个相对研究较少但未来研究前景广阔的候选脑区。CoA在奖赏和厌恶信号传导以及嗅觉相关行为中起着至关重要的作用,最近已被证明参与小鼠的酒精依赖饮酒行为。CoA直接投射到对AUD至关重要的脑区,如中央杏仁核、终纹床核和基底外侧杏仁核。这些投射可能传递关键的调节信号,驱动酒精依赖者过度饮酒。本综述总结了关于CoA的结构和连接性及其在AUD中潜在作用的现有知识。了解该区域对过度饮酒行为的贡献可能为AUD的病因和潜在治疗靶点提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/6b17b6c8850f/nihms-1993092-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/4f8926b48b89/nihms-1993092-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/f56d21e7d76e/nihms-1993092-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/13315dd5cfca/nihms-1993092-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/6b17b6c8850f/nihms-1993092-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/4f8926b48b89/nihms-1993092-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/f56d21e7d76e/nihms-1993092-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/13315dd5cfca/nihms-1993092-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a079/11371945/6b17b6c8850f/nihms-1993092-f0004.jpg

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本文引用的文献

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Biomedicines. 2023 Sep 7;11(9):2481. doi: 10.3390/biomedicines11092481.
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Chronic Intermittent Ethanol Vapor Exposure Paired with Two-Bottle Choice to Model Alcohol Use Disorder.慢性间歇性乙醇蒸气暴露与双瓶选择配对,以模拟酒精使用障碍。
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The impact of age on olfactory alcohol cue-reactivity: A functional magnetic resonance imaging study in adolescent and adult male drinkers.
年龄对嗅觉酒精线索反应性的影响:一项针对青少年和成年男性饮酒者的功能磁共振成像研究。
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Chemogenetic inhibition of a monosynaptic projection from the basolateral amygdala to the ventral hippocampus selectively reduces appetitive, but not consummatory, alcohol drinking-related behaviours.化学遗传抑制外侧杏仁核到腹侧海马体的单突触投射选择性地减少了与摄取性但非饱食性酒精相关的行为。
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Alcohol Dependence Modifies Brain Networks Activated During Withdrawal and Reaccess: A c-Fos-Based Analysis in Mice.酒精依赖改变戒断和复饮期间激活的大脑网络:基于 c-Fos 的小鼠分析。
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