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皮质纹状体可塑性、神经元集群与觅药行为的调控

Corticostriatal plasticity, neuronal ensembles, and regulation of drug-seeking behavior.

作者信息

Bobadilla Ana-Clara, Heinsbroek Jasper A, Gipson Cassandra D, Griffin William C, Fowler Christie D, Kenny Paul J, Kalivas Peter W

机构信息

Medical University of South Carolina, Charleston, SC, United States.

Arizona State University, Tempe, AZ, United States.

出版信息

Prog Brain Res. 2017;235:93-112. doi: 10.1016/bs.pbr.2017.07.013. Epub 2017 Oct 12.

Abstract

The idea that interconnected neuronal ensembles code for specific behaviors has been around for decades; however, recent technical improvements allow studying these networks and their causal role in initiating and maintaining behavior. In particular, the role of ensembles in drug-seeking behaviors in the context of addiction is being actively investigated. Concurrent with breakthroughs in quantifying ensembles, research has identified a role for synaptic glutamate spillover during relapse. In particular, the transient relapse-associated changes in glutamatergic synapses on accumbens neurons, as well as in adjacent astroglia and extracellular matrix, are key elements of the synaptic plasticity encoded by drug use and the metaplasticity induced by drug-associated cues that precipitate drug-seeking behaviors. Here, we briefly review the recent discoveries related to ensembles in the addiction field and then endeavor to link these discoveries with drug-induced striatal plasticity and cue-induced metaplasticity toward deeper neurobiological understandings of drug seeking.

摘要

相互连接的神经元集群编码特定行为这一观点已存在数十年;然而,最近的技术进步使得研究这些网络及其在启动和维持行为中的因果作用成为可能。特别是,成瘾背景下集群在觅药行为中的作用正在积极研究中。与量化集群的突破同时,研究发现了复发期间突触谷氨酸溢出的作用。特别是,伏隔核神经元上以及相邻星形胶质细胞和细胞外基质中与复发相关的谷氨酸能突触的短暂变化,是由药物使用编码的突触可塑性以及由引发觅药行为的药物相关线索诱导的元可塑性的关键要素。在此,我们简要回顾成瘾领域中与集群相关的最新发现,然后努力将这些发现与药物诱导的纹状体可塑性和线索诱导的元可塑性联系起来,以更深入地从神经生物学角度理解觅药行为。

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