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在短期或长期禁欲后,大鼠纹状体和大脑皮层中寻求可卡因行为的复发会差异性地增加活动调节基因的表达。

Relapse to cocaine-seeking increases activity-regulated gene expression differentially in the striatum and cerebral cortex of rats following short or long periods of abstinence.

作者信息

Hearing M C, See R E, McGinty J F

机构信息

Department of Neurosciences, Medical University of South Carolina, 173 Ashley Avenue BSB 403, Charleston, SC 29425, USA.

出版信息

Brain Struct Funct. 2008 Sep;213(1-2):215-27. doi: 10.1007/s00429-008-0182-4. Epub 2008 May 17.

DOI:10.1007/s00429-008-0182-4
PMID:18488248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5771260/
Abstract

One of the most insidious features of cocaine addiction is a high rate of relapse even after extended periods of abstinence. A wide variety of drug-associated stimuli, including the context in which a drug is taken, can gain incentive motivational properties that trigger drug desire and relapse to drug-seeking. Both animal and clinical studies suggest that extensive cocaine exposure may induce a transition from cortical to striatal control over decision-making as compulsive drug-seeking emerges. Using an animal model of relapse to cocaine-seeking, the present study investigated the expression patterns of three different activity-related genes (c-fos, zif/268, and arc) in cortical and striatal brain regions implicated in compulsive drug-seeking in order to determine the neuroadaptations that occur during context-induced relapse following brief or prolonged abstinence from cocaine self-administration. Re-exposure to the environment previously associated with cocaine self-administration following 22 h or 15 days of abstinence produced a significant increase in zif/268 and arc, but not c-fos mRNA, in the caudate-putamen and nucleus accumbens. With the exception of arc mRNA levels following 15 days of abstinence, all three genes were increased in the anterior cingulate cortex of animals with a cocaine history when they were re-exposed to the operant chamber. Additionally, c-fos, zif/268, and arc expression was differentially affected in the motor and sensory cortices at both timepoints. Together, these results support convergent evidence that drug-seeking induced by a cocaine-paired context changes the activity of corticostriatal circuits.

摘要

可卡因成瘾最隐匿的特征之一是即便经过长时间戒断,复发率仍很高。各种各样与药物相关的刺激因素,包括用药时的环境,都可能获得激发动机的特性,从而引发对药物的渴望并导致复吸。动物研究和临床研究均表明,随着强迫性觅药行为的出现,长期接触可卡因可能会导致决策控制从皮质向纹状体转变。本研究利用一个可卡因觅药复发的动物模型,调查了与强迫性觅药行为相关的皮质和纹状体脑区中三种不同的与活动相关基因(c-fos、zif/268和arc)的表达模式,以确定在短暂或长期停止可卡因自我给药后,情境诱导复发期间发生的神经适应性变化。在戒断22小时或15天后,重新暴露于先前与可卡因自我给药相关的环境中,会使尾状核-壳核和伏隔核中的zif/268和arc mRNA显著增加,但c-fos mRNA无此变化。除了戒断15天后的arc mRNA水平外,有可卡因使用史的动物在重新进入操作箱时,前扣带回皮质中的这三种基因均增加。此外,在两个时间点,运动皮质和感觉皮质中的c-fos、zif/268和arc表达均受到不同程度的影响。这些结果共同支持了趋同证据,即由可卡因配对情境诱导的觅药行为改变了皮质-纹状体回路的活动。

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本文引用的文献

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Increased expression of the immediate-early gene arc/arg3.1 reduces AMPA receptor-mediated synaptic transmission.即刻早期基因arc/arg3.1表达增加会降低AMPA受体介导的突触传递。
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Arc/Arg3.1 is essential for the consolidation of synaptic plasticity and memories.Arc/Arg3.1对于突触可塑性和记忆的巩固至关重要。
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