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突触可塑性介导可卡因复吸需要基质金属蛋白酶。

Synaptic plasticity mediating cocaine relapse requires matrix metalloproteinases.

机构信息

Department of Neurosciences, Medical University of South Carolina, Charleston, South Carolina, USA.

出版信息

Nat Neurosci. 2014 Dec;17(12):1655-7. doi: 10.1038/nn.3846. Epub 2014 Oct 19.

Abstract

Relapse to cocaine use necessitates remodeling excitatory synapses in the nucleus accumbens and synaptic reorganization requires matrix metalloproteinase (MMP) degradation of the extracellular matrix proteins. We found enduring increases in MMP-2 activity in rats after withdrawal from self-administered cocaine and transient increases in MMP-9 during cue-induced cocaine relapse. Cue-induced heroin and nicotine relapse increased MMP activity, and increased MMP activity was required for both cocaine relapse and relapse-associated synaptic plasticity.

摘要

可卡因使用的复发需要重塑伏隔核中的兴奋性突触,而突触重组需要基质金属蛋白酶(MMP)降解细胞外基质蛋白。我们发现,从自我给药可卡因戒断后的大鼠中发现 MMP-2 活性持续增加,而在提示诱导可卡因复吸期间 MMP-9 活性短暂增加。提示诱导的海洛因和尼古丁复吸增加了 MMP 活性,并且可卡因复吸和与复吸相关的突触可塑性都需要增加 MMP 活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38fc/4241163/86d9ae864380/nihms631482f1.jpg

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