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可卡因引起的突触增强效应的逆转重置了药物引起的适应性行为。

Reversal of cocaine-evoked synaptic potentiation resets drug-induced adaptive behaviour.

机构信息

Department of Basic Neurosciences, Medical Faculty, University of Geneva, CH-1211 Geneva, Switzerland.

出版信息

Nature. 2011 Dec 7;481(7379):71-5. doi: 10.1038/nature10709.

Abstract

Drug-evoked synaptic plasticity is observed at many synapses and may underlie behavioural adaptations in addiction. Mechanistic investigations start with the identification of the molecular drug targets. Cocaine, for example, exerts its reinforcing and early neuroadaptive effects by inhibiting the dopamine transporter, thus causing a strong increase in mesolimbic dopamine. Among the many signalling pathways subsequently engaged, phosphorylation of the extracellular signal-regulated kinase (ERK) in the nucleus accumbens is of particular interest because it has been implicated in NMDA-receptor and type 1 dopamine (D1)-receptor-dependent synaptic potentiation as well as in several behavioural adaptations. A causal link between drug-evoked plasticity at identified synapses and behavioural adaptations, however, is missing, and the benefits of restoring baseline transmission have yet to be demonstrated. Here we find that cocaine potentiates excitatory transmission in D1-receptor-expressing medium-sized spiny neurons (D1R-MSNs) in mice via ERK signalling with a time course that parallels locomotor sensitization. Depotentiation of cortical nucleus accumbens inputs by optogenetic stimulation in vivo efficiently restored normal transmission and abolished cocaine-induced locomotor sensitization. These findings establish synaptic potentiation selectively in D1R-MSNs as a mechanism underlying a core component of addiction, probably by creating an imbalance between distinct populations of MSNs in the nucleus accumbens. Our data also provide proof of principle that reversal of cocaine-evoked synaptic plasticity can treat behavioural alterations caused by addictive drugs and may inspire novel therapeutic approaches involving deep brain stimulation or transcranial magnetic stimulation.

摘要

药物诱发的突触可塑性在许多突触中都有观察到,可能是成瘾行为适应的基础。机制研究始于鉴定分子药物靶点。例如,可卡因通过抑制多巴胺转运体发挥其强化和早期神经适应作用,从而导致中脑边缘多巴胺的强烈增加。在随后涉及的许多信号通路中,核_accumbens 中的细胞外信号调节激酶(ERK)磷酸化特别有趣,因为它与 NMDA 受体和 1 型多巴胺(D1)受体依赖性突触增强以及几种行为适应有关。然而,在已确定的突触中药物诱发的可塑性与行为适应之间缺乏因果关系,恢复基线传递的益处尚未得到证明。在这里,我们发现可卡因通过 ERK 信号增强了表达 D1 受体的中型棘突神经元(D1R-MSN)中的兴奋性传递,其时间过程与运动敏化平行。体内光遗传刺激对皮质核_accumbens 输入的去极化有效地恢复了正常的传递,并消除了可卡因引起的运动敏化。这些发现确立了 D1R-MSN 中突触增强作为成瘾核心成分的一种机制,可能是通过在核_accumbens 中不同 MSN 群体之间造成不平衡。我们的数据还提供了可卡因诱发的突触可塑性逆转可以治疗成瘾药物引起的行为改变的原理证明,并可能激发涉及深部脑刺激或经颅磁刺激的新的治疗方法。

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