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GIRK通道可塑性及其对药物成瘾的影响。

GIRK Channel Plasticity and Implications for Drug Addiction.

作者信息

Marron Fernandez de Velasco Ezequiel, McCall Nora, Wickman Kevin

机构信息

Department of Pharmacology, University of Minnesota, Minneapolis, Minnesota, USA.

Department of Neuroscience, University of Minnesota, Minneapolis, Minnesota, USA.

出版信息

Int Rev Neurobiol. 2015;123:201-38. doi: 10.1016/bs.irn.2015.05.011. Epub 2015 Jun 22.

Abstract

Drugs of abuse can "hijack" synaptic plasticity, a physiological basis of learning and memory, establishing maladaptations that can promote drug addiction. A wealth of data supports the existence and importance of neuroadaptations in excitatory neurotransmission upon drug exposure. Recent discoveries, however, have shown that inhibitory neurotransmission mediated by G protein-gated inwardly rectifying potassium (K(+)) (GIRK/Kir3) channels is also subject to adaptation triggered by exposure to drugs of abuse. GIRK channels are expressed in neuronal populations relevant to reward and reward-related behaviors, where their activation by neurotransmitters such as GABA, dopamine, and adenosine reduces neuronal excitability. Studies in animal models have implicated GIRK channels in a number of behaviors including reward. Drugs of abuse also affect the inhibitory neurotransmission mediated by GIRK channels. These changes might be important for the development, maintenance, or relapse of addiction, making GIRK channels promising targets for novel addiction therapies.

摘要

滥用药物会“劫持”突触可塑性,即学习和记忆的生理基础,从而建立起可促进药物成瘾的适应不良。大量数据支持药物暴露后兴奋性神经传递中神经适应的存在及其重要性。然而,最近的发现表明,由G蛋白偶联内向整流钾(K(+))(GIRK/Kir3)通道介导的抑制性神经传递也会因接触滥用药物而发生适应性变化。GIRK通道在与奖赏及奖赏相关行为有关的神经元群体中表达,神经递质如γ-氨基丁酸、多巴胺和腺苷对其激活会降低神经元兴奋性。动物模型研究表明GIRK通道参与包括奖赏在内的多种行为。滥用药物也会影响由GIRK通道介导的抑制性神经传递。这些变化可能对成瘾的发展、维持或复发很重要,这使得GIRK通道成为新型成瘾疗法的有前景的靶点。

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