mGlu受体和药物成瘾。

Richard M Cleva, M Foster Olive
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引用次数: 17

摘要

从历史上看,脑儿茶酚胺系统一直是研究药物成瘾的神经基质的主要焦点。然而,在过去的二十年中,积累了大量的证据表明,谷氨酸能神经传递在介导成瘾行为以及与慢性药物使用相关的长期神经可塑性中起着关键作用。因此,人们对开发以谷氨酸为基础的治疗成瘾性疾病的疗法越来越感兴趣。代谢性谷氨酸(mGlu)受体被划分为I类(mGlu1和mGlu5)、II类(mGlu2和mGlu3)和III类(mGlu4、mGlu6、mGlu7和mGlu8),因其介导较慢的调节性兴奋性神经传递而受到广泛关注。与那些靶向嗜离子性谷氨酸(iGlu)受体的药物配体相比,靶向这些受体的药物配体已经证明其兴奋性毒性或严重不良副作用的发生率较低。行为遗传学和药理学研究已经探索了个体mGlu受体亚型在调节各种成瘾相关行为中的作用,并且一些mGlu受体配体已经成为其他医疗条件下临床测试的主题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
mGlu receptors and drug addiction.

Historically, brain catecholamine systems have been the primary focus of studies examining the neural substrates of drug addiction. In the past two decades, however, a wealth of evidence has accumulated indicating a pivotal role for glutamatergic neurotransmission in mediating addictive behaviors as well as long-term neuroplasticity associated with chronic drug use. As a result, there has been increased interest in developing glutamate-based therapies for the treatment of addictive disorders. Metabotropic glutamate (mGlu) receptors are classified into subcategories designated as Group I (mGlu1 and mGlu5), Group II (mGlu2 and mGlu3), and Group III (mGlu4, mGlu6, mGlu7, and mGlu8), and have received a great deal of attention due to their mediation of slower modulatory excitatory neurotransmission. Pharmacological ligands targeting these receptors have demonstrated reduced incidences of excitotoxicity or severe adverse side effects as compared to those targeting ionotropic glutamate (iGlu) receptors. Behavioral genetic and pharmacological studies have explored the role of individual mGlu receptor subtypes in regulating various addiction-related behaviours and several mGlu receptor ligands have been the subject of clinical testing for other medical conditions.

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