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I 型代谢型谷氨酸受体:在觅药和药物诱导的可塑性中的作用。

Group I metabotropic glutamate receptors: involvement in drug-seeking and drug-induced plasticity.

机构信息

Howard Florey Institute, University of Melbourne, Parkville, Victoria, 3010, Australia.

出版信息

Curr Mol Pharmacol. 2009 Jan;2(1):83-94. doi: 10.2174/1874467210902010083.

Abstract

L-glutamate is the principal excitatory neurotransmitter at fast synapses in the mammalian central nervous system, and signals though a number of ionotropic and metabotropic receptors. Among the latter are the group I metabotropic glutamate (mGlu1 and mGlu5) receptors that upon activation elevate intracellular calcium levels through activation of the phospholipase C pathway. The role of glutamatergic transmission in both the development of addiction and the phenomenon of relapse that may occur after prolonged abstinence, has come under intense scrutiny in recent times. While both mGlu1 and mGlu5 receptors have been implicated in certain aspects of the addictive state, the exact roles these receptors play in this process is, as yet, unclear. This review will introduce contemporary theories on drug addiction, including neural circuitry, before critically assessing the current body of knowledge on group I metabotropic glutamate receptors in this regard. This will involve an in-depth discussion of the distribution of these receptors in the brain, their presence in neural pathways known or postulated to be involved in addiction and their involvement in drug-related behavioral paradigms. The effect of acute and chronic drug administration on the activity and expression of group I metabotropic glutamate receptors will be investigated, as will the effect these receptors have on behavioral and biochemical responses to drugs of abuse. Finally, there will be a brief discussion on current and future therapeutic applications using our knowledge of these receptors, and the direction that future studies will need to take to close the gaps in our understanding.

摘要

L-谷氨酸是哺乳动物中枢神经系统快突触中主要的兴奋性神经递质,通过多种离子型和代谢型受体传递信号。其中包括 I 组代谢型谷氨酸(mGlu1 和 mGlu5)受体,其通过激活磷脂酶 C 途径来提高细胞内钙水平。谷氨酸能传递在成瘾的发展和长期戒断后可能发生的复发现象中起着重要作用,最近受到了广泛关注。虽然 mGlu1 和 mGlu5 受体都与成瘾状态的某些方面有关,但这些受体在这个过程中的确切作用尚不清楚。这篇综述将介绍药物成瘾的当代理论,包括神经回路,然后批判性地评估目前关于 I 组代谢型谷氨酸受体在这方面的知识体系。这将包括深入讨论这些受体在大脑中的分布、它们在已知或假设与成瘾有关的神经通路中的存在以及它们在与药物相关的行为范式中的参与。将研究急性和慢性药物给药对 I 组代谢型谷氨酸受体活性和表达的影响,以及这些受体对滥用药物的行为和生化反应的影响。最后,将简要讨论利用我们对这些受体的了解的当前和未来的治疗应用,以及未来研究需要采取的方向,以缩小我们理解中的差距。

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