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变构调节代谢型谷氨酸受体作为神经精神疾病治疗的新策略。

Allosteric Modulators of Metabotropic Glutamate Receptors as Novel Therapeutics for Neuropsychiatric Disease.

出版信息

Pharmacol Rev. 2022 Jul;74(3):630-661. doi: 10.1124/pharmrev.121.000540.

DOI:10.1124/pharmrev.121.000540
PMID:35710132
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9553119/
Abstract

Metabotropic glutamate (mGlu) receptors, a family of G-protein-coupled receptors, have been identified as novel therapeutic targets based on extensive research supporting their diverse contributions to cell signaling and physiology throughout the nervous system and important roles in regulating complex behaviors, such as cognition, reward, and movement. Thus, targeting mGlu receptors may be a promising strategy for the treatment of several brain disorders. Ongoing advances in the discovery of subtype-selective allosteric modulators for mGlu receptors has provided an unprecedented opportunity for highly specific modulation of signaling by individual mGlu receptor subtypes in the brain by targeting sites distinct from orthosteric or endogenous ligand binding sites on mGlu receptors. These pharmacological agents provide the unparalleled opportunity to selectively regulate neuronal excitability, synaptic transmission, and subsequent behavioral output pertinent to many brain disorders. Here, we review preclinical and clinical evidence supporting the utility of mGlu receptor allosteric modulators as novel therapeutic approaches to treat neuropsychiatric diseases, such as schizophrenia, substance use disorders, and stress-related disorders. SIGNIFICANCE STATEMENT: Allosteric modulation of metabotropic glutamate (mGlu) receptors represents a promising therapeutic strategy to normalize dysregulated cellular physiology associated with neuropsychiatric disease. This review summarizes preclinical and clinical studies using mGlu receptor allosteric modulators as experimental tools and potential therapeutic approaches for the treatment of neuropsychiatric diseases, including schizophrenia, stress, and substance use disorders.

摘要

代谢型谷氨酸(mGlu)受体是一类 G 蛋白偶联受体,大量研究表明它们在神经系统中的细胞信号转导和生理功能方面具有多样性,在调节认知、奖励和运动等复杂行为方面也发挥着重要作用,因此被认为是一种有前途的治疗靶点。目前,针对 mGlu 受体的亚型选择性变构调节剂的研究取得了进展,为通过靶向 mGlu 受体上不同于变构或内源性配体结合位点的独特位点,对大脑中单个 mGlu 受体亚型的信号进行高度特异性调节提供了前所未有的机会。这些药理学药物提供了独特的机会,可以选择性地调节神经元兴奋性、突触传递以及与许多脑部疾病相关的后续行为输出。本文综述了支持 mGlu 受体变构调节剂作为治疗神经精神疾病(如精神分裂症、物质使用障碍和应激相关障碍)的新型治疗方法的临床前和临床证据。

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Loss of mGluR5 in D1 Receptor-Expressing Neurons Improves Stress Coping.D1 受体表达神经元中 mGluR5 的缺失可改善应激应对。
Int J Mol Sci. 2021 Jul 22;22(15):7826. doi: 10.3390/ijms22157826.
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Developing breakthrough psychiatric treatments by modulating G protein-coupled receptors on prefrontal cortex somatostatin interneurons.通过调节前额叶皮质生长抑素中间神经元上的G蛋白偶联受体来开发突破性的精神疾病治疗方法。
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Loss of mGluR1-LTD following cocaine exposure accumulates Ca-permeable AMPA receptors and facilitates synaptic potentiation in the prefrontal cortex.可卡因暴露后 mGluR1-LTD 的丧失会积累通透性 AMPA 受体,并在前额叶皮层中促进突触增强。
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Activating mGlu Metabotropic Glutamate Receptors Rescues Schizophrenia-like Cognitive Deficits Through Metaplastic Adaptations Within the Hippocampus.激活 mGlu 代谢型谷氨酸受体通过海马内的形质变化适应性挽救精神分裂症样认知缺陷。
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