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代谢型谷氨酸受体5负变构调节剂的药理学、信号传导及治疗潜力

Pharmacology, Signaling and Therapeutic Potential of Metabotropic Glutamate Receptor 5 Negative Allosteric Modulators.

作者信息

Kos Jackson A, Langiu Monica, Hellyer Shane D, Gregory Karen J

机构信息

Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences and Department of Pharmacology, Monash University, Parkville, VIC 3052, Australia.

ARC Centre for Cryo-electron Microscopy of Membrane Proteins, Monash University, Parkville, VIC 3052, Australia.

出版信息

ACS Pharmacol Transl Sci. 2024 Nov 5;7(12):3671-3690. doi: 10.1021/acsptsci.4c00213. eCollection 2024 Dec 13.

Abstract

Metabotropic glutamate receptors are a family of eight class C G protein-coupled receptors regulating higher order brain functions including cognition and motion. Metabotropic glutamate receptors have thus been heavily investigated as potential drug targets for treating neurological disorders. Drug discovery efforts directed toward metabotropic glutamate receptor subtype 5 (mGlu) have been particularly fruitful, with a wealth of drug candidates and pharmacological tools identified. mGlu negative allosteric modulators (NAMs) are promising novel therapeutics for developmental, neuropsychiatric and neurodegenerative disorders (e.g., Alzheimer's Disease, Huntington's Disease, Parkinson's Disease, amyotrophic lateral sclerosis, autism spectrum disorders, substance use disorders, stroke, anxiety and depression) and show promise in ameliorating adverse effects induced by other medications (e.g., L-dopa induced dyskinesia in Parkinson's Disease). However, despite preclinical success, mGlu NAMs are yet to reach the market due to poor safety and efficacy profiles in clinical trials. Herein, we review the physiology and signal transduction of mGlu. We provide a comprehensive critique of therapeutic options with respect to mGlu5 inhibitors, spanning from orthosteric antagonists to NAMs. Finally, we address the challenges associated with drug development and highlight future directions to guide rational drug discovery of safe and effective novel therapeutics.

摘要

代谢型谷氨酸受体是一个由8种C类G蛋白偶联受体组成的家族,可调节包括认知和运动在内的高级脑功能。因此,代谢型谷氨酸受体作为治疗神经疾病的潜在药物靶点受到了广泛研究。针对代谢型谷氨酸受体5亚型(mGlu)的药物研发工作尤其富有成果,已鉴定出大量候选药物和药理学工具。mGlu负变构调节剂(NAMs)是治疗发育、神经精神和神经退行性疾病(如阿尔茨海默病、亨廷顿病、帕金森病、肌萎缩侧索硬化症、自闭症谱系障碍、物质使用障碍、中风、焦虑和抑郁)的有前景的新型疗法,并有望改善其他药物引起的不良反应(如帕金森病中左旋多巴诱导的运动障碍)。然而,尽管临床前研究取得了成功,但由于在临床试验中安全性和疗效不佳,mGlu NAMs尚未上市。在此,我们综述了mGlu的生理学和信号转导。我们对mGlu5抑制剂的治疗选择进行了全面批判,涵盖从正构拮抗剂到NAMs。最后,我们阐述了药物开发相关的挑战,并强调了未来的方向,以指导安全有效的新型疗法的合理药物研发。

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