代谢性谷氨酸受体5负变构调节剂的药理学、信号传导和治疗潜力。

IF 4.9 Q1 CHEMISTRY, MEDICINAL ACS Pharmacology and Translational Science Pub Date : 2024-11-05 eCollection Date: 2024-12-13 DOI:10.1021/acsptsci.4c00213
Jackson A Kos, Monica Langiu, Shane D Hellyer, Karen J Gregory
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引用次数: 0

摘要

代谢性谷氨酸受体是一个由8个C类G蛋白偶联受体组成的家族,调节包括认知和运动在内的高阶脑功能。因此,代谢性谷氨酸受体作为治疗神经系统疾病的潜在药物靶点已被大量研究。针对代谢性谷氨酸受体亚型5 (mGlu5)的药物发现工作尤其富有成果,已确定了大量候选药物和药理工具。mGlu5阴性变构调节剂(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)的有希望的新疗法,并有望改善其他药物引起的不良反应(如左旋多巴引起的帕金森病运动障碍)。然而,尽管临床前取得了成功,但由于临床试验中的安全性和有效性不佳,mGlu5 NAMs尚未进入市场。本文就mGlu5的生理和信号转导进行综述。我们提供了关于mGlu5抑制剂的治疗选择的综合批评,从正构拮抗剂到NAMs。最后,我们讨论了与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疗法的合理药物发现。
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Pharmacology, Signaling and Therapeutic Potential of Metabotropic Glutamate Receptor 5 Negative Allosteric Modulators.

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 (mGlu5) have been particularly fruitful, with a wealth of drug candidates and pharmacological tools identified. mGlu5 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, mGlu5 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 mGlu5. 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.

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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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