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代谢型谷氨酸受体5:神经性疼痛治疗的潜在靶点。

Metabotropic Glutamate Receptor 5: A Potential Target for Neuropathic Pain Treatment.

作者信息

Manengu Chalton, Zhu Chun-Hao, Zhang Guo-Dong, Tian Miao-Miao, Lan Xiao-Bing, Tao Li-Jun, Ma Lin, Liu Yue, Yu Jian-Qiang, Liu Ning

机构信息

College of Pharmacy, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750004, Ningxia Hui Autonomous Region, China.

School of International Education, Ningxia Medical University, 1160 Shengli Street, Yinchuan 750004, Ningxia Hui Autonomous Region, China.

出版信息

Curr Neuropharmacol. 2025;23(3):276-294. doi: 10.2174/1570159X23666241011163035.

DOI:10.2174/1570159X23666241011163035
PMID:39411936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11808587/
Abstract

Neuropathic pain, a multifaceted and incapacitating disorder, impacts a significant number of individuals globally. Despite thorough investigation, the development of efficacious remedies for neuropathic pain continues to be a formidable task. Recent research has revealed the potential of metabotropic glutamate receptor 5 (mGlu5) as a target for managing neuropathic pain. mGlu5 is a receptor present in the central nervous system that has a vital function in regulating synaptic transmission and the excitability of neurons. This article seeks to investigate the importance of mGlu5 in neuropathic pain pathways, analyze the pharmacological approach of targeting mGlu5 for neuropathic pain treatment, and review the negative allosteric mGlu5 modulators used to target mGlu5. By comprehending the role of mGlu5 in neuropathic pain, we can discover innovative treatment approaches to ease the distress endured by persons afflicted with this incapacitating ailment.

摘要

神经性疼痛是一种多方面且使人丧失能力的疾病,在全球影响着大量人群。尽管进行了深入研究,但开发有效的神经性疼痛治疗方法仍然是一项艰巨的任务。最近的研究揭示了代谢型谷氨酸受体5(mGlu5)作为治疗神经性疼痛靶点的潜力。mGlu5是一种存在于中枢神经系统中的受体,在调节突触传递和神经元兴奋性方面具有重要作用。本文旨在探讨mGlu5在神经性疼痛通路中的重要性,分析针对mGlu5治疗神经性疼痛的药理学方法,并综述用于靶向mGlu5的负变构mGlu5调节剂。通过理解mGlu5在神经性疼痛中的作用,我们可以发现创新的治疗方法,以减轻患有这种使人丧失能力疾病的患者所遭受的痛苦。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc2/11808587/c5747009847c/CN-23-3-276_F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc2/11808587/4f508498296b/CN-23-3-276_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc2/11808587/edd96b585df3/CN-23-3-276_F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc2/11808587/c5747009847c/CN-23-3-276_F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc2/11808587/4f508498296b/CN-23-3-276_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc2/11808587/edd96b585df3/CN-23-3-276_F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc2/11808587/c5747009847c/CN-23-3-276_F3.jpg

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本文引用的文献

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Elife. 2024 Aug 22;13:e94931. doi: 10.7554/eLife.94931.
2
Neuropathic pain: From actual pharmacological treatments to new therapeutic horizons.神经病理性疼痛:从实际的药理学治疗到新的治疗前景。
Pharmacol Ther. 2023 Nov;251:108546. doi: 10.1016/j.pharmthera.2023.108546. Epub 2023 Oct 11.
3
Metabotropic glutamate receptors (mGluRs) in epileptogenesis: an update on abnormal mGluRs signaling and its therapeutic implications.
代谢型谷氨酸受体(mGluRs)在癫痫发生中的作用:mGluRs异常信号传导及其治疗意义的最新进展
Neural Regen Res. 2024 Feb;19(2):360-368. doi: 10.4103/1673-5374.379018.
4
Exploring the molecular pathways and therapeutic implications of angiogenesis in neuropathic pain.探索神经病理性疼痛中血管生成的分子途径及其治疗意义。
Biomed Pharmacother. 2023 Jun;162:114693. doi: 10.1016/j.biopha.2023.114693. Epub 2023 Apr 14.
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Allosteric modulation of G protein-coupled receptor signaling.变构调节 G 蛋白偶联受体信号转导。
Front Endocrinol (Lausanne). 2023 Feb 16;14:1137604. doi: 10.3389/fendo.2023.1137604. eCollection 2023.
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Phosphorylation and regulation of group II metabotropic glutamate receptors (mGlu2/3) in neurons.神经元中II型代谢型谷氨酸受体(mGlu2/3)的磷酸化与调节
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