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神经疾病中的瞬时受体电位香草酸亚型4通道:从分子机制到治疗潜力

TRPV4 Channel in Neurological Disease: from Molecular Mechanisms to Therapeutic Potential.

作者信息

Zhang Feng, Mehta Hritik, Choudhary Hadi Hasan, Islam Rezwanul, Hanafy Khalid A

机构信息

Cooper Medical School at Rowan University, Camden, NJ, USA.

Cooper University Health Care, Camden, NJ, USA.

出版信息

Mol Neurobiol. 2025 Mar;62(3):3877-3891. doi: 10.1007/s12035-024-04518-5. Epub 2024 Sep 28.

Abstract

Transient Receptor Potential Vanilloid 4 (TRPV4) is a non-selective cation channel with pivotal roles in various physiological processes, including osmosensitivity, mechanosensation, neuronal development, vascular tone regulation, and bone homeostasis in human bodies. Recent studies have made significant progress in understanding the structure and functional role of TRPV4, shedding light on its involvement in pathological processes, particularly in the realm of neurological diseases. Here, we aim to provide a comprehensive exploration of the multifaceted contributions of TRPV4 to neurological diseases, spanning its intricate molecular mechanisms to its potential as a target for therapeutic interventions. We delve into the structural and functional attributes of TRPV4, scrutinize its expression profile, and elucidate the possible mechanisms through which it participates in the pathogenesis of neurological disorders. Furthermore, we discussed recent years' progress in therapeutic strategies aimed at harnessing TRPV4 for the treatment of these diseases. These insights will provide a basis for understanding and designing modality-specific pharmacological agents to treat TRPV4-associated disorders.

摘要

瞬时受体电位香草酸亚型4(TRPV4)是一种非选择性阳离子通道,在多种生理过程中发挥关键作用,包括人体的渗透压敏感性、机械感觉、神经元发育、血管张力调节和骨稳态。最近的研究在理解TRPV4的结构和功能作用方面取得了重大进展,揭示了其在病理过程中的参与情况,特别是在神经疾病领域。在此,我们旨在全面探讨TRPV4对神经疾病的多方面贡献,涵盖其复杂的分子机制以及作为治疗干预靶点的潜力。我们深入研究TRPV4的结构和功能特性,仔细审查其表达谱,并阐明其参与神经疾病发病机制的可能机制。此外,我们讨论了近年来旨在利用TRPV4治疗这些疾病的治疗策略进展。这些见解将为理解和设计针对TRPV4相关疾病的特定模态药理药物提供基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3244/11790740/834b96930032/12035_2024_4518_Fig1_HTML.jpg

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