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水通道蛋白4水通道及其作为阿尔茨海默病药物靶点潜力的最新进展。

The aquaporin-4 water channel and updates on its potential as a drug target for Alzheimer's disease.

作者信息

Silverglate Bret, Gao Xiaoyi, Lee Hannah P, Maliha Peter, Grossberg George T

机构信息

Division of Geriatric Psychiatry, St. Louis University School of Medicine, St. Louis, Missouri, USA.

Carolyn Wells-Peterson Geriatric Psychiatry Research Fellow, St. Louis University School of Medicine, St. Louis, Missouri, USA.

出版信息

Expert Opin Ther Targets. 2023 Jul-Dec;27(7):523-530. doi: 10.1080/14728222.2023.2240017. Epub 2023 Jul 27.

DOI:10.1080/14728222.2023.2240017
PMID:37475487
Abstract

INTRODUCTION

Although there are several FDA-approved treatments for Alzheimer's disease (AD), only recently have disease-modifying therapies received approval for use in patients. In this narrative review, we examine the history of aquaporin-4 (AQP4) as a therapeutic target for NMOSD (neuromyelitis optica spectrum disorder) and as a potential therapeutic target for AD.

AREAS COVERED

We review the basic science and discovery of AQP4, a transmembrane water-channel essential to regulating water balance in the central nervous system (CNS). We also review the pathogenesis of NMOSD, an autoimmune disease characterized by the destruction of cells that express AQP4. Then, we review how AQP4 is likely involved in the pathogenesis of Alzheimer's disease (AD). Finally, we discuss future challenges with drug design that would modulate AQP4 to potentially slow AD development. The literature search for this article consisted of searching Google Scholar and PubMed for permutations of the keywords 'Alzheimer's disease,' 'aquaporin-4,' 'neuromyelitis optica,' and their abbreviations.

EXPERT OPINION

We place research into AQP4 into context with other recent developments in AD research. A major difficulty with drug development for Alzheimer's is the lack of strategies to cleanly target the early pathogenesis of the disease. Targeting AQP4 may provide such a strategy.

摘要

引言

尽管美国食品药品监督管理局(FDA)已批准多种治疗阿尔茨海默病(AD)的方法,但直到最近疾病修饰疗法才获批用于患者。在这篇叙述性综述中,我们探讨水通道蛋白4(AQP4)作为视神经脊髓炎谱系障碍(NMOSD)治疗靶点以及作为AD潜在治疗靶点的历史。

涵盖领域

我们回顾AQP4的基础科学及发现,AQP4是一种对调节中枢神经系统(CNS)水平衡至关重要的跨膜水通道。我们还回顾了NMOSD的发病机制,NMOSD是一种以表达AQP4的细胞被破坏为特征的自身免疫性疾病。然后,我们回顾AQP4可能如何参与阿尔茨海默病(AD)的发病机制。最后,我们讨论药物设计未来面临的挑战,这些挑战涉及调节AQP4以潜在减缓AD发展。本文的文献检索包括在谷歌学术和PubMed上搜索关键词“阿尔茨海默病”、“水通道蛋白4”、“视神经脊髓炎”及其缩写的各种排列组合。

专家观点

我们将对AQP4的研究与AD研究的其他最新进展相结合进行探讨。阿尔茨海默病药物研发的一个主要困难在于缺乏精准靶向该疾病早期发病机制的策略。靶向AQP4可能提供这样一种策略。

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