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轴突起始段在精神障碍中的作用:功能、功能障碍和干预。

Role of the axonal initial segment in psychiatric disorders: function, dysfunction, and intervention.

机构信息

Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; Graduate Program in Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; M.D.-Ph.D. Combined Degree Program, The University of Texas Medical Branch at Galveston , Galveston, TX , USA.

Department of Pharmacology and Toxicology, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; Sealy Center for Molecular Medicine, The University of Texas Medical Branch at Galveston , Galveston, TX , USA.

出版信息

Front Psychiatry. 2014 Aug 21;5:109. doi: 10.3389/fpsyt.2014.00109. eCollection 2014.

Abstract

The progress of developing effective interventions against psychiatric disorders has been limited due to a lack of understanding of the underlying cellular and functional mechanisms. Recent research findings focused on exploring novel causes of psychiatric disorders have highlighted the importance of the axonal initial segment (AIS), a highly specialized neuronal structure critical for spike initiation of the action potential. In particular, the role of voltage-gated sodium channels, and their interactions with other protein partners in a tightly regulated macromolecular complex has been emphasized as a key component in the regulation of neuronal excitability. Deficits and excesses of excitability have been linked to the pathogenesis of brain disorders. Identification of the factors and regulatory pathways involved in proper AIS function, or its disruption, can lead to the development of novel interventions that target these mechanistic interactions, increasing treatment efficacy while reducing deleterious off-target effects for psychiatric disorders.

摘要

由于对潜在的细胞和功能机制缺乏了解,开发针对精神障碍的有效干预措施的进展一直受到限制。最近的研究结果集中在探索精神障碍的新病因,强调了轴突起始段(AIS)的重要性,AIS 是一种高度特化的神经元结构,对动作电位的尖峰起始至关重要。特别是,电压门控钠离子通道及其与其他蛋白质伴侣在紧密调节的大分子复合物中的相互作用,被强调为调节神经元兴奋性的关键组成部分。兴奋性的不足和过度与脑疾病的发病机制有关。鉴定适当的 AIS 功能或其破坏所涉及的因素和调节途径,可以导致针对这些机制相互作用的新干预措施的发展,提高治疗效果,同时减少精神障碍的有害脱靶效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3668/4139700/a09cf234dd0d/fpsyt-05-00109-g001.jpg

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