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血清素能系统与肌萎缩侧索硬化症:当前证据综述

The Serotonergic System and Amyotrophic Lateral Sclerosis: A Review of Current Evidence.

作者信息

Yang Lu, Cheng Yanfei, Zhu Yicheng, Cui Liying, Li Xiaoguang

机构信息

Department of Neurology, Peking Union Medical College Hospital (PUMCH), The Transformation Medical Center of PUMC, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, 100005, China.

Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.

出版信息

Cell Mol Neurobiol. 2023 Aug;43(6):2387-2414. doi: 10.1007/s10571-023-01320-0. Epub 2023 Feb 2.

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the premature death of motor neurons. Serotonin (5-HT) is a crucial neurotransmitter, and its dysfunction, whether as a contributor or by-product, has been implicated in ALS pathogenesis. Here, we summarize current evidence linking serotonergic alterations to ALS, including results from post-mortem and neuroimaging studies, biofluid testing, and studies of ALS animal models. We also discuss the possible role of 5-HT in modulating some important mechanisms of ALS (i.e. glutamate excitotoxity and neuroinflammation) and in regulating ALS phenotypes (i.e. breathing dysfunction and metabolic defects). Finally, we discuss the promise and limitations of the serotonergic system as a target for the development of ALS biomarkers and therapeutic approaches. However, due to a relative paucity of data and standardized methodologies in previous studies, proper interpretation of existing results remains a challenge. Future research is needed to unravel the mechanisms linking serotonergic pathways and ALS and to provide valid, reproducible, and translatable findings.

摘要

肌萎缩侧索硬化症(ALS)是一种神经退行性疾病,其特征是运动神经元过早死亡。血清素(5-羟色胺,5-HT)是一种关键的神经递质,其功能障碍,无论是作为致病因素还是副产物,都与ALS的发病机制有关。在此,我们总结了目前将血清素能改变与ALS联系起来的证据,包括尸检和神经影像学研究、生物流体检测以及ALS动物模型研究的结果。我们还讨论了5-HT在调节ALS的一些重要机制(即谷氨酸兴奋性毒性和神经炎症)以及调节ALS表型(即呼吸功能障碍和代谢缺陷)方面的可能作用。最后,我们讨论了血清素能系统作为开发ALS生物标志物和治疗方法靶点的前景和局限性。然而,由于先前研究中的数据相对较少且方法缺乏标准化,对现有结果的合理解读仍然是一项挑战。需要未来的研究来阐明血清素能途径与ALS之间的联系机制,并提供有效、可重复和可转化的研究结果。

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