肾上腺系统与肌萎缩性脊髓侧索硬化症

IF 6.7 2区 医学 Q1 NEUROSCIENCES
Andrew Eisen , Maiken Nedergaard , Emma Gray , Matthew C. Kiernan
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引用次数: 0

摘要

脑淋巴系统和脑膜淋巴管是运输溶质和清除脑内有毒物质的通道。与渐冻症特别相关的是,这适用于 TDP-43 和谷氨酸,两者都是疾病发病机制的主要因素。水流受动脉搏动、呼吸、姿势以及水蒸发素-4 通道(AQP4)的位置和比例的影响。非快速眼动期慢波睡眠是甘油排泄的关键,而清醒时甘油排泄会中断。在帕金森病和阿尔茨海默病中,睡眠障碍比特征性临床特征的出现要早数年,并且与有毒蛋白质产物的逐渐积累有关。虽然 ALS 中的睡眠问题已被充分描述,但临床前睡眠障碍或 ALS 中潜在的甘液系统衰竭却很少被考虑。在此,我们回顾一下糖尿系统可能对 ALS 产生的影响。临床前睡眠障碍是导致 ALS 的一个未被发现的主要风险因素,同时我们还探讨了改善甘液流动的潜在治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The glymphatic system and Amyotrophic lateral sclerosis

The glymphatic system and the meningeal lymphatic vessels provide a pathway for transport of solutes and clearance of toxic material from the brain. Of specific relevance to ALS, this is applicable for TDP-43 and glutamate, both major elements in disease pathogenesis. Flow is propelled by arterial pulsation, respiration, posture, as well as the positioning and proportion of aquaporin-4 channels (AQP4). Non-REM slow wave sleep is the is key to glymphatic drainage which discontinues during wakefulness. In Parkinson’s disease and Alzheimer’s disease, sleep impairment is known to predate the development of characteristic clinical features by several years and is associated with progressive accumulation of toxic proteinaceous products. While sleep issues are well described in ALS, consideration of preclinical sleep impairment or the potential of a failing glymphatic system in ALS has rarely been considered. Here we review how the glymphatic system may impact ALS. Preclinical sleep impairment as an unrecognized major risk factor for ALS is considered, while potential therapeutic options to improve glymphatic flow are explored.

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来源期刊
Progress in Neurobiology
Progress in Neurobiology 医学-神经科学
CiteScore
12.80
自引率
1.50%
发文量
107
审稿时长
33 days
期刊介绍: Progress in Neurobiology is an international journal that publishes groundbreaking original research, comprehensive review articles and opinion pieces written by leading researchers. The journal welcomes contributions from the broad field of neuroscience that apply neurophysiological, biochemical, pharmacological, molecular biological, anatomical, computational and behavioral analyses to problems of molecular, cellular, developmental, systems, and clinical neuroscience.
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