淋巴系统
肌萎缩侧索硬化
神经科学
疾病
医学
多发性硬化
清醒
水通道蛋白4
睡眠(系统调用)
病理
心理学
脑脊液
免疫学
脑电图
计算机科学
操作系统
作者
Andrew Eisen,Maiken Nedergaard,E. G. Gray,Matthew C. Kiernan
标识
DOI:10.1016/j.pneurobio.2024.102571
摘要
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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