脑脊液
冲程(发动机)
肿胀 的
水肿
医学
脑肿胀
去极化
神经退行性变
脑水肿
脑组织
病理
神经科学
麻醉
解剖
内科学
生物
机械工程
疾病
工程类
作者
Humberto Mestre,Ting Du,Amanda M. Sweeney,Guojun Liu,Andrew J. Samson,Weiguo Peng,Kristian Nygaard Mortensen,Frederik Filip Stæger,Peter A. R. Bork,Logan Bashford,Edna R. Toro,Jeffrey Tithof,Douglas H. Kelley,John H. Thomas,Poul G. Hjorth,Erik A. Martens,Rupal I. Mehta,Orestes E. Solis,Pablo Blinder,David Kleinfeld
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2020-01-31
卷期号:367 (6483)
被引量:474
标识
DOI:10.1126/science.aax7171
摘要
Stroke affects millions each year. Poststroke brain edema predicts the severity of eventual stroke damage, yet our concept of how edema develops is incomplete and treatment options remain limited. In early stages, fluid accumulation occurs owing to a net gain of ions, widely thought to enter from the vascular compartment. Here, we used magnetic resonance imaging, radiolabeled tracers, and multiphoton imaging in rodents to show instead that cerebrospinal fluid surrounding the brain enters the tissue within minutes of an ischemic insult along perivascular flow channels. This process was initiated by ischemic spreading depolarizations along with subsequent vasoconstriction, which in turn enlarged the perivascular spaces and doubled glymphatic inflow speeds. Thus, our understanding of poststroke edema needs to be revised, and these findings could provide a conceptual basis for development of alternative treatment strategies.
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