| Literature DB >> 32001524 |
Humberto Mestre1,2, Ting Du1,3, Amanda M Sweeney1, Guojun Liu1,4, Andrew J Samson5, Weiguo Peng5, Kristian Nygaard Mortensen5, Frederik Filip Stæger5, Peter A R Bork5,6, Logan Bashford7, Edna R Toro7, Jeffrey Tithof7, Douglas H Kelley7, John H Thomas7, Poul G Hjorth6, Erik A Martens6, Rupal I Mehta1,2,8,9, Orestes Solis2, Pablo Blinder10,11, David Kleinfeld12,13, Hajime Hirase5,14, Yuki Mori15, Maiken Nedergaard16,5.
Abstract
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.Entities:
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Year: 2020 PMID: 32001524 PMCID: PMC7375109 DOI: 10.1126/science.aax7171
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728