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Issue title: Selected Proceedings of the 6th Asian Congress for Mirocirculation (ACM'05) (Tokyo, February 25 and 26, 2005)
Article type: Research Article
Authors: Osada, Takashi; | Tomita, Minoru | Tanahashi, Norio | Takeda, Hidetaka | Nagai, Toshihiro | Suzuki, Norihiro
Affiliations: Department of Neurology, School of Medicine, Keio University, Tokyo, Japan | Department of Neurology, Saitama Medical School, Saitama, Japan | Department of Neurology, National Hospital Organization Saitama Hospital, Saitama, Japan | Laboratory of Electronmicroscopy, School of Medicine, Keio University, Tokyo, Japan
Note: [] Corresponding author. E-mail: osada@sc.itc.keio.ac.jp.
Abstract: The source and target of edema fluid for ischemic brain swelling clinically often observed in “malignant infarction” was examined in ex vivo. Wister rat brain hemispheres were removed and incubated air-tightly in a deoxygenated artificial cerebrospinal fluid at 37° for 30 min. Ionic movement into the brain tissue was calculated from their concentration changes in the incubation fluid. We found a weight increase by 11.3±2.5% (p<0.01) and a decrease in Na+ from 148.0 to 139.0±8.2 mEq/l (p<0.01) and an increase in K+ from 4.3 to 11.2±1.2 mEq/l. Video tape recording revealed that the brain swelling started immediately upon the incubation, and the electronmicroscopical investigation of the swollen cortical tissue revealed that the fluid moved mainly into astroglial cells. The astroglial swelling was quite similar to that of specimen taken from clinical cases at autopsy. The driving force of the water shift can be explained by discharge of thermodynamic potential, i.e., a coupled transport of water with Na+ across the cell membrane (anomalous osmosis). The swelling was not affected by addition of aquaporin blocker, mercuric chloride. It is concluded that cerebrospinal fluid bathing the brain in situ can be the source of edema fluid for ischemic brain swelling.
Keywords: Edema fluid, anomalous osmosis, membrane depolization, ischemic brain swelling
Journal: Clinical Hemorheology and Microcirculation, vol. 34, no. 1-2, pp. 223-226, 2006
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