Abstract
The purpose of this study was to determine whether treatment with high-dose human serum albumin (HSA) would offer protection in a model of high-grade transient forebrain ischemia. Twenty-six fasted Wistar rats underwent bilateral common carotid artery occlusion and severe hypotension (50 mmHg) for 10 min. The agent (25% HSA) or vehicle (0.9% NaCl) was administered i.v. 5 min after termination of ischemia. HSA-treated rats showed significantly improved neurological deficits throughout a 7-day survival period. Histologically, HSA-treated rats showed 2.4- to 5.3-fold increases in numbers of surviving CA1 hippocampal pyramidal neurons compared to saline-treated animals. These results document that high-dose albumin therapy instituted 5 min after global ischemia significantly improves neurological score and reduces histological damage. Copyright (C) 1999 Elsevier Science B.V.
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Belayev, L., Saul, I., Huh, P. W., Finotti, N., Zhao, W., Busto, R., & Ginsberg, M. D. (1999). Neuroprotective effect of high-dose albumin therapy against global ischemic brain injury in rats. Brain Research, 845(1), 107–111. https://doi.org/10.1016/S0006-8993(99)01952-6
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