外渗
医学
缺血
血脑屏障
水肿
病理
埃文斯蓝
脑水肿
血管闭塞
内皮
半影
白蛋白
脑血流
脑缺血
封堵器
血管通透性
脑水肿
麻醉
大脑中动脉
脑梗塞
神经保护
内科学
冲程(发动机)
水通道蛋白4
内皮干细胞
中枢神经系统
工程类
机械工程
作者
Martin Krueger,Bianca Mages,Constance Hobusch,Dominik Michalski
标识
DOI:10.1186/s40478-019-0671-0
摘要
In the setting of stroke, ischemia-related blood-brain barrier (BBB) dysfunction aggravates the cerebral edema, which critically impacts on the clinical outcome. Further, an impaired vascular integrity is associated with the risk of intracranial bleeding, especially after therapeutic recanalization. Therefore, the present study was aimed to investigate early vascular alterations from 30 min to 4 h after experimental middle cerebral artery occlusion (MCAO) in mice. Here, an extravasation of the permeability marker FITC-albumin was detectable in animals 2 and 4 h after MCAO. Thereby, BBB breakdown correlated with alterations of the endothelial surface, indicated by a discontinuous isolectin-B4 staining, while tight junction strands remained detectable using electron and immunofluorescence microscopy. Noteworthy, already 30 min after MCAO, up to 60% of the ischemia-affected vessels showed an endothelial edema, paralleled by edematous astrocytic endfeet, clearly preceding FITC-albumin extravasation. With increasing ischemic periods, scores of vascular damage significantly increased with up to 60% of the striatal vessels showing loss of endothelial integrity. Remarkably, comparison of permanent and transient ischemia did not provide significant differences 4 h after ischemia induction. As these degenerations also involved penumbral areas of potentially salvageable tissue, adjuvant approaches of endothelial protection may help to reduce the vasogenic edema after ischemic stroke.
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