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Endothelial edema precedes blood-brain barrier breakdown in early time points after experimental focal cerebral ischemia

机译:实验性局灶性脑缺血后的早期时间点内皮水肿先于血脑屏障破坏

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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.Electronic supplementary materialThe online version of this article (10.1186/s40478-019-0671-0) contains supplementary material, which is available to authorized users.
机译:在中风的情况下,缺血相关的血脑屏障(BBB)功能障碍加重了脑水肿,严重影响了临床结果。此外,血管完整性受损与颅内出血的风险有关,尤其是在治疗性再通气之后。因此,本研究旨在研究小鼠实验性大脑中动脉闭塞(MCAO)后30µmin至4µh的早期血管变化。在这里,在MCAO后2和4h,在动物中检测到渗透性标记物FITC-白蛋白的外渗。因此,BBB分解与内皮表面的改变相关,由不连续的异凝集素-B4染色指示,而紧密的连接链仍可使用电子和免疫荧光显微镜检出。值得注意的是,在MCAO后30分钟,高达60%受缺血影响的血管显示出了内皮水肿,并伴有水肿性星形胶质尾脚,明显是在FITC-白蛋白渗出之前。随着缺血期的增加,血管损伤的分数显着增加,多达60%的纹状体血管显示内皮完整性丧失。值得注意的是,永久性和短暂性缺血的比较在诱导缺血后4小时没有明显差异。由于这些变性还涉及潜在可挽救组织的半影区,因此内皮保护的辅助方法可能有助于减少缺血性中风后的血管性水肿。电子补充材料本文的在线版本(10.1186 / s40478-019-0671-0)包含补充材料,可供授权用户使用。

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