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Isoflurane Induces Endothelial Apoptosis of the Post-Hypoxic Blood-Brain Barrier in a Transdifferentiated Human Umbilical Vein Edothelial Cell Model

机译:异氟烷在转分化的人脐静脉内皮细胞模型中诱导缺氧后血脑屏障的内皮细胞凋亡。

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摘要

Isoflurane is a popular volatile anesthetic agent used in humans as well as in experimental animal research. In previous animal studies of the blood-brain barrier (BBB), observations towards an increased permeability after exposure to isoflurane are reported. In this study we investigated the effect of a 2-hour isoflurane exposure on apoptosis of the cerebral endothelium following 24 hours of hypoxia in an in vitro BBB model using astrocyte-conditioned human umbilical vein endothelial cells (AC-HUVECs). Apoptosis of AC-HUVECs was investigated using light microscopy of the native culture for morphological changes, Western blot (WB) analysis of Bax and Bcl-2, and a TUNEL assay. Treatment of AC-HUVECs with isoflurane resulted in severe cellular morphological changes and a significant dose-dependent increase in DNA fragmentation, which was observed during the TUNEL assay analysis. WB analysis confirmed increases in pro-apoptotic Bax levels at 4 hours and 24 hours and decreases in anti-apoptotic Bcl-2 in a dose-dependent manner compared with the control group. These negative effects of isoflurane on the BBB after a hypoxic challenge need to be taken into account not only in experimental stroke research, but possibly also in clinical practice.
机译:异氟烷是一种广泛用于人体以及实验动物研究的挥发性麻醉剂。在先前对血脑屏障(BBB)的动物研究中,据报道观察到异氟烷暴露后通透性增加。在这项研究中,我们研究了在星形胶质细胞条件下的人脐静脉内皮细胞(AC-HUVEC)体外BBB模型中,缺氧24小时后2小时异氟烷暴露对脑内皮细胞凋亡的影响。 AC-HUVECs的凋亡研究使用了自然培养物的光学显微镜进行形态学变化,Bax和Bcl-2的蛋白质印迹(WB)分析以及TUNEL分析。在TUNEL分析分析中观察到,用异氟烷处理AC-HUVEC会导致严重的细胞形态变化和DNA片段的剂量依赖性显着增加。 WB分析证实与对照组相比,促凋亡Bax水平在4小时和24小时增加,而抗凋亡Bcl-2以剂量依赖性方式降低。缺氧挑战后,异氟烷对血脑屏障的这些负面影响不仅需要在实验性卒中研究中加以考虑,而且在临床实践中也应予以考虑。

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