大鼠脑灌注LTB4时白细胞/内皮细胞相互作用和血脑屏障通透性。

L Schürer, S Corvin, F Röhrich, C Abels, A Baethmann
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引用次数: 6

摘要

本实验研究在模拟脑脊液中注入1.5 nM和15.0 nM LTB4之前、期间和之后,分析大鼠脑表面蛛网膜下腔血管舒张反应(动脉小动脉和小静脉直径的变化)和血脑屏障功能。白细胞动力学研究通过评估其中心线速度,滚动沿(“滚轮”)和附着(“贴纸”)静脉壁白细胞的罗达明6G静脉染色。在两种剂量水平下,脑内灌注LTB4导致小动脉扩张至130% (p < 0.001),而对照组小静脉扩张至117% (p < 0.001)。白细胞中心线速度从0.7 mm/s增加到0.9 mm/s,但只有在高剂量的LTB4灌注后才会增加。LTB4诱导白细胞呈剂量依赖性滚动(p < 0.01)和粘附(p < 0.001)。然而,观察到LTB4脑给药与白细胞滚动和粘附的最大反应之间约有60分钟的延迟。1.5 nM和15.0 nM LTB4脑灌注后,血脑屏障未被打开,而对于静脉注射Na(+)-荧光素,30.0 nM LTB4脑灌注可迅速引起血脑屏障渗漏。目前的研究结果表明,LTB4通过暴露的脑表面的灌注引起明显的血管舒张反应,而白细胞/内皮细胞相互作用的诱导则不那么令人印象深刻。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leukocyte/endothelial interactions and blood-brain barrier permeability in rats during cerebral superfusion with LTB4.

The experimental study analyses the vasomotor response (change of diameter of pial arterioles and venules), and blood-brain barrier function of the pia-arachnoidea at the rat brain surface before, during and after cerebral superfusion with 1.5 or 15.0 nM LTB4 in mock CSF. Leukocyte dynamics were studied by assessment of their centerline velocity, of rolling along ("roller") and attachment to ("sticker") the venular wall of white blood cells intravitally stained by Rhodamin 6G. Superfusion of the brain with LTB4 at both dose levels led to dilation of arterioles to 130% (p < 0.001), while of venules to 117% (p < 0.001) of control. The centerline velocity of leukocytes increased from 0.7 to 0.9 mm/s, however, only after superfusion with LTB4 at the high dose level. LTB4 induced a dose-dependent rolling (p < 0.01) and sticking of leukocytes (p < 0.001). Yet, a delay of about 60 min between cerebral administration of LTB4 and the maximal response of leukocyte rolling and sticking was observed. Whereas the blood-brain barrier was not opened by cerebral superfusion with 1.5 or 15.0 nM LTB4, for i.v. Na(+)-fluorescein, barrier leakage was promptly induced by 30.0 nM. The present findings demonstrate that cerebral administration of LTB4 by superfusion of the exposed brain surface is eliciting a pronounced vasomotor response, whereas the induction of leukocyte/endothelial interactions is less impressive.

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