Black K L, Hoff J T
Ann Neurol. 1985 Sep;18(3):349-51. doi: 10.1002/ana.410180313.
To examine whether leukotrienes could increase blood-brain barrier permeability, rats were anesthetized and injected intravenously with Evans blue. Ten microliters of vehicle, of leukotrienes B4, C4, or E4, or of arachidonic acid was injected over 1 hour directly into the brain parenchyma. The percentage of the total surface area of Evans blue extravasation in a coronal section of brain centered on the injection site was then determined as an estimate of blood-brain barrier permeability. Leukotrienes B4, C4, and E4, and arachidonic acid all increased blood-brain barrier permeability, but this effect was lost when the total dose was reduced to 20 ng. Increased blood-brain barrier permeability induced by arachidonic acid could be prevented by pretreatment with the lipoxygenase inhibitor BW755C, but not with indomethacin. Leukotrienes may play a role in the development of increased blood-brain barrier permeability after cerebral injury.
为研究白三烯是否会增加血脑屏障通透性,将大鼠麻醉后静脉注射伊文思蓝。在1小时内将10微升溶媒、白三烯B4、C4或E4,或花生四烯酸直接注射到脑实质中。然后测定以注射部位为中心的脑冠状切片中伊文思蓝外渗总面积的百分比,作为血脑屏障通透性的估计值。白三烯B4、C4和E4以及花生四烯酸均增加了血脑屏障通透性,但当总剂量降至20纳克时,这种作用消失。花生四烯酸诱导的血脑屏障通透性增加可通过用脂氧合酶抑制剂BW755C预处理来预防,但不能用吲哚美辛预防。白三烯可能在脑损伤后血脑屏障通透性增加的发展中起作用。