Rankin J A, Harris P
Pulmonary and Critical Care Section, Yale University School of Medicine, West Haven, Ct.
Prostaglandins. 1993 Jan;45(1):77-84. doi: 10.1016/0090-6980(93)90091-k.
Whereas we observed previously that concentrations of the lipoxygenase inhibitor nordihydroguaiaretic acid that inhibited leukotriene B4 release from lipopolysaccharide-stimulated human alveolar macrophages in vitro also inhibited subsequent interleukin-8 release, we hypothesized that leukotriene B4 release was required for the release of interleukin-8. Alveolar macrophages from normal nonsmoking volunteers were adhered to plastic and incubated with varying concentrations (25-250nM) of the 5-lipoxygenase activating protein inhibitor MK-886 prior to stimulation with lipopolysaccharide. MK-886 inhibited leukotriene B4 release in a concentration-dependent manner. The concentration of MK-886 that inhibited release by 50% was 53.3 +/- 23.1nM (mean +/- SD), n = 4. Interleukin-8 concentrations in 24hr supernatants were not inhibited by incubation of the cells with any concentration of MK-886, including those that inhibited leukotriene B4 release by > 95%. Thus, MK-886 is an effective inhibitor of human alveolar macrophage release of leukotriene B4, and the release of leukotriene B4 is not a prerequisite for alveolar macrophage release of interleukin-8.
鉴于我们之前观察到,在体外能抑制脂多糖刺激的人肺泡巨噬细胞释放白三烯B4的脂氧合酶抑制剂去甲二氢愈创木酸的浓度,也能抑制随后白细胞介素-8的释放,我们推测白细胞介素-8的释放需要白三烯B4的释放。来自正常不吸烟志愿者的肺泡巨噬细胞贴附于塑料培养皿上,在用脂多糖刺激之前,用不同浓度(25 - 250nM)的5-脂氧合酶激活蛋白抑制剂MK-886进行孵育。MK-886以浓度依赖的方式抑制白三烯B4的释放。抑制释放50%的MK-886浓度为53.3 +/- 23.1nM(平均值 +/- 标准差),n = 4。细胞与任何浓度的MK-886孵育,包括那些抑制白三烯B4释放>95%的浓度,24小时上清液中的白细胞介素-8浓度均未受到抑制。因此,MK-886是人类肺泡巨噬细胞释放白三烯B4的有效抑制剂,且白三烯B4的释放不是肺泡巨噬细胞释放白细胞介素-8的先决条件。