Shoam H, Razin E
Biochim Biophys Acta. 1985 Oct 23;837(1):1-5. doi: 10.1016/0005-2760(85)90078-5.
The inhibitory effect of the drug BW755C on the 5-lipoxygenase pathway was analyzed for bone marrow-derived murine mast cells, termed E-mast cells. The drug prevented the formation of 5-HETE from exogenous [14C]arachidonic acid when IgE-sensitized cells were challenged by the antigen. BW755C also prevented formation of leukotriene C4 in a dose-dependent fashion when IgE-sensitized mast cells, preincubated with the drug, were activated with either the specific antigen or the ionophore. Leukotriene C4 inhibition occurred with a minimal drug preincubation period of 1 min before the cells were subjected to antigen-dependent activation. BW755C did not affect the degranulation response of these cells. Thus in an intact cell system BW755C prevents 5-lipoxygenation of arachidonic acid. Furthermore, this study reveals that even with transmembrane activation of E-mast cells through their IgE-Fc receptors, granule secretion is not dependent upon corresponding metabolites from the 5-lipoxygenase pathway.
分析了药物BW755C对源自骨髓的小鼠肥大细胞(称为E肥大细胞)5-脂氧合酶途径的抑制作用。当用抗原刺激IgE致敏细胞时,该药物可阻止外源性[14C]花生四烯酸生成5-HETE。当用药物预孵育的IgE致敏肥大细胞用特异性抗原或离子载体激活时,BW755C还以剂量依赖的方式阻止白三烯C4的形成。在细胞进行抗原依赖性激活前,药物预孵育1分钟的最短时间即可出现白三烯C4抑制作用。BW755C不影响这些细胞的脱颗粒反应。因此,在完整细胞系统中,BW755C可阻止花生四烯酸的5-脂氧合作用。此外,本研究表明,即使通过E肥大细胞的IgE-Fc受体进行跨膜激活,颗粒分泌也不依赖于5-脂氧合酶途径的相应代谢产物。