肥大细胞
脂氧合酶
化学
组胺
花生四烯酸5-脂氧合酶
脱颗粒
类胰蛋白酶
免疫球蛋白E
花生四烯酸
生物
生物化学
细胞生物学
前列腺素D2
白三烯C4
嗜碱性粒细胞
桅杆(植物学)
分子生物学
作者
V. L. Cohan,Jane McKenzie‐White,Massimo Triggiani,William A. Massey,Anne Kagey‐Sobotka,Lawrence M. Lichtenstein
标识
DOI:10.1016/0006-2952(89)90656-4
摘要
The effects of a putatively specific 5-lipoxygenase inhibitor, 2(12-hydroxydodeca-5,10-dinyl)-3,5,6-trimethyl-1,4-benzoquin one (AA-861), and its major metabolite, M-I, were assessed using anti-IgE activated human basophils, lung mast cells and skin mast cells. In basophils and lung mast cells, no effects on histamine release were observed, whereas leukotriene C4 (LTC4) production was inhibited (IC50 values less than 1 microM). In addition, prostaglandin D2 (PGD2) production was inhibited in lung mast cells (IC50 congruent to 5 microM). In contrast, in skin mast cells both histamine release and PGD2 production were reduced by AA-861 and M-I, with IC50 values of congruent to 5 and 0.4 microM for histamine and PGD2, respectively. These data reveal biochemical heterogeneity among human histamine-containing cells and underscore the necessity of assessing a pharmacologic agonist in relevant cell systems.
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