Yamada K, Okano Y, Miura K, Nozawa Y
Biochim Biophys Acta. 1987 Feb 14;917(2):290-5.
Rat peritoneal mast cells respond to various secretagogues, such as ionophore A23187, concanavalin A (Ig E receptor cross-bridging) and compound 48/80 (membrane perturbing), to secrete histamine and to liberate arachidonic acid. Arachidonic acid release was made identifiable by pretreatment with BW755C, an inhibitor of both lipoxygenase and cyclo-oxygenase. The extent of arachidonic acid release varied among these three secretagogues. A23187 appeared to be most potent, whereas compound 48/80 was weakest. The sources of released arachidonic acids may be different depending on the types of stimulants. The stimulation with A23187 released arachidonic acid mainly from phosphatidylcholine and triacylglycerol. After treatment with concanavalin A and compound 48/80, in addition to phosphatidylcholine, phosphatidylinositol also appeared to serve as a donor of arachidonic acid.
大鼠腹膜肥大细胞对多种促分泌剂有反应,如离子载体A23187、伴刀豆球蛋白A(Ig E受体交联)和化合物48/80(膜扰动),以分泌组胺并释放花生四烯酸。通过用BW755C(一种脂氧合酶和环氧化酶的抑制剂)预处理,可使花生四烯酸的释放变得可识别。这三种促分泌剂中花生四烯酸的释放程度各不相同。A23187似乎最有效,而化合物48/80最弱。释放的花生四烯酸的来源可能因刺激物类型而异。用A23187刺激主要从磷脂酰胆碱和三酰甘油释放花生四烯酸。用伴刀豆球蛋白A和化合物48/80处理后,除磷脂酰胆碱外,磷脂酰肌醇似乎也作为花生四烯酸的供体。