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血小板活化因子刺激磷脂酰肌醇循环。磷脂酸的出现与马血小板中5-羟色胺的释放有关。

Platelet-activating factor stimulates the phosphatidylinositol cycle. Appearance of phosphatidic acid is associated with the release of serotonin in horse platelets.

作者信息

Lapetina E G

出版信息

J Biol Chem. 1982 Jul 10;257(13):7314-7.

PMID:7045103
Abstract

The addition of platelet-activating factor to horse platelets prelabeled with (32P)orthophosphate induces the rapid formation of [32P]phosphatidic acid. This is subsequently followed by a considerable increase in the labeling of phosphatidylinositol. Activation of the formation of phosphatidic acid by platelet-activating factor is evident at a concentration of 1 nM, is maximal at 0.1 microM, and independent of the presence or absence of plasma in the medium. In horse platelets prelabeled with [14C]arachidonic acid, platelet-activating factor stimulates the rapid formation of [14C]phosphatidic acid, [14C]arachidonic acid, and [14C]arachidonate metabolites. Concomitantly, there is a loss of radioactivity from phosphatidylinostiol., phosphatidylcholine, and phosphatidylethanolamine. Platelet-activating factor at a concentration of 1 nM stimulates formation of phosphatidic acid while the appearance of arachidonate metabolites is seen at a higher concentration (10 nM), without acetate in the 2-position, is unable to induce in platelets the formation of phosphatidic acid, arachidonate metabolites, or the release of [3H]serotonin and, in addition, does not antagonize the action of platelet-activating factor. the release of [3H]serotonin and [14C]arachidonate from platelets stimulated with platelet-activating factor is not affected by indomethacin. Trifluoperazine (50-100 microM) inhibits the platelet-activating factor-stimulated liberation of arachidonic acid from phospholipids, without affecting the formation of phosphatidic acid and the release of serotonin. Prostacyclin, on the other hand, inhibits the platelet-activating factor-induced release of serotonin, arachidonate metabolites, and formation of phosphatidic acid. These data indicate a close relationship between the formation of phosphatidic acid and the release of serotonin in platelets stimulated with the platelet-activating factor.

摘要

向预先用(32P)正磷酸盐标记的马血小板中添加血小板活化因子会诱导[32P]磷脂酸的快速形成。随后,磷脂酰肌醇的标记显著增加。血小板活化因子对磷脂酸形成的激活在1 nM浓度时明显,在0.1 microM时达到最大值,且与培养基中是否存在血浆无关。在用[14C]花生四烯酸预先标记的马血小板中,血小板活化因子刺激[14C]磷脂酸、[14C]花生四烯酸和[14C]花生四烯酸代谢物的快速形成。同时,磷脂酰肌醇、磷脂酰胆碱和磷脂酰乙醇胺中的放射性会损失。1 nM浓度的血小板活化因子刺激磷脂酸的形成,而花生四烯酸代谢物的出现则在更高浓度(10 nM)时可见,2位没有乙酸盐的情况下,无法诱导血小板中磷脂酸、花生四烯酸代谢物的形成或[3H]5-羟色胺的释放,此外,也不拮抗血小板活化因子的作用。血小板活化因子刺激血小板释放[3H]5-羟色胺和[14C]花生四烯酸不受吲哚美辛的影响。三氟拉嗪(50 - 100 microM)抑制血小板活化因子刺激的花生四烯酸从磷脂中的释放,而不影响磷脂酸的形成和5-羟色胺的释放。另一方面,前列环素抑制血小板活化因子诱导的5-羟色胺释放、花生四烯酸代谢物形成和磷脂酸形成。这些数据表明在血小板活化因子刺激的血小板中,磷脂酸的形成与5-羟色胺的释放之间存在密切关系。

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