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前列腺素E1和前列腺素内过氧化物PGG2对血小板环核苷酸含量的调节作用。

Modulation of platelet cyclic nucleotide content by PGE1 and the prostaglandin endoperoxide PGG2.

作者信息

Miller O V, Gorman R R

出版信息

J Cyclic Nucleotide Res. 1976;2(2):79-87.

PMID:177467
Abstract

The effects of prostaglandin E1 and prostaglandin G2, the prostaglandin endoperoxide, on platelet cyclic nucleotide concentrations were measured in platelet rich plasma (PRP), and in washed intact platelets. PGE1 was found to be a potent stimulator of platelet cAMP levels in both PRP and washed cells, and to inhibit aggregation in both systems. PGE1 did not change platelet cGMP levels in either PRP or washed cells. PGG2 which is a potent inducer of platelet aggregation, did not affect either the basal cAMP or the basal cGMP concentration. However, PGG2 was found to antagonize the increases in cAMP content in response to PGE1 in both PRP and washed platelets. The addition to our system of a cyclic nucleotide phosphodiesterase inhbitor, theophylline, did not change our findings. It is suggested that PGG2 may induce platelet aggregation by inhibiting PGE1-stimulated cAMP accumulation.

摘要

在富血小板血浆(PRP)和洗涤后的完整血小板中,测量了前列腺素E1、前列腺素G2(前列腺素内过氧化物)对血小板环核苷酸浓度的影响。发现PGE1在PRP和洗涤后的细胞中均为血小板cAMP水平的强效刺激剂,并在两个系统中均抑制聚集。PGE1在PRP或洗涤后的细胞中均未改变血小板cGMP水平。作为血小板聚集强效诱导剂的PGG2,对基础cAMP或基础cGMP浓度均无影响。然而,发现PGG2在PRP和洗涤后的血小板中均拮抗因PGE1导致的cAMP含量增加。在我们的系统中添加环核苷酸磷酸二酯酶抑制剂茶碱,并未改变我们的研究结果。提示PGG2可能通过抑制PGE1刺激的cAMP积累来诱导血小板聚集。

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