6-酮- pge1对血小板聚集的抑制作用对环GMP水平没有影响

Eugene G. Pontecorvo, Carl B. Myers, Howard L. Lippton , Philip J. Kadowitz
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引用次数: 2

摘要

研究了6-酮- pge1对人富血小板血浆(PRP)中花生四烯酸(AA)、二磷酸腺苷(ADP)和胶原聚集反应的影响。此外,我们还进行了实验,以确定这些作用是否与血小板环AMP和环GMP水平的变化有关。在PRP中培养的6-Keto-PGE1产生血小板环AMP水平的剂量相关升高,而血小板环GMP水平不变。AA和ADP诱导的对照聚集没有改变环AMP和环GMP水平,而胶原诱导的对照聚集升高了环GMP水平,而环AMP水平不变。6-Keto-PGE1对AA、ADP和胶原诱导的血小板聚集产生剂量依赖性抑制,这种抑制与剂量相关的环AMP水平升高相关。由于6-酮- pge1不会持续改变人PRP中的环GMP水平,因此目前的数据支持先前的研究,即6-酮- pge1通过刺激环AMP积累来抑制血小板聚集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of platelet aggregation by 6-keto-PGE1; lack of an effect on cyclic GMP levels

The effects of 6-keto-PGE1 on aggregatory responses to arachidonic acid (AA), adenosine diphosphate (ADP) and collagen were studied in human platelet-rich plasma (PRP). In addition, experiments were carried out to determine if these effects correlate with changes in platelet cyclic AMP and cyclic GMP levels. 6-Keto-PGE1 incubated in PRP produced dose-related increases in platelet cyclic AMP levels whereas platelet cyclic GMP levels were unchanged. Control aggregations induced by AA and ADP did not alter cyclic AMP and cyclic GMP levels whereas control aggregations induced by collagen elevated cyclic GMP levels while cyclic AMP levels were unchanged. 6-Keto-PGE1 produced a dose-dependent inhibition of platelet aggregation induced by AA, ADP and collagen and this inhibition correlated with a dose-related increase in cyclic AMP levels. Since 6-keto-PGE1 does not consistently alter cyclic GMP levels in human PRP, the present data support previous studies suggesting that 6-keto-PGE1 produces inhibition of platelet aggregation through the stimulation of cyclic AMP accumulation.

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