首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >Single-blind study of epoprostenol and 6-keto-prostaglandin E1 in man: effects of platelet aggregation and plasma renin.
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Single-blind study of epoprostenol and 6-keto-prostaglandin E1 in man: effects of platelet aggregation and plasma renin.

机译:人体中鬼臼烯醇和6-酮-前列腺素E1的单盲研究:血小板聚集和血浆肾素的影响。

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摘要

The effects of epoprostenol (PGI2, 2-8 ng kg-1 min-1) and 6-keto-prostaglandin E1 (6-keto-PGE1, 7.5-30 ng kg-1 min-1) on ADP-induced platelet aggregation, blood pressure (BP), heart rate and plasma renin activity (PRA) were studied in six healthy male volunteers. During graded intravenous administration of PGI2, platelet aggregation was inhibited at a minimum dose of 4 ng kg-1 min-1. The dose required to produce the same degree of platelet inhibition was approximately 15 ng kg-1 min-1 for 6-keto-PGE1. Diastolic BP was significantly reduced and PRA was increased by PGI2 at a dose greater than 8 ng kg-1 min-1. In contrast, 6-keto-PGE1 did not produce BP and PRA changes up to a dose of 30 ng kg-1 min-1. These data indicate that PGI2 has approximately four times more potent antiplatelet activity than 6-keto-PGE1 on a molar basis in man. The cardiovascular and PRA changes were less prominent for 6-keto-PGE1 than PGI2.
机译:Epoprostenol(PGI2,2-8 ng kg-1 min-1)和6-酮-前列腺素E1(6-keto-PGE1,7.5-30 ng kg-1 min-1)对ADP诱导的血小板聚集的影响,在六位健康的男性志愿者中研究了血压(BP),心率和血浆肾素活性(PRA)。在分阶段静脉内给予PGI2的过程中,最小4 ng kg-1 min-1的剂量抑制了血小板凝集。对于6-酮-PGE1,产生相同程度的血小板抑制作用所需的剂量约为15 ng kg-1 min-1。大于8 ng kg-1 min-1的剂量通过PGI2可使舒张压明显降低,PRA升高。相反,当剂量达到30 ng kg-1 min-1时,6-keto-PGE1不会产生BP和PRA变化。这些数据表明,按摩尔计算,人中PGI2的抗血小板活性约为6-酮-PGE1的四倍。 6-酮基-PGE1的心血管和PRA变化不如PGI2显着。

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