首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >A comparison of the abilities of acetylsalicylic acid flurbiprofen and indomethacin to inhibit the release reaction and prostaglandin synthesis in human blood platelets.
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A comparison of the abilities of acetylsalicylic acid flurbiprofen and indomethacin to inhibit the release reaction and prostaglandin synthesis in human blood platelets.

机译:乙酰水杨酸氟比洛芬和消炎痛抑制人体血小板释放反应和前列腺素合成的能力比较。

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摘要

1 A quantitative comparison has been made of the abilities of acetylsalicylic acid, flurbiprofen and indomethacin to inhibit the adenosine diphosphate (ADP)-induced platelet release reaction and to inhibit the synthesis of prostaglandins from arachidonic acid. 2 Experiments were carried out on human platelets that had been incubated with the agents in vitro and on platelets obtained from volunteers who had ingested standard doses of the drugs. 3 The results obtained for acetylsalicylic acid show that there is a close relation between the release reaction and the synthesis of prostaglandins in platelets. 4 Flurbiprofen and indomethacin appear to inhibit the release reaction rather more effectively than they inhibit the synthesis of prostaglandins. It is possible that these agents inhibit the release reaction by another mechanism.
机译:1定量比较了乙酰水杨酸,氟比洛芬和消炎痛抑制二磷酸腺苷(ADP)诱导的血小板释放反应和抑制花生四烯酸合成前列腺素的能力。 2实验是对已在体外与药剂孵育的人血小板以及从摄入了标准剂量药物的志愿者那里获得的血小板进行的。 3乙酰水杨酸的结果表明,释放反应与血小板中前列腺素的合成密切相关。 4氟比洛芬和消炎痛似乎比其抑制前列腺素的合成更有效地抑制了释放反应。这些试剂可能通过其他机理抑制释放反应。

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