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呋塞米对人血小板体外前列腺素生物合成的影响。

Effect of furosemide on the in vitro prostaglandin biosynthesis in human platelets.

作者信息

Srivastava K C, Awasthi K K

出版信息

Prostaglandins Leukot Med. 1982 Aug;9(2):211-21. doi: 10.1016/0262-1746(82)90010-5.

Abstract

Effect of furosemide at various concentrations (0.05-4 mM) was examined on the in vitro biosynthesis of prostaglandins in human platelets. At lower furosemide concentrations (0.05 and 0.1 mM) no effect was observed. At 1 and 2 mM concentrations, PGE2 significantly (P less than 0.01) increased. At 3 and 4 mM concentrations PGE2 increased though not significantly probably because of the small number of samples (n=5). A decrease in PGD2 formation was noted at 1-4 mM furosemide concentrations, though significantly only at 3 mM conc. At 1 and 2 mM concentrations, TxB2 and HHT increased whereas at 3 and 4 mM concentrations these metabolites were decreased. These effects were, however, not significant. No effect was observed on endoperoxide generation at 1 and 2 mM conc. Furosemide at 1 and 2 mM concentrations inhibited ADP- and arachidonic acid induced platelet aggregation. An increased platelet formation of PGE2 in the presence of furosemide may point to the fact that this drug shows its effect mainly on the formation of PGE2 which has been found to exert a profound effect on renal blood flow and thus ameliorates some forms of hypertension.

摘要

研究了不同浓度(0.05 - 4 mM)呋塞米对人血小板中前列腺素体外生物合成的影响。在较低的呋塞米浓度(0.05和0.1 mM)下未观察到影响。在1和2 mM浓度时,PGE2显著(P < 0.01)增加。在3和4 mM浓度时,PGE2虽有增加但不显著,可能是因为样本数量少(n = 5)。在呋塞米浓度为1 - 4 mM时,PGD2生成减少,不过仅在3 mM浓度时显著。在1和2 mM浓度时,TXB2和HHT增加,而在3和4 mM浓度时这些代谢产物减少。然而,这些影响并不显著。在1和2 mM浓度时未观察到对内过氧化物生成的影响。1和2 mM浓度的呋塞米抑制ADP和花生四烯酸诱导的血小板聚集。在呋塞米存在下血小板中PGE2生成增加可能表明该药物主要对PGE2的形成产生影响,而PGE2已被发现对肾血流量有深远影响,从而改善某些类型的高血压。

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