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萘普生对人体血栓素和前列环素体内合成的影响。

Effects of naproxen on the in vivo synthesis of thromboxane and prostacyclin in man.

作者信息

Vesterqvist O, Gréen K

机构信息

Department of Clinical Chemistry and Blood Coagulation, Karolinska Hospital, Stockholm, Sweden.

出版信息

Eur J Clin Pharmacol. 1989;37(6):563-5. doi: 10.1007/BF00562545.

Abstract

The effect of a single oral dose of 500 mg naproxen on the synthesis in vivo of thromboxane A2 and prostacyclin was studied in healthy volunteers. The synthesis of the prostanoids was assessed by measuring the urinary excretion of the metabolites 2,3-dinor-TxB2 and 2,3-dinor-6-keto-PGF1 alpha, respectively, using stable isotope dilution assays based on gas chromatography - mass spectrometry. Naproxen caused significant inhibition of the excretion of both metabolites for about two days. The reduction of the thromboxane metabolite was more pronounced (75% inhibition) than that of the prostacyclin metabolite (about 50% inhibition). The data support the idea that naproxen causes reversible inhibition of cyclooxygenase.

摘要

在健康志愿者中研究了单次口服500毫克萘普生对血栓素A2和前列环素体内合成的影响。通过基于气相色谱 - 质谱的稳定同位素稀释法分别测量代谢物2,3 - 二去甲 - TxB2和2,3 - 二去甲 - 6 - 酮 - PGF1α的尿排泄量来评估前列腺素的合成。萘普生在约两天内引起两种代谢物排泄的显著抑制。血栓素代谢物的减少比前列环素代谢物的减少更明显(75%抑制)(约50%抑制)。这些数据支持萘普生引起环氧化酶可逆性抑制的观点。

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