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环氧化酶选择性和非选择性抑制对速尿刺激的利钠作用的影响。

The effects of selective and non-selective inhibition of cyclo-oxygenase on frusemide-stimulated natriuresis.

作者信息

Wilkins M R, Woods K L, Kendall M J

出版信息

Int J Clin Pharmacol Ther Toxicol. 1986 Feb;24(2):55-7.

PMID:3082774
Abstract

The relative potency of four non-steroidal anti-inflammatory drugs (NSAIDs) - indomethacin, flurbiprofen, sulindac and piroxicam - in inhibiting frusemide-stimulated natriuresis and creatinine clearance was investigated in a placebo controlled cross-over study using healthy volunteers. All four drugs tested significantly inhibited the action of frusemide and they were equipotent in their effects. If it is accepted that sulindac is renal sparing with respect to inhibition of prostaglandin synthesis, our observations raise two possibilities concerning the underlying mechanism of antagonism: a) that inhibition of renal prostaglandin synthesis is not important; b) that sulindac interacts with frusemide in a manner different from other NSAIDs.

摘要

在一项使用健康志愿者的安慰剂对照交叉研究中,研究了四种非甾体抗炎药(NSAIDs)——吲哚美辛、氟比洛芬、舒林酸和吡罗昔康——抑制速尿刺激的利钠作用和肌酐清除率的相对效力。所测试的四种药物均显著抑制了速尿的作用,且它们的效力相当。如果认为舒林酸在抑制前列腺素合成方面对肾脏有保护作用,那么我们的观察结果就拮抗的潜在机制提出了两种可能性:a)抑制肾脏前列腺素合成并不重要;b)舒林酸与速尿的相互作用方式与其他NSAIDs不同。

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