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阿司匹林、甲芬那酸、二氢可待因、右丙氧芬和对乙酰氨基酚对内脏痛、呼吸频率及前列腺素生物合成的相对作用比较。

Comparison of the relative effects of aspirin, mefenamic acid, dihydrocodeine, dextropropoxyphene and paracetamol on visceral pain, respiratory rate and prostaglandin biosynthesis.

作者信息

Sewell R D, Gonzalez J P, Pugh J

出版信息

Arch Int Pharmacodyn Ther. 1984 Apr;268(2):325-34.

PMID:6732369
Abstract

A comparison was made between the relative effects of aspirin, mefenamic acid, dihydrocodeine , dextropropoxyphene and paracetamol on visceral pain (chemically-inducing writhing), respiratory rate and prostaglandin (PG) biosynthesis (cyclo-oxygenase activity). A close correlation was found to exist between inhibition of PG biosynthesis and inhibition of visceral pain for mefenamic acid, aspirin and paracetamol. Analysis of the complete activity profiles derived from evaluation of the test parameters yielded the following rank order of overall ratios of their beneficial anti-writhing/anti-cyclo-oxygenase to respiratory depressive activities: (1) mefenamic acid, (2) aspirin, (3) dihydrocodeine , (4) dextropropoxyphene and paracetamol.

摘要

对阿司匹林、甲芬那酸、二氢可待因、右丙氧芬和对乙酰氨基酚在内脏疼痛(化学诱导扭体反应)、呼吸频率及前列腺素(PG)生物合成(环氧化酶活性)方面的相对作用进行了比较。结果发现,甲芬那酸、阿司匹林和对乙酰氨基酚在抑制PG生物合成与抑制内脏疼痛之间存在密切相关性。通过对测试参数评估得出的完整活性谱进行分析,得出了它们有益的抗扭体反应/抗环氧化酶与呼吸抑制活性总体比值的以下排序:(1)甲芬那酸,(2)阿司匹林,(3)二氢可待因,(4)右丙氧芬和对乙酰氨基酚。

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