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苯恶洛芬的比较药理学

The comparative pharmacology of benoxaprofen.

作者信息

Dawson W

出版信息

J Rheumatol Suppl. 1980;6:5-11.

PMID:6771399
Abstract

Comparative studies with nonsteroidal antiinflammatory drugs (NSAIDs) have shown benoxaprofen to be moderately active in inhibiting carrageenin-induced pleurisy in rats and cellular migration in vitro. Benoxaprofen was also moderately active in inhibiting developing adjuvant-induced arthritis; however, it exhibited a potent response in established adjuvant arthritis, and it was the only compound tested which showed marked inhibition of the directional movement of mononuclear cells. Unlike other NSAIDs, it was a weak inhibitor of prostaglandin synthetase. The data suggested that there may be mechanisms of antiinflammatory activity which do not relate to inhibition of prostaglandin synthetase.

摘要

与非甾体抗炎药(NSAIDs)的对比研究表明,苯恶洛芬在抑制角叉菜胶诱导的大鼠胸膜炎及体外细胞迁移方面具有中等活性。苯恶洛芬在抑制佐剂诱导的关节炎发展方面也具有中等活性;然而,它在已形成的佐剂性关节炎中表现出强效反应,并且是所测试的唯一一种对单核细胞定向运动有显著抑制作用的化合物。与其他NSAIDs不同,它是一种较弱的前列腺素合成酶抑制剂。这些数据表明,可能存在与抑制前列腺素合成酶无关的抗炎活性机制。

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