非甾体抗炎药的历史概述。

V Wright
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引用次数: 0

摘要

非甾体类抗炎药(NSAIDs)已成为治疗关节炎的重要药物。Vane在1971年证实阿司匹林及相关药物的主要作用机制是抑制花生四烯酸合成前列腺素。虽然Vane的前列腺素假说已被普遍接受,但各种研究表明,其他机制可能在非甾体抗炎药的作用中起作用。随着可获得的非甾体抗炎药数量的增加以及有关非甾体抗炎药治疗相关副作用的最新信息,检查这些药物是否以最适当的方式使用变得很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Historical overview of NSAIDs.

Nonsteroidal anti-inflammatory drugs (NSAIDs) have become valuable therapeutic agents in the treatment of arthritic conditions. In 1971, Vane demonstrated that the primary mechanism of action of aspirin and related drugs was inhibition of synthesis of prostaglandins from arachidonic acid. Although Vane's prostaglandin hypothesis has been generally accepted, various studies have suggested that additional mechanisms may have a role in the effects of NSAIDs. With the increasing number of NSAIDs available and with recent information on the side effects associated with NSAID therapy, it becomes important to examine whether these drugs are being used in the most appropriate manner.

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