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[新型非甾体抗炎药:COX - 1、COX - 2,它们是怎么回事?]

[New NSAIDS: COX-1, COX-2, what about them?].

作者信息

Peretz A

机构信息

Clinique de Rhumatologie, Département de Médecine Interne, C.H.U. Brugmann, U.L.B.

出版信息

Rev Med Brux. 1998 Sep;19(4):A399-402.

PMID:9805982
Abstract

Non steroidal antiinflammatory (NSAID) drugs are the most widely prescribed drugs against pain and inflammation. Problems of tolerance, particularly gastrointestinal toxicity, limit their use. The central mechanism of NSAID action is the reduction of prostaglandin production from arachidonic acid through cyclooxygenase inhibition. Although such a mechanism was already described 25 years ago, the recent discovery of two isoforms of cyclooxygenase, the cyclooxygenase 1 (COX-1) constitutively expressed in most tissues and the cyclooxygenase 2 (COX-2), inducible, has prompted research in developing new NSAID that would be safer whilst maintaining their efficacy. Nevertheless, their long term efficacy and safety need to be demonstrated in clinical practice. There are still unsolved questions, especially about the physiological role of COX-2.

摘要

非甾体抗炎药(NSAID)是治疗疼痛和炎症最常用的处方药。耐受性问题,尤其是胃肠道毒性,限制了它们的使用。NSAID作用的核心机制是通过抑制环氧化酶减少花生四烯酸生成前列腺素。尽管这一机制在25年前就已被描述,但最近发现环氧化酶有两种同工型,即大多数组织中组成性表达的环氧化酶1(COX-1)和可诱导的环氧化酶2(COX-2),这促使人们研发新的NSAID,使其在保持疗效的同时更安全。然而,它们的长期疗效和安全性仍需在临床实践中得到证实。仍有一些未解决的问题,尤其是关于COX-2的生理作用。

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