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[选择性环氧化酶-2(COX-2)抑制剂:重要性与局限性]

[Selective cyclooxygenase-2 (COX-2) inhibitors: importance and limitations].

作者信息

Pairet M, Netter P

机构信息

Boehinger Ingelheim Pharma KG, Dept of Pulmonary Research, Ingelheim am Rhein, Germany.

出版信息

Therapie. 1999 Jul-Aug;54(4):433-45.

Abstract

The discovery of an inducible form of cyclooxygenase (COX-2) requires a refinement of the theory that inhibition of cyclooxygenase activity explains both therapeutic effects and side-effects of non-steroidal anti-inflammatory drugs (NSAIDs). Selective COX-2 inhibitors have demonstrated in clinical trials a significantly better gastrointestinal tolerability than classical NSAIDs, for the same anti-inflammatory activity. Their tolerability in patients with active ulcer or with a recent history of ulcer as well as in patients suffering from cardiovascular or renal diseases has still to be investigated in detail. Their therapeutic potential in several new indications, including pre-term labour, colorectal cancer and Alzheimer's disease, is currently being investigated.

摘要

环氧化酶-2(COX-2)诱导形式的发现,需要对以下理论进行完善:即环氧化酶活性的抑制可解释非甾体抗炎药(NSAIDs)的治疗效果和副作用。在临床试验中,对于相同的抗炎活性,选择性COX-2抑制剂已显示出比传统NSAIDs显著更好的胃肠道耐受性。它们在活动性溃疡患者、近期有溃疡病史的患者以及患有心血管或肾脏疾病的患者中的耐受性仍有待详细研究。目前正在研究它们在包括早产、结直肠癌和阿尔茨海默病在内的几种新适应症中的治疗潜力。

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