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[非甾体抗炎药导致胃黏膜损伤:特别提及环氧化酶-2]

[NSAIDs caused gastric mucosal injury: with a special reference to COX-2].

作者信息

Sakamoto Choitsu

机构信息

Department of Internal Medicine III, Nippon Medical School, Tokyo, Japan.

出版信息

J Nippon Med Sch. 2003 Feb;70(1):5-11. doi: 10.1272/jnms.70.5.

Abstract

Nonsteroidal antiinflammatory drugs (NSAIDs) have been shown to cause mucosal injury in the gastrointestinal tract as a side effect, occasionally turning out to be severe complications such as bleeding and perforation. So far NSAIDs-caused mucosal injury was attributed to their inhibitory effects on the activity of cyclooxygenase-1 (COX-1) which is expressed and shown to play a crucial role for the mucosal protection via producing prostaglandin E2 in the stomach. However, a recent progress of the understanding about COX physiology has revealed that NSAIDs cause gastric mucosal injury by inhibiting not only COX-1 but also COX-2 in the stomach. COX-1 inhibition alone has been demonstrated not to cause gastric mucosal injury. In addition, a selective COX-2 inhibitor which is demonstrated to have much less harmful effect in the stomach is now widely used as a safer NSAID in USA. Moreover, a selective COX-2 inhibitor is recently considered to have an inhibitory effect on growth of a certain type of cancers, thereby being in the spotlight as a chemopreventive agent.

摘要

非甾体抗炎药(NSAIDs)已被证明会引起胃肠道黏膜损伤这一副作用,偶尔还会导致诸如出血和穿孔等严重并发症。到目前为止,NSAIDs引起的黏膜损伤被认为是由于它们对环氧化酶-1(COX-1)活性的抑制作用,COX-1在胃中表达,并通过产生前列腺素E2对黏膜保护起着关键作用。然而,最近对COX生理学的认识进展表明,NSAIDs不仅通过抑制胃中的COX-1,还通过抑制COX-2来引起胃黏膜损伤。单独抑制COX-1已被证明不会导致胃黏膜损伤。此外,一种在胃中显示出危害小得多的选择性COX-2抑制剂,目前在美国作为一种更安全的NSAIDs被广泛使用。此外,最近有人认为选择性COX-2抑制剂对某种类型的癌症生长有抑制作用,因此作为一种化学预防剂受到关注。

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