新型非甾体抗炎药与胃十二指肠损伤。

G C Folco
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引用次数: 0

摘要

环氧合酶(COX)有两种异构体:COX-1是一种组成酶,在大多数组织中广泛表达;COX-2是一种诱导酶,在整个胃肠道中含量丰富。COX-2的表达可被炎症刺激局部诱导,并与局部前列腺素(PG)的产生一致。目前,非甾体类抗炎药(NSAIDs)广泛用于炎症性疾病的治疗;然而,由于抑制COX-1的显著副作用限制了它们的使用。COX-2抑制剂与非选择性非甾体抗炎药一样具有活性,可抑制炎症细胞中PG的合成。与其他非甾体抗炎药相比,选择性COX-2抑制剂不会引起胃溃疡或肠道溃疡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New NSAIDs and gastroduodenal damage.

Two isoforms of cyclooxygenase (COX) are described: COX-1 is a constitutive enzyme and is widely expressed in most tissues, COX-2 is an inducible enzyme and is abundant throughout the gastrointestinal tract. Expression of COX-2 can be induced locally by inflammatory stimuli and appears coincident with local prostaglandin (PG) production. Currently available non-steroidal antiinflammatory drugs (NSAIDs) are widely used for the treatment of inflammatory diseases; however, significant side-effects due to inhibition of COX-1 limit their use. Inhibitors of COX-2 are as active as non-selective NSAIDs and inhibit PG synthesis in inflammatory cells. In contrast to other NSAIDs, selective COX-2 inhibitors do not cause ulcers in the stomach or intestine.

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