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环氧化酶在胃黏膜保护中的作用。

The role of cyclooxygenase in gastric mucosal protection.

作者信息

Gudis Katya, Sakamoto Choitsu

机构信息

Third Department of Internal Medicine, Nippon Medical School, 1-1-5, Sendagi, Bunkyo-ku, Tokyo 113-8603, Japan.

出版信息

Dig Dis Sci. 2005 Oct;50 Suppl 1:S16-23. doi: 10.1007/s10620-005-2802-7.

Abstract

COX-1 and COX-2 are two cyclooxygenase enzymes responsible for prostanoid production. COX-2 is expressed in inflammatory cells and fibroblasts of the gastric mucosa, and through the production of various growth factors including hepatocyte growth factor (HGF) and vascular endothelial growth factor (VEGF), plays a key role in the tissue repair process. Aspirin induces and acetylates COX-2 to produce 15-(R)-epi-lipoxinA4, an anti-inflammatory mediator thought to protect the gastric mucosa against aspirin-induced injury. Recently, three different PGE synthases have been identified, that convert COX-2 metabolites into PGE2. mPGE synthase (mPGES)-1 has been shown to be inducible, and to colocalize with COX-2 in fibroblasts and macrophages infiltrating the gastric ulcer bed. cPGES and mPGES-2 have been found expressed in normal gastric mucosa, with no change in expression levels seen in gastritis or gastric ulcer tissue. Finally, this review discusses the role of these enzymes in the pathophysiology of the gastric mucosa, as well as the biologcal significance of their inhibition.

摘要

COX-1和COX-2是两种负责前列腺素生成的环氧化酶。COX-2在胃黏膜的炎症细胞和成纤维细胞中表达,并通过产生包括肝细胞生长因子(HGF)和血管内皮生长因子(VEGF)在内的多种生长因子,在组织修复过程中发挥关键作用。阿司匹林诱导并使COX-2乙酰化,生成15-(R)-表-脂氧素A4,这是一种抗炎介质,被认为可保护胃黏膜免受阿司匹林诱导的损伤。最近,已鉴定出三种不同的前列腺素E合酶,它们将COX-2代谢产物转化为前列腺素E2。微粒体前列腺素E合酶(mPGES)-1已被证明是可诱导的,并与COX-2在浸润胃溃疡床的成纤维细胞和巨噬细胞中共定位。胞质前列腺素E合酶(cPGES)和mPGES-2已在正常胃黏膜中发现表达,在胃炎或胃溃疡组织中未见表达水平变化。最后,本综述讨论了这些酶在胃黏膜病理生理学中的作用,以及其抑制的生物学意义。

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