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氧化应激和抗氧化防御在克罗恩病中的概念。

Concepts of oxidative stress and antioxidant defense in Crohn's disease.

机构信息

Mohammed A Alzoghaibi, Department of Physiology, College of Medicine, King Saud University, Riyadh 11461, Saudi Arabia.

出版信息

World J Gastroenterol. 2013 Oct 21;19(39):6540-7. doi: 10.3748/wjg.v19.i39.6540.

Abstract

Oxygen free radical and lipid peroxides (oxidative stress) are highly reactive and represent very damaging compounds. Oxidative stress could be a major contributing factor to the tissue injury and fibrosis that characterize Crohn's disease. An imbalance between increased reactive oxygen species levels and decreased antioxidant defenses occurs in Crohn's patients. Decreased blood levels of vitamins C and E and decreased intestinal mucosal levels of CuZn superoxide dismutase, glutathione, vitamin A, C, E, and β-carotene have been reported for Crohn's patients. Increased levels of proinflammatory cytokines, such as interleukin-1 and -8 and tumor necrosis factor, have been detected in inflammatory bowel disease. Oxidative stress significantly increased the production of neutrophils, chemokines, and interleukin-8. These effects were inhibited by antioxidant vitamins and arachidonic acid metabolite inhibitors in human intestinal smooth muscle cells isolated from the bowels of Crohn's disease patients. The main pathological feature of Crohn's disease is an infiltration of polymorphonuclear neutrophils and mononuclear cells into the affected part of the intestine. Activated neutrophils produce noxious substances that cause inflammation and tissue injury. Due to the physiological and biochemical actions of reactive oxygen species and lipid peroxides, many of the clinical and pathophysiological features of Crohn's disease might be explained by an imbalance of increased reactive oxygen species and a net decrease of antioxidant molecules. This review describes the general concepts of free radical, lipid peroxide and antioxidant activities and eventually illustrates their interferences in the development of Crohn's strictures.

摘要

氧自由基和脂质过氧化物(氧化应激)具有高度反应性,是非常有害的化合物。氧化应激可能是导致克罗恩病特征性组织损伤和纤维化的主要因素。在克罗恩病患者中,活性氧水平增加和抗氧化防御能力下降之间存在不平衡。据报道,克罗恩病患者的血液维生素 C 和 E 水平降低,肠黏膜铜锌超氧化物歧化酶、谷胱甘肽、维生素 A、C、E 和β-胡萝卜素水平降低。在炎症性肠病中,检测到促炎细胞因子如白细胞介素-1 和 -8 和肿瘤坏死因子水平升高。氧化应激显著增加中性粒细胞、趋化因子和白细胞介素-8 的产生。这些作用在克罗恩病患者肠道分离的人肠平滑肌细胞中被抗氧化维生素和花生四烯酸代谢物抑制剂抑制。克罗恩病的主要病理特征是多形核白细胞和单核细胞浸润肠道受影响的部位。活化的中性粒细胞产生有害物质,引起炎症和组织损伤。由于活性氧和脂质过氧化物的生理生化作用,许多克罗恩病的临床和病理生理特征可能可以通过活性氧增加和抗氧化分子净减少的不平衡来解释。本文综述了自由基、脂质过氧化物和抗氧化活性的一般概念,并最终说明了它们在克罗恩病狭窄发展中的相互干扰。

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