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首页> 外文期刊>Digestive Diseases and Sciences >CV-11974, angiotensin II type I receptor antagonist, reduces the severity of indomethacin-induced rat enteritis
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CV-11974, angiotensin II type I receptor antagonist, reduces the severity of indomethacin-induced rat enteritis

机译:CV-11974,血管紧张素II型I受体拮抗剂,可减轻消炎痛诱导的大鼠肠炎的严重性

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The aim of the present study was to examine the effect of angiotensin II type I receptor antagonist, CV-11974, on indomethacin-induced small intestinal injury in rats. Single administration of indomethacin provoked severe inflammatory lesions in the small intestine. The levels of thiobarbituric acid-reactive substances (TBARS), myeloperoxidase (MPO) activities and cytokine-induced neutrophil chemoattractant-1 (CINC-1) in the intestinal mucosa significantly increased in the indomethacin-treated group compared with the sham group. In addition, the angiotensin II type I receptor was increased in the small intestine after the administration of indomethacin. The development of intestinal lesions in response to indomethacin was prevented by pretreatment with CV-11974 together with significant suppression of the increased level of TBARS, MPO activities and CINC-1. These results indicate that CV-11974 protected against the small intestinal damage elicited by indomethacin, which suggests that angiotensin II/AT1 receptor interaction is involved in the pathogenesis of the intestinal inflammation associated with oxidative stress.
机译:本研究的目的是研究血管紧张素II型I受体拮抗剂CV-11974对消炎痛诱导的大鼠小肠损伤的作用。消炎痛的单次给药会引起小肠严重炎症性病变。与假手术组相比,在吲哚美辛治疗组的肠粘膜中硫代巴比妥酸反应性物质(TBARS),髓过氧化物酶(MPO)活性和细胞因子诱导的中性粒细胞趋化因子1(CINC-1)的水平显着增加。另外,消炎痛给药后小肠中的I型血管紧张素II受体增加。通过用CV-11974预处理以及显着抑制TBARS,MPO活性和CINC-1升高的水平,可以预防响应吲哚美辛的肠部病变的发展。这些结果表明,CV-11974可以抵抗吲哚美辛引起的小肠损害,这表明血管紧张素II / AT1受体的相互作用与氧化应激相关的肠道炎症的发病机制有关。

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