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Lansoprazole ameliorates intestinal mucosal damage induced by ischemia-reperfusion in rats

机译:兰索拉唑改善大鼠缺血再灌注引起的肠粘膜损伤

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AIM: To investigate the protective effect of lansoprazole on ischemia and reperfusion (I/R)-induced rat intestinal mucosal injury in vivo. METHODS: Intestinal damage was induced by clamping both the superior mesenteric artery and the celiac trunk for 30 min followed by reperfusion in male Sprague-Dawley rats. Lansoprazole was given to rats intra peritoneally 1 h before vascular clamping. RESULTS: Both the intraluminal hemoglobin and protein levels, as indices of mucosal damage, significantly increased in I/R-groups comparion with those of sham-operation groups. These increases in intraluminal hemoglobin and protein levels were significantly inhibited by the treatment with lansoprazole at a dose of 1 mg/kg. Small intestine exposed to I/R resulted in mucosal inflammation that was characterized by significant increases in thiobarbituric acid-reactive substances (TBARS), tissue-associated myeloperoxidase activity (MPO), and mucosal content of rat -cytokine-induced neutrophil chemoattractant-1 (CINC-1). These increases in TBARS, MPO activities and CINC-1 content in the intestinal mucosa after I/R were all inhibited by pretreatment with lansoprazole at a dose of 1 mg/kg. Furthermore, the CINC-1 mRNA expression was increased during intestinal I/R, and this increase in mRNA expression was inhibited by treatment with lansoprazole. CONCLUSION: Lansoprazole inhibits lipid peroxidation and reduces development of intestinal mucosal inflammation induced by I/R in rats, suggesting that lansoprazole may have a therapeutic potential for I/R injury.
机译:目的:探讨兰索拉唑对体内缺血再灌注(I / R)大鼠肠粘膜损伤的保护作用。方法:通过将肠系膜上动脉和腹腔干线夹住30分钟,然后再灌注雄性Sprague-Dawley大鼠,引起肠损伤。兰索拉唑在血管钳夹前1 h腹膜内给予大鼠。结果:与假手术组相比,I / R组的腔内血红蛋白和蛋白质水平(作为粘膜损伤的指标)均显着增加。管腔内血红蛋白和蛋白质水平的这些增加被兰索拉唑以1 mg / kg的剂量治疗显着抑制。暴露于I / R的小肠导致粘膜炎症,其特征是硫代巴比妥酸反应性物质(TBARS),组织相关的髓过氧化物酶活性(MPO)显着增加以及大鼠细胞因子诱导的中性白细胞趋化因子1( CINC-1)。 I / R后肠粘膜中TBARS,MPO活性和CINC-1含量的这些增加都通过用1 mg / kg的兰索拉唑预处理来抑制。此外,在肠I / R期间CINC-1 mRNA表达增加,而用兰索拉唑治疗抑制了mRNA表达的这种增加。结论:兰索拉唑可抑制脂质过氧化作用并减少I / R诱导的大鼠肠粘膜炎症的发展,提示Lansoprazole可能具有I / R损伤的治疗潜力。

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