首页> 外文期刊>Experimental and therapeutic medicine >Berberine alleviates dextran sodium sulfate-induced colitis by improving intestinal barrier function and reducing inflammation and oxidative stress
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Berberine alleviates dextran sodium sulfate-induced colitis by improving intestinal barrier function and reducing inflammation and oxidative stress

机译:小檗碱通过改善肠道阻隔功能并降低炎症和氧化应激来减轻葡聚糖硫酸钠诱导的结肠炎

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摘要

Berberine has demonstrated efficacy in alleviating experimental colitis in vivo and in vitro. However, the anti-colitis mechanisms of berberine that enable it to promote intestinal barrier function in vivo remain unclear. The present study aimed to evaluate the effect of berberine on intestinal epithelial barrier function, expression of tight junction proteins and the levels of inflammatory and oxidative stress factors in the intestinal mucosa of dextran sulfate sodium (DSS)-induced colitis mice. Berberine (100 mg/kg) was administered for five days to mice with established colitis, induced by administration of DSS (3% w/v) for six days. Intestinal barrier function and the presence of proinflammatory factors, oxidative stress and active signaling pathways in the colon were determined principally by western blotting and reverse transcription-quantitative polymerase chain reaction. It was observed that berberine reduced weight loss, shortening of the colon and colon damage in DSS-colitis mice. In addition, berberine significantly inhibited the increase of fluorescein isothiocyanate-dextran in serum and the decrease of zonula occluden-1 (also known as tight junction protein-1), occludin and epithelial cadherin expression in colonic tissue, relative to a DSS-treated control group. Berberine also significantly inhibited the expression of interleukin (IL)-1 beta, IL-6 and tumor necrosis factor-a mRNA and phosphorylation of signal transducer and activator of transcription 3. Furthermore, berberine reduced the levels of myeloperoxidase and increased the levels of superoxide dismutase and catalase in colon and serum samples relative to the control group. The expression of cluster of differentiation 68 in the colon of colitis mice was also reduced by berberine. Collectively, these data suggest that berberine alleviates colitis principally by improving intestinal barrier function and promoting anti-inflammatory and antioxidative stress responses. In turn these effects inhibit macrophage infiltration into the colon and thus may be central to the anti-colitis activity of berberine.
机译:小檗碱在减轻体内和体外缓解实验性结肠炎的疗效表明了疗效。然而,使其能够在体内促进肠道屏障功能的小檗碱的抗结肠炎机制仍不清楚。本研究旨在评估小檗碱对肠上皮屏障功能,紧密结蛋白表达的影响,葡萄糖粘膜粘膜粘膜粘膜粘膜粘膜粘膜中的炎症和氧化应激因子水平。将小檗碱(100mg / kg)施用5天,致小鼠与已建立的结肠炎,通过施用DSS(3%w / v)致六天。肠道屏障功能和促炎因子的存在,主要通过蛋白质印迹和逆转录定量聚合酶链反应来确定结肠中的氧化应激和活性信号传导途径。观察到,小檗碱减轻了减重,结肠缩短和DSS-结肠炎小鼠的结肠损伤。此外,小檗碱显着抑制血清中荧光素异硫氰酸酯 - 葡聚糖的增加和Zonula occluden-1(也称为紧密结蛋白-1),occludin和上皮钙粘蛋白在结肠组织中的表达,相对于DSS处理的对照团体。 Berberine也显着抑制了白细胞介素(IL)-1β,IL-6和肿瘤坏死因子的表达 - 信号传感器和转录激活剂的mRNA和磷酸化3.此外,小檗碱降低了髓过氧化物酶的水平并增加了超氧化物的水平结肠和血清样品中的歧化酶和过氧化氢酶相对于对照组。小檗碱还减少了结肠炎小鼠结肠癌中分化68的表达。总的来说,这些数据表明,小檗碱主要通过改善肠道阻隔功能并促进抗炎和抗氧化应激反应来减轻结肠炎。反过来,这些效果抑制巨噬细胞浸润到结肠中,因此可能是小檗碱的抗结肠炎活性的核心。

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