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首页> 外文期刊>Gastroenterology research and practice >Influence of Rosiglitazone on the Expression of PPARγ, NF-κB, and TNF-αin Rat Model of Ulcerative Colitis
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Influence of Rosiglitazone on the Expression of PPARγ, NF-κB, and TNF-αin Rat Model of Ulcerative Colitis

机译:罗格列酮对溃疡性结肠炎大鼠模型中PPARγ,NF-κB和TNF-α表达的影响

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Aim. To observe the disease activity index (DAI) and the colonic mucosa damage index (CMDI), detect the colonic mucosal expression of PPARγ, NF-κB, and TNF-αin rats with ulcerative colitis (UC), and to investigate the protective role of rosiglitazone in UC.Methods. Sprague-Dawley (SD) rats were divided into three groups: a control group, a rosiglitazone treatment group, and a UC model group. Rats were sacrificed on days 7, 14, 21, or 35 following administration of treatment after enema and DAI, CMDI and colonic expression of PPARγ, NF-κB, and TNF-αwere assessed.Results. In the UC model group, DAI, CDMI and the colonic expression of NF-κB and TNF-αincreased significantly compared to the control group at all timepoints, but PPARγdecreased significantly. Furthermore, in the rosiglitazone treatment group, DAI and CMDI decreased significantly on the 14-day, 21-day, and 35-day timepoints compared to the UC model group; the colonic expression of NF-κB and TNF-αdecreased compared to UC model group at all timepoints, but the PPARγexpression increased significantly.Conclusions. Rosiglitazone can alleviate colonic mucosal inflammation and have the protective role on UC by upregulating PPARγexpression and downregulating NF-κB and TNF-αexpression.
机译:目标。观察溃疡性结肠炎(UC)大鼠的疾病活动指数(DAI)和结肠黏膜损伤指数(CMDI),检测PPARγ,NF-κB和TNF-α的结肠黏膜表达,并研究其的保护作用。罗格列酮在UC.Methods。将Sprague-Dawley(SD)大鼠分为三组:对照组,罗格列酮治疗组和UC模型组。在灌肠和DAI,CMDI以及PPARγ,NF-κB和TNF-α的结肠表达后的治疗后第7、14、21或35天处死大鼠。在UC模型组中,与对照组相比,DAI,CDMI和结肠中NF-κB和TNF-α的表达在所有时间点均显着增加,但PPARγ显着降低。此外,在罗格列酮治疗组中,与UC模型组相比,DAI和CMDI在第14天,21天和35天的时间点显着下降。在所有时间点,NF-κB和TNF-α的结肠表达均较UC模型组降低,但PPARγ的表达明显增加。罗格列酮可通过上调PPARγ的表达,下调NF-κB和TNF-α的表达来减轻结肠黏膜炎症,对UC具有保护作用。

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