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Effect of Saccharomyces cerevisiae strain UFMG A-905 in experimental model of inflammatory bowel disease

机译:酿酒酵母菌株UFMG A-905在炎症性肠病实验模型中的作用

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摘要

In the present study, the protective potential of Saccharomyces cerevisiae strain UFMG A-905 was evaluated in a murine model of acute ulcerative colitis (UC). Six groups of Balb/c mice were used: not treated with yeast and not challenged with dextran sulphate sodium (DSS) (control); treated with S. cerevisiae UFMG A-905 (905); treated with the non-probiotic S. cerevisiae W303 (W303); challenged with DSS (DSS); treated with S. cerevisiae UFMG A-905 and challenged with DSS (905 + DSS); and treated with S. cerevisiae W303 and challenged with DSS (W303 + DSS). Seven days after induction of UC, mice were euthanised to remove colon for enzymatic, immunological, and histopathological analysis. In vivo intestinal permeability was also evaluated. An improvement of clinical manifestations of experimental UC was observed only in mice of the 905 + DSS group when compared to animals from DSS and W303 + DSS groups. This observation was confirmed by histological and morphometrical data and determination of myeloperoxidase and eosinophil peroxidase activities, intestinal permeability and some pro-inflammatory cytokines. S. cerevisiae UFMG A-905 showed to be a potential alternative treatment for UC when used in an experimental animal model of the disease.
机译:在本研究中,在急性溃疡性结肠炎(UC)的鼠模型中评估了酿酒酵母菌株UFMG A-905的保护潜力。使用六组Balb / c小鼠:未用酵母处理且未用右旋糖酐硫酸钠(DSS)攻击(对照组);未用酵母处理。用啤酒酵母UFMG A-905(905)处理;用非益生啤酒酵母W303(W303)处理;挑战DSS(DSS);用啤酒酵母UFMG A-905处理并用DSS(905 + DSS)攻击;并用酿酒酵母W303处理,并用DSS(W303 + DSS)攻击。 UC诱导7天后,对小鼠实施安乐死以去除结肠,以进行酶学,免疫学和组织病理学分析。还评估了体内肠道通透性。与来自DSS和W303 + DSS组的动物相比,仅在905 + DSS组的小鼠中观察到实验性UC临床表现的改善。组织学和形态计量学数据以及髓过氧化物酶和嗜酸性粒细胞过氧化物酶活性,肠道通透性和某些促炎细胞因子的测定证实了这一观察结果。当用于该疾病的实验动物模型中时,酿酒酵母UFMG A-905被证明是一种潜在的UC替代疗法。

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