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食品添加剂P-80影响小鼠肠道微生物群,促进肠道炎症、肥胖和肝功能障碍。

Food Additive P-80 Impacts Mouse Gut Microbiota Promoting Intestinal Inflammation, Obesity and Liver Dysfunction.

作者信息

Singh Ratnesh Kumar, Wheildon Nolan, Ishikawa Seiichi

机构信息

Janelia Research Campus, Howard Hughes Medical Institute.

Human Health and Nutritional Sciences, University of Guelph, ON, Canada.

出版信息

SOJ Microbiol Infect Dis. 2016;4(1). doi: 10.15226/sojmid/4/1/00148. Epub 2016 Jun 1.

Abstract

The increasing prevalence of obesity has emerged as one of the most important global public health issue. The change to the human microbiome as a result of changes in the quality and quantity of food intake over the past several decades has been implicated in the development of obesity and metabolic syndrome. We administered polysorbate-80 to mice via gavage. The researchers monitor liver noninvasively using a bioluminescence imaging. For the liver dysfunction we measure the liver enzymes and PAS stain on liver, electron microscopy liver mitochondria. For the assessment of intestinal inflammation we measured fecal LCN2, LPS, MPO and flagellin by ELISA and qPCR. We use confocal microscopy to detect closet bacteria near the epithelium. 16S sequence was used for the composition of microbiota. Compared with control mice, those receiving emulsifier, showed impaired glycemic tolerance, hyperinsulinemia, altered liver enzymes, larger mitochondria and increased gall bladder size. Additionally, mice in the experimental group showed higher levels of DCA, reduced Muc2 RNA expression, reduced mucus thickness in the intestinal epithelium and increased gut permeability. Intestinal bacteria of mice receiving P-80 were found deeper in the mucus and closer to the intestinal epithelium and had increased level of bioactive LPS, flagellin and LCN2 expression. The result of the study are supportive of evidence that emulsifier agents such as polysorbate-80, may be contributing to obesity related intestinal inflammation and progression of liver dysfunction and alternation of gut microbiota.

摘要

肥胖患病率的不断上升已成为全球最重要的公共卫生问题之一。过去几十年间,食物摄入的质量和数量发生变化,导致人类微生物群改变,这与肥胖和代谢综合征的发展有关。我们通过灌胃给小鼠施用聚山梨醇酯-80。研究人员使用生物发光成像对肝脏进行非侵入性监测。对于肝功能障碍,我们测量肝酶并对肝脏进行PAS染色、对肝线粒体进行电子显微镜检查。为了评估肠道炎症,我们通过ELISA和qPCR测量粪便中的LCN2、LPS、MPO和鞭毛蛋白。我们使用共聚焦显微镜检测上皮附近的紧密细菌。16S序列用于分析微生物群的组成。与对照小鼠相比,接受乳化剂的小鼠表现出糖耐量受损、高胰岛素血症、肝酶改变、线粒体更大以及胆囊增大。此外,实验组小鼠的脱氧胆酸水平更高,Muc2 RNA表达降低,肠上皮黏液厚度减小,肠道通透性增加。接受聚山梨醇酯-80的小鼠肠道细菌在黏液中更深且更靠近肠上皮,生物活性LPS、鞭毛蛋白和LCN2表达水平升高。该研究结果支持以下证据:聚山梨醇酯-80等乳化剂可能导致与肥胖相关的肠道炎症、肝功能障碍进展以及肠道微生物群改变。

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