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

Ratnesh Kumar Singh, Nolan Wheildon, Seiichi Ishikawa
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引用次数: 58

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.

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食品添加剂P-80对小鼠肠道菌群的影响促进肠道炎症、肥胖和肝功能障碍
肥胖症的日益流行已成为全球最重要的公共卫生问题之一。在过去的几十年里,由于食物摄入的质量和数量的变化,人类微生物组的变化与肥胖和代谢综合征的发展有关。我们给小鼠灌胃给予聚山梨酯-80。研究人员使用生物发光成像技术对肝脏进行无创监测。对肝功能障碍进行肝酶测定,肝PAS染色,电镜观察肝线粒体。为了评估肠道炎症,我们采用ELISA和qPCR检测粪便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壁橱细菌。微生物群组成采用16S序列。与对照组小鼠相比,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、线粒体增大和胆囊增大。此外,实验组小鼠DCA水平升高,Muc2 RNA表达降低,肠上皮粘液厚度降低,肠道通透性增加。注射P-80的小鼠肠道细菌在黏液中更深,更靠近肠上皮,生物活性LPS、鞭毛蛋白和LCN2表达水平升高。该研究结果支持了乳化剂如聚山梨酸酯-80可能导致肥胖相关的肠道炎症、肝功能障碍进展和肠道微生物群改变的证据。
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