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二甲双胍可减轻非酒精性脂肪性肝病的发生,并影响肠道微生物群和小肠屏障。

Metformin attenuates the onset of non-alcoholic fatty liver disease and affects intestinal microbiota and barrier in small intestine.

机构信息

Department of Nutritional Sciences, R.F. Molecular Nutritional Science, University of Vienna, 1090, Vienna, Austria.

Institute of Animal Science, University of Hohenheim, 70599, Stuttgart, Germany.

出版信息

Sci Rep. 2019 Apr 30;9(1):6668. doi: 10.1038/s41598-019-43228-0.

DOI:10.1038/s41598-019-43228-0
PMID:31040374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6491483/
Abstract

The antidiabetic drug metformin has been proposed to affect non-alcoholic fatty liver disease (NAFLD) through its effects on intestinal microbiota and barrier function. However, so far most studies focused on long-term effects and more progressed disease stages. The aim of this study was to assess in two experimental settings, if the onset of NAFLD is associated with changes of intestinal microbiota and barrier function and to determine effects of metformin herein. C57Bl/6J mice were fed a liquid control diet (C) or fat-, fructose- and cholesterol-rich diet (FFC) for four days or six weeks ±300 mg/kg BW/day metformin (Met). Markers of liver health, intestinal barrier function and microbiota composition were assessed. Metformin treatment markedly attenuated FFC-induced NAFLD in both experiments with markers of inflammation and lipidperoxidation in livers of FFC + Met-fed mice being almost at the level of controls. Metformin treatment attenuated the loss of tight junction proteins in small intestine and the increase of bacterial endotoxin levels in portal plasma. Changes of intestinal microbiota found in FFC-fed mice were also significantly blunted in FFC + Met-fed mice. Taken together, protective effects of metformin on the onset of NAFLD are associated with changes of intestinal microbiota composition and lower translocation of bacterial endotoxins.

摘要

二甲双胍作为一种抗糖尿病药物,据其对肠道微生物群和屏障功能的影响,被认为可以治疗非酒精性脂肪性肝病(NAFLD)。然而,到目前为止,大多数研究都集中在长期影响和更严重的疾病阶段。本研究旨在通过两种实验设置来评估:NAFLD 的发生是否与肠道微生物群和屏障功能的变化有关,并确定二甲双胍在此过程中的作用。C57Bl/6J 小鼠在食用液体对照饮食(C)或高脂肪、高果糖和高胆固醇饮食(FFC)四天或六周的同时,分别接受 300mg/kg BW/天的二甲双胍(Met)或不接受药物治疗。评估肝脏健康、肠道屏障功能和微生物群组成的标志物。在这两项实验中,二甲双胍治疗明显减轻了 FFC 诱导的 NAFLD,FFC+Met 喂养的小鼠肝脏的炎症和脂质过氧化标志物几乎与对照组水平相当。二甲双胍治疗还减轻了小肠紧密连接蛋白的丢失和门脉血浆中细菌内毒素水平的升高。FFC 喂养小鼠肠道微生物群的变化在 FFC+Met 喂养的小鼠中也明显减弱。总之,二甲双胍对 NAFLD 发病的保护作用与肠道微生物群组成的变化和细菌内毒素易位的减少有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/9f955ab5d804/41598_2019_43228_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/751f29a85c83/41598_2019_43228_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/e585951dd1c3/41598_2019_43228_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/8994f7ec5f68/41598_2019_43228_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/9f955ab5d804/41598_2019_43228_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/751f29a85c83/41598_2019_43228_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/e585951dd1c3/41598_2019_43228_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/8994f7ec5f68/41598_2019_43228_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/6491483/9f955ab5d804/41598_2019_43228_Fig4_HTML.jpg

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