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激活特定的肠道拟杆菌-叶酸-肝脏轴有益于缓解非酒精性肝脂肪变性。

Activation of a Specific Gut Bacteroides-Folate-Liver Axis Benefits for the Alleviation of Nonalcoholic Hepatic Steatosis.

作者信息

Qiao Shanshan, Bao Li, Wang Kai, Sun Shanshan, Liao Mingfang, Liu Chang, Zhou Nan, Ma Ke, Zhang Yuwei, Chen Yihua, Liu Shuang-Jiang, Liu Hongwei

机构信息

State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, No. 1 Beichenxi Road, Chaoyang District, Beijing 100101, P. R. China; Savaid Medical School, University of Chinese Academy of Sciences, Beijing 100049, P. R. China.

State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, No. 1 Beichenxi Road, Chaoyang District, Beijing 100101, P. R. China; School of Life Sciences, University of Science and Technology of China, No. 96 Jinzhai-Road, Hefei 230026, P. R. China.

出版信息

Cell Rep. 2020 Aug 11;32(6):108005. doi: 10.1016/j.celrep.2020.108005.

Abstract

A beneficial gut Bacteroides-folate-liver pathway regulating lipid metabolism is demonstrated. Oral administration of a Ganoderma meroterpene derivative (GMD) ameliorates nonalcoholic hepatic steatosis in the liver of fa/fa rats by reducing endotoxemia, enhancing lipid oxidation, decreasing de novo lipogenesis, and suppressing lipid export from the liver. An altered gut microbiota with an increase of butyrate and folate plays a causative role in the effects of GMD. The commensal bacteria Bacteroides xylanisolvens, Bacteroides thetaiotaomicron, Bacteroides dorei, and Bacteroides uniformis, which are enriched by GMD, are major contributors to the increased gut folate. Administration of live B. xylanisolvens reduces hepatic steatosis and enhances the folate-mediated signaling pathways in mice. Knockout of the folate biosynthetic folp gene in B. xylanisolvens blocks its folate production and beneficial effects. This work confirms the therapeutic potential of GMD and B. xylanisolvens in alleviating nonalcoholic hepatic steatosis and provides evidence for benefits of the gut Bacteroides-folate-liver pathway.

摘要

研究证实了一种有益的肠道拟杆菌-叶酸-肝脏途径可调节脂质代谢。口服灵芝杂萜衍生物(GMD)可通过降低内毒素血症、增强脂质氧化、减少从头脂肪生成以及抑制肝脏脂质输出,改善fa/fa大鼠肝脏中的非酒精性肝脂肪变性。肠道微生物群的改变以及丁酸和叶酸的增加在GMD的作用中起因果作用。GMD富集的共生细菌解木聚糖拟杆菌、多形拟杆菌、多雷拟杆菌和单形拟杆菌是肠道叶酸增加的主要贡献者。给小鼠施用活的解木聚糖拟杆菌可减轻肝脏脂肪变性并增强叶酸介导的信号通路。解木聚糖拟杆菌中叶酸生物合成folp基因的敲除会阻断其叶酸产生和有益作用。这项工作证实了GMD和解木聚糖拟杆菌在减轻非酒精性肝脂肪变性方面的治疗潜力,并为肠道拟杆菌-叶酸-肝脏途径的益处提供了证据。

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