| Literature DB >> 32783933 |
Shanshan Qiao1, Li Bao1, Kai Wang1, Shanshan Sun2, Mingfang Liao1, Chang Liu3, Nan Zhou3, Ke Ma1, Yuwei Zhang3, Yihua Chen3, Shuang-Jiang Liu4, Hongwei Liu5.
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.Entities:
Keywords: Bacteroides; Bacteroides xylanisolvens; a Ganoderma meroterpene derivative; a gut Bacteroides-folate-liver axis; folate; gut microbiota; nonalcoholic hepatic steatosis
Mesh:
Year: 2020 PMID: 32783933 DOI: 10.1016/j.celrep.2020.108005
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423