Naturally Occurring Stilbenoid TSG Reverses Non-Alcoholic Fatty Liver Diseases via Gut-Liver Axis
Identifieur interne : 000036 ( Main/Merge ); précédent : 000035; suivant : 000037Naturally Occurring Stilbenoid TSG Reverses Non-Alcoholic Fatty Liver Diseases via Gut-Liver Axis
Auteurs : Pei Lin ; Jianmei Lu ; Yanfang Wang ; Wen Gu ; Jie Yu ; Ronghua ZhaoSource :
- PLoS ONE [ 1932-6203 ] ; 2015.
Abstract
The gut-liver axis is largely involved in the development of non-alcoholic fatty liver disease (NAFLD). We investigated whether 2, 3, 5, 4′-tetrahydroxy-stilbene-2-
Url:
DOI: 10.1371/journal.pone.0140346
PubMed: 26474417
PubMed Central: 4608713
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PMC:4608713Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Naturally Occurring Stilbenoid TSG Reverses Non-Alcoholic Fatty Liver Diseases via Gut-Liver Axis</title>
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<author><name sortKey="Gu, Wen" sort="Gu, Wen" uniqKey="Gu W" first="Wen" last="Gu">Wen Gu</name>
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<author><name sortKey="Zhao, Ronghua" sort="Zhao, Ronghua" uniqKey="Zhao R" first="Ronghua" last="Zhao">Ronghua Zhao</name>
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<front><div type="abstract" xml:lang="en"><p>The gut-liver axis is largely involved in the development of non-alcoholic fatty liver disease (NAFLD). We investigated whether 2, 3, 5, 4′-tetrahydroxy-stilbene-2-<italic>O</italic>
-<italic>β</italic>
-<sc>D</sc>
-glucoside (TSG) could reverse NAFLD induced by a high-fat diet (HFD) and whether it did so via the gut-liver axis. Results showed that TSG could reduce the accumulation of FFA and it did so by reducing the expression of L-FABP and FATP4. TSG regulated gut microbiota balanced and increased the protein expression of ZO-1 and occludin, which could improve the function of the intestinal mucosal barrier and reduce serum LPS content by about 25%. TSG reduced TL4 levels by 56% and NF-κB expression by 23% relative to the NAFLD model group. This suggests that prevention of NAFLD by TSG in HFD-fed rats is mediated by modulation of the gut microbiota and TLR4/NF-κB pathway, which may alleviate chronic low-grade inflammation by reducing the exogenous antigen load on the host.</p>
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