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Resveratrol Improves Liver Steatosis and Insulin Resistance in Non-alcoholic Fatty Liver Disease in Association With the Gut Microbiota

Resveratrol (RSV) is a potential alternative therapy for non-alcoholic fatty liver disease (NAFLD) that has been evaluated in many clinical trials, but the mechanisms of RSV action have not been fully elucidated. Recent studies suggested that the gut microbiota is an important RSV target; therefore,...

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Autores principales: Du, Fan, Huang, Rongfeng, Lin, Dan, Wang, Yuying, Yang, Xiaohuang, Huang, Xiaoyun, Zheng, Biyun, Chen, Zhixin, Huang, Yuehong, Wang, Xiaozhong, Chen, Fenglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942199/
https://www.ncbi.nlm.nih.gov/pubmed/33708180
http://dx.doi.org/10.3389/fmicb.2021.611323
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author Du, Fan
Huang, Rongfeng
Lin, Dan
Wang, Yuying
Yang, Xiaohuang
Huang, Xiaoyun
Zheng, Biyun
Chen, Zhixin
Huang, Yuehong
Wang, Xiaozhong
Chen, Fenglin
author_facet Du, Fan
Huang, Rongfeng
Lin, Dan
Wang, Yuying
Yang, Xiaohuang
Huang, Xiaoyun
Zheng, Biyun
Chen, Zhixin
Huang, Yuehong
Wang, Xiaozhong
Chen, Fenglin
author_sort Du, Fan
collection PubMed
description Resveratrol (RSV) is a potential alternative therapy for non-alcoholic fatty liver disease (NAFLD) that has been evaluated in many clinical trials, but the mechanisms of RSV action have not been fully elucidated. Recent studies suggested that the gut microbiota is an important RSV target; therefore, we speculated that the gut microbiota might mediate the beneficial effects of RSV in NAFLD. To verify this hypothesis, we established a high-fat diet (HFD)-induced NAFLD mouse model, which was subjected to RSV gavage to evaluate the therapeutic effects. We observed that RSV reduced liver steatosis and insulin resistance in NAFLD. RSV significantly changed the diversity and composition of the gut microbiota according to 16S rRNA sequencing. Gut microbiota gene function prediction showed that the enrichment of pathways related to lipid and glucose metabolism decreased after RSV treatment. Furthermore, correlation analysis indicated that the improvements in NAFLD metabolic indicators were closely related to the altered gut microbiota. We further fermented RSV with the gut microbiota in vitro to verify that RSV directly affected the gut microbiota. Our data suggested that the gut microbiota might be an important target through which RSV exerts its anti-NAFLD effect.
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spelling pubmed-79421992021-03-10 Resveratrol Improves Liver Steatosis and Insulin Resistance in Non-alcoholic Fatty Liver Disease in Association With the Gut Microbiota Du, Fan Huang, Rongfeng Lin, Dan Wang, Yuying Yang, Xiaohuang Huang, Xiaoyun Zheng, Biyun Chen, Zhixin Huang, Yuehong Wang, Xiaozhong Chen, Fenglin Front Microbiol Microbiology Resveratrol (RSV) is a potential alternative therapy for non-alcoholic fatty liver disease (NAFLD) that has been evaluated in many clinical trials, but the mechanisms of RSV action have not been fully elucidated. Recent studies suggested that the gut microbiota is an important RSV target; therefore, we speculated that the gut microbiota might mediate the beneficial effects of RSV in NAFLD. To verify this hypothesis, we established a high-fat diet (HFD)-induced NAFLD mouse model, which was subjected to RSV gavage to evaluate the therapeutic effects. We observed that RSV reduced liver steatosis and insulin resistance in NAFLD. RSV significantly changed the diversity and composition of the gut microbiota according to 16S rRNA sequencing. Gut microbiota gene function prediction showed that the enrichment of pathways related to lipid and glucose metabolism decreased after RSV treatment. Furthermore, correlation analysis indicated that the improvements in NAFLD metabolic indicators were closely related to the altered gut microbiota. We further fermented RSV with the gut microbiota in vitro to verify that RSV directly affected the gut microbiota. Our data suggested that the gut microbiota might be an important target through which RSV exerts its anti-NAFLD effect. Frontiers Media S.A. 2021-02-23 /pmc/articles/PMC7942199/ /pubmed/33708180 http://dx.doi.org/10.3389/fmicb.2021.611323 Text en Copyright © 2021 Du, Huang, Lin, Wang, Yang, Huang, Zheng, Chen, Huang, Wang and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Du, Fan
Huang, Rongfeng
Lin, Dan
Wang, Yuying
Yang, Xiaohuang
Huang, Xiaoyun
Zheng, Biyun
Chen, Zhixin
Huang, Yuehong
Wang, Xiaozhong
Chen, Fenglin
Resveratrol Improves Liver Steatosis and Insulin Resistance in Non-alcoholic Fatty Liver Disease in Association With the Gut Microbiota
title Resveratrol Improves Liver Steatosis and Insulin Resistance in Non-alcoholic Fatty Liver Disease in Association With the Gut Microbiota
title_full Resveratrol Improves Liver Steatosis and Insulin Resistance in Non-alcoholic Fatty Liver Disease in Association With the Gut Microbiota
title_fullStr Resveratrol Improves Liver Steatosis and Insulin Resistance in Non-alcoholic Fatty Liver Disease in Association With the Gut Microbiota
title_full_unstemmed Resveratrol Improves Liver Steatosis and Insulin Resistance in Non-alcoholic Fatty Liver Disease in Association With the Gut Microbiota
title_short Resveratrol Improves Liver Steatosis and Insulin Resistance in Non-alcoholic Fatty Liver Disease in Association With the Gut Microbiota
title_sort resveratrol improves liver steatosis and insulin resistance in non-alcoholic fatty liver disease in association with the gut microbiota
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942199/
https://www.ncbi.nlm.nih.gov/pubmed/33708180
http://dx.doi.org/10.3389/fmicb.2021.611323
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