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Apigenin Alleviates Obesity-Associated Metabolic Syndrome by Regulating the Composition of the Gut Microbiome

The gut microbiota, often viewed as a “digestive organ,” can influence the development of obesity and related metabolic disorders. Diet is significantly important in shaping the structure and modulating the function of the gut microbiota. Apigenin (Api) widely exists in fruits and vegetables as a na...

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Autores principales: Qiao, Yuan, Zhang, Zhichun, Zhai, Yuanyuan, Yan, Xu, Zhou, Wenling, Liu, Hao, Guan, Lingling, Peng, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762173/
https://www.ncbi.nlm.nih.gov/pubmed/35046924
http://dx.doi.org/10.3389/fmicb.2021.805827
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author Qiao, Yuan
Zhang, Zhichun
Zhai, Yuanyuan
Yan, Xu
Zhou, Wenling
Liu, Hao
Guan, Lingling
Peng, Liang
author_facet Qiao, Yuan
Zhang, Zhichun
Zhai, Yuanyuan
Yan, Xu
Zhou, Wenling
Liu, Hao
Guan, Lingling
Peng, Liang
author_sort Qiao, Yuan
collection PubMed
description The gut microbiota, often viewed as a “digestive organ,” can influence the development of obesity and related metabolic disorders. Diet is significantly important in shaping the structure and modulating the function of the gut microbiota. Apigenin (Api) widely exists in fruits and vegetables as a naturally occurring flavonoid and has anti-obesogenic, anti-inflammatory, and anti-carcinogenic properties. Its low bioavailability means it has enough time to interact with the intestine thus becomes a potential substrate for the gut intestine; thus, contributing to gut health. Here, we show that Api reduces whole-body weight, low-grade inflammation, and insulin resistance in high-fat diet (HFD)-induced obese mice. Our results reflect that Api supplementation can substantially improve intestinal dysbiosis triggered by HFD and restores gut barrier damage by alleviating metabolic endotoxemia. Augmentation of Akkermansia and Incertae_Sedis along with reduction of Faecalibaculum and Dubosiella at the genus level potentially mediated the protective effects of Api on metabolic syndrome. Furthermore, we show that the impact of Api on the reduction of body weight and the modification of gut microbiota could be transferred from Api-administered mice to HFD-feeding mice via horizontal fecal microbiota transplantation. Taken together, our data highlight the prebiotic role of Api and show its contribution to the restraint of gut dysbiosis and metabolic deterioration associated with obesity in mice.
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spelling pubmed-87621732022-01-18 Apigenin Alleviates Obesity-Associated Metabolic Syndrome by Regulating the Composition of the Gut Microbiome Qiao, Yuan Zhang, Zhichun Zhai, Yuanyuan Yan, Xu Zhou, Wenling Liu, Hao Guan, Lingling Peng, Liang Front Microbiol Microbiology The gut microbiota, often viewed as a “digestive organ,” can influence the development of obesity and related metabolic disorders. Diet is significantly important in shaping the structure and modulating the function of the gut microbiota. Apigenin (Api) widely exists in fruits and vegetables as a naturally occurring flavonoid and has anti-obesogenic, anti-inflammatory, and anti-carcinogenic properties. Its low bioavailability means it has enough time to interact with the intestine thus becomes a potential substrate for the gut intestine; thus, contributing to gut health. Here, we show that Api reduces whole-body weight, low-grade inflammation, and insulin resistance in high-fat diet (HFD)-induced obese mice. Our results reflect that Api supplementation can substantially improve intestinal dysbiosis triggered by HFD and restores gut barrier damage by alleviating metabolic endotoxemia. Augmentation of Akkermansia and Incertae_Sedis along with reduction of Faecalibaculum and Dubosiella at the genus level potentially mediated the protective effects of Api on metabolic syndrome. Furthermore, we show that the impact of Api on the reduction of body weight and the modification of gut microbiota could be transferred from Api-administered mice to HFD-feeding mice via horizontal fecal microbiota transplantation. Taken together, our data highlight the prebiotic role of Api and show its contribution to the restraint of gut dysbiosis and metabolic deterioration associated with obesity in mice. Frontiers Media S.A. 2022-01-03 /pmc/articles/PMC8762173/ /pubmed/35046924 http://dx.doi.org/10.3389/fmicb.2021.805827 Text en Copyright © 2022 Qiao, Zhang, Zhai, Yan, Zhou, Liu, Guan and Peng. https://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
Qiao, Yuan
Zhang, Zhichun
Zhai, Yuanyuan
Yan, Xu
Zhou, Wenling
Liu, Hao
Guan, Lingling
Peng, Liang
Apigenin Alleviates Obesity-Associated Metabolic Syndrome by Regulating the Composition of the Gut Microbiome
title Apigenin Alleviates Obesity-Associated Metabolic Syndrome by Regulating the Composition of the Gut Microbiome
title_full Apigenin Alleviates Obesity-Associated Metabolic Syndrome by Regulating the Composition of the Gut Microbiome
title_fullStr Apigenin Alleviates Obesity-Associated Metabolic Syndrome by Regulating the Composition of the Gut Microbiome
title_full_unstemmed Apigenin Alleviates Obesity-Associated Metabolic Syndrome by Regulating the Composition of the Gut Microbiome
title_short Apigenin Alleviates Obesity-Associated Metabolic Syndrome by Regulating the Composition of the Gut Microbiome
title_sort apigenin alleviates obesity-associated metabolic syndrome by regulating the composition of the gut microbiome
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762173/
https://www.ncbi.nlm.nih.gov/pubmed/35046924
http://dx.doi.org/10.3389/fmicb.2021.805827
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