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Flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers

BACKGROUND: Flavonoids are a class of plant and fungus secondary metabolites and are the most common group of polyphenolic compounds in the human diet. In recent studies, flavonoids have been shown to induce browning of white adipocytes, increase energy consumption, inhibit high-fat diet (HFD)-induc...

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Autores principales: Zhang, Xuejun, Li, Xin, Fang, Huang, Guo, Fengjin, Li, Feng, Chen, Anmin, Huang, Shilong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637576/
https://www.ncbi.nlm.nih.gov/pubmed/31346342
http://dx.doi.org/10.1186/s12986-019-0370-7
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author Zhang, Xuejun
Li, Xin
Fang, Huang
Guo, Fengjin
Li, Feng
Chen, Anmin
Huang, Shilong
author_facet Zhang, Xuejun
Li, Xin
Fang, Huang
Guo, Fengjin
Li, Feng
Chen, Anmin
Huang, Shilong
author_sort Zhang, Xuejun
collection PubMed
description BACKGROUND: Flavonoids are a class of plant and fungus secondary metabolites and are the most common group of polyphenolic compounds in the human diet. In recent studies, flavonoids have been shown to induce browning of white adipocytes, increase energy consumption, inhibit high-fat diet (HFD)-induced obesity and improve metabolic status. Promoting the activity of brown adipose tissue (BAT) and inducing white adipose tissue (WAT) browning are promising means to increase energy expenditure and improve glucose and lipid metabolism. This review summarizes recent advances in the knowledge of flavonoid compounds and their metabolites. METHODS: We searched the following databases for all research related to flavonoids and WAT browning published through March 2019: PubMed, MEDLINE, EMBASE, and the Web of Science. All included studies are summarized and listed in Table 1. RESULT: We summarized the effects of flavonoids on fat metabolism and the specific underlying mechanisms in sub-categories. Flavonoids activated the sympathetic nervous system (SNS), promoted the release of adrenaline and thyroid hormones to increase thermogenesis and induced WAT browning through the AMPK-PGC-1α/Sirt1 and PPAR signalling pathways. Flavonoids may also promote brown preadipocyte differentiation, inhibit apoptosis and produce inflammatory factors in BAT. CONCLUSION: Flavonoids induced WAT browning and activated BAT to increase energy consumption and non-shivering thermogenesis, thus inhibiting weight gain and preventing metabolic diseases.
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spelling pubmed-66375762019-07-25 Flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers Zhang, Xuejun Li, Xin Fang, Huang Guo, Fengjin Li, Feng Chen, Anmin Huang, Shilong Nutr Metab (Lond) Review BACKGROUND: Flavonoids are a class of plant and fungus secondary metabolites and are the most common group of polyphenolic compounds in the human diet. In recent studies, flavonoids have been shown to induce browning of white adipocytes, increase energy consumption, inhibit high-fat diet (HFD)-induced obesity and improve metabolic status. Promoting the activity of brown adipose tissue (BAT) and inducing white adipose tissue (WAT) browning are promising means to increase energy expenditure and improve glucose and lipid metabolism. This review summarizes recent advances in the knowledge of flavonoid compounds and their metabolites. METHODS: We searched the following databases for all research related to flavonoids and WAT browning published through March 2019: PubMed, MEDLINE, EMBASE, and the Web of Science. All included studies are summarized and listed in Table 1. RESULT: We summarized the effects of flavonoids on fat metabolism and the specific underlying mechanisms in sub-categories. Flavonoids activated the sympathetic nervous system (SNS), promoted the release of adrenaline and thyroid hormones to increase thermogenesis and induced WAT browning through the AMPK-PGC-1α/Sirt1 and PPAR signalling pathways. Flavonoids may also promote brown preadipocyte differentiation, inhibit apoptosis and produce inflammatory factors in BAT. CONCLUSION: Flavonoids induced WAT browning and activated BAT to increase energy consumption and non-shivering thermogenesis, thus inhibiting weight gain and preventing metabolic diseases. BioMed Central 2019-07-18 /pmc/articles/PMC6637576/ /pubmed/31346342 http://dx.doi.org/10.1186/s12986-019-0370-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Zhang, Xuejun
Li, Xin
Fang, Huang
Guo, Fengjin
Li, Feng
Chen, Anmin
Huang, Shilong
Flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers
title Flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers
title_full Flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers
title_fullStr Flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers
title_full_unstemmed Flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers
title_short Flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers
title_sort flavonoids as inducers of white adipose tissue browning and thermogenesis: signalling pathways and molecular triggers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637576/
https://www.ncbi.nlm.nih.gov/pubmed/31346342
http://dx.doi.org/10.1186/s12986-019-0370-7
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