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Tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating COX-2 and iNOS expression in high fat-fed dogs

BACKGROUND: Tea polyphenols (TPs) attenuate obesity related liver inflammation; however, the anti-obesity effects and anti-inflammatory mechanisms are not clearly understood. This study aimed to determine whether the anti-obesity and anti-inflammatory TPs mechanisms associated with cyclooxygenase-2...

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Autores principales: Rahman, Sajid Ur, Huang, Yingying, Zhu, Lei, Chu, Xiaoyan, Junejo, Shahid Ahmed, Zhang, Yafei, Khan, Ibrar Muhammad, Li, Yu, Feng, Shibin, Wu, Jinjie, Wang, Xichun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346471/
https://www.ncbi.nlm.nih.gov/pubmed/32641048
http://dx.doi.org/10.1186/s12917-020-02448-7
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author Rahman, Sajid Ur
Huang, Yingying
Zhu, Lei
Chu, Xiaoyan
Junejo, Shahid Ahmed
Zhang, Yafei
Khan, Ibrar Muhammad
Li, Yu
Feng, Shibin
Wu, Jinjie
Wang, Xichun
author_facet Rahman, Sajid Ur
Huang, Yingying
Zhu, Lei
Chu, Xiaoyan
Junejo, Shahid Ahmed
Zhang, Yafei
Khan, Ibrar Muhammad
Li, Yu
Feng, Shibin
Wu, Jinjie
Wang, Xichun
author_sort Rahman, Sajid Ur
collection PubMed
description BACKGROUND: Tea polyphenols (TPs) attenuate obesity related liver inflammation; however, the anti-obesity effects and anti-inflammatory mechanisms are not clearly understood. This study aimed to determine whether the anti-obesity and anti-inflammatory TPs mechanisms associated with cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression levels, and obesity-related gene response in dogs. RESULTS: Dogs fed TPs displayed significantly decreased (p < 0.01) mRNA expression of tumor necrosis factor-α (TNF-α), interleukin-1 beta (IL-1β), and interleukin-6 (IL-6) compared to dogs that consumed high-fat diet (HFD) alone. TPs significantly (p < 0.01) inhibited COX-2 and iNOS expression level, and decreased liver fat content and degeneration. CONCLUSION: These results suggested that TPs act as a therapeutic agent for obesity, liver inflammation, and fat degeneration via COX-2 and iNOS inhibition, with TNF-α, IL-1β, and IL-6 involvement.
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spelling pubmed-73464712020-07-14 Tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating COX-2 and iNOS expression in high fat-fed dogs Rahman, Sajid Ur Huang, Yingying Zhu, Lei Chu, Xiaoyan Junejo, Shahid Ahmed Zhang, Yafei Khan, Ibrar Muhammad Li, Yu Feng, Shibin Wu, Jinjie Wang, Xichun BMC Vet Res Research Article BACKGROUND: Tea polyphenols (TPs) attenuate obesity related liver inflammation; however, the anti-obesity effects and anti-inflammatory mechanisms are not clearly understood. This study aimed to determine whether the anti-obesity and anti-inflammatory TPs mechanisms associated with cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression levels, and obesity-related gene response in dogs. RESULTS: Dogs fed TPs displayed significantly decreased (p < 0.01) mRNA expression of tumor necrosis factor-α (TNF-α), interleukin-1 beta (IL-1β), and interleukin-6 (IL-6) compared to dogs that consumed high-fat diet (HFD) alone. TPs significantly (p < 0.01) inhibited COX-2 and iNOS expression level, and decreased liver fat content and degeneration. CONCLUSION: These results suggested that TPs act as a therapeutic agent for obesity, liver inflammation, and fat degeneration via COX-2 and iNOS inhibition, with TNF-α, IL-1β, and IL-6 involvement. BioMed Central 2020-07-08 /pmc/articles/PMC7346471/ /pubmed/32641048 http://dx.doi.org/10.1186/s12917-020-02448-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Rahman, Sajid Ur
Huang, Yingying
Zhu, Lei
Chu, Xiaoyan
Junejo, Shahid Ahmed
Zhang, Yafei
Khan, Ibrar Muhammad
Li, Yu
Feng, Shibin
Wu, Jinjie
Wang, Xichun
Tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating COX-2 and iNOS expression in high fat-fed dogs
title Tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating COX-2 and iNOS expression in high fat-fed dogs
title_full Tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating COX-2 and iNOS expression in high fat-fed dogs
title_fullStr Tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating COX-2 and iNOS expression in high fat-fed dogs
title_full_unstemmed Tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating COX-2 and iNOS expression in high fat-fed dogs
title_short Tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating COX-2 and iNOS expression in high fat-fed dogs
title_sort tea polyphenols attenuate liver inflammation by modulating obesity-related genes and down-regulating cox-2 and inos expression in high fat-fed dogs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346471/
https://www.ncbi.nlm.nih.gov/pubmed/32641048
http://dx.doi.org/10.1186/s12917-020-02448-7
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