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Effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet

Nonalcoholic fatty liver disease (NAFLD) is considered as a severe threat to human health. It has been reported that tea has abundant bioactive compounds and beneficial effects. In our study, the effects of 12 tea extracts on NAFLD were assessed and compared at the dose of 200 mg/kg body weight in m...

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Autores principales: Mao, Qian‐Qian, Li, Bang‐Yan, Meng, Jin‐Ming, Gan, Ren‐You, Xu, Xiao‐Yu, Gu, Ying‐Ying, Wang, Xiao‐Hui, Li, Hua‐Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194756/
https://www.ncbi.nlm.nih.gov/pubmed/34136163
http://dx.doi.org/10.1002/fsn3.2255
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author Mao, Qian‐Qian
Li, Bang‐Yan
Meng, Jin‐Ming
Gan, Ren‐You
Xu, Xiao‐Yu
Gu, Ying‐Ying
Wang, Xiao‐Hui
Li, Hua‐Bin
author_facet Mao, Qian‐Qian
Li, Bang‐Yan
Meng, Jin‐Ming
Gan, Ren‐You
Xu, Xiao‐Yu
Gu, Ying‐Ying
Wang, Xiao‐Hui
Li, Hua‐Bin
author_sort Mao, Qian‐Qian
collection PubMed
description Nonalcoholic fatty liver disease (NAFLD) is considered as a severe threat to human health. It has been reported that tea has abundant bioactive compounds and beneficial effects. In our study, the effects of 12 tea extracts on NAFLD were assessed and compared at the dose of 200 mg/kg body weight in mice fed with a high‐fat diet (HFD) for 15 weeks. Enshi Yulu Tea, Fenghuang Narcissus Tea, and Yihong Tea showed strong effects in suppressing the accumulation of epididymal and perirenal adipose tissue as well as the increases of body weight and liver weight. The histopathological analysis revealed that hepatic steatosis and adipocyte hypertrophy induced by a HFD could be ameliorated by tea supplementation. In addition, Enshi Yulu Tea and Qing Brick Tea exerted more remarkable functions on decreasing the level of serum triglyceride and preventing hepatic fat accumulation, respectively. Furthermore, Fenghuang Narcissus Tea, Enshi Yulu Tea, and Qing Brick Tea could reverse the abnormal change in the levels of glutathione and superoxide dismutase. Moreover, 13 phytoconstituents were detected and quantified in these teas with high‐performance liquid chromatography (HPLC) method. The correlation analysis demonstrated that gallic acid might decrease MDA level, and the reduction of liver weight might be attributed to ellagic acid. However, it should be paid attention to some teas that showed hepatotoxicity with elevated levels of aspartate transaminase and alanine aminotransferase. Several teas showed strong effects in the prevention of NAFLD, which could be developed into functional foods against NAFLD.
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spelling pubmed-81947562021-06-15 Effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet Mao, Qian‐Qian Li, Bang‐Yan Meng, Jin‐Ming Gan, Ren‐You Xu, Xiao‐Yu Gu, Ying‐Ying Wang, Xiao‐Hui Li, Hua‐Bin Food Sci Nutr Original Research Nonalcoholic fatty liver disease (NAFLD) is considered as a severe threat to human health. It has been reported that tea has abundant bioactive compounds and beneficial effects. In our study, the effects of 12 tea extracts on NAFLD were assessed and compared at the dose of 200 mg/kg body weight in mice fed with a high‐fat diet (HFD) for 15 weeks. Enshi Yulu Tea, Fenghuang Narcissus Tea, and Yihong Tea showed strong effects in suppressing the accumulation of epididymal and perirenal adipose tissue as well as the increases of body weight and liver weight. The histopathological analysis revealed that hepatic steatosis and adipocyte hypertrophy induced by a HFD could be ameliorated by tea supplementation. In addition, Enshi Yulu Tea and Qing Brick Tea exerted more remarkable functions on decreasing the level of serum triglyceride and preventing hepatic fat accumulation, respectively. Furthermore, Fenghuang Narcissus Tea, Enshi Yulu Tea, and Qing Brick Tea could reverse the abnormal change in the levels of glutathione and superoxide dismutase. Moreover, 13 phytoconstituents were detected and quantified in these teas with high‐performance liquid chromatography (HPLC) method. The correlation analysis demonstrated that gallic acid might decrease MDA level, and the reduction of liver weight might be attributed to ellagic acid. However, it should be paid attention to some teas that showed hepatotoxicity with elevated levels of aspartate transaminase and alanine aminotransferase. Several teas showed strong effects in the prevention of NAFLD, which could be developed into functional foods against NAFLD. John Wiley and Sons Inc. 2021-04-09 /pmc/articles/PMC8194756/ /pubmed/34136163 http://dx.doi.org/10.1002/fsn3.2255 Text en © 2021 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Mao, Qian‐Qian
Li, Bang‐Yan
Meng, Jin‐Ming
Gan, Ren‐You
Xu, Xiao‐Yu
Gu, Ying‐Ying
Wang, Xiao‐Hui
Li, Hua‐Bin
Effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet
title Effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet
title_full Effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet
title_fullStr Effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet
title_full_unstemmed Effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet
title_short Effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet
title_sort effects of several tea extracts on nonalcoholic fatty liver disease in mice fed with a high‐fat diet
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194756/
https://www.ncbi.nlm.nih.gov/pubmed/34136163
http://dx.doi.org/10.1002/fsn3.2255
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