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Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats)
(-)-Epigallocatechin-3-gallate (EGCG) is the most abundant catechin with various biological activities found in tea. In this study, the effects of EGCG on the metabolism and toxicity of acetaminophen in rat liver were investigated. Male Sprague-Dawley rats were fed a controlled diet without or with...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
China Medical University
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531855/ https://www.ncbi.nlm.nih.gov/pubmed/26264479 http://dx.doi.org/10.7603/s40681-015-0015-8 |
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author | Yao, Hsien-Tsung Yang, Yu-Chi Chang, Chen-Hui Yang, Hui-Ting Yin, Mei-Chin |
author_facet | Yao, Hsien-Tsung Yang, Yu-Chi Chang, Chen-Hui Yang, Hui-Ting Yin, Mei-Chin |
author_sort | Yao, Hsien-Tsung |
collection | PubMed |
description | (-)-Epigallocatechin-3-gallate (EGCG) is the most abundant catechin with various biological activities found in tea. In this study, the effects of EGCG on the metabolism and toxicity of acetaminophen in rat liver were investigated. Male Sprague-Dawley rats were fed a controlled diet without or with EGCG (0.54 %, w/w) for 1 week and were then intraperitoneally injected with acetaminophen (1 g/kg body weight) and killed after 12 h. Concentrations of acetaminophen and its conjugates in plasma and liver were then determined. The cytochrome P450 (CYP) and phase II enzymes activities were also evaluated. Rats fed the EGCG diet had lower plasma alanine aminotransferase and aspartate aminotransferase activities, as indices of hepatotoxicity, after acetaminophen treatment. Morphological damage by acetaminophen was lower in rats fed the EGCG diet. In addition, EGCG significantly reduced hepatic activities of midazolam 1-hydroxylation (CYP3A), nitrophenol 6-hydroxylase (CYP2E1), UDP-glucurosyltransferase, and sulfotransferase. Finally, EGCG feeding reduced acetaminophen-glucuronate and acetaminophen-glutathione contents in plasma and liver. These results indicate that EGCG feeding may reduce the metabolism and toxicity of acetaminophen in rats. |
format | Online Article Text |
id | pubmed-4531855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | China Medical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-45318552015-08-12 Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats) Yao, Hsien-Tsung Yang, Yu-Chi Chang, Chen-Hui Yang, Hui-Ting Yin, Mei-Chin Biomedicine (Taipei) Article (-)-Epigallocatechin-3-gallate (EGCG) is the most abundant catechin with various biological activities found in tea. In this study, the effects of EGCG on the metabolism and toxicity of acetaminophen in rat liver were investigated. Male Sprague-Dawley rats were fed a controlled diet without or with EGCG (0.54 %, w/w) for 1 week and were then intraperitoneally injected with acetaminophen (1 g/kg body weight) and killed after 12 h. Concentrations of acetaminophen and its conjugates in plasma and liver were then determined. The cytochrome P450 (CYP) and phase II enzymes activities were also evaluated. Rats fed the EGCG diet had lower plasma alanine aminotransferase and aspartate aminotransferase activities, as indices of hepatotoxicity, after acetaminophen treatment. Morphological damage by acetaminophen was lower in rats fed the EGCG diet. In addition, EGCG significantly reduced hepatic activities of midazolam 1-hydroxylation (CYP3A), nitrophenol 6-hydroxylase (CYP2E1), UDP-glucurosyltransferase, and sulfotransferase. Finally, EGCG feeding reduced acetaminophen-glucuronate and acetaminophen-glutathione contents in plasma and liver. These results indicate that EGCG feeding may reduce the metabolism and toxicity of acetaminophen in rats. China Medical University 2015-08-12 /pmc/articles/PMC4531855/ /pubmed/26264479 http://dx.doi.org/10.7603/s40681-015-0015-8 Text en © China Medical University 2015 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided original author(s) and source are credited. |
spellingShingle | Article Yao, Hsien-Tsung Yang, Yu-Chi Chang, Chen-Hui Yang, Hui-Ting Yin, Mei-Chin Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats) |
title | Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats) |
title_full | Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats) |
title_fullStr | Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats) |
title_full_unstemmed | Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats) |
title_short | Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats) |
title_sort | protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531855/ https://www.ncbi.nlm.nih.gov/pubmed/26264479 http://dx.doi.org/10.7603/s40681-015-0015-8 |
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