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The Protective Effect of Resveratrol on Concanavalin-A-Induced Acute Hepatic Injury in Mice
Pharmacologic Relevance. Resveratrol, an antioxidant derived from grapes, has been reported to modulate the inflammatory process. In this study, we investigated the effects of resveratrol and its mechanism of protection on concanavalin-A- (ConA-) induced liver injury in mice. Materials and Methods....
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458299/ https://www.ncbi.nlm.nih.gov/pubmed/26089871 http://dx.doi.org/10.1155/2015/506390 |
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author | Zhou, Yingqun Chen, Kan He, Lei Xia, Yujing Dai, Weiqi Wang, Fan Li, Jingjing Li, Sainan Liu, Tong Zheng, Yuanyuan Wang, Jianrong Lu, Wenxia Yin, Qin Zhou, Yuqing Lu, Jie Teng, Hongfei Guo, Chuanyong |
author_facet | Zhou, Yingqun Chen, Kan He, Lei Xia, Yujing Dai, Weiqi Wang, Fan Li, Jingjing Li, Sainan Liu, Tong Zheng, Yuanyuan Wang, Jianrong Lu, Wenxia Yin, Qin Zhou, Yuqing Lu, Jie Teng, Hongfei Guo, Chuanyong |
author_sort | Zhou, Yingqun |
collection | PubMed |
description | Pharmacologic Relevance. Resveratrol, an antioxidant derived from grapes, has been reported to modulate the inflammatory process. In this study, we investigated the effects of resveratrol and its mechanism of protection on concanavalin-A- (ConA-) induced liver injury in mice. Materials and Methods. Acute autoimmune hepatitis was induced by ConA (20 mg/kg) in Balb/C mice; mice were treated with resveratrol (10, 20, and 30 mg/kg) daily by oral gavage for fourteen days prior to a single intravenous injection of ConA. Eight hours after injection, histologic grading, proinflammatory cytokine levels, and hedgehog pathway activity were determined. Results. After ConA injection, the cytokines IL-2, IL-6, and TNF-α were increased, and Sonic hedgehog (Shh), Glioblastoma- (Gli-) 1, and Patched (Ptc) levels significantly increased. Pretreatment with resveratrol ameliorated the pathologic effects of ConA-induced autoimmune hepatitis and significantly inhibited IL-2, IL-6, TNF-α, Shh, Gli-1, and Ptc. The effects of resveratrol on the hedgehog pathway were studied by western blotting and immunohistochemistry. Resveratrol decreased Shh expression, possibly by inhibiting Shh expression in order to reduce Gli-1 and Ptc expression. Conclusion. Resveratrol protects against ConA-induced autoimmune hepatitis by decreasing cytokines expression in mice. The decreases seen in Gli-1 and Ptc may correlate with the amelioration of hedgehog pathway activity. |
format | Online Article Text |
id | pubmed-4458299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-44582992015-06-18 The Protective Effect of Resveratrol on Concanavalin-A-Induced Acute Hepatic Injury in Mice Zhou, Yingqun Chen, Kan He, Lei Xia, Yujing Dai, Weiqi Wang, Fan Li, Jingjing Li, Sainan Liu, Tong Zheng, Yuanyuan Wang, Jianrong Lu, Wenxia Yin, Qin Zhou, Yuqing Lu, Jie Teng, Hongfei Guo, Chuanyong Gastroenterol Res Pract Research Article Pharmacologic Relevance. Resveratrol, an antioxidant derived from grapes, has been reported to modulate the inflammatory process. In this study, we investigated the effects of resveratrol and its mechanism of protection on concanavalin-A- (ConA-) induced liver injury in mice. Materials and Methods. Acute autoimmune hepatitis was induced by ConA (20 mg/kg) in Balb/C mice; mice were treated with resveratrol (10, 20, and 30 mg/kg) daily by oral gavage for fourteen days prior to a single intravenous injection of ConA. Eight hours after injection, histologic grading, proinflammatory cytokine levels, and hedgehog pathway activity were determined. Results. After ConA injection, the cytokines IL-2, IL-6, and TNF-α were increased, and Sonic hedgehog (Shh), Glioblastoma- (Gli-) 1, and Patched (Ptc) levels significantly increased. Pretreatment with resveratrol ameliorated the pathologic effects of ConA-induced autoimmune hepatitis and significantly inhibited IL-2, IL-6, TNF-α, Shh, Gli-1, and Ptc. The effects of resveratrol on the hedgehog pathway were studied by western blotting and immunohistochemistry. Resveratrol decreased Shh expression, possibly by inhibiting Shh expression in order to reduce Gli-1 and Ptc expression. Conclusion. Resveratrol protects against ConA-induced autoimmune hepatitis by decreasing cytokines expression in mice. The decreases seen in Gli-1 and Ptc may correlate with the amelioration of hedgehog pathway activity. Hindawi Publishing Corporation 2015 2015-05-24 /pmc/articles/PMC4458299/ /pubmed/26089871 http://dx.doi.org/10.1155/2015/506390 Text en Copyright © 2015 Yingqun Zhou et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhou, Yingqun Chen, Kan He, Lei Xia, Yujing Dai, Weiqi Wang, Fan Li, Jingjing Li, Sainan Liu, Tong Zheng, Yuanyuan Wang, Jianrong Lu, Wenxia Yin, Qin Zhou, Yuqing Lu, Jie Teng, Hongfei Guo, Chuanyong The Protective Effect of Resveratrol on Concanavalin-A-Induced Acute Hepatic Injury in Mice |
title | The Protective Effect of Resveratrol on Concanavalin-A-Induced Acute Hepatic Injury in Mice |
title_full | The Protective Effect of Resveratrol on Concanavalin-A-Induced Acute Hepatic Injury in Mice |
title_fullStr | The Protective Effect of Resveratrol on Concanavalin-A-Induced Acute Hepatic Injury in Mice |
title_full_unstemmed | The Protective Effect of Resveratrol on Concanavalin-A-Induced Acute Hepatic Injury in Mice |
title_short | The Protective Effect of Resveratrol on Concanavalin-A-Induced Acute Hepatic Injury in Mice |
title_sort | protective effect of resveratrol on concanavalin-a-induced acute hepatic injury in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458299/ https://www.ncbi.nlm.nih.gov/pubmed/26089871 http://dx.doi.org/10.1155/2015/506390 |
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