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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....

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
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.
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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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