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AMPK: a novel target for treating hepatic fibrosis

Fibrosis is a common process of excessive extracellular matrix (ECM) accumulation following inflammatory injury. Fibrosis is involved in the pathogenesis of almost all liver diseases for which there is no effective treatment. 5'-AMP-activated protein kinase (AMPK) is a cellular energy sensor th...

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Detalles Bibliográficos
Autores principales: Liang, Zhenxing, Li, Tian, Jiang, Shuai, Xu, Jing, Di, Wencheng, Yang, Zhi, Hu, Wei, Yang, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617548/
https://www.ncbi.nlm.nih.gov/pubmed/28977988
http://dx.doi.org/10.18632/oncotarget.19376
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author Liang, Zhenxing
Li, Tian
Jiang, Shuai
Xu, Jing
Di, Wencheng
Yang, Zhi
Hu, Wei
Yang, Yang
author_facet Liang, Zhenxing
Li, Tian
Jiang, Shuai
Xu, Jing
Di, Wencheng
Yang, Zhi
Hu, Wei
Yang, Yang
author_sort Liang, Zhenxing
collection PubMed
description Fibrosis is a common process of excessive extracellular matrix (ECM) accumulation following inflammatory injury. Fibrosis is involved in the pathogenesis of almost all liver diseases for which there is no effective treatment. 5'-AMP-activated protein kinase (AMPK) is a cellular energy sensor that can ameliorate the process of hepatic fibrogenesis. Given the existing evidence, we first introduce the basic background of AMPK and hepatic fibrosis and the actions of AMPK in hepatic fibrosis. Second, we discuss the three phases of hepatic fibrosis and potential drugs that target AMPK. Third, we analyze possible anti-fibrosis mechanisms and other benefits of AMPK on the liver. Finally, we summarize and briefly explain the current objections to targeting AMPK. This review may aid clinical and basic research on AMPK, which may be a novel drug candidate for hepatic fibrosis.
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spelling pubmed-56175482017-10-03 AMPK: a novel target for treating hepatic fibrosis Liang, Zhenxing Li, Tian Jiang, Shuai Xu, Jing Di, Wencheng Yang, Zhi Hu, Wei Yang, Yang Oncotarget Review Fibrosis is a common process of excessive extracellular matrix (ECM) accumulation following inflammatory injury. Fibrosis is involved in the pathogenesis of almost all liver diseases for which there is no effective treatment. 5'-AMP-activated protein kinase (AMPK) is a cellular energy sensor that can ameliorate the process of hepatic fibrogenesis. Given the existing evidence, we first introduce the basic background of AMPK and hepatic fibrosis and the actions of AMPK in hepatic fibrosis. Second, we discuss the three phases of hepatic fibrosis and potential drugs that target AMPK. Third, we analyze possible anti-fibrosis mechanisms and other benefits of AMPK on the liver. Finally, we summarize and briefly explain the current objections to targeting AMPK. This review may aid clinical and basic research on AMPK, which may be a novel drug candidate for hepatic fibrosis. Impact Journals LLC 2017-07-19 /pmc/articles/PMC5617548/ /pubmed/28977988 http://dx.doi.org/10.18632/oncotarget.19376 Text en Copyright: © 2017 Liang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Liang, Zhenxing
Li, Tian
Jiang, Shuai
Xu, Jing
Di, Wencheng
Yang, Zhi
Hu, Wei
Yang, Yang
AMPK: a novel target for treating hepatic fibrosis
title AMPK: a novel target for treating hepatic fibrosis
title_full AMPK: a novel target for treating hepatic fibrosis
title_fullStr AMPK: a novel target for treating hepatic fibrosis
title_full_unstemmed AMPK: a novel target for treating hepatic fibrosis
title_short AMPK: a novel target for treating hepatic fibrosis
title_sort ampk: a novel target for treating hepatic fibrosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617548/
https://www.ncbi.nlm.nih.gov/pubmed/28977988
http://dx.doi.org/10.18632/oncotarget.19376
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