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Alcoholic liver disease: Utility of animal models
Alcoholic liver disease (ALD) is a major cause of acute and chronic liver injury. Extensive evidence has been accumulated on the pathological process of ALD during the past decades. However, effective treatment options for ALD are very limited due to the lack of suitable in vivo models that recapitu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288648/ https://www.ncbi.nlm.nih.gov/pubmed/30568384 http://dx.doi.org/10.3748/wjg.v24.i45.5063 |
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author | Lamas-Paz, Arantza Hao, Fengjie Nelson, Leonard J Vázquez, Maria Teresa Canals, Santiago Gómez del Moral, Manuel Martínez-Naves, Eduardo Nevzorova, Yulia A Cubero, Francisco Javier |
author_facet | Lamas-Paz, Arantza Hao, Fengjie Nelson, Leonard J Vázquez, Maria Teresa Canals, Santiago Gómez del Moral, Manuel Martínez-Naves, Eduardo Nevzorova, Yulia A Cubero, Francisco Javier |
author_sort | Lamas-Paz, Arantza |
collection | PubMed |
description | Alcoholic liver disease (ALD) is a major cause of acute and chronic liver injury. Extensive evidence has been accumulated on the pathological process of ALD during the past decades. However, effective treatment options for ALD are very limited due to the lack of suitable in vivo models that recapitulate the full spectrum of ALD. Experimental animal models of ALD, particularly rodents, have been used extensively to mimic human ALD. An ideal animal model should recapitulate all aspects of the ALD process, including significant steatosis, hepatic neutrophil infiltration, and liver injury. A better strategy against ALD depends on clear diagnostic biomarkers, accurate predictor(s) of its progression and new therapeutic approaches to modulate stop or even reverse the disease. Numerous models employing rodent animals have been established in the last decades to investigate the effects of acute and chronic alcohol exposure on the initiation and progression of ALD. Although significant progress has been made in gaining better knowledge on the mechanisms and pathology of ALD, many features of ALD are unknown, and require further investigation, ideally with improved animal models that more effectively mimic human ALD. Although differences in the degree and stages of alcoholic liver injury inevitably exist between animal models and human ALD, the acquisition and translational relevance will be greatly enhanced with the development of new and improved animal models of ALD. |
format | Online Article Text |
id | pubmed-6288648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-62886482018-12-19 Alcoholic liver disease: Utility of animal models Lamas-Paz, Arantza Hao, Fengjie Nelson, Leonard J Vázquez, Maria Teresa Canals, Santiago Gómez del Moral, Manuel Martínez-Naves, Eduardo Nevzorova, Yulia A Cubero, Francisco Javier World J Gastroenterol Review Alcoholic liver disease (ALD) is a major cause of acute and chronic liver injury. Extensive evidence has been accumulated on the pathological process of ALD during the past decades. However, effective treatment options for ALD are very limited due to the lack of suitable in vivo models that recapitulate the full spectrum of ALD. Experimental animal models of ALD, particularly rodents, have been used extensively to mimic human ALD. An ideal animal model should recapitulate all aspects of the ALD process, including significant steatosis, hepatic neutrophil infiltration, and liver injury. A better strategy against ALD depends on clear diagnostic biomarkers, accurate predictor(s) of its progression and new therapeutic approaches to modulate stop or even reverse the disease. Numerous models employing rodent animals have been established in the last decades to investigate the effects of acute and chronic alcohol exposure on the initiation and progression of ALD. Although significant progress has been made in gaining better knowledge on the mechanisms and pathology of ALD, many features of ALD are unknown, and require further investigation, ideally with improved animal models that more effectively mimic human ALD. Although differences in the degree and stages of alcoholic liver injury inevitably exist between animal models and human ALD, the acquisition and translational relevance will be greatly enhanced with the development of new and improved animal models of ALD. Baishideng Publishing Group Inc 2018-12-07 2018-12-07 /pmc/articles/PMC6288648/ /pubmed/30568384 http://dx.doi.org/10.3748/wjg.v24.i45.5063 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Review Lamas-Paz, Arantza Hao, Fengjie Nelson, Leonard J Vázquez, Maria Teresa Canals, Santiago Gómez del Moral, Manuel Martínez-Naves, Eduardo Nevzorova, Yulia A Cubero, Francisco Javier Alcoholic liver disease: Utility of animal models |
title | Alcoholic liver disease: Utility of animal models |
title_full | Alcoholic liver disease: Utility of animal models |
title_fullStr | Alcoholic liver disease: Utility of animal models |
title_full_unstemmed | Alcoholic liver disease: Utility of animal models |
title_short | Alcoholic liver disease: Utility of animal models |
title_sort | alcoholic liver disease: utility of animal models |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288648/ https://www.ncbi.nlm.nih.gov/pubmed/30568384 http://dx.doi.org/10.3748/wjg.v24.i45.5063 |
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