Alcoholic liver disease: Utility of animal models

被引:6
作者
Arantza Lamas-Paz [1 ,2 ]
Fengjie Hao [1 ,2 ]
Leonard J Nelson [3 ]
Maria Teresa Vázquez [4 ]
Santiago Canals [5 ]
Manuel Gómez del Moral [6 ]
Eduardo Martínez-Naves [1 ,2 ]
Yulia A Nevzovova [2 ,7 ,8 ]
Francisco Javier Cubero [1 ,2 ]
机构
[1] Department of Immunology, Ophthalmology and ORL, Complutense University School of Medicine
[2] 12 de Octubre Health Research Institute (imas12)
[3] Institute for Bioengineering (IBioE), School of Engineering, Faraday Building, The University of Edinburgh
[4] Department of Human Anatomy and Embryology, Complutense University School of Medicine
[5] Instituto de Neurociencias, Consejo Superior de Investigaciones Científicas, Universidad Miguel Hernández
[6] Department of Cell Biology, Complutense University School of Medicine
[7] Department of Genetics, Physiology and Microbiology, Faculty of Biology, Universidad Complutense
[8] Department of Internal Medicine Ⅲ, University Hospital RWTH Aachen
关键词
Steatohepatitis; Cirrhosis; Hepatocellular carcinoma; Alcoholic liver disease; Reactive oxygen species;
D O I
暂无
中图分类号
R575 [肝及胆疾病]; R-332 [医用实验动物学];
学科分类号
1001 ; 1002 ; 100201 ;
摘要
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.
引用
收藏
页码:5063 / 5075
页数:13
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