Jacobs Ans, Warda Anne-Sophie, Verbeek Jef, Cassiman David, Spincemaille Pieter
Department of Hepatology, University Hospitals KU Leuven, Leuven, Belgium.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.
Curr Protoc Mouse Biol. 2016 Jun 1;6(2):185-200. doi: 10.1002/cpmo.3.
Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in the Western world. It is associated with obesity and type 2 diabetes and represents a spectrum of histological abnormalities ranging from simple steatosis to non-alcoholic steatohepatitis (NASH), which can further progress to fibrosis, cirrhosis, hepatocellular carcinoma (HCC), and liver failure. To gain insight into the pathogenesis and evaluate treatment options, mouse models of NAFLD/NASH are of utmost importance. There is a high phenotypical variety in the available mouse models, however, models that truly display the full spectrum of histopathological and metabolic features associated with human NASH are rare. In this review, we summarize the most important NAFLD/NASH mouse models that have been developed over the years and briefly highlight the pros and cons. Also, we illustrate the preclinical research in which these models have been used. © 2016 by John Wiley & Sons, Inc.
非酒精性脂肪性肝病(NAFLD)是西方世界最常见的慢性肝病。它与肥胖和2型糖尿病相关,代表了一系列组织学异常,从单纯性脂肪变性到非酒精性脂肪性肝炎(NASH),后者可进一步发展为纤维化、肝硬化、肝细胞癌(HCC)和肝衰竭。为深入了解发病机制并评估治疗方案,NAFLD/NASH小鼠模型至关重要。然而,现有的小鼠模型存在高度的表型多样性,真正展现出与人类NASH相关的完整组织病理学和代谢特征的模型却很罕见。在本综述中,我们总结了多年来开发的最重要的NAFLD/NASH小鼠模型,并简要突出其优缺点。此外,我们还阐述了使用这些模型的临床前研究。© 2016约翰威立国际出版公司