Tsukamoto Hidekazu, Machida Keigo, Dynnyk Alla, Mkrtchyan Hasmik
Southern California Research Center for ALPD and Cirrhosis, Keck School of Medicine of University of Southern California, Los Angeles, California 90033, USA.
Semin Liver Dis. 2009 May;29(2):178-87. doi: 10.1055/s-0029-1214373. Epub 2009 Apr 22.
Alcoholic liver disease (ALD) is a lifestyle disease with its pathogenesis and individual predisposition governed by gene-environment interactions. Based on the "second hit" or "multiple hits" hypothesis, patients are predisposed to progressive ALD when a magic combination of gene and environmental interactions exists. Reproduction of second or multiple hits in animal models serves to test a combination and to gain mechanistic insights into synergism achieved by such combination. Numerous environmental factors have been incorporated into animal models, largely classified into nutritional, xenobiotic/pharmacologic, hemodynamic, and viral groups. A loss or gain of function genetic model has become a popular experimental approach to test the role of a gene as a second hit. Future research will need to test more subtle or natural hits combined with excessive alcohol intake to test multiple hits in the genesis of ALD. Additionally, animal models of comorbidities are urgently needed particularly for synergistic liver disease and oncogenesis caused by alcohol, obesity, and hepatitis virus.
酒精性肝病(ALD)是一种生活方式疾病,其发病机制和个体易感性由基因 - 环境相互作用决定。基于“二次打击”或“多次打击”假说,当存在基因与环境相互作用的神奇组合时,患者易患进行性ALD。在动物模型中重现二次或多次打击有助于测试这种组合,并深入了解这种组合所实现的协同作用机制。许多环境因素已被纳入动物模型,主要分为营养、外源生物/药物、血流动力学和病毒组。功能丧失或获得性遗传模型已成为测试基因作为二次打击作用的常用实验方法。未来的研究需要测试更微妙或自然的打击与过量饮酒相结合的情况,以测试ALD发生过程中的多次打击。此外,迫切需要共病的动物模型,特别是针对由酒精、肥胖和肝炎病毒引起的协同性肝病和肿瘤发生的模型。