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用于非酒精性脂肪性肝病研究的基因修饰小鼠模型。

Genetically modified mouse models for the study of nonalcoholic fatty liver disease.

出版信息

World J Gastroenterol. 2012 Mar 21;18(11):1141-53. doi: 10.3748/wjg.v18.i11.1141.

DOI:10.3748/wjg.v18.i11.1141
PMID:22468076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3309902/
Abstract

Nonalcoholic fatty liver disease (NAFLD) is associated with obesity, insulin resistance, and type 2 diabetes. NAFLD represents a large spectrum of diseases ranging from (1) fatty liver (hepatic steatosis); (2) steatosis with inflammation and necrosis; to (3) cirrhosis. The animal models to study NAFLD/nonalcoholic steatohepatitis (NASH) are extremely useful, as there are still many events to be elucidated in the pathology of NASH. The study of the established animal models has provided many clues in the pathogenesis of steatosis and steatohepatitis, but these remain incompletely understood. The different mouse models can be classified in two large groups. The first one includes genetically modified (transgenic or knockout) mice that spontaneously develop liver disease, and the second one includes mice that acquire the disease after dietary or pharmacological manipulation. Although the molecular mechanism leading to the development of hepatic steatosis in the pathogenesis of NAFLD is complex, genetically modified animal models may be a key for the treatment of NAFLD. Ideal animal models for NASH should closely resemble the pathological characteristics observed in humans. To date, no single animal model has encompassed the full spectrum of human disease progression, but they can imitate particular characteristics of human disease. Therefore, it is important that the researchers choose the appropriate animal model. This review discusses various genetically modified animal models developed and used in research on NAFLD.

摘要

非酒精性脂肪性肝病(NAFLD)与肥胖、胰岛素抵抗和 2 型糖尿病有关。NAFLD 代表了一系列疾病,从(1)脂肪肝(肝脂肪变性);(2)脂肪变性伴炎症和坏死;到(3)肝硬化。研究 NAFLD/非酒精性脂肪性肝炎(NASH)的动物模型非常有用,因为 NASH 的病理仍然有许多事件需要阐明。对已建立的动物模型的研究为脂肪变性和脂肪性肝炎的发病机制提供了许多线索,但这些仍然不完全清楚。不同的小鼠模型可以分为两大类。第一类包括自发发生肝脏疾病的基因修饰(转基因或敲除)小鼠,第二类包括通过饮食或药理学处理获得疾病的小鼠。尽管导致 NAFLD 发病机制中肝脂肪变性的分子机制很复杂,但基因修饰动物模型可能是治疗 NAFLD 的关键。NASH 的理想动物模型应与人类观察到的病理特征非常相似。迄今为止,没有一种单一的动物模型涵盖了人类疾病进展的全部范围,但它们可以模仿人类疾病的某些特征。因此,研究人员选择合适的动物模型非常重要。这篇综述讨论了用于研究 NAFLD 的各种已开发和使用的基因修饰动物模型。

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