Comparison of Animal Models for the Study of Nonalcoholic Fatty Liver Disease

被引:8
作者
Zheng, Qing [1 ]
Zhu, Min [1 ]
Zeng, Xin [1 ]
Liu, Wen [2 ]
Fu, Fudong [2 ]
Li, Xiaoyu [2 ]
Liao, Guangneng [3 ]
Lu, Yanrong [1 ]
Chen, Younan [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Transplant Ctr, Regenerat Med Res Ctr,NHFPC, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Inst Syst Genet, Frontiers Sci Ctr Dis Related Mol Network, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, Anim Expt Ctr, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
high-fat diet; high-fat high-fructose and; high-cholesterol diet; nonalcoholic fatty liver disease; nonalcoholic steatohepatitis; FRUCTOSE; DYSREGULATION; ASSOCIATION; CHOLESTEROL; SEVERITY; INJURY; NAFLD; DIET; MICE;
D O I
10.1016/j.labinv.2023.100129
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Nonalcoholic fatty liver disease (NAFLD) is one of the most prevalent chronic liver diseases, and there is still no effective treatment for its advanced stage, nonalcoholic steatohepatitis (NASH). An ideal animal model of NAFLD/NASH is urgently needed for preclinical studies. However, the models reported previously are quite heterogeneous owing to differences in animal strains, feed formulations, and evaluation indicators, among others. In this study, we report 5 NAFLD mouse models we developed in previous studies and comprehensively compared their characteristics. The highfat diet (HFD) model was time-consuming and characterized by early insulin resistance and slight liver steatosis at 12 weeks. However, inflammation and fibrosis were rare, even at 22 weeks. The high-fat, high-fructose, and high-cholesterol diet (FFC) exacerbates glucose and lipid metabolism disorders, showing distinct hypercholesterolemia, steatosis, and mild inflammation at 12 weeks. An FFC diet combined with streptozotocin (STZ) was a novel model that speeds up the process of lobular inflammation and fibrosis. The STAM model also used a combination of FFC and STZ but used newborn mice and showed the fastest formation of fibrosis nodules. The HFD model was appropriate for the study of early NAFLD. FFC combined with STZ accelerated the pathologic process of NASH and might be the most promising model for NASH research and drug development.(c) 2023 United States & Canadian Academy of Pathology. Published by Elsevier Inc. All rights reserved.
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页数:14
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