Transplant Center and Key Laboratory of Transplant Engineering and Immunology, NHFPC, Regenerative Medicine Research Center, West China Hospital, Sichuan University, Chengdu, China.
Institutes for Systems Genetics, Frontiers Science Center for Disease-Related Molecular Network, West China Hospital, Sichuan University, Chengdu, China.
Lab Invest. 2023 Jul;103(7):100129. doi: 10.1016/j.labinv.2023.100129. Epub 2023 Mar 11.
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 high-fat 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.
非酒精性脂肪性肝病(NAFLD)是最常见的慢性肝病之一,其晚期阶段——非酒精性脂肪性肝炎(NASH)仍没有有效的治疗方法。迫切需要一种理想的 NAFLD/NASH 动物模型用于临床前研究。然而,由于动物品系、饲料配方和评估指标等方面的差异,以前报道的模型非常多样化。在本研究中,我们报告了我们之前在研究中开发的 5 种 NAFLD 小鼠模型,并对其特征进行了综合比较。高脂肪饮食(HFD)模型耗时较长,在 12 周时表现出早期胰岛素抵抗和轻微的肝脂肪变性。然而,炎症和纤维化很少见,即使在 22 周时也是如此。高脂肪、高果糖和高胆固醇饮食(FFC)加剧了糖和脂质代谢紊乱,在 12 周时表现出明显的高胆固醇血症、脂肪变性和轻度炎症。FFC 饮食与链脲佐菌素(STZ)联合使用是一种新型模型,可加速小叶炎症和纤维化的过程。STAM 模型也使用 FFC 和 STZ 的组合,但使用新生小鼠,表现出最快的纤维化结节形成。HFD 模型适用于早期 NAFLD 的研究。FFC 联合 STZ 加速了 NASH 的病理过程,可能是 NASH 研究和药物开发最有前途的模型。