Cui Xiao-Shan, Li Hong-Zheng, Li Liang, Xie Cheng-Zhi, Gao Jia-Ming, Chen Yuan-Yuan, Zhang Hui-Yu, Hao Wei, Fu Jian-Hua, Guo Hao
Institute of Basic Medical Sciences, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Guang'an men Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
J Gastroenterol Hepatol. 2025 Jan;40(1):48-66. doi: 10.1111/jgh.16749. Epub 2024 Sep 25.
Although significant progress has been made in developing preclinical models for metabolic dysfunction-associated steatotic liver disease (MASLD), few have encapsulated the essential biological and clinical outcome elements reflective of the human condition. We conducted a comprehensive literature review of English-language original research articles published from 1990 to 2023, sourced from PubMed, Embase, and Web of Science, aiming to collate studies that provided a comparative analysis of physiological, metabolic, and hepatic histological characteristics between MASLD models and control groups. The establishment of a robust metabolic dysfunction-associated steatotic liver rodent model hinges on various factors, including animal species and strains, sex, induction agents and methodologies, and the duration of induction. Through this review, we aim to guide researchers in selecting suitable induction methods and animal species for constructing preclinical models aligned with their specific research objectives and laboratory conditions. Future studies should strive to develop simple, reliable, and reproducible models, considering the model's sensitivity to factors such as light-dark cycles, housing conditions, and environmental temperature. Additionally, the potential of diverse in vitro models, including 3D models and liver organ technology, warrants further exploration as valuable tools for unraveling the cellular mechanisms underlying fatty liver disease.
尽管在开发代谢功能障碍相关脂肪性肝病(MASLD)的临床前模型方面已取得显著进展,但很少有模型能够囊括反映人类情况的基本生物学和临床结局要素。我们对1990年至2023年发表的英文原创研究文章进行了全面的文献综述,这些文章来源于PubMed、Embase和科学网,旨在整理那些对MASLD模型与对照组之间的生理、代谢和肝脏组织学特征进行比较分析的研究。建立一个强大的代谢功能障碍相关脂肪性肝病啮齿动物模型取决于多种因素,包括动物种类和品系、性别、诱导剂和方法,以及诱导持续时间。通过本综述,我们旨在指导研究人员根据其特定的研究目标和实验室条件,选择合适的诱导方法和动物种类来构建临床前模型。未来的研究应努力开发简单、可靠且可重复的模型,同时考虑模型对诸如昼夜节律、饲养条件和环境温度等因素的敏感性。此外,包括三维模型和肝脏器官技术在内的多种体外模型作为揭示脂肪肝疾病细胞机制的有价值工具,其潜力值得进一步探索。