Martin-Grau Maria, Marrachelli Vannina G, Monleon Daniel
Department of Pathology, University of Valencia, Valencia 46010, Spain.
Department of Physiology, University of Valencia, Valencia 46010, Spain.
World J Hepatol. 2022 Feb 27;14(2):304-318. doi: 10.4254/wjh.v14.i2.304.
Non-alcoholic fatty liver disease (NAFLD) prevalence has increased drastically in recent decades, affecting up to 25% of the world's population. NAFLD is a spectrum of different diseases that starts with asymptomatic steatosis and continues with development of an inflammatory response called steatohepatitis, which can progress to fibrosis. Several molecular and metabolic changes are required for the hepatocyte to finally vary its function; hence a "multiple hit" hypothesis seems a more accurate proposal. Previous studies and current knowledge suggest that in most cases, NAFLD initiates and progresses through most of nine hallmarks of the disease, although the triggers and mechanisms for these can vary widely. The use of animal models remains crucial for understanding the disease and for developing tools based on biological knowledge. Among certain requirements to be met, a good model must imitate certain aspects of the human NAFLD disorder, be reliable and reproducible, have low mortality, and be compatible with a simple and feasible method. Metabolism studies in these models provides a direct reflection of the workings of the cell and may be a useful approach to better understand the initiation and progression of the disease. Metabolomics seems a valid tool for studying metabolic pathways and crosstalk between organs affected in animal models of NAFLD and for the discovery and validation of relevant biomarkers with biological understanding. In this review, we provide a brief introduction to NAFLD hallmarks, the five groups of animal models available for studying NAFLD and the potential role of metabolomics in the study of experimental NAFLD.
近几十年来,非酒精性脂肪性肝病(NAFLD)的患病率急剧上升,影响了全球多达25%的人口。NAFLD是一系列不同的疾病,始于无症状脂肪变性,并随着一种称为脂肪性肝炎的炎症反应的发展而持续,脂肪性肝炎可进展为纤维化。肝细胞最终改变其功能需要几种分子和代谢变化;因此,“多重打击”假说似乎是一个更准确的提议。先前的研究和当前的知识表明,在大多数情况下,NAFLD通过该疾病的九个特征中的大多数开始并进展,尽管这些特征的触发因素和机制可能有很大差异。动物模型的使用对于理解该疾病和基于生物学知识开发工具仍然至关重要。在需要满足的某些要求中,一个好的模型必须模仿人类NAFLD疾病的某些方面,可靠且可重复,死亡率低,并且与简单可行的方法兼容。这些模型中的代谢研究直接反映了细胞的运作情况,可能是更好地理解该疾病的起始和进展的有用方法。代谢组学似乎是研究NAFLD动物模型中受影响器官之间的代谢途径和相互作用以及发现和验证具有生物学意义的相关生物标志物的有效工具。在这篇综述中,我们简要介绍了NAFLD的特征、可用于研究NAFLD的五类动物模型以及代谢组学在实验性NAFLD研究中的潜在作用。