代谢功能障碍相关性脂肪肝的发病机制:脂质代谢的重要作用

IF 3.1 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Xiaoxi Feng, Rutong Zhang, Zhenye Yang, Kaiguang Zhang, Jun Xing
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引用次数: 0

摘要

代谢功能障碍相关性脂肪性肝病(MASLD)以前被称为非酒精性脂肪肝,在全球发病率很高,可发展为代谢功能障碍相关性脂肪性肝炎、肝硬化和肝细胞癌。MASLD 的发病机制主要由肝脏脂质代谢紊乱引起,涉及六个关键过程:肝脏脂肪酸摄取增加、脂肪酸合成增强、脂肪酸氧化降解减少、胆固醇摄取增加、胆固醇合成增加和胆汁酸合成增加。因此,维持肝脏脂质代谢平衡对于有效控制 MASLD 至关重要。许多新型分子和中成药主要通过抑制脂质合成和促进脂质氧化来治疗 MASLD,已显示出良好的治疗潜力。在这篇综述中,我们总结了近年来有关MASLD的研究,阐明了脂质代谢紊乱导致MASLD发病的分子机制,并讨论了针对MASLD的各种脂质代谢靶向治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanism of Metabolic Dysfunction-associated Steatotic Liver Disease: Important role of lipid metabolism.

Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as non-alcoholic fatty liver disease, has a high global prevalence and can progress to metabolic dysfunction-associated steatohepatitis, cirrhosis, and hepatocellular carcinoma. The pathogenesis of MASLD is primarily driven by disturbances in hepatic lipid metabolism, involving six key processes: increased hepatic fatty acid uptake, enhanced fatty acid synthesis, reduced oxidative degradation of fatty acids, increased cholesterol uptake, elevated cholesterol synthesis, and increased bile acid synthesis. Consequently, maintaining hepatic lipid metabolic homeostasis is essential for effective MASLD management. Numerous novel molecules and Chinese proprietary medicines have demonstrated promising therapeutic potential in treating MASLD, primarily by inhibiting lipid synthesis and promoting lipid oxidation. In this review, we summarized recent research on MASLD, elucidated the molecular mechanisms by which lipid metabolism disorders contribute to MASLD pathogenesis, and discussed various lipid metabolism-targeted therapeutic approaches for MASLD.

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来源期刊
Journal of Clinical and Translational Hepatology
Journal of Clinical and Translational Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.40
自引率
2.80%
发文量
496
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