脂质代谢
脂肪性肝炎
脂肪肝
医学
脂代谢紊乱
发病机制
肝硬化
脂肪酸合成
新陈代谢
脂肪酸
胆固醇
疾病
生物化学
内科学
化学
血脂
作者
Xiaoxi Feng,Rutong Zhang,Zhenye Yang,Kaiguang Zhang,Jun Xing
出处
期刊:Journal of clinical and translational hepatology
[Xia & He Publishing]
日期:2024-09-03
卷期号:000 (000): 000-000
被引量:22
标识
DOI:10.14218/jcth.2024.00019
摘要
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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