Iron metabolism and ferroptosis in nonalcoholic fatty liver disease: what is our next step?

被引:3
|
作者
Shen, Xiang [1 ]
Yu, Ziqi [1 ]
Wei, Changli [2 ]
Hu, Chong [2 ]
Chen, Jianyong [2 ]
机构
[1] Ludwig Maximilian Univ Munich, Munich Med Res Sch, Munich, Germany
[2] Jiangxi Prov Peoples Hosp, Nanchang Med Coll, Affiliated Hosp 1, Dept Obstet & Reprod Hlth, Nanchang, Peoples R China
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2024年 / 326卷 / 06期
基金
中国国家自然科学基金;
关键词
ferroptosis; iron metabolism; lipid peroxidation; NAFLD; NASH; INSULIN-RESISTANCE; HOMEOSTASIS; ACTIVATION; FIBROSIS; PROGRESSION; EXPRESSION; PHLEBOTOMY; AUTOPHAGY; DEPLETION; HEPCIDIN;
D O I
10.1152/ajpendo.00260.2023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease with increasing prevalence worldwide. NAFLD could develop from simple hepatic steatosis to nonalcoholic steatohepatitis (NASH), NASH-related fibrosis, cirrhosis, and even hepatocellular carcinoma. However, the mechanism of NAFLD development has not yet been fully defined. Recently, emerging evidence shows that the dysregulated iron metabolism marked by elevated serum ferritin, and ferroptosis are involved in the NAFLD. Understanding iron metabolism and ferroptosis can shed light on the mechanisms of NAFLD development. Here, we summarized studies on iron metabolism and the ferroptosis process involved in NAFLD development to highlight potential medications and therapies for treating NAFLD.
引用
收藏
页码:E767 / E775
页数:9
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