Ceramide de novo synthesis in non-alcoholic fatty liver disease: Pathogenic mechanisms and therapeutic perspectives

被引:28
|
作者
Yu, Xiao-Dong [1 ,2 ]
Wang, Jiong-Wei [1 ,2 ,3 ,4 ,5 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Surg, Singapore, Singapore
[2] Natl Univ Singapore, Ctr Nanomed, Yong Loo Lin Sch Med, Nanomed Translat Res Programme, Singapore, Singapore
[3] Natl Univ Heart Ctr Singapore NUHCS, Cardiovasc Res Inst CVRI, Singapore, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore, Singapore
[5] Natl Univ Singapore, Dept Surg, 1E Kent Ridge Rd,NUHS Tower Block,Level 8, Singapore 119228, Singapore
基金
英国医学研究理事会;
关键词
Ceramide; Ceramide de novo synthesis; Non-alcoholic fatty liver disease; Non-alcoholic steatohepatitis; Sphingolipids; Therapeutic target; INDUCED INSULIN-RESISTANCE; NF-KAPPA-B; HEPATIC STEATOSIS; SERINE PALMITOYLTRANSFERASE; MOLECULAR-MECHANISMS; OXIDATIVE STRESS; VLDL SECRETION; PKC-ZETA; PROTEIN; INHIBITION;
D O I
10.1016/j.bcp.2022.115157
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease, and its advanced form nonalcoholic steatohepatitis (NASH) may progress to cirrhosis and hepatocellular carcinoma. Ceramides have been shown to exacerbate NAFLD development through enhancing insulin resistance, reactive oxygen species production, liver steatosis, lipotoxicity and hepatocyte apoptosis, and eventually causing hepatic inflammation and fibrosis. Emerging evidence indicates that ceramide production in NAFLD is predominantly attributed to activation of the de novo synthesis pathway of ceramides in hepatocytes. More importantly, pharmacological modulation of ceramide de novo synthesis in preclinical studies seems efficacious for the treatment of NAFLD. In this review, we provide an overview of the pathogenic mechanisms of ceramides in NAFLD, discuss recent advances and challenges in pharmacological interventions targeting ceramide de novo synthesis, and propose some research directions in the field.
引用
收藏
页数:12
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