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Silent information regulator 1 inhibition induces lipid metabolism disorders of hepatocytes and enhances hepatitis C virus replication
Author(s) -
Sun LiJie,
Li ShuChen,
Zhao YongHua,
Yu JianWu,
Kang Peng,
Yan BingZhu
Publication year - 2013
Publication title -
hepatology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.123
H-Index - 75
eISSN - 1872-034X
pISSN - 1386-6346
DOI - 10.1111/hepr.12089
Subject(s) - lipid metabolism , beta oxidation , nad+ kinase , biology , steatosis , cerulenin , activator (genetics) , fatty acid synthase , biochemistry , fatty acid , chemistry , microbiology and biotechnology , endocrinology , enzyme , gene
Aim Hepatic steatosis is an important histopathological feature of chronic hepatitis C virus ( HCV ) infection. Silent information regulator 1 ( SIRT1 ) plays key role in regulation of hepatic lipid metabolism. We investigated the possible effect of HCV replication on lipid metabolism of hepatocytes and expression of SIRT1 using H uh‐7.5 cells harboring HCV replicon. Methods The level of reactive oxygen species ( ROS ) and malondialdehyde ( MDA ), the activity of superoxide dismutase ( SOD ), and the value of nicotinamide adenine dinucleotide ( NAD + )/ NADH was detected. The level of triacylglycerol ( TG ), total cholesterol ( TC ) and fatty acid β‐oxidation rate was detected. The activity and expression levels of SIRT1 and expression of its downstream lipid‐metabolism genes were measured. Results In replicon cells, the level of ROS and MDA increased, SOD activity and the value of NAD + / NADH decreased, then the activity and expression level of m RNA and protein of SIRT1 reduced. Inhibition of SIRT1 decreased phosphorylation of forkhead box O1 ( FoxO1 ), which not only upregulated SREBP ‐1c, FAS , ACC , SREBP ‐2, HMGR and HMGS genes and increased fatty acid synthesis; but also downregulated PPAR ‐α and CPT1A genes and decreased fatty acid β‐oxidation. Interferon treatment restored aforementioned changes. SIRT1 activator improved lipid metabolism disorders by an increase in fatty acid β‐oxidation and a decrease in TG and TC synthesis and inhibited HCV replication. Conclusion HCV replication decreasing NAD + / NADH ratio may downregulate the activity and the expression of SIRT1 , then change the expression profile of lipid metabolism‐related genes, thereby cause lipid metabolism disorders of hepatocytes and promote HCV replication. Treatment with SIRT1 activator ameliorates lipid metabolic disorders and inhibits HCV replication.