Corn Oligopeptide Alleviates Nonalcoholic Fatty Liver Disease by Regulating the Sirtuin Signaling Pathway

被引:4
|
作者
Xu, Yali [1 ,2 ]
Su, Ting [2 ]
Mishra, Hricha [1 ]
Ando, Reiko [3 ]
Furutani, Yutaka [4 ]
Lu, Jun [5 ]
Cai, Muyi [5 ]
Suzuki, Harukazu [1 ]
Yu, Wenkui [2 ]
Qin, Xian-Yang [1 ]
机构
[1] RIKEN Ctr Integrat Med Sci, Lab Cellular Funct Convers Technol, Yokohama 2300045, Japan
[2] Nanjing Univ, Affiliated Drum Tower Hosp, Med Sch, Dept Intens Care Unit, Nanjing 210008, Peoples R China
[3] RIKEN Ctr Brain Sci, Res Resources Div, Support Unit Biomat Anal, Wako 3510106, Japan
[4] Jikei Univ, Sch Med, Dept Lab Med, Tokyo 1058461, Japan
[5] China Natl Res Inst Food & Fermentat Ind, Beijing 100016, Peoples R China
基金
日本学术振兴会;
关键词
corn oligopeptides; high-fat diet; nonalcoholicfatty liver disease; nonalcoholic steatohepatitis; oxidative stress; sirtuin; PEPTIDES; METABOLISM; INJURY; MECHANISMS; FIBROSIS; DEATH; MODEL;
D O I
10.1021/acs.jafc.3c09058
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Nonalcoholic fatty liver disease (NAFLD) represents the most prevalent type of chronic liver disease, spanning from simple steatosis to nonalcoholic steatohepatitis (NASH). Corn oligopeptide (CP) is a functional peptide known for its diverse pharmacological effects on metabolism. In this study, we evaluated the protective activity of CP against fatty liver disease. Oral administration of CP significantly reduced body weight gain by 2.95%, serum cholesterol by 22.54%, and liver injury, as evidenced by a reduction of 32.19% in serum aspartate aminotransferase (AST) and 49.10% in alanine aminotransferase (ALT) levels in mice subjected to a high-fat diet (HFD). In a streptozotocin/HFD-induced NASH mouse model, CP attenuated body weight gain by 5.11%, liver injury (with a 34.15% decrease in AST and 11.43% decrease in ALT), and, to some extent, liver inflammation and fibrosis. Proteomic analysis revealed the modulation of oxidative phosphorylation and sirtuin (SIRT) signaling pathways by CP. Remarkably, CP selectively inhibited the hepatic expression of mitochondrial SIRT3 and SIRT5 in both HFD and NASH models. In summary, CP demonstrates a preventive effect against metabolic-stress-induced NAFLD progression by modulating oxidative stress and the SIRT signaling pathway, suggesting the potential of CP as a therapeutic agent for the treatment of NAFLD and advanced-stage NASH.
引用
收藏
页码:6360 / 6371
页数:12
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