Corn Oligopeptide Alleviates Nonalcoholic Fatty Liver Disease by Regulating the Sirtuin Signaling Pathway.
Yali XuTing SuHricha MishraReiko AndoYutaka FurutaniJun LuMuyi CaiHarukazu SuzukiWenkui YuXian-Yang QinPublished in: Journal of agricultural and food chemistry (2024)
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.
Keyphrases
- high fat diet
- liver injury
- oxidative stress
- drug induced
- weight gain
- signaling pathway
- diabetic rats
- insulin resistance
- adipose tissue
- stress induced
- body mass index
- ischemia reperfusion injury
- mouse model
- birth weight
- induced apoptosis
- pi k akt
- dna damage
- poor prognosis
- weight loss
- high fat diet induced
- type diabetes
- risk assessment
- physical activity
- cell proliferation
- protein kinase
- heat shock
- endoplasmic reticulum stress