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Corn Oligopeptide Alleviates Nonalcoholic Fatty Liver Disease by Regulating the Sirtuin Signaling Pathway.
Xu, Yali; Su, Ting; Mishra, Hricha; Ando, Reiko; Furutani, Yutaka; Lu, Jun; Cai, Muyi; Suzuki, Harukazu; Yu, Wenkui; Qin, Xian-Yang.
Afiliação
  • Xu Y; Laboratory for Cellular Function Conversion Technology, RIKEN Center for Integrative Medical Sciences, Yokohama 2300045, Japan.
  • Su T; Department of Intensive Care Unit, The Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing 210008, China.
  • Mishra H; Department of Intensive Care Unit, The Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing 210008, China.
  • Ando R; Laboratory for Cellular Function Conversion Technology, RIKEN Center for Integrative Medical Sciences, Yokohama 2300045, Japan.
  • Furutani Y; Support Unit for Bio-Material Analysis, Research Resources Division, RIKEN Center for Brain Science, Wako 3510106, Japan.
  • Lu J; Department of Laboratory Medicine, The Jikei University School of Medicine, Tokyo 1058461, Japan.
  • Cai M; China National Research Institute of Food and Fermentation Industries, Beijing 100016, China.
  • Suzuki H; China National Research Institute of Food and Fermentation Industries, Beijing 100016, China.
  • Yu W; Laboratory for Cellular Function Conversion Technology, RIKEN Center for Integrative Medical Sciences, Yokohama 2300045, Japan.
  • Qin XY; Department of Intensive Care Unit, The Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing 210008, China.
J Agric Food Chem ; 72(12): 6360-6371, 2024 Mar 27.
Article em En | MEDLINE | ID: mdl-38489847
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sirtuínas / Hepatopatia Gordurosa não Alcoólica Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sirtuínas / Hepatopatia Gordurosa não Alcoólica Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article