免疫系统
急性胰腺炎
胰腺炎
生物
微生物学
免疫学
医学
胃肠病学
作者
Hao Chen,Xin Chen,Yan Ding,Qian Zhang,Wen Fu,Meixuan Wu,Feifei Ge,Jiangtuan Wang,LI Xiao-fen,Meiyu Geng,Jinheng Wang,Daolin Tang,Jinbao Liu
标识
DOI:10.1038/s41467-024-52398-z
摘要
Despite recent advances, severe acute pancreatitis (SAP) remains a lethal inflammation with limited treatment options. Here, we provide compelling evidence of GV-971 (sodium oligomannate), an anti-Alzheimer's medication, as being a protective agent in various male mouse SAP models. Microbiome sequencing, along with intestinal microbiota transplantation and mass cytometry technology, unveil that GV-971 reshapes the gut microbiota, increasing Faecalibacterium populations and modulating both peripheral and intestinal immune systems. A metabolomics analysis of cecal contents from GV-971-treated SAP mice further identifies short-chain fatty acids, including propionate and butyrate, as key metabolites in inhibiting macrophage M1 polarization and subsequent lethal inflammation by blocking the MAPK pathway. These findings suggest GV-971 as a promising therapeutic for SAP by targeting the microbiota metabolic immune axis.
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