GV-971 prevents severe acute pancreatitis by remodeling the microbiota-metabolic-immune axis

IF 3.784 3区 化学 Q1 Chemistry
Xi Chen, Xin Chen, Ding Yan, Na Zhang, Wen Fu, Meixuan Wu, Feifei Ge, Jiangtuan Wang, Xiaofen Li, Meiyu Geng, Jinheng Wang, Daolin Tang, Jinbao Liu
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引用次数: 0

Abstract

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.

Abstract Image

GV-971 通过重塑微生物群-代谢-免疫轴预防重症急性胰腺炎
尽管最近取得了一些进展,但重症急性胰腺炎(SAP)仍然是一种致命的炎症,治疗方法有限。在这里,我们提供了令人信服的证据,证明抗阿尔茨海默氏症药物 GV-971(低聚甘露酸钠)在各种雄性小鼠 SAP 模型中具有保护作用。微生物组测序以及肠道微生物群移植和质谱技术揭示,GV-971 能重塑肠道微生物群,增加粪杆菌数量,调节外周和肠道免疫系统。对经 GV-971 处理的 SAP 小鼠盲肠内容物进行的代谢组学分析进一步确定,丙酸和丁酸等短链脂肪酸是通过阻断 MAPK 通路抑制巨噬细胞 M1 极化和随后致命炎症的关键代谢物。这些研究结果表明,GV-971 可通过靶向微生物群代谢免疫轴来治疗 SAP。
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来源期刊
ACS Combinatorial Science
ACS Combinatorial Science CHEMISTRY, APPLIED-CHEMISTRY, MEDICINAL
自引率
0.00%
发文量
0
审稿时长
1 months
期刊介绍: The Journal of Combinatorial Chemistry has been relaunched as ACS Combinatorial Science under the leadership of new Editor-in-Chief M.G. Finn of The Scripps Research Institute. The journal features an expanded scope and will build upon the legacy of the Journal of Combinatorial Chemistry, a highly cited leader in the field.
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