亚精胺
益生元
结肠炎
转录组
化学
肠道菌群
生物化学
生物
信号转导
粪便
抗生素
多胺
细胞生物学
低聚糖
炎症性肠病
微生物学
细胞因子
新陈代谢
作者
Yijin Cai,J Sun,S. R. Wayne Chen,Dafeng Wang,Yulei Jing,Xin Jin,Zhen Li,Caiming Li,Xiaofeng Ban
标识
DOI:10.1021/acs.jafc.5c16297
摘要
Agarotriose (A3), a marine-derived oligosaccharide from agar, has shown anti-inflammatory potential, yet the involvement of gut microbiota remains incompletely understood. Using a dextran sulfate sodium-induced colitis mouse model combined with antibiotic depletion and fecal microbiota transplantation, we found that the protective effects of A3 were largely dependent on the gut microbiota. Integrated multiomics analyses indicated that A3 preferentially enriched Akkermansia muciniphila and was associated with increased intraluminal spermidine levels. Spermidine abundance correlated with A. muciniphila enrichment and improvement of colitis-related phenotypes. In vitro, A3 promoted the growth of A. muciniphila and enhanced spermidine production. Transcriptomic and cellular analyses further suggested that spermidine attenuated inflammatory responses, at least in part, through modulation of the PI3K/AKT/NF-κB signaling pathway. Collectively, these results support a potential “A3– A. muciniphila –spermidine–host signaling” axis and suggest that A3 may serve as a promising marine-derived prebiotic for intestinal health.
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