微泡
溃疡性结肠炎
下调和上调
结肠炎
治疗效果
肠道菌群
炎症
外体
巨噬细胞
药理学
调节器
免疫学
生物
炎症性肠病
小RNA
促炎细胞因子
信号转导
肠粘膜
骆驼奶
癌症研究
医学
化学
趋化因子
微生物学
功能性食品
作者
Siriguleng Yu,Chaoqun Liu,Hongqiang Yao,Zhijun Guo,Xiaoxuan Yan,Lijun Liu,Yang Xu,Qiuyue Yu
标识
DOI:10.1021/acs.jafc.5c11226
摘要
Camel milk contains abundant bioactive compounds, but the therapeutic potential of its exosomes as natural delivery systems for gut health remains unclear. This study investigated the therapeutic effects and underlying mechanisms of camel milk exosomes (CME) and their enriched miRNA cargo, miR-148a-3p, on dextran sodium sulfate (DSS)-induced ulcerative colitis (UC) in mice. Both CME and miR-148a-3p significantly alleviated colitis symptoms, including weight loss, colon shortening, and disease activity scores. These effects were achieved by suppressing pro-inflammatory cytokines and restoring intestinal barrier integrity through Zonula Occludens-1 (ZO-1) upregulation. Moreover, the treatments promoted M2 macrophage polarization, inhibited NF-κB signaling via silent information regulator T1 (SIRT1) upregulation and increased microbial diversity with the enrichment of beneficial taxa. Notably, the therapeutic effects of miR-148a-3p were comparable to those of CME, underscoring its role as a key functional component. These findings highlight CME as promising natural nanotherapeutics for UC, offering a novel, multitargeted strategy for managing intestinal inflammation.
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