粘蛋白
阿拉伯半乳聚糖
结肠炎
糖组学
聚糖
势垒函数
岩藻糖基化
微生物学
肠粘膜
多糖
毛螺菌科
化学
溃疡性结肠炎
细菌
生物
免疫学
生物化学
医学
糖蛋白
细胞生物学
内科学
遗传学
16S核糖体RNA
疾病
厚壁菌
作者
Tong Zhao,Sining Liu,Xiaoran Ma,Yang Shuai,Houde He,Tianfu Guo,Wenqi Huang,Qian Wang,Shan Liu,Zhongfu Wang,Guiping Gong,Linjuan Huang
标识
DOI:10.1016/j.carbpol.2024.121882
摘要
Structurally defined arabinogalactan (LBP-3) from Lycium barbarum have effect on improving intestinal barrier function. However, whether its intestinal barrier function depended on the changes of intestinal mucin O-glycans have not been investigated. A dextran sodium sulfate-induced acute colitis mouse model was employed to test prevention and treatment with LBP-3. The intestinal microbiota as well as colonic mucin O-glycan profiles were analyzed. Supplementation with LBP-3 inhibited harmful bacteria, including Desulfovibrionaceae, Enterobacteriaceae, and Helicobacteraceae while significantly increased the abundance of beneficial bacteria (e.g., Lachnospiraceae, Ruminococcaceae, and Lactobacillaceae). Notably, LBP-3 augmented the content of neutral O-glycans by stimulating the fucosylation glycoforms (F1H1N2 and F1H2N2), short-chain sulfated O-glycans (S1F1H1N2, S1H1N2, and S1H2N3), and sialylated medium- and long-chain O-glycans (F1H2N2A1, H2N3A1, and F1H3N2A1). In summary, we report that supplement LBP-3 significantly reduced pathological symptoms, restored the bacterial community, and promoted the expression of O-glycans to successfully prevent and alleviate colitis in a mouse model, especially in the LBP-3 prevention testing group. The underlying mechanism of action was investigated using glycomics to better clarify which the structurally defined LBP-3 were responsible for its beneficial effect against ulcerative colitis and assess its use as a functional food or pharmaceutical supplement.
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