Shaanxi Natural Carbohydrate Resource Engineering Research Center, College of Food Science and Technology, Northwest University, Xi'an 710069, China.
Tianren Goji Biotechnology Co., Ltd, Ningxia, China.
Carbohydr Polym. 2024 Apr 15;330:121882. doi: 10.1016/j.carbpol.2024.121882. Epub 2024 Jan 28.
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.
结构定义的枸杞阿拉伯半乳聚糖(LBP-3)对改善肠道屏障功能有作用。然而,其肠道屏障功能是否依赖于肠道粘蛋白 O-聚糖的变化尚未被研究。本研究采用葡聚糖硫酸钠诱导的急性结肠炎小鼠模型来测试 LBP-3 的预防和治疗作用。分析了肠道微生物群和结肠粘蛋白 O-聚糖谱。补充 LBP-3 可抑制有害细菌,包括脱硫弧菌科、肠杆菌科和螺旋杆菌科,而显著增加有益细菌(如lachnospiraceae、瘤胃球菌科和乳杆菌科)的丰度。值得注意的是,LBP-3 通过刺激岩藻糖基化糖型(F1H1N2 和 F1H2N2)、短链硫酸化 O-聚糖(S1F1H1N2、S1H1N2 和 S1H2N3)和唾液酸化中长链 O-聚糖(F1H2N2A1、H2N3A1 和 F1H3N2A1)来增加中性 O-聚糖的含量。总之,我们报告补充 LBP-3 可显著减轻病理症状,恢复细菌群落,并促进 O-聚糖的表达,成功预防和缓解结肠炎小鼠模型中的疾病,特别是在 LBP-3 预防试验组中。通过糖组学研究其作用机制,以更好地阐明结构定义的 LBP-3 对溃疡性结肠炎的有益作用及其作为功能性食品或药物补充剂的用途。