Jing Yongshuai, Wang Ziying, Cheng Wenjing, Fan Hanju, Zheng Kaiyan, Zheng Yuguang, Wu Lanfang
College of Chemical and Pharmaceutical Engineering, Hebei University of Science and Technology, 26 Yuxiang Street, Shijiazhuang 050018, China.
College of Pharmacy, Hebei University of Chinese Medicine, 3 Xingyuan Road, Shijiazhuang 050200, China.
Foods. 2025 Feb 23;14(5):753. doi: 10.3390/foods14050753.
Ulcerative colitis (UC) is on the rise all over the world. polysaccharide (ZOP-1) has good anti-inflammatory and antioxidant effects, but the therapeutic effect and mechanism of ZOP-1 on UC are still unclear.
ZOP-1 obtained by water extraction and alcohol precipitation was analyzed by methylation and NMR. At the same time, the mechanism of ZOP-1 in the treatment of UC was clarified by hematoxylin-eosin (HE) staining, metagenomics, immunohistochemistry, and protein blot (Wb).
ZOP-1 was the structure of the by →4,6)-β-Glcp-1→ and →3,6)-α-Galp-(1→ constitute the main chain, there were two branched chain by →4)-β-Glcp(1→, and α-Araf(1→ as the end group. ZOP-1 significantly improved the shortening and thickening of the colon, changed the index of immune organs, inhibited the production of inflammatory factors in mice with ulcerative colitis, changed the intestinal flora of mice, increased the content of short-chain fatty acids (SCFAs) in the intestine, and controlled the TLR4/NF-κB/MAPK signaling pathway, thus preventing and treating DSS-induced ulcerative colitis in mice.
ZOP-1 alleviated UC by controlling the expression of cytokines, thereby reducing intestinal inflammation and oxidative stress, enhancing intestinal integrity, modulating intestinal flora, and regulating the levels of SCFAs.
溃疡性结肠炎(UC)在全球范围内呈上升趋势。多糖(ZOP-1)具有良好的抗炎和抗氧化作用,但ZOP-1对UC的治疗效果及机制仍不清楚。
采用水提醇沉法获得ZOP-1,并通过甲基化和核磁共振进行分析。同时,通过苏木精-伊红(HE)染色、宏基因组学、免疫组织化学和蛋白质印迹(Wb)阐明ZOP-1治疗UC的机制。
ZOP-1的结构由→4,6)-β-Glcp-1→和→3,6)-α-Galp-(1→构成主链,有两条由→4)-β-Glcp(1→和α-Araf(1→作为端基的支链。ZOP-1显著改善了结肠炎小鼠结肠的缩短和增厚,改变了免疫器官指数,抑制了溃疡性结肠炎小鼠炎症因子的产生,改变了小鼠肠道菌群,增加了肠道中短链脂肪酸(SCFAs)的含量,并调控了TLR4/NF-κB/MAPK信号通路,从而防治了葡聚糖硫酸钠(DSS)诱导的小鼠溃疡性结肠炎。
ZOP-1通过控制细胞因子的表达减轻UC,从而减轻肠道炎症和氧化应激,增强肠道完整性,调节肠道菌群,并调节SCFAs水平。