Gong Xinwei, Cai Wanshuang, Yang Dezhao, Wang Wei, Che Hongxia, Li Hongyan
College of Marine Science and Biological Engineering, Shandong Provincial Key Laboratory of Biochemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
College of Marine Science and Biological Engineering, Shandong Provincial Key Laboratory of Biochemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Int J Biol Macromol. 2025 Jan;286:138525. doi: 10.1016/j.ijbiomac.2024.138525. Epub 2024 Dec 6.
An arabinogalactan (ICPA) was extracted from the medicinal and edible plant Ixeris chinensis (Thunb.) Nakai., and ICPA exhibited excellent immunomodulatory activity. In this research, the impact of ICPA on DSS-induced ulcerative colitis was investigated. The results indicated that ICPA ameliorated the symptoms of colitis mice including loss of body weight, decrease of disease activity index, shortness of colon length and reduction of spleen index that caused by DSS. After treatment with ICPA, inflammatory cell infiltration and crypt loss were alleviated, and the number of goblet epithelial cells was enriched. ICPA inhibited the overproduction of TNF-α, IL-1β, and NLRP3, and promoted the secretion of IL-10 in colon tissues. Meanwhile, the intestinal barrier integrity was restored through increasing the expression of ZO-1 and occludin. ICPA could also regulate the structure of gut microbiota through elevating the abundance of Turicibacter and Bifidobacterium, and decreasing the ratio of Bacteroidetes/Firmicutes. In addition, ICPA improved the depression-like behavior of UC mice, and reduced the expression of proteins NLRP3, GFAP, and Iba-1 in brain tissues. These results suggested ICPA had an alleviative effect on UC and accompanied depression-like behavior, and could be developed as a dietary supplement for the prevention and treatment of UC.
从药食两用植物中华苦荬菜(Ixeris chinensis (Thunb.) Nakai.)中提取了一种阿拉伯半乳聚糖(ICPA),且ICPA表现出优异的免疫调节活性。在本研究中,考察了ICPA对葡聚糖硫酸钠(DSS)诱导的溃疡性结肠炎的影响。结果表明,ICPA改善了结肠炎小鼠的症状,包括体重减轻、疾病活动指数降低、结肠长度缩短以及由DSS引起的脾脏指数下降。用ICPA治疗后,炎症细胞浸润和隐窝丢失得到缓解,杯状上皮细胞数量增加。ICPA抑制了结肠组织中肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和NLRP3的过量产生,并促进了白细胞介素-10(IL-10)的分泌。同时,通过增加紧密连接蛋白1(ZO-1)和闭合蛋白的表达恢复了肠道屏障完整性。ICPA还可通过提高Turicibacter和双歧杆菌的丰度以及降低拟杆菌门/厚壁菌门的比例来调节肠道微生物群的结构。此外,ICPA改善了溃疡性结肠炎小鼠的抑郁样行为,并降低了脑组织中NLRP3、胶质纤维酸性蛋白(GFAP)和离子钙结合衔接分子1(Iba-1)的蛋白表达。这些结果表明,ICPA对溃疡性结肠炎及伴发的抑郁样行为具有缓解作用,可开发为预防和治疗溃疡性结肠炎的膳食补充剂。