Huo Zeqi, Li Junxiang, Li Xiaofeng, Xiao Han, Lin Yang, Ma Yuchan, Li Jiaru, Yang Hui, Zhang Chunjiang
School of Life Sciences, Lanzhou University, Lanzhou 730000, China; Key Laboratory of Cell Activities and Stress Adaptations, Ministry of Education, Lanzhou University, Lanzhou 730000, China; Gansu Key Laboratory of Biomonitoring and Bioremediation for Environmental Pollution, Lanzhou University, Lanzhou 730000, China.
Lanzhou University Second Hospital, Lanzhou, Gansu 730030, China.
Int J Biol Macromol. 2024 Jun;271(Pt 1):132580. doi: 10.1016/j.ijbiomac.2024.132580. Epub 2024 May 23.
Ulcerative colitis (UC) is a chronic inflammatory disease of the intestine that is significantly influenced by an imbalance in the gut microbiota. Astragalus membranaceus, particularly its polysaccharide components, has shown therapeutic potential for the treatment of UC, although the specific active constituents and their mechanistic pathways remain to be fully elucidated. In this study, we investigated two molecular weight fractions of Astragalus polysaccharides (APS), APS1 (Mw < 10 kDa) and APS2 (10 kDa < Mw < 50 kDa), isolated by ultrafiltration, focusing on their prebiotic effects, effects on UC, and the underlying mechanism. Our results showed that both APS1 and APS2 exhibit prebiotic properties, with APS1 significantly outperforming APS2 in ameliorating UC symptoms. APS1 significantly attenuated weight loss and UC manifestations, reduced colonic pathology, and improved intestinal mucosal barrier integrity. In addition, APS1 significantly reduced the levels of inflammatory cytokines in the serum and colonic tissue, and downregulated colonic chemokines. Furthermore, APS1 ameliorated dextran sulfate sodium salt (DSS)-induced intestinal dysbiosis by promoting the growth of beneficial microbes and inhibiting the proliferation of potential pathogens, leading to a significant increase in short-chain fatty acids. In conclusion, this study highlights the potential of APS1 as a novel prebiotic for the prevention and treatment of UC.
溃疡性结肠炎(UC)是一种肠道慢性炎症性疾病,受肠道微生物群失衡的显著影响。黄芪,特别是其多糖成分,已显示出治疗UC的潜力,尽管具体的活性成分及其作用机制仍有待充分阐明。在本研究中,我们研究了通过超滤分离得到的两种分子量级分的黄芪多糖(APS),即APS1(Mw < 10 kDa)和APS2(10 kDa < Mw < 50 kDa),重点关注它们的益生元效应、对UC的影响及其潜在机制。我们的结果表明,APS1和APS2均具有益生元特性,在改善UC症状方面,APS1显著优于APS2。APS1显著减轻体重减轻和UC表现,减轻结肠病理变化,并改善肠道黏膜屏障完整性。此外,APS1显著降低血清和结肠组织中炎症细胞因子的水平,并下调结肠趋化因子。此外,APS1通过促进有益微生物的生长和抑制潜在病原体的增殖,改善葡聚糖硫酸钠(DSS)诱导的肠道菌群失调,导致短链脂肪酸显著增加。总之,本研究突出了APS1作为预防和治疗UC的新型益生元的潜力。