Zhang Yu, Ji Wenting, Qin Hailong, Chen Zehong, Zhou Yinxing, Zhou Zhihong, Wang Jinglin, Wang Kaiping
Department of Pharmacy, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 430030 Wuhan, PR China; Hubei Province Clinical Research Center for Precision Medicine for Critical Illness, 430030 Wuhan, PR China.
Hubei Key Laboratory of Nature Medicinal Chemistry and Resource Evaluation, Tongji Medical College of Pharmacy, Huazhong University of Science and Technology, 430030 Wuhan, PR China.
Carbohydr Polym. 2025 Feb 1;349(Pt A):122829. doi: 10.1016/j.carbpol.2024.122829. Epub 2024 Oct 3.
Natural polysaccharides from Astragalus membranaceus have been shown to relieve ulcerative colitis (UC). However, the mechanism and causal relationship between the gut microbiota and Astragalus polysaccharides (APS) treatment of UC are unclear. The results of the present study showed that APS ameliorated colonic injury and the disruption of the gut microbiota and restored intestinal immune homeostasis in mice with DSS-induced colitis. Meanwhile, we found that APS treatment was ineffective in antibiotic-treated colitis mice but was effective when FMT (Fecal microbiota transplantation) was performed on UC mice using APS-treated mice as donors. APS increased the proportion of relevant microbiota that produce SCFAs and both direct administration of APS and administration of APS-adjusted gut microbiota significantly promoted the production of SCFAs in colitis mice. We demonstrated that APS dually inhibited NF-κB activation via the TLR4 and HDAC3 pathways and improved the balance in Th17/Treg cells in UC mice. In conclusion, our study revealed that APS is a promising prebiotic agent for the maintenance of intestinal health and demonstrated that APS may ameliorate colitis in a gut microbiota-dependent manner.
黄芪中的天然多糖已被证明可缓解溃疡性结肠炎(UC)。然而,肠道微生物群与黄芪多糖(APS)治疗UC之间的机制和因果关系尚不清楚。本研究结果表明,APS可改善DSS诱导的结肠炎小鼠的结肠损伤和肠道微生物群紊乱,并恢复肠道免疫稳态。同时,我们发现APS治疗在抗生素处理的结肠炎小鼠中无效,但当以APS处理的小鼠为供体对UC小鼠进行粪便微生物群移植(FMT)时有效。APS增加了产生短链脂肪酸(SCFA)的相关微生物群的比例,直接给予APS和给予经APS调节的肠道微生物群均显著促进了结肠炎小鼠中SCFA的产生。我们证明,APS通过TLR4和HDAC3途径双重抑制NF-κB激活,并改善UC小鼠中Th17/Treg细胞的平衡。总之,我们的研究表明,APS是一种有前途的益生元制剂,可维持肠道健康,并证明APS可能以肠道微生物群依赖的方式改善结肠炎。