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甘露寡糖通过调节LGALS3治疗炎症性肠病的新型抗炎特性。

Novel anti-inflammatory properties of mannose oligosaccharides in the treatment of inflammatory bowel disease via LGALS3 modulation.

作者信息

Du Yaqi, Fan Yan, Li Xin, Chen Fenqin

机构信息

Department of Gastroenterology, The First Hospital of China Medical University, Shenyang, P.R. China.

Department of Pediatrics, The First Hospital of China Medical University, Shenyang, P.R. China.

出版信息

NPJ Biofilms Microbiomes. 2025 Feb 8;11(1):26. doi: 10.1038/s41522-025-00648-3.

Abstract

This study investigates the role of Gum Arabic Mannose Oligosaccharides (GA-MOS) in modulating gut microbiota and alleviating symptoms of Inflammatory Bowel Disease (IBD). Employing both in vitro and in vivo models, we explored how GA-MOS influences microbial communities, particularly focusing on their capacity to enhance health-associated bacteria and reduce pathogenic species within the gut environment. Our findings reveal that GA-MOS treatment significantly altered the gut microbiota composition, increasing the abundance of anti-inflammatory bacteria while decreasing pro-inflammatory species, thus contributing to a reduction in gut inflammation and an improvement in intestinal barrier function. Detailed molecular analyses further demonstrated that these changes in microbiota were associated with modifications in the host's immune response, particularly through the suppression of key inflammatory pathways and cytokines involved in IBD progression. These results underscore the potential of dietary polysaccharides like GA-MOS as therapeutic agents in managing dysbiosis and inflammatory conditions in the gut, offering a promising approach for enhancing microbial health and overall disease management in IBD. This study provides novel insights into the bioactive properties of MOS and their interactions with gut microbiota, suggesting broader implications for their use in microbiome-centered therapies.

摘要

本研究调查了阿拉伯胶甘露寡糖(GA-MOS)在调节肠道微生物群和缓解炎症性肠病(IBD)症状中的作用。我们采用体外和体内模型,探究了GA-MOS如何影响微生物群落,特别关注其在肠道环境中增强与健康相关细菌并减少致病物种的能力。我们的研究结果表明,GA-MOS处理显著改变了肠道微生物群的组成,增加了抗炎细菌的丰度,同时减少了促炎物种,从而有助于减轻肠道炎症并改善肠道屏障功能。详细的分子分析进一步表明,微生物群的这些变化与宿主免疫反应的改变有关,特别是通过抑制IBD进展中涉及的关键炎症途径和细胞因子。这些结果强调了像GA-MOS这样的膳食多糖作为治疗肠道菌群失调和炎症性疾病的治疗剂的潜力,为改善IBD中的微生物健康和整体疾病管理提供了一种有前景的方法。本研究为MOS的生物活性特性及其与肠道微生物群的相互作用提供了新的见解,表明其在以微生物群为中心的治疗中的应用具有更广泛的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4656/11806110/4b657cd6968f/41522_2025_648_Fig1_HTML.jpg

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