Using gut microbiota and non-targeted metabolomics techniques to study the effect of xylitol on alleviating DSS-induced inflammatory bowel disease in mice.

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Peng Ma, Wen Sun, Chang Sun, Jiajun Tan, Xueyun Dong, Jiayuan He, Asmaa Ali, Min Chen, Leilei Zhang, Liang Wu, Pingping Wang
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引用次数: 0

Abstract

Background: Inflammatory bowel disease (IBD) has become a global healthcare issue, with its incidence continuing to rise, but currently there is no complete cure. Xylitol is a widely used sweetener in various foods and beverages, but there is limited research on the effects of xylitol on IBD symptoms.

Aim: Study on the effect of oral xylitol in improving intestinal inflammation and damage in IBD mice, further explore the mechanism of xylitol in alleviating IBD symptoms using intestinal microbiota and non-targeted metabolomics techniques.

Methods: An IBD mouse model was induced using sodium dextran sulfate (DSS). After 30 days of oral administration of xylitol, we assessed the disease activity index (DAI) scores of mice in each group. The expression levels of inflammatory factors in the colon tissues were measured using qPCR. Additionally, we examined the damage to the intestinal mucosa and tight junction structures through HE staining and immunohistochemical staining. Finally, the alterations in the gut microbiota of the mice were analyzed using 16S rDNA sequencing technology.The production of three main short-chain fatty acids (SCFAs, including acetate, propionic acid and butyric acid) in feces and the changes of serum metabolomics were measured by non-targeted metabolomics techniques.

Results: The findings indicated that xylitol effectively mitigated weight loss and improved the DAI score in mice with IBD. Moreover, xylitol reduced the expressions of Caspase-1, IL-1β, and TNF-α in the colon tissue of the mice, and increased the expressions of ZO-1 and occludin in intestinal mucosal. Xylitol could enhance the variety of intestinal bacteria in IBD mice and influenced the abundance of different bacterial species. Additionally, metabolomic analysis revealed that oral xylitol increased the levels of three main SCFAs in the feces of IBD mice, while also impacting serum metabolites.

Conclusions: Our findings suggest that xylitol can help improve IBD symptoms. Xylitol can improve the intestinal flora of IBD mice and increase the production of SCFAs to play an anti-inflammatory role and protect the mucosal tight junction barrier. These discoveries present a fresh prophylactic treatment of IBD.

Clinical trial number: Not applicable.

利用肠道微生物群和非靶向代谢组学技术研究木糖醇对减轻dss诱导的小鼠炎症性肠病的作用。
背景:炎症性肠病(IBD)已成为一个全球性的卫生保健问题,其发病率持续上升,但目前还没有完全治愈。木糖醇是一种广泛用于各种食品和饮料的甜味剂,但关于木糖醇对IBD症状影响的研究有限。目的:研究口服木糖醇对IBD小鼠肠道炎症和损伤的改善作用,利用肠道菌群和非靶向代谢组学技术进一步探讨木糖醇缓解IBD症状的机制。方法:用葡聚糖硫酸钠(DSS)建立IBD小鼠模型。口服木糖醇30天后,对各组小鼠进行疾病活动指数(DAI)评分。采用qPCR检测结肠组织中炎症因子的表达水平。此外,我们还通过HE染色和免疫组织化学染色检测了肠黏膜和紧密连接结构的损伤。最后,使用16S rDNA测序技术分析小鼠肠道微生物群的变化。采用非靶向代谢组学技术检测粪便中3种主要短链脂肪酸(SCFAs,包括乙酸、丙酸和丁酸)的生成以及血清代谢组学的变化。结果:木糖醇能有效减轻IBD小鼠的体重减轻,提高DAI评分。木糖醇降低小鼠结肠组织Caspase-1、IL-1β和TNF-α的表达,增加肠黏膜ZO-1和occludin的表达。木糖醇可以增加IBD小鼠肠道细菌的多样性,影响不同细菌种类的丰度。此外,代谢组学分析显示,口服木糖醇增加了IBD小鼠粪便中三种主要SCFAs的水平,同时也影响了血清代谢物。结论:我们的研究结果表明木糖醇可以帮助改善IBD症状。木糖醇可以改善IBD小鼠肠道菌群,增加SCFAs的产生,起到抗炎作用,保护粘膜紧密连接屏障。这些发现为IBD提供了一种新的预防性治疗方法。临床试验号:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Immunology
BMC Immunology 医学-免疫学
CiteScore
5.50
自引率
0.00%
发文量
54
审稿时长
1 months
期刊介绍: BMC Immunology is an open access journal publishing original peer-reviewed research articles in molecular, cellular, tissue-level, organismal, functional, and developmental aspects of the immune system as well as clinical studies and animal models of human diseases.
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