补充低聚果糖可缓解 DSS 诱导的急性结肠炎小鼠的病理性免疫反应,防止肠道屏障受损。

Fructooligosaccharide supplementation alleviated the pathological immune response and prevented the impairment of intestinal barrier in DSS-induced acute colitis mice.

机构信息

Department of Medical Laboratory, School of Medicine, Hunan Normal University, Changsha 410013, China.

School of Life Science, Hunan Normal University, Changsha 410018, China.

出版信息

Food Funct. 2021 Oct 19;12(20):9844-9854. doi: 10.1039/d1fo01147b.

Abstract

The dysbiosis of gut microbiota is closely related to the occurrence and development of inflammatory bowel disease (IBD). The manipulation of intestinal flora through prebiotics or probiotics is expected to induce and maintain the remission of IBD symptoms. 6-week-old C57BL/J mice were daily gavaged with fructooligosaccharides (FOS) or the synbiotic two weeks before the administration of dextran sulfate sodium (DSS). The supplementation of FOS or synbiotic could significantly ameliorate the body weight loss and colon histological damage in DSS-induced acute colitis mice. The altered composition of gut microbiota in acute colitis mice was reversed by FOS or Synbiotic supplementation, with a characteristic of decreased abundance of . Both FOS and synbiotic mitigated DSS-induced loss of mucus protein (MUC2) and epithelium tight junction proteins (ZO-1, Occluding, Claudin1) in colon mucosa. The expression of pro-inflammatory cytokines (IL-6 and TNF-α) was decreased by FOS or synbiotic treatment, while the expression of Tbx21 and IL-10 was increased. The results suggested that the modulation of gut microbiota by FOS or synbiotic supplementation could decrease the inflammation potential of colonized commensals, which prevented the impairment of the intestinal barrier and induced a regulation of immune response in DSS-induced acute colitis mice.

摘要

肠道微生物群落的失调与炎症性肠病(IBD)的发生和发展密切相关。通过使用益生元或益生菌来操纵肠道菌群,有望诱导和维持 IBD 症状的缓解。在给予葡聚糖硫酸钠(DSS)之前两周,每天用低聚果糖(FOS)或合生元对 6 周龄 C57BL/J 小鼠进行灌胃。FOS 或合生元的补充可显著改善 DSS 诱导的急性结肠炎小鼠的体重减轻和结肠组织学损伤。FOS 或合生元的补充可逆转急性结肠炎小鼠肠道微生物群落的组成改变,其特征为丰度降低。FOS 和合生元均减轻了 DSS 诱导的结肠黏膜中粘蛋白(MUC2)和上皮紧密连接蛋白(ZO-1、Occluding、Claudin1)的丢失。FOS 或合生元处理可降低促炎细胞因子(IL-6 和 TNF-α)的表达,而增加 Tbx21 和 IL-10 的表达。结果表明,通过 FOS 或合生元补充来调节肠道微生物群落可以降低定植共生菌的炎症潜能,从而防止肠道屏障受损,并在 DSS 诱导的急性结肠炎小鼠中诱导免疫反应的调节。

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