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Protective effect of baicalin on the regulation of Treg/Th17 balance, gut microbiota and short-chain fatty acids in rats with ulcerative colitis

机译:黄芩苷对溃疡性结肠炎大鼠TREG / TH17平衡,肠道微生物脂肪酸和短链脂肪酸调控的保护作用

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摘要

Baicalin is reported as an effective drug for ulcerative colitis (UC). However, its effect on gut microbiota and short-chain fatty acids (SCFAs) remains unknown. In this study, we investigated the role of baicalin on Th17/Treg balance, gut microbiota community, and SCFAs levels in trinitrobenzene sulphonic acid (TNBS)-induced UC rat model. We found the DAI scores were significantly increased in the TNBS-treated rats, while reduced in the baicalin-treated group in a dose-dependent manner, accompanied with the alleviation of mucosal injury, the reduction of ZO-1, Occludin, and MUC2 expression. At the meanwhile, baicalin repressed the increased levels of reactive oxygen species (ROS) and MDA, while deceased the GSH and SOD levels in colon tissue of rats treated with TNBS. On the other hand, administration of baicalin attenuated the TNBS-induced upregulations of Th17/Treg ratio, indicating a strong amelioration in the colorectal inflammation. More importantly, pyrosequencing of the V4 regions of 16S rRNA genes in rat feces revealed a deviation of the gut microbiota in response to baicalin treatment. In particular, the decreased Firmicutes-to-Bacteroidetes ratios and endotoxin-bearing Proteobacteria levels indicated that baicalin reversed TNBS-induced gut dysbiosis OTUs. In addition, we further investigated the fecal levels of major SCFAs in rats and found that baicalin significantly resorted the fecal butyrate levels in rats treated with TNBS. The increased butyrate levels were in consistent with the higher abundance of butyrate-producing species such as Butyricimonas spp., Roseburia spp., Subdoligranulum spp., and Eubacteriu spp. in baicalin-treated group. In conclusion, our findings suggest that baicalin possibly protected rats against ulcerative colitis by regulation of Th17/Treg balance, and modulation of both gut microbiota and SCFAs. Baicalin may be used as a prebiotic agent to treat ulcerative colitis-associated inflammation and gut dysbiosis.
机译:据报道,黄芩苷作为溃疡性结肠炎(UC)的有效药物。然而,它对肠道微生物群和短链脂肪酸(SCFA)的影响仍然未知。在这项研究中,我们研究了黄芩苷对Th17 / Treg平衡,肠道微生物群落和三硝基苯磺酸(TNB)诱导的UC大鼠模型中的SCFA水平的作用。在TNBS治疗的大鼠中发现DAI评分显着增加,同时以剂量依赖性方式在黄芩苷治疗组中减少,伴随着缓解粘膜损伤,减少ZO-1,occludin和MUC2表达。同时,黄芩苷抑制了活性氧物质(ROS)和MDA的增加水平,同时死于用TNB处理的大鼠的大鼠结肠组织中的GSH和SOD水平。另一方面,疾病诱导的TNICIN诱导的TN17 / TREG比率的上调,表明结直肠炎症中的强劲改善。更重要的是,大鼠粪便中16S rRNA基因的v4区域的焦磷酸测序显示肠道微生物酵母响应于黄芩苷处理的偏差。特别地,降低的致力致细胞率降低和内毒素承重的植物水平表明,黄芩苷逆转TNBS诱导的肠道脱肠病OTU。此外,我们进一步调查了大鼠的主要SCFA的粪便水平,发现黄芩苷在用TNB处理的大鼠中显着诉诸粪便丁酸碱水平。丁酸盐水平的增加与丁霉素生产种类的较高丰度,如丁霉素SPP。,Roseburia SPP,Subdoligranulum SPP。和eubacteriu spp。在黄芩苷治疗组中。总之,我们的研究结果表明,通过调节Th17 / Treg平衡和调节肠道微生物群和SCFA的调节,BACICALIN可能受到免受溃疡性结肠炎的大鼠。黄芩苷可以用作益生元剂以治疗溃疡性结肠炎相关的炎症和肠道脱泻。

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