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首页> 外文期刊>World Journal of Gastroenterology >Moxibustion treatment modulates the gut microbiota and immune function in a dextran sulphate sodium-induced colitis rat model
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Moxibustion treatment modulates the gut microbiota and immune function in a dextran sulphate sodium-induced colitis rat model

机译:艾灸治疗可调节葡聚糖硫酸钠诱导的结肠炎大鼠模型的肠道菌群和免疫功能

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AIM To investigate the effect and mechanism of moxibustion in rats with ulcerative colitis. METHODS A rat colitis model was established by administering 4% dextran sulphate sodium solution. Seventy male rats were randomly divided into seven groups: Healthy controls (HC), ulcerative colitis model group (UC), UC with 7 d of moxibustion (UC-7), UC with 14 d of moxibustion (UC-14), UC with mesalazine gavage (UC-W), HC with 7 d of moxibustion (HC-7), HC with 14 d of moxibustion (HC-14). Moxibustion was applied to the bilateral Tianshu (ST25). Gut microbiome profiling was conducted by 16S rRNA amplicon sequencing, and PCR and ELISA determined the expression of inflammatory cytokines in colon mucosa and serum, respectively. RESULTS Moxibustion treatment restored the colonic mucosa and decreased submucosal inflammatory cell infiltration in colitis rats. Rats treated with moxibustion and mesalazine had significantly lower levels of the dominant phyla Proteobacteria and the genera Saccharibacteria , Sphingomonas and Barnesiella than colitis rats, and they could restore the microbiome to levels similar to those observed in healthy rats. UC rats had reduced alpha diversity, which could be alleviated by moxibustion therapy, and UC-7 had a higher alpha diversity than UC-14. This finding suggests that short-term (7 d) but no longer term (14 d) moxibustion treatment may significantly affect the gut microbiome. The potential bacterial functions affected by moxibustion may be ascorbate and aldarate metabolism, and amino acid metabolism. Compared with HC group, the levels of the cytokines interleukin-12 (IL-12) ( P < 0.05) and IL-6, IL-17, IL-23, interferon-γ, lipopolysaccharide, IgA, tumour necrosis factor-α and its receptors 1 (TNFR1) and TNFR2 ( P < 0.01) were all increased, whereas anti-inflammatory cytokine IL-2 and IL-10 ( P < 0.01) and transforming growth factor-β ( P < 0.05) were decreased in UC rats. These changes were reversed by moxibustion. CONCLUSION Our findings suggest that moxibustion exerts its therapeutic effect by repairing mucosal tissue damage and modulating the gut microbiome and intestinal mucosal immunity.
机译:目的探讨艾灸对溃疡性结肠炎大鼠的治疗作用及其机制。方法采用4%的葡聚糖硫酸钠溶液建立大鼠结肠炎模型。将70只雄性大鼠随机分为7组:健康对照组(HC),溃疡性结肠炎模型组(UC),加艾灸7 d的UC(UC-7),加艾灸14 d的UC(UC-14),加艾灸的UC。美沙拉嗪管(UC-W),HC灸7 d(HC-7),HC灸14 d(HC-14)。艾灸应用于双边天枢(ST25)。通过16S rRNA扩增子测序进行肠道微生物组谱分析,PCR和ELISA分别测定了结肠黏膜和血清中炎性细胞因子的表达。结果艾灸治疗可恢复结肠炎大鼠的结肠黏膜并减少其黏膜下炎性细胞浸润。用艾灸和美沙拉嗪治疗的大鼠的肠道菌群,糖杆菌属,鞘氨醇单胞菌和巴氏杆菌属的水平明显低于结肠炎大鼠,并且可以使微生物组恢复到与健康大鼠相似的水平。 UC大鼠的α多样性降低,可通过艾灸疗法缓解,并且UC-7的α多样性高于UC-14。该发现表明短期(7 d)但不长期(14 d)的艾灸治疗可能会显着影响肠道微生物组。受艾灸影响的潜在细菌功能可能是抗坏血酸和藻酸盐代谢以及氨基酸代谢。与HC组相比,细胞因子IL-12,IL-6,IL-17,IL-23,干扰素-γ,脂多糖,IgA,肿瘤坏死因子-α和IL-6水平(P <0.05)。 UC大鼠其受体1(TNFR1)和TNFR2(P <0.01)均增加,而抗炎细胞因子IL-2和IL-10(P <0.01)和转化生长因子-β(P <0.05)降低。 。艾灸逆转了这些变化。结论我们的研究结果表明,艾灸通过修复粘膜组织损伤,调节肠道微生物组和肠道粘膜免疫来发挥其治疗作用。

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