Moxibustion treatment modulates the gut microbiota and immune function in a dextran sulphate sodium-induced colitis rat model

被引:68
作者
Qi, Qin [1 ]
Liu, Ya-Nan [1 ]
Jin, Xiao-Ming [2 ,3 ]
Zhang, Lin-Shuang [4 ]
Wang, Cun [1 ]
Bao, Chun-Hui [5 ]
Liu, Hui-Rong [5 ]
Wu, Huan-Gan [5 ]
Wang, Xiao-Mei [5 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Yueyang Clin Med Coll, Shanghai 200437, Peoples R China
[2] Indiana Univ Sch Med, Stark Neurosci Res Inst, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Dept Anat & Cell Biol, Indianapolis, IN 46202 USA
[4] Zhejiang Inst Food & Drug Control, Hangzhou 310052, Zhejiang, Peoples R China
[5] Shanghai Univ Tradit Chinese Med, Shanghai Res Inst Acupuncture Moxibust & Meridian, 650 South Wanping Rd, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金;
关键词
Ulcerative colitis; Moxibustion; 16S rRNA; Gut microbiome; Inflammatory cytokine; INFLAMMATORY-BOWEL-DISEASE; ULCERATIVE-COLITIS; FECAL MICROBIOTA; HUMAN HEALTH; FLORA; ELECTROACUPUNCTURE; COMMUNITIES; EXPRESSION; BACTERIA; MUCOSA;
D O I
10.3748/wjg.v24.i28.3130
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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-gamma, lipopolysaccharide, IgA, tumour necrosis factor-alpha 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-beta (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.
引用
收藏
页码:3130 / 3144
页数:15
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