Xuesanqi ameliorates DSS-induced colitis in mice by mediating gut microbiota dysbiosis and modulating MAPK/ERK/JNK pathway

被引:0
作者
Su, Qiyuan [1 ]
Hu, Qian [2 ]
Wu, Songtao [3 ]
Yang, Suqin [4 ]
Su, Hanwen [5 ]
Zhang, Zhengjun [6 ,7 ,8 ]
Ling, Chengxiu [1 ]
机构
[1] Xian Jiaotong Liverpool Univ, Wisdom Lake Acad Pharm, Suzhou 215123, Jiangsu, Peoples R China
[2] Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Wuhan 430016, Hubei, Peoples R China
[3] Hubei Univ Chinese Med, Fac Pharm, 16 Huangjiahu West Rd, Wuhan 430065, Hubei, Peoples R China
[4] South Cent Minzu Univ, Sch Pharmaceut Sci, Wuhan 430074, Hubei, Peoples R China
[5] Wuhan Univ, Renmin Hosp, Dept Clin Lab, Wuhan 430060, Hubei, Peoples R China
[6] Univ Wisconsin Madison, Dept Stat, Madison, WI 53706 USA
[7] Univ Chinese Acad Sci, Chinese Acad Sci, Ctr Forecasting Sci, Sch Econ & Management, Beijing 100049, Peoples R China
[8] Univ Chinese Acad Sci, Chinese Acad Sci, Ctr Forecasting Sci, MOE Social Sci Lab Digital Econ Forecasts & Policy, Beijing 100049, Peoples R China
关键词
Colitis; Xuesanqi; Gut microbiota; Short chain fatty acids (SCFas); MAPK/ERK/JNK signaling pathway; Tight junction (TJ) protein; PANAX-NOTOGINSENG SAPONINS; ULCERATIVE-COLITIS; KAPPA-B; INFLAMMATION; BACTERIA;
D O I
10.1007/s13659-024-00482-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study aimed to evaluate the therapeutic properties of the traditional Chinese medicine Xuesanqi (XSQ, from the rhizome of Polygonum amplexicaule D. Don) in treating ulcerative colitis. We hypothesized that its many active components can alleviate symptoms of colitis by regulating the gut microbiota, its metabolites, and various signaling pathways. To test our hypotheses, we designed a DSS- induced colitis model in C57BL/6 male mice. Apparent metrics were evaluated in each group of mice and performed histological analysis of relevant tissues. The gut microbial composition was analyzed by 16S rRNA sequencing of bacteria. Simultaneously, the SCFAs content was detected by gas chromatography, inflammatory factor secretion was evaluated by ELISA or western-blot, the expression of tight junction protein and key proteins of the MAPK signaling pathway were analyzed by western-blot. Our result showed that the treatment with XSQ alleviated significant various symptoms such as weight loss, blood in stool, and shortening of colon. In addition, XSQ treatment restored the dysregulated gut microbiota in colitis mice, increased short chain fatty acids (SCFAs) and normalized the MAPK/ERK/JNK signaling pathways, promoted expression of tight junction protein Occludin, Claudin-1, and E-cadherin proteins. Furthermore, we also observed a dose-dependent pattern in these treatment responses. These findings demonstrated the active components of XSQ is a promising new treatment platform for ulcerative colitis.
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页数:17
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