Curcumin alleviated dextran sulfate sodium-induced ulcerative colitis via inhibition of the Wnt/(3-catenin signaling pathway and regulation of the differentiation of intestinal stem cells

被引:1
|
作者
Liang, Shaojie [1 ,2 ]
Wang, Kun [1 ]
Mao, Dabin [1 ]
Ouyang, Qianqian [2 ,3 ]
Lv, Xiaoping [4 ]
Xie, Liwei [5 ]
Zhu, Dajian [1 ]
机构
[1] Guangdong Med Univ, Shunde Maternal & Childrens Hosp, Maternal & Childrens Hlth Res Inst, Foshan 528300, Peoples R China
[2] Marine Biomed Res Inst Guangdong Zhanjiang, Zhanjiang 524023, Peoples R China
[3] Guangdong Med Univ, Marine Biomed Res Inst Guangdong Zhanjiang, Zhanjiang 524023, Peoples R China
[4] Guangxi Med Univ, Dept Gastroenterol, Affiliated Hosp 1, Nanning 530021, Peoples R China
[5] Guangdong Acad Sci, Inst Microbiol,Guangdong Open Lab Appl Microbiol, State Key Lab Appl Microbiol Southern China, Guangdong Prov Key Lab Microbial Culture Collect &, Guangzhou 510075, Peoples R China
关键词
Ulcerative colitis; Curcumin; Intestinal stem cell; Wnt/(3-catenin; SOX9;
D O I
10.1016/j.taap.2024.117175
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, we investigated the regulatory role of curcumin in the differentiation of intestinal stem cells (ISCs) in dextran sulfate sodium (DSS)-induced ulcerative colitis (UC) model mice and explored whether this effect was mediated by the Wnt/(3-catenin signaling pathway. We conducted experiments in DSS-induced UC model mice to observe changes in intestinal morphology through HE staining and detect the expression of key proteins in the Wnt/(3-catenin signaling pathway. According to these findings, curcumin was found to have a significant impact on the differentiation of ISCs. These results indicated that curcumin inhibited the Wnt/(3-catenin signaling pathway and restored ISC differentiation. The effects of curcumin on the Wnt/(3-catenin signaling pathway were further confirmed using Wnt/(3-catenin agonists. These findings provide a new perspective for understanding the behavior of ISCs in the context of inflammation and offer new insights into the development of novel therapeutic strategies and drugs for UC.
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页数:11
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