波形蛋白
上皮-间质转换
肿瘤坏死因子α
溃疡性结肠炎
医学
结肠炎
脂多糖
药理学
免疫学
化学
免疫组织化学
内科学
癌症
疾病
转移
作者
Yaxin Qi,Meng Wang,Lijuan Chai,Min Zhang,Sitong Jia,Nuttapong Wichai,Lin Wang,Yujing Wang,Jixiang Song,Han Zhang,Yi Wang,Peng Zhang,Lin Miao
标识
DOI:10.1097/hm9.0000000000000064
摘要
Objective: To investigate the inhibitory effect and mechanism of Wei Chang An pill (WCA) on ulcerative colitis (UC). Methods: A 2,4,6-trinitro-benzenesulfonic acid (TNBS)-induced UC model was established, and WCA was administered orally for 1 week. Body weight, colon length, disease activity index (DAI) score, and colon mucosa damage index (CMDI) score were recorded. Cytokine expression in lipopolysaccharide (LPS)-stimulated THP-1 cells was evaluated to determine the anti-inflammatory effects of WCA and its active ingredients. Immunohistochemistry and immunofluorescence were performed to detect the expression of epithelial-mesenchymal transition (EMT) markers E-cadherin and vimentin in rat UC and WCA groups, and in Caco-2 cells stimulated with conditioned medium (CM) from THP-1 cells, with or without LPS or WCA. Results: WCA significantly inhibited body weight loss, decreased DAI and CMDI scores, blocked colon length shortening, and improved histological damage in UC rats. Furthermore, both myeloperoxidase (MPO) activities and cytokine expression in UC tissues were significantly suppressed by WCA as well. In THP-1 cells, the mRNA expression of interferon-inducible protein (IP)-10, tumor necrosis factor-α (TNF-α), interleukin (IL)-6, and NF-κB inhibitor α (IκBα) was significantly suppressed by WCA and its active ingredients. E-cadherin expression in UC rats and CM-stimulated Caco-2 cells was downregulated and vimentin expression was upregulated, whereas both were blocked when administered with WCA. Conclusions: Our data showed that WCA alleviated UC progression by inhibiting inflammation-induced EMT progression. Graphical abstract: http://links.lww.com/AHM/A56
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