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
{"title":"胃肠安丸通过抑制上皮-间质转化过程减轻2,4,6-三硝基苯磺酸诱导的溃疡性结肠炎","authors":"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","doi":"10.1097/HM9.0000000000000064","DOIUrl":null,"url":null,"abstract":"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","PeriodicalId":93856,"journal":{"name":"Acupuncture and herbal medicine","volume":"280 1","pages":"107 - 115"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Wei Chang An pill alleviates 2,4,6-trinitro-benzenesulfonic acid-induced ulcerative colitis by inhibiting epithelial-mesenchymal transition process\",\"authors\":\"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\",\"doi\":\"10.1097/HM9.0000000000000064\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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. 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引用次数: 2
摘要
目的:探讨胃肠安丸对溃疡性结肠炎(UC)的抑制作用及其机制。方法:建立2,4,6-三硝基苯磺酸(TNBS)致UC模型,口服WCA 1周。记录体重、结肠长度、疾病活动指数(DAI)评分、结肠黏膜损伤指数(CMDI)评分。通过观察脂多糖(LPS)刺激THP-1细胞中细胞因子的表达,确定WCA及其有效成分的抗炎作用。采用免疫组织化学和免疫荧光法检测UC组和WCA组大鼠上皮间质转化(EMT)标志物E-cadherin和vimentin的表达,以及THP-1细胞条件培养基(CM)刺激Caco-2细胞(LPS或WCA)的表达。结果:WCA显著抑制UC大鼠体重减轻,降低DAI和CMDI评分,阻断结肠长度缩短,改善UC大鼠组织学损伤。此外,WCA还能显著抑制UC组织中髓过氧化物酶(MPO)活性和细胞因子表达。WCA及其有效成分显著抑制THP-1细胞中干扰素诱导蛋白(IP)-10、肿瘤坏死因子-α (TNF-α)、白细胞介素(IL)-6、NF-κB抑制剂α (i -κB α) mRNA表达。在UC大鼠和cm刺激的Caco-2细胞中,E-cadherin表达下调,vimentin表达上调,而在WCA的作用下,两者均被阻断。结论:我们的数据显示WCA通过抑制炎症诱导的EMT进展来缓解UC进展。图形摘要:http://links.lww.com/AHM/A56
Wei Chang An pill alleviates 2,4,6-trinitro-benzenesulfonic acid-induced ulcerative colitis by inhibiting epithelial-mesenchymal transition process
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