Treatment of ulcerative colitis with Wu-Mei-Wan by inhibiting intestinal inflammatory response and repairing damaged intestinal mucosa

• Published in: Phytomedicine (Stuttgart) Vol. 105; p. 154362
• Main Authors: Yan, Shuguang, Wang, Ping, Wei, Hailiang, Jia, Rui, Zhen, Meijia, Li, Qian, Xue, Chang, Li, Jingtao
• Format: Journal Article
• Language: English
• Published: Elsevier GmbH 01-10-2022
• Subjects: Hippo/YAP pathway; Macrophages; Notch/NF-κB/NLRP3 pathway; Ulcerative colitis; Wu-Mei-Wan; WMW; PCNA; p-NF-kBp65; Notch/NF-κB/NLRP3 pathway; Macrophages; UC; IκB; NF-κB; p-IkBα; ISCs; CCL2; Wu-Mei-Wan; HPLC; CCR2; Hippo/YAP pathway; DSS; IL-1; H&E; DAI; STAT; TNF-α; IL-18; 5-ASA; Axin2; Lgr5; Ulcerative colitis; ELISA
• ISSN: 0944-7113; 1618-095X
• DOI: 10.1016/j.phymed.2022.154362

Wu-Mei-Wan (WMW), a traditional Chinese medicine, has been applied in the treatment of gastrointestinal diseases with long-term diarrhea and mucopurulent bloody stool as the main symptoms since ancient times. Studies have shown that WMW inhibits intestinal inflammation, repairs damaged intestinal mucosa, resists colon necrosis, and resists intestinal fibrosis. However, the specific mechanism of action is not yet clear.
Ulcerative colitis (UC), an intestinal disease with intestinal inflammation and injury as the main pathological manifestations, is one of the high-risk factors for colon cancer. Inhibiting the inflammatory response and promoting colonic epithelial repair are critical to the treatment of UC. However, there is still a lack of remedies with satisfactory curative effects. In this study, the role of WMW in dextran sulfate sodium (DSS)-induced colitis in mice and its related mechanisms are discussed from two aspects: intestinal inflammation and tissue repair.
DSS was used to induce colitis in mice and the therapeutic effect of WMW was analyzed by disease activity score, histopathological score, colon length measurement, serum cytokine detection, and flow cytometry. Macrophage activation and colonic stem cell proliferation were observed by immunohistochemistry. The expression of critical molecules in macrophage activation and colonic stem cell proliferation signaling pathways in colon tissue was detected with immunohistochemistry, immunofluorescence staining, RT-qPCR, and Western blot.
WMW could significantly alleviate DSS-induced colitis. We showed that WMW could reduce disease activity, reduce pathological scores, limit weight loss, inhibit colon shortening, inhibit inflammatory factor secretion, attenuate inflammatory response, and promote the repair of damaged colonic epithelium. WMW inhibited the activation of colonic macrophages, and its mechanism might be inhibiting the Notch/NF-κB/NLRP3 pathway; WMW promoted the proliferation of colonic stem cells, and its mechanism was associated with the regulation of the Hippo/YAP signaling pathway.
The results of this study suggested that WMW could treat UC via a mechanism that inhibited the intestinal inflammatory response and repaired damaged intestinal mucosa.