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乌梅丸通过调节巨噬细胞极化改善小鼠溃疡性结肠炎。

Wu-Mei-Wan Ameliorates Murine Ulcerative Colitis by Regulating Macrophage Polarization.

作者信息

Yan Shuguang, Wei Hailiang, Jia Rui, Zhen Meijia, Bao Shengchuan, Wang Wenba, Liu Fanrong, Li Jingtao

机构信息

College of Basic Medicine, Shaanxi University of Chinese Medicine, Xianyang, China.

Key Laboratory of Gastrointestinal Diseases and Prescriptions in Shaanxi Province, Shaanxi University of Chinese Medicine, Xianyang, China.

出版信息

Front Pharmacol. 2022 Mar 21;13:859167. doi: 10.3389/fphar.2022.859167. eCollection 2022.

DOI:10.3389/fphar.2022.859167
PMID:35387334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8978603/
Abstract

An increasing body of evidence shows that macrophages play an important role in the pathogenesis of ulcerative colitis (UC). Macrophage polarization and changes in related signaling pathways are reported to have a protective effect on intestinal inflammation. The well-known Chinese medicine Wumeiwan (WMW) has been used to treat diarrhea, one of the main symptoms of colitis, for more than 2,000 years. Increasing evidence shows that WMW can inhibit intestinal inflammation and repair damaged intestinal mucosa, but its effector mechanisms are unknown. Therefore, we studied the prophylactic effects of WMW in dextran sulfate sodium (DSS)-induced UC and its effects on macrophage mechanisms and polarization. The results show that colitis was significantly alleviated in mice in the WMW group, and the secretion and expression of pro-inflammatory factors TNF-, IL-1, and IL-6 were inhibited in the serum and colonic tissues of mice with WMW-treated colitis, whereas anti-inflammatory factors IL-10, Arg-1, and TGF-1 were increased. Subsequent studies found that WMW could inhibit M1 polarization and promote M2 polarization in colonic macrophages in DSS-induced colitis mice. Network pharmacology was used to predict potential targets and pathways, and further studies confirmed the related targets The results showed that WMW gradually inhibits the activation of the P38MAPK and NF-κB signaling pathways and further activates the STAT6 signaling pathway. In summary, WMW interferes with the p38MAPK, NF-κB and STAT6 signaling pathways to regulate M1/M2 polarization in macrophages, thereby protecting mice against DSS-induced colitis.

摘要

越来越多的证据表明,巨噬细胞在溃疡性结肠炎(UC)的发病机制中起重要作用。据报道,巨噬细胞极化及相关信号通路的变化对肠道炎症具有保护作用。著名的中药乌梅丸(WMW)用于治疗结肠炎的主要症状之一腹泻已有2000多年的历史。越来越多的证据表明,WMW可以抑制肠道炎症并修复受损的肠黏膜,但其作用机制尚不清楚。因此,我们研究了WMW对葡聚糖硫酸钠(DSS)诱导的UC的预防作用及其对巨噬细胞机制和极化的影响。结果表明,WMW组小鼠的结肠炎明显减轻,WMW治疗的结肠炎小鼠血清和结肠组织中促炎因子TNF-、IL-1和IL-6的分泌及表达受到抑制,而抗炎因子IL-10、Arg-1和TGF-1则增加。随后的研究发现,WMW可以抑制DSS诱导的结肠炎小鼠结肠巨噬细胞的M1极化并促进M2极化。利用网络药理学预测潜在靶点和通路,进一步研究证实了相关靶点。结果表明,WMW逐渐抑制P38MAPK和NF-κB信号通路的激活,并进一步激活STAT6信号通路。综上所述,WMW通过干扰p38MAPK、NF-κB和STAT6信号通路来调节巨噬细胞的M1/M2极化,从而保护小鼠免受DSS诱导的结肠炎。

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