Ding Yuxuan, Chen Mingjun, Wang Qiying, Gao Lu, Feng Yang, Wang Shida, Song Zitian, Tong Zhanqi
Department of Traditional Chinese Medicine and Acupuncture, The Second Medical Centre, Chinese People's Liberation Army General Hospital, National Clinical Research Center for Geriatric Diseases, Beijing 100853, China.
The Graduate School of Chinese PLA General Hospital, Beijing 100853, China.
Evid Based Complement Alternat Med. 2020 Apr 20;2020:9521073. doi: 10.1155/2020/9521073. eCollection 2020.
Ulcerative colitis (UC) has multifactorial pathogenesis that acts synergistically, such as immune system dysregulation and expansion of infectious gut microbiota. Therefore, a multicomponent treatment derived from Chinese herbal medicine that interacts with multiple targets synergistically is needed. Composite sophora colon-soluble capsule (CSCC) is a Chinese herbal formula that has shown therapeutic efficacy against UC in randomized clinical trials. However, its bioactive components and potential target genes against UC remain unclear. Here, we used a network pharmacology approach to detect component-target-pathway interactions of CSCC against UC. A total of 29 gene targets, 91 bioactive components, and 20 enriched pathways of CSCC were identified. The IL-17 signaling pathway activated by infectious gastrointestinal microbes and predicted by the network analysis to be a major pathway modulated by CSCC against UC was studied in a dextran sulfate sodium-induced colitis model. CSCC showed remarkable efficacy against UC with respect to the attenuation of colon length, body weight loss, and disease activity index through gut microbiota recovery and intestinal immune homeostasis. The rectal administration of CSCC reduced the numbers of Th17 cells isolated from both mesenteric lymph nodes and lamina propria mononuclear cells and the levels of IL-17A, IL-6, IL-1, and TNF-. Additionally, the percentage of Treg cells and the levels of their hallmark cytokines were upregulated. Rectal administration of CSCC led to microbiota regulation with a significant correlation between suppression of Verrucomicrobiaceae and Ruminococcaceae, as well as the elevation of Lactobacillaceae, and CSCC administration via microbiome correlation heatmaps and cooccurrence network analysis at multiple time points. Thus, our study presents an effective herbal formula, CSCC, for UC treatment and explores its components and mechanisms of efficacy through the examination of gut microbiota and hallmark cytokines in the IL-17 pathway.
溃疡性结肠炎(UC)具有多因素协同作用的发病机制,如免疫系统失调和肠道感染性微生物群的扩张。因此,需要一种源自中药的多成分协同作用于多个靶点的治疗方法。复方苦参结肠溶胶囊(CSCC)是一种中药配方,在随机临床试验中已显示出对UC的治疗效果。然而,其针对UC的生物活性成分和潜在靶基因仍不清楚。在此,我们采用网络药理学方法来检测CSCC针对UC的成分-靶点-通路相互作用。共鉴定出CSCC的29个基因靶点、91种生物活性成分和20条富集通路。在葡聚糖硫酸钠诱导的结肠炎模型中,研究了由感染性胃肠道微生物激活并经网络分析预测为CSCC针对UC调节的主要通路的IL-17信号通路。CSCC通过恢复肠道微生物群和肠道免疫稳态,在减轻结肠长度、体重减轻和疾病活动指数方面显示出对UC的显著疗效。直肠给药CSCC减少了从肠系膜淋巴结和固有层单核细胞中分离出的Th17细胞数量以及IL-17A、IL-6、IL-1和TNF-的水平。此外,Treg细胞的百分比及其标志性细胞因子的水平上调。直肠给药CSCC导致微生物群调节,疣微菌科和瘤胃球菌科的抑制与乳酸杆菌科的升高之间存在显著相关性,并且通过在多个时间点的微生物组相关热图和共现网络分析进行CSCC给药。因此,我们的研究提出了一种用于UC治疗的有效中药配方CSCC,并通过检查肠道微生物群和IL-17通路中的标志性细胞因子来探索其成分和疗效机制。