Wang Zihao, Linghu Ke-Gang, Hu Yuanjia, Zuo Huali, Yi Hao, Xiong Shi-Hang, Lu Jinjian, Chan Ging, Yu Hua, Huang Run-Yue
State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macau, China.
Department of Rheumatology and Immunology, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, China.
Front Pharmacol. 2019 Sep 23;10:1065. doi: 10.3389/fphar.2019.01065. eCollection 2019.
Rheumatoid arthritis is a chronic inflammatory autoimmune disease, causing articular and extra-articular dysfunctions among patients, and it could result in irreversible joint damages or disability if untreated. A traditional Chinese medicine formula, Huayu-Qiangshen-Tongbi (HT) formula, has been observed successful in controlling rheumatoid arthritis progression in traditional Chinese medicine clinics. In this study, we conducted a systematic analysis of the HT formula with a purpose of proposing for its potential mechanism of action using network pharmacological methods. The potential targets of the formula were collected and screened according to the topological features of their protein-protein interaction network, and we subsequently validated our prediction results through experiments. We proposed that the HT formula could interfere with the bone metabolism and the inflammatory pathways of the body. The experimental validation results indicated that HT formula could exhibit anti-inflammatory effects by regulating several signaling pathways specifically the Toll-like receptor signaling pathway, phosphoinositide-3-kinase-Akt signaling pathway, hypoxia-inducible factor 1 signaling pathway, mitogen-activated protein kinase signaling pathway and activator protein 1 signaling pathway.
类风湿性关节炎是一种慢性炎症性自身免疫疾病,可导致患者出现关节及关节外功能障碍,若不治疗可导致不可逆转的关节损伤或残疾。在中医临床实践中,一种中药配方——化瘀强身通痹(HT)方,已被观察到在控制类风湿性关节炎进展方面取得成功。在本研究中,我们对HT方进行了系统分析,目的是利用网络药理学方法揭示其潜在作用机制。根据其蛋白质-蛋白质相互作用网络的拓扑特征收集并筛选该配方的潜在靶点,随后通过实验验证我们的预测结果。我们提出HT方可能会干扰机体的骨代谢和炎症途径。实验验证结果表明,HT方可以通过调节多种信号通路发挥抗炎作用,特别是Toll样受体信号通路、磷脂酰肌醇-3-激酶-蛋白激酶B信号通路、缺氧诱导因子1信号通路、丝裂原活化蛋白激酶信号通路和活化蛋白1信号通路。