School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China.
Periodicals Publishing Center, Beijing University of Chinese Medicine, Beijing, 100029, China.
Sci Rep. 2018 Nov 26;8(1):17362. doi: 10.1038/s41598-018-35791-9.
Maxing Ganshi Decoction (MXGSD) is used widely for asthma over thousands of years, but its underlying pharmacological mechanisms remain unclear. In this study, systematic and comprehensive network pharmacology was utilized for the first time to reveal the potential pharmacological mechanisms of MXGSD on asthma. Specifically, we collected 141 bioactive components from the 600 components in MXGSD, which shared 52 targets common to asthma-related ones. In-depth network analysis of these 52 common targets indicated that asthma might be a manifestation of systemic neuro-immuno-inflammatory dysfunction in the respiratory system, and MXGSD could treat asthma through relieving airway inflammation, improving airway remodeling, and increasing drug responsiveness. After further cluster and enrichment analysis of the protein-protein interaction network of MXGSD bioactive component targets and asthma-related targets, we found that the neurotrophin signaling pathway, estrogen signaling pathway, PI3K-Akt signaling pathway, and ErbB signaling pathway might serve as the key points and principal pathways of MXGSD gene therapy for asthma from a systemic and holistic perspective, and also provides a novel idea for the development of new drugs for asthma.
麻杏甘石汤(MXGSD)在治疗哮喘方面已有数千年的应用历史,但其中的潜在药理学机制尚不清楚。本研究首次采用系统全面的网络药理学方法来揭示 MXGSD 治疗哮喘的潜在药理学机制。具体来说,我们从 MXGSD 的 600 种成分中收集了 141 种生物活性成分,这些成分与哮喘相关的成分共享 52 个共同靶点。对这 52 个共同靶点的深入网络分析表明,哮喘可能是呼吸系统全身神经免疫炎症功能障碍的一种表现,而 MXGSD 可以通过缓解气道炎症、改善气道重塑和提高药物反应性来治疗哮喘。进一步对 MXGSD 生物活性成分靶点和哮喘相关靶点的蛋白质-蛋白质相互作用网络进行聚类和富集分析后,我们发现从系统和整体的角度来看,神经生长因子信号通路、雌激素信号通路、PI3K-Akt 信号通路和 ErbB 信号通路可能是 MXGSD 治疗哮喘的基因治疗的关键点和主要通路,为哮喘新药的开发提供了新的思路。