School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Bei San Huan East Road, Beijing, 100029, China.
Pharmaceutical Informatics Institute, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, 310058, China.
Pharmacol Res. 2020 Jul;157:104820. doi: 10.1016/j.phrs.2020.104820. Epub 2020 Apr 29.
The Coronavirus Disease 2019 (COVID-19) pandemic has become a huge threaten to global health, which raise urgent demand of developing efficient therapeutic strategy. The aim of the present study is to dissect the chemical composition and the pharmacological mechanism of Qingfei Paidu Decoction (QFPD), a clinically used Chinese medicine for treating COVID-19 patients in China. Through comprehensive analysis by liquid chromatography coupled with high resolution mass spectrometry (MS), a total of 129 compounds of QFPD were putatively identified. We also constructed molecular networking of mass spectrometry data to classify these compounds into 14 main clusters, in which exhibited specific patterns of flavonoids (45 %), glycosides (15 %), carboxylic acids (10 %), and saponins (5 %). The target network model of QFPD, established by predicting and collecting the targets of identified compounds, indicated a pivotal role of Ma Xing Shi Gan Decoction (MXSG) in the therapeutic efficacy of QFPD. Supportively, through transcriptomic analysis of gene expression after MXSG administration in rat model of LPS-induced pneumonia, the thrombin and Toll-like receptor (TLR) signaling pathway were suggested to be essential pathways for MXSG mediated anti-inflammatory effects. Besides, changes in content of major compounds in MXSG during decoction were found by the chemical analysis. We also validate that one major compound in MXSG, i.e. glycyrrhizic acid, inhibited TLR agonists induced IL-6 production in macrophage. In conclusion, the integration of in silico and experimental results indicated that the therapeutic effects of QFPD against COVID-19 may be attributed to the anti-inflammatory effects of MXSG, which supports the rationality of the compatibility of TCM.
新型冠状病毒病(COVID-19)大流行已成为全球健康的巨大威胁,这迫切需要开发有效的治疗策略。本研究旨在剖析清肺排毒汤(QFPD)的化学成分和药理机制,QFPD 是一种在中国用于治疗 COVID-19 患者的临床中药。通过液相色谱与高分辨质谱联用(LC-HRMS)的综合分析,共推测出 129 种 QFPD 化合物。我们还构建了质谱数据的分子网络,将这些化合物分为 14 个主要簇,其中显示出黄酮类(45%)、糖苷类(15%)、羧酸类(10%)和皂苷类(5%)的特定模式。通过预测和收集鉴定化合物的靶点,建立 QFPD 的靶向网络模型,表明麻杏石甘汤(MXSG)在 QFPD 治疗功效中起着关键作用。支持性的,通过 LPS 诱导肺炎大鼠模型中 MXSG 给药后的转录组学分析,表明凝血酶和 Toll 样受体(TLR)信号通路是 MXSG 介导抗炎作用的重要途径。此外,通过化学分析发现 MXSG 在煎煮过程中主要化合物的含量发生变化。我们还验证了 MXSG 中的一种主要化合物,即甘草酸,可抑制 TLR 激动剂诱导的巨噬细胞中 IL-6 的产生。总之,计算和实验结果的综合表明,QFPD 治疗 COVID-19 的疗效可能归因于 MXSG 的抗炎作用,这支持了中药配伍的合理性。