王琨, 颜海燕, 吴硕, 王辉强, 李玉环, 蒋建东. 清肺排毒汤的体外抗冠状病毒作用研究J. 药学学报, 2021,56(5): 1400-1408. doi: 10.16438/j.0513-4870.2020-1879
引用本文: 王琨, 颜海燕, 吴硕, 王辉强, 李玉环, 蒋建东. 清肺排毒汤的体外抗冠状病毒作用研究J. 药学学报, 2021,56(5): 1400-1408. doi: 10.16438/j.0513-4870.2020-1879
WANG Kun, YAN Hai-yan, WU Shuo, WANG Hui-qiang, LI Yu-huan, JIANG Jian-dong. Inhibitory effect of Qing-Fei-Pai-Du decoction on coronavirus in vitroJ. Acta Pharmaceutica Sinica, 2021,56(5): 1400-1408. doi: 10.16438/j.0513-4870.2020-1879
Citation: WANG Kun, YAN Hai-yan, WU Shuo, WANG Hui-qiang, LI Yu-huan, JIANG Jian-dong. Inhibitory effect of Qing-Fei-Pai-Du decoction on coronavirus in vitroJ. Acta Pharmaceutica Sinica, 2021,56(5): 1400-1408. doi: 10.16438/j.0513-4870.2020-1879

清肺排毒汤的体外抗冠状病毒作用研究

Inhibitory effect of Qing-Fei-Pai-Du decoction on coronavirus in vitro

  • 摘要: 清肺排毒汤由中医经典方剂组合而成,在新冠肺炎的治疗中发挥了重要作用。本研究主要考察了清肺排毒汤(Qing-Fei-Pai-Du decoction,QFPDD)对冠状病毒的抑制作用及其作用机制。本研究采用PrestoBlue细胞活性检测试剂检测QFPDD的细胞毒性;实时荧光定量PCR法(quantitive reverse transcription PCR,qRT-PCR)和免疫荧光法(immunofluorescence assay,IF)检测QFPDD在RNA和蛋白水平对冠状病毒的抑制作用;qRT-PCR检测QFPDD对冠状病毒吸附和穿入的作用;qRT-PCR检测QFPDD对干扰素(interferon,IFN)以及干扰素刺激基因(interferon stimulated genes,ISGs)的作用。本课题研究结果表明,在RNA和蛋白水平,QFPDD在无毒浓度下可剂量依赖性地抑制冠状病毒复制,时间进程分析发现,QFPDD主要在冠状病毒感染的早期阶段发挥作用。此外,初步机制研究表明,QFPDD一方面可以通过抑制病毒的吸附阻碍其入胞过程,另一方面QFPDD也通过上调IFN和ISGs的表达发挥抗病毒作用。本研究为QFPDD的临床应用提供了理论基础。

     

    Abstract: Qing-Fei-Pai-Du decoction (QFPDD) is a combination of traditional Chinese medicine and plays an important role in the treatment of coronavirus disease 2019 (COVID-19). This study investigated the inhibitory effect of QFPDD on coronavirus replication and antiviral mechanism. The cytotoxicity of QFPDD was determined by PrestoBlue cell viability assay. Quantitive reverse transcription PCR (qRT-PCR) and immunofluorescence assay (IF) were used to detect the inhibitory effects of QFPDD on coronavirus at RNA and protein levels. qRT-PCR was used to detect the adsorption and penetration of coronavirus after QFPDD treatment. The effects of QFPDD on interferon (IFN) and interferon-stimulated genes (ISGs) were also detected by qRT-PCR. The results showed that QFPDD inhibited coronavirus at RNA and protein levels in a dose-dependent manner at non-toxic concentration, and QFPDD targeted in the early stages of coronavirus infection cycle. Preliminary mechanism studies have shown that QFPDD can directly block the virus entry into the cell by inhibiting virus adsorption, and QFPDD can also play an antiviral role by up-regulating the expression of IFN and ISGs. These results indicate QFPDD as a drug potential to treat coronavirus infection.

     

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