Yeh Yuan-Chieh, Doan Ly Hien, Huang Zi-Yi, Chu Li-Wei, Shi Tzu-Hau, Lee Ying-Ray, Wu Cheng-Tao, Lin Chao-Hsiung, Chiang Shu-Tuan, Liu Hui-Kang, Chuang Tsung-Hsien, Ping Yueh-Hsin, Liu Hsiao-Sheng, Huang Chi-Ying F
Department of Traditional Chinese Medicine, Chang Gung Memorial Hospital, Keelung, Taiwan.
Program in Molecular Medicine, College of Life Sciences, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Front Pharmacol. 2022 Mar 25;12:765553. doi: 10.3389/fphar.2021.765553. eCollection 2021.
COVID-19 is threatening human health worldwide but no effective treatment currently exists for this disease. Current therapeutic strategies focus on the inhibition of viral replication or using anti-inflammatory/immunomodulatory compounds to improve host immunity, but not both. Traditional Chinese medicine (TCM) compounds could be promising candidates due to their safety and minimal toxicity. In this study, we have developed a novel bioinformatics workflow that integrates multiple databases to predict the use of honeysuckle () and Huangqi () as potential anti-SARS-CoV-2 agents. Using extracts from honeysuckle and Huangqi, these two herbs upregulated a group of microRNAs including , , and , which are critical to reduce the pathogenesis of SARS-CoV-2. Moreover, these herbs suppressed pro-inflammatory cytokines including IL-6 or TNF-α, which were both identified in the cytokine storm of acute respiratory distress syndrome, a major cause of COVID-19 death. Furthermore, both herbs partially inhibited the fusion of SARS-CoV-2 spike protein-transfected BHK-21 cells with the human lung cancer cell line Calu-3 that was expressing ACE2 receptors. These herbs inhibited SARS-CoV-2 M activity, thereby alleviating viral entry as well as replication. In conclusion, our findings demonstrate that honeysuckle and Huangqi have the potential to be used as an inhibitor of SARS-CoV-2 virus entry that warrants further analysis and functional assessment of miRNAs to confirm their clinical importance. This fast-screening platform can also be applied to other drug discovery studies for other infectious diseases.
新型冠状病毒肺炎正在全球范围内威胁人类健康,但目前尚无针对该疾病的有效治疗方法。当前的治疗策略主要集中在抑制病毒复制或使用抗炎/免疫调节化合物来提高宿主免疫力,但无法兼顾二者。中药化合物因其安全性和低毒性,有望成为治疗药物的候选者。在本研究中,我们开发了一种新型生物信息学工作流程,整合多个数据库来预测金银花和黄芪作为潜在抗新型冠状病毒药物的用途。使用金银花和黄芪的提取物,这两种草药上调了一组微小RNA,包括miR-122-5p、miR-148a-3p和miR-223-3p,这些微小RNA对于降低新型冠状病毒的致病性至关重要。此外,这些草药抑制了包括白细胞介素-6或肿瘤坏死因子-α在内的促炎细胞因子,这两种细胞因子均在急性呼吸窘迫综合征的细胞因子风暴中被发现,而急性呼吸窘迫综合征正是新型冠状病毒肺炎死亡的主要原因。此外,这两种草药均部分抑制了表达血管紧张素转换酶2受体的人肺癌细胞系Calu-3与新型冠状病毒刺突蛋白转染的BHK-21细胞的融合。这些草药抑制了新型冠状病毒M蛋白的活性,从而减轻了病毒的侵入和复制。总之,我们的研究结果表明,金银花和黄芪有潜力作为新型冠状病毒病毒侵入的抑制剂,这需要对微小RNA进行进一步分析和功能评估,以确认它们的临床重要性。这个快速筛选平台也可应用于其他传染病的药物发现研究。