State Key Laboratory of Respiratory Disease for Allergy at Shenzhen University, Shenzhen Key Laboratory of Allergy & Immunology, Shenzhen University School of Medicine, Shenzhen University, Shenzhen, 518020, China; Department of Respirology & Allergy. Third Affiliated Hospital of Shenzhen University. Shenzhen University, Shenzhen, 518020, China.
Musculoskeletal Research Laboratory, Department of Orthopaedics & Traumatology, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, 999077, Hong Kong, China.
Comput Biol Med. 2022 Sep;148:105845. doi: 10.1016/j.compbiomed.2022.105845. Epub 2022 Jul 14.
The emergence of the novel coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has led to millions of infections and is exerting an unprecedented impact on society and economies worldwide. The evidence showed that heart failure (HF) is a clinical syndrome that could be encountered at different stages during the progression of COVID-19. Shenfu injection (SFI), a traditional Chinese medicine (TCM) formula has been widely used for heart failure therapy in China and was suggested to treat critical COVID-19 cases based on the guideline for diagnosis and treatment of COVID-19 (the 7th version) issued by National Health Commission of the People's Republic of China. However, the active components, potential targets, related pathways, and underlying pharmacology mechanism of SFI against COVID-19 combined with HF remain vague.
To investigate the effectiveness and possible pharmacological mechanism of SFI for the prevention and treatment of COVID-19 combined with HF.
In the current study, a network analysis approach integrating active compound screening (drug-likeness, lipophilicity, and aqueous solubility models), target fishing (Traditional Chinese Medicine Systems Pharmacology, fingerprint-based Similarity Ensemble Approach, and PharmMapper databases), compound-target-disease network construction (Cytoscape software), protein-protein interaction network construction (STRING and Cytoscape software), biological process analysis (STRING and Cytoscape plug-in Clue GO) and pathway analysis (Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis) was developed to decipher the active ingredients, potential targets, relevant pathways, and the therapeutic mechanisms of SFI for preventing and treating COVID-19 combined with HF.
Finally, 20 active compounds (DL ≥ 0.18, 1≤Alog P ≤ 5, and -5≤LogS ≤ -1) and 164 relevant targets of SFI were identified related to the development of COVID-19 combined with HF, which were mainly involved in three biological processes including metabolic, hemostasis, and cytokine signaling in immune system. The C-T-D network and reactome pathway analysis indicated that SFI probably regulated the pathological processes of heart failure, respiratory failure, lung injury, and inflammatory response in patients with COVID-19 combined with HF through acting on several targets and pathways. Moreover, the venn diagram was used to identify 54 overlapped targets of SFI, COVID-19, and HF. KEGG pathway enrichment analysis showed that 54 overlapped targets were highly enriched to several COVID-19 and HF related pathways, such as IL-17 signaling pathway, Th17 cell differentiation, and NF-kappa B signaling pathway.
A comprehensive network analysis approach framework was developed to systematically elucidate the potential pharmacological mechanism of SFI for the prevention and treatment of SFI against COVID-19 combined with HF. The current study may not only provide in-depth understanding of the pharmacological mechanisms of SFI, but also a scientific basis for the application of SFI against COVID-19 combined with HF.
新型冠状病毒病 2019(COVID-19)的出现是由严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)引起的,导致了数百万人感染,并对全球社会和经济造成了前所未有的影响。有证据表明,心力衰竭(HF)是一种可以在 COVID-19 进展的不同阶段出现的临床综合征。参附注射液(SFI)是一种中药(TCM)配方,在中国已广泛用于心力衰竭治疗,并根据中华人民共和国国家卫生健康委员会发布的 COVID-19 诊断和治疗指南(第 7 版)建议用于治疗严重 COVID-19 病例。然而,SFI 对 COVID-19 合并 HF 的作用成分、潜在靶点、相关途径和潜在药理学机制仍不清楚。
探讨参附注射液防治 COVID-19 合并 HF 的有效性及可能的药理学机制。
本研究采用网络分析方法,整合活性化合物筛选(类药性、亲脂性和水溶性模型)、靶点捕捞(中药系统药理学、基于指纹的相似性集成方法和 PharmMapper 数据库)、化合物-靶点-疾病网络构建(Cytoscape 软件)、蛋白质-蛋白质相互作用网络构建(STRING 和 Cytoscape 软件)、生物过程分析(STRING 和 Cytoscape 插件 ClueGO)和通路分析(京都基因与基因组百科全书通路富集分析),以揭示 SFI 防治 COVID-19 合并 HF 的活性成分、潜在靶点、相关通路和治疗机制。
最终,确定了 20 种参附注射液的活性成分(DL≥0.18、1≤Alog P≤5 和-5≤LogS≤-1)和 164 个与 COVID-19 合并 HF 相关的潜在靶点,这些靶点主要涉及代谢、止血和细胞因子信号转导免疫三个生物学过程。C-T-D 网络和反应组通路分析表明,参附注射液可能通过作用于多个靶点和通路,调节 COVID-19 合并 HF 患者心力衰竭、呼吸衰竭、肺损伤和炎症反应的病理过程。此外,通过使用维恩图来识别参附注射液、COVID-19 和 HF 的 54 个重叠靶点。KEGG 通路富集分析表明,54 个重叠靶点高度富集到 COVID-19 和 HF 相关的多个通路,如 IL-17 信号通路、Th17 细胞分化和 NF-kappa B 信号通路。
本研究采用综合网络分析方法框架,系统阐明了参附注射液防治 COVID-19 合并 HF 的潜在药理学机制。本研究不仅可以深入了解参附注射液的药理学机制,还可为参附注射液防治 COVID-19 合并 HF 提供科学依据。