Study on novel coronavirus pneumonia (COVID-19) mechanism by Huashi Baidu Formula based on network pharmacology
Objective: To explore novel coronavirus pneumonia (COVID-19) by the method of network pharmacology. Methods: The compounds contained in the Huashi Baidu Formula were searched by TCMSP database, the active components and their action targets were screened, and the proteins were standardized by Uni...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Editorial Board of Journal of Hainan Medical University
2020-06-01
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Series: | Journal of Hainan Medical University |
Subjects: | |
Online Access: | http://www.hnykdxxb.com/PDF/202011/02.pdf |
Summary: | Objective: To explore novel coronavirus pneumonia (COVID-19) by the method of network
pharmacology. Methods: The compounds contained in the Huashi Baidu Formula were
searched by TCMSP database, the active components and their action targets were screened,
and the proteins were standardized by Uniprot database, and the drug-active ingredienttarget
network was constructed by Cytoscape3.7.2 software. The targets related to COVID-
19 were screened by GeneCards database. STRING database and DAVID database were used
to construct and analyze PPI network, GO analysis and KEGG enrichment analysis(P < 0.05).
Results: The "drug-active ingredient-target" network of Huashi Baidu Formula consists of
176 components and 149targets, including AR, ESR1, PTGS2, PPARG, NOS2 and so on. 251
targets related to COVID-19. GO functional enrichment analysis showed that there were 179
biological processes, mainly related to inflammation, regulation of apoptosis and immune
response, and 82 KEGG related signaling pathways were obtained, including HIF-1, TNF,
small cell lung cancer, non-small cell lung cancer, tuberculosis, PI3K-Akt, NF- κ B, MAPK
and so on. Conclusion: Huashi Baidu Formula may regulate the immune and inflammatory
response of the body by acting on AR, ESR1, PTGS2, PPARG, NOS2 and other targets, which
is the result of multi-component, multi-target and multi-channel interaction. |
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ISSN: | 1007-1237 1007-1237 |