| Literature DB >> 35403089 |
Junfeng Cao1, Lianglei Li2, Li Xiong1, Chaochao Wang1, Yijun Chen1, Xiao Zhang2.
Abstract
Purpose Pulmonary fibrosis caused by COVID-19 pneumonia is a serious complication of COVID-19 infection, there is a lack of effective treatment methods clinically. This article explored the mechanism of action of berberine in the treatment of COVID-19 (Corona Virus Disease 2019, COVID-19) pneumonia pulmonary fibrosis with the help of the network pharmacology and molecular docking. Methods We predicted the role of berberine protein targets with the Pharmmapper database and the 3D structure of berberine in the Pubchem database. And GeneCards database was used in order to search disease target genes and screen common target genes. Then we used STRING web to construct PPI interaction network of common target protein. The common target genes were analyzed by GO and KEGG by DAVID database. The disease-core target gene-drug network was established and molecular docking was used for prediction. We also analyzed the binding free energy and simulates molecular dynamics of complexes. Results Berberine had 250 gene targets, COVID-19 pneumonia pulmonary fibrosis had 191 gene targets, the intersection of which was 23 in common gene targets. Molecular docking showed that berberine was associated with CCl2, IL-6, STAT3 and TNF-α. GO and KEGG analysis reveals that berberine mainly plays a vital role by the signaling pathways of influenza, inflammation and immune response. Conclusion Berberine acts on TNF-α, STAT3, IL-6, CCL2 and other targets to inhibit inflammation and the activation of fibrocytes to achieve the purpose of treating COVID-19 pneumonia pulmonary fibrosis.Entities:
Keywords: ARDS, acute respiratory distress syndrome; BP, biological process; Berberine; CC, cellular component; CCL2, chemokine ligand2; COVID-19; COVID-19 pneumonia; COVID-19, corona virus disease 2019; ECM, extracellular matrix; EMT, epithelial-mesenchymal cell transformation; FOXM1, forkhead box M1; Fsp1, fibroblast-specific protein 1; GO, gene ontology; HIF-1, hypoxia inducible factor; IBD, inflammatory bowel disease; IL-12, interleukin 12; IL-6, interleukin 6; JAK, Janus kinase; KEGG, Kyoto encyclopedia of genes and genomes; LR-MSCs, mesenchymal stem cells; MF, molecular function; MMP14, matrix metalloproteinase 14; MMP7, matrix metalloproteinase 7; Molecular docking; NF-κB, nuclear transcription factor; NOS, nitric oxide synthase; Network pharmacology; OTUB1, deubiquitinase; PAI-1, plasminogen activator inhibitor 1; PPI, protein-protein interaction; Pulmonary fibrosis; STAT3, transcription activator; TGF-β, transforming growth factor-β; TNF-α, tumor necrosis factor-α; sIL-6R, interleukin 6 receptor; α-SMA, α-smooth muscle actin
Year: 2022 PMID: 35403089 PMCID: PMC8895682 DOI: 10.1016/j.phyplu.2022.100252
Source DB: PubMed Journal: Phytomed Plus ISSN: 2667-0313