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10.1016/j.compbiomed.2021.104293

http://scihub22266oqcxt.onion/10.1016/j.compbiomed.2021.104293
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suck abstract from ncbi


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pmid33662681      Comput+Biol+Med 2021 ; 131 (ä): 104293
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  • Network pharmacology and RNA-sequencing reveal the molecular mechanism of Xuebijing injection on COVID-19-induced cardiac dysfunction #MMPMID33662681
  • He DD; Zhang XK; Zhu XY; Huang FF; Wang Z; Tu JC
  • Comput Biol Med 2021[Apr]; 131 (ä): 104293 PMID33662681show ga
  • BACKGROUND: Coronavirus disease 2019 (COVID-19) is an emerging infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Up to 20%-30% of patients hospitalized with COVID-19 have evidence of cardiac dysfunction. Xuebijing injection is a compound injection containing five traditional Chinese medicine ingredients, which can protect cells from SARS-CoV-2-induced cell death and improve cardiac function. However, the specific protective mechanism of Xuebijing injection on COVID-19-induced cardiac dysfunction remains unclear. METHODS: The therapeutic effect of Xuebijing injection on COVID-19 was validated by the TCM Anti COVID-19 (TCMATCOV) platform. RNA-sequencing (RNA-seq) data from GSE150392 was used to find differentially expressed genes (DEGs) from human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) infected with SARS-CoV-2. Data from GSE151879 was used to verify the expression of Angiotensin I Converting Enzyme 2 (ACE2) and central hub genes in both human embryonic-stem-cell-derived cardiomyocytes (hESC-CMs) and adult human CMs with SARS-CoV-2 infection. RESULTS: A total of 97 proteins were identified as the therapeutic targets of Xuebijing injection for COVID-19. There were 22 DEGs in SARS-CoV-2 infected hiPSC-CMs overlapped with the 97 therapeutic targets, which might be the therapeutic targets of Xuebijing injection on COVID-19-induced cardiac dysfunction. Based on the bioinformatics analysis, 7 genes (CCL2, CXCL8, FOS, IFNB1, IL-1A, IL-1B, SERPINE1) were identified as central hub genes and enriched in pathways including cytokines, inflammation, cell senescence and oxidative stress. ACE2, the receptor of SARS-CoV-2, and the 7 central hub genes were differentially expressed in at least two kinds of SARS-CoV-2 infected CMs. Besides, FOS and quercetin exhibited the tightest binding by molecular docking analysis. CONCLUSION: Our study indicated the underlying protective effect of Xuebijing injection on COVID-19, especially on COVID19-induced cardiac dysfunction, which provided the theoretical basis for exploring the potential protective mechanism of Xuebijing injection on COVID19-induced cardiac dysfunction.
  • |*RNA-Seq[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |COVID-19/*metabolism[MESH]
  • |Cell Line[MESH]
  • |Drugs, Chinese Herbal/*pharmacology[MESH]
  • |Gene Expression Regulation/*drug effects[MESH]
  • |Human Embryonic Stem Cells/metabolism/pathology/virology[MESH]
  • |Humans[MESH]
  • |Induced Pluripotent Stem Cells/metabolism/pathology/virology[MESH]
  • |Myocytes, Cardiac/*metabolism/pathology/virology[MESH]


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