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10.1038/s41598-021-92293-x

http://scihub22266oqcxt.onion/10.1038/s41598-021-92293-x
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suck abstract from ncbi


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pmid34140611      Sci+Rep 2021 ; 11 (1): 12787
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  • ELV-N32 and RvD6 isomer decrease pro-inflammatory cytokines, senescence programming, ACE2 and SARS-CoV-2-spike protein RBD binding in injured cornea #MMPMID34140611
  • Pham TL; He J; Kakazu AH; Calandria J; Do KV; Nshimiyimana R; Lam TF; Petasis NA; Bazan HEP; Bazan NG
  • Sci Rep 2021[Jun]; 11 (1): 12787 PMID34140611show ga
  • The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection that causes coronavirus disease 2019 (COVID-19) has resulted in a pandemic affecting the most vulnerable in society, triggering a public health crisis and economic collapse around the world. Effective treatments to mitigate this viral infection are needed. Since the eye is a route of virus entrance, we use an in vivo rat model of corneal inflammation as well as human corneal epithelial cells (HCEC) in culture challenged with IFNgamma as models of the eye surface to study this issue. We explore ways to block the receptor-binding domain (RBD) of SARS-CoV-2 Spike (S) protein to angiotensin-converting enzyme 2 (ACE2). We found that the lipid mediators, elovanoid (ELV)-N32 or Resolvin D6-isomer (RvD6i) decreased the expression of the ACE2 receptor, furin, and integrins in damaged corneas or IFNgamma-stimulated HCEC. There was also a concomitant decrease in the binding of Spike RBD with the lipid treatments. Using RNA-seq analysis, we uncovered that the lipid mediators also attenuated the expression of pro-inflammatoy cytokines participating in hyper-inflammation and senescence programming. Thus, the bioactivity of these lipid mediators will contribute to open therapeutic avenues to counteract virus attachment and entrance to the body.
  • |*Protein Domains[MESH]
  • |Angiotensin-Converting Enzyme 2/*metabolism[MESH]
  • |Animals[MESH]
  • |COVID-19/metabolism/virology[MESH]
  • |Cells, Cultured[MESH]
  • |Cellular Senescence/*drug effects[MESH]
  • |Corneal Injuries/*metabolism[MESH]
  • |Cytokines/*metabolism[MESH]
  • |Disease Models, Animal[MESH]
  • |Docosahexaenoic Acids/*analogs & derivatives/*pharmacology[MESH]
  • |Drug Discovery/*methods[MESH]
  • |Epithelial Cells/drug effects/metabolism[MESH]
  • |Epithelium, Corneal/cytology[MESH]
  • |Humans[MESH]
  • |Lipoxins/pharmacology[MESH]
  • |Male[MESH]
  • |Protein Binding[MESH]
  • |Rats[MESH]
  • |Rats, Sprague-Dawley[MESH]
  • |SARS-CoV-2/metabolism[MESH]
  • |Signal Transduction/*drug effects[MESH]
  • |Spike Glycoprotein, Coronavirus/chemistry/*metabolism[MESH]
  • |Virus Attachment/drug effects[MESH]


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