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10.1016/j.yjmcc.2020.06.007

http://scihub22266oqcxt.onion/10.1016/j.yjmcc.2020.06.007
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32562701!7299869!32562701
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suck abstract from ncbi

pmid32562701      J+Mol+Cell+Cardiol 2020 ; 145 (ä): 84-87
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  • Apelin-potential therapy for COVID-19? #MMPMID32562701
  • Saeedi Saravi SS; Beer JH
  • J Mol Cell Cardiol 2020[Aug]; 145 (ä): 84-87 PMID32562701show ga
  • We believe that, in parallel to the attempts for direct blockade of the SARS-CoV-2 penetration into host cell and repurposing drugs, finding new therapeutic strategies for patients with lung injury or cardiovascular complications/coagulopathies associated with COVID-19 should be paid particular attention. Apelin or its receptor agonists are of great potential treatment for COVID-19 through suppressing angiotensin-converting enzyme (ACE) and angiotensin II (Ang-II) production, as well as, down-regulating angiotensin receptor 1 (AT1R) and ACE2 up-regulation. These drugs have potential to improve acute lung injury and cardiovascular/coagulopathy complications in COVID-19 which are associated with elevated Ang-II/Ang(1-7) ratio.
  • |Angiotensin I/metabolism[MESH]
  • |Angiotensin II Type 1 Receptor Blockers/*therapeutic use[MESH]
  • |Angiotensin II/biosynthesis/blood[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Angiotensin-Converting Enzyme Inhibitors/*therapeutic use[MESH]
  • |Animals[MESH]
  • |Apelin Receptors/agonists/metabolism/*therapeutic use[MESH]
  • |Apelin/metabolism/*therapeutic use[MESH]
  • |Betacoronavirus/*metabolism[MESH]
  • |COVID-19[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |Coronavirus Infections/*drug therapy/virology[MESH]
  • |Drug Repositioning/methods[MESH]
  • |Humans[MESH]
  • |Mice[MESH]
  • |Pandemics[MESH]
  • |Peptide Fragments/metabolism[MESH]
  • |Peptidyl-Dipeptidase A/*metabolism[MESH]
  • |Pneumonia, Viral/*drug therapy/virology[MESH]
  • |Receptor, Angiotensin, Type 1/metabolism[MESH]
  • |Renin-Angiotensin System/drug effects/immunology[MESH]


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