Abstract
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.
Keywords:
Apelin; COVID-19; Renin-angiotensin system.
Copyright © 2020 Elsevier Ltd. All rights reserved.
MeSH terms
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Angiotensin I / metabolism
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Angiotensin II / biosynthesis
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Angiotensin II / blood
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Angiotensin II Type 1 Receptor Blockers / therapeutic use*
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Angiotensin-Converting Enzyme 2
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Angiotensin-Converting Enzyme Inhibitors / therapeutic use*
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Animals
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Apelin / metabolism
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Apelin / therapeutic use*
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Apelin Receptors / agonists
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Apelin Receptors / metabolism
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Apelin Receptors / therapeutic use*
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Betacoronavirus / metabolism*
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COVID-19
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COVID-19 Drug Treatment
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Coronavirus Infections / drug therapy*
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Coronavirus Infections / virology
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Drug Repositioning / methods
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Humans
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Mice
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Pandemics
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Peptide Fragments / metabolism
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Peptidyl-Dipeptidase A / metabolism*
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Pneumonia, Viral / drug therapy*
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Pneumonia, Viral / virology
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Receptor, Angiotensin, Type 1 / metabolism
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Renin-Angiotensin System / drug effects
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Renin-Angiotensin System / immunology
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SARS-CoV-2
Substances
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APLNR protein, human
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Angiotensin II Type 1 Receptor Blockers
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Angiotensin-Converting Enzyme Inhibitors
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Apelin
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Apelin Receptors
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Peptide Fragments
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Receptor, Angiotensin, Type 1
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Angiotensin II
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Angiotensin I
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Peptidyl-Dipeptidase A
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ACE2 protein, human
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Ace2 protein, mouse
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Angiotensin-Converting Enzyme 2
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angiotensin I (1-7)