dc.creatorMalhotra, Atul
dc.creatorHepokoski, Mark
dc.creatorMcCowen, Karen C.
dc.creatorY-J Shyy, John
dc.date.accessioned2020-08-12T14:25:33Z
dc.date.accessioned2022-09-23T18:52:56Z
dc.date.available2020-08-12T14:25:33Z
dc.date.available2022-09-23T18:52:56Z
dc.date.created2020-08-12T14:25:33Z
dc.identifier2589-0042
dc.identifierhttps://doi.org/10.1016/j.isci.2020.101425
dc.identifierhttp://hdl.handle.net/20.500.12010/11857
dc.identifierhttps://doi.org/10.1016/j.isci.2020.101425
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3509072
dc.description.abstractCOVID-19 is becoming a leading cause of mortality throughout the world, and few effective therapies are currently available. Angiotensin converting enzyme 2 (ACE2) is essential to COVID-19 pathogenesis, as the binding of SARS-CoV-2 spike protein (S protein) is required for viral entry and development of COVID-19. ACE2 regulates the protective arm of the reninangiotensin-aldosterone system (RAAS) that endows anti-hypertensive and anti-inflammatory effects in the cardiovascular and pulmonary systems. Preclinical data suggest ACE2 might be downregulated after SARS-CoV-2 binding, and treatments that increase ACE2 may prevent cardiopulmonary injury. Development, testing, and mass production of novel ACE2 therapies may take years, while more effective treatments for COVID-19 are needed urgently. Metformin is a widely available anti-diabetic agent that has an excellent safety profile, and clinical and preclinical data suggest metformin may offer cardiopulmonary protection in COVID-19 via enhanced ACE2 expression.
dc.publisherISCIENCE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAbierto (Texto Completo)
dc.sourcereponame:Expeditio Repositorio Institucional UJTL
dc.sourceinstname:Universidad de Bogotá Jorge Tadeo Lozano
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subjectNovel ACE2
dc.titleACE2, Metformin, and COVID-19


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