eLife · 2020 · 149 citations · 31 references
MedicinePharmacologyPharmacotherapyCardiovascular PharmacotherapyPharmacodynamicsRenal PathophysiologyAcute Respiratory Distress SyndromeCardiac MedicationsRespiratory PharmacologyCovid-19-associated Acute Respiratory Distress SyndromeRenin-angiotensin System InhibitorsRenin-angiotensin-aldosterone System ActivationRenin-angiotensin-aldosterone System BlockadeRenin-angiotensin-aldosterone System InhibitionRenin-angiotensin-aldosterone System InhibitorsSars-cov-2 InfectionSevere Acute Respiratory Syndrome
The discovery of angiotensin converting enzyme-2 (ACE-2) as the receptor for SARS- CoV-2 (Severe Acute Respiratory Syndrome Coronavirus-2) has implicated the renin-angiotensin-aldosterone system in acute respiratory distress syndrome (ARDS) and respiratory failure in patients with coronavirus disease-19 (COVID-19). The angiotensin converting enzyme-1–angiotensin II–angiotensin AT 1 receptor pathway contributes to the pathophysiology of ARDS, whereas activation of the ACE-2–angiotensin(1-7)-angiotensin AT 2 receptor and the ACE-2–angiotensin(1-7)–Mas receptor pathways have been shown to be protective. Here we propose and discuss therapeutic considerations how to increase soluble ACE-2 in plasma in order for ACE-2 to capture and thereby inactivate SARS-CoV-2. This could be achieved by administering recombinant soluble ACE-2. We also discuss why and how ACEIs and ARBs provide cardiovascular, renal and also pulmonary protection in SARS-CoV-2- associated ARDS. Discontinuing these medications in COVID-19 patients may therefore potentially be harmful.
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