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Angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers: potential allies in the COVID-19 pandemic instead of a threat?
Simko, Fedor; Baka, Tomas.
  • Simko F; Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava 81108, Slovak Republic.
  • Baka T; Third Department of Internal Medicine, Faculty of Medicine, Comenius University, Bratislava 83305, Slovak Republic.
Clin Sci (Lond) ; 135(8): 1009-1014, 2021 04 30.
Article in English | MEDLINE | ID: covidwho-1195632
ABSTRACT
Angiotensin-converting enzyme 2 (ACE2) is the leading player of the protective renin-angiotensin system (RAS) pathway but also the entry receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). RAS inhibitors seemed to interfere with the ACE2 receptor, and their safety was addressed in COVID-19 patients. Pedrosa et al. (Clin. Sci. (Lond.) (2021), 135, 465-481) showed in rats that captopril and candesartan up-regulated ACE2 expression and the protective RAS pathway in lung tissue. In culture of pneumocytes, the captopril/candesartan-induced ACE2 up-regulation was associated with inhibition of ADAM17 activity, counterbalancing increased ACE2 expression, which was associated with reduced SARS-CoV-2 spike protein entry. If confirmed in humans, these results could become the pathophysiological background for justifying RAS inhibitors as cornerstone cardiovascular protectives even during COVID-19 pandemic.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Angiotensin-Converting Enzyme Inhibitors / COVID-19 Limits: Animals / Humans Language: English Journal: Clin Sci (Lond) Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Angiotensin-Converting Enzyme Inhibitors / COVID-19 Limits: Animals / Humans Language: English Journal: Clin Sci (Lond) Year: 2021 Document Type: Article