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Drugs Modulating Renin-Angiotensin System in COVID-19 Treatment. | LitMetric

Drugs Modulating Renin-Angiotensin System in COVID-19 Treatment.

Biomedicines

Research Center for Molecular Medicine and Chronic Diseases (CIMUS), IDIS, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain.

Published: February 2022

AI Article Synopsis

  • A global vaccination campaign is the primary tool against COVID-19, but drug treatments, particularly antivirals and those targeting disease aggravation mechanisms, are also important.
  • The renin-angiotensin system (RAS), especially the role of ACE2, is linked to COVID-19 severity and has influenced treatment considerations, leading to initial concerns over the use of ACE inhibitors (ACEIs) and angiotensin type-1 receptor blockers (ARBs).
  • Recent studies suggest that ACEIs and ARBs may actually improve COVID-19 outcomes by reducing inflammation and blocking viral entry, while new strategies targeting RAS are being researched.

Article Abstract

A massive worldwide vaccination campaign constitutes the main tool against the COVID-19 pandemic. However, drug treatments are also necessary. Antivirals are the most frequently considered treatments. However, strategies targeting mechanisms involved in disease aggravation may also be effective. A major role of the tissue renin-angiotensin system (RAS) in the pathophysiology and severity of COVID-19 has been suggested. The main link between RAS and COVID-19 is angiotensin-converting enzyme 2 (ACE2), a central RAS component and the primary binding site for SARS-CoV-2 that facilitates the virus entry into host cells. An initial suggestion that the susceptibility to infection and disease severity may be enhanced by angiotensin type-1 receptor blockers (ARBs) and ACE inhibitors (ACEIs) because they increase ACE2 levels, led to the consideration of discontinuing treatments in thousands of patients. More recent experimental and clinical data indicate that ACEIs and, particularly, ARBs can be beneficial for COVID-19 outcome, both by reducing inflammatory responses and by triggering mechanisms (such as ADAM17 inhibition) counteracting viral entry. Strategies directly activating RAS anti-inflammatory components such as soluble ACE2, Angiotensin 1-7 analogues, and Mas or AT2 receptor agonists may also be beneficial. However, while ACEIs and ARBs are cheap and widely used, the second type of strategies are currently under study.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962306PMC
http://dx.doi.org/10.3390/biomedicines10020502DOI Listing

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