Drugs Modulating Renin-Angiotensin System in COVID-19 Treatment

Jose L Labandeira-Garcia1,2, Carmen M Labandeira1,3, Rita Valenzuela1,2

  • 1Research Center for Molecular Medicine and Chronic Diseases (CIMUS), IDIS, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain.

Biomedicines
|February 25, 2022
PubMed

Insights

Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs) show promise in treating COVID-19 by reducing inflammation and viral entry. Further research into other renin-angiotensin system (RAS) strategies is ongoing.

Area of Science:

  • Cardiovascular Research
  • Infectious Diseases
  • Pharmacology

Background:

  • The renin-angiotensin system (RAS) plays a significant role in COVID-19 severity.
  • Angiotensin-converting enzyme 2 (ACE2) is the primary SARS-CoV-2 binding site, influencing viral entry.
  • Initial concerns suggested ACE inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs) might worsen COVID-19 outcomes due to increased ACE2 levels.

Purpose of the Study:

  • To evaluate the role of RAS modulators in COVID-19 pathophysiology.
  • To investigate the therapeutic potential of ACEIs and ARBs in COVID-19.
  • To explore novel RAS-targeted strategies for COVID-19 treatment.

Main Methods:

  • Review of experimental and clinical data on RAS inhibitors in COVID-19.
  • Analysis of mechanisms by which ACEIs and ARBs affect viral entry and inflammation.
  • Exploration of emerging RAS-targeted therapies.

Main Results:

  • Recent data suggest ACEIs and particularly ARBs are beneficial for COVID-19 outcomes.
  • ACEIs and ARBs can reduce inflammatory responses and inhibit viral entry mechanisms (e.g., ADAM17).
  • Strategies activating anti-inflammatory RAS components are under investigation.

Conclusions:

  • ACEIs and ARBs represent a viable and accessible therapeutic option for COVID-19.
  • Targeting the RAS offers promising avenues for managing COVID-19 severity.
  • Further research is needed for novel RAS-based treatments like Angiotensin 1-7 analogues and Mas or AT2 receptor agonists.

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