Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Nov 17;4(4):e440.
doi: 10.1002/hsr2.440. eCollection 2021 Dec.

COVID-19 and renin angiotensin aldosterone system: Pathogenesis and therapy

Affiliations
Review

COVID-19 and renin angiotensin aldosterone system: Pathogenesis and therapy

Fatemeh Babajani et al. Health Sci Rep. .

Abstract

Aims: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) binds to the ACE2 component of the renin-angiotensin aldosterone system (RAAS) and infects the human cells. The aims of the present review were to look at the role and alteration of the RAAS components in SARS-CoV-2 infection, therapeutic approaches, and clinical trials in this field.

Methods: We surveyed the literature (PubMed, Web of Science, and Scopus) till August 18, 2021, and 59 published papers regarding the components of the RAAS and their role and alterations in SARS-CoV-2 infection along with various COVID-19 therapies based on the RASS components were included in the study.

Results: ACE inhibitors, angiotensin receptor blockers, and mineralocorticoid receptor inhibitors are agents that significantly enhance the ACE2 and Ang-(1-7) levels, which can be suggestive for their role as therapeutics against SARS-CoV-2 infection. Beta-adrenergic blockers, which negatively regulate renin release from juxtaglomerular cells, and vitamin D, as a regulator of the RAAS and renin expression, are proposed therapeutics in the treatment of COVID-19. Some antihyperglycemic agents could be potentially protective against COVID-19-induced lung injury. Also, the inhibition of the Janus kinase/signal transducer and activator of the transcription pathway as a potential treatment for COVID-19 has been suggested. Finally, resveratrol, an antioxidant that can suppress Ang II, has been suggested as an adjunct to other therapies.

Conclusion: Regarding the suggested potential therapies for COVID-19, there are many clinical trials whose results might change the treatment strategies of SARS-CoV-2 infection. So, the results of well-organized clinical trials on the efficacy and safety of the mentioned agents in the treatment of COVID-19 will be useful in the management and therapy of the disease.

Keywords: ACE2; COVID‐19; Janus kinase inhibitors; RAAS inhibitors; SARS‐CoV‐2; antihyperglycemic drugs.

PubMed Disclaimer

Conflict of interest statement

None.

References

    1. Ebrahimi A, Sayad B, Rahimi Z. COVID‐19 and psoriasis: biologic treatment and challenges. J Dermatol Treat. 2020;1‐5. - PubMed
    1. Touyz RM, Li H, Delles C. ACE2 the Janus‐Faced protein–from cardiovascular protection to severe acute respiratory syndrome‐coronavirus and COVID‐19. Clin Sci (Lond). 2020;134(7):747‐750. - PubMed
    1. Kolberg ES. ACE2, COVID19 and serum ACE as a possible biomarker to predict severity of disease. J Clin Virol. 2020;126:104350. - PMC - PubMed
    1. Costa LB, Perez LG, Palmeira VA, et al. Insights on SARS‐CoV‐2 molecular interactions with the renin‐angiotensin system. Front Cell Dev Biol. 2020;8:559841. - PMC - PubMed
    1. Santos RA, Passaglio KT, Pesquero JB, Bader M, Simões e Silva AC. Interactions between angiotensin‐(1‐7), kinins, and angiotensin II in kidney and blood vessels. Hypertension. 2001;38(3):660‐664. - PubMed

LinkOut - more resources