SARS-CoV-2 – the Hidden Agonist of the Pressor Arm Within the Renin-Angiotensin System: Considerations for Statins and Propionate Derivatives

Author:

Cismaru Cosmin Andrei1,Cismaru Gabriel Laurențiu2,Burz Claudia Cristina3,Nutu Andreea4,Berindan Neagoe Ioana5

Affiliation:

1. Department of Oncology, University of Medicine and Pharmacy "Iuliu Hațieganu", Cluj-Napoca, Romania

2. "5th Department of Internal Medicine, Cardiology-Rehabilitation, “Iuliu Hatieganu” University of Medicine and Pharmacy, Cluj-Napoca, Romania."

3. "Institute of Oncology ""Prof. Dr. Ion Chiricuță"", Cluj-Napoca, Romania Department of Oncology, University of Medicine and Pharmacy ""Iuliu Hațieganu"", Cluj-Napoca, Romania"

4. "Research Center for functional Genomics, Biomedicine and Translational Medicine, “Iuliu Hatieganu”, University of Medicine and Pharmacy, Cluj-Napoca, Romania. University of Medicine and Pharmacy, Cluj-Napoca, Romania."

5. "Research Center for functional Genomics, Biomedicine and Translational Medicine, “Iuliu Hatieganu” University of Medicine and Pharmacy, Cluj-Napoca, Romania."

Abstract

"Coronavirus disease 2019 (COVID-19) has become a serious healthcare problem, causing more than 2 million fatalities worldwide. Several treatments used for the management of chronic diseases such as hypertension, cardiovascular disease, diabetes and arthritis were shown to increase the expression of the receptor exploited by the virus, the angiotensin-converting enzyme 2 (ACE2), in vitro. This raises concerns on the safety of continuing such drugs or switching to other classes that don’t interfere with the receptor exploited by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here we emphasize the mechanisms behind the regulation of ACE2 expression by several widely used drugs with possible interactions with COVID-19. Moreover, we discuss how the physiological mechanisms of attenuating inflammation and fibrosis can lead to increased expression of the receptor exploited by the virus and how this expression is further influenced be statins, propionate derivative nonsteroidal antiinflamatory drugs (NSAIDs) and renin-angiotensin system (RAS) blockers."

Publisher

Asociatia Societatea Transdisciplinara de Oncologie Personalizata Pentru Combaterea Cancerului - Stop Cancer

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