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Role of Angiotensin II in Cardiovascular Diseases: Introducing Bisartans as a Novel Therapy for Coronavirus 2019

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BIOMOLECULES
卷 13, 期 5, 页码 -

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MDPI
DOI: 10.3390/biom13050787

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angiotensin-converting enzyme 2; angiotensin II; bisartans; cardiovascular diseases; coronavirus 2019; severe acute respiratory syndrome coronavirus 2; renin-angiotensin system

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Cardiovascular diseases (CVDs) and COVID-19 share overlapping pathophysiological complications. CVDs have been identified as major risk factors for severe and fatal COVID-19 states. Dysregulation of the renin-angiotensin system (RAS) in CVDs contributes to the development of COVID-19. Inhibiting RAS signaling through angiotensin receptor blockers (ARBs) has been indicated as a promising therapeutic approach for COVID-19 treatment.
Cardiovascular diseases (CVDs) are the main contributors to global morbidity and mortality. Major pathogenic phenotypes of CVDs include the development of endothelial dysfunction, oxidative stress, and hyper-inflammatory responses. These phenotypes have been found to overlap with the pathophysiological complications of coronavirus disease 2019 (COVID-19). CVDs have been identified as major risk factors for severe and fatal COVID-19 states. The renin-angiotensin system (RAS) is an important regulatory system in cardiovascular homeostasis. However, its dysregulation is observed in CVDs, where upregulation of angiotensin type 1 receptor (AT(1)R) signaling via angiotensin II (AngII) leads to the AngII-dependent pathogenic development of CVDs. Additionally, the interaction between the spike protein of severe acute respiratory syndrome coronavirus 2 with angiotensin-converting enzyme 2 leads to the downregulation of the latter, resulting in the dysregulation of the RAS. This dysregulation favors AngII/AT(1)R toxic signaling pathways, providing a mechanical link between cardiovascular pathology and COVID-19. Therefore, inhibiting AngII/AT(1)R signaling through angiotensin receptor blockers (ARBs) has been indicated as a promising therapeutic approach to the treatment of COVID-19. Herein, we review the role of AngII in CVDs and its upregulation in COVID-19. We also provide a future direction for the potential implication of a novel class of ARBs called bisartans, which are speculated to contain multifunctional targeting towards COVID-19.

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