New perspectives on natural flavonoids on COVID-19-induced lung injuries
- PMID: 33928690
- PMCID: PMC8242604
- DOI: 10.1002/ptr.7131
New perspectives on natural flavonoids on COVID-19-induced lung injuries
Abstract
The SARS-CoV-2 virus, responsible for COVID-19, spread rapidly worldwide and became a pandemic in 2020. In some patients, the virus remains in the respiratory tract, causing pneumonia, respiratory failure, acute respiratory distress syndrome (ARDS), and sepsis, leading to death. Natural flavonoids (aglycone and glycosides) possess broad biological activities encompassing antiinflammatory, antiviral, antitumoral, antiallergic, antiplatelet, and antioxidant effects. While many studies have focused on the effects of natural flavonoids in experimental models, reports based on clinical trials are still insufficient. In this review, we highlight the effects of flavonoids in controlling pulmonary diseases, particularly the acute respiratory distress syndrome, a consequence of COVID-19, and their potential use in coronavirus-related diseases. Furthermore, we also focus on establishing a relationship between biological potential and chemical aspects of related flavonoids and discuss several possible mechanisms of action, pointing out some possible effects on COVID-19.
Keywords: ACE2; COVID-19; SARS-CoV-2; acute lung injury; flavonoids.
© 2021 John Wiley & Sons Ltd.
Conflict of interest statement
The authors have no conflicts of interest to declare related to the data shown on this publication.
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References
-
- Akbari, H. , Tabrizi, R. , Lankarani, K. B. , Aria, H. , Vakili, S. , Asadian, F. , … Faramarz, S. (2020). The role of cytokine profile and lymphocyte subsets in the severity of coronavirus disease 2019 (COVID‐19): A systematic review and meta‐analysis. Life Sciences, 258, 118167–118175. - PMC - PubMed
-
- Alexopoulou, L. , Holt, A. C. , Medzhitov, R. , & Flavell, R. A. (2001). Recognition of double‐stranded RNA and activation of NF‐κB by Toll‐like receptor 3. Nature, 413, 732–738. - PubMed
-
- Aloufi, N. , Traboulsi, H. , Ding, J. , Fonseca, G. J. , Nair, P. , Huang, S. K. , … Baglole, C. J. (2020). Angiotensin‐converting enzyme 2 (ACE2) expression in COPD and IPF fibroblasts—The forgotten cell in COVID‐19. American Journal of Physiology. Lung Cellular and Molecular Physiology, 320, L152–L157. - PMC - PubMed
-
- Anand, K. , Ziebuhr, J. , Wadhwani, P. , Mesters, J. R. , & Hilgenfeld, R. (2003). Coronavirus main proteinase (3CLpro) structure: Basis for design of anti‐SARS drugs. Science, 300, 1763–1767. - PubMed
-
- Arendse, L. B. , Jan Danser, A. H. , Poglitsch, M. , Touyz, R. M. , Burnett, J. C. , Llorens‐Cortes, C. , … Sturrock, E. D. (2019). Novel therapeutic approaches targeting the renin‐angiotensin system and associated peptides in hypertension and heart failure. Pharmacological Reviews, 71, 539–570. - PMC - PubMed
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