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Pirfenidone: A novel hypothetical treatment for COVID-19

Cytokine storm, multiorgan failure, and particularly acute respiratory distress syndrome (ARDS) is the leading cause of mortality and morbidity in patients with COVID-19. A fulminant ARDS kills the majority of COVID-19 victims. Pirfenidone (5-methyl-1-phenyl-2-[1H]-pyridone), is a novel anti-fibroti...

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Autor principal: Seifirad, Soroush
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297676/
https://www.ncbi.nlm.nih.gov/pubmed/32575019
http://dx.doi.org/10.1016/j.mehy.2020.110005
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author Seifirad, Soroush
author_facet Seifirad, Soroush
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description Cytokine storm, multiorgan failure, and particularly acute respiratory distress syndrome (ARDS) is the leading cause of mortality and morbidity in patients with COVID-19. A fulminant ARDS kills the majority of COVID-19 victims. Pirfenidone (5-methyl-1-phenyl-2-[1H]-pyridone), is a novel anti-fibrotic agent with trivial adverse effects. Pirfenidone is approved for the treatment of Idiopathic Pulmonary Fibrosis (IPF) for patients with mild to moderate disease. Pirfenidone could inhibit apoptosis, downregulate ACE receptors expression, decrease inflammation by several mechanisms and ameliorate oxidative stress and hence protect pneumocytes and other cells from COVID-19 invasion and cytokine storm simultaneously. Based on the pirfenidone mechanism of action and the known pathophysiology of COVID-19, I believe that pirfenidone has the potential for the treatment of COVID-19 patients.
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spelling pubmed-72976762020-06-17 Pirfenidone: A novel hypothetical treatment for COVID-19 Seifirad, Soroush Med Hypotheses Article Cytokine storm, multiorgan failure, and particularly acute respiratory distress syndrome (ARDS) is the leading cause of mortality and morbidity in patients with COVID-19. A fulminant ARDS kills the majority of COVID-19 victims. Pirfenidone (5-methyl-1-phenyl-2-[1H]-pyridone), is a novel anti-fibrotic agent with trivial adverse effects. Pirfenidone is approved for the treatment of Idiopathic Pulmonary Fibrosis (IPF) for patients with mild to moderate disease. Pirfenidone could inhibit apoptosis, downregulate ACE receptors expression, decrease inflammation by several mechanisms and ameliorate oxidative stress and hence protect pneumocytes and other cells from COVID-19 invasion and cytokine storm simultaneously. Based on the pirfenidone mechanism of action and the known pathophysiology of COVID-19, I believe that pirfenidone has the potential for the treatment of COVID-19 patients. Elsevier Ltd. 2020-11 2020-06-17 /pmc/articles/PMC7297676/ /pubmed/32575019 http://dx.doi.org/10.1016/j.mehy.2020.110005 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Seifirad, Soroush
Pirfenidone: A novel hypothetical treatment for COVID-19
title Pirfenidone: A novel hypothetical treatment for COVID-19
title_full Pirfenidone: A novel hypothetical treatment for COVID-19
title_fullStr Pirfenidone: A novel hypothetical treatment for COVID-19
title_full_unstemmed Pirfenidone: A novel hypothetical treatment for COVID-19
title_short Pirfenidone: A novel hypothetical treatment for COVID-19
title_sort pirfenidone: a novel hypothetical treatment for covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297676/
https://www.ncbi.nlm.nih.gov/pubmed/32575019
http://dx.doi.org/10.1016/j.mehy.2020.110005
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