Small molecule therapeutics for COVID-19: repurposing of inhaled furosemide.

Anti-inflammatory COVID-19 Coronavirus Cytokine storm Furosemide Hypercytokinemia

Journal

PeerJ
ISSN: 2167-8359
Titre abrégé: PeerJ
Pays: United States
ID NLM: 101603425

Informations de publication

Date de publication:
2020
Historique:
received: 13 04 2020
accepted: 23 06 2020
entrez: 25 7 2020
pubmed: 25 7 2020
medline: 25 7 2020
Statut: epublish

Résumé

The novel coronavirus SARS-CoV-2 has become a global health concern. The morbidity and mortality of the potentially lethal infection caused by this virus arise from the initial viral infection and the subsequent host inflammatory response. The latter may lead to excessive release of pro-inflammatory cytokines, IL-6 and IL-8, as well as TNF-α ultimately culminating in hypercytokinemia ("cytokine storm"). To address this immuno-inflammatory pathogenesis, multiple clinical trials have been proposed to evaluate anti-inflammatory biologic therapies targeting specific cytokines. However, despite the obvious clinical utility of such biologics, their specific applicability to COVID-19 has multiple drawbacks, including they target only one of the multiple cytokines involved in COVID-19's immunopathy. Therefore, we set out to identify a small molecule with broad-spectrum anti-inflammatory mechanism of action targeting multiple cytokines of innate immunity. In this study, a library of small molecules endogenous to the human body was assembled, subjected to in silico molecular docking simulations and a focused in vitro screen to identify anti-pro-inflammatory activity via interleukin inhibition. This has enabled us to identify the loop diuretic furosemide as a candidate molecule. To pre-clinically evaluate furosemide as a putative COVID-19 therapeutic, we studied its anti-inflammatory activity on RAW264.7, THP-1 and SIM-A9 cell lines stimulated by lipopolysaccharide (LPS). Upon treatment with furosemide, LPS-induced production of pro-inflammatory cytokines was reduced, indicating that furosemide suppresses the M1 polarization, including IL-6 and TNF-α release. In addition, we found that furosemide promotes the production of anti-inflammatory cytokine products (IL-1RA, arginase), indicating M2 polarization. Accordingly, we conclude that furosemide is a reasonably potent inhibitor of IL-6 and TNF-α that is also safe, inexpensive and well-studied. Our pre-clinical data suggest that it may be a candidate for repurposing as an inhaled therapy against COVID-19.

Identifiants

pubmed: 32704455
doi: 10.7717/peerj.9533
pii: 9533
pmc: PMC7350920
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e9533

Informations de copyright

© 2020 Wang et al.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

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Auteurs

Zhiyu Wang (Z)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.
Faculty of Pharmacy, University of Toronto, Toronto, ON, Canada.

Yanfei Wang (Y)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Prachi Vilekar (P)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Seung-Pil Yang (SP)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Mayuri Gupta (M)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Myong In Oh (MI)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Autumn Meek (A)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Lisa Doyle (L)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Laura Villar (L)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Anja Brennecke (A)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Imindu Liyanage (I)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.
Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Mark Reed (M)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.
Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.

Christopher Barden (C)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Donald F Weaver (DF)

Krembil Research Institute, University Health Network, Toronto, ON, Canada.
Faculty of Pharmacy, University of Toronto, Toronto, ON, Canada.
Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Classifications MeSH