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Antiviral Properties of the NSAID Drug Naproxen Targeting the Nucleoprotein of SARS-CoV-2 Coronavirus

Authors :
Olivier Terrier
Sébastien Dilly
Andrés Pizzorno
Dominika Chalupska
Jana Humpolickova
Evžen Bouřa
Francis Berenbaum
Stéphane Quideau
Bruno Lina
Bruno Fève
Frédéric Adnet
Michèle Sabbah
Manuel Rosa-Calatrava
Vincent Maréchal
Julien Henri
Anny Slama-Schwok
Source :
Molecules, Vol 26, Iss 9, p 2593 (2021)
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

There is an urgent need for specific antiviral treatments directed against SARS-CoV-2 to prevent the most severe forms of COVID-19. By drug repurposing, affordable therapeutics could be supplied worldwide in the present pandemic context. Targeting the nucleoprotein N of the SARS-CoV-2 coronavirus could be a strategy to impede viral replication and possibly other essential functions associated with viral N. The antiviral properties of naproxen, a non-steroidal anti-inflammatory drug (NSAID) that was previously demonstrated to be active against Influenza A virus, were evaluated against SARS-CoV-2. Intrinsic fluorescence spectroscopy, fluorescence anisotropy, and dynamic light scattering assays demonstrated naproxen binding to the nucleoprotein of SARS-Cov-2 as predicted by molecular modeling. Naproxen impeded recombinant N oligomerization and inhibited viral replication in infected cells. In VeroE6 cells and reconstituted human primary respiratory epithelium models of SARS-CoV-2 infection, naproxen specifically inhibited viral replication and protected the bronchial epithelia against SARS-CoV-2-induced damage. No inhibition of viral replication was observed with paracetamol or the COX-2 inhibitor celecoxib. Thus, among the NSAID tested, only naproxen combined antiviral and anti-inflammatory properties. Naproxen addition to the standard of care could be beneficial in a clinical setting, as tested in an ongoing clinical study.

Details

Language :
English
ISSN :
14203049
Volume :
26
Issue :
9
Database :
Directory of Open Access Journals
Journal :
Molecules
Publication Type :
Academic Journal
Accession number :
edsdoj.b9cc3f495e4edab8a5cc709db997e4
Document Type :
article
Full Text :
https://doi.org/10.3390/molecules26092593