Evidence map›Paper›PMID 36706864›Full record

ArticleNitric oxide : biology and chemistry2023

Gaseous nitric oxide failed to inhibit the replication cycle of SARS-CoV-2 in vitro.

Audrey Rousseaud, Matthieu Prot, Etienne Simon Loriere, Ira Katz, Juan Fernando Ramirez-Gil, Géraldine Farjot

Open access · greenAbstract read
In one paragraph

Article in Nitric oxide : biology and chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Audrey RousseaudAir Liquide Healthcare, Paris Innovation Center, 1 Chemin de la Porte des Loges, 78354, Jouy-en-Josas, France. Electronic address: audrey.rssd@gmail.com.
Matthieu ProtInstitut Pasteur, 25-28 Rue du Dr Roux, 75015, Paris, France. Electronic address: matthieu.prot@pasteur.fr.
Etienne Simon LoriereInstitut Pasteur, 25-28 Rue du Dr Roux, 75015, Paris, France. Electronic address: etienne.simon-loriere@pasteur.fr.
Ira KatzAir Liquide Healthcare, Paris Innovation Center, 1 Chemin de la Porte des Loges, 78354, Jouy-en-Josas, France. Electronic address: ira.katz.fr@gmail.com.
Juan Fernando Ramirez-GilAir Liquide Healthcare, Paris Innovation Center, 1 Chemin de la Porte des Loges, 78354, Jouy-en-Josas, France. Electronic address: juanfernando.ramirezMD@gmail.com.
Géraldine FarjotAir Liquide Healthcare, Paris Innovation Center, 1 Chemin de la Porte des Loges, 78354, Jouy-en-Josas, France. Electronic address: gfarjot@gmail.com.
Air Liquide (France) · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nitric oxide (NO) has been shown to have antimicrobial activity in vitro and in some in vivo models, while the virucidal activity of NO remains elusive. Some studies using NO donors have suggested that NO could be a potential candidate to treat SARS-CoV infection. The Covid-19 pandemic raised the hypothesis that NO gas might have an impact on Sars-CoV-2 replication cycle and might be considered as a candidate therapy to treat COVID-19. To our knowledge, there are no in vitro preclinical studies demonstrating a virucidal effect of gaseous NO on SARS-CoV-2. This study aims to determine whether gaseous NO has an impact on the replication cycle of SARS-CoV-2 in vitro. To that end, SARS-CoV-2 infected epithelial (VeroE6) and pulmonary (A549-hACE2) cells were treated with repeated doses of gaseous NO at different concentrations known to be efficient against bacteria. Our results show that exposing SARS-CoV-2 infected-cells to NO gas even at high doses (160 ppm, 6 h) does not influence the replication cycle of the virus in vitro. We report here that NO gas has no antiviral properties in vitro on SARS-COV-2. Therefore, there is no rationale for its usage in clinical settings to treat COVID-19 patients for direct antiviral purposes, which does not exclude other potential physiological benefits of this gas.

Indexed as

COVID-19SARS-CoV-2AnimalsAntiviral AgentsChlorocebus aethiopsHumansNitric OxidePandemicsVero CellsVirus ReplicationAntiviral AgentsNitric OxideCOVID-19Gaseous nitric oxideSARS-CoV-2

Identifiers

PMID36706864
PMCPMC9873364
OpenAlexW4317936549

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.