Evidence map›Paper›PMID 17478622›Full record

ArticleAmerican journal of respiratory and critical care medicine2007

Inhaled ethyl nitrite prevents hyperoxia-impaired postnatal alveolar development in newborn rats.

Richard L Auten, Stanley N Mason, Mary H Whorton, William R Lampe, W Michael Foster, Ronald N Goldberg, Bo Li, Jonathan S Stamler, Kathryn M Auten

Retracted Registry-linked trialOpen access · greenAbstract readComparative Study
In one paragraph

Article in American journal of respiratory and critical care medicine, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. It is linked to trial NCT03926741 (Methods to Identify and Treat Severe Asthma Patients Project 1), which is not on this map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.6field-weighted citation impact, top 4% 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.

NCT03926741 early_phase1completednot on this mapstarted 2019, after this paper: background citation

Methods to Identify and Treat Severe Asthma Patients Project 1: GSNOR Phenotyping and GSNO Challenge

TypeinterventionalSponsorJames ReynoldsRan2019 to 2024Enrolled48ConditionsAsthmaArmsGSNO Challenge
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 70 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Bronchopulmonary Dysplasia and Pulmonary Hypertension. The Role of Smooth MuscleAmerican journal of respiratory cell and molecular biology · 2021
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Observational
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. The thioredoxin system in neonatal lung disease.Antioxidants & redox signaling · 2014
    Review
  18. Oxidative Stress and Therapeutic Development in Lung Diseases.Journal of pulmonary & respiratory medicine · 2014
    Article
  19. Article
  20. Postnatal inflammation in the pathogenesis of bronchopulmonary dysplasia.Birth defects research. Part A, Clinical and molecular teratology · 2014
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Richard L AutenDivision of Neonatal Medicine, Department of Pediatrics, Neonatal-Perinatal Research Institute, University Medical Center, Durham, North Carolina 27710, USA. auten@duke.edu
Stanley N Mason
Mary H Whorton
William R Lampe
W Michael Foster
Ronald N Goldberg
Bo Li
Jonathan S Stamler
Kathryn M Auten
Duke University · USDurham University · GB

Funding

Research Core 3: Environmental Health PolicyP30ES011961 · NIEHS · DUKE UNIVERSITY · PI DI GIULIO, RICHARD · 2004 to 2009
$4.1M
gClqR/p33 in S. Aureus Endovascular PathogenesisR01HL067211 · NHLBI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI PEERSCHKE, ELLINOR I · 2002 to 2005
$1.2M
NHLBI NIH HHS HL 067211NIEHS NIH HHS ES 011961
6 · The paper itself

Abstract

rationaleInhaled nitric oxide (NO) has been used to prevent bronchopulmonary dysplasia, but with variable results. Ethyl nitrite (ENO) forms S-nitrosothiols more readily than does NO, and resists higher-order nitrogen oxide formation. Because S-nitrosylation is a key pathway mediating many NO biological effects, treatment with inhaled ENO may better protect postnatal lung development from oxidative stress than NO.

objectivesTo compare inhaled NO and ENO on hyperoxia-impaired postnatal lung development.

methodsWe treated newborn rats beginning at birth to air or 95% O(2) +/- 0.2-20.0 ppm ENO for 8 days, or to 10 ppm NO for 8 days. Pups treated with the optimum ENO dose, 10 ppm, and pups treated with 10 ppm NO were recovered in room air for 6 more days. MEASUREMENTS AND MAIN

resultsENO and NO partly prevented 95% O(2)-induced airway neutrophil influx in lavage, but ENO had a greater effect than did NO in prevention of lung myeloperoxidase accumulation, and in expression of cytokine-induced neutrophil chemoattractant-1. Treatment with 10 ppm ENO, but not NO, for 8 days followed by recovery in air for 6 days prevented 95% O(2)-induced impairments of body weight, lung compliance, and alveolar development.

conclusionsInhaled ENO conferred protection superior to inhaled NO against hyperoxia-induced inflammation. ENO prevented hyperoxia impairments of lung compliance and postnatal alveolar development in newborn rats.

Indexed as

Administration, InhalationAnimalsAnimals, NewbornBronchodilator AgentsBronchopulmonary DysplasiaDisease Models, AnimalHumansHyperoxiaInfant, NewbornInflammationNitric OxideNitritesOxidative StressPulmonary AlveoliRatsRats, Sprague-DawleyBronchodilator Agentsethyl nitriteNitric OxideNitrites

Identifiers

PMID17478622
PMCPMC1994219
OpenAlexW2017967134

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.