Evidence map›Paper›PMID 23499839›Full record

ArticleFree radical biology & medicine2013

Developmental differences in hyperoxia-induced oxidative stress and cellular responses in the murine lung.

Sara K Berkelhamer, Gina A Kim, Josiah E Radder, Stephen Wedgwood, Lyubov Czech, Robin H Steinhorn, Paul T Schumacker

Abstract read
In one paragraph

Article in Free radical biology & medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 89 citations in OpenAlex.

  1. Trial
  2. Role of ROS, soluble guanylate cyclase and cGMP in mouse lung development during hyperoxia.American journal of physiology. Heart and circulatory physiology · 2026
    Article
  3. Cannabidiol Protects the Neonatal Mouse Heart from Hyperoxia-Induced Injury.International journal of molecular sciences · 2025
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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

7 authors at 1 institution in 1 country.

Sara K BerkelhamerDepartment of Pediatrics, Northwestern University, Chicago, IL 60611, USA. Electronic address: s-berkelhamer@northwestern.edu.
Gina A KimDepartment of Pediatrics, Northwestern University, Chicago, IL 60611, USA.
Josiah E RadderDepartment of Pulmonary and Critical Care Medicine, Northwestern University, Chicago, IL 60611, USA.
Stephen WedgwoodDepartment of Pediatrics, Northwestern University, Chicago, IL 60611, USA.
Lyubov CzechDepartment of Pediatrics, Northwestern University, Chicago, IL 60611, USA.
Robin H SteinhornDepartment of Pediatrics, Northwestern University, Chicago, IL 60611, USA.
Paul T SchumackerDepartment of Pediatrics, Northwestern University, Chicago, IL 60611, USA.
Northwestern University · US

Funding

Respiratory and Metabolic Adaptation to HypoxiaR01HL035440 · NHLBI · UNIVERSITY OF CHICAGO · PI SCHUMACKER, PAUL T · 1986 to 2018
$5.0M
REDOX REGULATION IN THE PERINATAL PULMONARY VASCULATURER01HL054705 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI STEINHORN, ROBIN H. · 2001 to 2013
$4.8M
Faculty Development Program for Pediatric Clinician-ScientistsK12HD052902 · NICHD · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI GREEN, THOMAS P. · 2006 to 2010
$1.6M
Monitoring cellular redox signaling and oxidant stress in vivoR21RR025355 · NCRR · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHUMACKER, PAUL T · 2009 to 2010
$511k
NCRR NIH HHS R21 RR025355NHLBI NIH HHS HL35440NHLBI NIH HHS R01 HL035440NHLBI NIH HHS R01 HL054705NICHD NIH HHS K12 HD052902NICHD NIH HHS K12HD052902
6 · The paper itself

Abstract

Exposure of newborn mice to high inspired oxygen elicits a distinct phenotype of compromised alveolar and vascular development, although lethality during long-term exposure is lower in newborns compared to adults. As the effects of hyperoxia are mediated by excessive reactive oxygen species (ROS) generation, we hypothesized that newborn mice may exhibit enhanced expression of antioxidant defenses or attenuated ROS generation compared with adults. We measured subcellular oxidant responses to acute hyperoxia in lung slices and alveolar epithelial cells at varying time points during postnatal murine lung development. Oxidant stress was assessed using RoGFP, a ratiometric protein thiol redox sensor, targeted to the cytosol or the mitochondrial matrix. In contrast to newborn resistance to oxygen-induced mortality, cells of lung slices from younger mice demonstrated exaggerated mitochondrial matrix oxidant stress compared to adults, whereas oxidant stress responses in the cytosol were absent. Cell death in lung slices from newborn mice exposed to 48h of hyperoxia was also greater than for adults. Consistent with these findings, expression of antioxidant enzymes in newborn lungs was lower than in adults, and induction of antioxidant levels and activity during 24h of in vivo exposure was absent. However, expression of the reactive oxygen species-generating enzyme NADPH oxidase 1 was increased with hyperoxic exposure in the young but not the adult lung. Collectively, these results suggest that the greater lethality in adult animals may be more likely attributed to processes such as inflammation than to differences in antioxidant defenses. Therapies for neonatal and adult oxidative lung injury should therefore consider and address developmental differences in oxidative stress responses.

Indexed as

Oxidative StressAge FactorsAnimalsFemaleHyperoxiaLungMiceMice, Inbred C57BLNADH, NADPH OxidoreductasesNADPH Oxidase 1Reactive Oxygen SpeciesSuperoxide DismutaseNADH, NADPH OxidoreductasesNADPH Oxidase 1Reactive Oxygen SpeciesSuperoxide DismutaseDevelopmental differencesFree radicalsLung developmentMitochondrial oxidative stressNADPH oxidase 1Oxidative lung injurySubcellular response

Identifiers

PMID23499839
PMCPMC3723750
OpenAlexW1979881414

What OpenQuestion holds

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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.