Evidence map›Paper›PMID 22565502›Full record

ArticlePediatric research2012

Isoprostanes as physiological mediators of transition to newborn life: novel mechanisms regulating patency of the term and preterm ductus arteriosus.

Jian-Xiong Chen, Patrick W O'Mara, Stanley D Poole, Naoko Brown, Noah J Ehinger, James C Slaughter, Bibhash C Paria, Judy L Aschner, Jeff Reese

Abstract readComparative Study
In one paragraph

Article in Pediatric research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Review
  2. A novel role for PGEAmerican journal of physiology. Heart and circulatory physiology · 2023
    Article
  3. Oxygen for the Newborn: Friend or Foe?Children (Basel, Switzerland) · 2023
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Observational
  11. Review
  12. Predictors of successful closure of patent ductus arteriosus with indomethacin.Journal of perinatology : official journal of the California Perinatal Association · 2015
    Observational
  13. The isoprostanes--25 years later.Biochimica et biophysica acta · 2015
    Review
  14. 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

9 authors.

Jian-Xiong ChenDepartment of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson, USA.
Patrick W O'Mara
Stanley D Poole
Naoko Brown
Noah J Ehinger
James C Slaughter
Bibhash C Paria
Judy L Aschner
Jeff Reese

Funding

Regulation of vascular maturation/regression in diabetesR01HL102042 · NHLBI · VANDERBILT UNIVERSITY · PI CHEN, JIAN-XIONG · 2010 to 2020
$3.0M
Genes contributing to patent ductus arteriosus susceptibility in preterm newbornsR01HL109199 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CLYMAN, RONALD I · 2011 to 2014
$3.0M
Mechanisms of Ductus Arteriosus RegulationR01HL077395 · NHLBI · VANDERBILT UNIVERSITY · PI REESE, JOHN JEFFREY · 2006 to 2010
$2.0M
Role of natriuretic peptides in the ductus arteriosusR01HL096967 · NHLBI · VANDERBILT UNIVERSITY · PI REESE, JOHN JEFFREY · 2010 to 2013
$1.5M
Hsp90/Client Protein Interactions in the Newborn LungR01HL075511 · NHLBI · VANDERBILT UNIVERSITY · PI ASCHNER, JUDY LYNN · 2005 to 2008
$1.5M
NHLBI NIH HHS HL075511NHLBI NIH HHS HL102042NHLBI NIH HHS HL77395NHLBI NIH HHS HL96967NHLBI NIH HHS R01 HL075511NHLBI NIH HHS R01 HL077395NHLBI NIH HHS R01 HL096967NHLBI NIH HHS R01 HL102042NHLBI NIH HHS R01 HL109199
6 · The paper itself

Abstract

backgroundIncreased oxygen tension at birth regulates physiologic events that are essential to postnatal survival, but the accompanying oxidative stress may also generate isoprostanes. We hypothesized that isoprostanes regulate ductus arteriosus (DA) function during postnatal vascular transition.

methodsIsoprostanes were measured by gas chromatography-mass spectrometry. DA tone was assessed by pressure myography. Gene expression was measured by quantitative PCR.

resultsOxygen exposure was associated with increased 8-iso-prostaglandin (PG)F2α in newborn mouse lungs. Both 8-iso-PGE2 and 8-iso-PGF2α induced concentration-dependent constriction of the isolated term DA, which was reversed by the thromboxane A2 (TxA2) receptor antagonist SQ29548. SQ29548 pretreatment unmasked an isoprostane-induced DA dilation mediated by the EP4 PG receptor. Exposure of the preterm DA to 8-iso-PGE2 caused unexpected DA relaxation that was reversed by EP4 antagonism. In contrast, exposure to 8-iso-PGF2α caused preterm DA constriction via TxA2 receptor activation. Further investigation revealed the predominance of the TxA2 receptor at term, whereas the EP4 receptor was expressed and functionally active from mid-gestation onward.

conclusionThis study identifies a novel physiological role for isoprostanes during postnatal vascular transition and provide evidence that oxidative stress may act on membrane lipids to produce vasoactive mediators that stimulate physiological DA closure at birth or induce pathological patency of the preterm DA.

Indexed as

Analysis of VarianceAnimalsAnimals, NewbornBridged Bicyclo Compounds, HeterocyclicDinoprostDinoprostoneDuctus ArteriosusDuctus Arteriosus, PatentFatty Acids, UnsaturatedFemaleGas Chromatography-Mass SpectrometryGene Expression ProfilingHydrazinesIsoprostanesMiceMyography8-epi-prostaglandin F2alpha8-isoprostaglandin E2Bridged Bicyclo Compounds, HeterocyclicDinoprostDinoprostoneFatty Acids, UnsaturatedHydrazinesIsoprostanesOxygenReceptors, Prostaglandin E, EP4 SubtypeReceptors, Thromboxane A2, Prostaglandin H2SQ 29548

Identifiers

PMID22565502
PMCPMC3586272

What OpenQuestion holds

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Registered trials

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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.