Evidence map›Paper›PMID 22962015›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2012

Decreases in manganese superoxide dismutase expression and activity contribute to oxidative stress in persistent pulmonary hypertension of the newborn.

Adeleye J Afolayan, Annie Eis, Ru-Jeng Teng, Ivane Bakhutashvili, Sushma Kaul, Jonathan M Davis, Girija G Konduri

Abstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.9field-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.

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

43 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
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  5. Review
  6. Insights into Manganese Superoxide Dismutase and Human Diseases.International journal of molecular sciences · 2022
    Review
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  8. Review
  9. Article
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  12. Article
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  16. Article
  17. Optimal oxygenation and role of free radicals in PPHN.Free radical biology & medicine · 2019
    Review
  18. Article
  19. Article
  20. 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

7 authors at 3 institutions in 1 country.

Adeleye J AfolayanDepartment of Pediatrics, Cardiovascular Research Center and Children’s Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Annie Eis
Ru-Jeng Teng
Ivane Bakhutashvili
Sushma Kaul
Jonathan M Davis
Girija G Konduri
Medical College of Wisconsin · USChildren's Hospital of Wisconsin · USTufts Medical Center · US

Funding

REGULATION OF PULMONARY CIRCULATION IN FETUS AND NEWBORNR01HL057268 · NHLBI · WAYNE STATE UNIVERSITY · PI KONDURI, GIRIJA G. · 1998 to 2013
$2.0M
Oxidative stress in pulmonary circulation during birth related transitionR03HD065841 · NICHD · MEDICAL COLLEGE OF WISCONSIN · PI KONDURI, GIRIJA G. · 2010 to 2011
$150k
NHLBI NIH HHS R01 HL-057268NHLBI NIH HHS R01 HL057268NICHD NIH HHS R03 HD-065841NICHD NIH HHS R03 HD065841
6 · The paper itself

Abstract

A rapid increase in the synthesis and release of nitric oxide (NO) facilitates the pulmonary vasodilation that occurs during birth-related transition. Alteration of this transition in persistent pulmonary hypertension of the newborn (PPHN) is associated with impaired function of endothelial nitric oxide synthase (eNOS) and an increase in oxidative stress. We investigated the hypothesis that a decrease in expression and activity of mitochondrial localized manganese superoxide dismutase (MnSOD) in pulmonary artery endothelial cells (PAEC) increases oxidative stress and impairs eNOS function in PPHN. We isolated PAEC and pulmonary arteries from fetal lambs with PPHN induced by prenatal ductus arteriosus ligation or sham ligation (control). We investigated MnSOD expression and activity, tyrosine nitration of MnSOD, and mitochondrial O(2)(-) levels in PAEC from control and PPHN lambs. We introduced exogenous MnSOD via an adenoviral vector (ad-MnSOD) transduction into PAEC and pulmonary arteries of PPHN lambs. The effect of ad-MnSOD was investigated on: mitochondrial O(2)(-) levels, MnSOD and eNOS expression and activity, intracellular hydrogen peroxide (H(2)O(2)) levels, and catalase expression in PAEC. MnSOD mRNA and protein levels and activity were decreased and MnSOD tyrosine nitration was increased in PPHN-PAEC. ad-MnSOD transduction of PPHN-PAEC increased its activity two- to threefold, decreased mitochondrial O(2)(-) levels, and increased H(2)O(2) levels and catalase expression. ad-MnSOD transduction improved eNOS expression and function and the relaxation response of PPHN pulmonary arteries. Our observations suggest that decreased MnSOD expression and activity contribute to the endothelial dysfunction observed in PPHN.

Indexed as

Gene Expression Regulation, EnzymologicOxidative StressAdenoviridaeAnimalsDisease Models, AnimalEndothelial CellsGenetic VectorsHumansHydrogen PeroxideInfant, NewbornMitochondriaNitric OxideNitric Oxide Synthase Type IIIPersistent Fetal Circulation SyndromePulmonary ArteryRNA, MessengerHydrogen PeroxideNitric OxideNitric Oxide Synthase Type IIIRNA, MessengerSuperoxide DismutaseSuperoxides

Identifiers

PMID22962015
PMCPMC3517675
OpenAlexW2029658224

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.