Evidence map›Paper›PMID 25517730›Full record

ArticlePloS one2014

Intestinal NADPH oxidase 2 activity increases in a neonatal rat model of necrotizing enterocolitis.

Scott R Welak, Rebecca M Rentea, Ru-Jeng Teng, Nathan Heinzerling, Ben Biesterveld, Jennifer L Liedel, Kirkwood A Pritchard, Katherine M Fredrich, David M Gourlay

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Scott R WelakDivision of Neonatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Children's Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Translational Vascular Biology Program, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Rebecca M RenteaChildren's Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Division of Pediatric Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Ru-Jeng TengDivision of Neonatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Children's Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Translational Vascular Biology Program, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Nathan HeinzerlingChildren's Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Division of Pediatric Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Ben BiesterveldChildren's Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Division of Pediatric Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Jennifer L LiedelDivision of Neonatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Children's Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Division of Critical Care, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Kirkwood A PritchardTranslational Vascular Biology Program, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Division of Pediatric Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Katherine M FredrichTranslational Vascular Biology Program, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Division of Pediatric Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
David M GourlayChildren's Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Translational Vascular Biology Program, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America; Division of Pediatric Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Medical College of Wisconsin · USChildren's Hospital of Wisconsin · US

Funding

Biophysics of HDL DysfunctionR01HL112270 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI PRITCHARD, KIRKWOOD ARTHUR, SORCI-THOMAS, MARY G · 2012 to 2015
$2.5M
NHLBI NIH HHS R01 HL112270
6 · The paper itself

Abstract

Necrotizing enterocolitis (NEC) is a complication of prematurity. The etiology is unknown, but is related to enteral feeding, ischemia, infection, and inflammation. Reactive oxygen species production, most notably superoxide, increases in NEC. NADPH oxidase (NOX) generates superoxide, but its activity in NEC remains unknown. We hypothesize that NOX-derived superoxide production increases in NEC. Newborn Sprague-Dawley rats were divided into control, formula-fed, formula/LPS, formula/hypoxia, and NEC (formula, hypoxia, and LPS). Intestinal homogenates were analyzed for NADPH-dependent superoxide production. Changes in superoxide levels on days 0-4 were measured. Inhibitors for nitric oxide synthase (L-NAME) and NOX2 (GP91-ds-tat) were utilized. RT-PCR for eNOS, NOX1, GP91phox expression was performed. Immunofluorescence studies estimated the co-localization of p47phox and GP91phox in control and NEC animals on D1, D2, and D4. NEC pups generated more superoxide than controls on D4, while all other groups were unchanged. NADPH-dependent superoxide production was greater in NEC on days 0, 3, and 4. GP91-ds-tat decreased superoxide production in both groups, with greater inhibition in NEC. L-NAME did not alter superoxide production. Temporally, superoxide production varied minimally in controls. In NEC, superoxide generation was decreased on day 1, but increased on days 3-4. GP91phox expression was higher in NEC on days 2 and 4. NOX1 and eNOS expression were unchanged from controls. GP91phox and p47phox had minimal co-localization in all control samples and NEC samples on D1 and D2, but had increased co-localization on D4. In conclusion, this study proves that experimentally-induced NEC increases small intestinal NOX activity. All components of NEC model are necessary for increased NOX activity. NOX2 is the major source, especially as the disease progresses.

Indexed as

Disease Models, AnimalAnimalsAnimals, NewbornEnteral NutritionEnterocolitis, NecrotizingEnzyme InhibitorsFemaleFluorescent Antibody TechniqueHypoxiaIntestinesMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide SynthaseCybb protein, ratEnzyme InhibitorsMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide SynthaseRNA, MessengerSuperoxidesTumor Necrosis Factor-alpha

Identifiers

PMID25517730
PMCPMC4269454
OpenAlexW2050108722

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.