Evidence map›Paper›PMID 26266917›Full record

ArticleIntensive care medicine experimental2014

Regulation of lung oxidative damage by endogenous superoxide dismutase in sepsis.

Larissa Constantino, Renata Casagrande Gonçalves, Vinícius Renê Giombelli, Cristiane Damiani Tomasi, Francieli Vuolo, Luiza Wilges Kist, Giovanna Medeiros Tavares de Oliveira, Matheus Augusto de Bittencourt Pasquali, Maurício Reis Bogo, Thais Mauad and 6 more

Open access · goldAbstract read
In one paragraph

Article in Intensive care medicine experimental, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
  5. Review
  6. Review
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  8. Article
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

16 authors at 5 institutions in 1 country.

Larissa ConstantinoLaboratório de Fisiopatologia Experimenta e Instituto Nacional de Ciência e Tecnologia Translacional em Medicina (INCT-TM), Programa de Pós-Graduação de Ciências da Saúde, Universidade do Extremo Sul Catarinense, Avenida Universitária, 1105, Criciúma, SC, 88806-000, Brazil, larissa.constantino@gmail.com.
Renata Casagrande Gonçalves
Vinícius Renê Giombelli
Cristiane Damiani Tomasi
Francieli Vuolo
Luiza Wilges Kist
Giovanna Medeiros Tavares de Oliveira
Matheus Augusto de Bittencourt Pasquali
Maurício Reis Bogo
Thais Mauad
Adolfo Horn
Karen V Melo
Christiane Fernandes
José Cláudio Fonseca Moreira
Cristiane Ritter
Felipe Dal-Pizzol
Universidade do Extremo Sul Catarinense · BRPontifícia Universidade Católica do Rio Grande do Sul · BRState University of Norte Fluminense · BRUniversidade Federal do Rio Grande do Sul · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe purpose of this research is to study the relationship between superoxide dismutase (SOD) and lung redox state in an animal model of sepsis.

methodsSepsis was induced in rats by the cecal ligation and perforation model (CLP). After 3, 6, and 12 h, CLP protein content and expression of SOD1, SOD2, and SOD3 were evaluated, and SOD activity was assessed. Oxidative damage was determined by quantifying nitrotyrosine content. Lung localization of SOD3 was performed by immunohistochemistry. The protective effect of a SOD mimetic on oxidative damage, inflammation, and lung permeability was assessed 12 and 24 h after sepsis induction.

resultsLung levels of SOD1 decreased 3 and 12 h after sepsis, but SOD2 and SOD3 increased, as well as SOD activity. These alterations were not associated with changes in sod gene expression. Nitrotyrosine levels increased 3 and 12 h after sepsis. The administration of a SOD mimetic decreased nitrotyrosine and proinflammatory cytokine levels and improved lung permeability.

conclusionsSOD2 and SOD3 increased after sepsis induction, but this was insufficient to protect the lung. Treatments based on SOD mimetics could have a role in lung injury associated with sepsis.

Identifiers

PMID26266917
PMCPMC4513028
OpenAlexW2167524498

What OpenQuestion holds

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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.