Evidence map›Paper›PMID 39699515›Full record

ArticleJornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia2024

Hyperventilation worsens inflammatory lung injury in spontaneously breathing rats.

Juliana Dias Nascimento Ferreira, Maycon Moura Reboredo, Eduardo Leite Vieira Costa, Lídia Maria Carneiro da Fonseca, Jaime Retamal, Fabrício Júnio Mendes Santos, Flavia de Paoli, Adenilson de Souza da Fonseca, Leda Marília Fonseca Lucinda, Bruno Valle Pinheiro

Abstract read
In one paragraph

Article in Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Juliana Dias Nascimento Ferreira. Divisão de Pneumologia e Terapia Intensiva, Hospital Universitário, Universidade Federal de Juiz de Fora, Juiz de Fora (MG), Brasil.ORCID 0000-0002-4781-7814
Maycon Moura Reboredo. Divisão de Pneumologia e Terapia Intensiva, Hospital Universitário, Universidade Federal de Juiz de Fora, Juiz de Fora (MG), Brasil.ORCID 0000-0001-8155-7414
Eduardo Leite Vieira Costa. Laboratório de Pneumologia, Laboratório de Investigação Médica 09, Disciplina de Pneumologia, Instituto do Coração, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo (SP), Brasil.ORCID 0000-0002-6941-3626
Lídia Maria Carneiro da Fonseca. Divisão de Pneumologia e Terapia Intensiva, Hospital Universitário, Universidade Federal de Juiz de Fora, Juiz de Fora (MG), Brasil.ORCID 0000-0002-9624-2359
Jaime Retamal. Departamento de Medicina Intensiva, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID 0000-0002-6817-3659
Fabrício Júnio Mendes Santos. Divisão de Pneumologia e Terapia Intensiva, Hospital Universitário, Universidade Federal de Juiz de Fora, Juiz de Fora (MG), Brasil.ORCID 0000-0003-2365-1271
Flavia de Paoli. Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Juiz de Fora, Juiz de Fora (MG), Brasil.ORCID 0000-0002-9849-8323
Adenilson de Souza da Fonseca. Departamento de Biofísica e Biometria, Instituto de Biologia Roberto Alcantara Gomes, Universidade Estadual do Rio de Janeiro, Rio de Janeiro (RJ), Brasil.ORCID 0000-0002-4441-4008
Leda Marília Fonseca Lucinda. Divisão de Pneumologia e Terapia Intensiva, Hospital Universitário, Universidade Federal de Juiz de Fora, Juiz de Fora (MG), Brasil.ORCID 0000-0002-0975-9350
Bruno Valle Pinheiro. Divisão de Pneumologia e Terapia Intensiva, Hospital Universitário, Universidade Federal de Juiz de Fora, Juiz de Fora (MG), Brasil.ORCID 0000-0002-5288-3533

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesHere, we investigated the effects of hyperventilation on acute lung injury (ALI) in spontaneously breathing rats.

methodsWistar rats were randomized to receive either intraperitoneal lipopolysaccharides (LPS) or saline, and intravenous infusion of NH4Cl (to induce metabolic acidosis and hyperventilation) or saline. Four groups were established: control-control (C-C), control-hyperventilation (C-HV), LPS-control (LPS-C), and LPS-hyperventilation (LPS-HV). Venous blood gases were collected before and after NH4Cl infusion and analyzed to confirm the presence of metabolic acidosis and hyperventilation. After euthanasia, lung injury was assessed using the ALI score, morphometric quantification of perivascular edema, neutrophil counts in the bronchoalveolar lavage, and mRNA expression of biological markers in the lung tissue.

resultsHyperventilation induced inflammatory lung injury in previously healthy lungs and exacerbated injuries previously induced by LPS (ALI score: C-C=0.14 [IQR 0.12; 0.14]; C-HV=0.36 [IQR 0.31; 0.37]; LPS-C=0.51 [IQR 0.50; 0.54]; LPS-HV=0.58 [IQR 0.56; 0.62]; p<0.01). Perivascular edema, neutrophil counts in bronchoalveolar lavage, and amphiregulin mRNA expression were higher in the LPS-HV group compared to the control group.

conclusionsHyperventilation increased inflammatory injury in rats with ALI during spontaneous ventilation. These results suggest that the impact of vigorous spontaneous breathing efforts on worsening inflammatory lung injury warrants further investigation.

Indexed as

Acute Lung InjuryHyperventilationLipopolysaccharidesRats, WistarAnimalsBronchoalveolar Lavage FluidDisease Models, AnimalMaleNeutrophilsRandom AllocationRatsLipopolysaccharides

Identifiers

PMID39699515
PMCPMC11601074

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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.