Evidence map›Paper›PMID 39020115›Full record

ArticleLung2024

Lung Volumes in a Mouse Model of Pulmonary Allergic Inflammation.

Andrés Rojas-Ruiz, Magali Boucher, Cyndi Henry, Rosalie Packwood, Jorge Soliz, Ynuk Bossé

Abstract read
In one paragraph

Article in Lung, 2024. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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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

6 authors.

Andrés Rojas-RuizInstitut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ), Université Laval, Pavillon M, Room 2687, 2725, Chemin Sainte-Foy, Québec, QC, G1V 4G5, Canada.
Magali BoucherInstitut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ), Université Laval, Pavillon M, Room 2687, 2725, Chemin Sainte-Foy, Québec, QC, G1V 4G5, Canada.
Cyndi HenryInstitut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ), Université Laval, Pavillon M, Room 2687, 2725, Chemin Sainte-Foy, Québec, QC, G1V 4G5, Canada.
Rosalie PackwoodInstitut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ), Université Laval, Pavillon M, Room 2687, 2725, Chemin Sainte-Foy, Québec, QC, G1V 4G5, Canada.
Jorge SolizInstitut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ), Université Laval, Pavillon M, Room 2687, 2725, Chemin Sainte-Foy, Québec, QC, G1V 4G5, Canada.
Ynuk BosséInstitut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ), Université Laval, Pavillon M, Room 2687, 2725, Chemin Sainte-Foy, Québec, QC, G1V 4G5, Canada. ynuk.bosse@criucpq.ulaval.ca.ORCID 0000-0002-2023-3130

Funding

CIHR 508356-202209PJTNatural Sciences and Engineering Research Council of Canada RGPIN-2020-06355
6 · The paper itself

Abstract

purposeAir trapping, often attested in humans by elevated residual volume (RV) and ratio of RV on total lung capacity (RV/TLC), is frequently observed in asthma. Confirming these alterations in experimental asthma would be important for translational purposes. Herein, lung volumes were investigated in a mouse model of pulmonary allergic inflammation.

methodsEight- to 10-week-old male C57BL/6 and BALB/c mice were exposed once daily to intranasal house dust mite (HDM) for 10 consecutive days. All readouts were measured 24 h after the last exposure. Lung volumes were assessed with the flexiVent using a new automated method consisting of degassing the lungs followed by a full-range pressure-volume maneuver. The weight and the volume of the lungs were also measured ex vivo and a lobe was further processed for histological analyses.

resultsHDM exposure led to tissue infiltration with inflammatory cells, goblet cell hyperplasia, thickening of the airway epithelium, and elevated ex vivo lung weight and volume. It also decreased TLC and vital capacity but without affecting RV and RV/TLC. These observations were similar between the two mouse strains.

conclusionAlterations of lung volumes in a murine model of pulmonary allergic inflammation are inconsistent with observations made in human asthma. These discrepancies reflect the different means whereby lung volumes are measured between species. The invasive method used herein enables RV to be measured more precisely and without the confounding effect of air trapping, suggesting that changes in RV and RV/TLC using this method in mice should be interpreted differently than in humans.

Indexed as

Disease Models, AnimalLungLung Volume MeasurementsMice, Inbred BALB CMice, Inbred C57BLPyroglyphidaeAnimalsAsthmaGoblet CellsHyperplasiaMaleMiceOrgan SizePneumoniaResidual VolumeTotal Lung CapacityAir trappingLung mechanicsMouse modelsResidual volumeTotal lung capacity

Identifiers

PMID39020115
PMCPMC11427586

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.