Evidence map›Paper›PMID 30284390›Full record

ArticlePhysiological reports2018

Application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice.

Melissa Preissner, Rhiannon P Murrie, Catherine Bresee, Richard P Carnibella, Andreas Fouras, E Kenneth Weir, Stephen Dubsky, Isaac P Pinar, Heather D Jones

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

9 authors at 4 institutions in 2 countries.

Melissa PreissnerDepartment of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
Rhiannon P MurrieDepartment of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
Catherine BreseeCedars-Sinai Medical Center, Biostatistics & Bioinformatics Research Institute, Los Angeles, California.
Richard P Carnibella4Dx Limited, Melbourne, Victoria, Australia.
Andreas FourasDepartment of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
E Kenneth WeirDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota.
Stephen DubskyDepartment of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
Isaac P PinarDepartment of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
Heather D JonesDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Biomedical Imaging Research Institute, Los Angeles, California.
Monash University · AUCedars-Sinai Medical Center · USNovita Healthcare (Australia) · AUUniversity of Minnesota · US

Funding

IL-1beta in the Development of Hypoxemia in Acute Lung InjuryK08HL125806 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI JONES, HEATHER · 2015 to 2019
$822k
NHLBI NIH HHS K08 HL125806NHLBI NIH HHS K08HL125806NIH HHS
6 · The paper itself

Abstract

Noninvasive imaging of the murine pulmonary vasculature is challenging due to the small size of the animal, limits of resolution of the imaging technology, terminal nature of the procedure, or the need for intravenous contrast. We report the application of laboratory-based high-speed, high-resolution x-ray imaging, and image analysis to detect quantitative changes in the pulmonary vascular tree over time in the same animal without the need for intravenous contrast. Using this approach, we detected an increased number of vessels in the pulmonary vascular tree of animals after 30 min of recovery from a brief exposure to inspired gas with 10% oxygen plus 5% carbon dioxide (mean ± standard deviation: 2193 ± 382 at baseline vs. 6177 ± 1171 at 30 min of recovery; P < 0.0001). In a separate set of animals, we showed that the total pulmonary blood volume increased (P = 0.0412) while median vascular diameter decreased from 0.20 mm (IQR: 0.15-0.28 mm) to 0.18 mm (IQR: 0.14-0.26 mm; P = 0.0436) over the respiratory cycle from end-expiration to end-inspiration. These findings suggest that the noninvasive, nonintravenous contrast imaging approach reported here can detect dynamic responses of the murine pulmonary vasculature and may be a useful tool in studying these responses in models of disease.

Indexed as

Pulmonary CirculationAnimalsFemaleImaging, Three-DimensionalLungMiceMice, Inbred BALB CRespiration, ArtificialX-Ray Microtomography4DCTin vivo imagingmicro-CTpulmonary vasculature

Identifiers

PMID30284390
PMCPMC6170880
OpenAlexW2895295808

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.