Evidence map›Paper›PMID 22363613›Full record

ArticlePloS one2012

In vivo MR imaging of pulmonary perfusion and gas exchange in rats via continuous extracorporeal infusion of hyperpolarized 129Xe.

Zackary I Cleveland, Harald E Möller, Laurence W Hedlund, John C Nouls, Matthew S Freeman, Yi Qi, Bastiaan Driehuys

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Improved preclinical hyperpolarizedNMR in biomedicine · 2021
    Article
  4. Article
  5. Nanoparticle-Based Contrast Agents forContrast media & molecular imaging · 2019
    Review
  6. Magnetic resonance in medicine · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Perspectives of hyperpolarized noble gas MRI beyond 3He.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2013
    Review
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

7 authors at 2 institutions in 2 countries.

Zackary I ClevelandDepartment of Radiology, Duke University Medical Center, Durham, North Carolina, United States of America.
Harald E Möller
Laurence W Hedlund
John C Nouls
Matthew S Freeman
Yi Qi
Bastiaan Driehuys
Duke Medical Center · USDuke University · US

Funding

X-RAY RESEARCH AND DEVELOPMENT WITH/WITHOUT LIVE ANIMALSP41RR005959 · NCRR · DUKE UNIVERSITY · PI MCCONNELL, GEORGE C · 1990 to 2011
$16.0M
Sensitive and Specific Molecular Imaging of Pulmonary NodulesR01CA142842 · NCI · DUKE UNIVERSITY · PI BRANCA, ROSA TAMARA, DRIEHUYS, BASTIAAN · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA142842NCRR NIH HHS P41 RR005959
6 · The paper itself

Abstract

backgroundHyperpolarized (HP) (129)Xe magnetic resonance imaging (MRI) permits high resolution, regional visualization of pulmonary ventilation. Additionally, its reasonably high solubility (>10%) and large chemical shift range (>200 ppm) in tissues allow HP (129)Xe to serve as a regional probe of pulmonary perfusion and gas transport, when introduced directly into the vasculature. In earlier work, vascular delivery was accomplished in rats by first dissolving HP (129)Xe in a biologically compatible carrier solution, injecting the solution into the vasculature, and then detecting HP (129)Xe as it emerged into the alveolar airspaces. Although easily implemented, this approach was constrained by the tolerable injection volume and the duration of the HP (129)Xe signal. METHODS AND PRINCIPAL

findingsHere, we overcome the volume and temporal constraints imposed by injection, by using hydrophobic, microporous, gas-exchange membranes to directly and continuously infuse (129)Xe into the arterial blood of live rats with an extracorporeal (EC) circuit. The resulting gas-phase (129)Xe signal is sufficient to generate diffusive gas exchange- and pulmonary perfusion-dependent, 3D MR images with a nominal resolution of 2×2×2 mm(3). We also show that the (129)Xe signal dynamics during EC infusion are well described by an analytical model that incorporates both mass transport into the blood and longitudinal relaxation.

conclusionsExtracorporeal infusion of HP (129)Xe enables rapid, 3D MR imaging of rat lungs and, when combined with ventilation imaging, will permit spatially resolved studies of the ventilation-perfusion ratio in small animals. Moreover, EC infusion should allow (129)Xe to be delivered elsewhere in the body and make possible functional and molecular imaging approaches that are currently not feasible using inhaled HP (129)Xe.

Indexed as

PerfusionAnimalsComputer SimulationExtracorporeal CirculationLungMagnetic Resonance ImagingMaleModels, BiologicalPulmonary Gas ExchangeRatsRats, Sprague-DawleyRespirationSignal Processing, Computer-AssistedXenonXenon IsotopesXenonXenon Isotopes

Identifiers

PMID22363613
PMCPMC3283644
OpenAlexW2030159355

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.