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Application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice.
Preissner, Melissa; Murrie, Rhiannon P; Bresee, Catherine; Carnibella, Richard P; Fouras, Andreas; Weir, E Kenneth; Dubsky, Stephen; Pinar, Isaac P; Jones, Heather D.
Afiliação
  • Preissner M; Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
  • Murrie RP; Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
  • Bresee C; Cedars-Sinai Medical Center, Biostatistics & Bioinformatics Research Institute, Los Angeles, California.
  • Carnibella RP; 4Dx Limited, Melbourne, Victoria, Australia.
  • Fouras A; Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
  • Weir EK; 4Dx Limited, Melbourne, Victoria, Australia.
  • Dubsky S; Department of Biomedical Sciences, Cedars-Sinai Medical Center, Biomedical Imaging Research Institute, Los Angeles, California.
  • Pinar IP; Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
  • Jones HD; Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
Physiol Rep ; 6(19): e13875, 2018 09.
Article em En | MEDLINE | ID: mdl-30284390
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Circulação Pulmonar / Imageamento Tridimensional / Microtomografia por Raio-X / Pulmão Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Circulação Pulmonar / Imageamento Tridimensional / Microtomografia por Raio-X / Pulmão Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article