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

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‐resolutio...

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Autores principales: Preissner, Melissa, Murrie, Rhiannon P., Bresee, Catherine, Carnibella, Richard P., Fouras, Andreas, Weir, E. Kenneth, Dubsky, Stephen, Pinar, Isaac P., Jones, Heather D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170880/
https://www.ncbi.nlm.nih.gov/pubmed/30284390
http://dx.doi.org/10.14814/phy2.13875
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author Preissner, Melissa
Murrie, Rhiannon P.
Bresee, Catherine
Carnibella, Richard P.
Fouras, Andreas
Weir, E. Kenneth
Dubsky, Stephen
Pinar, Isaac P.
Jones, Heather D.
author_facet Preissner, Melissa
Murrie, Rhiannon P.
Bresee, Catherine
Carnibella, Richard P.
Fouras, Andreas
Weir, E. Kenneth
Dubsky, Stephen
Pinar, Isaac P.
Jones, Heather D.
author_sort Preissner, Melissa
collection PubMed
description 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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spelling pubmed-61708802018-10-10 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. Physiol Rep Original Research 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. John Wiley and Sons Inc. 2018-10-04 /pmc/articles/PMC6170880/ /pubmed/30284390 http://dx.doi.org/10.14814/phy2.13875 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Preissner, Melissa
Murrie, Rhiannon P.
Bresee, Catherine
Carnibella, Richard P.
Fouras, Andreas
Weir, E. Kenneth
Dubsky, Stephen
Pinar, Isaac P.
Jones, Heather D.
Application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice
title Application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice
title_full Application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice
title_fullStr Application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice
title_full_unstemmed Application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice
title_short Application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice
title_sort application of a novel in vivo imaging approach to measure pulmonary vascular responses in mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170880/
https://www.ncbi.nlm.nih.gov/pubmed/30284390
http://dx.doi.org/10.14814/phy2.13875
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