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Technical Note: Contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source
PURPOSE: In vivo imaging of the pulmonary vasculature in small animals is difficult yet highly desirable in order to allow study of the effects of a host of dynamic biological processes such as hypoxic pulmonary vasoconstriction. Here the authors present an approach for the quantification of changes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association of Physicists in Medicine
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074996/ https://www.ncbi.nlm.nih.gov/pubmed/27806595 http://dx.doi.org/10.1118/1.4964794 |
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author | Samarage, Chaminda R. Carnibella, Richard Preissner, Melissa Jones, Heather D. Pearson, James T. Fouras, Andreas Dubsky, Stephen |
author_facet | Samarage, Chaminda R. Carnibella, Richard Preissner, Melissa Jones, Heather D. Pearson, James T. Fouras, Andreas Dubsky, Stephen |
author_sort | Samarage, Chaminda R. |
collection | PubMed |
description | PURPOSE: In vivo imaging of the pulmonary vasculature in small animals is difficult yet highly desirable in order to allow study of the effects of a host of dynamic biological processes such as hypoxic pulmonary vasoconstriction. Here the authors present an approach for the quantification of changes in the vasculature. METHODS: A contrast free angiography technique is validated in silico through the use of computer-generated images and in vivo through microcomputed tomography (μCT) of live mice conducted using a laboratory-based x-ray source. Subsequent image processing on μCT data allowed for the quantification of the caliber of pulmonary vasculature without the need for external contrast agents. These measures were validated by comparing with quantitative contrast microangiography in the same mice. RESULTS: Quantification of arterial diameters from the method proposed in this study is validated against laboratory-based x-ray contrast microangiography. The authors find that there is a high degree of correlation (R = 0.91) between measures from microangiography and their contrast free method. CONCLUSIONS: A technique for quantification of murine pulmonary vasculature without the need for contrast is presented. As such, this technique could be applied for longitudinal studies of animals to study changes to vasculature without the risk of premature death in sensitive mouse models of disease. This approach may also be of value in the clinical setting. |
format | Online Article Text |
id | pubmed-5074996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Association of Physicists in Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-50749962016-10-28 Technical Note: Contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source Samarage, Chaminda R. Carnibella, Richard Preissner, Melissa Jones, Heather D. Pearson, James T. Fouras, Andreas Dubsky, Stephen Med Phys QUANTITATIVE IMAGING AND IMAGE PROCESSING PURPOSE: In vivo imaging of the pulmonary vasculature in small animals is difficult yet highly desirable in order to allow study of the effects of a host of dynamic biological processes such as hypoxic pulmonary vasoconstriction. Here the authors present an approach for the quantification of changes in the vasculature. METHODS: A contrast free angiography technique is validated in silico through the use of computer-generated images and in vivo through microcomputed tomography (μCT) of live mice conducted using a laboratory-based x-ray source. Subsequent image processing on μCT data allowed for the quantification of the caliber of pulmonary vasculature without the need for external contrast agents. These measures were validated by comparing with quantitative contrast microangiography in the same mice. RESULTS: Quantification of arterial diameters from the method proposed in this study is validated against laboratory-based x-ray contrast microangiography. The authors find that there is a high degree of correlation (R = 0.91) between measures from microangiography and their contrast free method. CONCLUSIONS: A technique for quantification of murine pulmonary vasculature without the need for contrast is presented. As such, this technique could be applied for longitudinal studies of animals to study changes to vasculature without the risk of premature death in sensitive mouse models of disease. This approach may also be of value in the clinical setting. American Association of Physicists in Medicine 2016-11 2016-10-18 /pmc/articles/PMC5074996/ /pubmed/27806595 http://dx.doi.org/10.1118/1.4964794 Text en © 2016 Author(s). 0094-2405/2016/43(11)/6017/7/$0.00 All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | QUANTITATIVE IMAGING AND IMAGE PROCESSING Samarage, Chaminda R. Carnibella, Richard Preissner, Melissa Jones, Heather D. Pearson, James T. Fouras, Andreas Dubsky, Stephen Technical Note: Contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source |
title | Technical Note: Contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source |
title_full | Technical Note: Contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source |
title_fullStr | Technical Note: Contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source |
title_full_unstemmed | Technical Note: Contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source |
title_short | Technical Note: Contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source |
title_sort | technical note: contrast free angiography of the pulmonary vasculature in live mice using a laboratory x-ray source |
topic | QUANTITATIVE IMAGING AND IMAGE PROCESSING |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074996/ https://www.ncbi.nlm.nih.gov/pubmed/27806595 http://dx.doi.org/10.1118/1.4964794 |
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