Understanding Vasomotion of Lung Microcirculation by In Vivo Imaging

The balance of lung extravascular water depends upon the control of blood flow in the alveolar distribution vessels that feed downstream two districts placed in parallel, the corner vessels and the alveolar septal network. The occurrence of an edemagenic condition appears critical as an increase in...

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Main Authors: Enrico Mazzuca, Andrea Aliverti, Giuseppe Miserocchi
Format: Article
Language:English
Published: MDPI AG 2019-01-01
Series:Journal of Imaging
Subjects:
Online Access:https://www.mdpi.com/2313-433X/5/2/22
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spelling doaj-170f23fa71514a23bb2326903e6474db2020-11-25T02:46:21ZengMDPI AGJournal of Imaging2313-433X2019-01-01522210.3390/jimaging5020022jimaging5020022Understanding Vasomotion of Lung Microcirculation by In Vivo ImagingEnrico Mazzuca0Andrea Aliverti1Giuseppe Miserocchi2Department of Electronics, Information and Bioengineering, Politecnico di Milano, 20133 Milan, ItalyDepartment of Electronics, Information and Bioengineering, Politecnico di Milano, 20133 Milan, ItalyDepartment of Experimental Medicine, Università di Milano Bicocca, 20900 Milan, ItalyThe balance of lung extravascular water depends upon the control of blood flow in the alveolar distribution vessels that feed downstream two districts placed in parallel, the corner vessels and the alveolar septal network. The occurrence of an edemagenic condition appears critical as an increase in extravascular water endangers the thinness of the air⁻blood barrier, thus negatively affecting the diffusive capacity of the lung. We exposed anesthetized rabbits to an edemagenic factor (12% hypoxia) for 120 min and followed by in vivo imaging the micro-vascular morphology through a “pleural window„ using a stereo microscope at a magnification of 15× (resolution of 7.2 μm). We measured the change in diameter of distribution vessels (50⁻200 μm) and corner vessels (<50 μm). On average, hypoxia caused a significant decrease in diameter of both smaller distribution vessels (about ~50%) and corner vessels (about ~25%) at 30 min. After 120 min, reperfusion occurred. Regional differences in perivascular interstitial volume were observed and could be correlated with differences in blood flow control. To understand such difference, we modelled imaged alveolar capillary units, obtained by Voronoi method, integrating microvascular pressure parameters with capillary filtration. Results of the analysis suggested that at 120 min, alveolar blood flow was diverted to the corner vessels in larger alveoli, which were found also to undergo a greater filtration indicating greater proneness to develop lung edema.https://www.mdpi.com/2313-433X/5/2/22in vivo microscopylung capillariesedemaimage-based modeling
collection DOAJ
language English
format Article
sources DOAJ
author Enrico Mazzuca
Andrea Aliverti
Giuseppe Miserocchi
spellingShingle Enrico Mazzuca
Andrea Aliverti
Giuseppe Miserocchi
Understanding Vasomotion of Lung Microcirculation by In Vivo Imaging
Journal of Imaging
in vivo microscopy
lung capillaries
edema
image-based modeling
author_facet Enrico Mazzuca
Andrea Aliverti
Giuseppe Miserocchi
author_sort Enrico Mazzuca
title Understanding Vasomotion of Lung Microcirculation by In Vivo Imaging
title_short Understanding Vasomotion of Lung Microcirculation by In Vivo Imaging
title_full Understanding Vasomotion of Lung Microcirculation by In Vivo Imaging
title_fullStr Understanding Vasomotion of Lung Microcirculation by In Vivo Imaging
title_full_unstemmed Understanding Vasomotion of Lung Microcirculation by In Vivo Imaging
title_sort understanding vasomotion of lung microcirculation by in vivo imaging
publisher MDPI AG
series Journal of Imaging
issn 2313-433X
publishDate 2019-01-01
description The balance of lung extravascular water depends upon the control of blood flow in the alveolar distribution vessels that feed downstream two districts placed in parallel, the corner vessels and the alveolar septal network. The occurrence of an edemagenic condition appears critical as an increase in extravascular water endangers the thinness of the air⁻blood barrier, thus negatively affecting the diffusive capacity of the lung. We exposed anesthetized rabbits to an edemagenic factor (12% hypoxia) for 120 min and followed by in vivo imaging the micro-vascular morphology through a “pleural window„ using a stereo microscope at a magnification of 15× (resolution of 7.2 μm). We measured the change in diameter of distribution vessels (50⁻200 μm) and corner vessels (<50 μm). On average, hypoxia caused a significant decrease in diameter of both smaller distribution vessels (about ~50%) and corner vessels (about ~25%) at 30 min. After 120 min, reperfusion occurred. Regional differences in perivascular interstitial volume were observed and could be correlated with differences in blood flow control. To understand such difference, we modelled imaged alveolar capillary units, obtained by Voronoi method, integrating microvascular pressure parameters with capillary filtration. Results of the analysis suggested that at 120 min, alveolar blood flow was diverted to the corner vessels in larger alveoli, which were found also to undergo a greater filtration indicating greater proneness to develop lung edema.
topic in vivo microscopy
lung capillaries
edema
image-based modeling
url https://www.mdpi.com/2313-433X/5/2/22
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