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Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling
The neurovascular mechanisms underpinning the local regulation of cerebral blood flow (CBF) and oxygen transport remain elusive. In this study we have combined novel in vivo imaging of cortical microvascular and mural cell architecture with mathematical modelling of blood flow and oxygen transport,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778006/ https://www.ncbi.nlm.nih.gov/pubmed/29358701 http://dx.doi.org/10.1038/s41598-017-19086-z |
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author | Sweeney, Paul W. Walker-Samuel, Simon Shipley, Rebecca J. |
author_facet | Sweeney, Paul W. Walker-Samuel, Simon Shipley, Rebecca J. |
author_sort | Sweeney, Paul W. |
collection | PubMed |
description | The neurovascular mechanisms underpinning the local regulation of cerebral blood flow (CBF) and oxygen transport remain elusive. In this study we have combined novel in vivo imaging of cortical microvascular and mural cell architecture with mathematical modelling of blood flow and oxygen transport, to provide new insights into CBF regulation that would be inaccessible in a conventional experimental context. Our study indicates that vasoconstriction of smooth muscle actin-covered vessels, rather than pericyte-covered capillaries, induces stable reductions in downstream intravascular capillary and tissue oxygenation. We also propose that seemingly paradoxical observations in the literature around reduced blood velocity in response to arteriolar constrictions might be caused by a propagation of constrictions to upstream penetrating arterioles. We provide support for pericytes acting as signalling conduits for upstream smooth muscle activation, and erythrocyte deformation as a complementary regulatory mechanism. Finally, we caution against the use of blood velocity as a proxy measurement for flow. Our combined imaging-modelling platform complements conventional experimentation allowing cerebrovascular physiology to be probed in unprecedented detail. |
format | Online Article Text |
id | pubmed-5778006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57780062018-01-31 Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling Sweeney, Paul W. Walker-Samuel, Simon Shipley, Rebecca J. Sci Rep Article The neurovascular mechanisms underpinning the local regulation of cerebral blood flow (CBF) and oxygen transport remain elusive. In this study we have combined novel in vivo imaging of cortical microvascular and mural cell architecture with mathematical modelling of blood flow and oxygen transport, to provide new insights into CBF regulation that would be inaccessible in a conventional experimental context. Our study indicates that vasoconstriction of smooth muscle actin-covered vessels, rather than pericyte-covered capillaries, induces stable reductions in downstream intravascular capillary and tissue oxygenation. We also propose that seemingly paradoxical observations in the literature around reduced blood velocity in response to arteriolar constrictions might be caused by a propagation of constrictions to upstream penetrating arterioles. We provide support for pericytes acting as signalling conduits for upstream smooth muscle activation, and erythrocyte deformation as a complementary regulatory mechanism. Finally, we caution against the use of blood velocity as a proxy measurement for flow. Our combined imaging-modelling platform complements conventional experimentation allowing cerebrovascular physiology to be probed in unprecedented detail. Nature Publishing Group UK 2018-01-22 /pmc/articles/PMC5778006/ /pubmed/29358701 http://dx.doi.org/10.1038/s41598-017-19086-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sweeney, Paul W. Walker-Samuel, Simon Shipley, Rebecca J. Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling |
title | Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling |
title_full | Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling |
title_fullStr | Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling |
title_full_unstemmed | Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling |
title_short | Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling |
title_sort | insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778006/ https://www.ncbi.nlm.nih.gov/pubmed/29358701 http://dx.doi.org/10.1038/s41598-017-19086-z |
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