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Autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain
Impairment of cerebrovascular autoregulation (CAR) is common after brain injury, although the pathophysiology remains elusive. The mechanisms of vascular dysregulation, their impact on brain function, and potential therapeutic implications are still incompletely understood. Clinical assessment of CA...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746693/ https://www.ncbi.nlm.nih.gov/pubmed/31527671 http://dx.doi.org/10.1038/s41598-019-50046-x |
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author | Klein, S. P. De Sloovere, V. Meyfroidt, G. Depreitere, B. |
author_facet | Klein, S. P. De Sloovere, V. Meyfroidt, G. Depreitere, B. |
author_sort | Klein, S. P. |
collection | PubMed |
description | Impairment of cerebrovascular autoregulation (CAR) is common after brain injury, although the pathophysiology remains elusive. The mechanisms of vascular dysregulation, their impact on brain function, and potential therapeutic implications are still incompletely understood. Clinical assessment of CAR remains challenging. Observational studies suggest that CAR impairment is associated with worse outcomes, and that optimization of cerebral blood flow (CBF) by individual arterial blood pressure (ABP) targets could potentially improve outcome. We present a porcine closed cranial window model that measures the hemodynamic response of pial arterioles, the main site of CBF control, based on changes in their diameter and red blood cell velocity. This quantitative direct CAR assessment is compared to laser Doppler flow (LDF). CAR breakpoints are determined by segmented regression analysis and validated using LDF and brain tissue oxygen pressure. Using a standardized cortical impact, CAR impairment in traumatic brain injury can be studied using our method of combining pial arteriolar diameter and RBC velocity to quantify RBC flux in a large animal model. The model has numerous potential applications to investigate CAR physiology and pathophysiology of CAR impairment after brain injury, the impact of therapeutic interventions, drugs, and other confounders, or to develop personalized ABP management strategies. |
format | Online Article Text |
id | pubmed-6746693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67466932019-09-27 Autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain Klein, S. P. De Sloovere, V. Meyfroidt, G. Depreitere, B. Sci Rep Article Impairment of cerebrovascular autoregulation (CAR) is common after brain injury, although the pathophysiology remains elusive. The mechanisms of vascular dysregulation, their impact on brain function, and potential therapeutic implications are still incompletely understood. Clinical assessment of CAR remains challenging. Observational studies suggest that CAR impairment is associated with worse outcomes, and that optimization of cerebral blood flow (CBF) by individual arterial blood pressure (ABP) targets could potentially improve outcome. We present a porcine closed cranial window model that measures the hemodynamic response of pial arterioles, the main site of CBF control, based on changes in their diameter and red blood cell velocity. This quantitative direct CAR assessment is compared to laser Doppler flow (LDF). CAR breakpoints are determined by segmented regression analysis and validated using LDF and brain tissue oxygen pressure. Using a standardized cortical impact, CAR impairment in traumatic brain injury can be studied using our method of combining pial arteriolar diameter and RBC velocity to quantify RBC flux in a large animal model. The model has numerous potential applications to investigate CAR physiology and pathophysiology of CAR impairment after brain injury, the impact of therapeutic interventions, drugs, and other confounders, or to develop personalized ABP management strategies. Nature Publishing Group UK 2019-09-16 /pmc/articles/PMC6746693/ /pubmed/31527671 http://dx.doi.org/10.1038/s41598-019-50046-x Text en © The Author(s) 2019 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 Klein, S. P. De Sloovere, V. Meyfroidt, G. Depreitere, B. Autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain |
title | Autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain |
title_full | Autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain |
title_fullStr | Autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain |
title_full_unstemmed | Autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain |
title_short | Autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain |
title_sort | autoregulation assessment by direct visualisation of pial arterial blood flow in the piglet brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746693/ https://www.ncbi.nlm.nih.gov/pubmed/31527671 http://dx.doi.org/10.1038/s41598-019-50046-x |
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