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Enduring Disturbances in Regional Cerebral Blood Flow and Brain Oxygenation at 24 Hours after Asphyxial Cardiac Arrest in Developing Rats
BACKGROUND: Disturbances in cerebral blood flow (CBF) and brain oxygenation (PbO(2)) are present early after pediatric cardiac arrest (CA). CBF-targeted therapies improved neurological outcome in our CA model. To assess the therapeutic window for CBF- and PbO(2)-targeted therapies, we propose to det...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287715/ https://www.ncbi.nlm.nih.gov/pubmed/27636898 http://dx.doi.org/10.1038/pr.2016.175 |
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author | Foley, Lesley M. Clark, Robert S.B. Vazquez, Alberto L. Hitchens, T. Kevin Alexander, Henry Ho, Chien Kochanek, Patrick M. Manole, Mioara D. |
author_facet | Foley, Lesley M. Clark, Robert S.B. Vazquez, Alberto L. Hitchens, T. Kevin Alexander, Henry Ho, Chien Kochanek, Patrick M. Manole, Mioara D. |
author_sort | Foley, Lesley M. |
collection | PubMed |
description | BACKGROUND: Disturbances in cerebral blood flow (CBF) and brain oxygenation (PbO(2)) are present early after pediatric cardiac arrest (CA). CBF-targeted therapies improved neurological outcome in our CA model. To assess the therapeutic window for CBF- and PbO(2)-targeted therapies, we propose to determine if CBF and PbO(2) disturbances persist at 24 h after experimental pediatric CA. METHODS: Regional CBF and PbO(2) were measured at 24 h after asphyxial CA in immature rats (n=26, 6–8/group) using arterial spin label MRI and tissue electrodes, respectively. Results. In all regions but the thalamus CBF recovered to sham values by 24 h; thalamic CBF was >32% higher after CA vs. sham. PbO(2) values at 24 h after CA in cortex and thalamus were similar to shams in rats who received supplemental oxygen, however, on room air, cortical PbO(2) was lower after CA vs. shams. CONCLUSION: CBF remains increased in the thalamus at 24 h after CA and PbO(2) is decreased to hypoxic levels in cortex at 24 h after CA in rats who do not receive supplemental oxygen. Given the enduring disturbances in this model and the lack of routine CBF or PbO(2) monitoring in patients, our data suggest then need for clinical correlation. |
format | Online Article Text |
id | pubmed-5287715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-52877152017-03-16 Enduring Disturbances in Regional Cerebral Blood Flow and Brain Oxygenation at 24 Hours after Asphyxial Cardiac Arrest in Developing Rats Foley, Lesley M. Clark, Robert S.B. Vazquez, Alberto L. Hitchens, T. Kevin Alexander, Henry Ho, Chien Kochanek, Patrick M. Manole, Mioara D. Pediatr Res Article BACKGROUND: Disturbances in cerebral blood flow (CBF) and brain oxygenation (PbO(2)) are present early after pediatric cardiac arrest (CA). CBF-targeted therapies improved neurological outcome in our CA model. To assess the therapeutic window for CBF- and PbO(2)-targeted therapies, we propose to determine if CBF and PbO(2) disturbances persist at 24 h after experimental pediatric CA. METHODS: Regional CBF and PbO(2) were measured at 24 h after asphyxial CA in immature rats (n=26, 6–8/group) using arterial spin label MRI and tissue electrodes, respectively. Results. In all regions but the thalamus CBF recovered to sham values by 24 h; thalamic CBF was >32% higher after CA vs. sham. PbO(2) values at 24 h after CA in cortex and thalamus were similar to shams in rats who received supplemental oxygen, however, on room air, cortical PbO(2) was lower after CA vs. shams. CONCLUSION: CBF remains increased in the thalamus at 24 h after CA and PbO(2) is decreased to hypoxic levels in cortex at 24 h after CA in rats who do not receive supplemental oxygen. Given the enduring disturbances in this model and the lack of routine CBF or PbO(2) monitoring in patients, our data suggest then need for clinical correlation. 2016-09-16 2017-01 /pmc/articles/PMC5287715/ /pubmed/27636898 http://dx.doi.org/10.1038/pr.2016.175 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Foley, Lesley M. Clark, Robert S.B. Vazquez, Alberto L. Hitchens, T. Kevin Alexander, Henry Ho, Chien Kochanek, Patrick M. Manole, Mioara D. Enduring Disturbances in Regional Cerebral Blood Flow and Brain Oxygenation at 24 Hours after Asphyxial Cardiac Arrest in Developing Rats |
title | Enduring Disturbances in Regional Cerebral Blood Flow and Brain Oxygenation at 24 Hours after Asphyxial Cardiac Arrest in Developing Rats |
title_full | Enduring Disturbances in Regional Cerebral Blood Flow and Brain Oxygenation at 24 Hours after Asphyxial Cardiac Arrest in Developing Rats |
title_fullStr | Enduring Disturbances in Regional Cerebral Blood Flow and Brain Oxygenation at 24 Hours after Asphyxial Cardiac Arrest in Developing Rats |
title_full_unstemmed | Enduring Disturbances in Regional Cerebral Blood Flow and Brain Oxygenation at 24 Hours after Asphyxial Cardiac Arrest in Developing Rats |
title_short | Enduring Disturbances in Regional Cerebral Blood Flow and Brain Oxygenation at 24 Hours after Asphyxial Cardiac Arrest in Developing Rats |
title_sort | enduring disturbances in regional cerebral blood flow and brain oxygenation at 24 hours after asphyxial cardiac arrest in developing rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287715/ https://www.ncbi.nlm.nih.gov/pubmed/27636898 http://dx.doi.org/10.1038/pr.2016.175 |
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