Cargando…

The Time of Maximum Post-Ischemic Hyperperfusion Indicates Infarct Growth Following Transient Experimental Ischemia

After recanalization, cerebral blood flow (CBF) can increase above baseline in cerebral ischemia. However, the significance of post-ischemic hyperperfusion for tissue recovery remains unclear. To analyze the course of post-ischemic hyperperfusion and its impact on vascular function, we used magnetic...

Descripción completa

Detalles Bibliográficos
Autores principales: Wegener, Susanne, Artmann, Judith, Luft, Andreas R., Buxton, Richard B., Weller, Michael, Wong, Eric C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669346/
https://www.ncbi.nlm.nih.gov/pubmed/23741488
http://dx.doi.org/10.1371/journal.pone.0065322
_version_ 1782271738156941312
author Wegener, Susanne
Artmann, Judith
Luft, Andreas R.
Buxton, Richard B.
Weller, Michael
Wong, Eric C.
author_facet Wegener, Susanne
Artmann, Judith
Luft, Andreas R.
Buxton, Richard B.
Weller, Michael
Wong, Eric C.
author_sort Wegener, Susanne
collection PubMed
description After recanalization, cerebral blood flow (CBF) can increase above baseline in cerebral ischemia. However, the significance of post-ischemic hyperperfusion for tissue recovery remains unclear. To analyze the course of post-ischemic hyperperfusion and its impact on vascular function, we used magnetic resonance imaging (MRI) with pulsed arterial spin labeling (pASL) and measured CBF quantitatively during and after a 60 minute transient middle cerebral artery occlusion (MCAO) in adult rats. We added a 5% CO(2) - challenge to analyze vasoreactivity in the same animals. Results from MRI were compared to histological correlates of angiogenesis. We found that CBF in the ischemic area recovered within one day and reached values significantly above contralateral thereafter. The extent of hyperperfusion changed over time, which was related to final infarct size: early (day 1) maximal hyperperfusion was associated with smaller lesions, whereas a later (day 4) maximum indicated large lesions. Furthermore, after initial vasoparalysis within the ischemic area, vasoreactivity on day 14 was above baseline in a fraction of animals, along with a higher density of blood vessels in the ischemic border zone. These data provide further evidence that late post-ischemic hyperperfusion is a sequel of ischemic damage in regions that are likely to undergo infarction. However, it is transient and its resolution coincides with re-gaining of vascular structure and function.
format Online
Article
Text
id pubmed-3669346
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36693462013-06-05 The Time of Maximum Post-Ischemic Hyperperfusion Indicates Infarct Growth Following Transient Experimental Ischemia Wegener, Susanne Artmann, Judith Luft, Andreas R. Buxton, Richard B. Weller, Michael Wong, Eric C. PLoS One Research Article After recanalization, cerebral blood flow (CBF) can increase above baseline in cerebral ischemia. However, the significance of post-ischemic hyperperfusion for tissue recovery remains unclear. To analyze the course of post-ischemic hyperperfusion and its impact on vascular function, we used magnetic resonance imaging (MRI) with pulsed arterial spin labeling (pASL) and measured CBF quantitatively during and after a 60 minute transient middle cerebral artery occlusion (MCAO) in adult rats. We added a 5% CO(2) - challenge to analyze vasoreactivity in the same animals. Results from MRI were compared to histological correlates of angiogenesis. We found that CBF in the ischemic area recovered within one day and reached values significantly above contralateral thereafter. The extent of hyperperfusion changed over time, which was related to final infarct size: early (day 1) maximal hyperperfusion was associated with smaller lesions, whereas a later (day 4) maximum indicated large lesions. Furthermore, after initial vasoparalysis within the ischemic area, vasoreactivity on day 14 was above baseline in a fraction of animals, along with a higher density of blood vessels in the ischemic border zone. These data provide further evidence that late post-ischemic hyperperfusion is a sequel of ischemic damage in regions that are likely to undergo infarction. However, it is transient and its resolution coincides with re-gaining of vascular structure and function. Public Library of Science 2013-05-31 /pmc/articles/PMC3669346/ /pubmed/23741488 http://dx.doi.org/10.1371/journal.pone.0065322 Text en © 2013 Wegener et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wegener, Susanne
Artmann, Judith
Luft, Andreas R.
Buxton, Richard B.
Weller, Michael
Wong, Eric C.
The Time of Maximum Post-Ischemic Hyperperfusion Indicates Infarct Growth Following Transient Experimental Ischemia
title The Time of Maximum Post-Ischemic Hyperperfusion Indicates Infarct Growth Following Transient Experimental Ischemia
title_full The Time of Maximum Post-Ischemic Hyperperfusion Indicates Infarct Growth Following Transient Experimental Ischemia
title_fullStr The Time of Maximum Post-Ischemic Hyperperfusion Indicates Infarct Growth Following Transient Experimental Ischemia
title_full_unstemmed The Time of Maximum Post-Ischemic Hyperperfusion Indicates Infarct Growth Following Transient Experimental Ischemia
title_short The Time of Maximum Post-Ischemic Hyperperfusion Indicates Infarct Growth Following Transient Experimental Ischemia
title_sort time of maximum post-ischemic hyperperfusion indicates infarct growth following transient experimental ischemia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669346/
https://www.ncbi.nlm.nih.gov/pubmed/23741488
http://dx.doi.org/10.1371/journal.pone.0065322
work_keys_str_mv AT wegenersusanne thetimeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT artmannjudith thetimeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT luftandreasr thetimeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT buxtonrichardb thetimeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT wellermichael thetimeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT wongericc thetimeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT wegenersusanne timeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT artmannjudith timeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT luftandreasr timeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT buxtonrichardb timeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT wellermichael timeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia
AT wongericc timeofmaximumpostischemichyperperfusionindicatesinfarctgrowthfollowingtransientexperimentalischemia