Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental Model
BackgroundCerebral microcirculation after severe head injury is heterogeneous and temporally variable. Microcirculation is dependent upon the severity of injury, and it is unclear how histology relates to cerebral regional blood flow.ObjectiveThis study assesses the changes of cerebral microcirculat...
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Frontiers Media S.A.
2018-05-01
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Series: | Frontiers in Neurology |
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Online Access: | http://journal.frontiersin.org/article/10.3389/fneur.2018.00277/full |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Judith Bellapart Kylie Cuthbertson Kimble Dunster Kimble Dunster Sara Diab Sara Diab David G. Platts David G. Platts Owen Christopher Raffel Owen Christopher Raffel Levon Gabrielian Levon Gabrielian Adrian Barnett Adrian Barnett Jenifer Paratz Rob Boots John F. Fraser John F. Fraser John F. Fraser John F. Fraser |
spellingShingle |
Judith Bellapart Kylie Cuthbertson Kimble Dunster Kimble Dunster Sara Diab Sara Diab David G. Platts David G. Platts Owen Christopher Raffel Owen Christopher Raffel Levon Gabrielian Levon Gabrielian Adrian Barnett Adrian Barnett Jenifer Paratz Rob Boots John F. Fraser John F. Fraser John F. Fraser John F. Fraser Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental Model Frontiers in Neurology anemia amyloid precursor protein staining histology microcirculation microspheres |
author_facet |
Judith Bellapart Kylie Cuthbertson Kimble Dunster Kimble Dunster Sara Diab Sara Diab David G. Platts David G. Platts Owen Christopher Raffel Owen Christopher Raffel Levon Gabrielian Levon Gabrielian Adrian Barnett Adrian Barnett Jenifer Paratz Rob Boots John F. Fraser John F. Fraser John F. Fraser John F. Fraser |
author_sort |
Judith Bellapart |
title |
Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental Model |
title_short |
Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental Model |
title_full |
Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental Model |
title_fullStr |
Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental Model |
title_full_unstemmed |
Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental Model |
title_sort |
cerebral microcirculation and histological mapping after severe head injury: a contusion and acceleration experimental model |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Neurology |
issn |
1664-2295 |
publishDate |
2018-05-01 |
description |
BackgroundCerebral microcirculation after severe head injury is heterogeneous and temporally variable. Microcirculation is dependent upon the severity of injury, and it is unclear how histology relates to cerebral regional blood flow.ObjectiveThis study assesses the changes of cerebral microcirculation blood flow over time after an experimental brain injury model in sheep and contrasts these findings with the histological analysis of the same regions with the aim of mapping cerebral flow and tissue changes after injury.MethodsMicrocirculation was quantified using flow cytometry of color microspheres injected under intracardiac ultrasound to ensure systemic and homogeneous distribution. Histological analysis used amyloid precursor protein staining as a marker of axonal injury. A mapping of microcirculation and axonal staining was performed using adjacent layers of tissue from the same anatomical area, allowing flow and tissue data to be available from the same anatomical region. A mixed effect regression model assessed microcirculation during 4 h after injury, and those results were then contrasted to the amyloid staining qualitative score.ResultsMicrocirculation values for each subject and tissue region over time, including baseline, ranged between 20 and 80 ml/100 g/min with means that did not differ statistically from baseline flows. However, microcirculation values for each subject and tissue region were reduced from baseline, although their confidence intervals crossing the horizontal ratio of 1 indicated that such reduction was not statistically significant. Histological analysis demonstrated the presence of moderate and severe score on the amyloid staining throughout both hemispheres.ConclusionMicrocirculation at the ipsilateral and contralateral site of a contusion and the ipsilateral thalamus and medulla showed a consistent decline over time. Our data suggest that after severe head injury, microcirculation in predefined areas of the brain is reduced from baseline with amyloid staining in those areas reflecting the early establishment of axonal injury. |
topic |
anemia amyloid precursor protein staining histology microcirculation microspheres |
url |
http://journal.frontiersin.org/article/10.3389/fneur.2018.00277/full |
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doaj-f7ee7951f693439c819e246219c45e022020-11-24T22:39:19ZengFrontiers Media S.A.Frontiers in Neurology1664-22952018-05-01910.3389/fneur.2018.00277332909Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental ModelJudith Bellapart0Kylie Cuthbertson1Kimble Dunster2Kimble Dunster3Sara Diab4Sara Diab5David G. Platts6David G. Platts7Owen Christopher Raffel8Owen Christopher Raffel9Levon Gabrielian10Levon Gabrielian11Adrian Barnett12Adrian Barnett13Jenifer Paratz14Rob Boots15John F. Fraser16John F. Fraser17John F. Fraser18John F. Fraser19Department of Intensive Care, Royal Brisbane and Women’s Hospital, Brisbane, QLD, AustraliaDepartment of Histopathology, Royal Brisbane and Women’s Hospital, Brisbane, QLD, AustraliaCritical Care Research Group, University of Queensland, Brisbane, QLD, AustraliaMedical Engineering Research Facility, Queensland University of Technology, Brisbane, QLD, AustraliaCritical Care Research Group, University of Queensland, Brisbane, QLD, AustraliaMedical Engineering Research Facility, Queensland University of Technology, Brisbane, QLD, AustraliaCritical Care Research Group, University of Queensland, Brisbane, QLD, AustraliaDepartment of Cardiology, The Prince Charles Hospital, Chermside, QLD, AustraliaCritical Care Research Group, University of Queensland, Brisbane, QLD, AustraliaDepartment of Cardiology, The Prince Charles Hospital, Chermside, QLD, AustraliaMedical School, University of South Australia, Adelaide, SA, AustraliaMedical Research Centre, Adelaide, SA, AustraliaCritical Care Research Group, University of Queensland, Brisbane, QLD, AustraliaInstitute of Health and Biomedical Innovation & School of Public Health and Social Work, Queensland University of Technology, Brisbane, QLD, AustraliaDepartment of Intensive Care, Royal Brisbane and Women’s Hospital, Brisbane, QLD, AustraliaDepartment of Intensive Care, Royal Brisbane and Women’s Hospital, Brisbane, QLD, AustraliaCritical Care Research Group, University of Queensland, Brisbane, QLD, AustraliaMedical Engineering Research Facility, Queensland University of Technology, Brisbane, QLD, AustraliaInstitute of Health and Biomedical Innovation & School of Public Health and Social Work, Queensland University of Technology, Brisbane, QLD, AustraliaDepartment of Intensive Care, The Prince Charles Hospital, Chermside, QLD, AustraliaBackgroundCerebral microcirculation after severe head injury is heterogeneous and temporally variable. Microcirculation is dependent upon the severity of injury, and it is unclear how histology relates to cerebral regional blood flow.ObjectiveThis study assesses the changes of cerebral microcirculation blood flow over time after an experimental brain injury model in sheep and contrasts these findings with the histological analysis of the same regions with the aim of mapping cerebral flow and tissue changes after injury.MethodsMicrocirculation was quantified using flow cytometry of color microspheres injected under intracardiac ultrasound to ensure systemic and homogeneous distribution. Histological analysis used amyloid precursor protein staining as a marker of axonal injury. A mapping of microcirculation and axonal staining was performed using adjacent layers of tissue from the same anatomical area, allowing flow and tissue data to be available from the same anatomical region. A mixed effect regression model assessed microcirculation during 4 h after injury, and those results were then contrasted to the amyloid staining qualitative score.ResultsMicrocirculation values for each subject and tissue region over time, including baseline, ranged between 20 and 80 ml/100 g/min with means that did not differ statistically from baseline flows. However, microcirculation values for each subject and tissue region were reduced from baseline, although their confidence intervals crossing the horizontal ratio of 1 indicated that such reduction was not statistically significant. Histological analysis demonstrated the presence of moderate and severe score on the amyloid staining throughout both hemispheres.ConclusionMicrocirculation at the ipsilateral and contralateral site of a contusion and the ipsilateral thalamus and medulla showed a consistent decline over time. Our data suggest that after severe head injury, microcirculation in predefined areas of the brain is reduced from baseline with amyloid staining in those areas reflecting the early establishment of axonal injury.http://journal.frontiersin.org/article/10.3389/fneur.2018.00277/fullanemiaamyloid precursor protein staininghistologymicrocirculationmicrospheres |