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Type: Journal article
Title: Cerebral microcirculation during experimental normovolaemic anemia
Author: Bellapart, J.
Cuthbertson, K.
Dunster, K.
Diab, S.
Platts, D.G.
Raffel, O.C.
Gabrielian, L.
Barnett, A.
Paratz, J.
Boots, R.
Fraser, J.F.
Citation: Frontiers in Neurology, 2016; 7(FEB):6-1-6-9
Publisher: Frontiers Media
Issue Date: 2016
ISSN: 1664-2295
Statement of
Judith Bellapart, Kylie Cuthbertson, Kimble Dunster, Sara Diab, David G. Platts, O. Christopher Raffel, Levon Gabrielian, Adrian Barnett, Jenifer Paratz, Rob Boots and John F. Fraser
Abstract: Anemia is accepted among critically ill patients as an alternative to elective blood transfusion. This practice has been extrapolated to head injury patients with only one study comparing the effects of mild anemia on neurological outcome. There are no studies quantifying microcirculation during anemia. Experimental studies suggest that anemia leads to cerebral hypoxia and increased rates of infarction, but the lack of clinical equipoise, when testing the cerebral effects of transfusion among critically injured patients, supports the need of experimental studies. The aim of this study was to quantify cerebral microcirculation and the potential presence of axonal damage in an experimental model exposed to normovolaemic anemia, with the intention of describing possible limitations within management practices in critically ill patients. Under non-recovered anesthesia, six Merino sheep were instrumented using an intracardiac transeptal catheter to inject coded microspheres into the left atrium to ensure systemic and non-chaotic distribution. Cytometric analyses quantified cerebral microcirculation at specific regions of the brain. Amyloid precursor protein staining was used as an indicator of axonal damage. Animals were exposed to normovolaemic anemia by blood extractions from the indwelling arterial catheter with simultaneous fluid replacement through a venous central catheter. Simultaneous data recording from cerebral tissue oxygenation, intracranial pressure, and cardiac output was monitored. A regression model was used to examine the effects of anemia on microcirculation with a mixed model to control for repeated measures. Homogeneous and normal cerebral microcirculation with no evidence of axonal damage was present in all cerebral regions, with no temporal variability, concluding that acute normovolaemic anemia does not result in short-term effects on cerebral microcirculation in the ovine brain.
Keywords: APP staining; anemia; histology; microcirculation; microspheres
Rights: © 2016 Bellapart, Cuthbertson, Dunster, Diab, Platts, Raffel, Gabrielian, Barnett, Paratz, Boots and Fraser. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
RMID: 0030045958
DOI: 10.3389/fneur.2016.00006
Appears in Collections:Medicine publications

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