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Type: Journal article
Title: Temporal characterisation of pro- and anti-apoptotic mechanisms following diffuse traumatic brain injury in rats
Author: Cernak, I.
Chapman, S.
Hamlin, G.
Vink, R.
Citation: Journal of Clinical Neuroscience, 2002; 9(5):565-572
Publisher: Churchill Livingstone
Issue Date: 2002
ISSN: 0967-5868
Statement of
Ibolja Cernak, Sarah M. Chapman, Gary P. Hamlin and Robert Vink
Abstract: Few studies have characterised apoptosis in a brain injury model that causes a significant degree of diffuse axonal injury. Such characterisation is essential from a clinical viewpoint since diffuse axonal injury is a major component of human head injury. The present study therefore, examines the expression of active and proactive caspase-3, and the bax, bcl-2 and bcl-x members of the bcl-2 family, to characterise the temporal profile of apoptosis in a model of traumatic brain injury in rats that produces significant diffuse axonal injury. Pentobarbital anaesthetised male Sprague-Dawley rats were injured using the 2m impact-acceleration model of diffuse traumatic brain injury. After injury, diffuse trauma resulted in an increased bax expression followed by induction of caspase-3. The increase in caspase-3 was simultaneous with an increase in anti-apoptotic bcl-2 expression. Bcl-x levels were increased after induction of caspase-3 and the increased levels of bcl-x were sustained to the end of the 5-day observation period. Increased active caspase-3 expression was associated with the appearance of TUNEL positive cells. These cells were detected in different brain regions at different times, with some regions showing no apoptotic cells until 3 days after injury. No TUNEL positive cells were detected at 7 and 14 days after injury. DNA electrophoresis confirmed that DNA fragmentation was maximal at 3 days after injury. Increased active caspase-3 levels were also significantly correlated with increased bcl-2 levels (r=0.80; P<0.001) suggesting that the apoptotic cascade after diffuse traumatic brain injury is a carefully controlled cellular homeostatic response. Pharmacological manipulation of this balance may offer a therapeutic approach for preventing cell death and improving outcome after diffuse traumatic brain injury.
Keywords: Neurons
Rats, Sprague-Dawley
Brain Injuries
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-bcl-2
Electrophoresis, Agar Gel
In Situ Nick-End Labeling
DNA Fragmentation
bcl-2-Associated X Protein
Caspase 3
Rights: Copyright © 2002 Elsevier Science Ltd. All rights reserved.
DOI: 10.1054/jocn.2002.1132
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Appears in Collections:Aurora harvest
Pathology publications

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