Kernspintomographische Untersuchungen nach "controlled cortical impact injury"
Abstract (Summary)
Objective: The controlled cortical impact injury (CCII) device, as described by Dixon
1991, was used to investigate the brain tissue damage in an animal model of severe traumatic
brain injury. Magnetic resonance imaging (MRI) techniques including diffusion
weighted imaging (DWI) have been applied to analyse the time course and the characteristics
of edema formation and to detect blood-brain-barrier disruption. Furthermore MRI
has been used to investigate a neuroprotective effect of the NO-synthase pathway modulator
lubeluzole, which has proved markedly beneficial in a model of cerebral ischemia in
rats.
Material and Methods: a left parieto-temporal cortical contusion was inflicted upon 46
Sprague Dawley rats. Animals have been examined up to 7 days following trauma by
MRI. 36 animals have been administered lubeluzole resp. placebo.
Results: The most pronounced edema formation has been shown in T2-weighed imaging
at 24 - 48 hours post trauma. DWI was able to distinguish between a contusion core and
a contusion rim. The contusion core was marked by a decrease in the apparent diffusion
coefficient (ADC) up to 48 hours post trauma, indicating cytotoxic edema, whereas the
contusion rim has been characterised by vasogenic edema, as indicated by ADC-increase
over the entire investigation period. In T1-weighted imaging contrast agent extravasation
indicated a sustained blood brain barrier disruption up to 7 days after trauma. Compared
to placebo administered rats in lubeluzole-treated animals no significant differences
in ADC-changes, edema-extension or physiological parameters as blood pressure, intracranial
pressure or brain swelling could be demonstrated.
Conclusion: CCII induced traumatic brain injury is characterised by a cytotoxic edema
up to 48 hours encircled by a vasogenic contusion rim accompanied by a sustained blood
brain barrier disruption. In the model of CCII lubeluzole did not reveal a neuroprotective
effect in the applied dosage.
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Source Type:Master's Thesis
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