Recovery Time between Multiple Mild Photothrombotic Strokes Affects Brain Damage

atmire.migration.oldid1902
dc.contributor.advisorTuor, Ursula
dc.contributor.authorDeng, Qinbo
dc.date.accessioned2014-02-12T16:47:15Z
dc.date.available2014-03-15T07:00:21Z
dc.date.issued2014-02-12
dc.date.submitted2014en
dc.description.abstractPrior to stroke, patients often experience a transient ischemic attack (TIA) or minor stroke with a high recurrence within the first week. The initial episode of ischemia, traditionally considered to causing little permanent damage to brain, is poorly understood for its role in subsequent ischemic events. We hypothesized that despite functional recovery following TIA/minor stroke, there can be sparse tissue damage that alters the brain response to a secondary mild stroke, with the final tissue fate being dependent on the recovery time between recurrent strokes. Thus, the first objective of this thesis was to establish a rat model of TIA/minor stroke using modifications of a phothothrombotic (PT) occlusion of the cerebral microvasculature. The effect of varied light intensities and illumination durations were examined on the severity of stroke. Multiple sequences (T2, Apparent Diffusion Coefficient (ADC), Perfusion Weighted Imaging) of Magnetic Resonance Imaging (MRI) were performed to evaluate the tissue damage. We found that a 5-min illumination at approximate 35,000 Lux of light intensity was optimal to produce a mild tissue damage associated with a transient ischemia measured by Laser-Doppler Flowmetry. The T2 signatures measured at 24h were good predictors of graded ischemic injury confirmed by histology. Compared with ADC measures, T2 provided a better diagnosis of mild damage (scattered necrosis). The second objective was to use this modified PT model to produce a recurrent stroke and to investigate if the outcome differed depending on the interval between insults – i.e. 1day, 2days, 3days and 1week. Using this novel model, we demonstrated that a mild recurrent stroke produced more deleterious injury with acute intervals (1 day to 3 day) than a subacute one (1week). This enhancement of damage was characterized by an increase of T2 and a decrease of perfusion. In contrast, the 1week interval produced tissue damage similar to a single mild stroke, associated with similar changes of MR. Together, our finding revealed a temporal change of brain susceptibility to ischemia, implying the importance of early treatment after TIA/minor stroke for reduction of damage with stroke recurrence.en_US
dc.identifier.citationDeng, Q. (2014). Recovery Time between Multiple Mild Photothrombotic Strokes Affects Brain Damage (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/27565en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/27565
dc.identifier.urihttp://hdl.handle.net/11023/1374
dc.language.isoeng
dc.publisher.facultyGraduate Studies
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.subjectNeuroscience
dc.subjectPsychology--Experimental
dc.subject.classificationAnimal Modelen_US
dc.subject.classificationRecurrent Strokeen_US
dc.subject.classificationTransient Ischemic Attacken_US
dc.subject.classificationMagnetic Resonance Imagingen_US
dc.subject.classificationApparent Diffusion Coeficienten_US
dc.subject.classificationT2-weighted Imagingen_US
dc.subject.classificationDiffusion-weighted Imagingen_US
dc.subject.classificationPerfusion-weighted Imagingen_US
dc.subject.classificationScattered Necrosisen_US
dc.subject.classificationCerebral Blood Flowen_US
dc.titleRecovery Time between Multiple Mild Photothrombotic Strokes Affects Brain Damage
dc.typemaster thesis
thesis.degree.disciplineNeuroscience
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameMaster of Science (MSc)
ucalgary.item.requestcopytrue
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