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dc.contributor.authorSpratt, Neil Jen
dc.contributor.authorAckerman, Uween
dc.contributor.authorTochon-Danguy, Henri Jen
dc.contributor.authorDonnan, Geoffrey Aen
dc.contributor.authorHowells, David Williamen
dc.date.accessioned2015-05-15T23:32:05Z
dc.date.available2015-05-15T23:32:05Z
dc.date.issued2006-06-08en
dc.identifier.citationStroke; A Journal of Cerebral Circulation 2006; 37(7): 1862-7en
dc.identifier.govdoc16763190en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/10169en
dc.description.abstract[18F]fluoromisonidazole (FMISO) positron emission tomography has been used to image hypoxia early after human stroke. To further study the role of hypoxia in stroke and the binding characteristics of FMISO, we aimed to develop [3H]FMISO autoradiography in an animal stroke model. We hypothesized that [3H]FMISO binding is prolonged, allowing correlation with 24-hour histology, and that there is no FMISO binding after effective reperfusion.Temporary middle cerebral artery (MCA) occlusion was performed in rats, followed by [3H]FMISO administration. Tissue preparation for autoradiography and histology (from the same sections) was performed 2.5 hours after MCA occlusion (MCAo; replicating [18F]FMISO studies). Then, otherwise identical cohorts with tissue preparation at 2.5 or 24 hours were prepared. For reperfusion studies, animals had 1-hour MCAo, with [3H]FMISO administered 1 hour after reperfusion.[3H]FMISO autoradiography provided a high-resolution image of hypoxia throughout the ischemic territory. Delaying animal death from 2.5 to 24 hours allowed histological changes of stroke to develop, without significantly altering either relative intensity (1.88+/-0.06 and 2.02+/-0.11, respectively) or volume (25+/-6 mm3 and 28+/-5 mm3, respectively) of hypoxic binding. [3H]FMISO binding did not occur after effective reperfusion, despite histological injury from the preceding MCAo.[3H]FMISO autoradiography of hypoxia in experimental stroke offers several advantages. Bound FMISO is retained in tissues long term, enabling direct correlation with 24-hour histology. It is not bound after effective reperfusion. Therefore, positive [18F]FMISO positron emission tomography studies in stroke patients are indicative of ongoing tissue hypoxia, not merely recent tissue injury.en
dc.language.isoenen
dc.subject.otherAnimalsen
dc.subject.otherAutoradiography.methodsen
dc.subject.otherBrain.pathologyen
dc.subject.otherCell Hypoxiaen
dc.subject.otherCerebrovascular Circulationen
dc.subject.otherContrast Media.pharmacokineticsen
dc.subject.otherFluorine Radioisotopes.pharmacokineticsen
dc.subject.otherHypoxia, Brain.etiology.pathology.radionuclide imagingen
dc.subject.otherInfarction, Middle Cerebral Artery.complications.pathology.physiopathology.radionuclide imagingen
dc.subject.otherLaser-Doppler Flowmetryen
dc.subject.otherMisonidazole.analogs & derivatives.analysis.pharmacokineticsen
dc.subject.otherPositron-Emission Tomographyen
dc.subject.otherProtein Bindingen
dc.subject.otherRadioactive Tracersen
dc.subject.otherRatsen
dc.subject.otherRats, Sprague-Dawleyen
dc.subject.otherReperfusionen
dc.subject.otherTime Factorsen
dc.titleCharacterization of fluoromisonidazole binding in stroke.en
dc.typeJournal Articleen
dc.identifier.journaltitleStrokeen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, and National Stroke Research Institute, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1161/01.STR.0000226908.93295.9den
dc.description.pages1862-7en
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/16763190en
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