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dc.contributor.authorBardutzky, Juergen F.
dc.contributor.authorShen, Qiang
dc.contributor.authorHenninger, Nils
dc.contributor.authorBouley, James P.
dc.contributor.authorDuong, Timothy Q.
dc.contributor.authorFisher, Marc
dc.date2022-08-11T08:09:28.000
dc.date.accessioned2022-08-23T16:32:02Z
dc.date.available2022-08-23T16:32:02Z
dc.date.issued2005-09-25
dc.date.submitted2008-04-07
dc.identifier.citationStroke. 2005 Sep;36(9):2000-5. Epub 2005 Jul 21. <a href="http://dx.doi.org/10.1161/01.STR.0000177486.85508.4d">Link to article on publisher's site</a>
dc.identifier.issn1524-4628 (Electronic)
dc.identifier.doi10.1161/01.STR.0000177486.85508.4d
dc.identifier.pmid16040589
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37793
dc.description.abstractBACKGROUND AND PURPOSE: Interstrain differences in the temporal evolution of ischemia after middle cerebral artery occlusion (MCAO) in rats may considerably influence the results of experimental stroke research. We investigated, in 2 commonly used rat strains (Sprague-Dawley [SD] and Wistar-Kyoto [WK]), the spatiotemporal evolution of ischemia after permanent suture MCAO using diffusion and perfusion imaging. METHODS: Serial measurements of quantitative cerebral blood flow (CBF) and apparent diffusion coefficient (ADC) were performed up to 210 min after MCAO. Lesion volumes were calculated by using previously established viability thresholds and correlated with infarct volume defined by 2,3,5-triphenyltetrazolium chloride staining 24 hours after MCAO. RESULTS: While the ADC-derived lesion volume increased rapidly during the first 120 min after MCAO and essentially stopped growing after 3 hours in SD rats, ADC lesion in WK rats increased progressively during the entire 210-min period and was significantly smaller at all time points (PCONCLUSIONS: This study demonstrated substantial differences in acute ischemic lesion evolution between SD and WK rats. These interstrain variations must be taken into account when assessing new therapeutic approaches on ischemic lesion evolution in the rat MCAO model.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16040589&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1161/01.STR.0000177486.85508.4d
dc.subjectAnimals
dc.subjectBrain Ischemia
dc.subjectCerebrovascular Circulation
dc.subjectColoring Agents
dc.subjectDiffusion
dc.subjectDiffusion Magnetic Resonance Imaging
dc.subjectDisease Models, Animal
dc.subjectInfarction, Middle Cerebral Artery
dc.subjectIschemia
dc.subjectMagnetic Resonance Angiography
dc.subjectMale
dc.subjectRats
dc.subjectRats, Inbred WKY
dc.subjectRats, Sprague-Dawley
dc.subjectSpecies Specificity
dc.subjectTetrazolium Salts
dc.subjectTime Factors
dc.subjectNeurology
dc.subjectNeuroscience and Neurobiology
dc.titleDifferences in ischemic lesion evolution in different rat strains using diffusion and perfusion imaging
dc.typeJournal Article
dc.source.journaltitleStroke; a journal of cerebral circulation
dc.source.volume36
dc.source.issue9
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neuro_pp/61
dc.identifier.contextkey483785
html.description.abstract<p>BACKGROUND AND PURPOSE: Interstrain differences in the temporal evolution of ischemia after middle cerebral artery occlusion (MCAO) in rats may considerably influence the results of experimental stroke research. We investigated, in 2 commonly used rat strains (Sprague-Dawley [SD] and Wistar-Kyoto [WK]), the spatiotemporal evolution of ischemia after permanent suture MCAO using diffusion and perfusion imaging.</p> <p>METHODS: Serial measurements of quantitative cerebral blood flow (CBF) and apparent diffusion coefficient (ADC) were performed up to 210 min after MCAO. Lesion volumes were calculated by using previously established viability thresholds and correlated with infarct volume defined by 2,3,5-triphenyltetrazolium chloride staining 24 hours after MCAO.</p> <p>RESULTS: While the ADC-derived lesion volume increased rapidly during the first 120 min after MCAO and essentially stopped growing after 3 hours in SD rats, ADC lesion in WK rats increased progressively during the entire 210-min period and was significantly smaller at all time points (PCONCLUSIONS: This study demonstrated substantial differences in acute ischemic lesion evolution between SD and WK rats. These interstrain variations must be taken into account when assessing new therapeutic approaches on ischemic lesion evolution in the rat MCAO model.</p>
dc.identifier.submissionpathneuro_pp/61
dc.contributor.departmentDepartment of Neurology
dc.source.pages2000-5


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