Show simple item record

dc.contributor.authorHenninger, Nils
dc.contributor.authorSicard, Kenneth M.
dc.contributor.authorSchmidt, Karl F.
dc.contributor.authorBardutzky, Juergen F.
dc.contributor.authorFisher, Marc
dc.date2022-08-11T08:09:28.000
dc.date.accessioned2022-08-23T16:32:03Z
dc.date.available2022-08-23T16:32:03Z
dc.date.issued2006-03-25
dc.date.submitted2008-04-07
dc.identifier.citationStroke. 2006 May;37(5):1283-7. Epub 2006 Mar 23. <a href="http://dx.doi.org/10.1161/01.STR.0000217223.72193.98">Link to article on publisher's site</a>
dc.identifier.issn1524-4628 (Electronic)
dc.identifier.doi10.1161/01.STR.0000217223.72193.98
dc.identifier.pmid16556883
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37795
dc.description<p>Co-author Karl F. Schmidt is a student in the Neuroscience program in the Graduate School of Biomedical Sciences (GSBS) at UMass Medical School.</p>
dc.description.abstractBACKGROUND AND PURPOSE: Differences among models in the temporal evolution of ischemia after middle cerebral artery occlusion (MCAO) in rats may considerably influence the results of experimental stroke research. Using diffusion and perfusion imaging, we compared the spatiotemporal evolution of ischemia in Sprague Dawley rats after permanent suture MCAO (sMCAO; n=8) and embolic MCAO (eMCAO; n=8). METHODS: Serial measurements of quantitative cerebral blood flow (CBF) and the apparent diffusion coefficient (ADC) were performed up to 180 minutes after MCAO. ADC and CBF values within 5 different brain regions were analyzed. ADC and CBF 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: Compared with sMCAO animals, the threshold-derived CBF lesion volume was significantly larger in eMCAO at all time points (P<0.01), remained relatively constant over time, and was highly correlated with the 2,3,5-triphenyltetrazolium chloride-defined infarct size. The ADC lesion volume did not differ between models at any time point. A diffusion/perfusion mismatch was present significantly longer in eMCAO animals (P<0.05), and these rats demonstrated larger absolute mismatch volumes that were statistically significant at 30, 60, and 90 minutes (P<0.05). In both models, CBF and ADC declines were highly correlated. CONCLUSIONS: This study demonstrated substantial differences in acute ischemic lesion evolution between the eMCAO and sMCAO models.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16556883&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1161/01.STR.0000217223.72193.98
dc.subjectAnimals
dc.subjectDiffusion Magnetic Resonance Imaging
dc.subject*Disease Models, Animal
dc.subjectEmbolism
dc.subjectInfarction, Middle Cerebral Artery
dc.subjectMale
dc.subjectMiddle Cerebral Artery
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectNeurology
dc.subjectNeuroscience and Neurobiology
dc.titleComparison of ischemic lesion evolution in embolic versus mechanical middle cerebral artery occlusion in Sprague Dawley rats using diffusion and perfusion imaging
dc.typeJournal Article
dc.source.journaltitleStroke; a journal of cerebral circulation
dc.source.volume37
dc.source.issue5
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neuro_pp/63
dc.identifier.contextkey483787
html.description.abstract<p>BACKGROUND AND PURPOSE: Differences among models in the temporal evolution of ischemia after middle cerebral artery occlusion (MCAO) in rats may considerably influence the results of experimental stroke research. Using diffusion and perfusion imaging, we compared the spatiotemporal evolution of ischemia in Sprague Dawley rats after permanent suture MCAO (sMCAO; n=8) and embolic MCAO (eMCAO; n=8).</p> <p>METHODS: Serial measurements of quantitative cerebral blood flow (CBF) and the apparent diffusion coefficient (ADC) were performed up to 180 minutes after MCAO. ADC and CBF values within 5 different brain regions were analyzed. ADC and CBF 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: Compared with sMCAO animals, the threshold-derived CBF lesion volume was significantly larger in eMCAO at all time points (P<0.01), remained relatively constant over time, and was highly correlated with the 2,3,5-triphenyltetrazolium chloride-defined infarct size. The ADC lesion volume did not differ between models at any time point. A diffusion/perfusion mismatch was present significantly longer in eMCAO animals (P<0.05), and these rats demonstrated larger absolute mismatch volumes that were statistically significant at 30, 60, and 90 minutes (P<0.05). In both models, CBF and ADC declines were highly correlated.</p> <p>CONCLUSIONS: This study demonstrated substantial differences in acute ischemic lesion evolution between the eMCAO and sMCAO models.</p>
dc.identifier.submissionpathneuro_pp/63
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.contributor.departmentDepartment of Neurology
dc.source.pages1283-7


This item appears in the following Collection(s)

Show simple item record