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dc.contributor.authorLi, Fuhai
dc.contributor.authorIrie, Katsumi
dc.contributor.authorAnwer, M. Sawkat
dc.contributor.authorFisher, Marc
dc.date2022-08-11T08:09:26.000
dc.date.accessioned2022-08-23T16:31:06Z
dc.date.available2022-08-23T16:31:06Z
dc.date.issued1997-10-01
dc.date.submitted2008-04-17
dc.identifier.citationJ Cereb Blood Flow Metab. 1997 Oct;17(10):1132-5. <a href="http://dx.doi.org/10.1097/00004647-199710000-00016">Link to article on publisher's site</a>
dc.identifier.issn0271-678X (Print)
dc.identifier.doi10.1097/00004647-199710000-00016
dc.identifier.pmid9346439
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37566
dc.description.abstractSixteen of 24 Sprague-Dawley rats with permanent middle cerebral artery occlusion for 24 hours were subjected to immediate or 8-hour delayed 2,3,5-triphenyltetrazolium chloride (TTC) staining (n = 8 at each time point); the other 8 animals were subjected to immediate or 8-hour delayed measurement of succinate dehydrogenase activity (n = 4 at each time point). The TTC staining was of good quality good in all animals, and the infarcted region could be distinguished easily from normal tissue. There was no significant difference in corrected infarct volume between the two groups (263.8 +/- 43.1 versus 264.4 +/- 54.8 mm3 [mean +/- standard deviation]). The activity of succinate dehydrogenase was not significantly different when normal or infarcted tissue was measured immediately after death or with an 8 hour delay, although less activity was detected at both time points in the infarcted tissue. These results demonstrate that an 8-hour delay of TTC staining is reliable for evaluating brain infarct volume in a rat stroke model and this probably is attributable to the slow deterioration of mitochondrial enzyme activity in nonischemic brain over this time period.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9346439&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1097/00004647-199710000-00016
dc.subjectAnimals
dc.subjectBrain
dc.subjectCerebral Infarction
dc.subjectColoring Agents
dc.subjectMale
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectStaining and Labeling
dc.subjectSuccinate Dehydrogenase
dc.subject*Tetrazolium Salts
dc.subjectTime Factors
dc.subjectNervous System Diseases
dc.subjectNeurology
dc.titleDelayed triphenyltetrazolium chloride staining remains useful for evaluating cerebral infarct volume in a rat stroke model
dc.typeJournal Article
dc.source.journaltitleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
dc.source.volume17
dc.source.issue10
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neuro_pp/105
dc.identifier.contextkey492211
html.description.abstract<p>Sixteen of 24 Sprague-Dawley rats with permanent middle cerebral artery occlusion for 24 hours were subjected to immediate or 8-hour delayed 2,3,5-triphenyltetrazolium chloride (TTC) staining (n = 8 at each time point); the other 8 animals were subjected to immediate or 8-hour delayed measurement of succinate dehydrogenase activity (n = 4 at each time point). The TTC staining was of good quality good in all animals, and the infarcted region could be distinguished easily from normal tissue. There was no significant difference in corrected infarct volume between the two groups (263.8 +/- 43.1 versus 264.4 +/- 54.8 mm3 [mean +/- standard deviation]). The activity of succinate dehydrogenase was not significantly different when normal or infarcted tissue was measured immediately after death or with an 8 hour delay, although less activity was detected at both time points in the infarcted tissue. These results demonstrate that an 8-hour delay of TTC staining is reliable for evaluating brain infarct volume in a rat stroke model and this probably is attributable to the slow deterioration of mitochondrial enzyme activity in nonischemic brain over this time period.</p>
dc.identifier.submissionpathneuro_pp/105
dc.contributor.departmentDepartment of Neurology
dc.source.pages1132-5


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