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dc.contributor.authorSirlak, Mustafa
dc.contributor.authorEryilmaz, Sadik
dc.contributor.authorInan, Mustafa Bahadir
dc.contributor.authorSirin, Yusuf Sinan
dc.contributor.authorBesalti, Omer
dc.contributor.authorYazicioglu, Levent
dc.contributor.authorOzyurda, Umit
dc.date.accessioned2020-06-21T15:13:01Z
dc.date.available2020-06-21T15:13:01Z
dc.date.issued2008
dc.identifier.issn0022-5223
dc.identifier.urihttps://doi.org/10.1016/j.jtcvs.2007.12.068
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19160
dc.descriptionBesalti, Omer/0000-0002-7819-9094; Erdemli, Esra/0000-0002-9737-269X; Elhan, Atilla Halil/0000-0003-3324-248Xen_US
dc.descriptionWOS: 000260314800034en_US
dc.descriptionPubMed: 18954647en_US
dc.description.abstractBackground: Prophylactic treatment with carbamazepine has been shown to reduce the cerebral damage and neurologic deficit in ischemic conditions. A randomized controlled study based on a rabbit model was designed to study the effect of carbamazepine on a spinal cord ischemic reperfusion injury. Methods: Thirty New Zealand rabbits were randomly assigned to 1 of the 2 groups (n = 15 per group): group I (control group) and group II (carbamazepine group). Spinal cord ischemia was induced by infrarenal aortic crossclamp for 25 minutes in both groups. Functional evaluation with the Tarlov score during a 2-day observation period and histopathologic assessment of the lumbar spinal cord were performed. Changes in spinal cord morphology were observed with hematoxylin-eosin staining and electron microscopy. Gray matter damage was assessed on the basis of the number of normal neurons in the ventral horn. Results: Diffuse destruction of gray matter with moderate to severe vacuolization and essentially no normal ganglion cells was observed in the spinal cord of rabbits in the control group, whereas specimens of rabbits assigned to the carbamazepine group showed ganglion cells with normal nuclei and cytoplasm (P < .0001). Neurologic impairment was significantly attenuated in the carbamazepine group compared with the Tarlov scores of the control group (P < .0001 at day 2). Conclusion: Carbamazepine may protect the spinal cord from ischemic reperfusion injury that is associated with ameliorated neurologic and histopathologic results.en_US
dc.description.sponsorshipTurkish Society of Vascular Surgeryen_US
dc.description.sponsorshipFinancial support was provided by the Turkish Society of Vascular Surgery.en_US
dc.language.isoengen_US
dc.publisherMosby-Elsevieren_US
dc.relation.isversionof10.1016/j.jtcvs.2007.12.068en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleEffects of carbamazepine on spinal cord ischemiaen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume136en_US
dc.identifier.issue4en_US
dc.identifier.startpage1038en_US
dc.identifier.endpageU18en_US
dc.relation.journalJournal of Thoracic and Cardiovascular Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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