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dc.contributor.authorColak, A.
dc.contributor.authorKaya, M.
dc.contributor.authorKaraoglan, A.
dc.contributor.authorSagmanligil, A.
dc.contributor.authorAkdemir, O.
dc.contributor.authorSahan, E.
dc.contributor.authorCelik, Oe
dc.date.accessioned19.07.201910:50:10
dc.date.accessioned2019-07-19T15:55:13Z
dc.date.available19.07.201910:50:10
dc.date.available2019-07-19T15:55:13Z
dc.date.issued2009
dc.identifier.issn1130-1473
dc.identifier.urihttps://hdl.handle.net/20.500.12415/2239
dc.descriptionWOS: 000268685000002en_US
dc.descriptionPubMed ID: 19575128en_US
dc.description.abstractBackground. An increase in the level of intracellular calcium activates the calcium-dependent neutral protease calpain, which in turn leads to cellular dysfunction and cell death after an insult to the central nervous system. fit this study, we evaluated the effect of a calpain inhibitor, AK 295, on spinal cord structure, neurologic function, and apoptosis after spinal cord injury (SCI) in a murine model. Methods. Thirty albino Wistar rats were divided into 3 groups of 10 each: the sham-operated control group (group 1), the spinal cord trauma group (group 2), and the spinal cord trauma plus AK 295 treatment group (group 3). After having received a combination of ketamine 60 mg/kg and xylazine 9 mg/kg to induce anesthesia, the rats in groups 2 and 3 were subjected to thoracic trauma by the weight drop technique (40 g-cm). One hour after having been subjected to that trauma, the rats in groups 2 and 3 were treated with an intraperitoneal injection of either dimethyl sulfoxide 2 mg/kg or AK 295 2 mg/kg. The effects of the injury and the efficacy of AK 295 were determined by an assessment of the TUNEL technique and the results of examination with a light microscope. The neurologic performance of 5 rats from group 2 and 5 from group 3 was assessed by means of the inclined plane technique and the modified Tarlov's motor grading scale 1, 3, and 5 days after spinal cord trauma. Findings. Light-microscopic examination of spinal cord specimens from group 2 revealed hemorrhage, edema, necrosis, and vascular thrombi 24 : hours after trauma. Similar (but less prominent) features were seen in specimens obtained from group 3 rats. Twenty-four hours after injury, the mean apoptotie cell numbers in groups I and 2 were zero and 4.57 +/- 0.37 cells, respectively. In group 3, the mean apoptotic cell number was 2.30 +/- 0.34 cells, a value significantly lower than that in group 2 (P < .05). Five days after trauma, the injured rats in group 2 demonstrated significant motor dysfunction (P < .05). In comparison, the motor scores exhibited by group 3 rats were markedly better (P < .05). Conclusions. AK 295 inhibited apoptosis via calpain-dependent pathway's and provided neuroprotection and improved neurologic function in a rat model of SCI. To our knowledge, this is the first study to evaluate the use of AK 295, a calpain inhibitor, after SCI. Our data suggest that AK 295 might be a novel therapeutic compound for the neuroprotection of tissue and the recovery of function in patients with a SCI.en_US
dc.language.isoengen_US
dc.publisherSOC ESPANOLA NEUROCIRUGIAen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAK 295en_US
dc.subjectApoptosisen_US
dc.subjectCalpain inhibitoren_US
dc.subjectSecondary damageen_US
dc.subjectSpinal cord traumaen_US
dc.titleCalpain inhibitor AK 295 inhibits calpain-induced apoptosis and improves neurologic function after traumatic spinal cord injury in ratsen_US
dc.typearticleen_US
dc.relation.journalNEUROCIRUGIAen_US
dc.contributor.departmentMaltepe Üniversitesien_US
dc.identifier.volume20en_US
dc.identifier.issue3en_US
dc.identifier.startpage245en_US
dc.identifier.endpage254en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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