Effects of Atorvastatin on Experimental Spinal Cord lschemia-Reperfusion Injury in Rabbits

dc.contributor.authorKardes, Ozgur
dc.contributor.authorCivi, Soner
dc.contributor.authorTufan, Kadir
dc.contributor.authorOz Oyar, Eser
dc.contributor.authorOmeroglu, Suna
dc.contributor.authorAykol, Sukru
dc.contributor.orcID0000-0003-2854-941Xen_US
dc.contributor.pubmedID27593815en_US
dc.contributor.researcherIDP-5895-2018en_US
dc.date.accessioned2019-06-11T16:37:19Z
dc.date.available2019-06-11T16:37:19Z
dc.date.issued2017
dc.description.abstractAIM: Extent of secondary injury is the determinant of tissue destruction and functional worsening after primary spinal cord injury (SCI). Data have accumulated on alleviation of secondary injury in SCI from many studies on the subject. Besides its cholesterol lowering effects, statins are known to have anti-inflammatory and anti-oxidant effects which are the main targets of spinal cord research. This study aims to evaluate the effects of atorvastatin on experimental spinal cord ischemia-reperfusion injury. MATERIAL and METHODS: Thirty adult male New Zealand rabbits were allocated into control, ischemia-reperfusion (I/R) and treatment groups. Treatment group received 5 mg/kg of atorvastatin via lavage for the preceding 14 days. Other groups received placebo during the same time period. After two weeks, animals in the I/R and treatment groups underwent abdominal temporary aorta occlusion for 30 minutes. Neurological condition of the animals was recorded during the 48 hours of observation. Afterwards, animals were sacrificed and levels of malondialdehyde, glutathione and nitric oxide in spinal cord tissue and plasma and the histopathological tissue changes were determined. RESULTS: Animals in the treatment groups demonstrated significantly better results than the I/R group regarding biochemical markers. Neurological evaluation using the Tarlov scale demonstrated significantly better results at the 48th hour in treatment group. Histopathological results were also better in the treatment groups. CONCLUSION: Results of this study demonstrate the neuroprotective effects of atorvastatin. Atorvastatin has favorable effects on biochemical markers of oxidative stress in SCI. Further studies with larger cohorts and different time periods are also needed.en_US
dc.identifier.endpage602en_US
dc.identifier.issn1019-5149
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-85021377302en_US
dc.identifier.startpage594en_US
dc.identifier.urihttp://turkishneurosurgery.org.tr/pdf/pdf_JTN_1879.pdf
dc.identifier.urihttp://hdl.handle.net/11727/3468
dc.identifier.volume27en_US
dc.identifier.wos000406170300014en_US
dc.language.isoengen_US
dc.relation.isversionof10.5137/1019-5149.JTN.16627-15.2en_US
dc.relation.journalTURKISH NEUROSURGERYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAtorvastatinen_US
dc.subjectlschemia/reperfusion injuryen_US
dc.subjectStatinen_US
dc.subjectSpinal cord injuryen_US
dc.titleEffects of Atorvastatin on Experimental Spinal Cord lschemia-Reperfusion Injury in Rabbitsen_US
dc.typearticleen_US

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