Publication:
Myelin Basic Protein Profile of Central Nervous System in Experimentally Induced Demyelination and Remyelination

dc.authorscopusid6506699286
dc.authorscopusid56005973000
dc.authorscopusid15755525400
dc.authorscopusid25925857500
dc.contributor.authorYarim, G.F.
dc.contributor.authorYarm, M.
dc.contributor.authorÇiftçi, G.
dc.contributor.authorKarayiǧit, M.O.
dc.date.accessioned2020-06-21T14:16:32Z
dc.date.available2020-06-21T14:16:32Z
dc.date.issued2013
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Yarim] Gül Fatma, Department of Biochemistry, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yarm] Murat, Department of Pathology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Çiftçi] Gülay, Department of Biochemistry, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Karayiǧit] Mehmet Önder, Department of Pathology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractObjective: The aim of the present study was to assess myelin basic protein (MBP) profiles of central nervous system in experimentally induced demyelination and remyelination. Materials and Methods: Sixty 8-10 weeks old male C57Bl/6 mice were used for this study. Twenty mice were selected as control and 40 mice as experimental group. Experimental group was fed ad libitum with a 0.3% cuprizone diet for 6 weeks. At the end of 6 weeks, 20 mice from the experimental group and 10 mice from the control group were euthanasied and the remaining of the experimental group was fed cuprizone-free diet for more 4 weeks and then 10 mice in the control group and 20 mice in the experimental group were sacrificed. Corpus callosum sections were removed and protein extraction was performed in all samples. The MBP profiles were evaluated by sodium dodecyl sulphate - polyacrylamide gel electrophoresis and Western-blot analysis. Results and Conclusion: Decreased intensity of the MBP isoforms below the 26.6 kDa was observed in demyelinated group as compared with controls. In the remylinated group, intensity of MBP approached to values of control group. This study will contribute to the understanding of the mechanisms of demyelination and remyelination as well as will serve a base for the future studies investigating diseases characterized by demyelination in human and animals.en_US
dc.identifier.doi10.5505/tjb.2013.37232
dc.identifier.endpage456en_US
dc.identifier.issn0250-4685
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-84892618475
dc.identifier.scopusqualityQ4
dc.identifier.startpage451en_US
dc.identifier.urihttps://doi.org/10.5505/tjb.2013.37232
dc.identifier.volume38en_US
dc.identifier.wosWOS:000329577500013
dc.identifier.wosqualityQ4
dc.language.isoenen_US
dc.publisherWalter de Gruyter GmbHen_US
dc.relation.ispartofTurkish Journal of Biochemistry-Turk Biyokimya Dergisien_US
dc.relation.journalTurkish Journal of Biochemistry-Turk Biyokimya Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDemyelinationen_US
dc.subjectMiceen_US
dc.subjectMyelin Basic Proteinen_US
dc.subjectRemyelination Conflict of Interest: Authors Declare No Conflict of Interesten_US
dc.titleMyelin Basic Protein Profile of Central Nervous System in Experimentally Induced Demyelination and Remyelinationen_US
dc.title.alternativeDeneysel Demiyelinasyon Ve Remiyelinasyonda Merkezi Sinir Sisteminin N Miyelin Temel Protein Profilien_US
dc.typeArticleen_US
dspace.entity.typePublication

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