Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/34600
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dc.contributor.authorGül, Zülfiye-
dc.contributor.authorBüyükuysal, M. Çağatay-
dc.date.accessioned2023-10-26T12:49:38Z-
dc.date.available2023-10-26T12:49:38Z-
dc.date.issued2020-03-03-
dc.identifier.citationGül, Z. vd. (2020). "Brain slice viability determined under normoxic and oxidative stress conditions: Involvement of slice quantity in the medium". Neurological Research, 42(3), 228-238.en_US
dc.identifier.issn0161-6412-
dc.identifier.issn1743-1328-
dc.identifier.urihttps://doi.org/10.1080/01616412.2020.1723299-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/01616412.2020.1723299-
dc.identifier.urihttp://hdl.handle.net/11452/34600-
dc.description.abstractObjective: In vitro acute adult brain slice methods are instruments in developing our knowledge of the nervous system. Optimization of this method for obtaining high-quality brain slices is extremely important in terms of consistency and reliability of the experimental results. Although some important topics such as slice thickness, temperature, and composition of the physiological medium have been studied for optimization, involvement of slice quantity in medium on tissue viability has not been investigated yet. Methods: Different number of slices (1, 3, or 6 slices) were incubated under normoxic or some prooxidant stress conditions induced by oxygen-glucose deprivation (OGD), H2O2, FeSO4+ ascorbic acid, or menadione to evaluate the effect of slice density on tissue viability. Results:Slice quantity in the normoxic incubation medium caused a significant increase in 2,3,5-triphenyltetrazolium chloride (TTC) staining intensity of the slices. Similarly, increase in the slice quantity in the medium also protected the slices against either OGD, H2O2, FeSO4, or menadione-induced decrease in TTC staining. In addition to TTC staining, lactate dehydrogenase leakage or malondialdehyde and reactive oxygen species production under normoxic or ischemia-like conditions were also attenuated by increasing slice quantity in the medium. Conclusion: These results show that when using brain slices method for investigating the structural and functional features of brain at the molecular and cellular levels, both slice quantity in the medium and incubation volume should be considered first. Increasing slice quantity or decreasing incubation volume probably causes an increase in the concentration of endogenous substance(s) involved in neuroprotection.en_US
dc.description.sponsorshipBahçeşehir Üniversitesitr_TR
dc.description.sponsorshipGökçe Kızılkaya Yabancı Dil Okulutr_TR
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNeurosciences & neurologyen_US
dc.subjectBrain slicesen_US
dc.subjectIncubation volumeen_US
dc.subjectSlice quantityen_US
dc.subjectOxidative stressen_US
dc.subjectTtc stainingen_US
dc.subjectRat striatal slicesen_US
dc.subjectCortical slicesen_US
dc.subjectIn-vitroen_US
dc.subjectProtectsen_US
dc.subjectLactateen_US
dc.subjectAciden_US
dc.subjectReceptorsen_US
dc.subjectPyruvateen_US
dc.subjectHypoxiaen_US
dc.subjectNetworken_US
dc.subject.meshAnimalsen_US
dc.subject.meshBrainen_US
dc.subject.meshCulture mediaen_US
dc.subject.meshFemaleen_US
dc.subject.meshOrgan culture techniquesen_US
dc.subject.meshOxidative stressen_US
dc.subject.meshRats, sprague-dawleyen_US
dc.subject.meshReactive oxygen speciesen_US
dc.titleBrain slice viability determined under normoxic and oxidative stress conditions: Involvement of slice quantity in the mediumen_US
dc.typeArticleen_US
dc.identifier.wos000514503900001tr_TR
dc.identifier.scopus2-s2.0-85079699250tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Farmakoloji Anabilim Dalı.tr_TR
dc.relation.bapHDP(T)-2014/33tr_TR
dc.identifier.startpage228tr_TR
dc.identifier.endpage238tr_TR
dc.identifier.volume42tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalNeurological Researchen_US
dc.contributor.buuauthorBüyükuysal, R. Levent-
dc.contributor.researcheridAAH-1657-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed32065058tr_TR
dc.subject.wosClinical neurologyen_US
dc.subject.wosNeurosciencesen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3 (Clinical neurology)en_US
dc.wos.quartileQ4 (Neurosciences)en_US
dc.contributor.scopusid6602686612tr_TR
dc.subject.scopusSevoflurane; Brain ischemia; Animalsen_US
dc.subject.emtreeAscorbic aciden_US
dc.subject.emtreeLactate dehydrogenaseen_US
dc.subject.emtreeMalonaldehydeen_US
dc.subject.emtreeMenadioneen_US
dc.subject.emtreeReactive oxygen metaboliteen_US
dc.subject.emtreeTriphenyltetrazoliumen_US
dc.subject.emtreeReactive oxygen metaboliteen_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeAnimal modelen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBrain homogenateen_US
dc.subject.emtreeBrain sizeen_US
dc.subject.emtreeBrain sliceen_US
dc.subject.emtreeCell densityen_US
dc.subject.emtreeCell viabilityen_US
dc.subject.emtreeComparative studyen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeEnergy metabolismen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeIn vitro studyen_US
dc.subject.emtreeLipid peroxidationen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNeuroprotectionen_US
dc.subject.emtreeNeurotransmitter releaseen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeOxidative stressen_US
dc.subject.emtreeRaten_US
dc.subject.emtreeReoxygenationen_US
dc.subject.emtreeTissue injuryen_US
dc.subject.emtreeAnimalen_US
dc.subject.emtreeBrainen_US
dc.subject.emtreeCulture mediumen_US
dc.subject.emtreeMetabolismen_US
dc.subject.emtreeOrgan culture techniqueen_US
dc.subject.emtreeProceduresen_US
dc.subject.emtreeSprague dawley raten_US
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