Publication:
Brain slice viability determined under normoxic and oxidative stress conditions: Involvement of slice quantity in the medium

dc.contributor.authorGül, Zülfiye
dc.contributor.authorBüyükuysal, M. Çağatay
dc.contributor.buuauthorBüyükuysal, R. Levent
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Farmakoloji Ana Bilim Dalı
dc.contributor.researcheridAAH-1657-2021
dc.contributor.scopusid6602686612
dc.date.accessioned2023-10-26T12:49:38Z
dc.date.available2023-10-26T12:49:38Z
dc.date.issued2020-03-03
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.
dc.description.sponsorshipBahçeşehir Üniversitesi
dc.description.sponsorshipGökçe Kızılkaya Yabancı Dil Okulu
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.
dc.identifier.endpage238
dc.identifier.issn0161-6412
dc.identifier.issn1743-1328
dc.identifier.issue3
dc.identifier.pubmed32065058
dc.identifier.scopus2-s2.0-85079699250
dc.identifier.startpage228
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.identifier.volume42
dc.identifier.wos000514503900001
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherTaylor & Francis
dc.relation.bapHDP(T)-2014/33
dc.relation.collaborationYurt içi
dc.relation.journalNeurological Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectNeurosciences & neurology
dc.subjectBrain slices
dc.subjectIncubation volume
dc.subjectSlice quantity
dc.subjectOxidative stress
dc.subjectTtc staining
dc.subjectRat striatal slices
dc.subjectCortical slices
dc.subjectIn-vitro
dc.subjectProtects
dc.subjectLactate
dc.subjectAcid
dc.subjectReceptors
dc.subjectPyruvate
dc.subjectHypoxia
dc.subjectNetwork
dc.subject.emtreeAscorbic acid
dc.subject.emtreeLactate dehydrogenase
dc.subject.emtreeMalonaldehyde
dc.subject.emtreeMenadione
dc.subject.emtreeReactive oxygen metabolite
dc.subject.emtreeTriphenyltetrazolium
dc.subject.emtreeReactive oxygen metabolite
dc.subject.emtreeAnimal experiment
dc.subject.emtreeAnimal model
dc.subject.emtreeArticle
dc.subject.emtreeBrain homogenate
dc.subject.emtreeBrain size
dc.subject.emtreeBrain slice
dc.subject.emtreeCell density
dc.subject.emtreeCell viability
dc.subject.emtreeComparative study
dc.subject.emtreeControlled study
dc.subject.emtreeEnergy metabolism
dc.subject.emtreeFemale
dc.subject.emtreeIn vitro study
dc.subject.emtreeLipid peroxidation
dc.subject.emtreeMale
dc.subject.emtreeNeuroprotection
dc.subject.emtreeNeurotransmitter release
dc.subject.emtreeNonhuman
dc.subject.emtreeOxidative stress
dc.subject.emtreeRat
dc.subject.emtreeReoxygenation
dc.subject.emtreeTissue injury
dc.subject.emtreeAnimal
dc.subject.emtreeBrain
dc.subject.emtreeCulture medium
dc.subject.emtreeMetabolism
dc.subject.emtreeOrgan culture technique
dc.subject.emtreeProcedures
dc.subject.emtreeSprague dawley rat
dc.subject.meshAnimals
dc.subject.meshBrain
dc.subject.meshCulture media
dc.subject.meshFemale
dc.subject.meshOrgan culture techniques
dc.subject.meshOxidative stress
dc.subject.meshRats, sprague-dawley
dc.subject.meshReactive oxygen species
dc.subject.scopusSevoflurane; Brain ischemia; Animals
dc.subject.wosClinical neurology
dc.subject.wosNeurosciences
dc.titleBrain slice viability determined under normoxic and oxidative stress conditions: Involvement of slice quantity in the medium
dc.typeArticle
dc.wos.quartileQ3 (Clinical neurology)
dc.wos.quartileQ4 (Neurosciences)
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Farmakoloji Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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