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http://hdl.handle.net/11452/34600
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Gül, Zülfiye | - |
dc.contributor.author | Büyükuysal, M. Çağatay | - |
dc.date.accessioned | 2023-10-26T12:49:38Z | - |
dc.date.available | 2023-10-26T12:49:38Z | - |
dc.date.issued | 2020-03-03 | - |
dc.identifier.citation | Gül, 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.issn | 0161-6412 | - |
dc.identifier.issn | 1743-1328 | - |
dc.identifier.uri | https://doi.org/10.1080/01616412.2020.1723299 | - |
dc.identifier.uri | https://www.tandfonline.com/doi/full/10.1080/01616412.2020.1723299 | - |
dc.identifier.uri | http://hdl.handle.net/11452/34600 | - |
dc.description.abstract | Objective: 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.sponsorship | Bahçeşehir Üniversitesi | tr_TR |
dc.description.sponsorship | Gökçe Kızılkaya Yabancı Dil Okulu | tr_TR |
dc.language.iso | en | en_US |
dc.publisher | Taylor & Francis | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Neurosciences & neurology | en_US |
dc.subject | Brain slices | en_US |
dc.subject | Incubation volume | en_US |
dc.subject | Slice quantity | en_US |
dc.subject | Oxidative stress | en_US |
dc.subject | Ttc staining | en_US |
dc.subject | Rat striatal slices | en_US |
dc.subject | Cortical slices | en_US |
dc.subject | In-vitro | en_US |
dc.subject | Protects | en_US |
dc.subject | Lactate | en_US |
dc.subject | Acid | en_US |
dc.subject | Receptors | en_US |
dc.subject | Pyruvate | en_US |
dc.subject | Hypoxia | en_US |
dc.subject | Network | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Brain | en_US |
dc.subject.mesh | Culture media | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Organ culture techniques | en_US |
dc.subject.mesh | Oxidative stress | en_US |
dc.subject.mesh | Rats, sprague-dawley | en_US |
dc.subject.mesh | Reactive oxygen species | en_US |
dc.title | Brain slice viability determined under normoxic and oxidative stress conditions: Involvement of slice quantity in the medium | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000514503900001 | tr_TR |
dc.identifier.scopus | 2-s2.0-85079699250 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Farmakoloji Anabilim Dalı. | tr_TR |
dc.relation.bap | HDP(T)-2014/33 | tr_TR |
dc.identifier.startpage | 228 | tr_TR |
dc.identifier.endpage | 238 | tr_TR |
dc.identifier.volume | 42 | tr_TR |
dc.identifier.issue | 3 | tr_TR |
dc.relation.journal | Neurological Research | en_US |
dc.contributor.buuauthor | Büyükuysal, R. Levent | - |
dc.contributor.researcherid | AAH-1657-2021 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.identifier.pubmed | 32065058 | tr_TR |
dc.subject.wos | Clinical neurology | en_US |
dc.subject.wos | Neurosciences | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q3 (Clinical neurology) | en_US |
dc.wos.quartile | Q4 (Neurosciences) | en_US |
dc.contributor.scopusid | 6602686612 | tr_TR |
dc.subject.scopus | Sevoflurane; Brain ischemia; Animals | en_US |
dc.subject.emtree | Ascorbic acid | en_US |
dc.subject.emtree | Lactate dehydrogenase | en_US |
dc.subject.emtree | Malonaldehyde | en_US |
dc.subject.emtree | Menadione | en_US |
dc.subject.emtree | Reactive oxygen metabolite | en_US |
dc.subject.emtree | Triphenyltetrazolium | en_US |
dc.subject.emtree | Reactive oxygen metabolite | en_US |
dc.subject.emtree | Animal experiment | en_US |
dc.subject.emtree | Animal model | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Brain homogenate | en_US |
dc.subject.emtree | Brain size | en_US |
dc.subject.emtree | Brain slice | en_US |
dc.subject.emtree | Cell density | en_US |
dc.subject.emtree | Cell viability | en_US |
dc.subject.emtree | Comparative study | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Energy metabolism | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | In vitro study | en_US |
dc.subject.emtree | Lipid peroxidation | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Neuroprotection | en_US |
dc.subject.emtree | Neurotransmitter release | en_US |
dc.subject.emtree | Nonhuman | en_US |
dc.subject.emtree | Oxidative stress | en_US |
dc.subject.emtree | Rat | en_US |
dc.subject.emtree | Reoxygenation | en_US |
dc.subject.emtree | Tissue injury | en_US |
dc.subject.emtree | Animal | en_US |
dc.subject.emtree | Brain | en_US |
dc.subject.emtree | Culture medium | en_US |
dc.subject.emtree | Metabolism | en_US |
dc.subject.emtree | Organ culture technique | en_US |
dc.subject.emtree | Procedures | en_US |
dc.subject.emtree | Sprague dawley rat | en_US |
Appears in Collections: | Scopus Web of Science |
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