Protective Effects of Cyclosativene on H2O2-Induced Injury in Cultured Rat Primary Cerebral Cortex Cells

dc.contributor.author Turkez, Hasan
dc.contributor.author Togar, Basak
dc.contributor.author Di Stefano, Antonio
dc.contributor.author Taspinar, Numan
dc.contributor.author Sozio, Piera
dc.date.accessioned 2026-03-26T14:49:43Z
dc.date.available 2026-03-26T14:49:43Z
dc.date.issued 2015
dc.description Di Stefano, Antonio/0000-0002-3042-2234; en_US
dc.description.abstract Sesquiterpenes have attracted much interest with respect to their protective effect against oxidative damage that may be the cause of many diseases including several neurodegenerative disorders and cancer. Our previous unpublished work suggested that cyclosativene (CSV), a tetracyclic sesquiterpene, has antioxidant and anticarcinogenic features. However, little is known about the effects of CSV on oxidative stress induced neurotoxicity. We used hydrogen peroxide (H2O2) exposure for 6 h to model oxidative stress. Therefore, this experimental design allowed us to explore the neuroprotective potential of CSV in H2O2-induced toxicity in new-born rat cerebral cortex cell cultures for the first time. For this aim, MTT and lactate dehydrogenase release assays were carried out to evaluate cytotoxicity. Total antioxidant capacity (TAC) and total oxidative stress (TOS) parameters were used to evaluate oxidative changes. In addition to determining of 8-hydroxy-2-deoxyguanosine (8-OH-dG) levels, the single cell gel electrophoresis (or Comet assay) was also performed for measuring the resistance of neuronal DNA to H2O2-induced challenge. Our results showed that survival and TAC levels of the cells decreased, while TOS, 8-OH-dG levels and the mean values of the total scores of cells showing DNA damage (Comet assay) increased in the H2O2 alone treated cultures. But pre-treatment of CSV suppressed the cytotoxicity, genotoxicity and oxidative stress which were increased by H2O2. On the basis of these observations, it is suggested that CSV as a natural product with an antioxidant capacity in mitigating oxidative injuries in the field of neurodegenerative disorders. en_US
dc.identifier.doi 10.1007/s10616-013-9685-9
dc.identifier.issn 0920-9069
dc.identifier.issn 1573-0778
dc.identifier.scopus 2-s2.0-84942303233
dc.identifier.uri https://doi.org/10.1007/s10616-013-9685-9
dc.identifier.uri https://hdl.handle.net/20.500.14901/2257
dc.language.iso en en_US
dc.publisher Springer en_US
dc.relation.ispartof Cytotechnology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Cyclosativene en_US
dc.subject Neuroprotection en_US
dc.subject H2O2 en_US
dc.subject Primary Neuron en_US
dc.subject DNA Damage en_US
dc.subject Oxidative Stress en_US
dc.title Protective Effects of Cyclosativene on H2O2-Induced Injury in Cultured Rat Primary Cerebral Cortex Cells en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Di Stefano, Antonio/0000-0002-3042-2234
gdc.author.scopusid 9134233800
gdc.author.scopusid 36551575900
gdc.author.scopusid 35742643400
gdc.author.scopusid 56019884800
gdc.author.scopusid 6506763869
gdc.author.wosid Di Stefano, Antonio/Jbj-1293-2023
gdc.author.wosid Türkez, Hasan/Aaq-4905-2020
gdc.author.wosid Taşpınar, Numan/Abg-2334-2021
gdc.description.department Erzurum Technical University en_US
gdc.description.departmenttemp [Turkez, Hasan] Erzurum Tech Univ, Dept Mol Biol & Genet, Fac Sci, Erzurum, Turkey; [Togar, Basak] Ataturk Univ, Dept Biol, Fac Sci, TR-25240 Erzurum, Turkey; [Di Stefano, Antonio; Sozio, Piera] Univ G DAnnunzio, Dipartimento Farm, I-66100 Chieti, Italy; [Taspinar, Numan] Ataturk Univ, Dept Med Pharmacol, Fac Med, TR-25240 Erzurum, Turkey en_US
gdc.description.endpage 309 en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 299 en_US
gdc.description.volume 67 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q4
gdc.identifier.pmid 24493068
gdc.identifier.wos WOS:000349768500012

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