Zingiberene Attenuates Hydrogen Peroxide-Induced Toxicity in Neuronal Cells
| dc.contributor.author | Togar, B. | |
| dc.contributor.author | Turkez, H. | |
| dc.contributor.author | Stefano, A. D. | |
| dc.contributor.author | Tatar, A. | |
| dc.contributor.author | Cetin, D. | |
| dc.date.accessioned | 2026-03-26T14:49:40Z | |
| dc.date.available | 2026-03-26T14:49:40Z | |
| dc.date.issued | 2015 | |
| dc.description | Di Stefano, Antonio/0000-0002-3042-2234; | en_US |
| dc.description.abstract | In this experimental design, we explored the neuroprotective potential of zingiberene (ZGB), a monocyclic sesquiterpene, in hydrogen peroxide (H2O2)-induced toxicity in newborn rat cerebral cortex cell cultures for the first time. The rats were exposed to H2O2 for 6 h to determine the oxidative stress levels. To evaluate cell viability, both 3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyltetrazolium bromide and lactate dehydrogenase assays were carried out. Total antioxidant capacity (TAC) and total oxidative stress (TOS) parameters were used to evaluate oxidative changes. Besides determining 8-hydroxy-2-deoxyguanosine (8-OH-dG) levels in vitro, single-cell gel electrophoresis was also performed to measure the resistance of neuronal DNA to H2O2- exposed rats. 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 increased in the H2O2 alone-treated cultures. But pretreatment of ZGB suppressed the cytotoxicity, genotoxicity and oxidative stress that were increased by H2O2. Based on these observations, it is suggested that the sesquiterpene ZGB can be used as a novel and natural potential therapeutic in counteracting oxidative damages in the field of neurodegenerative disorders. | en_US |
| dc.identifier.doi | 10.1177/0960327114538987 | |
| dc.identifier.issn | 0960-3271 | |
| dc.identifier.issn | 1477-0903 | |
| dc.identifier.scopus | 2-s2.0-84921968296 | |
| dc.identifier.uri | https://doi.org/10.1177/0960327114538987 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14901/2254 | |
| dc.language.iso | en | en_US |
| dc.publisher | Sage Publications Ltd | en_US |
| dc.relation.ispartof | Human & Experimental Toxicology | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Zingiberene | en_US |
| dc.subject | Neuroprotective Action | en_US |
| dc.subject | H2O2 | en_US |
| dc.subject | Cultured Neuron | en_US |
| dc.subject | DNA Damage | en_US |
| dc.subject | Oxidative Stress | en_US |
| dc.title | Zingiberene Attenuates Hydrogen Peroxide-Induced Toxicity in Neuronal 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 | 36551575900 | |
| gdc.author.scopusid | 9134233800 | |
| gdc.author.scopusid | 35742643400 | |
| gdc.author.scopusid | 8530113400 | |
| gdc.author.scopusid | 56341724000 | |
| gdc.author.wosid | Di Stefano, Antonio/Jbj-1293-2023 | |
| gdc.author.wosid | Türkez, Hasan/Aaq-4905-2020 | |
| gdc.author.wosid | Tatar, Abdulgani/I-6300-2012 | |
| gdc.bip.impulseclass | C5 | |
| gdc.bip.influenceclass | C5 | |
| gdc.bip.popularityclass | C4 | |
| gdc.collaboration.industrial | false | |
| gdc.description.department | Erzurum Technical University | en_US |
| gdc.description.departmenttemp | [Togar, B.] Ataturk Univ, Dept Biol, Fac Sci, TR-25240 Erzurum, Turkey; [Turkez, H.] Erzurum Tech Univ, Dept Mol Biol & Genet, Fac Sci, Erzurum, Turkey; [Stefano, A. D.] Univ G DAnnunzio, Dept Pharmacol, Chieti, Italy; [Tatar, A.] Ataturk Univ, Dept Med Genet, Fac Med, TR-25240 Erzurum, Turkey; [Cetin, D.] Ataturk Univ, Dept Med Pharmacol, Fac Med, TR-25240 Erzurum, Turkey | en_US |
| gdc.description.endpage | 144 | en_US |
| gdc.description.issue | 2 | en_US |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| gdc.description.scopusquality | N/A | |
| gdc.description.startpage | 135 | en_US |
| gdc.description.volume | 34 | en_US |
| gdc.description.woscitationindex | Science Citation Index Expanded | |
| gdc.description.wosquality | Q2 | |
| gdc.identifier.openalex | W1974404739 | |
| gdc.identifier.pmid | 24925361 | |
| gdc.identifier.wos | WOS:000349087600003 | |
| gdc.index.type | PubMed | |
| gdc.oaire.diamondjournal | false | |
| gdc.oaire.impulse | 3.0 | |
| gdc.oaire.influence | 2.9072134E-9 | |
| gdc.oaire.isgreen | false | |
| gdc.oaire.keywords | Cerebral Cortex | |
| gdc.oaire.keywords | Neurons | |
| gdc.oaire.keywords | L-Lactate Dehydrogenase | |
| gdc.oaire.keywords | Cell Survival | |
| gdc.oaire.keywords | Deoxyguanosine | |
| gdc.oaire.keywords | Hydrogen Peroxide | |
| gdc.oaire.keywords | Antioxidants | |
| gdc.oaire.keywords | Rats | |
| gdc.oaire.keywords | Monocyclic Sesquiterpenes | |
| gdc.oaire.keywords | Rats, Sprague-Dawley | |
| gdc.oaire.keywords | Animals, Newborn | |
| gdc.oaire.keywords | 8-Hydroxy-2'-Deoxyguanosine | |
| gdc.oaire.keywords | cultured neuron; DNA damage | |
| gdc.oaire.keywords | Animals | |
| gdc.oaire.keywords | Comet Assay | |
| gdc.oaire.keywords | Sesquiterpenes | |
| gdc.oaire.keywords | Cells, Cultured | |
| gdc.oaire.keywords | DNA Damage | |
| gdc.oaire.popularity | 8.395182E-9 | |
| gdc.oaire.publicfunded | false | |
| gdc.oaire.sciencefields | 0301 basic medicine | |
| gdc.oaire.sciencefields | 0303 health sciences | |
| gdc.oaire.sciencefields | 03 medical and health sciences | |
| gdc.openalex.collaboration | International | |
| gdc.openalex.fwci | 1.5298 | |
| gdc.openalex.normalizedpercentile | 0.82 | |
| gdc.opencitations.count | 18 | |
| gdc.plumx.crossrefcites | 14 | |
| gdc.plumx.mendeley | 38 | |
| gdc.plumx.pubmedcites | 5 | |
| gdc.plumx.scopuscites | 21 | |
| gdc.scopus.citedcount | 21 | |
| gdc.wos.citedcount | 15 |
