Publication:
3-Nitrotyrosine Levels in Dichlorvos-Induced Neurotoxicity

dc.authorscopusid16238460900
dc.authorscopusid16237906700
dc.authorscopusid23476782200
dc.authorscopusid36058260100
dc.authorscopusid25230622200
dc.contributor.authorGüvenç, D.
dc.contributor.authorAksoy, A.
dc.contributor.authorDas, Y.K.
dc.contributor.authorAtmaca, E.
dc.contributor.authorYavuz, O.
dc.date.accessioned2020-06-21T13:57:43Z
dc.date.available2020-06-21T13:57:43Z
dc.date.issued2014
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Güvenç] Dilek, Department of Pharmacology and Toxicology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aksoy] Abdurrahman, Department of Pharmacology and Toxicology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Das] Y. K., Department of Pharmacology and Toxicology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Atmaca] Enes, Department of Pharmacology and Toxicology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yavuz] Oguzhan, Department of Pharmacology and Toxicology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractThe aim of this study was to evaluate dichlorvos toxicity in terms of nitro-oxidative stress by determining 3-nitrotyrosine (3-NT) levels in the fore, mid, and hindbrain regions in acutely exposed rats. Male Sprague-Dawley rats were randomly allocated to three groups of eight. Group 1 was administered a single intraperitoneal dichlorvos dose of 1.8 mg kg-1 (0.1×LD<inf>50</inf>) and group 2 a dose of 9 mg kg-1 (0.5×LD<inf>50</inf>). The control group received 0.5 mL saline solution via the same route. 3-NT and tyrosine (TYR) levels were measured using high performance liquid chromatography with a photodiode array detector (HPLC-PDA) and expressed as a ratio of 3-NT to TYR. The 3-NT/1000 TYR ratios increased significantly in the fore-, mid- and hindbrains of the exposed groups compared to control (p<0.01). In the forebrain, the increase was also significant between the treated groups. Our study has confirmed that acute exposure to dichlorvos leads to nitro-oxidative stress in the brain and that 3-NT may play a role in the mechanism of dichlorvos neurotoxicity.en_US
dc.identifier.doi10.2478/10004-1254-65-2014-2416
dc.identifier.endpage112en_US
dc.identifier.issn0004-1254
dc.identifier.issn1848-6312
dc.identifier.issue1en_US
dc.identifier.pmid24535296
dc.identifier.scopus2-s2.0-84899890581
dc.identifier.scopusqualityQ3
dc.identifier.startpage109en_US
dc.identifier.urihttps://doi.org/10.2478/10004-1254-65-2014-2416
dc.identifier.volume65en_US
dc.identifier.wosWOS:000333849700011
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherInstitute for Medical Research and Occupational Healthen_US
dc.relation.ispartofArhiv Za Higijenu Rada I Toksikologiju-Archives of Industrial Hygiene and Toxicologyen_US
dc.relation.journalArhiv Za Higijenu Rada I Toksikologiju-Archives of Industrial Hygiene and Toxicologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBrainen_US
dc.subjectHPLCen_US
dc.subjectNitro-Oxidative Stressen_US
dc.subjectPesticidesen_US
dc.subjectRatsen_US
dc.title3-Nitrotyrosine Levels in Dichlorvos-Induced Neurotoxicityen_US
dc.typeArticleen_US
dspace.entity.typePublication

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