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dc.contributor.authorAvci, Bahattin
dc.contributor.authorBilge, S. Sirri
dc.contributor.authorArslan, Gokhan
dc.contributor.authorAlici, Omer
dc.contributor.authorDarakci, Ozge
dc.contributor.authorBaratzada, Turkhan
dc.contributor.authorBozkurt, Ayhan
dc.date.accessioned2020-06-21T13:11:47Z
dc.date.available2020-06-21T13:11:47Z
dc.date.issued2018
dc.identifier.issn0748-2337
dc.identifier.issn1477-0393
dc.identifier.urihttps://doi.org/10.1177/0748233717737646
dc.identifier.urihttps://hdl.handle.net/20.500.12712/11763
dc.descriptionBilge, S.Sirri/0000-0003-2878-6968; Arslan, Gokhan/0000-0003-4186-2478; Ciftcioglu, Engin/0000-0003-4402-3004en_US
dc.descriptionWOS: 000425176300001en_US
dc.descriptionPubMed: 29141517en_US
dc.description.abstractIn this study, we aimed to study the possible preventive effect of docosahexaenoic acid (DHA), a dietary omega-3 fatty acid, on toxicity caused by chlorpyrifos (CPF). Six groups of Sprague Dawley rats (200-250 g) consisting of equal numbers of males and females (n = 8) were assigned to study. The rats were orally given for 5 days. The control group was administered pure olive oil, which was the vehicle for CPF. The CPF challenge groups were administered oral physiological saline, pure olive oil, or DHA (50, 100 and 400 mg/kg dosages) for 5 days. The animals were weighed on the sixth day and then administered CPF (279 mg/kg, subcutaneously). The rats were weighed again 24 h following CPF administration. The body temperatures and locomotor activities of the rats were also measured. Blood samples, brain and liver tissues were collected for biochemical, histopathological and immunohistochemical examinations. A comparison with the control group demonstrated that CPF administration increased malondialdehyde (MDA) levels in blood, brain and liver, while it reduced catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPx) concentrations (p < 0.05-0.001). Advanced oxidation protein products (AOPPs) increased only in the brain (p < 0.001). DHA reduced these changes in MDA and AOPP values (p < 0.05-0.001), while it increased CAT, SOD and GPx concentrations (p < 0.05-0.001). Similarly, DHA prevented the decreases in body weight, body temperature and locomotor activities caused by CPF at 100 mg/kg and 400 mg/kg dosages (p < 0.05-0.001). Similar to the physiological and biochemical changes, the histopathological damage scores, which increased with CPF (p < 0.05-0.01), decreased at all three dosages of DHA (p < 0.05-0.01). Our findings suggest that DHA, by supporting the antioxidant mechanism, reduces toxicity caused by CPF.en_US
dc.description.sponsorshipOndokuz Mayis University Research FundOndokuz Mayis University [PYO. TIP. 1901.13.013]en_US
dc.description.sponsorshipThe author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by Ondokuz Mayis University Research Fund. PYO. TIP. 1901.13.013.en_US
dc.language.isoengen_US
dc.publisherSage Publications Incen_US
dc.relation.isversionof10.1177/0748233717737646en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectOrganophosphateen_US
dc.subjectoxidative stressen_US
dc.subjectpesticide toxicologyen_US
dc.subjectchlorpyrifosen_US
dc.subjectdocosahexaenoic aciden_US
dc.subjectomega-3 fatty acidsen_US
dc.titleProtective effects of dietary omega-3 fatty acid supplementation on organophosphate poisoningen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume34en_US
dc.identifier.issue2en_US
dc.identifier.startpage69en_US
dc.identifier.endpage82en_US
dc.relation.journalToxicology and Industrial Healthen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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