Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4628
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dc.contributor.authorDugeroglu, Harun-
dc.contributor.authorOzgenoglu, Murat-
dc.date.accessioned2024-03-15T12:05:36Z-
dc.date.available2024-03-15T12:05:36Z-
dc.date.issued2023-
dc.identifier.citationDügeroglu, H., Özgenoglu, M. (2023). HEPATORENAL PROTECTIVE EFFECTS OF WALNUT OIL AGAINST ANTICANCER DRUG METHOTREXATE IN EXPERIMENTALLY INDUCED LIVER AND KIDNEY TOXICITY IN RATS. C. R. Acad. Bulg. Sci., 76(10), 1609-1616. https://doi.org/10.7546/CRABS.2023.10.15en_US
dc.identifier.issn1310-1331-
dc.identifier.urihttp://dx.doi.org/10.7546/CRABS.2023.10.15-
dc.identifier.urihttps://www.webofscience.com/wos/woscc/full-record/WOS:001145903300005-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4628-
dc.descriptionWoS Categories: Multidisciplinary Sciencesen_US
dc.descriptionWeb of Science Index: Science Citation Index Expanded (SCI-EXPANDED)en_US
dc.descriptionResearch Areas: Science & Technology - Other Topicsen_US
dc.description.abstractThe aim of this study was to investigate the hepatorenal protective effects of walnut oil (WO) against anticancer drug methotrexate (MTX)-induced kidney and liver toxicity.In our study, 40 male Sprague Dawley rats weighing between 200-250 g were used. The rats were randomly divided into four groups; Group 1, control group (corn oil by gavage for 14 days and intraperitoneal (i.p.) physiological saline on the third day, n = 10), Group 2, WO group (2 ml/kg WO by gavage for 14 days and i.p. physiological saline on the third day, n = 10), Group 3, MTX group (corn oil by gavage for 14 days and 20 mg/kg MTX single dose i.p. on the third day, n = 10), Group 4, MTX + WO group (2 ml/kg WO by gavage for 14 days and 20 mg/kg MTX single dose i.p. on the third day, n = 10). At the end of the experiment, the rats were decapitated. Kidney and liver were preserved at -86 degrees C and biochemical measurements were performed.Thiobarbituric acid reactive substances (TBARS) levels increased and superoxide dismutase (SOD), glutathione (GSH), glutathione peroxidase (GPx) and catalase (CAT) activities decreased in kidney and liver tissues in the methotrexate alone group compared to the control group. In the MTX + WO treated group, TBARS level decreased and GSH, CAT, SOD and GPx activities increased significantly compared to the MTX alone treated group.It was found that MTX caused oxidative damage in kidney and liver tissues and WO prevented this damage. Walnut oil is protective against MTX-induced kidney and liver toxicity.en_US
dc.language.isoengen_US
dc.publisherPUBL HOUSE BULGARIAN ACAD SCI-SOFIAen_US
dc.relation.isversionof10.7546/CRABS.2023.10.15en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectkidney, liver, methotrexate, oxidative damage, walnut oilen_US
dc.subjectINDUCED HEPATOTOXICITY, ACID, NEPHROTOXICITY, INJURYen_US
dc.titleHEPATORENAL PROTECTIVE EFFECTS OF WALNUT OIL AGAINST ANTICANCER DRUG METHOTREXATE IN EXPERIMENTALLY INDUCED LIVER AND KIDNEY TOXICITY IN RATSen_US
dc.typearticleen_US
dc.relation.journalCOMPTES RENDUS DE L ACADEMIE BULGARE DES SCIENCESen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.identifier.volume76en_US
dc.identifier.issue10en_US
dc.identifier.startpage1609en_US
dc.identifier.endpage1616en_US
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