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HEPATORENAL PROTECTIVE EFFECTS OF WALNUT OIL AGAINST ANTICANCER DRUG METHOTREXATE IN EXPERIMENTALLY INDUCED LIVER AND KIDNEY TOXICITY IN RATS

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dc.contributor.author Dugeroglu, Harun
dc.contributor.author Ozgenoglu, Murat
dc.date.accessioned 2024-03-15T12:05:36Z
dc.date.available 2024-03-15T12:05:36Z
dc.date.issued 2023
dc.identifier.citation Dügeroglu, 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.2023.10.15 en_US
dc.identifier.issn 1310-1331
dc.identifier.uri http://dx.doi.org/10.7546/CRABS.2023.10.15
dc.identifier.uri https://www.webofscience.com/wos/woscc/full-record/WOS:001145903300005
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4628
dc.description WoS Categories: Multidisciplinary Sciences en_US
dc.description Web of Science Index: Science Citation Index Expanded (SCI-EXPANDED) en_US
dc.description Research Areas: Science & Technology - Other Topics en_US
dc.description.abstract The 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.iso eng en_US
dc.publisher PUBL HOUSE BULGARIAN ACAD SCI-SOFIA en_US
dc.relation.isversionof 10.7546/CRABS.2023.10.15 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject kidney, liver, methotrexate, oxidative damage, walnut oil en_US
dc.subject INDUCED HEPATOTOXICITY, ACID, NEPHROTOXICITY, INJURY en_US
dc.title HEPATORENAL PROTECTIVE EFFECTS OF WALNUT OIL AGAINST ANTICANCER DRUG METHOTREXATE IN EXPERIMENTALLY INDUCED LIVER AND KIDNEY TOXICITY IN RATS en_US
dc.type article en_US
dc.relation.journal COMPTES RENDUS DE L ACADEMIE BULGARE DES SCIENCES en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.identifier.volume 76 en_US
dc.identifier.issue 10 en_US
dc.identifier.startpage 1609 en_US
dc.identifier.endpage 1616 en_US


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