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dc.contributor.authorErboğa, Mustafa
dc.contributor.authorAktaş, Cevat
dc.contributor.authorErboğa, Zeynep Fidanol
dc.contributor.authorDönmez, Yeliz Bozdemir
dc.contributor.authorGürel, Ahmet
dc.date.accessioned2022-05-11T14:09:57Z
dc.date.available2022-05-11T14:09:57Z
dc.date.issued2015
dc.identifier.issn0886-022X
dc.identifier.issn1525-6049
dc.identifier.urihttps://doi.org/10.3109/0886022X.2015.1074521
dc.identifier.urihttps://hdl.handle.net/20.500.11776/5214
dc.description.abstractBackground: In the present study, the protective and therapeutic effects of quercetin (QE) on renal injury induced by methotrexate (MTX) have been examined. Materials and methods: A total of 24 male rats were divided into the following three groups: control group, MTX group, and MTX+QE group. Rats in MTX group received 20mg/kg of single dose of MTX, while those in MTX+QE group received 20mg/kg of single dose MTX, in addition to 15mg/kg of QE administered 30min prior to MTX and in the following 5-day period as a single daily dose. At the end of the experimental period, renal tissues were removed for histopathological and biochemical assessments. Results: Light microscopic examination showed a disruption of the renal structure in rats in MTX group in the form of tubular degeneration and dilation, with shedding of the tubular epithelial cells into the lumen. QE treatment was associated with less marked degenerative changes, with a similar histological appearance to that of controls. Furthermore, QE treatment resulted in decreased the number of apoptotic cells. Biochemical assessments showed significantly higher malondialdehyde (MDA) levels in MTX group as compared to control and MTX+QE groups. superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) levels showed a significant decrease in MTX group as compared to controls. However, QE significantly suppressed MDA level, compensated deficits in the anti-oxidant defenses [reduced SOD, GSH-Px, and CAT levels] in kidney tissue resulted from MTX administration. Conclusions: In conclusion, renal toxic effects of MTX may be alleviated by QE.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.identifier.doi10.3109/0886022X.2015.1074521
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectApoptosisen_US
dc.subjectmethotrexateen_US
dc.subjectnephrotoxicityen_US
dc.subjectoxidative stressen_US
dc.subjectquercetinen_US
dc.subjectInduced Nephrotoxicityen_US
dc.subjectAdenosine-Deaminaseen_US
dc.subjectDna-Damageen_US
dc.subjectInjuryen_US
dc.subjectAciden_US
dc.subjectToxicityen_US
dc.subjectProtectsen_US
dc.subjectKidneyen_US
dc.titleQuercetin ameliorates methotrexate-induced renal damage, apoptosis and oxidative stress in ratsen_US
dc.typearticleen_US
dc.relation.ispartofRenal Failureen_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Histoloji ve Embriyoloji Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Biyoistatistik Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyokimya Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyokimya Ana Bilim Dalıen_US
dc.identifier.volume37en_US
dc.identifier.issue9en_US
dc.identifier.startpage1492en_US
dc.identifier.endpage1497en_US
dc.institutionauthorErboğa, Mustafa
dc.institutionauthorAktaş, Cevat
dc.institutionauthorErboğa, Zeynep Fidanol
dc.institutionauthorDönmez, Yeliz Bozdemir
dc.institutionauthorGürel, Ahmet
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid36023238400
dc.authorscopusid24436194200
dc.authorscopusid56816914100
dc.authorscopusid55134339900
dc.authorscopusid36866111300
dc.authorwosidAktas, Cevat/D-8468-2011
dc.identifier.wosWOS:000369740900017en_US
dc.identifier.scopus2-s2.0-84944165976en_US
dc.identifier.pmid26338102en_US


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