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dc.contributor.authorSutcuoglu, Osman
dc.contributor.authorDerici, Mehmet Kursat
dc.contributor.authorPasaoglu, Ozge Tugce
dc.contributor.authorDumludag, Burak
dc.contributor.authorHelvaci, Ozant
dc.contributor.authorOgut, Betul
dc.contributor.authorDerici, Ulver
dc.date.accessioned2020-06-25T18:33:59Z
dc.date.available2020-06-25T18:33:59Z
dc.date.issued2019
dc.identifier.citationclosedAccessen_US
dc.identifier.issn0301-1623
dc.identifier.issn1573-2584
dc.identifier.urihttps://doi.org/10.1007/s11255-019-02194-2
dc.identifier.urihttps://hdl.handle.net/20.500.12587/7724
dc.descriptionDerici, Mehmet Kursat/0000-0002-8260-7492; Ogut, Betul/0000-0002-1385-7324en_US
dc.descriptionWOS: 000477631100016en_US
dc.descriptionPubMed: 31190296en_US
dc.description.abstractPurposeContrast-induced nephropathy (CIN) is one of the side effects of diagnostic procedures. Oxidative stress plays an important role in CIN's pathophysiology. Dexpanthenol (Dexp) is a substance with antioxidant efficacy. We investigated the likely protective effects of dexpanthenol for CIN.MethodsTwenty-four Sprague-Dawley rats were divided randomly into four groups of 6 rats; control (group 1), Dexp (group 2), CIN (group 3) and Dexp+CIN (group 4). All rats were restricted of water moderately to facilitate of nephrotoxicity. Dexp was administered into the intraperitoneally at a dose of 500mg/kg for 5days in groups 2 and 4. The same amount of saline was applied via intraperitoneally to group 1 and 3. In CIN and Dexp+CIN groups, L-NAME (10mg/kg), tenoxicam (0.5mg/kg) and sodium amidotrizoate (10ml/kg) were administered on the 4th day via the tail vein for CIN. All rats were euthanized on the 6th day and samples for biochemical and pathological evaluations were collected.ResultsWhen the Dexp+CIN group and the CIN group were compared, it was found to be provide a significant decline at the level of acute tubular injury and necrosis in kidney biopsies by dexp. Furthermore Dexp significantly reduced the serum cystatin C (Cys-C) levels, not serum creatinine. There was no statistically significant difference between the groups in total oxidant and antioxidant levels.ConclusionsDexpanthenol did not have significant effect on oxidative stress of acute kidney injury on this rat model. However, it has ameliorated serum Cys-C levels and histopathological findings of CIN.en_US
dc.description.sponsorshipTurkish Society of Hypertension and Kidney Diseaseen_US
dc.description.sponsorshipThis study was supported by Turkish Society of Hypertension and Kidney Disease.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.relation.isversionof10.1007/s11255-019-02194-2en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectRadiocontrast mediaen_US
dc.subjectNephrotoxicityen_US
dc.subjectDexpanthenolen_US
dc.subjectCystatin Cen_US
dc.subjectApoptosisen_US
dc.titleIs it possible to prevent contrast-induced nephropathy with dexpanthenol?en_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume51en_US
dc.identifier.issue8en_US
dc.identifier.startpage1387en_US
dc.identifier.endpage1394en_US
dc.relation.journalInternational Urology And Nephrologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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