The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin

dc.authorid0000-0002-5444-557X
dc.authorid0000-0003-3048-6489
dc.authorid0000-0003-2099-2273
dc.authorid0000-0001-9497-3468
dc.authorid0000-0002-0346-8704
dc.contributor.authorToplu, Yuksel
dc.contributor.authorSapmaz, Emrah
dc.contributor.authorParlakpinar, Hakan
dc.contributor.authorKelles, Mehmet
dc.contributor.authorKalcıoğlu, M. Tayyar
dc.contributor.authorTanbek, Kevser
dc.contributor.authorKizilay, Ahmet
dc.date.accessioned2025-05-10T19:35:27Z
dc.date.issued2016
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractObjectives. This study was aimed to investigate the protective effects of dexpanthenol (Dxp) on against cisplatin-induced ototoxicity. Methods. To examine this effect, distortion product otoacoustic emissions (DPOAEs) measurements and serum levels of oxidative and antioxidant status (including malondialdehyde, superoxide dismutase, catalase, glutathione, glutathione peroxidase, total oxidant status, total antioxidant status, and oxidative stress index) were evaluated. Thirty-two adult female Wistar albino rats were randomly divided into 4 equal groups; control (K), cisplatin (C), cisplatin plus Dxp (CD), and Dxp (D). In all groups DPOAEs measurements, between 996 and 10,078 Hz as DPOAEs and input/output functions, were performed on days 0, 1th, 5th, and 12th. Prior to death, the last DPOAEs measurements and blood samples were taken. Results. In the C group, statistically significant differences were detected at all frequencies between 0 and 5 days and 0 and 12 days measurements (P <0.05). Serum level of oxidant and antioxidant status were detected statistically significantly changed in this group versus K group (P<0.05). Contrary to the C group, in the CD group hearing ability was seen largely preserved at many frequencies and serum levels of all biochemical parameters were shifted toward normal values, similar to the K group. No significant differences were detected in the either D or K group's measurements. Conclusion. According to these results, Dxp may prevent cisplatin-induced ototoxicity.
dc.identifier.doi10.21053/ceo.2016.9.1.14
dc.identifier.endpage20
dc.identifier.issn1976-8710
dc.identifier.issn2005-0720
dc.identifier.issue1
dc.identifier.pmid26976021
dc.identifier.scopus2-s2.0-84960445390
dc.identifier.scopusqualityQ1
dc.identifier.startpage14
dc.identifier.urihttps://doi.org/10.21053/ceo.2016.9.1.14
dc.identifier.urihttps://hdl.handle.net/20.500.14730/8874
dc.identifier.volume9
dc.identifier.wosWOS:000372773000003
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherKorean Soc Otorhinolaryngol
dc.relation.ispartofClinical and Experimental Otorhinolaryngology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectCisplatin
dc.subjectOtotoxicity
dc.subjectDexpanthenol
dc.subjectOtoacoustic Emissions
dc.subjectBiomarkers
dc.titleThe Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin
dc.typeArticle

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