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dc.contributor.authorSimsek, Goekce
dc.contributor.authorTas, Burak Mustafa
dc.contributor.authorMuluk, Nuray Bayar
dc.contributor.authorAzman, Musa
dc.contributor.authorKilic, Rahmi
dc.date.accessioned2020-06-25T18:30:22Z
dc.date.available2020-06-25T18:30:22Z
dc.date.issued2019
dc.identifier.citationclosedAccessen_US
dc.identifier.issn0937-4477
dc.identifier.issn1434-4726
dc.identifier.urihttps://doi.org/10.1007/s00405-019-05635-x
dc.identifier.urihttps://hdl.handle.net/20.500.12587/7624
dc.descriptionSIMSEK, GOKCE/0000-0001-5281-0986en_US
dc.descriptionWOS: 000496697400005en_US
dc.descriptionPubMed: 31531774en_US
dc.description.abstractPurpose The main aim of this study was to compare the efficacy of intratympanic administration of dexamethasone and resveratrol in preventing cisplatin ototoxicity by measuring acoustic brainstem response (ABR) and distortion product otoacoustic emission (DPOAE). Methods Forty rats (80 ears) were divided into five groups. Cisplatin was administered intraperitoneally to the first group (n = 8). Group 2 (n = 8) received cisplatin after resveratrol had been administered intratympanically. Group 3 (n = 8) received cisplatin after dexamethasone had been administered intratympanically. Group 4 (n = 8) received cisplatin after sodium chloride (NaCl) had been given intratympanically. Group 5 (n = 8) received cisplatin after dimethylsulfoxide (DMSO) had been given intratympanically. ABR and DPOAE tests were performed on all groups before and 72 h after the procedure. Results ABR threshold values in rats that received dexamethasone and resveratrol were found to be less affected than those observed in the other post-cisplatin groups. ABR-IV and ABR-I-IV interval values were significantly reduced in rats that had been given dexamethasone and resveratrol compared to the other groups. After cisplatin treatment, otoacoustic emission (OAE) amplitudes were significantly decreased in Groups 1, 4, and 5 for all frequencies, while OAE values were sustained in the resveratrol and dexamethasone groups (Groups 2 and 3). At OAE frequency 5652, dexamethasone was more significantly associated with protective than resveratrol was, while no significant difference was found between the two groups at other OAE frequencies. Conclusion In conclusion, intratympanic dexamethasone and intratympanic resveratrol treatments may provide a significant protection against cisplatin-induced ototoxicity.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.relation.isversionof10.1007/s00405-019-05635-xen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCisplatinen_US
dc.subjectDexamethasoneen_US
dc.subjectIntratympanicen_US
dc.subjectOtotoxicityen_US
dc.subjectResveratrolen_US
dc.titleComparison of the protective efficacy between intratympanic dexamethasone and resveratrol treatments against cisplatin-induced ototoxicity: an experimental studyen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume276en_US
dc.identifier.issue12en_US
dc.identifier.startpage3287en_US
dc.identifier.endpage3293en_US
dc.relation.journalEuropean Archives Of Oto-Rhino-Laryngologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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