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dc.contributor.authorSoyalic, Harun
dc.contributor.authorGevrek, Fikret
dc.contributor.authorKoc, Sema
dc.contributor.authorAvcu, Mustafa
dc.contributor.authorMetin, Mehmet
dc.contributor.authorAladag, Ibrahim
dc.date.accessioned2019-11-24T21:01:09Z
dc.date.available2019-11-24T21:01:09Z
dc.date.issued2016
dc.identifier.issn0165-5876
dc.identifier.issn1872-8464
dc.identifier.urihttps://dx.doi.org/10.1016/j.ijporl.2016.08.012
dc.identifier.urihttps://hdl.handle.net/20.500.12513/3495
dc.descriptionWOS: 000383933500034en_US
dc.descriptionPubMed ID: 27619052en_US
dc.description.abstractIntroduction: Cisplatin ototoxicity is characterized by irreversible, progressive, bilateral sensorineural hearing loss at high frequencies, accompanied by tinnitus. The aim of this study is to demonstrate the protective action of curcumin alone or in combination with vitamin E against cisplatin-induced ototoxicity in animal models. Material and methods: The study included 42 rats. Experimental animals were randomized into 6 groups. In the first group, intra-peritoneal cisplatin was administered alone. In the second group, intra-peritoneal cisplatin and curcumin were administered together. In the third group, intra-peritoneal cisplatin and vitamin E were administered together. In the fourth group, intra-peritoneal cisplatin was administered together with curcumin in combination with vitamin E. In the fifth group, intra-peritoneal curcumin was administered alone. The sixth group was sacrificed directly without administration of any drugs. A distortion product otoacoustic emission (DPOAE) test was applied to both ears of all experimental animals. Curcumin was administered 1 h before cisplatin treatment continued for three successive days. Vitamin E was administered only as a single dose 30 min prior to cisplatin. All animals were sacrificed following DPOAE testing on the 5th day of cisplatin administration. Histopathological findings included a TUNEL (TdT-mediated deoxyuridine triphosphate nick end-labeling) assay, and the percentage of apoptotic cells was calculated. DPOAE values and the percentage of apoptotic cells were compared before and after treatment and between experimental groups. Results: In Group 1, DPOAE values were significantly decreased at all frequencies (3000 Hz, 4000 Hz and 6000 Hz; P < 0.05). In Groups 2, 3, 4 and 5 there was no significant difference between the pre- and post-treatment DPOAE results (p > 0.05). Apoptotic index values were lower in all treatment groups compared to the cisplatin group, however the difference was only statistically significant in group 3 (p = 0.009). Conclusion: In rats, cisplatin ototoxicity can be prevented with curcumin or curcumin-vitamin E combination. (C) 2016 Elsevier Ireland Ltd. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherELSEVIER IRELAND LTDen_US
dc.relation.isversionof10.1016/j.ijporl.2016.08.012en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCisplatinen_US
dc.subjectOtotoxicityen_US
dc.subjectCurcuminen_US
dc.subjectVitamin Een_US
dc.subjectDistortion product otoacoustic emissionen_US
dc.subjectApoptosisen_US
dc.titleIntraperitoneal curcumin and vitamin E combination for the treatment of cisplatin-induced ototoxicity in ratsen_US
dc.typearticleen_US
dc.relation.journalINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGYen_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri, Kulak-Burun ve Boğaz Hastalıkları ABDen_US
dc.identifier.volume89en_US
dc.identifier.startpage173en_US
dc.identifier.endpage178en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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