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The protective role of molsidomine on the cisplatin Induced ototoxicity

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dc.contributor.author Toplu, Yüksel
dc.contributor.author Parlakpınar, Hakan
dc.contributor.author Sapmaz, Emrah
dc.contributor.author Karataş, Erkan
dc.contributor.author Polat, Alaattin
dc.contributor.author Kızılay, Ahmet
dc.date.accessioned 2017-05-29T13:59:01Z
dc.date.available 2017-05-29T13:59:01Z
dc.date.issued 2014
dc.identifier.citation Toplu, Y. Parlakpınar, H. Sapmaz, E. Karataş, E. Polat, A. Kızılay, A. (2014). The Protective Role of Molsidomine on the Cisplatin Induced Ototoxicity. Indian Journal of Otolaryngology and Head & Neck Surgery, 66(3), 314–319. tr_TR
dc.identifier.issn 2231-3796
dc.identifier.uri http://link.springer.com/10.1007/s12070-014-0718-2
dc.identifier.uri http://hdl.handle.net/11616/6993
dc.description.abstract This experimental study was designed to investigate the protective effects of molsidomine (MOL) on against cisplatin-induced ototoxicity (CIO). To examine this effect, distortion product otoacoustic emissions (DPOAEs) measurements and serum levels of oxidative and antioxidant status [including malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione (GSH), glutathione peroxidase (GPX), total oxidant status (TOS), total antioxidant status (TAS), and oxidative stress index (OSI)] were evaluated. Thirty-two female wistar albino rats were divided into four groups including; control (Group K), cisplatin (Group C), cisplatin plus MOL group (Group CM), and MOL group (Group M). DPOAEs measurements between 0.9961 and 8.0003 Hz as DP-gram and input/output (I/O) functions were performed in the same (left) ear of all rats on days 0, 1st, 5th and 12th. Prior to death, the last DPOAEs measurements and blood samples were taken. In the C group, statistically significant DPOAE amplitude reductions were detected at 2.5195, 3.1758, 3.9961, 5.0391, 6.3516 and 8.0039 Hz frequencies (p\0.05) between 0th and 1st, 0th and 5th and 0th and 12th days’ measurements (p\0.05). Serum level of MDA, TAC and OSI levels were significantly higher in the C group versus K group (p\0.05). In the CM group, there were no significant differences at all frequencies between 0th and other days’ measurements (p[0.05) and the serum levels of all biochemical parameters were shifted toward normal values, similar to the K group (p\0.05). No significant differences were detected in the either M or K group’s measurements. According to these results, cisplatin-related ototoxicity has been significantly prevented by MOL. tr_TR
dc.language.iso eng tr_TR
dc.publisher Indian Journal of Otolaryngology and Head & Neck Surgery tr_TR
dc.relation.isversionof 10.1007/s12070-014-0718-2 tr_TR
dc.rights info:eu-repo/semantics/openAccess tr_TR
dc.subject Cisplatin tr_TR
dc.subject Molsidomine tr_TR
dc.subject Otoacoustic emissions tr_TR
dc.subject Oxidative status tr_TR
dc.subject Ototoxicity tr_TR
dc.title The protective role of molsidomine on the cisplatin Induced ototoxicity tr_TR
dc.type article tr_TR
dc.relation.journal Indian Journal of Otolaryngology and Head & Neck Surgery tr_TR
dc.contributor.department İnönü Üniversitesi tr_TR
dc.identifier.volume 66 tr_TR
dc.identifier.issue 3 tr_TR
dc.identifier.startpage 314 tr_TR
dc.identifier.endpage 319 tr_TR


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