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The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin

OBJECTIVES: 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 malon...

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Autores principales: Toplu, Yuksel, Sapmaz, Emrah, Parlakpinar, Hakan, Kelles, Mehmet, Kalcioglu, M. Tayyar, Tanbek, Kevser, Kizilay, Ahmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Otorhinolaryngology-Head and Neck Surgery 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792246/
https://www.ncbi.nlm.nih.gov/pubmed/26976021
http://dx.doi.org/10.21053/ceo.2016.9.1.14
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author Toplu, Yuksel
Sapmaz, Emrah
Parlakpinar, Hakan
Kelles, Mehmet
Kalcioglu, M. Tayyar
Tanbek, Kevser
Kizilay, Ahmet
author_facet Toplu, Yuksel
Sapmaz, Emrah
Parlakpinar, Hakan
Kelles, Mehmet
Kalcioglu, M. Tayyar
Tanbek, Kevser
Kizilay, Ahmet
author_sort Toplu, Yuksel
collection PubMed
description OBJECTIVES: 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.
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spelling pubmed-47922462016-03-17 The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin Toplu, Yuksel Sapmaz, Emrah Parlakpinar, Hakan Kelles, Mehmet Kalcioglu, M. Tayyar Tanbek, Kevser Kizilay, Ahmet Clin Exp Otorhinolaryngol Original Article OBJECTIVES: 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. Korean Society of Otorhinolaryngology-Head and Neck Surgery 2016-03 2016-03-07 /pmc/articles/PMC4792246/ /pubmed/26976021 http://dx.doi.org/10.21053/ceo.2016.9.1.14 Text en Copyright © 2016 by Korean Society of Otorhinolaryngology-Head and Neck Surgery. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Toplu, Yuksel
Sapmaz, Emrah
Parlakpinar, Hakan
Kelles, Mehmet
Kalcioglu, M. Tayyar
Tanbek, Kevser
Kizilay, Ahmet
The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin
title The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin
title_full The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin
title_fullStr The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin
title_full_unstemmed The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin
title_short The Effect of Dexpanthenol on Ototoxicity Induced by Cisplatin
title_sort effect of dexpanthenol on ototoxicity induced by cisplatin
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792246/
https://www.ncbi.nlm.nih.gov/pubmed/26976021
http://dx.doi.org/10.21053/ceo.2016.9.1.14
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