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The ototoxic effect of intratympanic terbinafine applied in the middle ear of rats

BACKGROUND: Otomycosis is defined as an infection of the external ear canal with fungal agents. The treatment of the disease is cleansing and drying of the external ear canal, identification and treatment of any predisposing factors and application of topical antifungal agents. Terbinafine is used a...

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Autores principales: Sagit, Mustafa, Somdas, Mehmet Akıf, Korkmaz, Ferhat, Akcadag, Alper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650939/
https://www.ncbi.nlm.nih.gov/pubmed/23663536
http://dx.doi.org/10.1186/1916-0216-42-13
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author Sagit, Mustafa
Somdas, Mehmet Akıf
Korkmaz, Ferhat
Akcadag, Alper
author_facet Sagit, Mustafa
Somdas, Mehmet Akıf
Korkmaz, Ferhat
Akcadag, Alper
author_sort Sagit, Mustafa
collection PubMed
description BACKGROUND: Otomycosis is defined as an infection of the external ear canal with fungal agents. The treatment of the disease is cleansing and drying of the external ear canal, identification and treatment of any predisposing factors and application of topical antifungal agents. Terbinafine is used as an antifungal agent to treat otomycosis. We proposed to investigate the probable ototoxic effect of terbinafine solution on auditory brain stem response (ABR) and distortion product otoacoustic emission (DPOAE) when applied intratympanically in the middle ear of rats. METHODS: The experiment was performed on 30 female Wistar albino rats. Thirty animals were divided into three groups of 10 animals each. 1% terbinafine solution was administered to the first group (group T). The second group (group G) was administered 40 mg/ml gentamicin solution (ototoxic control). The third group (group S) was administered saline solution (negative control). Baseline DPOAE measurements and ABR testing from the left ears were obtained from the animals in all groups under general anesthesia. Ear solutions were applied in the middle ear intratympanically with a dental needle. Treatment was initiated after baseline measurements and repeated once every two days for fifteen days. RESULTS: Pre and post-treatment DPOAE responses for all tested frequencies of group T and Group S showed no statistically significant difference. However, the group G demonstrated a significant change in ABR thresholds and DPOAE responses. CONCLUSIONS: Terbinafine solution is a broad spectrum antifungal agent effective in the treatment of otomycosis. The present study demonstrated that its direct administration in the middle ear of rats does not affect inner ear function as measured by ABR and DPOAE responses.
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spelling pubmed-36509392013-05-14 The ototoxic effect of intratympanic terbinafine applied in the middle ear of rats Sagit, Mustafa Somdas, Mehmet Akıf Korkmaz, Ferhat Akcadag, Alper J Otolaryngol Head Neck Surg Original Research Article BACKGROUND: Otomycosis is defined as an infection of the external ear canal with fungal agents. The treatment of the disease is cleansing and drying of the external ear canal, identification and treatment of any predisposing factors and application of topical antifungal agents. Terbinafine is used as an antifungal agent to treat otomycosis. We proposed to investigate the probable ototoxic effect of terbinafine solution on auditory brain stem response (ABR) and distortion product otoacoustic emission (DPOAE) when applied intratympanically in the middle ear of rats. METHODS: The experiment was performed on 30 female Wistar albino rats. Thirty animals were divided into three groups of 10 animals each. 1% terbinafine solution was administered to the first group (group T). The second group (group G) was administered 40 mg/ml gentamicin solution (ototoxic control). The third group (group S) was administered saline solution (negative control). Baseline DPOAE measurements and ABR testing from the left ears were obtained from the animals in all groups under general anesthesia. Ear solutions were applied in the middle ear intratympanically with a dental needle. Treatment was initiated after baseline measurements and repeated once every two days for fifteen days. RESULTS: Pre and post-treatment DPOAE responses for all tested frequencies of group T and Group S showed no statistically significant difference. However, the group G demonstrated a significant change in ABR thresholds and DPOAE responses. CONCLUSIONS: Terbinafine solution is a broad spectrum antifungal agent effective in the treatment of otomycosis. The present study demonstrated that its direct administration in the middle ear of rats does not affect inner ear function as measured by ABR and DPOAE responses. BioMed Central 2013-02-04 /pmc/articles/PMC3650939/ /pubmed/23663536 http://dx.doi.org/10.1186/1916-0216-42-13 Text en Copyright © 2013 Sagit et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Sagit, Mustafa
Somdas, Mehmet Akıf
Korkmaz, Ferhat
Akcadag, Alper
The ototoxic effect of intratympanic terbinafine applied in the middle ear of rats
title The ototoxic effect of intratympanic terbinafine applied in the middle ear of rats
title_full The ototoxic effect of intratympanic terbinafine applied in the middle ear of rats
title_fullStr The ototoxic effect of intratympanic terbinafine applied in the middle ear of rats
title_full_unstemmed The ototoxic effect of intratympanic terbinafine applied in the middle ear of rats
title_short The ototoxic effect of intratympanic terbinafine applied in the middle ear of rats
title_sort ototoxic effect of intratympanic terbinafine applied in the middle ear of rats
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650939/
https://www.ncbi.nlm.nih.gov/pubmed/23663536
http://dx.doi.org/10.1186/1916-0216-42-13
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