Evaluation of the Protective Effect of Beta Glucan on Amikacin Ototoxicity Using Distortion Product Otoacoustic Emission Measurements in Rats

dc.authorid0000-0003-4150-5016
dc.authorid0000-0001-8557-0886
dc.contributor.authorBayindir, Tuba
dc.contributor.authorFiliz, Aliye
dc.contributor.authorIraz, Mustafa
dc.contributor.authorKaya, Serdar
dc.contributor.authorTan, Mehmet
dc.contributor.authorKalcıoğlu, Mahmut Tayyar
dc.date.accessioned2025-05-10T19:36:35Z
dc.date.issued2013
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractObjectives. This experimental study investigated the possible protective effect of beta glucans on amikacin ototoxicity. Methods. Thirty-eight rats with normal distortion product otoacoustic emissions (DPOAEs) were divided into four groups. Group K was the control group. Group A was injected intramuscularly (i.m.) with amikacin 600 mg/kg/day between days 1-15. Group AB was given beta glucan gavage 1 mg/kg/day on days 0-15 and given amikacin 600 mg/kg/day i.m. on days 1-15. Group B was administered only beta glucan gavage, 1 mg/kg/day, on days 0-15.The DPOAEs were elicited in different frequency regions between 2,003 and 9,515 Hz, as distortion product diagrams (DPgrams), before and after the medication was administered, in all groups, on days 1, 5, 10, and 15. Results. No significant changes in the DPgrams were observed in group K. In group A, significant deterioration was observed at the 8,003 and 9,515 Hz frequencies on day 10, and at the 3,991, 4,557, 5,660, 6,726, 8,003, and 9,515 Hz frequencies on day 15. For group AB, statistically significant deterioration was observed at the 2,824, 8,003, and 9,515 Hz frequencies on day 15. The results for group B showed a significant improvement of hearing at the 2,378, 2,824, 3,363, and 3,991 Hz frequencies on day 1, at the 3,363, 3,991, and 8,003 Hz frequencies on day 10, and at the 8,003 Hz frequency on day 15. Conclusion. This study suggests that amikacin-induced hearing loss in rats may be limited to some extent by concomitant use of beta glucan.
dc.identifier.doi10.3342/ceo.2013.6.1.1
dc.identifier.endpage6
dc.identifier.issn1976-8710
dc.identifier.issn2005-0720
dc.identifier.issue1
dc.identifier.pmid23525870
dc.identifier.scopusqualityQ1
dc.identifier.startpage1
dc.identifier.urihttps://doi.org/10.3342/ceo.2013.6.1.1
dc.identifier.urihttps://hdl.handle.net/20.500.14730/9239
dc.identifier.volume6
dc.identifier.wosWOS:000317157200001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherKorean Soc Otorhinolaryngol
dc.relation.ispartofClinical and Experimental Otorhinolaryngology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectBeta glucan
dc.subjectAmikacin
dc.subjectOtoacoustic emission measurement
dc.titleEvaluation of the Protective Effect of Beta Glucan on Amikacin Ototoxicity Using Distortion Product Otoacoustic Emission Measurements in Rats
dc.typeArticle

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