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Acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus

As a common debilitating disorder worldwide, tinnitus requires objective assessment. In the auditory brainstem response (ABR) test, auditory potentials can be evoked by acoustic or optoacoustic (induced by laser light) stimulations. In order to use the ABR test in the objective assessment of tinnitu...

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Autores principales: Montazeri, Katayoon, Farhadi, Mohammad, Akbarnejad, Zeinab, Asadpour, Abdoreza, Majdabadi, Abbas, Fekrazad, Reza, Mahmoudian, Saeid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366222/
https://www.ncbi.nlm.nih.gov/pubmed/37488197
http://dx.doi.org/10.1038/s41598-023-39033-5
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author Montazeri, Katayoon
Farhadi, Mohammad
Akbarnejad, Zeinab
Asadpour, Abdoreza
Majdabadi, Abbas
Fekrazad, Reza
Mahmoudian, Saeid
author_facet Montazeri, Katayoon
Farhadi, Mohammad
Akbarnejad, Zeinab
Asadpour, Abdoreza
Majdabadi, Abbas
Fekrazad, Reza
Mahmoudian, Saeid
author_sort Montazeri, Katayoon
collection PubMed
description As a common debilitating disorder worldwide, tinnitus requires objective assessment. In the auditory brainstem response (ABR) test, auditory potentials can be evoked by acoustic or optoacoustic (induced by laser light) stimulations. In order to use the ABR test in the objective assessment of tinnitus, in this study, acoustic ABR (aABR) and optoacoustic ABR (oABR) were compared in the control and tinnitus groups to determine the changes caused by sodium salicylate (SS)-induced tinnitus in rat. In both aABR and oABR, wave II was the most prominent waveform, and the amplitude of wave II evoked by oABR was significantly higher than that of aABR. Brainstem transmission time (BTT), which represents the time required for a neural stimulation to progress from the auditory nerve ending to the inferior colliculus, was significantly shorter in oABR. In the tinnitus group, there was a significant increase in the threshold of both ABRs and a significant decrease in the amplitude of wave II only in the oABR. Based on our findings, the ABR test has the potential to be used in the assessment of SS-induced tinnitus, but oABR has the advantages of producing more prominent waveforms and significantly reducing the amplitude of wave II in tinnitus.
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spelling pubmed-103662222023-07-26 Acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus Montazeri, Katayoon Farhadi, Mohammad Akbarnejad, Zeinab Asadpour, Abdoreza Majdabadi, Abbas Fekrazad, Reza Mahmoudian, Saeid Sci Rep Article As a common debilitating disorder worldwide, tinnitus requires objective assessment. In the auditory brainstem response (ABR) test, auditory potentials can be evoked by acoustic or optoacoustic (induced by laser light) stimulations. In order to use the ABR test in the objective assessment of tinnitus, in this study, acoustic ABR (aABR) and optoacoustic ABR (oABR) were compared in the control and tinnitus groups to determine the changes caused by sodium salicylate (SS)-induced tinnitus in rat. In both aABR and oABR, wave II was the most prominent waveform, and the amplitude of wave II evoked by oABR was significantly higher than that of aABR. Brainstem transmission time (BTT), which represents the time required for a neural stimulation to progress from the auditory nerve ending to the inferior colliculus, was significantly shorter in oABR. In the tinnitus group, there was a significant increase in the threshold of both ABRs and a significant decrease in the amplitude of wave II only in the oABR. Based on our findings, the ABR test has the potential to be used in the assessment of SS-induced tinnitus, but oABR has the advantages of producing more prominent waveforms and significantly reducing the amplitude of wave II in tinnitus. Nature Publishing Group UK 2023-07-24 /pmc/articles/PMC10366222/ /pubmed/37488197 http://dx.doi.org/10.1038/s41598-023-39033-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Montazeri, Katayoon
Farhadi, Mohammad
Akbarnejad, Zeinab
Asadpour, Abdoreza
Majdabadi, Abbas
Fekrazad, Reza
Mahmoudian, Saeid
Acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus
title Acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus
title_full Acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus
title_fullStr Acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus
title_full_unstemmed Acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus
title_short Acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus
title_sort acoustic and optoacoustic stimulations in auditory brainstem response test in salicylate induced tinnitus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366222/
https://www.ncbi.nlm.nih.gov/pubmed/37488197
http://dx.doi.org/10.1038/s41598-023-39033-5
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