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Vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin

Todd et al. (2014ab) have recently demonstrated the presence of vestibular-dependent contributions to auditory evoked potentials (AEPs) when passing through the vestibular threshold as determined by vestibular evoked myogenic potentials (VEMPs), including a particular deflection labeled as an N42/P5...

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Autores principales: Todd, N.P.M., Govender, S., Colebatch, J.G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier/North-Holland Biomedical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090052/
https://www.ncbi.nlm.nih.gov/pubmed/27498399
http://dx.doi.org/10.1016/j.heares.2016.07.017
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author Todd, N.P.M.
Govender, S.
Colebatch, J.G.
author_facet Todd, N.P.M.
Govender, S.
Colebatch, J.G.
author_sort Todd, N.P.M.
collection PubMed
description Todd et al. (2014ab) have recently demonstrated the presence of vestibular-dependent contributions to auditory evoked potentials (AEPs) when passing through the vestibular threshold as determined by vestibular evoked myogenic potentials (VEMPs), including a particular deflection labeled as an N42/P52 prior to the long-latency AEPs N1 and P2. In this paper we report the results of an experiment to determine the effect of inter-stimulus interval (ISI) and regularity on potentials recorded above and below VEMP threshold. Five healthy, right-handed subjects were recruited and evoked potentials were recorded to binaurally presented sound stimulation, above and below vestibular threshold, at seven stimulus rates with ISIs of 212, 300, 424, 600, 848, 1200 and 1696 ms. The inner five intervals, i.e. 300, 424, 600, 848, 1200 ms, were presented twice in both regular and irregular conditions. ANOVA on the global field power (GFP) were conducted for each of four waves, N42, P52, N1 and P2 with factors of intensity, ISI and regularity. Both N42 and P52 waves showed significant ANOVA effects of intensity but no other main effects or interactions. In contrast both N1 and P2 showed additional effects of ISI, as well as intensity, and evidence of non-linear interactions between ISI and intensity. A source analysis was carried out consistent with prior work suggesting that when above vestibular threshold, in addition to bilateral superior temporal cortex, ocular, cerebellar and cingulate sources are recruited. Further statistical analysis of the source currents indicated that the origin of the interactions with intensity may be the ISI sensitivity of the vestibular-dependent sources. This in turn may reflect a specific vestibular preference for stimulus rates associated with locomotion, i.e. rates close to 2 Hz, or ISIs close to 500 ms, where saccular afferents show increased gain and the corresponding reflexes are most sensitive.
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spelling pubmed-50900522016-11-07 Vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin Todd, N.P.M. Govender, S. Colebatch, J.G. Hear Res Research Paper Todd et al. (2014ab) have recently demonstrated the presence of vestibular-dependent contributions to auditory evoked potentials (AEPs) when passing through the vestibular threshold as determined by vestibular evoked myogenic potentials (VEMPs), including a particular deflection labeled as an N42/P52 prior to the long-latency AEPs N1 and P2. In this paper we report the results of an experiment to determine the effect of inter-stimulus interval (ISI) and regularity on potentials recorded above and below VEMP threshold. Five healthy, right-handed subjects were recruited and evoked potentials were recorded to binaurally presented sound stimulation, above and below vestibular threshold, at seven stimulus rates with ISIs of 212, 300, 424, 600, 848, 1200 and 1696 ms. The inner five intervals, i.e. 300, 424, 600, 848, 1200 ms, were presented twice in both regular and irregular conditions. ANOVA on the global field power (GFP) were conducted for each of four waves, N42, P52, N1 and P2 with factors of intensity, ISI and regularity. Both N42 and P52 waves showed significant ANOVA effects of intensity but no other main effects or interactions. In contrast both N1 and P2 showed additional effects of ISI, as well as intensity, and evidence of non-linear interactions between ISI and intensity. A source analysis was carried out consistent with prior work suggesting that when above vestibular threshold, in addition to bilateral superior temporal cortex, ocular, cerebellar and cingulate sources are recruited. Further statistical analysis of the source currents indicated that the origin of the interactions with intensity may be the ISI sensitivity of the vestibular-dependent sources. This in turn may reflect a specific vestibular preference for stimulus rates associated with locomotion, i.e. rates close to 2 Hz, or ISIs close to 500 ms, where saccular afferents show increased gain and the corresponding reflexes are most sensitive. Elsevier/North-Holland Biomedical Press 2016-11 /pmc/articles/PMC5090052/ /pubmed/27498399 http://dx.doi.org/10.1016/j.heares.2016.07.017 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Todd, N.P.M.
Govender, S.
Colebatch, J.G.
Vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin
title Vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin
title_full Vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin
title_fullStr Vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin
title_full_unstemmed Vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin
title_short Vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin
title_sort vestibular-dependent inter-stimulus interval effects on sound evoked potentials of central origin
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090052/
https://www.ncbi.nlm.nih.gov/pubmed/27498399
http://dx.doi.org/10.1016/j.heares.2016.07.017
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