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Temporal Pitch Sensitivity in an Animal Model: Psychophysics and Scalp Recordings: Temporal Pitch Sensitivity in Cat

Cochlear implant (CI) users show limited sensitivity to the temporal pitch conveyed by electric stimulation, contributing to impaired perception of music and of speech in noise. Neurophysiological studies in cats suggest that this limitation is due, in part, to poor transmission of the temporal fine...

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Autores principales: Richardson, Matthew L., Guérit, François, Gransier, Robin, Wouters, Jan, Carlyon, Robert P., Middlebrooks, John C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437162/
https://www.ncbi.nlm.nih.gov/pubmed/35668206
http://dx.doi.org/10.1007/s10162-022-00849-z
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author Richardson, Matthew L.
Guérit, François
Gransier, Robin
Wouters, Jan
Carlyon, Robert P.
Middlebrooks, John C.
author_facet Richardson, Matthew L.
Guérit, François
Gransier, Robin
Wouters, Jan
Carlyon, Robert P.
Middlebrooks, John C.
author_sort Richardson, Matthew L.
collection PubMed
description Cochlear implant (CI) users show limited sensitivity to the temporal pitch conveyed by electric stimulation, contributing to impaired perception of music and of speech in noise. Neurophysiological studies in cats suggest that this limitation is due, in part, to poor transmission of the temporal fine structure (TFS) by the brainstem pathways that are activated by electrical cochlear stimulation. It remains unknown, however, how that neural limit might influence perception in the same animal model. For that reason, we developed non-invasive psychophysical and electrophysiological measures of temporal (i.e., non-spectral) pitch processing in the cat. Normal-hearing (NH) cats were presented with acoustic pulse trains consisting of band-limited harmonic complexes that simulated CI stimulation of the basal cochlea while removing cochlear place-of-excitation cues. In the psychophysical procedure, trained cats detected changes from a base pulse rate to a higher pulse rate. In the scalp-recording procedure, the cortical-evoked acoustic change complex (ACC) and brainstem-generated frequency following response (FFR) were recorded simultaneously in sedated cats for pulse trains that alternated between the base and higher rates. The range of perceptual sensitivity to temporal pitch broadly resembled that of humans but was shifted to somewhat higher rates. The ACC largely paralleled these perceptual patterns, validating its use as an objective measure of temporal pitch sensitivity. The phase-locked FFR, in contrast, showed strong brainstem encoding for all tested pulse rates. These measures demonstrate the cat’s perceptual sensitivity to pitch in the absence of cochlear-place cues and may be valuable for evaluating neural mechanisms of temporal pitch perception in the feline animal model of stimulation by a CI or novel auditory prostheses.
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spelling pubmed-94371622022-09-03 Temporal Pitch Sensitivity in an Animal Model: Psychophysics and Scalp Recordings: Temporal Pitch Sensitivity in Cat Richardson, Matthew L. Guérit, François Gransier, Robin Wouters, Jan Carlyon, Robert P. Middlebrooks, John C. J Assoc Res Otolaryngol Research Article Cochlear implant (CI) users show limited sensitivity to the temporal pitch conveyed by electric stimulation, contributing to impaired perception of music and of speech in noise. Neurophysiological studies in cats suggest that this limitation is due, in part, to poor transmission of the temporal fine structure (TFS) by the brainstem pathways that are activated by electrical cochlear stimulation. It remains unknown, however, how that neural limit might influence perception in the same animal model. For that reason, we developed non-invasive psychophysical and electrophysiological measures of temporal (i.e., non-spectral) pitch processing in the cat. Normal-hearing (NH) cats were presented with acoustic pulse trains consisting of band-limited harmonic complexes that simulated CI stimulation of the basal cochlea while removing cochlear place-of-excitation cues. In the psychophysical procedure, trained cats detected changes from a base pulse rate to a higher pulse rate. In the scalp-recording procedure, the cortical-evoked acoustic change complex (ACC) and brainstem-generated frequency following response (FFR) were recorded simultaneously in sedated cats for pulse trains that alternated between the base and higher rates. The range of perceptual sensitivity to temporal pitch broadly resembled that of humans but was shifted to somewhat higher rates. The ACC largely paralleled these perceptual patterns, validating its use as an objective measure of temporal pitch sensitivity. The phase-locked FFR, in contrast, showed strong brainstem encoding for all tested pulse rates. These measures demonstrate the cat’s perceptual sensitivity to pitch in the absence of cochlear-place cues and may be valuable for evaluating neural mechanisms of temporal pitch perception in the feline animal model of stimulation by a CI or novel auditory prostheses. Springer US 2022-06-06 2022-08 /pmc/articles/PMC9437162/ /pubmed/35668206 http://dx.doi.org/10.1007/s10162-022-00849-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Research Article
Richardson, Matthew L.
Guérit, François
Gransier, Robin
Wouters, Jan
Carlyon, Robert P.
Middlebrooks, John C.
Temporal Pitch Sensitivity in an Animal Model: Psychophysics and Scalp Recordings: Temporal Pitch Sensitivity in Cat
title Temporal Pitch Sensitivity in an Animal Model: Psychophysics and Scalp Recordings: Temporal Pitch Sensitivity in Cat
title_full Temporal Pitch Sensitivity in an Animal Model: Psychophysics and Scalp Recordings: Temporal Pitch Sensitivity in Cat
title_fullStr Temporal Pitch Sensitivity in an Animal Model: Psychophysics and Scalp Recordings: Temporal Pitch Sensitivity in Cat
title_full_unstemmed Temporal Pitch Sensitivity in an Animal Model: Psychophysics and Scalp Recordings: Temporal Pitch Sensitivity in Cat
title_short Temporal Pitch Sensitivity in an Animal Model: Psychophysics and Scalp Recordings: Temporal Pitch Sensitivity in Cat
title_sort temporal pitch sensitivity in an animal model: psychophysics and scalp recordings: temporal pitch sensitivity in cat
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437162/
https://www.ncbi.nlm.nih.gov/pubmed/35668206
http://dx.doi.org/10.1007/s10162-022-00849-z
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