Cargando…

Neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats

BACKGROUND: Primary auditory cortex (AI) neurons show qualitatively distinct response features to successive acoustic signals depending on the inter-stimulus intervals (ISI). Such ISI-dependent AI responses are believed to underlie, at least partially, categorical perception of click trains (element...

Descripción completa

Detalles Bibliográficos
Autores principales: Sakai, Masashi, Chimoto, Sohei, Qin, Ling, Sato, Yu
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2679037/
https://www.ncbi.nlm.nih.gov/pubmed/19208233
http://dx.doi.org/10.1186/1471-2202-10-10
_version_ 1782166871993221120
author Sakai, Masashi
Chimoto, Sohei
Qin, Ling
Sato, Yu
author_facet Sakai, Masashi
Chimoto, Sohei
Qin, Ling
Sato, Yu
author_sort Sakai, Masashi
collection PubMed
description BACKGROUND: Primary auditory cortex (AI) neurons show qualitatively distinct response features to successive acoustic signals depending on the inter-stimulus intervals (ISI). Such ISI-dependent AI responses are believed to underlie, at least partially, categorical perception of click trains (elemental vs. fused quality) and stop consonant-vowel syllables (eg.,/da/-/ta/continuum). METHODS: Single unit recordings were conducted on 116 AI neurons in awake cats. Rectangular clicks were presented either alone (single click paradigm) or in a train fashion with variable ISI (2–480 ms) (click-train paradigm). Response features of AI neurons were quantified as a function of ISI: one measure was related to the degree of stimulus locking (temporal modulation transfer function [tMTF]) and another measure was based on firing rate (rate modulation transfer function [rMTF]). An additional modeling study was performed to gain insight into neurophysiological bases of the observed responses. RESULTS: In the click-train paradigm, the majority of the AI neurons ("synchronization type"; n = 72) showed stimulus-locking responses at long ISIs. The shorter cutoff ISI for stimulus-locking responses was on average ~30 ms and was level tolerant in accordance with the perceptual boundary of click trains and of consonant-vowel syllables. The shape of tMTF of those neurons was either band-pass or low-pass. The single click paradigm revealed, at maximum, four response periods in the following order: 1st excitation, 1st suppression, 2nd excitation then 2nd suppression. The 1st excitation and 1st suppression was found exclusively in the synchronization type, implying that the temporal interplay between excitation and suppression underlies stimulus-locking responses. Among these neurons, those showing the 2nd suppression had band-pass tMTF whereas those with low-pass tMTF never showed the 2nd suppression, implying that tMTF shape is mediated through the 2nd suppression. The recovery time course of excitability suggested the involvement of short-term plasticity. The observed phenomena were well captured by a single cell model which incorporated AMPA, GABA(A), NMDA and GABA(B )receptors as well as short-term plasticity of thalamocortical synaptic connections. CONCLUSION: Overall, it was suggested that ISI-dependent responses of the majority of AI neurons are configured through the temporal interplay of excitation and suppression (inhibition) along with short-term plasticity.
format Text
id pubmed-2679037
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-26790372009-05-08 Neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats Sakai, Masashi Chimoto, Sohei Qin, Ling Sato, Yu BMC Neurosci Research Article BACKGROUND: Primary auditory cortex (AI) neurons show qualitatively distinct response features to successive acoustic signals depending on the inter-stimulus intervals (ISI). Such ISI-dependent AI responses are believed to underlie, at least partially, categorical perception of click trains (elemental vs. fused quality) and stop consonant-vowel syllables (eg.,/da/-/ta/continuum). METHODS: Single unit recordings were conducted on 116 AI neurons in awake cats. Rectangular clicks were presented either alone (single click paradigm) or in a train fashion with variable ISI (2–480 ms) (click-train paradigm). Response features of AI neurons were quantified as a function of ISI: one measure was related to the degree of stimulus locking (temporal modulation transfer function [tMTF]) and another measure was based on firing rate (rate modulation transfer function [rMTF]). An additional modeling study was performed to gain insight into neurophysiological bases of the observed responses. RESULTS: In the click-train paradigm, the majority of the AI neurons ("synchronization type"; n = 72) showed stimulus-locking responses at long ISIs. The shorter cutoff ISI for stimulus-locking responses was on average ~30 ms and was level tolerant in accordance with the perceptual boundary of click trains and of consonant-vowel syllables. The shape of tMTF of those neurons was either band-pass or low-pass. The single click paradigm revealed, at maximum, four response periods in the following order: 1st excitation, 1st suppression, 2nd excitation then 2nd suppression. The 1st excitation and 1st suppression was found exclusively in the synchronization type, implying that the temporal interplay between excitation and suppression underlies stimulus-locking responses. Among these neurons, those showing the 2nd suppression had band-pass tMTF whereas those with low-pass tMTF never showed the 2nd suppression, implying that tMTF shape is mediated through the 2nd suppression. The recovery time course of excitability suggested the involvement of short-term plasticity. The observed phenomena were well captured by a single cell model which incorporated AMPA, GABA(A), NMDA and GABA(B )receptors as well as short-term plasticity of thalamocortical synaptic connections. CONCLUSION: Overall, it was suggested that ISI-dependent responses of the majority of AI neurons are configured through the temporal interplay of excitation and suppression (inhibition) along with short-term plasticity. BioMed Central 2009-02-10 /pmc/articles/PMC2679037/ /pubmed/19208233 http://dx.doi.org/10.1186/1471-2202-10-10 Text en Copyright © 2009 Sakai 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 Research Article
Sakai, Masashi
Chimoto, Sohei
Qin, Ling
Sato, Yu
Neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats
title Neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats
title_full Neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats
title_fullStr Neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats
title_full_unstemmed Neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats
title_short Neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats
title_sort neural mechanisms of interstimulus interval-dependent responses in the primary auditory cortex of awake cats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2679037/
https://www.ncbi.nlm.nih.gov/pubmed/19208233
http://dx.doi.org/10.1186/1471-2202-10-10
work_keys_str_mv AT sakaimasashi neuralmechanismsofinterstimulusintervaldependentresponsesintheprimaryauditorycortexofawakecats
AT chimotosohei neuralmechanismsofinterstimulusintervaldependentresponsesintheprimaryauditorycortexofawakecats
AT qinling neuralmechanismsofinterstimulusintervaldependentresponsesintheprimaryauditorycortexofawakecats
AT satoyu neuralmechanismsofinterstimulusintervaldependentresponsesintheprimaryauditorycortexofawakecats