Cargando…

Vocal Tract Images Reveal Neural Representations of Sensorimotor Transformation During Speech Imitation

Imitating speech necessitates the transformation from sensory targets to vocal tract motor output, yet little is known about the representational basis of this process in the human brain. Here, we address this question by using real-time MR imaging (rtMRI) of the vocal tract and functional MRI (fMRI...

Descripción completa

Detalles Bibliográficos
Autores principales: Carey, Daniel, Miquel, Marc E., Evans, Bronwen G., Adank, Patti, McGettigan, Carolyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939209/
https://www.ncbi.nlm.nih.gov/pubmed/28334401
http://dx.doi.org/10.1093/cercor/bhx056
_version_ 1783320918751182848
author Carey, Daniel
Miquel, Marc E.
Evans, Bronwen G.
Adank, Patti
McGettigan, Carolyn
author_facet Carey, Daniel
Miquel, Marc E.
Evans, Bronwen G.
Adank, Patti
McGettigan, Carolyn
author_sort Carey, Daniel
collection PubMed
description Imitating speech necessitates the transformation from sensory targets to vocal tract motor output, yet little is known about the representational basis of this process in the human brain. Here, we address this question by using real-time MR imaging (rtMRI) of the vocal tract and functional MRI (fMRI) of the brain in a speech imitation paradigm. Participants trained on imitating a native vowel and a similar nonnative vowel that required lip rounding. Later, participants imitated these vowels and an untrained vowel pair during separate fMRI and rtMRI runs. Univariate fMRI analyses revealed that regions including left inferior frontal gyrus were more active during sensorimotor transformation (ST) and production of nonnative vowels, compared with native vowels; further, ST for nonnative vowels activated somatomotor cortex bilaterally, compared with ST of native vowels. Using test representational similarity analysis (RSA) models constructed from participants’ vocal tract images and from stimulus formant distances, we found that RSA searchlight analyses of fMRI data showed either type of model could be represented in somatomotor, temporal, cerebellar, and hippocampal neural activation patterns during ST. We thus provide the first evidence of widespread and robust cortical and subcortical neural representation of vocal tract and/or formant parameters, during prearticulatory ST.
format Online
Article
Text
id pubmed-5939209
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-59392092018-05-10 Vocal Tract Images Reveal Neural Representations of Sensorimotor Transformation During Speech Imitation Carey, Daniel Miquel, Marc E. Evans, Bronwen G. Adank, Patti McGettigan, Carolyn Cereb Cortex Original Articles Imitating speech necessitates the transformation from sensory targets to vocal tract motor output, yet little is known about the representational basis of this process in the human brain. Here, we address this question by using real-time MR imaging (rtMRI) of the vocal tract and functional MRI (fMRI) of the brain in a speech imitation paradigm. Participants trained on imitating a native vowel and a similar nonnative vowel that required lip rounding. Later, participants imitated these vowels and an untrained vowel pair during separate fMRI and rtMRI runs. Univariate fMRI analyses revealed that regions including left inferior frontal gyrus were more active during sensorimotor transformation (ST) and production of nonnative vowels, compared with native vowels; further, ST for nonnative vowels activated somatomotor cortex bilaterally, compared with ST of native vowels. Using test representational similarity analysis (RSA) models constructed from participants’ vocal tract images and from stimulus formant distances, we found that RSA searchlight analyses of fMRI data showed either type of model could be represented in somatomotor, temporal, cerebellar, and hippocampal neural activation patterns during ST. We thus provide the first evidence of widespread and robust cortical and subcortical neural representation of vocal tract and/or formant parameters, during prearticulatory ST. Oxford University Press 2017-05 2017-03-18 /pmc/articles/PMC5939209/ /pubmed/28334401 http://dx.doi.org/10.1093/cercor/bhx056 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Carey, Daniel
Miquel, Marc E.
Evans, Bronwen G.
Adank, Patti
McGettigan, Carolyn
Vocal Tract Images Reveal Neural Representations of Sensorimotor Transformation During Speech Imitation
title Vocal Tract Images Reveal Neural Representations of Sensorimotor Transformation During Speech Imitation
title_full Vocal Tract Images Reveal Neural Representations of Sensorimotor Transformation During Speech Imitation
title_fullStr Vocal Tract Images Reveal Neural Representations of Sensorimotor Transformation During Speech Imitation
title_full_unstemmed Vocal Tract Images Reveal Neural Representations of Sensorimotor Transformation During Speech Imitation
title_short Vocal Tract Images Reveal Neural Representations of Sensorimotor Transformation During Speech Imitation
title_sort vocal tract images reveal neural representations of sensorimotor transformation during speech imitation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939209/
https://www.ncbi.nlm.nih.gov/pubmed/28334401
http://dx.doi.org/10.1093/cercor/bhx056
work_keys_str_mv AT careydaniel vocaltractimagesrevealneuralrepresentationsofsensorimotortransformationduringspeechimitation
AT miquelmarce vocaltractimagesrevealneuralrepresentationsofsensorimotortransformationduringspeechimitation
AT evansbronweng vocaltractimagesrevealneuralrepresentationsofsensorimotortransformationduringspeechimitation
AT adankpatti vocaltractimagesrevealneuralrepresentationsofsensorimotortransformationduringspeechimitation
AT mcgettigancarolyn vocaltractimagesrevealneuralrepresentationsofsensorimotortransformationduringspeechimitation