» Articles » PMID: 7150957

Speech Evoked Activity in the Auditory Radiations and Cortex of the Awake Monkey

Overview
Journal Brain Res
Specialty Neurology
Date 1982 Dec 9
PMID 7150957
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

To determine whether phonetic features of human speech are reflected in activity patterns of the auditory cortex and its thalamic afferents, concurrent recordings of multiple unit activity (MUA) and averaged evoked potentials (AEP) to 3 synthetic syllables: /da/,/ba/ and /ta/, were performed in awake monkeys. Using clicks, responses from thalamocortical axons and cortical cells were differentiated on the basis of their response latency, spatial distribution, and relationships to AEP components. Voice onset time was reflected in MUA time-locked to consonant release and voicing onset, and phase-locked to the syllables' fundamental frequency. Place of articulation was reflected in discriminative 'on' and phase-locked responses occurring to the formant transitions of the syllables. Duration of the voiced formant transitions was represented by an accentuation of the phase-locked responses occurring to this period. Activity of thalamocortical fibers and cortical cells differed. Thalamocortical fibers were more responsive to speech sounds, as well as responding more frequently with a phase-locked response pattern. Cortical cells responded with sustained activity to a greater degree. Responses to identical portions of the vowels were biased by the preceding consonant. The spatial extent and timing of the responses demonstrate that speech sounds are processed along parallel, but not synchronous, channels. Relevance to human psychoacoustical phenomena is discussed.

Citing Articles

Laminar differences in response to simple and spectro-temporally complex sounds in the primary auditory cortex of ketamine-anesthetized gerbils.

Schaefer M, Kossl M, Hechavarria J PLoS One. 2017; 12(8):e0182514.

PMID: 28771568 PMC: 5542772. DOI: 10.1371/journal.pone.0182514.


Increasing diversity of neural responses to speech sounds across the central auditory pathway.

Ranasinghe K, Vrana W, Matney C, Kilgard M Neuroscience. 2013; 252:80-97.

PMID: 23954862 PMC: 3795858. DOI: 10.1016/j.neuroscience.2013.08.005.


Neural mechanisms supporting robust discrimination of spectrally and temporally degraded speech.

Ranasinghe K, Vrana W, Matney C, Kilgard M J Assoc Res Otolaryngol. 2012; 13(4):527-42.

PMID: 22549175 PMC: 3387312. DOI: 10.1007/s10162-012-0328-1.


Different timescales for the neural coding of consonant and vowel sounds.

Perez C, Engineer C, Jakkamsetti V, Carraway R, Perry M, Kilgard M Cereb Cortex. 2012; 23(3):670-83.

PMID: 22426334 PMC: 3563339. DOI: 10.1093/cercor/bhs045.


The representation of voice onset time in the cortical auditory evoked potentials of young children.

King K, Campbell J, Sharma A, Martin K, Dorman M, Langran J Clin Neurophysiol. 2008; 119(12):2855-61.

PMID: 18980862 PMC: 3726214. DOI: 10.1016/j.clinph.2008.09.015.