|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA
* To whom correspondence should be addressed. E-mail: xwang{at}bme.jhu.edu.
Little is known about sensory-motor interaction in the auditory cortex of primates at the level of single neurons and its role in supporting vocal communication. The present study investigated single-unit activities in the auditory cortex of a vocal primate, the common marmoset (Callithrix jacchus), during self-initiated vocalizations. We found that 1) self-initiated vocalizations resulted in suppression of neural discharges in a majority of auditory cortical units. The vocalization-induced inhibition suppressed both spontaneous and stimulus-driven discharges. Suppressed units responded poorly to external acoustic stimuli during vocalization. 2) Vocalization-induced suppression began several hundred milliseconds prior to the onset of vocalization. 3) The suppression of cortical discharges reduced neural firings to below the rates expected from a unit's rate-level function, adjusted for known subcortical attenuation, and therefore was likely not entirely caused by known subcortical attenuation mechanisms. 4) A second, smaller, type of responses by auditory cortical neurons were increased discharges during self-initiated vocalizations. This vocalization-related excitation began after the onset of vocalization and is likely the result of acoustic feedback. Units showing this excitation responded nearly normally to external stimuli during vocalization. Based on these findings we propose that the suppression of auditory cortical neurons, possibly originating from cortical vocal production centers, acts to increase the dynamic range of cortical responses to vocalization feedback for self monitoring. The excitatory responses, on the other hand, likely play a role in maintaining sensitivity to the external acoustic environment during vocalization.
This article has been cited by other articles:
![]() |
J. T. Sakata and M. S. Brainard Online Contributions of Auditory Feedback to Neural Activity in Avian Song Control Circuitry J. Neurosci., October 29, 2008; 28(44): 11378 - 11390. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. L. Towle, H.-A. Yoon, M. Castelle, J. C. Edgar, N. M. Biassou, D. M. Frim, J.-P. Spire, and M. H. Kohrman ECoG gamma activity during a language task: differentiating expressive and receptive speech areas Brain, August 1, 2008; 131(8): 2013 - 2027. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. S. Shaevitz and F. E. Theunissen Functional Connectivity Between Auditory Areas Field L and CLM and Song System Nucleus HVC in Anesthetized Zebra Finches J Neurophysiol, November 1, 2007; 98(5): 2747 - 2764. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Ford, B. J. Roach, W. O. Faustman, and D. H. Mathalon Synch Before You Speak: Auditory Hallucinations in Schizophrenia Am J Psychiatry, March 1, 2007; 164(3): 458 - 466. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. H. Heinks-Maldonado, D. H. Mathalon, J. F. Houde, M. Gray, W. O. Faustman, and J. M. Ford Relationship of Imprecise Corollary Discharge in Schizophrenia to Auditory Hallucinations Arch Gen Psychiatry, March 1, 2007; 64(3): 286 - 296. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. Eliades and X. Wang Dynamics of Auditory-Vocal Interaction in Monkey Auditory Cortex Cereb Cortex, October 1, 2005; 15(10): 1510 - 1523. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Brosch, E. Selezneva, and H. Scheich Nonauditory Events of a Behavioral Procedure Activate Auditory Cortex of Highly Trained Monkeys J. Neurosci., July 20, 2005; 25(29): 6797 - 6806. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. W. Cheung, S. S. Nagarajan, C. E. Schreiner, P. H. Bedenbaugh, and A. Wong Plasticity in Primary Auditory Cortex of Monkeys with Altered Vocal Production J. Neurosci., March 9, 2005; 25(10): 2490 - 2503. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. H. Martikainen, K.-i. Kaneko, and R. Hari Suppressed Responses to Self-triggered Sounds in the Human Auditory Cortex Cereb Cortex, March 1, 2005; 15(3): 299 - 302. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Tian and J. P. Rauschecker Processing of Frequency-Modulated Sounds in the Lateral Auditory Belt Cortex of the Rhesus Monkey J Neurophysiol, November 1, 2004; 92(5): 2993 - 3013. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Visit Other APS Journals Online |