|
|
||||||||
Journal of Neurophysiology, Vol 72, Issue 3 1270-1277, Copyright © 1994 by APS
ARTICLES |
N. Kraus, T. McGee, T. Littman, T. Nicol and C. King
Northwestern University, Department of Communication Sciences and Disorders, Evanston, Illinois 60208-3550.
1. The mismatch response, or mismatch negativity (MMN), is a neurophysiologic response to stimulus change. In humans and other animals, the MMN may underlie the ability to discriminate acoustic differences, a fundamental aspect of auditory perception. 2. This study investigated the role of the thalamus in the generation of a tone-evoked MMN in guinea pigs. Electrodes were placed in the caudomedial (nonprimary) and ventral (primary) subdivisions of the auditory thalamus (medial geniculate nucleus). Surface epidural electrodes were placed at the midline and over the temporal lobe. The MMN was elicited by a deviant stimulus (2,450-Hz tone burst) embedded in a sequence of standard stimuli (2,300-Hz tone bursts). 3. A tone-evoked MMN was present in nonprimary thalamus but was absent in the primary thalamus. Surface-recorded MMNs were measured at the midline but not over the temporal lobe. The correspondence between nonprimary thalamic responses and midline surface potentials, and between primary thalamic responses and temporal surface potentials, is consistent with data reported for the auditory middle latency responses in guinea pigs. 4. The results demonstrate that the nonprimary auditory thalamus contributes to the generation of a tone-evoked MMN in the guinea pig. Furthermore, the data indicate that the guinea pig is a feasible model for investigating central auditory processes underlying acoustic discrimination.
This article has been cited by other articles:
![]() |
R. S. Ehrlichman, C. R. Maxwell, S. Majumdar, and S. J. Siegel Deviance-elicited Changes in Event-related Potentials are Attenuated by Ketamine in Mice J. Cogn. Neurosci., August 1, 2008; 20(8): 1403 - 1414. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Tervaniemi, A. J. Szameitat, S. Kruck, E. Schroger, K. Alter, W. De Baene, and A. D. Friederici From Air Oscillations to Music and Speech: Functional Magnetic Resonance Imaging Evidence for Fine-Tuned Neural Networks in Audition. J. Neurosci., August 23, 2006; 26(34): 8647 - 8652. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Edwards, M. Soltani, L. Y. Deouell, M. S. Berger, and R. T. Knight High Gamma Activity in Response to Deviant Auditory Stimuli Recorded Directly From Human Cortex J Neurophysiol, December 1, 2005; 94(6): 4269 - 4280. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Rosburg, P. Trautner, T. Dietl, O. A. Korzyukov, N. N. Boutros, C. Schaller, C. E. Elger, and M. Kurthen Subdural recordings of the mismatch negativity (MMN) in patients with focal epilepsy Brain, April 1, 2005; 128(4): 819 - 828. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. H. Fitch and P. Tallal Neural Mechanisms of Language-Based Learning Impairments: Insights from Human Populations and Animal Models Behav Cogn Neurosci Rev, September 1, 2003; 2(3): 155 - 178. [Abstract] [PDF] |
||||
![]() |
M. Atienza, J. L. Cantero, and E. Dominguez-Marin The Time Course of Neural Changes Underlying Auditory Perceptual Learning Learn. Mem., May 1, 2002; 9(3): 138 - 150. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. G. Clark, G. D. Rosen, P. Tallal, and R. H. Fitch Impaired Processing of Complex Auditory Stimuli in Rats with Induced Cerebrocortical Microgyria: An Animal Model of Developmental Language Disabilities J. Cogn. Neurosci., September 1, 2000; 12(5): 828 - 839. [Abstract] [Full Text] |
||||
![]() |
T. J. Bellis, T. Nicol, and N. Kraus Aging Affects Hemispheric Asymmetry in the Neural Representation of Speech Sounds J. Neurosci., January 15, 2000; 20(2): 791 - 797. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |