Neural changes in cat auditory cortex after a transient pure-tone trauma

Journal of Neurophysiology

Volumn 90, Issue 4, 2003, Pages 2387-2401

  Noreña, Arnaud J ^a   Tomita, Masahiko ^a   Eggermont, Jos J ^a,b  

^a UNIVERSITY OF CALGARY   (Canada)

^b UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUDITORY CORTEX; AUDITORY MASKING; AUDITORY STIMULATION; AUDITORY THRESHOLD; BRAIN CELL; CAT; CONTROLLED STUDY; EAR INJURY; LOW FREQUENCY NOISE; NERVE CELL PLASTICITY; NERVE EXCITABILITY; NONHUMAN; PRIORITY JOURNAL; PURE TONE AUDIOMETRY; STIMULUS RESPONSE; TONOTOPY;

ACOUSTIC STIMULATION; ACTION POTENTIALS; ANIMALS; AUDITORY CORTEX; CATS; HEARING LOSS, NOISE-INDUCED; NEURONS;

EID: 0142027018     PISSN: 00223077     EISSN: None     Source Type: Journal    
DOI: 10.1152/jn.00139.2003     Document Type: Article

References (43)

1. Boettcher FA and Salvi RJ. Functional changes in the ventral cochlear nucleus following acute acoustic overstimulation. J Acoust Soc Am 94: 2123-2134, 1993.
2. Buonomano DV and Merzenich MM. Cortical plasticity: from synapses to maps. Annu Rev Neurosci 21: 149-186, 1998.
3. Calford MB, Rajan R, and Irvine DRF. Rapid changes in the frequency tuning of neurons in cat auditory cortex resulting from pure-tone-induced temporary threshold shift. Neuroscience 55: 953-964, 1993.
4. Dallos P and Harris D. Properties of auditory nerve responses in absence of outer hair cells. J Neurophysiol 41: 365-383, 1978.
5. Eggermont JJ. The correlative brain. In: Theory and Experiment in Neural Interaction. Berlin: Springer-Verlag, 1990.
6. Eggermont JJ. How homogeneous is cat primary auditory cortex? Evidence from simultaneous single-unit recordings. Audit Neurosci 2: 76-96, 1996.
7. Eggermont JJ and Komiya H. Moderate noise trauma in juvenile cats results in profound cortical topographic map changes in adulthood. Hear Res 141: 89-101, 2000.
8. Gilbert CD, Das A, Ito M, Kapidia M, and Westheimer G. Spatial integration and cortical dynamics. Proc Natl Acad Sci USA 92: 615-622, 1996.
9. Giraudet F, Horner KC, and Cazals Y. Similar half-octave TTS protection of the cochlea by xylazine/ketamine or sympathectomy. Hear Res 174: 239-248, 2002.
10. Jones EG. The role of afferent activity in the maintenance of primate neocortical function. J Exp Biol 153: 155-176, 1990.
11. Kaltenbach JA, Czaja J, and Kaplan CR. Changes in the tonotopic map of the dorsal cochlear nucleus following induction of cochlear lesions by exposure to intense sound. Hear Res 59: 213-233, 1992.
12. Kiang NYS, Moxon EC, and Levin RA. Auditory-nerve activity in cats normal and abnormal cochleas. In: Sensorineural Hearing Loss, edited by Wolstenholme GEW and Knight J. London: Churchill, 1970, p. 241-273.
13. Kimura M and Eggermont JJ. Effects of acute pure tone induced hearing loss on response properties in three auditory cortical fields in cat. Hear Res 135: 146-162, 1999.
14. Liberman MC. Chronic ultrastructural changes in acoustic trauma: serial-section reconstruction of stereocilia and cuticular plates. Hear Res 26: 65-88, 1987.
15. Liberman MC and Dodds LW. Single-neuron labeling and chronic cochlear pathology. II. Stereocilia damage and alterations of spontaneous discharge rates. Hear Res 16: 43-53, 1984.
16. Liberman MC and Dodds LW. Acute ultrastructural changes in acoustic trauma: serial-section reconstruction of stereocilia and cuticular plates. Hear Res 26: 45-64, 1987.
17. Lonsbury-Martin BL and Martin GK. Effects of moderately intense sound on auditory sensitivity in rhesus monkeys: behavioral and neural observations. J Neurophysiol 46: 563-586, 1981.
18. Lonsbury-Martin BL and Meikle MB. Neural correlates of auditory fatigue: frequency-dependent changes in activity of single cochlear nerve fibers. J Neurophysiol 41: 987-1006, 1978.
19. Mitzdorf U. Current source-density method and application in cat cerebral cortex: investigation of evoked potential and EEG phenomena. Physiol Rev 65: 37-99, 1985.
20. Muller CM and Scheich H. Contribution of GABAergic inhibition to the response characteristics of auditory units in the avian forebrain. J Neurophysiol 59: 1673-1689, 1988.
21. Noreña A and Eggermont JJ. Comparison between local field potentials and unit cluster activity in primary auditory cortex and anterior auditory field in the cat. Hear Res 166: 202-213, 2002.
22. Phillips DP and Hall SE. Multiplicity of inputs in the afferent path to cat auditory cortex neurons revealed by tone-on-tone masking. Cereb Cortex 2: 425-433, 1992.
23. Puel JL. Chemical synaptic transmission in the cochlea. Prog Neurobiol 447: 449-476, 1995.
24. Rajan R. Receptor organ damage causes loss of cortical surround inhibition without topographic map plasticity. Nat Neurosci 1: 138-143, 1998.
25. Rajan R. Plasticity of excitation and inhibition in the receptive field of primary auditory cortical neurons after limited receptor organ damage. Cereb Cortex 11: 171-182, 2001.
26. Rajan R and Irvine DRF. Absence of plasticity of the frequency map in dorsal cochlear nucleus of adult cats after unilateral partial cochlear lesions. J Comp Neurol 399: 35-46, 1998.
27. Rajan R, Irvine DRF, Wise LZ, and Heil P. Effects of unilateral partial cochlear lesions in adult cats on the representation of the lesioned and unlesioned cochleas in primary auditory cortex. J Comp Neurol 338: 17-49, 1993.
28. Robertson D and Irvine DRF. Plasticity of frequency organization in auditory cortex of guinea pig with partial unilateral deafness. J Comp Neurol 282: 456-471, 1989.
29. Salvi RJ, Saunders SS, Gratton MA, Arehole S, and Powers N. Enhanced evoked response amplitudes in the inferior colliculus of the chanchilla following acoustic trauma. Hear Res 50: 245-258, 1990.
30. Salvi RJ, Wang J, and Powers N. Rapid functional reorganization in the inferior colliculus and cochlear nucleus after acute cochlear damage. In: Auditory System Plasticity and Regeneration, edited by Salvi R, Henderson D, Fiorino F, and Colletti V. New York: Thieme, 1996, p. 275-296.
31. Salvi RJ, Wang J, and Ding D. Auditory plasticity and hyperactivity following cochlear damage. Hear Res 147: 261-274, 2000.
32. Seki S and Eggermont JJ. Changes in cat primary auditory cortex after minor-to-moderate pure-tone induced hearing loss. Hear Res 173: 172-186, 2002.
33. Shamma SA and Symmes D. Patterns of inhibition in auditory cortical cells in awake squirrel monkeys. Hear Res 19: 1-13, 1985.
34. Snyder RL and Sinex DG. Immediate changes in tuning of inferior colliculus neurons following acute lesions of cat spiral ganglion. J Neurophysiol 87: 434-452, 2002.
35. Snyder RL, Sinex DG, McGee JD, and Walsh EJ. Acute spiral ganglion lesions change the tuning and tonotopic organization of cat inferior colliculus neurons. Hear Res 147: 221-241, 2000.
36. Sutter ML, Schreiner CE, McLean M, O'Connor KN, and Loftus WC. Organization of inhibitory frequency receptive fields in cat primary auditory cortex. J Neurophysiol 82: 2358-2371, 1999.
37. van Heusden E and Smoorenburg GF. Responses from the AVCN units in the cat before and after inducement of an acute noise trauma. Hear Res 11: 295-326, 1983.
38. Volkov IO and Galazjuk AV. Formation of spikes response to sound tones in cat auditory cortex neurons: interaction of excitatory and inhibitory effects. Neuroscience 43: 307-321, 1991.
39. Wang J, Caspary D, and Salvi R. GABA-A antagonist causes dramatic expansion of tuning in primary auditory cortex. Neuroreport 11: 1137-1140, 2000.
40. Wang J, Ding D, and Salvi RJ. Functional reorganization in chinchilla inferior colliculus associated with chronic and acute cochlear damage. Hear Res 168: 238-249, 2002a.
41. Wang J, McFadden SL, Caspary D, and Salvi R. Gamma-aminobutyric acid circuits shape response properties of auditory cortex neurons. Brain Res 944: 219-231, 2002b.
42. Wang J, Salvi RJ, and Powers N. Plasticity of response properties of inferior colliculus neurons following acute cochlear damage. J Neurophysiol 75: 171-183, 1996.
43. Willott JF, Aitkin LM, and McFadden SM. Plasticity of auditory cortex associated with sensorineural hearing loss in adult C57BL/6J mice. J Comp Neurol 329: 402-411, 1993.