Perceptual consequences of peripheral hearing loss: Do edge effects exist for abrupt cochlear lesions?

Hearing Research

Volumn 125, Issue 1-2, 1998, Pages 98-108

  Buss, E ^a   Hall III, J W ^a   Grose, J H ^a   Hatch, D R ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

Hearing; Hearing loss; Plasticity

Indexed keywords

ADULT; ARTICLE; AUDITORY DISCRIMINATION; AUDITORY THRESHOLD; CLINICAL ARTICLE; COCHLEA INJURY; FEMALE; HEARING LOSS; HUMAN; MALE; NOISE; PRIORITY JOURNAL; SOUND INTENSITY;

ACOUSTIC STIMULATION; ADULT; AUDITORY PERCEPTION; AUDITORY THRESHOLD; CASE-CONTROL STUDIES; FEMALE; HEARING LOSS, HIGH-FREQUENCY; HUMANS; MALE; MIDDLE AGED; MODELS, BIOLOGICAL; PSYCHOACOUSTICS;

EID: 0031760191     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(98)00131-2     Document Type: Article

References (43)

1. Arlinger S.D., Jerlvall L.B., Holmgren E.C. Thresholds for linear frequency ramps of a continuous pure tone. Acta Otolaryngol. 83:1977;317-327.
2. Calford M.B., Rajan R., Irvine D.R.F. Rapid changes in the frequency tuning of neurons in cat auditory cortex resulting from pure-tone-induced temporary threshold shift. Neuroscience. 44:1993;953-964.
3. Chambers R.D., Feth L.L., Burns E.M. The relation between the human frequency-following response and the low pitch of complex tones. J. Acoust. Soc. Am. 80:1986;1673-1680.
4. Clopton B.M., Silverman M.S. Plasticity of binaural interaction. II Critical period and changes in midline response. J. Neurophysiol. 40:1977;1275-1280.
5. Dooley G.J., Moore B.C.J. Detection of linear frequency glides as a function of frequency and duration. J. Acoust. Soc. Am. 84:1988;2045-2057.
6. Eddins D.A., Hall J.W. III, Grose J.H. The detection of temporal gaps as a function of frequency region and absolute noise bandwidth. J. Acoust. Soc. Am. 91:1992;1069-1077.
7. Fitzgibbons P.J., Gordon-Salant S. Age effects on measures of auditory duration discrimination. J. Speech Hear. 37:1994;662-670.
8. Gatehouse S. The time course and magnitude of perceptual acclimatization to frequency responses: Evidence from monaural fitting of hearing aids. J. Acoust. Soc. Am. 92:1992;1258-1268.
9. Hall, J.W. III, 1992. Handbook of Auditory Evoked Responses. Allyn and Bacon, Boston, MA.
10. Harrison R.V., Nagasawa A., Smith D.W., Stanton S., Mount R.J. Reorganization of auditory cortex after neonatal high frequency cochlear hearing loss. Hear. Res. 54:1991;11-19.
11. Harrison, R.V., Smith, D.W., Nagasawa, A., Stanton, S., Mount, R.J., 1992. Developmental plasticity of auditory cortex in cochlear hearing loss: Physiological and psychophysical findings. In: Cazals, Y., Horner, K., Demany, L. (Eds.), Advances in the Biosciences, Vol. 83. Pergamon Press, Oxford, pp. 625-633.
12. Harrison R.V., Gordon D.C., Nagasawa A., Stanton S., Ibrahim D., Mount R.J. Auditory evoked potentials in cats with neonatal high frequency hearing loss. Acta Otolaryngol. 113:1993;31-38.
13. Harrison R.V., Stanton S.G., Ibrahim D., Nagasawa A., Mount R.J. Neonatal cochlear hearing loss results in developmental abnormalities of the central auditory pathways. Acta Otolaryngol. 113:1993;296-302.
14. Harrison R.V., Stanton S.G., Nagasawa A., Ibrahim D., Mount R.J. The effects of long-term cochlear hearing loss on the functional organization of central auditory pathways. J. Otolaryngol. 22:1993;4-11.
15. Hellman R.P. Relation between the growth of loudness and high-frequency excitation. J. Acoust. Soc. Am. 96:1994;2655-2663.
16. Hellman, R., Meiselman, C.H., 1986. Is high-frequency hearing necessary for normal loudness growth at low frequencies. In: Proceedings of the 12th International Congress on Acoustics, Vol. 1. Beauregard Press, Baton Rouge, LA, B11-5.
17. Irvine D.R.F., Rajan R. Injury- and use-related plasticity in the primary sensory cortex of adult mammals: possible relationship to perceptual learning. Clin. Exp. Pharmacol. Physiol. 23:1996;939-947.
18. Jesteadt W., Wier C.C., Green D.M. Intensity discrimination as a function of frequency and sensation level. J. Acoust. Soc. Am. 61:1977;169-177.
19. Knudsen E.L., Knudsen P.F., Esterly S.D. A critical period for recovery of sound localization accuracy following monaural occlusion in the barn owl. J. Neurosci. 4:1984;1012-1020.
20. Levitt H. Transformed up-down methods in psychoacoustics. J. Acoust. Soc. Am. 49:1971;467-477.
21. Mäkelä J.P., Hari R. Evidence for cortical origin of the 40-Hz auditory evoked response in man. Electroenceph. Clin. Neurophysiol. 66:1987;539-546.
22. Moore D.R. Postnatal development of the mammalian central auditory system and the neural consequences of auditory deprivation. Acta Otolaryngol. 421:1985;19-30.
23. Mount R.J., Harrison R.V., Stanton S.G., Nagasawa A. Correlation of cochlear pathology with auditory brainstem and cortical responses in cats with high frequency hearing loss. Scanning Microsc. 5:1991;1105-1113.
24. Nelson D.A., Schroder A.C. Release from upward spread of masking in regions of high-frequency hearing loss. J. Acoust. Soc. Am. 100:1996;2266-2277.
25. Nelson D.A., Schroder A.C. Linearized response growth inferred from growth-of-masking slopes in ears with cochlear hearing loss. J. Acoust. Soc. Am. 101:1997;2186-2201.
26. Plourde G., Stapells D.R., Picton T.W. The human auditory steady-state evoked potentials. Acta Otolaryngol. 491:1991;153-160.
27. Ponton C.W., Done M., Eggermont J.J., Waring M.D., Kwong B., Masuda A. Auditory system plasticity in children after long periods of complete deafness. NeuroReport. 8:1996;61-65.
28. Rajan, R., Irvine, D.R.F., Calford, M.B., Wise, L.Z., 1992. Effect of frequency-specific losses in cochlear neural sensitivity on the processing and representation of frequency in primary auditory cortex. In: Dancer, A.L., Henderson, D.R., Salvi, J., Hamernik, R.P. (Eds.), Noise-Induced Hearing Loss. Mosby Year Book, St. Louis, MO, pp. 119-129.
29. Rajan R., Irvine D.R.F., Wise L.Z., Heil P. Effect of unilateral partial cochlear lesions in adult cats on the representation of lesioned and unlesioned cochleas in primary auditory cortex. J. Comp. Neurol. 338:1993;17-49.
30. Reale R.A., Brugge J.F., Chan J.C.K. Maps of auditory cortex in cats reared after unilateral cochlear ablation in the neonatal period. Dev. Brain Res. 34:1987;281-290.
31. Recanzone G.H., Schreiner C.E., Merzenich M.M. Plasticity in the frequency representation of primary auditory cortex following discrimination training in adult owl monkeys. J. Neurosci. 13:1993;87-103.
32. Robertson D., Irvine D.R.F. Plasticity of frequency organization in auditory cortex of guinea pigs with partial unilateral deafness. J. Comp. Neurol. 282:1989;456-471.
33. Robinson K., Gatehouse S. Changes in intensity discrimination following monaural long-term use of a hearing aid. J. Acoust. Soc. Am. 97:1995;1183-1190.
34. Rodriguez R., Picton T., Linden D., Hamel G., Laframboise G. Human auditory steady state responses: Effects of intensity and frequency. Ear Hear. 7:1986;300-313.
35. Romand R. Modification of tonotopic representation in the auditory system during development. Prog. Neurobiol. 51:1997;1-17.
36. Scheich H. Auditory cortex: comparative aspects of maps and plasticity. Curr. Opin. Neurobiol. 1:1991;236-247.
37. Schroder A.C., Viemeister N.F., Nelson D.A. Intensity discrimination in normal-hearing and hearing-impaired listeners. J. Acoust. Soc. Am. 96:1994;2683-2693.
38. Schwaber M.K., Garraghty P.E., Kaas J.H. Neuroplasticity of the adult primate auditory cortex following cochlear hearing loss. Am. J. Otolaryngol. 14:1993;252-258.
39. Silman S., Silverman C.A., Emmer M.B., Gelfand S.A. Adult-onset auditory deprivation. J. Am. Audiol. 3:1992;390-396.
40. Tyler R.S., Summerfield Q., Wood E.J., Fernandes M.A. Psychoacoustic and phonetic temporal processing in normal and hearing-impaired listeners. J. Acoust. Soc. Am. 72:1982;740-752.
41. Vasama J.P., Mäkeä J.P. Auditory pathway plasticity in adult humans after unilateral idiopathic sudden sensorineural hearing loss. Hear. Res. 87:1995;132-140.
42. Willott J.F., Aitkin L.M., McFadden S.L. Plasticity of auditory cortex associated with sensorineural hearing loss in adult C57BL/6J mice. J. Comp. Neurol. 329:1993;402-411.
43. Wong, D., 1991. Cellular organization of the cat's auditory cortex. In: Altschuler, R.A., Bobbin, R.P., Clopton, B.M., Hoffman, D.W. (Eds.), Neurobiology of Hearing: The Central Auditory System. Raven Press, New York, pp. 367-387.