Functional and activity-dependent plasticity mechanisms in the adult and developing auditory brain;Mecanismos de plasticidad (funcional y dependiente de actividad) en el cerebro auditivo adulto y en desarrollo

Revista de Neurologia

Volumn 48, Issue 8, 2009, Pages 421-429

  Izquierdo, M A ^a,b   Oliver, D L ^a,c   Malmierca, M S ^a,b  

^a UNIVERSITY OF SALAMANCA   (Spain)

^b UNIVERSITY OF SALAMANCA   (Spain)

^c UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

Author keywords

Acoustic trauma; Activity dependent plasticity; Best frequency; Critical period; Functional plasticity; Stability; Tonotopic map

Indexed keywords

ARTICLE; AUDITORY CORTEX; AUDITORY STIMULATION; AUDITORY SYSTEM; BASAL GANGLION; BRAIN; COCHLEAR NERVE; CORTI ORGAN; EVOKED AUDITORY RESPONSE; HEARING LOSS; HUMAN; NERVE CELL PLASTICITY; NERVE LESION; NEUROBIOLOGY; NEUROEPITHELIUM; NOISE INJURY; NONHUMAN; TINNITUS; TONOTOPY;

EID: 65449143979     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.4808.2009038     Document Type: Article

References (78)

1. Malmierca MS. The structure and physiology of the rat auditory system: an overview. Int Rev Neurobiol 2003; 56: 147-211.
2. Hubel DH, Wiesel TN. The period of susceptibility to the physiological effects of unilateral eye closure in kittens. J Physiol 1970; 206: 419-36.
3. Blakemore C, Van Sluyters RC. Reversal of the physiological effects of monocular deprivation in kittens: further evidence for a sensitive period. J Physiol 1974; 237: 195-216.
4. Merzenich MM, Kaas JH, Wall J, Nelson RJ, Sur M, Felleman D. Topographic reorganization of somatosensory cortical areas 3b and 1 in adult monkeys following restricted deafferentation. Neuroscience 1983; 8:33-55.
5. Merzenich MM, Kaas JH, Wall JT, Sur M, Nelson RJ, Felleman DJ. Progression of change following median nerve section in the cortical representation of the hand in areas 3b and 1 in adult owl and squirrel monkeys. Neuroscience 1983; 10: 639-65.
6. Robertson D, Irvine DR. Plasticity of frequency organization in auditory cortex of guinea pigs with partial unilateral deafness. J Comp Neurol 1989; 282: 456-71.
7. Recanzone GH, Schreiner CE, Merzenich MM. Plasticity in the frequency representation of primary auditory cortex following discrimination training in adult owl monkeys. J Neurosci 1993; 13: 87-103.
8. Irvine DR, Wright BA. Plasticity of spectral processing. Int Rev Neurobiol 2005; 70: 435-72.
9. Ryugo DK, Weinberger NM. Differential plasticity of morphologically distinct neuron populations in the medical geniculate body of the cat during classical conditioning. Behav Biol 1978; 22: 275-301.
10. Weinberger NM. Associative representational plasticity in the auditory cortex: a synthesis of two disciplines. Learn Mem 2007; 14: 1-16.
11. Tsukahara N. Synaptic plasticity in the mammalian central nervous system. Annu Rev Neurosci 1981; 4: 351-79.
12. Rajan R, Irvine DR, Wise LZ, Heil P. Effect of unilateral partial co-chlear lesions in adult cats on the representation of lesioned and unlesioned cochleas in primary auditory cortex. J Comp Neurol 1993; 338:17-49.
13. Calford MB. Dynamic representational plasticity in sensory cortex. Neuroscience 2002; 111: 709-38.
14. Calford MB, Rajan R, Irvine DR. Rapid changes in the frequency tuning of neurons in cat auditory cortex resulting from pure-tone-induced temporary threshold shift. Neuroscience 1993; 55: 953-64.
15. Gómez-Palacio Schjetnan A, Escobar-Rodríguez ML. Codificación y retention de la memoria: el factor neurotrófico derivado del cerebro (BDNF) en la plasticidad sináptica. Rev Neurol 2007; 45: 409-17.
16. Rodríguez-De la Rosa L, Contreras-Rodríguez J, Cediel-Algovia R, León Y, Sánchez-Calderón H, Murillo-Cuesta S, et al. Acciones neurotróficas del factor de crecimiento similar a la insulina de tipo I en el oído interno. Rev Neurol 2007; 45: 245-50.
17. Morales B, Rozas C, Pancetti F, Kirkwood A. Períodos críticos de plasticidad cortical. Rev Neurol 2003; 37: 739-43.
18. Hebb DO. The organization of behavior. New York: John Wiley; 1949.
19. Singer W. Development and plasticity of cortical processing architectures. Science 1995; 270: 758-64.
20. Merzenich MM, Nelson RJ, Kaas JH, Stryker MP, Jenkins WM, Zook JM, et al. Variability in hand surface representations in areas 3b and 1 in adult owl and squirrel monkeys. J Comp Neurol 1987; 258: 281-96.
21. Rajan R. Receptor organ damage causes loss of cortical surround inhibition without topographic map plasticity. Nat Neurosci 1998; 1: 138-43.
22. Palombi PS, Caspary DM. GABA inputs control discharge rate primrily within frequency receptive fields of inferior colliculus neurons. J Neurophysiol 1996; 75: 2211-9.
23. Scholl B, Wehr M. Disruption of balanced cortical excitation and inhibition by acoustic trauma. J Neurophysiol 2008; 2: 646-56.
24. Hernández O, Espinosa,N, Pérez-González D, Malmierca MS. The inferior colliculus of the rat: a quantitative analysis of monaural frequency response areas. Neuroscience 2005; 132: 203-17.
25. LeBeau FE, Malmierca MS, Rees A. Iontophoresis in vivo demonstrates a key role for GABA(A) and glycinergic inhibition in shaping frequency response areas in the inferior colliculus of guinea pig. J Neurosci 2001; 21: 7303-12.
26. Wang J, Salvi RJ, Powers N. Plasticity of response properties of inferior colliculus neurons following acute cochlear damage. J Neurophysiol 1996; 75: 171-83.
27. De Villers-Sidani E, Chang EF, Bao S, Merzenich MM. Critical period window for spectral tuning defined in the primary auditory cortex (A1) in the rat. J Neurosci 2007; 27: 180-9.
28. Zhang LI, Bao S, Merzenich MM. Persistent and specific influences of early acoustic environments on primary auditory cortex. Nat Neurosci 2001; 4: 1123-30.
29. Bao S, Chang EF, Davis JD, Gobeske KT, Merzenich MM. Progressive degradation and subsequent refinement of acoustic representations in the adult auditory cortex. J Neurosci 2003; 23: 10765-75.
30. Izquierdo MA, Gutiérrez-Conde PM, Merchan MA, Malmierca MS. Non- plastic reorganization of frequency coding in the inferior colliculus of the rat following noise-induced hearing loss. Neuroscience 2008; 154:355-69.
31. Loftus WC, Malmierca MS, Bishop DC, Oliver DL. The cytoarchitecture of the inferior colliculus revisited: a common organization of the lateral cortex in rat and cat. Neuroscience 2008; 154: 196-205.
32. Buonomano DV, Merzenich MM. Cortical plasticity: from synapses to maps. Annu Rev Neurosci 1998; 21: 149-86.
33. Kaltenbach JA, Czaja JM, Kaplan CR. Changes in the tonotopic map of the dorsal cochlear nucleus following induction of cochlear lesions by exposure to intense sound. Hear Res 1992; 59: 213-23.
34. Rajan R, Irvine DR. Absence of plasticity of the frequency map in dorsal cochlear nucleus of adult cats after unilateral partial cochlear lesions. J Comp Neurol 1998; 399: 35-46.
35. Irvine DR, Rajan R, Smith S. Effects of restricted cochlear lesions in adult cats on the frequency organization of the inferior colliculus. J Comp Neurol 2003; 467: 354-74.
36. Kim JJ, Gross J, Potashner SJ, Morest DK. Fine structure of long-term changes in the cochlear nucleus after acoustic overstimulation: chronic degeneration and new growth of synaptic endings. J Neurosci Res 2004; 77: 817-28.
37. Bilak M, Kim J, Potashner SJ, Bohne BA, Morest DK. New growth of axons in the cochlear nucleus of adult chinchillas after acoustic trauma. Exp Neurol 1997; 147: 256-68.
38. Kim JJ, Gross J, Morest DK, Potashner SJ. Quantitative study of degeneration and new growth of axons and synaptic endings in the chinchilla cochlear nucleus after acoustic overstimulation. J Neurosci Res 2004; 77: 829-42.
39. Kamke MR, Brown M, Irvine DR. Plasticity in the tonotopic organization of the medial geniculate body in adult cats following restricted unilateral cochlear lesions. J Comp Neurol 2003; 459: 355-67.
40. Chang EF, Merzenich MM. Environmental noise retards auditory cortical development. Science 2003; 300: 498-502.
41. Seidl AH, Grothe B. Development of sound localization mechanisms in the Mongolian gerbil is shaped by early acoustic experience. J Neurophysiol 2005; 94: 1028-36.
42. Muhlnickel W, Elbert T, Taub E, Flor H. Reorganization of auditory cortex in tinnitus. Proc Natl Acad Sci U S A 1998; 95: 10340-3.
43. Kandler K. Activity-dependent organization of inhibitory circuits: lessons from the auditory system. Curr Opin Neurobiol 2004; 14: 96-104.
44. Kandler K, Gillespie DC. Developmental refinement of inhibitory sound- localization circuits. Trends Neurosci 2005; 28: 290-6.
45. Lomber SG, Eggermont JJ. Reprogramming the cerebral cortex: adaptive plasticity following central and peripheral lesions. Oxford: Oxford University Press; 2006.
46. Irvine DR. Auditory cortical plasticity: does it provide evidence for cognitive processing in the auditory cortex? Hear Res 2007; 229: 158-70.
47. Gilbert CD. Adult cortical dynamics. Physiol Rev 1998; 78: 467-85.
48. Liberman MC, Dodds LW. Single-neuron labeling and chronic cochlear pathology. III. Stereocilia damage and alterations of threshold tuning curves. Hear Res 1984; 16: 55-74.
49. Liberman MC. Single-neuron labeling and chronic cochlear pathology. I. Threshold shift and characteristic-frequency shift. Hear Res 1984; 16: 33-41.
50. Bohne BA, Harding GW, Nordmann AS, Tseng CJ, Liang GE, Bahadori RS. Survival-fixation of the cochlea: a technique for following time-dependent degeneration and repair in noise-exposed chinchillas. Hear Res 1999; 134: 163-78.
51. Holme RH, Steel KP. Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation. J Assoc Res Otolaryngol 2004; 5: 66-79.
52. Wang J, Ding D, Salvi RJ. Functional reorganization in chinchilla inferior colliculus associated with chronic and acute cochlear damage. Hear Res 2002; 168: 238-49.
53. Yoshida N, Hequembourg SJ, Atencio CA, Rosowski JJ, Liberman MC. Acoustic injury in mice: 129/SvEv is exceptionally resistant to noise induced hearing loss. Hear Res 2000; 141: 97-106.
54. Cody AR, Robertson, D. Variability of noise-induced damage in the guinea pig cochlea: electrophysiological and morphological correlates after strictly controlled exposures. Hear Res 1983; 9: 55-70.
55. Malmierca MS, Izquierdo MA, Cristaudo S, Hernandez O, Perez-Gonzalez D, Covey E, et al. A discontinuous tonotopic organization in the inferior colliculus of the rat. J Neurosci 2008; 28: 4767-76.
56. Cody AR, Johnstone BM. Acoustic trauma: single neuron basis for the 'half-octave shift'. J Acoust Soc Am 1981; 70: 707-11.
57. Le Page EL, Johnstone BM. Nonlinear mechanical behaviour of the basilar membrane in the basal turn of the guinea pig cochlea. Hear Res 1980; 2: 183-9.
58. Snyder RL, Sinex DG, McGee JD, Walsh EW. Acute spiral ganglion lesions change the tuning and tonotopic organization of cat inferior colliculus neurons. Hear Res 2000; 147: 200-20.
59. Snyder RL, Sinex DG. Immediate changes in tuning of inferior colliculus neurons following acute lesions of cat spiral ganglion. J Neurophysiol 2002; 87: 434-52.
60. Harrison RV. Age-related tonotopic map plasticity in the central auditory pathways. Scand Audiol Suppl 2001; 53: 8-14.
61. Kral A. Unimodal and cross-modal plasticity in the 'deaf' auditory cortex. Int J Audiol 2007; 46: 479-93.
62. Jusczyk PW, Hohne EA. Infants' memory for spoken words. Science 1997; 277: 1984-6.
63. Oliver DL, Izquierdo MA, Malmierca MS. Early sound exposure modifies function in the inferior colliculus (IC) of the rat. Annual Meeting Society for Neuroscience. Atlanta, EE. UU., octubre de 2006.
64. Izquierdo MA, Malmierca MS, Oliver DL. Early sound exposure alters frequency coding in the inferior colliculus (IC) of the rat. ARO Mid Winter Meeting. Denver, EE. UU., febrero de 2007.
65. Oliver DL, Izquierdo MA, Malmierca MS. Early sound exposure alters frequency coding in the inferior colliculus. The Auditory Brain -a tribute to Dexter Irvine. Lorne, Australia, julio de 2007.
66. Eggermont JJ. The role of sound in adult and developmental auditory cortical plasticity. Ear Hear 2008; 29: 819-29.
67. Jastreboff PJ, Brennan JF, Coleman JK, Sasaki CT. Phantom auditory sensation in rats: an animal model for tinnitus. Behav Neurosci 1988; 102: 811-22.
68. Eggermont JJ. Tinnitus: neurobiological substrates. Drug Discov Today 2005; 10: 1283-90.
69. Bauer CA, Brozoski TJ, Holder TM, Caspary DM. Effects of chronic salicylate on GABAergic activity in rat inferior colliculus. Hear Res 2000; 147: 175-82.
70. Milbrandt JC, Holder TM, Wilson MC, Salvi RJ, Caspary DM. GAD levels and muscimol binding in rat inferior colliculus following acoustic trauma. Hear Res 2000; 147: 251-60.
71. Abbott SD, Hughes LF, Bauer CA, Salvi R, Caspary DM. Detection of glutamate decarboxylase isoforms in rat inferior colliculus following acoustic exposure. Neuroscience 1999; 93: 1375-81.
72. Harris JA, Hardie NA, Bermingham-McDonogh O, Rubel EW. Gene expression differences over a critical period of afferent-dependent neuron survival in the mouse auditory brainstem. J Comp Neurol 2005; 493:460-74.
73. Harris JA, Rubel EW. Afferent regulation of neuron number in the cochlear nucleus: cellular and molecular analyses of a critical period. Hear Res 2006; 216-217: 127-37.
74. Turrigiano GG, Nelson SB. Homeostatic plasticity in the developing nervous system. Nat Rev Neurosci 2004; 5: 97-107.
75. Rauschecker JP, Shannon RV. Sending sound to the brain. Science 2002; 295: 1025-9.
76. Lenarz M, Lim HH, Lenarz T, Reich U, Marquardt N, Klingberg MN, et al. Auditory midbrain implant: histomorphologic effects of long- term implantation and electric stimulation of a new deep brain stimulation array. Otol Neurotol 2007; 28: 1045-52.
77. Kamke MR, Brown M, Irvine DR. Basal forebrain cholinergic input is not essential for lesion-induced plasticity in mature auditory cortex. Neuron 2005; 48: 675-86.
78. Kaltenbach JA, Meleca RJ, Falzarano PR. Alterations in the tonotopic map of the cochlear nucleus following cochlear damage. In Salvi RJ, Henderson D, Fiorino F, Colleti V, eds. Auditory system plasticity and regeneration. New York: Thieme Medical Publishers; 1996. p. 317-32.