Specific plasticity responses to unilaterally decreased or increased hearing intensity in the adult cochlear nucleus and beyond

Hearing Research

Volumn 216-217, Issue 1-2, 2006, Pages 189-197

  Illing, Robert Benjamin ^a   Reisch, Adrian ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

Author keywords

c Fos; Cochlear implant; Cochlear lesion; GAP 43; Synaptic remodeling

Indexed keywords

ADAPTATION; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; AUDITORY SYSTEM; BRAIN STEM; COCHLEAR NUCLEUS; ELECTROSTIMULATION; EVOKED BRAIN STEM AUDITORY RESPONSE; EXPERIENCE; HEARING; HEARING LOSS; MAMMAL; MORPHOLOGY; NERVE CELL NETWORK; NOISE INJURY; NONHUMAN; PLASTICITY; PRIORITY JOURNAL; RAT; ULTRASTRUCTURE;

ANIMALS; COCHLEA; COCHLEAR IMPLANTS; COCHLEAR NUCLEUS; ELECTRIC STIMULATION; GAP-43 PROTEIN; HEARING LOSS; IMMUNOHISTOCHEMISTRY; MICROSCOPY, ELECTRON; NEURONAL PLASTICITY; RATS; RATS, WISTAR; SYNAPSES; SYNAPTIC TRANSMISSION;

EID: 33745010239     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.heares.2005.12.014     Document Type: Article

References (32)

1. Abrahams W.C., Christie B.R., Logan B., Lawlor P., and Dragunow M. Immediate early gene expression associated with the persistence of heterosynaptic long-term depression in the hippocampus. Proc. Natl. Acad. Sci. USA 91 (1994) 10049-10053
2. Benowitz L.I., and Routtenberg A. GAP-43: an intrinsic determinant of neuronal development and plasticity. Trends Neurosci. 20 (1997) 84-91
3. Cole A.J., Saffen D.W., Baraban J.M., and Worley P.F. Rapid increase of an immediate early gene messenger RNA in hippocampal neurons by synaptic NMDA receptor activation. Nature 340 (1989) 474-476
4. Demmer J., Dragunow M., Lawlor P.A., Mason S.E., Leah J.D., Abraham W.C., and Tate W.P. Differential expression of immediate early genes after hippocampal long-term potentiation in awake rats. Brain Res. Mol. Brain Res. 17 (1993) 279-286
5. Fleischmann A., Hvalby O., Jensen V., Strekalova T., Zacher C., Layer L.E., Kvello A., Reschke M., Spanagel R., Sprengel R., Wagner E.F., and Gass P. Impaired long-term memory and NR2A-type NMDA receptor-dependent synaptic plasticity in mice lacking c-Fos in the CNS. J. Neurosci. 23 (2003) 9116-9122
6. Förster C.R., and Illing R.B. Redistribution of NMDA receptors in the cochlear nucleus following cochleotomy. NeuroReport 9 (1998) 3531-3535
7. Illing R.B., Cao Q.L., Förster C.R., and Laszig R. Auditory brainstem: development and plasticity of GAP-43 mRNA expression in the rat. J. Comp. Neurol. 412 (1999) 353-372
8. Illing R.B., and Horváth M. Re-emergence of GAP-43 in cochlear nucleus and superior olive following cochlear ablation in the rat. Neurosci. Lett. 194 (1995) 9-12
9. Illing R.B., Horváth M., and Laszig R. Plasticity of the auditory brainstem: effects of cochlear lesions on GAP-43 immunoreactivity in the rat. J. Comp. Neurol. 382 (1997) 116-138
10. Illing R.B., Kraus K.S., and Meidinger M.A. Reconnecting neuronal networks in the auditory brainstem following unilateral deafening. Hear. Res. 206 (2005) 185-199
11. Illing R.B., and Michler S.A. Modulation of P-CREB and expression of c-Fos in cochlear nucleus and superior olive following electrical intracochlear stimulation. NeuroReport 12 (2001) 875-878
12. Illing R.B., Michler S.A., Kraus K.S., and Laszig R. Transcription factor modulation and expression in the rat auditory brainstem following electrical intracochlear stimulation. Exp. Neurol. 175 (2002) 226-244
13. Jones M.W., Errington M.S., French P.J., Fine A., Bliss T.V.P., Garel S., Charnay P., Bozon B., Laroche S., and Davis S. A requirement for the immediate early gene zif268 in the expression of late LTP and long term memories. Nature Neurosci. 4 (2001) 289-296
14. Kaczmarek L. Expression of c-fos and other genes encoding transcription factors in long-term potentiation. Behav. Neural Biol. 57 (1992) 263-266
15. Kaczmarek L. Molecular biology of vertebrate learning: Is c-fos a new beginning?. J. Neurosci. Res. 34 (1993) 377-381
16. Koerber K.C., Pfeiffer R.P., Warr W.B., and Kiang N.Y.S. Spontaneous spike discharges from single units in the cochlear nucleus after destruction of the cochlea. Exp. Neurol. 16 (1966) 119-130
17. Kraus K.S., and Illing R.B. Superior olivary contributions to auditory system plasticity: medial but not lateral olivocochlear neurons are the source of cochleotomy-induced GAP-43 expression in the ventral cochlear nucleus. J. Comp. Neurol. 475 (2004) 374-390
18. Kuhl P.K., Williams K.A., Lacerda F., Stevens K.N., and Lindblom B. Linguistic experience alters phonetic perception in infants by 6 months of age. Science 255 (1992) 606-608
19. Lund R.D. Development and Plasticity of the Brain (1978), Oxford University Press, New York
20. Michler S.A., and Illing R.B. Acoustic trauma induces re-emergence of the growth and plasticity associated protein GAP-43 in the rat auditory brainstem. J. Comp. Neurol. 451 (2002) 250-266
21. Michler S.A., and Illing R.B. Modulation of plasticity related molecules in the auditory brainstem of the rat following acoustic overstimulation. Audiol. Neurootol. 8 (2003) 190-206
22. Moller A.R. Symptoms and signs caused by neural plasticity. Neurol. Res. 23 (2001) 565-572
23. Moller A.R. Neurophysiologic basis for cochlear and auditory brainstem implants. Am. J. Audiol. 10 (2001) 68-77
24. Moore J.K., and Guan Y.L. Cytoarchitectural and axonal maturation in human auditory cortex. J. Assoc. Res. Otolaryngol. 2 (2001) 297-311
25. Pena M., Maki A., Kovacic D., Dehaene-Lambertz G., Koizumi H., Bouquet F., and Mehler J. Sounds and silence: an optical topography study of language recognition at birth. Proc. Natl. Acad. Sci. USA 100 (2003) 11702-11705
26. Purves D., and Lichtman J.W. Principles of Neural Development (1985), Sinauer Assoc., Inc., Sunderland
27. Robertson H.A. Immediate-early genes, neuronal plasticity, and memory. Biochem. Cell Biol. 70 (1992) 729-737
28. Sumner C.J., Tucci D.L., and Shore S.E. Responses of ventral cochlear nucleus neurons to contralateral sound after conductive hearing loss. J. Neurophysiol. 94 (2005) 4234-4243
29. Vetter D.E., Adams J.C., and Mugnaini E. Chemically distinct rat olivocochlear neurons. Synapse 7 (1991) 21-43
30. Warr W.B. Organization of olivocochlear efferent systems in mammals. In: Webster D.B., Popper A.N., and Fay R.R. (Eds). The Mammalian Auditory Pathway: Neuroanatomy (1992), Springer, New York
31. Worley P.F., Bhat R.V., Baraban J.M., Erickson C.A., McNaughton B.L., and Barnes C.A. Thresholds for synaptic activation of transcription factors in hippocampus: correlation with long-term enhancement. J. Neurosci. 13 (1993) 4776-4786
32. Yao W., and Godfrey D.A. Autoradiographic distribution of muscarinic acetylcholine receptor subtypes in rat cochlear nucleus. Aud. Neurosci. 2 (1996) 241-255