Changes in neuronal activity and gene expression in guinea-pig auditory brainstem after unilateral partial hearing loss

Neuroscience

Volumn 159, Issue 3, 2009, Pages 1164-1174

  Dong, S ^a   Mulders, W H A M ^a   Rodger, J ^a   Robertson, D ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

cochlear nucleus; deafness; inferior colliculus; neurotransmitter; plasticity

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; GABA A RECEPTOR SUBUNIT ALPHA 1; GLUTAMATE DECARBOXYLASE; GLUTAMATE DECARBOXYLASE 1; GLYCINE RECEPTOR; GLYCINE RECEPTOR SUBUNIT ALPHA 1; MESSENGER RNA; POTASSIUM CHANNEL; POTASSIUM CHANNEL SUBFAMILY K MEMBER 15; RAB PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; COCHLEAR NUCLEUS; CONTROLLED STUDY; EVOKED BRAIN STEM AUDITORY RESPONSE; EXCITABLE MEMBRANE; GENE; GENE EXPRESSION; GUINEA PIG; HYPERACTIVITY; INFERIOR COLLICULUS; NERVE CELL; NEUROTRANSMISSION; NONHUMAN; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; REAL TIME POLYMERASE CHAIN REACTION; SYNAPTIC TRANSMISSION; UNILATERAL HEARING LOSS;

ACTION POTENTIALS; ANIMALS; COCHLEA; COCHLEAR NUCLEUS; GENE EXPRESSION; GLUTAMATE DECARBOXYLASE; GUINEA PIGS; HEARING LOSS, UNILATERAL; INFERIOR COLLICULI; NEURONS; POTASSIUM CHANNELS, TANDEM PORE DOMAIN; RAB3A GTP-BINDING PROTEIN; RANDOM ALLOCATION; RECEPTORS, AMPA; RECEPTORS, GABA-A; RECEPTORS, GLYCINE; RECEPTORS, N-METHYL-D-ASPARTATE; RNA, MESSENGER;

EID: 62549156612     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2009.01.043     Document Type: Article

References (51)

1. Asako M., Holt A.G., Griffith R.D., Buras E.D., and Altschuler R.A. Deafness-related decreases in glycine-immunoreactive labeling in the rat cochlear nucleus. J Neurosci Res 81 (2005) 102-109
2. Bauer C.A. Animal models of tinnitus. Otolaryngol Clin North Am 36 (2003) 267-285 vi
3. Brozoski T.J., Bauer C.A., and Caspary D.M. Elevated fusiform cell activity in the dorsal cochlear nucleus of chinchillas with psychophysical evidence of tinnitus. J Neurosci 22 (2002) 2383-2390
4. Brozoski T.J., Ciobanu L., and Bauer C.A. Central neural activity in rats with tinnitus evaluated with manganese-enhanced magnetic resonance imaging (MEMRI). Hear Res 228 (2007) 168-179
5. Campos M.L., de Cabo C., Wisden W., Juiz J.M., and Merlo D. Expression of GABA(A) receptor subunits in rat brainstem auditory pathways: cochlear nuclei, superior olivary complex and nucleus of the lateral lemniscus. Neuroscience 102 (2001) 625-638
6. Caspary D.M., Holder T.M., Hughes L.F., Milbrandt J.C., McKernan R.M., and Naritoku D.K. Age-related changes in GABA(A) receptor subunit composition and function in rat auditory system. Neuroscience 93 (1999) 307-312
7. Caspary D.M., Raza A., Lawhorn Armour B.A., Pippin J., and Arneric S.P. Immunocytochemical and neurochemical evidence for age-related loss of GABA in the inferior colliculus: implications for neural presbycusis. J Neurosci 10 (1990) 2363-2372
8. Cui Y.L., Holt A.G., Lomax C.A., and Altschuler R.A. Deafness associated changes in two-pore domain potassium channels in the rat inferior colliculus. Neuroscience 149 (2007) 421-433
9. Ebert U. Noradrenaline enhances the activity of cochlear nucleus neurons in the rat. Eur J Neurosci 8 (1996) 1306-1314
10. Eggermont J.J., and Roberts L.E. The neuroscience of tinnitus. Trends Neurosci 27 (2004) 676-682
11. Gonzalez-Hernandez T., Mantolan-Sarmiento B., Gonzalez-Gonzalez B., and Perez-Gonzalez H. Sources of GABAergic input to the inferior colliculus of the rat. J Comp Neurol 372 (1996) 309-326
12. 2+ permeability of KA-AMPA-gated glutamate receptor channels depends on subunit composition. Science 252 (1991) 851-853
13. Holt A.G., Asako M., Duncan R.K., Lomax C.A., Juiz J.M., and Altschuler R.A. Deafness associated changes in expression of two-pore domain potassium channels in the rat cochlear nucleus. Hear Res 216-217 (2006) 146-153
14. Holt A.G., Asako M., Lomax C.A., MacDonald J.W., Tong L., Lomax M.I., and Altschuler R.A. Deafness-related plasticity in the inferior colliculus: gene expression profiling following removal of peripheral activity. J Neurochem 93 (2005) 1069-1086
15. Johnstone J.R., Alder V.A., Johnstone B.M., Robertson D., and Yates G.K. Cochlear action potential threshold and single unit thresholds. J Acoust Soc Am 65 (1979) 254-257
16. Jordens I., Marsman M., Kuijl C., and Neefjes J. Rab proteins, connecting transport and vesicle fusion. Traffic 6 (2005) 1070-1077
17. Kaltenbach J.A., and Afman C.E. Hyperactivity in the dorsal cochlear nucleus after intense sound exposure and its resemblance to tone-evoked activity: a physiological model for tinnitus. Hear Res 140 (2000) 165-172
18. Kaltenbach J.A., Godfrey D.A., Neumann J.B., McCaslin D.L., Afman C.E., and Zhang J. Changes in spontaneous neural activity in the dorsal cochlear nucleus following exposure to intense sound: relation to threshold shift. Hear Res 124 (1998) 78-84
19. Kaltenbach J.A., Zhang J., and Afman C.E. Plasticity of spontaneous neural activity in the dorsal cochlear nucleus after intense sound exposure. Hear Res 147 (2000) 282-292
20. Karschin C., Wischmeyer E., Preisig-Muller R., Rajan S., Derst C., Grzeschik K.H., Daut J., and Karschin A. Expression pattern in brain of TASK-1, TASK-3, and a tandem pore domain K(+) channel subunit, TASK-5, associated with the central auditory nervous system. Mol Cell Neurosci 18 (2001) 632-648
21. Ketchum K.A., Joiner W.J., Sellers A.J., Kaczmarek L.K., and Goldstein S.A.N. A new family of outwardly rectifying potassium channel proteins with two pore domains in tandem. Nature (Lond) 376 (1995) 690-695
22. Li L., and Chin L.S. The molecular machinery of synaptic vesicle exocytosis. Cell Mol Life Sci 60 (2003) 942-960
23. Livak K.J., and Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-delta delta C(T)) method. Methods 25 (2001) 402-408
24. Ma W.L., Hidaka H., and May B.J. Spontaneous activity in the inferior colliculus of CBA/J mice after manipulations that induce tinnitus. Hear Res 212 (2006) 9-21
25. Merrill E.G., and Ainsworth A. Glass-coated platinum-plated tungsten microelectrodes. Med Biol Eng 10 (1972) 662-672
26. Moller A.R. Neural plasticity and disorders of the nervous system (2006), Cambridge University Press, Cambridge
27. Mossop J.E., Wilson M.J., Caspary D.M., and Moore D.R. Downregulation of inhibition following unilateral deafening. Hear Res 147 (2000) 183-187
28. Mugnaini E. GABA neurons in the superficial layers of the rat dorsal cochlear nucleus: light and electron microscopic immunocytochemistry. J Comp Neurol 235 (1985) 61-81
29. Ostapoff E.M., Benson C.G., and Saint Marie R.L. GABA- and glycine-immunoreactive projections from the superior olivary complex to the cochlear nucleus in guinea pig. J Comp Neurol 381 (1997) 500-512
30. Pereira-Leal J.B., and Seabra M.C. Evolution of the Rab family of small GTP-binding proteins. J Mol Biol 313 (2001) 889-901
31. Piechotta K., Weth F., Harvey R.J., and Friauf E. Localization of rat glycine receptor alpha1 and alpha2 subunit transcripts in the developing auditory brainstem. J Comp Neurol 438 (2001) 336-352
32. Plant L.D., Rajan S., and Goldstein S.A. K2P channels and their protein partners. Curr Opin Neurobiol 15 (2005) 326-333
33. Robertson D., and Irvine D.R. Plasticity of frequency organization in auditory cortex of guinea pigs with partial unilateral deafness. J Comp Neurol 282 (1989) 456-471
34. Sakane A., Manabe S., Ishizaki H., Tanaka-Okamoto M., Kiyokage E., Toida K., Yoshida T., Miyoshi J., Kamiya H., Takai Y., and Sasaki T. Rab3 GTPase-activating protein regulates synaptic transmission and plasticity through the inactivation of Rab3. Proc Natl Acad Sci U S A 103 (2006) 10029-10034
35. Salvi R.J., Wang J., and Ding D. Auditory plasticity and hyperactivity following cochlear damage. Hear Res 147 (2000) 261-274
36. Sato K., Kuriyama H., and Altschuler R.A. Expression of glycine receptor subunit mRNAs in the rat cochlear nucleus. Hear Res 144 (2000) 47-52
37. Sato K., Shiraishi S., Nakagawa H., Kuriyama H., and Altschuler R.A. Diversity and plasticity in amino acid receptor subunits in the rat auditory brain stem. Hear Res 147 (2000) 137-144
38. Schluter O.M., Schmitz F., Jahn R., Rosenmund C., and Sudhof T.C. A complete genetic analysis of neuronal Rab3 function. J Neurosci 24 (2004) 6629-6637
39. Seluakumaran K., Mulders W.H., and Robertson D. Effects of medial olivocochlear efferent stimulation on the activity of neurons in the auditory midbrain. Exp Brain Res 186 (2008) 161-174
40. Shneiderman A., Oliver D.L., and Henkel C.K. Connections of the dorsal nucleus of the lateral lemniscus: an inhibitory parallel pathway in the ascending auditory system?. J Comp Neurol 276 (1988) 188-208
41. Suneja S.K., Potashner S.J., and Benson C.G. Plastic changes in glycine and GABA release and uptake in adult brain stem auditory nuclei after unilateral middle ear ossicle removal and cochlear ablation. Exp Neurol 151 (1998) 273-288
42. Suneja S.K., Potashner S.J., and Benson C.G. AMPA receptor binding in adult guinea pig brain stem auditory nuclei after unilateral cochlear ablation. Exp Neurol 165 (2000) 355-369
43. Syka J. Plastic changes in the central auditory system after hearing loss, restoration of function, and during learning. Physiol Rev 82 (2002) 601-636
44. Tan J., Ruttiger L., Panford-Walsh R., Singer W., Schulze H., Kilian S.B., Hadjab S., Zimmermann U., Kopschall I., Rohbock K., and Knipper M. Tinnitus behavior and hearing function correlate with the reciprocal expression patterns of BDNF and Arg31/Arc in auditory neurons following acoustic trauma. Neuroscience 145 (2007) 715-726
45. Thompson J.D., Higgins D.G., and Gibson T.J. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22 (1994) 4673-4680
46. Vale C., Juiz J.M., Moore D.R., and Sanes D.H. Unilateral cochlear ablation produces greater loss of inhibition in the contralateral inferior colliculus. Eur J Neurosci 20 (2004) 2133-2140
47. Vio M.M., and Holme R.H. Hearing loss and tinnitus: 250 million people and a US$10 billion potential market. Drug Discov Today 10 (2005) 1263-1265
48. Willott J.F., Milbrandt J.C., Bross L.S., and Caspary D.M. Glycine immunoreactivity and receptor binding in the cochlear nucleus of C57BL/6J and CBA/CaJ mice: effects of cochlear impairment and aging. J Comp Neurol 385 (1997) 405-414
49. Wynne B., Harvey A.R., Robertson D., and Sirinathsinghji D.J. Neurotransmitter and neuromodulator systems of the rat inferior colliculus and auditory brainstem studied by in situ hybridization. J Chem Neuroanat 9 (1995) 289-300
50. Yang W., Wu W., and Fang Y. [Changes of GABA immunoreactivity in aged rat cochlear nucleus]. Zhonghua Yi Xue Za Zhi 78 (1998) 30-32
51. Zhang J.S., and Kaltenbach J.A. Increases in spontaneous activity in the dorsal cochlear nucleus of the rat following exposure to high-intensity sound. Neurosci Lett 250 (1998) 197-200