GAD levels and muscimol binding in rat inferior colliculus following acoustic trauma

Hearing Research

Volumn 147, Issue 1-2, 2000, Pages 251-260

  Milbrandt, J C ^a,b   Holder, T M ^a   Wilson, M C ^a   Salvi, R J ^c   Caspary, D M ^a  

^a SOUTHERN ILLINOIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF ILLINOIS   (United States)

^c UNIVERSITY AT BUFFALO   (United States)

Author keywords

Glutamic acid decarboxylase; Inferior colliculus; Noise exposure; Rat; Aminobutyric acid

Indexed keywords

4 AMINOBUTYRIC ACID; GLUTAMATE DECARBOXYLASE; MUSCIMOL;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDITORY NERVOUS SYSTEM; AUDITORY STIMULATION; CELL LOSS; COCHLEA INJURY; CONTROLLED STUDY; ENZYME ACTIVITY; HAIR CELL; IMMUNOREACTIVITY; INFERIOR COLLICULUS; INHIBITION KINETICS; MALE; NERVE CELL PLASTICITY; NEUROTRANSMISSION; NOISE INJURY; NONHUMAN; PRIORITY JOURNAL; RAT; RECEPTOR BINDING;

ANIMALS; COCHLEA; GAMMA-AMINOBUTYRIC ACID; GLUTAMATE DECARBOXYLASE; HAIR CELLS; HEARING LOSS, NOISE-INDUCED; INFERIOR COLLICULUS; MALE; MUSCIMOL; NEURONAL PLASTICITY; RATS; RATS, INBRED F344; RECEPTORS, GABA-A; SYNAPTIC TRANSMISSION;

EID: 0033842863     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(00)00135-0     Document Type: Article

References (56)

1. Abbott S.D., Hughes L.F., Bauer C.A., Salvi R., Caspary D.M. Detection of glutamic acid decarboxylase isoforms in rat inferior colliculus following acoustic exposure. Neuroscience. 93:1999;1375-1381.
2. Bledsoe S.C., Nagase S., Miller J.M., Altschuler R.A. Deafness-induced plasticity in the mature central auditory system. NeuroReport. 7:1995;225-229.
3. Bu D.-F., Erlander M.G., Hitz B.C., Tillakaratne N.J.K., Kaufman D.L., Wagner-McPherson C.B., Evans G.A., Tobin A.J. Two human glutamate decarboxylases, 65-kDa GAD and 67-kDa GAD, are each encoded by a single gene. Proc. Natl. Acad. Sci. USA. 89:1992;2115-2119.
4. Caspary D.M., Raza A., Armour B.A., Pippen J., Arnerič 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.
5. Caspary, D.M., Blomquist, T.S., Wilson, M.C., Salvi, R., Milbrandt, J.C., 1996. GAD immunoreactivity in the inferior colliculus following acute sound exposure: Loss of inhibition? 19th Midwinter Research Meeting ARO, St. Petersburg Beach, FL.
6. A receptor subunit composition and function in rat auditory system. Neuroscience. 93:1999;307-312.
7. Dumoulin A., Alonso G., Privat A., Feldblum S. Biphasic response of spinal GABAergic neurons after a lumbar rhizotomy in the adult rat. Eur. J. Neurosci. 8:1996;2553-2563.
8. Dupont, J., Bonneau, J.M., Altschuler, R.A., Aran, J.-M., 1994. GABA and glycine changes in the guinea pig brainstem auditory nuclei after total destruction of the inner ear. 17th Midwinter Research Meeting ARO, St. Petersburg Beach, FL.
9. Erlander M.G., Tobin A.J. The structural and functional heterogeneity of glutamic acid decarboxylase: a review. Neurochem. Res. 16:1991;215-226.
10. Esclapez M., Tillakaratne N.J.K., Tobin A.J., Houser C.R. Comparative localization of mRNAs encoding two forms of glutamic acid decarboxylase with nonradioactive in situ hybridization methods. J. Comp. Neurol. 331:1993;339-362.
11. Esclapez M., Tillakaratne N.J.K., Kaufman D.L., Tobin A.J., Houser C.R. Comparative localization of two forms of glutamic acid decarboxylase and their mRNAs in rat brain supports the concept of functional differences between the forms. J. Neurosci. 14:1994;1834-1855.
12. Faye-Lund H., Osen K.K. Anatomy of the inferior colliculus in rat. Anat. Embryol. 171:1985;1-20.
13. 67 mRNA suggest that two glutamate decarboxylases play distinctive functional roles. J. Neurosci. Res. 34:1993;689-706.
14. Fuchs J.L., Salazar E. Effects of whisker trimming on GABA(A) receptor binding in the barrel cortex of developing and adult rats. J. Comp. Neurol. 395:1998;209-216.
15. Gerken G.M., Saunders S.S., Paul R.E. Hypersensitivity to electrical stimulation of auditory nuclei follows hearing loss in cats. Hear. Res. 13:1984;249-259.
16. Gerken, G.M., Simhadri-Sumithra, R., Bhat, K.H.V., 1986. Increase in central auditory responsiveness during continuous tone stimulation or following hearing loss. In: Salvi, R.J., Henderson, D., Hamernik, R.P., Colletti, V. (Eds.), Basic and Applied Aspects of Noise Induced Hearing:oss. Plenum, New York, pp. 195-211.
17. Gold B.I., Roth R.H. Glutamate decarboxylase activity in striatal slices: Characterization of the increase following depolarization. J. Neurochem. 32:1979;883-888.
18. Griffith W.H., Murchison D.A. Enhancement of GABA-activated membrane currents in aged Fischer 344 rat basal forebrain neurons. J. Neurosci. 14:1995;7469-7477.
19. Hofstetter P., Ding D., Salvi R. Magnitude and pattern of inner and outer hair cell loss in chinchilla as a function of carboplatin dose. Audiology. 36:1997;301-311.
20. Kaufman D.L., Houser C.R., Tobin A.J. Two forms of gamma-aminobutyric acid synthetic enzyme glutamate decarboxylase have distinct intraneuronal distributions and cofactor interactions. J. Neurochem. 56:1991;720-723.
21. Krenning J., Hughes L.F., Caspary D.M., Helfert R.H. Age-related glycine receptor subunit changes in the cochlear nucleus of Fischer-344 rats. Laryngoscope. 108:1998;26-31.
22. 2+/calmodulin-dependent protein kinase II gene expression in rat cerebral cortex. Exp. Brain Res. 110:1996;163-174.
23. Liberman M.C., Dodds L.W. Single-neuron labeling and chronic cochlear pathology. II. Stereocilia damage and alterations of spontaneous discharge rates. Hear. Res. 16:1984;45-53.
24. Liberman M.C., Dodds L.W. Single-neuron labeling and chronic cochear pathology. III. Stereocilia damage and alterations of threshold tuning curves. Hear. Res. 16:1984;55-74.
25. Litwak J., Mercugliano M., Chesselet M.F., Oltmans G.A. Increased glutamic acid decarboxylase (GAD) mRNA and GAD activity in cerebellar Purkinje cells following lesion-induced increases in cell firing. Neurosci. Lett. 116:1990;179-183.
26. Lonsbury-Martin B.L., Martin G.K. Effects of moderately intense sound on auditory sensitivity in rhesus monkeys: behavioral and neural observations. J. Neurophysiol. 46:1981;563-586.
27. Martin D.L., Rimvall K. Regulation of gamma-aminobutyric acid synthesis in the brain. J. Neurochem. 60:1993;395-407.
28. Martin D.L., Martin S.B., Wu S.J., Espina N. Cofactor interactions and the regulation of glutamate decarboxylase activity. Neurochem. Res. 16:1991;243-249.
29. Martin D.L., Martin S.B., Wu S.J., Espina N. Regulatory properties of brain glutamate decarboxylase (GAD): the apoenzyme of GAD is present principally as the smaller of two molecular forms of GAD in brain. J. Neurosci. 11:1991;2725-2731.
30. Mercugliano M., Soghomonian J.-J., Quin Y., Nguyen H.Q., Fledblum S., Erlander M.G., Tobin A.J., Chesselet M.-F. Comparative distribution of messenger RNAs encoding glutamic acid decarboxylases (Mr 65,000 and Mr 67,000) in the basal ganglia of the rat. J. Comp. Neurol. 318:1992;245-254.
31. A receptor binding in the aging rat inferior colliculus. Neuroscience. 73:1996;449-458.
32. Milbrandt J.C., Hunter C., Caspary D.M. Alterations of GABA receptor subunit mRNA levels in the aging Fischer 344 rat inferior colliculus. J. Comp. Neurol. 379:1997;455-465.
33. Morest D.K., Kim J., Potashner S.J., Bohne B.A. Long-term degeneration in the cochlear nerve and cochlear nucleus of the adult chinchilla following acoustic overstimulation. Microsc. Res. Tech. 41:1998;205-216.
34. Palombi P.S., Caspary D.M. Physiology of the aged Fischer 344 rat inferior colliculus: responses to contralateral monaural stimuli. J. Neurophysiol. 76:1996;3114-3125.
35. 3H]muscimol binding in substantia nigra, entopeduncular nucleus, globus pallidus, and thalamus after striatal lesions as demonstrated by quantitative receptor autoradiography. J. Neurosci. 3:1983;1189-1198.
36. Paxinos, G., Watson, C., 1986. The Rat Brain in Stereotaxic Coordinates, 2nd edn. Academic Press, Orlando, FL.
37. 3H]Ro15-4513 specific binding in the superficial gray layer of the rat superior colliculus induced by visual deafferentation. Brain Res. 543:1991;287-295.
38. Popelar J., Erre J.P., Aran J.M., Cazals Y. Plastic changes in ipsi-contralateral differences of auditory cortex and inferior colliculus evoked potentials after injury to one ear in adult guinea pig. Hear. Res. 72:1994;125-134.
39. Raza A., Arnerič S.P., Milbrandt J.C., Caspary D.M. Age-related changes in brainstem auditory neurotransmitters: measures of GABA and acetylcholine function. Hear. Res. 77:1994;221-230.
40. 67 protein is highly sensitive to small increases in intraneuronal gamma-aminobutyric acid levels. J. Neurochem. 62:1994;1375-1381.
41. Rimvall K., Sheikh S.N., Martin D.L. Effects of increased gamma-aminobutyric acid levels on GAD67 protein and mRNA levels in rat cerebral cortex. J. Neurochem. 60:1993;714-720.
42. Salvi, R.J., Wang, J., 1997. Evidence for rapid functional reorganization in inferior colliculus and cochlear nucleus. In: Syka, J. (Ed.), Acoustical Signal Processing in the Central Auditory System. Plenum Press, New York, pp. 477-488.
43. Salvi, R.J., Perry, J., Hamernik, R.P., Henderson, D., 1982. Relationship between cochlear pathologies and auditory nerve and behavioral responses following acoustic trauma. In: Hamernik, R.P., Henderson, D., Salvi, R.J. (Eds.), New Perspectives on Noise-Induced Hearing Loss. Raven Press, New York, pp. 165-188.
44. Salvi R.J., Saunders S.S., Gratton M.A., Arehole S., Powers N. Enhanced evoked response amplitudes in the inferior colliculus of the chinchilla following acoustic trauma. Hear. Res. 50:1990;245-258.
45. Sanna E., Motzo C., Usala M., Pau D., Cagetti E., Biggio G. Functional changes in rat nigral GABA(A) receptors induced by degeneration of the striatonigral GABAergic pathway: an electrophysiological study of receptors incorporated into Xenopus oocytes. J. Neurochem. 70:1998;2539-2544.
46. - ion channels modulated by multiple drug-binding sites. Trends Pharmacol. Sci. 13:1992;446-450.
47. Spoendlin, H., 1976. Anatomical changes following various noise exposures. In: Henderson, D., Hamernik, R.P., Mills, J., Dosanjh, D. (Eds.), Effects of Noise on Hearing. Raven Press, New York, pp. 69-89.
48. Sponger V.P., Flood D.G., Frisina R.D., Salvi R.J. Quantitative measures of hair cell loss in CBA and C57BL/6 mice throughout their life spans. J. Acoust. Soc. Am. 101:1997;3546-3553.
49. Suneja S.K., Benson C.G., Potashner S.J. Glycine receptors in adult guinea pig brain stem auditory nuclei: regulation after unilateral cochlear ablation. Exp. Neurol. 154:1998;473-488.
50. Suneja S.K., Potashner S.J., 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.
51. Szczepaniak W.S., Møller A.R. Evidence of decreased GABAergic influence on temporal integration in the inferior colliculus following acute noise exposure: a study of evoked potentials in the rat. Neurosci. Lett. 196:1995;77-80.
52. Szczepaniak W.S., Møller A.R. Evidence of neuronal plasticity within the inferior colliculus after noise exposure: a study of evoked potentials in the rat. Electroencephalogr. Clin. Neurophysiol. 100:1996;158-164.
53. Willott J.F., Lu S.-M. Noise-induced hearing loss can alter neural coding and increase excitability in the central nervous system. Science. 216:1982;1331-1332.
54. Willott J.F., Parham K., Hunter K.P. Response properties of inferior colliculus neurons in young and very old CBA/J mice. Hear. Res. 37:1988;1-14.
55. Wyborski R.J., Bond R.W., Gottlieb D.I. Characterization of a cDNA coding for rat glutamic acid decarboxylase. Mol. Brain Res. 8:1990;193-198.
56. Zhang J., 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;1-4.