A dynamic relationship is hypothesized between the auditory periphery and the regulation of synaptic biochemistry in pathways of the central auditory nervous system. This predicts that changes in the acoustic efficacy of the ear, for example, after the cochlear trauma or long exposure to abnormally low or high levels of sound, should adjust the synaptic biochemistry of auditory pathways. Persistent changes of synaptic structure in the medial nucleus of the trapezoid body and of neuronal discharge in the inferior colliculus, medial geniculate nucleus, and auditory cortex were reported after procedures that decrease the acoustic efficacy of one ear. These changes may reflect a regulatory process that begins in the ascending brain stem auditory pathways. Knowledge of these phenomena will be valuable in understanding the synaptic basis of auditory functions, controlling pathology, and rehabilitating the central auditory system after insult. We propose to elucidate the hypothesized regulatory relationship. FIRST, we will identify the ascending auditory brain stem projections that use transmitters such as glutamate, aspartate, homocysteic acid, cysteine sulfanilic acid, GABA, glycine, and acetylcholine. Transmitters have been suggested for only one or two of the ascending auditory pathways. To determine the transmitters used by the others, ascending tracts will be lesioned to destroy their synaptic endings. At each projection site, we will measure changes in the evoked release and the high affinity uptake of the putative transmitters and quantify the binding activity of synaptic receptors. SECOND, we will determine the effect of cochlear lesions on the synaptic transmitter biochemistry in the brain stem auditory nuclei. High frequency hearing loss will be produced by acoustic trauma and surgical lesions of the cochlea. Then, synaptic biochemical activities, such as transmitter release, high-affinity uptake, and receptor binding, will be compared in the projection sites of the ascending auditory pathways of hearing-impaired and unlesioned cases. THIRD, we will determine the effect of exposure to different levels of sound on the synaptic transmitter biochemistry in the brain stem auditory nuclei. Three levels of environmental noise will provide different levels of cochlear activity without cochlear damage. We will compare synaptic biochemical activities in animals with bilateral ossiculectomies, intact animals kept in a 'normal' environment, and intact animals kept in a 'noisy' environment.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
2R01DC000199-08
Application #
3216086
Study Section
Hearing Research Study Section (HAR)
Project Start
1990-12-01
Project End
1997-11-30
Budget Start
1990-12-01
Budget End
1991-11-30
Support Year
8
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Connecticut
Department
Type
Schools of Dentistry
DUNS #
City
Farmington
State
CT
Country
United States
Zip Code
06030
Yan, Leqin; Suneja, Sanoj K; Potashner, Steven J (2007) Protein kinases regulate glycine receptor binding in brain stem auditory nuclei after unilateral cochlear ablation. Brain Res 1135:102-6
Zhang, J; Suneja, S K; Potashner, S J (2004) Protein kinase A and calcium/calmodulin-dependent protein kinase II regulate glycine and GABA release in auditory brain stem nuclei. J Neurosci Res 75:361-70
Muly, S M; Gross, J S; Potashner, S J (2004) Noise trauma alters D-[3H]aspartate release and AMPA binding in chinchilla cochlear nucleus. J Neurosci Res 75:585-96
Zhang, J; Suneja, S K; Potashner, S J (2003) Protein kinase C regulation of glycine and gamma-aminobutyric acid release in brain stem auditory nuclei. Exp Neurol 182:75-86
Zhang, J; Suneja, S K; Potashner, S J (2003) Protein kinase A and calcium/calmodulin-dependent protein kinase II regulate D-[3H]aspartate release in auditory brain stem nuclei. J Neurosci Res 74:81-90
Zhang, J; Suneja, S K; Potashner, S J (2002) Protein kinase C regulates [3H]D-aspartate release in auditory brain stem nuclei. Exp Neurol 175:245-56
Saint Marie, R L; Benson, C G; Ostapoff, E M et al. (1991) Glycine immunoreactive projections from the dorsal to the anteroventral cochlear nucleus. Hear Res 51:11-28