The long-term goal of this research is to discover the structural features of sensory neurons that define their capacities to code Information. The emphasis Is on the cytological design and pattern of connections of specific types of auditory neurons and their synaptic contacts at the levels of the cochlear nucleus, superior olive, and cochlea.
The specific aims are to define the synaptic organization of certain types of neurons In the cochlear nucleus that Initiate the ascending monaural and binaural pathways. to define their connections with other neuronal types In the cochlea and superior olive, Including their Inhibitory and excitatory synapses, and to relate these findings to the circuits responsible for binaural processing. The key morphological concept In this effort Is the synaptic profile, which quantitates the concentration of the different kinds of synaptic endings on each part of a cell. The hypothesis Is that each population of neurons defined In this way will differ with respect to one or more other features, morphological, neurochemical, and electrophysiological. The synaptic profile provides a map on which to plot the locations of the endings with respect to their origins from other nuclei or neuronal types and the neurotransmitters contained In the endings, and for quantitative comparisons between the results of different kinds of experiments. Light and electron microscopic methods are used. Sufficient details are obtained to correlate with physiological recordings from these neuron types in related studies. Anterograde or retrograde labeling of neurons with cellular tracers will be combined with immunocytochemical labeling methods to define the connections of specific types of neurons and to show which of these are associated with the known Inhibitory transmitters. This will provide a cellular basis for pursuing an understanding of the normal and abnormal function of the central auditory system, and ultimately a biological basis for neurochemical or prosthetic therapies of nerve deafness.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC000127-16
Application #
2124731
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1979-07-01
Project End
1996-11-30
Budget Start
1993-12-01
Budget End
1994-11-30
Support Year
16
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Connecticut
Department
Anatomy/Cell Biology
Type
Schools of Dentistry
DUNS #
City
Farmington
State
CT
Country
United States
Zip Code
06030
Leung, Alan W; Kent Morest, D; Li, James Y H (2013) Differential BMP signaling controls formation and differentiation of multipotent preplacodal ectoderm progenitors from human embryonic stem cells. Dev Biol 379:208-20
García-Hernández, Sofía; Potashner, Steven J; Morest, D Kent (2013) Role of fibroblast growth factor 8 in neurite outgrowth from spiral ganglion neurons in vitro. Brain Res 1529:39-45
Feng, J; Bendiske, J; Morest, D K (2012) Degeneration in the ventral cochlear nucleus after severe noise damage in mice. J Neurosci Res 90:831-41
Feng, J; Bendiske, J; Morest, D K (2010) Postnatal development of NT3 and TrkC in mouse ventral cochlear nucleus. J Neurosci Res 88:86-94
Wang, S J; Furusho, M; D'Sa, C et al. (2009) Inactivation of fibroblast growth factor receptor signaling in myelinating glial cells results in significant loss of adult spiral ganglion neurons accompanied by age-related hearing impairment. J Neurosci Res 87:3428-37
Hill, Gerhard W; Morest, D Kent; Parham, Kourosh (2008) Cisplatin-induced ototoxicity: effect of intratympanic dexamethasone injections. Otol Neurotol 29:1005-11
D'Sa, Chrystal; Gross, Julia; Francone, Victor P et al. (2007) Plasticity of synaptic endings in the cochlear nucleus following noise-induced hearing loss is facilitated in the adult FGF2 overexpressor mouse. Eur J Neurosci 26:666-80
Hurd, L B; Hutson, K A; Morest, D K (1999) Cochlear nerve projections to the small cell shell of the cochlear nucleus: the neuroanatomy of extremely thin sensory axons. Synapse 33:83-117
Bilak, S R; Morest, D K (1998) Differential expression of the metabotropic glutamate receptor mGluR1alpha by neurons and axons in the cochlear nucleus: in situ hybridization and immunohistochemistry. Synapse 28:251-70
Josephson, E M; Morest, D k (1998) A quantitative profile of the synapses on the stellate cell body and axon in the cochlear nucleus of the chinchilla. J Neurocytol 27:841-64

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