The proposed work is part of a continuing effort to understand how integrative tasks are performed in the mammalian cochlear nuclear complex. We hope to contribute to an understanding of what strategies the brain uses to process acoustic information by examining how neurons are interconnected. In the coming grant period two goals will be pursued. First, experiments will be performed to examine the pattern of convergence and divergence. On the basis of previous work which showed that anatomical cell types can be identified by their physiology and which revealed the location of local collaterals, we will inject pairs of cells that are likely to be connected. Estimates will be made of the proportion of terminals of one cell that are apposed to labeled processes of the other at the light microscopic level. We will also combine the labeling of single cochlear nuclear neurons intracellularly with intraaxonal or small extracellular injections to examine the innervation of cochlear nuclear neurons by auditory nerve fibers. With these experiments we will visualize connections between cells and relate them to synaptic responses recorded in these and in previous studies. Second, we will focus on the physiology of granule cells. These cells are numerous and occupy prominent positions in the cochlear nuclei of most mammals, yet it is not known how they are driven. The small size of granule cells makes electrophysiological studies difficult. We will attempt to measure extracellularly their spontaneous activity and their synaptic responses to shocks of various parts of the slice. We will also develop patch-clamping techniques to record from them intracellularly.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC000176-17
Application #
2608239
Study Section
Hearing Research Study Section (HAR)
Project Start
1981-07-01
Project End
1999-11-30
Budget Start
1997-12-01
Budget End
1998-11-30
Support Year
17
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Physiology
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Ison, James R; Allen, Paul D; Oertel, Donata (2017) Deleting the HCN1 Subunit of Hyperpolarization-Activated Ion Channels in Mice Impairs Acoustic Startle Reflexes, Gap Detection, and Spatial Localization. J Assoc Res Otolaryngol 18:427-440
Oertel, Donata; Cao, Xiao-Jie; Ison, James R et al. (2017) Cellular Computations Underlying Detection of Gaps in Sounds and Lateralizing Sound Sources. Trends Neurosci 40:613-624
Cao, Xiao-Jie; Oertel, Donata (2017) Genetic perturbations suggest a role of the resting potential in regulating the expression of the ion channels of the KCNA and HCN families in octopus cells of the ventral cochlear nucleus. Hear Res 345:57-68
Wright, Samantha; Hwang, Youngdeok; Oertel, Donata (2014) Synaptic transmission between end bulbs of Held and bushy cells in the cochlear nucleus of mice with a mutation in Otoferlin. J Neurophysiol 112:3173-88
McGinley, Matthew J; Liberman, M Charles; Bal, Ramazan et al. (2012) Generating synchrony from the asynchronous: compensation for cochlear traveling wave delays by the dendrites of individual brainstem neurons. J Neurosci 32:9301-11
Golding, Nace L; Oertel, Donata (2012) Synaptic integration in dendrites: exceptional need for speed. J Physiol 590:5563-9
Oertel, Donata; Wright, Samantha; Cao, Xiao-Jie et al. (2011) The multiple functions of T stellate/multipolar/chopper cells in the ventral cochlear nucleus. Hear Res 276:61-9
Oertel, Donata (2011) GluA4 sustains sensing of sounds through stable, speedy, sumptuous, spineless synapses. J Physiol 589:4089-90
Cao, Xiao-Jie; Oertel, Donata (2011) The magnitudes of hyperpolarization-activated and low-voltage-activated potassium currents co-vary in neurons of the ventral cochlear nucleus. J Neurophysiol 106:630-40
Cao, Xiao-Jie; Oertel, Donata (2010) Auditory nerve fibers excite targets through synapses that vary in convergence, strength, and short-term plasticity. J Neurophysiol 104:2308-20

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