The conceptual issue addressed in this proposal is how neurons in the lateral superior olive (LSO) obtain their selectivity for interaural intensity disparities (IIDs), and whether neurons with different IID selectivities are arranged in an orderly fashion within isofrequency contours of the LSO. The impetus for this proposal derives from the success that investigators have had in discovering how medial superior olivary (MSO) neurons, and their avian analogue in the nucleus laminaris, obtain their selectivity for a particular interaural time disparity and how those features are systematically represented with those nuclei. In contrast, the way in which LSO cells obtain their individual sensitivity for a particular IID and the degree to which an orderly arrangement of IID sensitivities might exist in the LSO are issues that have received little attention and are poorly understood. Only Reed and Blum have proposed a hypothesis that addresses both the issue of how LSO cells obtain their individual IID selectivity and what structural features could also impart an orderly arrangement of IID selectivity within isofrequency contours. Their hypothesis, however, has never been tested experimentally. Moreover, it relies only on the differences in thresholds of the inputs from the two ears, and thus it does not incorporate a number of other important features of the LSO, such as latency and time-intensity trading.
The aims of this proposal are to test the Reed and Blum hypothesis and fill in the gaps in our knowledge about how LSO neurons obtain their particular IID selectivity. The first series of experiments has two goals: 1) To survey the LSO and obtain an overall view of the prevalence of neurons whose IID selectivities are predicted by threshold differences between the excitatory and inhibitory ears. 2) To distinguish between the hypothesis based on threshold differences, and alternative hypotheses which predict that IID selectivity is determined by differences in the relative strengths of the excitatory and inhibitory inputs, differences in arrival times from the two ears, or by some combination of threshold, strength and latency differences. These hypotheses will be evaluated by obtaining indices of input thresholds, strengths and latencies for each ear and then confirming their relative contributions for creating the neuron s IID selectivity through time-intensity trading experiments. A second series of experiments will reveal the degree to which IID selectivities are arranged in an orderly fashion within one isofrequency contour in the LSO. These experiments will exploit the greatly hypertrophied 60 kHz isofrequency contour of the mustache bat s LSO, yielding data from a large number of cells within one isofrequency contour.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29DC002850-04
Application #
6175372
Study Section
Hearing Research Study Section (HAR)
Program Officer
Luethke, Lynn E
Project Start
1997-05-01
Project End
2002-04-30
Budget Start
2000-05-01
Budget End
2001-04-30
Support Year
4
Fiscal Year
2000
Total Cost
$105,869
Indirect Cost
Name
University of Illinois at Chicago
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
Park, Thomas J; Brand, Antje; Koch, Ursula et al. (2008) Dynamic changes in level influence spatial coding in the lateral superior olive. Hear Res 238:58-67
Smith, Timothy D; Bhatnagar, Kunwar P; Dennis, John C et al. (2007) Growth-deficient vomeronasal organs in the naked mole-rat (Heterocephalus glaber). Brain Res 1132:78-83
Hetling, John R; Baig-Silva, Monica S; Comer, Christopher M et al. (2005) Features of visual function in the naked mole-rat Heterocephalus glaber. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 191:317-30
Park, Thomas J; Klug, Achim; Holinstat, Michael et al. (2004) Interaural level difference processing in the lateral superior olive and the inferior colliculus. J Neurophysiol 92:289-301
Crish, Samuel D; Rice, Frank L; Park, Thomas J et al. (2003) Somatosensory organization and behavior in naked mole-rats I: vibrissa-like body hairs comprise a sensory array that mediates orientation to tactile stimuli. Brain Behav Evol 62:141-51
Park, Thomas J; Comer, Christopher; Carol, Andrew et al. (2003) Somatosensory organization and behavior in naked mole-rats: II. Peripheral structures, innervation, and selective lack of neuropeptides associated with thermoregulation and pain. J Comp Neurol 465:104-20
Pollak, George D; Burger, R Michael; Park, Thomas J et al. (2002) Roles of inhibition for transforming binaural properties in the brainstem auditory system. Hear Res 168:60-78
Klug, A; Khan, A; Burger, R M et al. (2000) Latency as a function of intensity in auditory neurons: influences of central processing. Hear Res 148:107-23
Oswald, J P; Klug, A; Park, T J (1999) Interaural intensity difference processing in auditory midbrain neurons: effects of a transient early inhibitory input. J Neurosci 19:1149-63
Park, T J; Klug, A; Oswald, J P et al. (1998) A novel circuit in the bat's midbrain recruits neurons into sound localization processing. Naturwissenschaften 85:176-9

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