Literature DB >> 6631473

Binaural interaction in low-frequency neurons in inferior colliculus of the cat. I. Effects of long interaural delays, intensity, and repetition rate on interaural delay function.

S Kuwada, T C Yin.   

Abstract

Detailed, quantitative studies were made of the interaural phase sensitivity of 197 neurons with low best frequency in the inferior colliculus (IC) of the barbiturate-anesthetized cat. We analyzed the responses of single cells to interaural delays in which tone bursts were delivered to the two ears via sealed earphones and the onset of the tone to one ear with respect to the other was varied. For most (80%) cells the discharge rate is a cyclic function of interaural delay at a period corresponding to that of the stimulating frequency. The cyclic nature of the interaural delay curve indicates that these cells are sensitive to the interaural phase difference. These cells are distributed throughout the low-frequency zone of the IC, but they are less numerous in the medial and caudal zones. Cells with a wide variety of response patterns will exhibit interaural phase sensitivities at stimulating frequencies up to 3,100 Hz, although above 2,500 Hz the number of such cells decrease markedly. Using dichotic stimuli we could study the cell's sensitivity to the onset delay and interaural phase independently. The large majority of IC cells respond only to changes in interaural phase, with no sensitivity to the onset delay. However, a small number (7%) of cells exhibit a sensitivity to the onset delay as well as to the interaural phase disparity, and most of these cells show an onset response. The effects of changing the stimulus intensity equally to both ears or of changing the interaural intensity difference on the mean interaural phase were studied. While some neurons are not affected by level changes, others exhibit systematic phase shifts for both average and interaural intensity variations, and there is a continuous distribution of sensitivities between these extremes. A few cells also showed systematic changes in the shape of the interaural delay curves as a function of interaural intensity difference, especially at very long delays. These shifts can be interpreted as a form of time-intensity trading. A few cells demonstrated orderly changes in the interaural delay curve as the repetition rate of the stimulus was varied. Some of these changes are consonant with an inhibitory effect that occurs at stimulus offset. The responses of the neurons show a strong bias for stimuli that would originate from he contralateral sound field; 77% of the responses display mean interaural phase angles that are less than 0.5 of a cycle, which are delays to the ipsilateral tone.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1983        PMID: 6631473     DOI: 10.1152/jn.1983.50.4.981

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  33 in total

1.  Ongoing temporal coding of a stochastic stimulus as a function of intensity: time-intensity trading.

Authors:  Pascal Michelet; Damir Kovacić; Philip X Joris
Journal:  J Neurosci       Date:  2012-07-11       Impact factor: 6.167

2.  Trading of interaural differences in high-rate Gabor click trains.

Authors:  G Christopher Stecker
Journal:  Hear Res       Date:  2010-06-12       Impact factor: 3.208

Review 3.  Creating a sense of auditory space.

Authors:  David McAlpine
Journal:  J Physiol       Date:  2005-03-10       Impact factor: 5.182

4.  Neural correlates and mechanisms of spatial release from masking: single-unit and population responses in the inferior colliculus.

Authors:  Courtney C Lane; Bertrand Delgutte
Journal:  J Neurophysiol       Date:  2005-04-27       Impact factor: 2.714

5.  Phase locking of auditory-nerve fibers to the envelopes of high-frequency sounds: implications for sound localization.

Authors:  Anna Dreyer; Bertrand Delgutte
Journal:  J Neurophysiol       Date:  2006-06-28       Impact factor: 2.714

6.  Sensitivity to interaural time differences in the inferior colliculus with bilateral cochlear implants.

Authors:  Zachary M Smith; Bertrand Delgutte
Journal:  J Neurosci       Date:  2007-06-20       Impact factor: 6.167

7.  Learning-induced plasticity in auditory spatial representations revealed by electrical neuroimaging.

Authors:  Lucas Spierer; Eric Tardif; Holger Sperdin; Micah M Murray; Stephanie Clarke
Journal:  J Neurosci       Date:  2007-05-16       Impact factor: 6.167

8.  Representation of dynamic interaural phase difference in auditory cortex of awake rhesus macaques.

Authors:  Brian H Scott; Brian J Malone; Malcolm N Semple
Journal:  J Neurophysiol       Date:  2009-01-21       Impact factor: 2.714

9.  Interaural time difference discrimination thresholds for single neurons in the inferior colliculus of Guinea pigs.

Authors:  Trevor M Shackleton; Bernt C Skottun; Robert H Arnott; Alan R Palmer
Journal:  J Neurosci       Date:  2003-01-15       Impact factor: 6.167

10.  Neural population encoding and decoding of sound source location across sound level in the rabbit inferior colliculus.

Authors:  Mitchell L Day; Bertrand Delgutte
Journal:  J Neurophysiol       Date:  2015-10-21       Impact factor: 2.714

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