Literature DB >> 9744940

Physiological studies of the precedence effect in the inferior colliculus of the cat. II. Neural mechanisms.

R Y Litovsky1, T C Yin.   

Abstract

We studied the responses of neurons in the inferior colliculus (IC) of cats to stimuli known to evoke the precedence effect (PE). This paper focuses on stimulus conditions that probe the neural mechanisms underlying the PE but that are not usually encountered in a natural situation. Experiments were conducted under both free-field (anechoic chamber) and dichotic (headphones) conditions. We found that in free field the amount of suppression of the lagging response depended on the location of the leading source. With stimuli in the azimuthal plane, the majority (84%) of units showed stronger suppression of the lagging response for a leading stimulus placed in the cell's responsive area as compared with a lead in the unresponsive field. A smaller number of units showed stronger suppression for a lead placed in the unresponsive field, and a few showed little effect of the lead location. In the elevational plane, there was less sensitivity of the leading source to changes in location, but for those cells in which there was sensitivity, suppression was always stronger when the lead was in the cell's responsive area. Studies on stimulus locations also were conducted under dichotic conditions by varying the interaural differences in time (ITD) of the leading source. Results were consistent with those obtained in free field, suggesting that ITDs play an important role in determining the amount of suppression that was observed as a function of leading stimulus location. In addition to location and ITD, we also studied the effect of varying the relative levels of the lead and lag as well as stimulus duration. For all units studied, increasing the level of the leading stimulus while holding the lagging stimulus constant resulted in increased suppression. Similar effects of leading source level were observed in azimuth and elevation. The effect of varying the duration of the leading source also showed that longer duration stimuli produce stronger suppression; this finding was observed both in azimuth and elevation. We also compared the suppression observed under binaural and monaural contralateral conditions and found a mixed effect: some neurons show stronger suppression under binaural conditions, others to monaural contralateral conditions, and still others show no effect. The results presented here support the hypothesis that the PE reflects a long-lasting inhibition evoked by the leading stimulus. Five possible sources for the inhibition are considered: the auditory nerve, intrinsic circuits in the cochlear nucleus, medial and lateral nuclei of the trapezoid body inhibition to the medial superior olive, dorsal nucleus of the lateral lemniscus (DNLL) inhibition to the ICC, and intrinsic circuits in the ICC itself.

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Year:  1998        PMID: 9744940     DOI: 10.1152/jn.1998.80.3.1302

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


  24 in total

1.  Reversible inactivation of the dorsal nucleus of the lateral lemniscus reveals its role in the processing of multiple sound sources in the inferior colliculus of bats.

Authors:  R M Burger; G D Pollak
Journal:  J Neurosci       Date:  2001-07-01       Impact factor: 6.167

2.  Evidence for a neural source of the precedence effect in sound localization.

Authors:  Andrew D Brown; Heath G Jones; Alan Kan; Tanvi Thakkar; G Christopher Stecker; Matthew J Goupell; Ruth Y Litovsky
Journal:  J Neurophysiol       Date:  2015-09-23       Impact factor: 2.714

3.  Short-latency, goal-directed movements of the pinnae to sounds that produce auditory spatial illusions.

Authors:  Daniel J Tollin; Elizabeth M McClaine; Tom C T Yin
Journal:  J Neurophysiol       Date:  2009-11-04       Impact factor: 2.714

4.  Failure of the precedence effect with a noise-band vocoder.

Authors:  Bernhard U Seeber; Ervin R Hafter
Journal:  J Acoust Soc Am       Date:  2011-03       Impact factor: 1.840

Review 5.  The precedence effect in sound localization.

Authors:  Andrew D Brown; G Christopher Stecker; Daniel J Tollin
Journal:  J Assoc Res Otolaryngol       Date:  2014-12-06

6.  Physiological and psychophysical modeling of the precedence effect.

Authors:  Jing Xia; Andrew Brughera; H Steven Colburn; Barbara Shinn-Cunningham
Journal:  J Assoc Res Otolaryngol       Date:  2010-04-01

7.  Forward masking in the medial nucleus of the trapezoid body of the rat.

Authors:  Fei Gao; Albert S Berrebi
Journal:  Brain Struct Funct       Date:  2015-04-29       Impact factor: 3.270

8.  Coding of electric pulse trains presented through cochlear implants in the auditory midbrain of awake rabbit: comparison with anesthetized preparations.

Authors:  Yoojin Chung; Kenneth E Hancock; Sung-Il Nam; Bertrand Delgutte
Journal:  J Neurosci       Date:  2014-01-01       Impact factor: 6.167

9.  Behavior and modeling of two-dimensional precedence effect in head-unrestrained cats.

Authors:  Yan Gai; Janet L Ruhland; Tom C T Yin
Journal:  J Neurophysiol       Date:  2015-07-01       Impact factor: 2.714

10.  Transient gain adjustment in the inferior colliculus is serotonin- and calcium-dependent.

Authors:  Ilona J Miko; Dan H Sanes
Journal:  Hear Res       Date:  2009-02-20       Impact factor: 3.208

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