Literature DB >> 7061349

Response properties of type II and type III units in dorsal cochlear nucleus.

E D Young, H F Voigt.   

Abstract

Type II and type III units in the dorsal cochlear nucleus (DCN) of unanesthetized (decerebrate) cats are those with excitatory responses to best frequency (BF) tones at all levels above threshold. They are distinguished from type IV units which give predominantly inhibitory responses to tones. Type II and type III units are distinguished from one another by their rates of spontaneous activity. Type II units have low rates of spontaneous activity (below 2.5 spikes/s), whereas type III units are spontaneously active at rates up to 95 spikes/s. In this paper we show that segregation of units according to spontaneous activity produces a segregation of several other properties as well. A typical type II unit responds vigorously to BF tones (median maximum rate of 242 spikes/s), has slightly nonmonotonic rate versus level function, and responds weakly or not at all to broadband noise. These units tend to be located in the deep layer of the DCN. Type III units tend to respond to BF tones at moderate rates (median maximum driven rate of 124 spikes/s), have monotonic or nonmonotonic rate versus level functions, and respond to noise at rates comparable to their tone rates. They are distributed somewhat more uniformly in all DCN layers, but a majority were found in the fusiform cell and molecular layers. Most evidence indicates that type II units are recorded from inhibitory interneurons in the DCN.

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Year:  1982        PMID: 7061349     DOI: 10.1016/0378-5955(82)90051-x

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  23 in total

1.  Dorsal cochlear nucleus response properties following acoustic trauma: response maps and spontaneous activity.

Authors:  Wei-Li Diana Ma; Eric D Young
Journal:  Hear Res       Date:  2006-04-19       Impact factor: 3.208

2.  Onset neurones in the anteroventral cochlear nucleus project to the dorsal cochlear nucleus.

Authors:  Robert H Arnott; Mark N Wallace; Trevor M Shackleton; Alan R Palmer
Journal:  J Assoc Res Otolaryngol       Date:  2004-06

3.  A modeling study of notch noise responses of type III units in the gerbil dorsal cochlear nucleus.

Authors:  Xiaohan Zheng; Herbert F Voigt
Journal:  Ann Biomed Eng       Date:  2006-12       Impact factor: 3.934

4.  The role of broadband inhibition in the rate representation of spectral cues for sound localization in the inferior colliculus.

Authors:  Bradford J May; Michael Anderson; Matthew Roos
Journal:  Hear Res       Date:  2008-01-26       Impact factor: 3.208

5.  On the role of the wideband inhibitor in the dorsal cochlear nucleus: a computational modeling study.

Authors:  Oleg Lomakin; Kevin A Davis
Journal:  J Assoc Res Otolaryngol       Date:  2008-08-14

6.  A discontinuous tonotopic organization in the inferior colliculus of the rat.

Authors:  Manuel S Malmierca; Marco A Izquierdo; Salvatore Cristaudo; Olga Hernández; David Pérez-González; Ellen Covey; Douglas L Oliver
Journal:  J Neurosci       Date:  2008-04-30       Impact factor: 6.167

7.  Temporal and binaural properties in dorsal cochlear nucleus and its output tract.

Authors:  P X Joris; P H Smith
Journal:  J Neurosci       Date:  1998-12-01       Impact factor: 6.167

8.  Synaptic connections in the dorsal cochlear nucleus of mice, in vitro.

Authors:  J A Hirsch; D Oertel
Journal:  J Physiol       Date:  1988-02       Impact factor: 5.182

9.  Response classes in the dorsal cochlear nucleus and its output tract in the chloralose-anesthetized cat.

Authors:  P X Joris
Journal:  J Neurosci       Date:  1998-05-15       Impact factor: 6.167

10.  Computer simulation of shared input among projection neurons in the dorsal cochlear nucleus.

Authors:  K A Davis; H F Voigt
Journal:  Biol Cybern       Date:  1996-05       Impact factor: 2.086

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