Literature DB >> 3360996

Tonotopic projection from the dorsal to the anteroventral cochlear nucleus of mice.

R E Wickesberg1, D Oertel.   

Abstract

To understand how auditory information is processed in the cochlear nuclei, it is crucial to know what circuitry exists and how it functions. In slice preparations, horseradish peroxidase (HRP) injections into the anteroventral cochlear nucleus (AVCN) reveal two circuits: a connection between the dorsal cochlear nucleus (DCN) and AVCN and a local circuit confined to the AVCN. Extracellular injection in the AVCN labels a band of cells in the DCN. The labeled cells in the DCN lie within a band of auditory nerve fiber terminals that are labeled by the same injection, showing that the connection from the DCN to the AVCN is frequency specific. The injections into the AVCN also labeled a cluster of neurons in the AVCN dorsal to the injection site. These cells may be interneurons that relay information from areas encoding higher frequencies to areas encoding lower frequencies within the AVCN. In the parasagittal plane, the AVCN is organized along two orthogonal axes that are indicated with HRP labeling of fibers and cell bodies. The tonotopic axis runs approximately dorsoventrally; the isofrequency axis runs approximately rostrocaudally. The axons of labeled DCN neurons and the cluster lie along the tonotopic axis, whereas the labeled auditory nerve fibers define the isofrequency axis. Where they cross is where HRP is taken up by the fibers. The area of uptake is small and lies in the middle of the darkly stained injection site.

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Year:  1988        PMID: 3360996     DOI: 10.1002/cne.902680308

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  31 in total

1.  Time course and permeation of synaptic AMPA receptors in cochlear nuclear neurons correlate with input.

Authors:  S M Gardner; L O Trussell; D Oertel
Journal:  J Neurosci       Date:  1999-10-15       Impact factor: 6.167

2.  Correlation of AMPA receptor subunit composition with synaptic input in the mammalian cochlear nuclei.

Authors:  S M Gardner; L O Trussell; D Oertel
Journal:  J Neurosci       Date:  2001-09-15       Impact factor: 6.167

3.  Neural modeling of intrinsic and spike-discharge properties of cochlear nucleus neurons.

Authors:  J E Arle; D O Kim
Journal:  Biol Cybern       Date:  1991       Impact factor: 2.086

4.  A phenomenological model of peripheral and central neural responses to amplitude-modulated tones.

Authors:  Paul C Nelson; Laurel H Carney
Journal:  J Acoust Soc Am       Date:  2004-10       Impact factor: 1.840

5.  Influence of inhibitory inputs on rate and timing of responses in the anteroventral cochlear nucleus.

Authors:  Yan Gai; Laurel H Carney
Journal:  J Neurophysiol       Date:  2008-01-16       Impact factor: 2.714

6.  Age-related changes in glycine receptor subunit composition and binding in dorsal cochlear nucleus.

Authors:  H Wang; J G Turner; L Ling; J L Parrish; L F Hughes; D M Caspary
Journal:  Neuroscience       Date:  2009-02-13       Impact factor: 3.590

7.  Short-term synaptic depression and recovery at the mature mammalian endbulb of Held synapse in mice.

Authors:  Yong Wang; Paul B Manis
Journal:  J Neurophysiol       Date:  2008-07-16       Impact factor: 2.714

8.  Pitfalls in behavioral estimates of basilar-membrane compression in humans.

Authors:  Magdalena Wojtczak; Andrew J Oxenham
Journal:  J Acoust Soc Am       Date:  2009-01       Impact factor: 1.840

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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