Literature DB >> 8132870

Auditory nerve terminals in the cochlear nucleus magnocellularis: differences between low and high frequencies.

C Köppl1.   

Abstract

Primary auditory nerve fibers were labelled in the barn owl by localized horseradish peroxidase (HRP) injections into the cochlear nucleus angularis. They were followed to their terminal sites in the hearing organ (basilar papilla), confirming that they were auditory, and to the cochlear nucleus magnocellularis. The terminal sites of low-frequency fibers within nucleus magnocellularis always included an area previously described as the lagenar part, i.e., an area receiving primary input which is probably only vestibular. Furthermore, a number of differences were recognized between these low-frequency (up to 0.64 kHz) and the high-frequency (1.8 kHz and above) auditory nerve projections to nucleus magnocellularis. Most importantly, the collaterals given off by low-frequency fibers into the nucleus typically showed multiple terminal branching, with both en passant and terminal bouton-like swellings. High-frequency fiber collaterals, in contrast, terminated unbranched in a single endbulb of Held. Nucleus magnocellularis is the first station in a brainstem auditory pathway processing stimulus timing information, coded through neuronal phase locking. The prominent difference in terminal shape found between its low- and high-frequency input fibers is interpreted as reflecting different requirements of the absolute temporal precision for significant phase locking. Terminals in the shape of endbulbs of Held are probably a specialization to improve the temporal precision of synaptic transmission, allowing phase locking to higher frequencies.

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Year:  1994        PMID: 8132870     DOI: 10.1002/cne.903390310

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


  18 in total

1.  The superior olivary nucleus and its influence on nucleus laminaris: a source of inhibitory feedback for coincidence detection in the avian auditory brainstem.

Authors:  L Yang; P Monsivais; E W Rubel
Journal:  J Neurosci       Date:  1999-03-15       Impact factor: 6.167

2.  Roles of axonal sodium channels in precise auditory time coding at nucleus magnocellularis of the chick.

Authors:  Hiroshi Kuba; Harunori Ohmori
Journal:  J Physiol       Date:  2008-11-10       Impact factor: 5.182

Review 3.  Sound localization in the alligator.

Authors:  Hilary S Bierman; Catherine E Carr
Journal:  Hear Res       Date:  2015-06-03       Impact factor: 3.208

Review 4.  The modulation by intensity of the processing of interaural timing cues for localizing sounds.

Authors:  Eri Nishino; Harunori Ohmori
Journal:  Mol Neurobiol       Date:  2009-07-11       Impact factor: 5.590

Review 5.  Structural tuning and plasticity of the axon initial segment in auditory neurons.

Authors:  Hiroshi Kuba
Journal:  J Physiol       Date:  2012-10-01       Impact factor: 5.182

6.  Short-term synaptic depression is topographically distributed in the cochlear nucleus of the chicken.

Authors:  Stefan N Oline; R Michael Burger
Journal:  J Neurosci       Date:  2014-01-22       Impact factor: 6.167

7.  Spatiotemporal Analysis of Cochlear Nucleus Innervation by Spiral Ganglion Neurons that Serve Distinct Regions of the Cochlea.

Authors:  Jennifer L Scheffel; Samiha S Mohammed; Chloe K Borcean; Annie J Parng; Hyun Ju Yoon; Darwin A Gutierrez; Wei-Ming Yu
Journal:  Neuroscience       Date:  2020-08-29       Impact factor: 3.590

8.  Excitatory-Inhibitory Synaptic Coupling in Avian Nucleus Magnocellularis.

Authors:  Mohammed Al-Yaari; Rei Yamada; Hiroshi Kuba
Journal:  J Neurosci       Date:  2019-11-14       Impact factor: 6.167

9.  Connections of the auditory brainstem in a songbird, Taeniopygia guttata. I. Projections of nucleus angularis and nucleus laminaris to the auditory torus.

Authors:  Nils O E Krützfeldt; Priscilla Logerot; M Fabiana Kubke; J Martin Wild
Journal:  J Comp Neurol       Date:  2010-06-01       Impact factor: 3.215

10.  Postnatal development of the endbulb of held in congenitally deaf cats.

Authors:  Christa A Baker; Karen L Montey; Tan Pongstaporn; David K Ryugo
Journal:  Front Neuroanat       Date:  2010-05-21       Impact factor: 3.856

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