Literature DB >> 8326065

Regularity of cochlear nucleus stellate cells: a computational modeling study.

M J Hewitt1, R Meddis.   

Abstract

This article reports on a computational modeling study designed to investigate the generation of the transient chopper response of cochlear nucleus stellate cells. The model is based on a simulation of the auditory periphery which feeds a generic stellate-cell model. Physiological recordings of transient chopper units in response to short, best frequency, tone bursts show a brief initial period (typically < 10 ms) of rapid rate adaptation as evidenced by a rapid rise in mean interspike interval. Associated with this rate adaptation is a significant increase in firing irregularity. The changes in rate and irregularity have recently been attributed to the activation of noisy inhibitory inputs on the cell [e.g., Banks and Sachs, J. Neurophysiol. 65, 606-629 (1991)]. However, the results show that the transient chopper response pattern can be generated without the need for inhibitory inputs. The transience of the initial chopping pattern is sensitive to the following model parameters: (a) the firing threshold of the cell, (b) the number of excitatory inputs that converge on the cell, and (c) the magnitude of the current delivered to the cell for each active input. The response was also found to be relatively insensitive to changes in the degree of dendritic filtering imposed on the auditory-nerve input. The results of each simulation can be explained by considering the pattern of depolarization the cell receives during the course of a tone burst.

Mesh:

Year:  1993        PMID: 8326065     DOI: 10.1121/1.405694

Source DB:  PubMed          Journal:  J Acoust Soc Am        ISSN: 0001-4966            Impact factor:   1.840


  8 in total

1.  Physiological correlates of comodulation masking release in the mammalian ventral cochlear nucleus.

Authors:  D Pressnitzer; R Meddis; R Delahaye; I M Winter
Journal:  J Neurosci       Date:  2001-08-15       Impact factor: 6.167

2.  Auditory nerve inputs to cochlear nucleus neurons studied with cross-correlation.

Authors:  E D Young; M B Sachs
Journal:  Neuroscience       Date:  2008-02-05       Impact factor: 3.590

3.  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

4.  Mode-locked spike trains in responses of ventral cochlear nucleus chopper and onset neurons to periodic stimuli.

Authors:  Jonathan Laudanski; Stephen Coombes; Alan R Palmer; Christian J Sumner
Journal:  J Neurophysiol       Date:  2009-12-30       Impact factor: 2.714

5.  Emergence of band-pass filtering through adaptive spiking in the owl's cochlear nucleus.

Authors:  Bertrand Fontaine; Katrina M MacLeod; Susan T Lubejko; Louisa J Steinberg; Christine Köppl; Jose L Peña
Journal:  J Neurophysiol       Date:  2014-04-30       Impact factor: 2.714

6.  Somatosensory inputs modify auditory spike timing in dorsal cochlear nucleus principal cells.

Authors:  Seth D Koehler; Shashwati Pradhan; Paul B Manis; Susan E Shore
Journal:  Eur J Neurosci       Date:  2010-12-29       Impact factor: 3.386

7.  A biophysical modelling platform of the cochlear nucleus and other auditory circuits: From channels to networks.

Authors:  Paul B Manis; Luke Campagnola
Journal:  Hear Res       Date:  2017-12-28       Impact factor: 3.208

8.  Neuronal spike-train responses in the presence of threshold noise.

Authors:  S Coombes; R Thul; J Laudanski; A R Palmer; C J Sumner
Journal:  Front Life Sci       Date:  2012-03-26       Impact factor: 2.000

  8 in total

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