Literature DB >> 8991457

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

K A Davis1, H F Voigt.   

Abstract

Computer simulations of a network model of an isofrequency patch of the dorsal cochlear nucleus (DCN) were run to explore possible mechanisms for the level-dependent features observed in the cross-correlograms of pairs of type IV units in the cat and nominal type IV units in the gerbil DCN. The computer model is based on the conceptual model (of a cat) that suggests two sources of shared input to DCN's projection neurons (type IV units): excitatory input for auditory nerves and inhibitory input from interneurons (type II units). Use of tonal stimuli is thought to cause competition between these sources resulting in the decorrelation of type IV unit activities at low levels. In the model, P-cells (projection neurons), representing type IV units, receive inhibitory input from I-cells (interneurons), representing type II units. Both sets of model neurons receive a simulated excitatory auditory nerve (AN) input from same-CF AN fibers, where the AN input is modeled as a dead-time modified Poisson process whose intensity is given by a computationally tractable discharge rate versus sound pressure level function. Subthreshold behavior of each model neuron is governed by a set of normalized state equations. The computer mode has previously been shown to reproduce the major response properties of both type IV and type II units (e.g., rate-level curves and peri-stimulus time histograms) and the level-dependence of the functional type II-type IV inhibitory interaction. This model is adapted for the gerbil by simulating a reduced population of I-cells. Simulations were carried out for several auditory nerve input levels, and cross-correlograms were computed from the activities of pairs of P-cells for a complete (cat model) and reduced (gerbil model) population of I-cells. The resultant correlograms show central mounds (CMs), indicative of either shared excitatory or inhibitory input, for both spontaneous and tone-evoked driven activities. Similar to experimental results, CM amplitudes are a non-monotonic function of level and CM widths decrease as a function of level. These results are consistent with the hypothesis that shared excitatory input correlates the spontaneous activities of type IV units adn shared inhibitory input correlates their driven activities. The results also suggest that the decorrelation of the activities of type IV units can result from a reduced effectiveness of the AN input as a function of increasing level. Thus, competition between the excitatory and inhibitory inputs is not required.

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Year:  1996        PMID: 8991457     DOI: 10.1007/bf00206708

Source DB:  PubMed          Journal:  Biol Cybern        ISSN: 0340-1200            Impact factor:   2.086


  41 in total

1.  Responses to tones and noise of single cells in dorsal cochlear nucleus of unanesthetized cats.

Authors:  E D Young; W E Brownell
Journal:  J Neurophysiol       Date:  1976-03       Impact factor: 2.714

2.  Morphology and physiology of cells in slice preparations of the dorsal cochlear nucleus of mice.

Authors:  D Oertel; S H Wu
Journal:  J Comp Neurol       Date:  1989-05-08       Impact factor: 3.215

3.  A model for repetitive firing in neurons.

Authors:  R J MacGregor; R M Oliver
Journal:  Kybernetik       Date:  1974

4.  The responses of single neurones in the cochlear nucleus of the cat as a function of their location and the anaesthetic state.

Authors:  E F Evans; P G Nelson
Journal:  Exp Brain Res       Date:  1973-06-29       Impact factor: 1.972

5.  Stellate neurons in rat dorsal cochlear nucleus studies with combined Golgi impregnation and electron microscopy: synaptic connections and mutual coupling by gap junctions.

Authors:  F G Wouterlood; E Mugnaini; K K Osen; A L Dahl
Journal:  J Neurocytol       Date:  1984-08

6.  Excitatory/inhibitory response types in the cochlear nucleus: relationships to discharge patterns and responses to electrical stimulation of the auditory nerve.

Authors:  W P Shofner; E D Young
Journal:  J Neurophysiol       Date:  1985-10       Impact factor: 2.714

7.  Stimulus dependent neural correlation: an example from the cochlear nucleus.

Authors:  H F Voigt; E D Young
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

8.  Identification of response properties of ascending axons from dorsal cochlear nucleus.

Authors:  E D Young
Journal:  Brain Res       Date:  1980-10-27       Impact factor: 3.252

9.  Neural modeling of the dorsal cochlear nucleus: cross-correlation analysis of short-duration tone-burst responses.

Authors:  K A Davis; H F Voigt
Journal:  Biol Cybern       Date:  1994       Impact factor: 2.086

10.  Distribution and targets of the cartwheel cell axon in the dorsal cochlear nucleus of the guinea pig.

Authors:  A S Berrebi; E Mugnaini
Journal:  Anat Embryol (Berl)       Date:  1991
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