Evidence map›Paper›PMID 31881018›Full record

ArticlePLoS computational biology2019

Neuronal population model of globular bushy cells covering unit-to-unit variability.

Go Ashida, Helen T Heinermann, Jutta Kretzberg

Abstract read
In one paragraph

Article in PLoS computational biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Go AshidaCluster of Excellence "Hearing4all", Department of Neuroscience, University of Oldenburg, Oldenburg, Germany.ORCID 0000-0002-8886-1213
Helen T HeinermannCluster of Excellence "Hearing4all", Department of Neuroscience, University of Oldenburg, Oldenburg, Germany.
Jutta KretzbergCluster of Excellence "Hearing4all", Department of Neuroscience, University of Oldenburg, Oldenburg, Germany.ORCID 0000-0001-9153-9324

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Computations of acoustic information along the central auditory pathways start in the cochlear nucleus. Bushy cells in the anteroventral cochlear nucleus, which innervate monaural and binaural stations in the superior olivary complex, process and transfer temporal cues relevant for sound localization. These cells are categorized into two groups: spherical and globular bushy cells (SBCs/GBCs). Spontaneous rates of GBCs innervated by multiple auditory nerve (AN) fibers are generally lower than those of SBCs that receive a small number of large AN synapses. In response to low-frequency tonal stimulation, both types of bushy cells show improved phase-locking and entrainment compared to AN fibers. When driven by high-frequency tones, GBCs show primary-like-with-notch or onset-L peristimulus time histograms and relatively irregular spiking. However, previous in vivo physiological studies of bushy cells also found considerable unit-to-unit variability in these response patterns. Here we present a population of models that can simulate the observed variation in GBCs. We used a simple coincidence detection model with an adaptive threshold and systematically varied its six parameters. Out of 567000 parameter combinations tested, 7520 primary-like-with-notch models and 4094 onset-L models were selected that satisfied a set of physiological criteria for a GBC unit. Analyses of the model parameters and output measures revealed that the parameters of the accepted model population are weakly correlated with each other to retain major GBC properties, and that the output spiking patterns of the model are affected by a combination of multiple parameters. Simulations of frequency-dependent temporal properties of the model GBCs showed a reasonable fit to empirical data, supporting the validity of our population modeling. The computational simplicity and efficiency of the model structure makes our approach suitable for future large-scale simulations of binaural information processing that may involve thousands of GBC units.

Indexed as

Models, NeurologicalAcoustic StimulationAction PotentialsAnimalsAuditory PathwaysCochlear NerveCochlear NucleusComputational BiologyNeuronsSynaptic Transmission

Identifiers

PMID31881018
PMCPMC6934273

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.