Evidence map›Paper›PMID 41984937›Full record

ArticlePLoS computational biology2026

On the role of L-type Ca2+ and BK channels in a biophysical model of cartwheel interneurons.

Matteo Martin, Jonathan E Rubin, Morten Gram Pedersen

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Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Matteo MartinDepartment of Information Engineering, University of Padova, Padova, Italy.
Jonathan E RubinDepartment of Mathematics, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.ORCID 0000-0002-1513-1551
Morten Gram PedersenDepartment of Information Engineering, University of Padova, Padova, Italy.ORCID 0000-0002-2639-2394

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cartwheel interneurons (CWCs) in the auditory system, which contribute to auditory processing and pathologies, exhibit a range of activity patterns, including bursting, spiking, and complex spiking. Although experiments have shown how these patterns can vary across individual neurons, the field has lacked a computational framework in which to explore the contributions of particular currents to these observations and to generate new predictions about the effects of pharmacological manipulations. We present a conductance-based CWC computational model, which captures the diversity of CWC activity patterns observed experimentally and suggests parameter changes that may underlie differences across cells. Specifically, we show using direct simulations and bifurcation diagrams that one parameter tuning yields a regular spiking phenotype in which the onset of activity, as input current is increased, takes the form of regular spiking and other tuning that gives a complex spiking phenotype in which bursting occurs at the spike onset and regular spiking only occurs over a narrow input range before it gives way to complex spiking. We next investigate the effects of the BK-type potassium current blocker iberiotoxin and the L-type calcium current blocker nifedipine. Our model reproduces the transitions to complex spiking and regular spiking, respectively, observed experimentally when these drugs are administered. In addition to the full model, we present a reduced model that preserves CWC dynamic regimes. We classify the reduced model variables in terms of distinct dynamic timescales and show that the key transitions in dynamic patterns under administration of iberiotoxin and nifedipine can be explained based on equilibria of the averaged dynamics of the slowest model variables, in a regime where the faster model variables exhibit oscillations. Overall, this study predicts how changes in parameters will influence CWC behavior, suggests how bifurcations contribute to changes in CWC dynamics, and provides a theoretical foundation that supports our simulation findings.

Indexed as

Calcium Channels, L-TypeInterneuronsLarge-Conductance Calcium-Activated Potassium ChannelsModels, NeurologicalAction PotentialsAnimalsComputational BiologyComputer SimulationNifedipinePeptidesCalcium Channels, L-TypeiberiotoxinLarge-Conductance Calcium-Activated Potassium ChannelsNifedipinePeptides

Identifiers

PMID41984937
PMCPMC13143179

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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.