Evidence map›Paper›PMID 42584764›Full record

ArticleJournal of the Association for Research in Otolaryngology : JARO2026

Impacts of Kv3.1 Channels on Action Potentials in Fusiform Neurons From the Dorsal Cochlear Nucleus of Mice Before and After Hearing Onset.

Mario Henrique Lopes Duarte de Oliveira, Alan Eidi Sasaki, Leonardo Calaça Arruda Vanderlei, Ricardo Mauricio Leão

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Article in Journal of the Association for Research in Otolaryngology : JARO, 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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5 · Who and what money

Authors and funding

4 authors.

Mario Henrique Lopes Duarte de OliveiraLaboratory of Neurophysiology and Synapse, Department of Physiology, School of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.
Alan Eidi SasakiLaboratory of Neurophysiology and Synapse, Department of Physiology, School of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.
Leonardo Calaça Arruda VanderleiLaboratory of Neurophysiology and Synapse, Department of Physiology, School of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.
Ricardo Mauricio LeãoLaboratory of Neurophysiology and Synapse, Department of Physiology, School of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil. leaor@fmrp.usp.br.ORCID http://orcid.org/0000-0002-3829-3342

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Finance code-0001Fundação de Amparo à Pesquisa do Estado de São Paulo 2022/14196-3
6 · The paper itself

Abstract

purposeKv3.1 channels are high-voltage-activated potassium channels that facilitate high-frequency firing in auditory brainstem neurons. Fusiform neurons in the dorsal cochlear nucleus (DCN) can fire rapid trains of action potentials and express Kv3.1 channels. Their ability to fire high-frequency action potential trains increases after hearing onset at postnatal day 14. Simultaneously, the action potentials become shorter and faster. We tested whether Kv3.1 channels drive the developmental maturation of action potentials in DCN fusiform neurons.

methodsWe used Swiss female mice from postnatal day 8 to 25 and divided them into pre-hearing (< P14) and post-hearing (> P14). We measured Kv currents and action potentials in whole-cell patch-clamp. Tetraethylammonium (TEA) was applied at a concentration of 1-5 mM to block Kv3 channels, and we detected the expression of Kv3.1b channel subunits by immunocytochemistry.

resultsWe found increased Kv3.1b subunit expression in the DCN after hearing onset, suggesting that this subunit could be responsible for the electrophysiological changes in post-hearing fusiform neurons. TEA-sensitive high-threshold currents were a significant component of voltage-dependent potassium currents in both pre- and post-hearing fusiform neurons, with similar magnitudes in both groups. However, blocking Kv3 currents with 1-5 mM TEA broadens action potential waveforms in neurons from both groups while maintaining the developmental differences between groups. On the other hand, TEA was more effective at reducing the firing of post-hearing neurons.

conclusionsWe conclude that the rise in Kv3.1b channel expression in DCN fusiform neurons after hearing does not account for the shorter, faster action potentials observed at that time, but could contribute to their ability to fire action potentials at high frequencies.

Indexed as

Action potentialCochlear nucleusDevelopmentHearingKv3

Identifiers

PMID42584764

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