Evidence map›Paper›PMID 41556370›Full record

ArticleJournal of neurochemistry2026

Sevoflurane Inhibits Layer 5 Pyramidal Neurons via Kv1.2-Dependent Modulation of Subthreshold Currents.

Aelton S Araujo, Gabriel M de Queiroz, Sérgio Ruschi B Silva, Werner Treptow, Katarina E Leao

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Aelton S AraujoHearing and Neuronal Activity Lab, Brain Institute, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0000-0001-5960-996X
Gabriel M de QueirozHearing and Neuronal Activity Lab, Brain Institute, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0009-0008-6685-5649
Sérgio Ruschi B SilvaHearing and Neuronal Activity Lab, Brain Institute, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0000-0003-0677-0439
Werner TreptowLaboratório de Biologia Teórica e Computacional, Departamento de Biologia Celular, Universidade de Brasília, Brasília, Brazil.ORCID https://orcid.org/0000-0003-4564-3205
Katarina E LeaoHearing and Neuronal Activity Lab, Brain Institute, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0000-0001-7295-1233

Funding

Conselho Nacional de Desenvolvimento Científico e TecnológicoCoordenação de Aperfeiçoamento de Pessoal de Nível SuperiorFundação de Apoio à Pesquisa do Distrito Federal 00193-00001721/2024-66
6 · The paper itself

Abstract

General anesthetics reduce cortical activity and disrupt consciousness, yet the molecular mechanisms underlying their effects on neocortical neurons remain incompletely understood. Recent evidence implicates layer 5 pyramidal neurons (L5 PNs) as critical targets, particularly through anesthetic-induced decoupling of distal apical dendritic inputs from somatic output. While several anesthetics impair L5 excitability, the ion channels mediating this effect have yet to be clearly identified. Voltage-gated Kv1.2 potassium channels have emerged as compelling candidates due to their high expression in L5 PNs and their known potentiation by volatile anesthetics. In this study, we investigated the effects of low-dose sevoflurane (~22 μM) on L5 PNs in the primary auditory cortex of adult mice using whole-cell patch-clamp recordings. Sevoflurane significantly suppressed firing and induced cell-type-specific changes in membrane properties: depolarizing the resting potential in type A neurons and increasing input resistance and altering action potential shape in type B neurons. Application of the selective Kv1.2 blocker TsTX-Kα partially reversed these effects at subthreshold membrane potentials, implicating Kv1.2 channel potentiation in the modulation of neuronal excitability. Supporting that view, NEURON simulations using a detailed biophysical model of thick-tufted L5b pyramidal neurons further revealed a significant sevoflurane-induced increase in persistent K

Indexed as

Anesthetics, InhalationKv1.2 Potassium ChannelPyramidal CellsSevofluraneAction PotentialsAnimalsAuditory CortexMaleMembrane PotentialsMiceMice, Inbred C57BLPatch-Clamp TechniquesAnesthetics, InhalationKv1.2 Potassium ChannelSevofluraneKv1.2layer 5primary auditory cortexpyramidal neuronsSevofluranevoltage‐gated potassium channels

Identifiers

PMID41556370
PMCPMC12817328

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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 Socratic graph.