Evidence map›Paper›PMID 41187206›Full record

ArticlePLoS biology2025

Zebrafish fast muscle contractions avoid the mammalian requirement for voltage-gated Na+ channels.

Léa Demesmay, Romane Idoux, Christine Berthier, Claire Bernat, Léon Espinosa, Vincent Jacquemond, Frédéric Brunet, Angel Maunier-Mercier, Philippe Lory, Sophie Nicole and 1 more

Abstract read
In one paragraph

Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Léa DemesmayPhysiopathologie et Génétique du Neurone et du Muscle, CNRS 5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.
Romane IdouxPhysiopathologie et Génétique du Neurone et du Muscle, CNRS 5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.
Christine BerthierPhysiopathologie et Génétique du Neurone et du Muscle, CNRS 5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.
Claire BernatIGF, Univ Montpellier, CNRS, Inserm, Montpellier, France.
Léon EspinosaLaboratoire de chimie bactérienne, CNRS 7283, Aix-Marseille Université, Marseille, France.
Vincent JacquemondPhysiopathologie et Génétique du Neurone et du Muscle, CNRS 5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.
Frédéric BrunetInstitut de Génomique Fonctionnelle de Lyon, ENS Lyon, CNRS 5242, INRA USC1370, Université Claude Bernard Lyon 1, Lyon, France.
Angel Maunier-MercierIGF, Univ Montpellier, CNRS, Inserm, Montpellier, France.
Philippe LoryIGF, Univ Montpellier, CNRS, Inserm, Montpellier, France.
Sophie NicoleIGF, Univ Montpellier, CNRS, Inserm, Montpellier, France.
Bruno AllardPhysiopathologie et Génétique du Neurone et du Muscle, CNRS 5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.

Funding

Centre National de la Recherche ScientifiqueInstitut National de la Santé et de la Recherche MédicaleInstitut National de Recherche pour l’Agriculture
6 · The paper itself

Abstract

Fast skeletal muscle fibers from zebrafish share a number of functional properties with mammalian twitch muscle fibers, making this vertebrate a precious model to investigate the pathophysiology of neuromuscular disorders. We previously reported that action potentials (APs) from zebrafish fast fibers exhibit low amplitude and require unusually strong negative resting membrane voltage levels to be elicited. In this study, using voltage-clamp and current-clamp techniques, we explored the properties of voltage-gated Na+ channels (NaV) responsible for initiation and propagation of AP in isolated adult zebrafish fast skeletal muscle fibers and compared them to mouse fast-twitch muscle fibers using the same experimental conditions. We found that kinetics of activation and inactivation of NaV were faster in zebrafish fibers and, overall, that the voltage-dependence of inactivation was shifted by 25 mV toward negative voltages as compared to mouse fibers, yielding a mean half-inactivation potential of -90 mV. In agreement with these findings, recording of APs at various resting membrane potentials indicated that APs vanished for resting membrane potentials less negative than -80 mV in zebrafish, whereas APs could still be elicited from resting membrane potentials as low as -60 mV in mice. In addition, Ca2+ transients induced by field stimulation were insensitive to Na+ current blockade in zebrafish but not in mouse fibers. Fluorescence labeling of nicotinic acetylcholine receptors showed that zebrafish fast fibers were multi-innervated with a mean distance between extra-synaptic sarcolemma and motor endplates of 14 µm, expected to lead to negligible attenuation of depolarization propagated from endplates. Finally, knock out of the two genes encoding pore-forming NaV subunits in zebrafish muscles did not induce any change in locomotion and escape behavior of the animals. Taken together, these data question the role of NaV and the occurrence of APs in zebrafish fast muscle.

Indexed as

Muscle ContractionMuscle Fibers, Fast-TwitchVoltage-Gated Sodium ChannelsZebrafishAction PotentialsAnimalsCalciumMembrane PotentialsMicePatch-Clamp TechniquesZebrafish ProteinsCalciumVoltage-Gated Sodium ChannelsZebrafish Proteins

Identifiers

PMID41187206
PMCPMC12604801

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.