Evidence map›Paper›PMID 24336653›Full record

ArticleAmerican journal of physiology. Cell physiology2014

Acid-sensing ion channels 1a (ASIC1a) inhibit neuromuscular transmission in female mice.

Francisco J Urbano, Noelia G Lino, Carlota M F González-Inchauspe, Laura E González, Natalia Colettis, Lucas G Vattino, Amanda M Wunsch, John A Wemmie, Osvaldo D Uchitel

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.4field-weighted citation impact, top 35% of its field
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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Acid-sensing ion channels as sensors of brain metabolic state.Pflugers Archiv : European journal of physiology · 2026
    Review
  2. Article
  3. Postsynaptic Calcium Extrusion at the Mouse Neuromuscular Junction Alkalinizes the Synaptic Cleft.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. TheThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  11. Acid-Sensing Ion Channels Activated by Evoked Released Protons Modulate Synaptic Transmission at the Mouse Calyx of Held Synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  12. Article
  13. 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

9 authors at 3 institutions in 2 countries.

Francisco J UrbanoLaboratorio de Fisiología y Biología Molecular (LFBM), Instituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE, UBA-CONICET), Intendente Güiraldes 2160, Ciudad Universitaria, Buenos Aires, Argentina; and.
Noelia G Lino
Carlota M F González-Inchauspe
Laura E González
Natalia Colettis
Lucas G Vattino
Amanda M Wunsch
John A Wemmie
Osvaldo D Uchitel
Experimental Medicine and Biology Institute · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARUniversity of Iowa · US

Funding

Brain pH and Acid Sensing in Depression-Related BehaviorI01BX000741 · VA · IOWA CITY VA MEDICAL CENTER · PI WEMMIE, JOHN A · 2011 to 2018
–
BLRD VA I01 BX000741Wellcome Trust 068941/Z/02/Z
6 · The paper itself

Abstract

Acid-sensing ion channels (ASIC) open in response to extracellular acidosis. ASIC1a, a particular subtype of these channels, has been described to have a postsynaptic distribution in the brain, being involved not only in ischemia and epilepsy, but also in fear and psychiatric pathologies. High-frequency stimulation of skeletal motor nerve terminals (MNTs) can induce presynaptic pH changes in combination with an acidification of the synaptic cleft, known to contribute to muscle fatigue. Here, we studied the role of ASIC1a channels on neuromuscular transmission. We combined a behavioral wire hanging test with electrophysiology, pharmacological, and immunofluorescence techniques to compare wild-type and ASIC1a lacking mice (ASIC1a (-/-) knockout). Our results showed that 1) ASIC1a (-/-) female mice were weaker than wild type, presenting shorter times during the wire hanging test; 2) spontaneous neurotransmitter release was reduced by ASIC1a activation, suggesting a presynaptic location of these channels at individual MNTs; 3) ASIC1a-mediated effects were emulated by extracellular local application of acid saline solutions (pH = 6.0; HEPES/MES-based solution); and 4) immunofluorescence techniques revealed the presence of ASIC1a antigens on MNTs. These results suggest that ASIC1a channels might be involved in controlling neuromuscular transmission, muscle contraction and fatigue in female mice.

Indexed as

Synaptic TransmissionAcid Sensing Ion ChannelsAnimalsBehavior, AnimalElectric StimulationEvoked Potentials, MotorFemaleHand StrengthHydrogen-Ion ConcentrationMaleMiceMice, KnockoutMotor EndplateMotor NeuronsMuscle ContractionMuscle FatigueAcid Sensing Ion ChannelsASIC1 protein, mouseacid-sensing ion channelsextracellular acidosismotor nerve transmissionpresynaptic modulationwire hanging

Identifiers

PMID24336653
PMCPMC3919981
OpenAlexW2007897339

What OpenQuestion 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 OpenQuestion graph.