Evidence map›Paper›PMID 29928032›Full record

ArticlePloS one2018

Activation of TREK currents by riluzole in three subgroups of cultured mouse nodose ganglion neurons.

Diego Fernández-Fernández, Alba Cadaveira-Mosquera, Lola Rueda-Ruzafa, Salvador Herrera-Pérez, Emma L Veale, Antonio Reboreda, Alistair Mathie, J Antonio Lamas

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Pulmonary Sensory Receptors.Advances in anatomy, embryology, and cell biology · 2021
    Article
  6. Article
  7. Functional Exploration of the Pulmonary NEB ME.Advances in anatomy, embryology, and cell biology · 2021
    Article
  8. Review
  9. Are TREK Channels Temperature Sensors?Frontiers in cellular neuroscience · 2021
    Review
  10. Article
  11. Review
  12. Ion Channels and Thermosensitivity: TRP, TREK, or Both?International journal of molecular sciences · 2019
    Review
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

8 authors at 2 institutions in 2 countries.

Diego Fernández-FernándezDepartment of Functional Biology and Health Sciences, Faculty of Biology-CINBIO, University of Vigo, Vigo, Galicia, Spain.ORCID 0000-0003-1431-3705
Alba Cadaveira-MosqueraDepartment of Functional Biology and Health Sciences, Faculty of Biology-CINBIO, University of Vigo, Vigo, Galicia, Spain.
Lola Rueda-RuzafaDepartment of Functional Biology and Health Sciences, Faculty of Biology-CINBIO, University of Vigo, Vigo, Galicia, Spain.
Salvador Herrera-PérezDepartment of Functional Biology and Health Sciences, Faculty of Biology-CINBIO, University of Vigo, Vigo, Galicia, Spain.
Emma L VealeMedway School of Pharmacy, University of Kent, Chatham Maritime, Kent, United Kingdom.ORCID 0000-0002-6778-9929
Antonio ReboredaDepartment of Functional Biology and Health Sciences, Faculty of Biology-CINBIO, University of Vigo, Vigo, Galicia, Spain.
Alistair MathieMedway School of Pharmacy, University of Kent, Chatham Maritime, Kent, United Kingdom.
J Antonio LamasDepartment of Functional Biology and Health Sciences, Faculty of Biology-CINBIO, University of Vigo, Vigo, Galicia, Spain.
Universidade de Vigo · ESMedway School of Pharmacy · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two-pore domain potassium channels (K2P) constitute major candidates for the regulation of background potassium currents in mammalian cells. Channels of the TREK subfamily are also well positioned to play an important role in sensory transduction due to their sensitivity to a large number of physiological and physical stimuli (pH, mechanical, temperature). Following our previous report describing the molecular expression of different K2P channels in the vagal sensory system, here we confirm that TREK channels are functionally expressed in neurons from the mouse nodose ganglion (mNG). Neurons were subdivided into three groups (A, Ah and C) based on their response to tetrodotoxin and capsaicin. Application of the TREK subfamily activator riluzole to isolated mNG neurons evoked a concentration-dependent outward current in the majority of cells from all the three subtypes studied. Riluzole increased membrane conductance and hyperpolarized the membrane potential by approximately 10 mV when applied to resting neurons. The resting potential was similar in all three groups, but C cells were clearly less excitable and showed smaller hyperpolarization-activated currents at -100 mV and smaller sustained currents at -30 mV. Our results indicate that the TREK subfamily of K2P channels might play an important role in the maintenance of the resting membrane potential in sensory neurons of the autonomic nervous system, suggesting its participation in the modulation of vagal reflexes.

Indexed as

Action PotentialsAnimalsCapsaicinCells, CulturedHumansIon Channel GatingMiceNeuronsNodose GanglionPotassium Channels, Tandem Pore DomainRiluzoleTetrodotoxinCapsaicinPotassium Channels, Tandem Pore DomainRiluzoleTetrodotoxin

Identifiers

PMID29928032
PMCPMC6013220
OpenAlexW2808926562

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.