Evidence map›Paper›PMID 37068087›Full record

ArticlePLoS computational biology2023

Dual contribution of ASIC1a channels in the spinal processing of pain information by deep projection neurons revealed by computational modeling.

Magda Chafaï, Ariane Delrocq, Perrine Inquimbert, Ludivine Pidoux, Kevin Delanoe, Maurizio Toft, Frederic Brau, Eric Lingueglia, Romain Veltz, Emmanuel Deval

Abstract read
In one paragraph

Article in PLoS computational biology, 2023. 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

10 authors.

Magda ChafaïUniversité Côte d'Azur, CNRS, IPMC, LabEx ICST, FHU InovPain, France.
Ariane DelrocqUniversité Côte d'Azur, CNRS, IPMC, LabEx ICST, FHU InovPain, France.ORCID 0000-0002-8641-0857
Perrine InquimbertUniversité de Strasbourg, CNRS, Institut des Neurosciences Cellulaires et Intégratives, Strasbourg, France.
Ludivine PidouxUniversité Côte d'Azur, CNRS, IPMC, LabEx ICST, FHU InovPain, France.ORCID 0000-0002-5268-4067
Kevin DelanoeUniversité Côte d'Azur, CNRS, IPMC, LabEx ICST, FHU InovPain, France.ORCID 0000-0001-6138-101X
Maurizio ToftUniversité Côte d'Azur, CNRS, IPMC, LabEx ICST, FHU InovPain, France.
Frederic BrauUniversité Côte d'Azur, CNRS, IPMC, LabEx ICST, FHU InovPain, France.
Eric LinguegliaUniversité Côte d'Azur, CNRS, IPMC, LabEx ICST, FHU InovPain, France.ORCID 0000-0003-3902-3405
Romain VeltzInria Center of University Côte d'Azur, France, Valbonne, France.
Emmanuel DevalUniversité Côte d'Azur, CNRS, IPMC, LabEx ICST, FHU InovPain, France.ORCID 0000-0002-0215-9379

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dorsal horn of the spinal cord is an important crossroad of pain neuraxis, especially for the neuronal plasticity mechanisms that can lead to chronic pain states. Windup is a well-known spinal pain facilitation process initially described several decades ago, but its exact mechanism is still not fully understood. Here, we combine both ex vivo and in vivo electrophysiological recordings of rat spinal neurons with computational modeling to demonstrate a role for ASIC1a-containing channels in the windup process. Spinal application of the ASIC1a inhibitory venom peptides mambalgin-1 and psalmotoxin-1 (PcTx1) significantly reduces the ability of deep wide dynamic range (WDR) neurons to develop windup in vivo. All deep WDR-like neurons recorded from spinal slices exhibit an ASIC current with biophysical and pharmacological characteristics consistent with functional expression of ASIC1a homomeric channels. A computational model of WDR neuron supplemented with different ASIC1a channel parameters accurately reproduces the experimental data, further supporting a positive contribution of these channels to windup. It also predicts a calcium-dependent windup decrease for elevated ASIC conductances, a phenomenon that was experimentally validated using the Texas coral snake ASIC-activating toxin (MitTx) and calcium-activated potassium channel inhibitory peptides (apamin and iberiotoxin). This study supports a dual contribution to windup of calcium permeable ASIC1a channels in deep laminae projecting neurons, promoting it upon moderate channel activity, but ultimately leading to calcium-dependent windup inhibition associated to potassium channels when activity increases.

Indexed as

CalciumPainAnimalsApaminComputer SimulationNeuronsPeptidesRatsApaminCalciumiberiotoxinPeptides

Identifiers

PMID37068087
PMCPMC10109503

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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.