Evidence map›Paper›PMID 25239455›Full record

ArticleThe Journal of physiology2014

The properties, distribution and function of Na(+)-Ca(2+) exchanger isoforms in rat cutaneous sensory neurons.

N N Scheff, E Yilmaz, M S Gold

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Role of NaInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Trafficking of Na+/Ca2+ exchanger to the site of persistent inflammation in nociceptive afferents.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    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

3 authors at 1 institution in 1 country.

N N ScheffThe Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, USA Department of Anesthesiology, University of Pittsburgh, Pittsburgh, PA, USA Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA, USA.
E YilmazThe Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, USA Department of Anesthesiology, University of Pittsburgh, Pittsburgh, PA, USA Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA, USA.
M S GoldThe Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, USA Department of Anesthesiology, University of Pittsburgh, Pittsburgh, PA, USA Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA, USA msg22@pitt.edu.
University of Pittsburgh · US

Funding

Mechanisms and Treatment of Dental PainR01DE018252 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GOLD, MICHAEL S · 2009 to 2013
$2.4M
NIDCR NIH HHS R01 DE018252NINDS NIH HHS F31-NS08466-1
6 · The paper itself

Abstract

The Na(+)-Ca(2+) exchanger (NCX) appears to play an important role in the regulation of the high K(+)-evoked Ca(2+) transient in putative nociceptive dorsal root ganglion (DRG) neurons. The purpose of the present study was to (1) characterize the properties of NCX activity in subpopulations of DRG neurons, (2) identify the isoform(s) underlying NCX activity, and (3) begin to assess the function of the isoform(s) in vivo. In retrogradely labelled neurons from the glabrous skin of adult male Sprague-Dawley rats, NCX activity, as assessed with fura-2-based microfluorimetry, was only detected in putative nociceptive IB4+ neurons. There were two modes of NCX activity: one was evoked in response to relatively large and long lasting (∼325 nm for >12 s) increases in the concentration of intracellular Ca(2+) ([Ca(2+)]i), and a second was active at resting [Ca(2+)]i > ∼150 nm. There also were two modes of evoked activity: one that decayed relatively rapidly (<5 min) and a second that persisted (>10 min). Whereas mRNA encoding all three NCX isoforms (NCX1-3) was detected in putative nociceptive cutaneous neurons with single cell PCR, pharmacological analysis and small interfering RNA (siRNA) knockdown of each isoform in vivo suggested that NCX2 and 3 were responsible for NCX activity. Western blot analyses suggested that NCX isoforms were differentially distributed within sensory neurons. Functional assays of excitability, action potential propagation, and nociceptive behaviour suggest NCX activity has little influence on excitability per se, but instead influences axonal conduction velocity, resting membrane potential, and nociceptive threshold. Together these results indicate that the function of NCX in the regulation of [Ca(2+)]i in putative nociceptive neurons may be unique relative to other cells in which these exchanger isoforms have been characterized and it has the potential to influence sensory neuron properties at multiple levels.

Indexed as

Action PotentialsAnimalsAxonsCalcium SignalingCells, CulturedMaleNociceptorsProtein IsoformsProtein TransportRatsRats, Sprague-DawleyRNA, MessengerSkinSodium-Calcium ExchangerProtein IsoformsRNA, MessengerSlc8a2 protein, ratSlc8a3 protein, ratSodium-Calcium Exchanger

Identifiers

PMID25239455
PMCPMC4259538
OpenAlexW1481528481

What OpenQuestion holds

Textmetadata
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.