Evidence map›Paper›PMID 22673325›Full record

ArticleJournal of neurophysiology2012

Sphingosine 1-phosphate receptor 2 antagonist JTE-013 increases the excitability of sensory neurons independently of the receptor.

Chao Li, Xian Xuan Chi, Wenrui Xie, J A Strong, J-M Zhang, G D Nicol

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. S1PScientific reports · 2019
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Chemical and genetic tools to explore S1P biology.Current topics in microbiology and immunology · 2014
    Review
  9. Article
  10. Synthesis and characterization of [Nuclear medicine and biology
    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

6 authors at 2 institutions in 1 country.

Chao LiMedical Neuroscience Program, School of Medicine, Indiana University, Indianapolis, IN, USA.
Xian Xuan Chi
Wenrui Xie
J A Strong
J-M Zhang
G D Nicol
Indiana University – Purdue University Indianapolis · USUniversity of Cincinnati Medical Center · US

Funding

EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR015481 · NCRR · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIFE, ROSE S · 2001 to 2001
$1.6M
Neurotrophic factors and excitabilityR01NS046084 · NINDS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI NICOL, GRANT D · 2003 to 2007
$1.3M
Sphingosine 1-Phosphate Receptors and Sensitization of Sensory NeuronsR01NS060853 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI NICOL, GRANT D · 2009 to 2010
$1.1M
NCRR NIH HHS C06 RR-015481-01NINDS NIH HHS R01 NS-046084NINDS NIH HHS R01 NS046084NINDS NIH HHS R01 NS-060853NINDS NIH HHS R01 NS060853
6 · The paper itself

Abstract

Previously we demonstrated that sphingosine 1-phosphate receptor 1 (S1PR(1)) played a prominent, but not exclusive, role in enhancing the excitability of small-diameter sensory neurons, suggesting that other S1PRs can modulate neuronal excitability. To examine the potential role of S1PR(2) in regulating neuronal excitability we used the established selective antagonist of S1PR(2), JTE-013. Here we report that exposure to JTE-013 alone produced a significant increase in excitability in a time- and concentration-dependent manner in 70-80% of recorded neurons. Internal perfusion of sensory neurons with guanosine 5'-O-(2-thiodiphosphate) (GDP-β-S) via the recording pipette inhibited the sensitization produced by JTE-013 as well as prostaglandin E(2). Pretreatment with pertussis toxin or the selective S1PR(1) antagonist W146 blocked the sensitization produced by JTE-013. These results indicate that JTE-013 might act as an agonist at other G protein-coupled receptors. In neurons that were sensitized by JTE-013, single-cell RT-PCR studies demonstrated that these neurons did not express the mRNA for S1PR(2). In behavioral studies, injection of JTE-013 into the rat's hindpaw produced a significant increase in the mechanical sensitivity in the ipsilateral, but not contralateral, paw. Injection of JTE-013 did not affect the withdrawal latency to thermal stimulation. Thus JTE-013 augments neuronal excitability independently of S1PR(2) by unknown mechanisms that may involve activation of other G protein-coupled receptors such as S1PR(1). Clearly, further studies are warranted to establish the causal nature of this increased sensitivity, and future studies of neuronal function using JTE-013 should be interpreted with caution.

Indexed as

Action PotentialsAnalysis of VarianceAnilidesAnimalsCapsaicinCell Line, TumorCell MovementDinoprostoneDose-Response Relationship, DrugDrug InteractionsGanglia, SpinalGuanosine DiphosphateHyperalgesiaLysophospholipidsMaleMelanoma3-amino-4-(3-hexylphenylamino)-4-oxobutylphosphonic acidAnilidesCapsaicinDinoprostoneguanosine 5'-O-(2-thiodiphosphate)Guanosine DiphosphateJTE 013LysophospholipidsOrganophosphonatesPertussis ToxinPyrazolesPyridinesReceptors, LysosphingolipidSensory System AgentsSphingosinesphingosine 1-phosphateThionucleotides

Identifiers

PMID22673325
PMCPMC3544961
OpenAlexW2079483965

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.