Evidence map›Paper›PMID 29282613›Full record

ReviewNeuroscience bulletin2018

Regulation of Pain and Itch by TRP Channels.

Carlene Moore, Rupali Gupta, Sven-Eric Jordt, Yong Chen, Wolfgang B Liedtke

Open access · greenAbstract readReview
In one paragraph

Review in Neuroscience bulletin, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 188 papers.

0numbers the graph read from it
0cells of the map it votes in
188citing papers in PubMed
12.2field-weighted citation impact, top 1% 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

188 citing papers in PubMed, 306 citations in OpenAlex.

  1. [Efficacy analysis of anti-migraine therapy for acute low-frequency hearing loss and investigation of its mechanisms].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2025
    Trial
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  12. Molecular divergence ofZoological research · 2026
    Article
  13. Article
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  18. Article
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128 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Carlene MooreDepartment of Neurology, Duke University Medical Center, Durham, NC, 27710, USA.
Rupali GuptaDepartment of Neurology, Duke University Medical Center, Durham, NC, 27710, USA.
Sven-Eric JordtDepartment of Anesthesiology, Duke University Medical Center, Durham, NC, 27710, USA.
Yong ChenDepartment of Neurology, Duke University Medical Center, Durham, NC, 27710, USA. yong.chen@duke.edu.ORCID http://orcid.org/0000-0001-8824-7187
Wolfgang B LiedtkeDepartment of Neurology, Duke University Medical Center, Durham, NC, 27710, USA. liedt001@duke.edu.ORCID http://orcid.org/0000-0003-4166-5394
Duke Medical Center · USDuke University · US

Funding

Duke CTSA (Composite)UL1TR001117 · NCATS · DUKE UNIVERSITY · PI BOULWARE, LEIGH E, LI, JENNIFER S · 2013 to 2017
$41.3M
Mechanical and Osmotic Signaling in ChondrocytesR01AR048182 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2003 to 2013
$3.0M
Role of trpv4 in trigeminally mediated nociceptionR01DE018549 · NIDCR · DUKE UNIVERSITY · PI LIEDTKE, WOLFGANG B. · 2007 to 2011
$2.5M
Biomedical Researcher Development Program in TMJD and Orofacial PainK12DE022793 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIM, PEI FENG, MAIXNER, WILLIAM · 2012 to 2016
$1.3M
Tissue Procurement and Analysis CoreP30AR066527 · NIAMS · DUKE UNIVERSITY · PI HALL, RUSSELL P. · 2014 to 2015
$1.3M
Masticatory sensitization of trigeminal ganglion sensory neuronsF33DE024668 · NIDCR · DUKE UNIVERSITY · PI CHEN, YONG · 2014 to 2014
$53k
NCATS NIH HHS UL1 TR001117NIAMS NIH HHS P30 AR066527NIAMS NIH HHS R01 AR048182NIDCR NIH HHS F33 DE024668NIDCR NIH HHS K12 DE022793NIDCR NIH HHS R01 DE018549
6 · The paper itself

Abstract

Nociception is an important physiological process that detects harmful signals and results in pain perception. In this review, we discuss important experimental evidence involving some TRP ion channels as molecular sensors of chemical, thermal, and mechanical noxious stimuli to evoke the pain and itch sensations. Among them are the TRPA1 channel, members of the vanilloid subfamily (TRPV1, TRPV3, and TRPV4), and finally members of the melastatin group (TRPM2, TRPM3, and TRPM8). Given that pain and itch are pro-survival, evolutionarily-honed protective mechanisms, care has to be exercised when developing inhibitory/modulatory compounds targeting specific pain/itch-TRPs so that physiological protective mechanisms are not disabled to a degree that stimulus-mediated injury can occur. Such events have impeded the development of safe and effective TRPV1-modulating compounds and have diverted substantial resources. A beneficial outcome can be readily accomplished via simple dosing strategies, and also by incorporating medicinal chemistry design features during compound design and synthesis. Beyond clinical use, where compounds that target more than one channel might have a place and possibly have advantageous features, highly specific and high-potency compounds will be helpful in mechanistic discovery at the structure-function level.

Indexed as

AnimalsHumansPainPruritusTransient Receptor Potential ChannelsTransient Receptor Potential ChannelsAllodyniaHyperalgesiaInflammationItchLipidsMechanotransductionNerve damageNeuropathic painNociceptorsPainTemperatureTRP channels

Identifiers

PMID29282613
PMCPMC5799130
OpenAlexW2776648429

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.