Evidence map›Paper›PMID 29561265›Full record

ArticleeLife2018

A zebrafish and mouse model for selective pruritus via direct activation of TRPA1.

Kali Esancy, Logan Condon, Jing Feng, Corinna Kimball, Andrew Curtright, Ajay Dhaka

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 49 citations in OpenAlex.

  1. TRPA1 Channels as Multimodal Environmental Sensors: Structure-Function Insights From Aquatic Organisms.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  2. The Pro- But Not Antinociceptive Effects of Cannabidiol Depend on Trpa1b in Larval Zebrafish.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
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  6. Single-Cell Analysis of Rohon-Beard Neurons Implicates Fgf Signaling in Axon Maintenance and Cell Survival.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  7. Article
  8. Heterocyclic chalcone (3 Biotech · 2023
    Article
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  11. Frontiers in physiology · 2023
    Article
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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 1 institution in 1 country.

Kali Esancy *Department of Biological Structure, University of Washington, Seattle, United States.
Logan Condon *Department of Biological Structure, University of Washington, Seattle, United States.
Jing Feng *Center for the Study of Itch, Washington University, St. Louis, United States.
Corinna KimballDepartment of Biological Structure, University of Washington, Seattle, United States.
Andrew CurtrightDepartment of Biological Structure, University of Washington, Seattle, United States.
Ajay DhakaDepartment of Biological Structure, University of Washington, Seattle, United States.ORCID http://orcid.org/0000-0001-5783-8582
University of Washington · US

Funding

A genetic screen for modulators of nociceptionR01DE023730 · NIDCR · UNIVERSITY OF WASHINGTON · PI DHAKA, AJAY K · 2013 to 2017
$1.9M
NIDCR NIH HHS R01 DE023730NIH HHS R01DE23730
6 · The paper itself

Abstract

Little is known about the capacity of lower vertebrates to experience itch. A screen of itch-inducing compounds (pruritogens) in zebrafish larvae yielded a single pruritogen, the TLR7 agonist imiquimod, that elicited a somatosensory neuron response. Imiquimod induced itch-like behaviors in zebrafish distinct from those induced by the noxious TRPA1 agonist, allyl isothiocyanate. In the zebrafish, imiquimod-evoked somatosensory neuronal responses and behaviors were entirely dependent upon TRPA1, while in the mouse TRPA1 was required for the direct activation of somatosensory neurons and partially responsible for behaviors elicited by this pruritogen. Imiquimod was found to be a direct but weak TRPA1 agonist that activated a subset of TRPA1 expressing neurons. Imiquimod-responsive TRPA1 expressing neurons were significantly more sensitive to noxious stimuli than other TRPA1 expressing neurons. Together, these results suggest a model for selective itch via activation of a specialized subpopulation of somatosensory neurons with a heightened sensitivity to noxious stimuli.

Indexed as

Disease Models, AnimalAnimalsAnimals, Genetically ModifiedEvoked Potentials, SomatosensoryHEK293 CellsHumansImiquimodIsothiocyanatesLarvaMembrane PotentialsMiceNeuronsPruritusTRPA1 Cation ChannelZebrafishZebrafish Proteinsallyl isothiocyanateImiquimodIsothiocyanatesTRPA1 Cation ChannelZebrafish ProteinsE. colihumanimiquimoditchmouseneurosciencepainsomatosensoryTRPA1zebrafish

Identifiers

PMID29561265
PMCPMC5912907
OpenAlexW2791294509

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.