Evidence map›Paper›PMID 24473265›Full record

ReviewNature neuroscience2014

Why we scratch an itch: the molecules, cells and circuits of itch.

Diana M Bautista, Sarah R Wilson, Mark A Hoon

Open access · greenAbstract readReview
In one paragraph

Review in Nature neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 155 papers.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed
34.1field-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

155 citing papers in PubMed, 328 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Immunopathogenesis of itch: an integrative framework for chronic pruritus.JID innovations : skin science from molecules to population health · 2026
    Review
  5. Article
  6. Review
  7. Endosomal MrGPRX1 signaling sensitizes TRPV1 to enhance itch.Frontiers in molecular neuroscience · 2026
    Article
  8. Article
  9. Article
  10. Endosomal MrGPRX1 signaling sensitizes TRPV1 to enhance itch.bioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Review
  13. Keratinocyte-TRPV1 sensory neuron interactions in a genetically controllable mouse model of chronic neuropathic itch.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The peripheral neuroimmune system.Journal of leukocyte biology · 2024
    Review
  19. Cell Type-Specific Modulation of Acute Itch Processing in the Anterior Cingulate Cortex.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  20. Neuroimmune recognition of allergens.Current opinion in immunology · 2024
    Review

95 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

3 authors at 2 institutions in 1 country.

Diana M Bautista1] Department of Molecular and Cell Biology, University of California Berkeley, Berkeley, California, USA. [2] Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, California, USA.
Sarah R Wilson1] Department of Molecular and Cell Biology, University of California Berkeley, Berkeley, California, USA. [2] Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, California, USA.
Mark A HoonMolecular Genetics Unit, Laboratory of Sensory Biology, National Institute of Dental and Craniofacial Research/NIH, Bethesda, Maryland, USA.
University of California, Berkeley · USNational Institute of Dental and Craniofacial Research · US

Funding

Molecular Genetic Studies of SomatosensationZIADE000721 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI HOON, MARK · 2009 to 2025
$26.6M
New approaches to identify molecular mechanisms of touch and pain in mammalsDP2OD007123 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI BAUTISTA, DIANA MICHELE · 2010 to 2010
$2.3M
Roles and functions of ion channels that mediate mammalian touch transduction.R01AR059385 · NIAMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BAUTISTA, DIANA MICHELE · 2011 to 2015
$1.7M
Intramural NIH HHSNIAMS NIH HHS AR059385NIAMS NIH HHS R01 AR059385NIH HHS DP2 OD007123
6 · The paper itself

Abstract

Itch is described as an irritating sensation that triggers a desire to scratch. However, this definition hardly seems fitting for the millions of people who suffer from intractable itch. Indeed, the Buddhist philosopher Nāgārjuna more aptly stated, "There is pleasure when an itch is scratched. But to be without an itch is more pleasurable still." Chronic itch is widespread and very difficult to treat. In this review we focus on the molecules, cells and circuits in the peripheral and central nervous systems that drive acute and chronic itch transmission. Understanding the itch circuitry is critical to developing new therapies for this intractable disease.

Indexed as

SensationAnimalsCentral Nervous SystemHumansModels, BiologicalPeripheral NervesPruritusSignal Transduction

Identifiers

PMID24473265
PMCPMC4364402
OpenAlexW2085720841

What OpenQuestion holds

Textmetadata
LicenceTDM
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.