Evidence map›Paper›PMID 37187829›Full record

ReviewTemperature (Austin, Tex.)2023

Neuronal and non-neuronal TRPA1 as therapeutic targets for pain and headache relief.

Luigi F Iannone, Romina Nassini, Riccardo Patacchini, Pierangelo Geppetti, Francesco De Logu

Open access · greenAbstract readReview
In one paragraph

Review in Temperature (Austin, Tex.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Observational
  11. Article
  12. Article
  13. Role of TRP Channels in Cancer-Induced Bone Pain.International journal of molecular sciences · 2025
    Review
  14. Article
  15. Review
  16. TRPA1-Related Diseases and Applications of Nanotherapy.International journal of molecular sciences · 2024
    Review
  17. Review
  18. Article
  19. Review
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 3 institutions in 1 country.

Luigi F IannoneHeadache Center and Clinical Pharmacology Unit, Careggi University Hospital, Florence, Italy.ORCID https://orcid.org/0000-0003-3598-0195
Romina NassiniSection of Clinical Pharmacology and Oncology, Department of Health Sciences, University of Florence, Florence, Italy.ORCID https://orcid.org/0000-0002-9223-8395
Riccardo PatacchiniCorporate Drug Development, Chiesi Farmaceutici S.p.A, Nuovo Centro Ricerche, Parma, Italy.
Pierangelo GeppettiHeadache Center and Clinical Pharmacology Unit, Careggi University Hospital, Florence, Italy.ORCID https://orcid.org/0000-0003-3797-8371
Francesco De LoguSection of Clinical Pharmacology and Oncology, Department of Health Sciences, University of Florence, Florence, Italy.ORCID https://orcid.org/0000-0001-8360-6929
Azienda Ospedaliero-Universitaria Careggi · ITUniversity of Florence · ITChiesi (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transient receptor potential ankyrin 1 (TRPA1), a member of the TRP superfamily of channels, has a major role in different types of pain. TRPA1 is primarily localized to a subpopulation of primary sensory neurons of the trigeminal, vagal, and dorsal root ganglia. This subset of nociceptors produces and releases the neuropeptide substance P (SP) and calcitonin gene-related peptide (CGRP), which mediate neurogenic inflammation. TRPA1 is characterized by unique sensitivity for an unprecedented number of reactive byproducts of oxidative, nitrative, and carbonylic stress and to be activated by several chemically heterogenous, exogenous, and endogenous compounds. Recent preclinical evidence has revealed that expression of TRPA1 is not limited to neurons, but its functional role has been reported in central and peripheral glial cells. In particular, Schwann cell TRPA1 was recently implicated in sustaining mechanical and thermal (cold) hypersensitivity in mouse models of macrophage-dependent and macrophage-independent inflammatory, neuropathic, cancer, and migraine pain. Some analgesics and herbal medicines/natural products widely used for the acute treatment of pain and headache have shown some inhibitory action at TRPA1. A series of high affinity and selective TRPA1 antagonists have been developed and are currently being tested in phase I and phase II clinical trials for different diseases with a prominent pain component.

Indexed as

CGRPnociceptionpainTRPA1TRP channels

Identifiers

PMID37187829
PMCPMC10177743
OpenAlexW4280564606

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.