Evidence map›Paper›PMID 31948011›Full record

ReviewInternational journal of molecular sciences2020

TRP Channels in the Focus of Trigeminal Nociceptor Sensitization Contributing to Primary Headaches.

Mária Dux, Judit Rosta, Karl Messlinger

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. 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
6.7field-weighted citation impact, top 2% 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, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. OnabotulinumtoxinA effects on trigeminal nociceptors.Cephalalgia : an international journal of headache · 2023
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

3 authors at 2 institutions in 2 countries.

Mária DuxDepartment of Physiology, University of Szeged, Dóm tér 10, H-6720 Szeged, Hungary.ORCID 0000-0002-9941-8188
Judit RostaDepartment of Physiology, University of Szeged, Dóm tér 10, H-6720 Szeged, Hungary.
Karl MesslingerInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University Erlangen-Nürnberg, Universitätsstr. 17, D-91054 Erlangen, Germany.
University of Szeged · HUFriedrich-Alexander-Universität Erlangen-Nürnberg · DE

Funding

Alexander von Humboldt Foundation Research Group Linkage ProgramHungarian National Research, Development and Innovation Office GINOP-2.3.2-15-2016-00034Hungarian National Research, Development and Innovation Office K119597University of Szeged Open Access Fund 4514
6 · The paper itself

Abstract

Pain in trigeminal areas is driven by nociceptive trigeminal afferents. Transduction molecules, among them the nonspecific cation channels transient receptor potential vanilloid 1 (TRPV1) and ankyrin 1 (TRPA1), which are activated by endogenous and exogenous ligands, are expressed by a significant population of trigeminal nociceptors innervating meningeal tissues. Many of these nociceptors also contain vasoactive neuropeptides such as calcitonin gene-related peptide (CGRP) and substance P. Release of neuropeptides and other functional properties are frequently examined using the cell bodies of trigeminal neurons as models of their sensory endings. Pathophysiological conditions cause phosphorylation, increased expression and trafficking of transient receptor potential (TRP) channels, neuropeptides and other mediators, which accelerate activation of nociceptive pathways. Since nociceptor activation may be a significant pathophysiological mechanism involved in both peripheral and central sensitization of the trigeminal nociceptive pathway, its contribution to the pathophysiology of primary headaches is more than likely. Metabolic disorders and medication-induced painful states are frequently associated with TRP receptor activation and may increase the risk for primary headaches.

Indexed as

CalciumCortical Spreading DepressionHeadacheHumansMeningesMetabolic DiseasesNeuronsNeuropeptidesNociceptorsTransient Receptor Potential ChannelsCalciumNeuropeptidesTransient Receptor Potential Channelscalcitonin gene-related peptidenociceptionprimary headachestransient receptor potential ankyrin 1transient receptor potential vanilloid 1trigeminal system

Identifiers

PMID31948011
PMCPMC6981722
OpenAlexW2998584474

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.