Evidence map›Paper›PMID 19505980›Full record

ArticleThe Journal of physiology2009

Peripheral sensitisation of nociceptors via G-protein-dependent potentiation of mechanotransduction currents.

Stefan G Lechner, Gary R Lewin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Piezo 1 and Piezo 2 in the Chemosensory Organs of Zebrafish (International journal of molecular sciences · 2024
    Article
  5. Article
  6. Article
  7. Peripheral mechanisms of chronic pain.Medical review (2021) · 2022
    Review
  8. Article
  9. The Form and Function of PIEZO2.Annual review of biochemistry · 2021
    Review
  10. Structure-guided examination of the mechanogating mechanism of PIEZO2.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  11. Nociceptor Signalling through ion Channel Regulation via GPCRs.International journal of molecular sciences · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Phosphoinositide signaling in somatosensory neurons.Advances in biological regulation · 2016
    Review
  17. Article
  18. P2Y Receptors Sensitize Mouse and Human Colonic Nociceptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  19. Sensory mechanotransduction at membrane-matrix interfaces.Pflugers Archiv : European journal of physiology · 2015
    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

2 authors at 1 institution in 1 country.

Stefan G LechnerDepartment of Neuroscience, Max-Delbrück-Center for Molecular Medicine, Robert Rössle Str. 10, 3125 Berlin, Germany.
Gary R Lewin
Max Delbrück Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanical stimuli impinging on the skin are converted into electrical signals by mechanically gated ion channels located at the peripheral nerve endings of dorsal root ganglion (DRG) neurons. Under inflammatory conditions sensory neurons are commonly sensitised to mechanical stimuli; a putative mechanism that may contribute to such sensitisation of sensory neurons is enhanced responsiveness of mechanotransduction ion channels. Here we show that the algogens UTP and ATP potentiate mechanosensitive RA currents in peptidergic nociceptive DRG neurons and reduce thresholds for mechanically induced action potential firing in these neurones. Pharmacological characterisation suggests that this effect is mediated by the Gq-coupled P2Y(2) nucleotide receptor. Moreover, using the in vitro skin nerve technique, we show that UTP also increases action potential firing rates in response to mechanical stimuli in a subpopulation of skin C-fibre nociceptors. Together our findings suggest that UTP sensitises a subpopulation of cutaneous C-fibre nociceptors via a previously undescribed G-protein-dependent potentiation of mechanically activated RA-type currents.

Indexed as

Adenosine TriphosphateAnimalsCells, CulturedGTP-Binding ProteinsLong-Term PotentiationMechanotransduction, CellularMembrane PotentialsMiceMice, Inbred C57BLNociceptorsPhysical StimulationSensory Receptor CellsSkinSkin Physiological PhenomenaUridine TriphosphateAdenosine TriphosphateGTP-Binding ProteinsUridine Triphosphate

Identifiers

PMID19505980
PMCPMC2742277
OpenAlexW1884196201

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.