Evidence map›Paper›PMID 23266932›Full record

ArticleThe Journal of physiology2013

The modality-specific contribution of peptidergic and non-peptidergic nociceptors is manifest at the level of dorsal horn nociresponsive neurons.

Jie Zhang, Daniel J Cavanaugh, Michael I Nemenov, Allan I Basbaum

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06030297 (Diode Laser as a Biomarker for Neuropathic Pain of Peripheral Origin.), which is not on this map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.4field-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.

NCT06030297 nacompletednot on this mapstarted 2023, after this paper: background citation

Diode Laser as a Biomarker for Neuropathic Pain of Peripheral Origin.

TypeinterventionalSponsorUniversity of UtahRan2023 to 2026Enrolled75ConditionsPeripheral NeuropathyArmsDiode Laser fiber type Selective Stimulator, ZTlido 1.8 % Topical System, PeriCam PSI NR, Medoc Quantitative Sensory Testing, Inactive Topical System
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
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  12. Spinal Inhibitory Interneurons: Gatekeepers of Sensorimotor Pathways.International journal of molecular sciences · 2021
    Review
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  15. Review
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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

4 authors at 2 institutions in 1 country.

Jie ZhangDepartment of Anatomy, University of California San Francisco, San Francisco, CA 94158, USA.
Daniel J Cavanaugh
Michael I Nemenov
Allan I Basbaum
University of California, San Francisco · USLasmed (United States) · US

Funding

BRAINSTEM CONTROL OF PAIN TRANSMISSIONR01NS014627 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BASBAUM, ALLAN I. · 1985 to 2016
$3.9M
Brainstem control of pain transmissionR37NS014627 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BASBAUM, ALLAN I. · 2008 to 2014
$3.6M
Multiple Opioid Receptors and the Control of PainR01DA029204 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BASBAUM, ALLAN I. · 2011 to 2015
$1.9M
Laser Diode for Ion Channel StimulationR44NS046951 · NINDS · LASMED, LLC · PI NEMENOV, MIKHAIL I. · 2007 to 2008
$1.0M
Laser Device for Ion Channel ActivationR43NS046951 · NINDS · LASMED, LLC · PI NEMENOV, MIKHAIL I. · 2003 to 2003
$100k
NIDA NIH HHS DA 29204NIDA NIH HHS R01 DA029204NINDS NIH HHS NS046951NINDS NIH HHS R01 NS014627NINDS NIH HHS R37 NS014627NINDS NIH HHS R37NS14627NINDS NIH HHS R43 NS046951NINDS NIH HHS R44 NS046951
6 · The paper itself

Abstract

We previously demonstrated that genetic and/or pharmacological ablation of the TRPV1+/peptidergic or the MrgprD+/non-peptidergic subset of nociceptors produced selective, modality-specific deficits in the behavioural responses to heat and mechanical stimuli, respectively. To assess whether this modality-specific contribution is also manifest at the level of spinal cord neuron responsiveness, here we made extracellular recordings from lumbar dorsal horn neurons of the mouse in response to graded thermal and mechanical stimulation. We found that, following intrathecal injection of capsaicin to eliminate the central terminals of TRPV1+ nociceptors, neurons in the region of laminae I and V of the spinal cord lost responsiveness to noxious heat (whether generated by a contact heat probe or diode laser), with no change in their response to noxious mechanical stimulation. In contrast, ablation of MrgprD+ afferents did not alter the response to noxious heat, but reduced the firing of superficial dorsal horn nociceptive-specific neurons in response to graded mechanical stimulation and decreased the relative number of wide dynamic range neurons that were exclusively mechanosensitive. Neither ablation procedure reduced the number of dorsal horn neurons that responded to noxious cold. These findings support the conclusion that TRPV1+ nociceptors are necessary and probably sufficient for noxious heat activation of dorsal horn neurons and that, despite their polymodal properties, TRPV1+ and MrgprD+ nociceptors provide modality-specific contributions to the response properties of spinal cord neurons.

Indexed as

AnimalsHot TemperatureMiceMice, Inbred C57BLNociceptorsPeptidesPhysical StimulationPosterior Horn CellsReceptors, G-Protein-CoupledTRPV Cation ChannelsMrgprd protein, mousePeptidesReceptors, G-Protein-CoupledTRPV1 protein, mouseTRPV Cation Channels

Identifiers

PMID23266932
PMCPMC3591717
OpenAlexW1543890890

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.