Evidence map›Paper›PMID 26240991›Full record

ArticleNeuroscience letters2015

Pain from intra-articular NGF or joint injury in the rat requires contributions from peptidergic joint afferents.

Jeffrey V Kras, Christine L Weisshaar, Parul S Pall, Beth A Winkelstein

Abstract read
In one paragraph

Article in Neuroscience letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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.

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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Opioid-Induced Hyperalgesic Priming in Single Nociceptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  5. Review
  6. Role of Nociceptor Toll-like Receptor 4 (TLR4) in Opioid-Induced Hyperalgesia and Hyperalgesic Priming.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Fentanyl Induces Rapid Onset Hyperalgesic Priming: Type I at Peripheral and Type II at Central Nociceptor Terminals.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

4 authors at 1 institution in 1 country.

Jeffrey V KrasDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
Christine L WeisshaarDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
Parul S PallDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
Beth A WinkelsteinDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA; Department of Neurosurgery, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: winkelst@seas.upenn.edu.
University of Pennsylvania · US

Funding

Nociceptive Mechanisms In Whiplash InjuryR01AR056288 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI WINKELSTEIN, BETH A · 2009 to 2013
$1.6M
NIAMS NIH HHS AR056288NIAMS NIH HHS R01 AR056288
6 · The paper itself

Abstract

Non-physiological stretch of the cervical facet joint's capsular ligament induces persistent behavioral hypersensitivity and spinal neuronal hyperexcitability via an intra-articular NGF-dependent mechanism. Although that ligament is innervated by nociceptors, it is unknown if a subpopulation is exclusively responsible for the behavioral and spinal neuronal responses to intra-articular NGF and/or facet joint injury. This study ablated joint afferents using the neurotoxin saporin targeted to neurons involved in either peptidergic ([Sar(9),Met (O2)(11)]-substance P-saporin (SSP-Sap)) or non-peptidergic (isolectin B4-saporin (IB4-Sap)) signaling to investigate the contributions of those neuronal populations to facet-mediated pain. SSP-Sap, but not IB4-Sap, injected into the bilateral C6/C7 facet joints 14 days prior to an intra- articular NGF injection prevents NGF-induced mechanical and thermal hypersensitivity in the forepaws. Similarly, only SSP- Sap prevents the increase in mechanical forepaw stimulation- induced firing of spinal neurons after intra-articular NGF. In addition, intra-articular SSP-Sap prevents both behavioral hypersensitivity and upregulation of NGF in the dorsal root ganglion after a facet joint distraction that normally induces pain. These findings collectively suggest that disruption of peptidergic signaling within the joint may be a potential treatment for facet pain, as well as other painful joint conditions associated with elevated NGF, such as osteoarthritis.

Indexed as

Action PotentialsAnimalsBehavior, AnimalHyperalgesiaLectinsMaleNerve Growth FactorNeurons, AfferentNeuropeptidesPain ThresholdPhysical StimulationRats, Sprague-DawleyRibosome Inactivating Proteins, Type 1SaporinsSignal TransductionSpinal Cord Dorsal HornIB4-saporin conjugateLectinsNerve Growth FactorNeuropeptidesRibosome Inactivating Proteins, Type 1SaporinsSubstance PAfferentFacet jointNeuronal hyperexcitabilityNGFPainTrauma

Identifiers

PMID26240991
PMCPMC4568150
OpenAlexW1006549038

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.