Evidence map›Paper›PMID 19285119›Full record

ArticleNeuroscience2009

Glial cell line-derived neurotrophic factor family ligands enhance capsaicin-stimulated release of calcitonin gene-related peptide from sensory neurons.

B S Schmutzler, S Roy, C M Hingtgen

Abstract read
In one paragraph

Article in Neuroscience, 2009. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Cutaneous TRPV1Cell · 2019
    Article
  4. Review
  5. Article
  6. Presynaptic modulation of spinal nociceptive transmission by glial cell line-derived neurotrophic factor (GDNF).The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  7. Article
  8. Article
  9. Artemin, a glial cell line-derived neurotrophic factor family member, induces TRPM8-dependent cold pain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  10. TRPV1 and TRPA1 function and modulation are target tissue dependent.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  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

3 authors.

B S SchmutzlerDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Stark Neurosciences Research Institute, 950 West Walnut Street, Research Building 2, Room 444, Indianapolis, IN 46202, USA. bschmutz@iupui.edu
S Roy
C M Hingtgen

Funding

Actions of GTPase-Activating Proteins on Sensory NeuronsR01NS051668 · NINDS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI HINGTGEN, CYNTHIA M · 2006 to 2010
$2.4M
NINDS NIH HHS R01 NS051668
6 · The paper itself

Abstract

The glial cell line-derived neurotrophic factor (GDNF) family ligands (GFLs) are a group of peptides that have been implicated as important factors in inflammation, since they are released in increased amounts during inflammation and induce thermal hyperalgesia upon injection. Mouse isolated sensory neurons in culture and freshly dissociated spinal cord slices were used to examine the enhancement in stimulated-release of the neuropeptide, calcitonin gene-related peptide (CGRP), as a measure of sensitization. Exposure of isolated sensory neurons in culture to GDNF, neurturin, and artemin enhanced the capsaicin-stimulated release of immunoreactive calcitonin gene-related peptide (iCGRP) two- to threefold, but did not increase potassium-stimulated release of iCGRP. A similar profile of sensitization was observed in freshly dissociated spinal cord slices. Persephin, another member of the GFL family thought to be important in development, was unable to induce an enhancement in the release of iCGRP. These results demonstrate that specific GFLs are important mediators affecting sensory neuronal sensitivity, likely through modulation of the capsaicin receptor. The sensitization of sensory neurons during inflammation, and the pain and neurogenic inflammation resulting from this sensitization, may be due in part to the effects of these selected GFLs.

Indexed as

AnimalsCalcitonin Gene-Related PeptideCapsaicinCells, CulturedGlial Cell Line-Derived Neurotrophic FactorsIn Vitro TechniquesMiceMice, Inbred C57BLSensory Receptor CellsSpinal CordCalcitonin Gene-Related PeptideCapsaicinGlial Cell Line-Derived Neurotrophic Factors

Identifiers

PMID19285119
PMCPMC2832305

What OpenQuestion holds

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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.