Evidence map›Paper›PMID 22713358›Full record

ArticleMolecular pain2012

Regulation of Wnt signaling by nociceptive input in animal models.

Yuqiang Shi, Subo Yuan, Bei Li, Jigong Wang, Susan M Carlton, Kyungsoon Chung, Jin Mo Chung, Shao-Jun Tang

Open access · goldAbstract read
In one paragraph

Article in Molecular pain, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

44 citing papers in PubMed, 65 citations in OpenAlex.

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  14. Unleashing Intrinsic Growth Pathways in Regenerating Peripheral Neurons.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Review
  17. The role of Wnt/mTOR signaling in spinal cord injury.Journal of clinical orthopaedics and trauma · 2022
    Review
  18. Lunatic Fringe-GFP Marks Lamina-Specific Astrocytes That Regulate Sensory Processing.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  19. Article
  20. Review
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

8 authors at 1 institution in 1 country.

Yuqiang ShiDepartment of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Subo Yuan
Bei Li
Jigong Wang
Susan M Carlton
Kyungsoon Chung
Jin Mo Chung
Shao-Jun Tang
The University of Texas Medical Branch at Galveston · US

Funding

VISCERAL PAINP01NS011255 · NINDS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CHUNG, JIN M · 1985 to 2012
$13.6M
Mechanisms of Neuropathic PainR01NS031680 · NINDS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CHUNG, JIN M · 1994 to 2016
$4.1M
PERIPHERAL GLUTAMATE RECEPTORS IN INFLAMMATORY PAINR01NS027910 · NINDS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CARLTON, SUSAN M · 1995 to 2013
$3.8M
SPINAL CORD PLASTICITY IN PERIPHERAL NEUROPATHYR29NS027910 · NINDS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CARLTON, SUSAN M · 1990 to 1994
–
NINDS NIH HHS NS011255NINDS NIH HHS NS027910NINDS NIH HHS NS031680NINDS NIH HHS P01 NS011255
6 · The paper itself

Abstract

backgroundCentral sensitization-associated synaptic plasticity in the spinal cord dorsal horn (SCDH) critically contributes to the development of chronic pain, but understanding of the underlying molecular pathways is still incomplete. Emerging evidence suggests that Wnt signaling plays a crucial role in regulation of synaptic plasticity. Little is known about the potential function of the Wnt signaling cascades in chronic pain development.

resultsFluorescent immunostaining results indicate that β-catenin, an essential protein in the canonical Wnt signaling pathway, is expressed in the superficial layers of the mouse SCDH with enrichment at synapses in lamina II. In addition, Wnt3a, a prototypic Wnt ligand that activates the canonical pathway, is also enriched in the superficial layers. Immunoblotting analysis indicates that both Wnt3a a β-catenin are up-regulated in the SCDH of various mouse pain models created by hind-paw injection of capsaicin, intrathecal (i.t.) injection of HIV-gp120 protein or spinal nerve ligation (SNL). Furthermore, Wnt5a, a prototypic Wnt ligand for non-canonical pathways, and its receptor Ror2 are also up-regulated in the SCDH of these models.

conclusionOur results suggest that Wnt signaling pathways are regulated by nociceptive input. The activation of Wnt signaling may regulate the expression of spinal central sensitization during the development of acute and chronic pain.

Indexed as

NociceptionWnt Signaling PathwayAnimalsbeta CateninCapsaicinDisease Models, AnimalGanglia, SpinalHIV Envelope Protein gp120MaleMiceMice, Inbred C57BLNeuralgiaPosterior Horn CellsProtein TransportUp-RegulationWnt3A Proteinbeta CateninCapsaicinHIV Envelope Protein gp120Wnt3A ProteinWnt3a protein, mouseWnt-5a ProteinWnt5a protein, mouseWnt Proteins

Identifiers

PMID22713358
PMCPMC3472283
OpenAlexW2153973840

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.