Evidence map›Paper›PMID 22458630›Full record

ArticleMolecular pain2012

Satellite glial cell P2Y12 receptor in the trigeminal ganglion is involved in lingual neuropathic pain mechanisms in rats.

Ayano Katagiri, Masamichi Shinoda, Kuniya Honda, Akira Toyofuku, Barry J Sessle, Koichi Iwata

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 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 112 citations in OpenAlex.

  1. Glial cells in neuropathic pain.Physiological reviews · 2026
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  6. Progress in study on animal models of trigeminal neuralgia.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
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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

6 authors at 3 institutions in 2 countries.

Ayano KatagiriDepartment of Physiology, Nihon University School of Dentistry, Tokyo, Japan.
Masamichi Shinoda
Kuniya Honda
Akira Toyofuku
Barry J Sessle
Koichi Iwata
Nihon University · JPTokyo Medical and Dental University · JPUniversity of Toronto · CA

Funding

PERIPHERAL NMDA RECEPTORS AND TMD PAIN MECHANISMSR01DE015420 · NIDCR · UNIVERSITY OF TORONTO · PI SESSLE, BARRY J. · 2003 to 2006
$1.2M
Canadian Institutes of Health ResearchNIDCR NIH HHS DE015420
6 · The paper itself

Abstract

backgroundIt has been reported that the P2Y12 receptor (P2Y12R) is involved in satellite glial cells (SGCs) activation, indicating that P2Y12R expressed in SGCs may play functional roles in orofacial neuropathic pain mechanisms. However, the involvement of P2Y12R in orofacial neuropathic pain mechanisms is still unknown. We therefore studied the reflex to noxious mechanical or heat stimulation of the tongue, P2Y12R and glial fibrillary acidic protein (GFAP) immunohistochemistries in the trigeminal ganglion (TG) in a rat model of unilateral lingual nerve crush (LNC) to evaluate role of P2Y12R in SGC in lingual neuropathic pain.

resultsThe head-withdrawal reflex thresholds to mechanical and heat stimulation of the lateral tongue were significantly decreased in LNC-rats compared to sham-rats. These nocifensive effects were apparent on day 1 after LNC and lasted for 17 days. On days 3, 9, 15 and 21 after LNC, the mean relative number of TG neurons encircled with GFAP-immunoreactive (IR) cells significantly increased in the ophthalmic, maxillary and mandibular branch regions of TG. On day 3 after LNC, P2Y12R expression occurred in GFAP-IR cells but not neuronal nuclei (NeuN)-IR cells (i.e. neurons) in TG. After 3 days of successive administration of the P2Y12R antagonist MRS2395 into TG in LNC-rats, the mean relative number of TG neurons encircled with GFAP-IR cells was significantly decreased coincident with a significant reversal of the lowered head-withdrawal reflex thresholds to mechanical and heat stimulation of the tongue compared to vehicle-injected rats. Furthermore, after 3 days of successive administration of the P2YR agonist 2-MeSADP into the TG in naïve rats, the mean relative number of TG neurons encircled with GFAP-IR cells was significantly increased and head-withdrawal reflex thresholds to mechanical and heat stimulation of the tongue were significantly decreased in a dose-dependent manner compared to vehicle-injected rats.

conclusionsThe present findings provide the first evidence that the activation of P2Y12R in SGCs of TG following lingual nerve injury is involved in the enhancement of TG neuron activity and nocifensive reflex behavior, resulting in neuropathic pain in the tongue.

Indexed as

AnimalsAntigens, NuclearGlial Fibrillary Acidic ProteinImmunohistochemistryLingual Nerve InjuriesMaleNerve Tissue ProteinsNeuralgiaRatsRats, Sprague-DawleyReceptors, Purinergic P2Receptors, Purinergic P2Y1Receptors, Purinergic P2Y12Trigeminal GanglionAntigens, NuclearGlial Fibrillary Acidic ProteinNerve Tissue ProteinsP2ry13 protein, ratRbfox3 protein, ratReceptors, Purinergic P2Receptors, Purinergic P2Y1Receptors, Purinergic P2Y12

Identifiers

PMID22458630
PMCPMC3386019
OpenAlexW2142819716

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LicenceCC BY
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Registered trials

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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.