Evidence map›Paper›PMID 25279551›Full record

ArticlePloS one2014

Involvement of trigeminal transition zone and laminated subnucleus caudalis in masseter muscle hypersensitivity associated with tooth inflammation.

Kohei Shimizu, Kunihito Matsumoto, Noboru Noma, Shingo Matsuura, Kinuyo Ohara, Hiroki Komiya, Tetsuro Watase, Bunnai Ogiso, Yoshiyuki Tsuboi, Masamichi Shinoda and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

13 authors at 1 institution in 1 country.

Kohei ShimizuDepartment of Endodontics, Nihon University School of Dentistry, Tokyo, Japan; Divisions of Advanced Dental Treatment, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
Kunihito MatsumotoDepartment of Radiology, Nihon University School of Dentistry, Tokyo, Japan; Divisions of Advanced Dental Treatment, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
Noboru NomaDepartment of Oral Diagnosis, Nihon University School of Dentistry, Tokyo, Japan; Divisions of Clinical Research, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
Shingo MatsuuraDepartment of Endodontics, Nihon University School of Dentistry, Tokyo, Japan.
Kinuyo OharaDepartment of Endodontics, Nihon University School of Dentistry, Tokyo, Japan.
Hiroki KomiyaDepartment of Endodontics, Nihon University School of Dentistry, Tokyo, Japan.
Tetsuro WataseDepartment of Endodontics, Nihon University School of Dentistry, Tokyo, Japan.
Bunnai OgisoDepartment of Endodontics, Nihon University School of Dentistry, Tokyo, Japan; Divisions of Advanced Dental Treatment, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
Yoshiyuki TsuboiDepartment of Physiology, Nihon University School of Dentistry, Tokyo, Japan; Division of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
Masamichi ShinodaDepartment of Physiology, Nihon University School of Dentistry, Tokyo, Japan; Division of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
Keisuke HatoriDepartment of Endodontics, Nihon University School of Dentistry, Tokyo, Japan; Divisions of Advanced Dental Treatment, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
Yuka NakayaDepartment of Oral Diagnosis, Nihon University School of Dentistry, Tokyo, Japan.
Koichi IwataDepartment of Physiology, Nihon University School of Dentistry, Tokyo, Japan; Division of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan; Division of Applied System Neuroscience Advanced Medical Research Center, Nihon University Graduate School of Medical Science, Tokyo, Japan.
Nihon University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A rat model of pulpitis/periapical periodontitis was used to study mechanisms underlying extraterritorial enhancement of masseter response associated with tooth inflammation. Periapical bone loss gradually increased and peaked at 6 weeks after complete Freund's adjuvant (CFA) application to the upper molar tooth pulp (M1). On day 3, the number of Fos-immunoreactive (IR) cells was significantly larger in M1 CFA rats compared with M1 vehicle (veh) rats in the trigeminal subnucleus interpolaris/caudalis transition zone (Vi/Vc). The number of Fos-IR cells was significantly larger in M1 CFA and masseter (Mass) capsaicin applied (M1 CFA/Mass cap) rats compared with M1 veh/Mass veh rats in the contralateral Vc and Vi/Vc. The number of phosphorylated extracellular signal-regulated kinase (pERK)-IR cells was significantly larger in M1 CFA/Mass cap and M1 veh/Mass cap rats compared to Mass-vehicle applied rats with M1 vehicle or CFA in the Vi/Vc. Pulpal CFA application caused significant increase in the number of Fos-IR cells in the Vi/Vc but not Vc on week 6. The number of pERK-IR cells was significantly lager in the rats with capsaicin application to the Mass compared to Mass-vehicle treated rats after pulpal CFA- or vehicle-application. However, capsaicin application to the Mass did not further affect the number of Fos-IR cells in the Vi/Vc in pulpal CFA-applied rats. The digastric electromyographic (d-EMG) activity after Mass-capsaicin application was significantly increased on day 3 and lasted longer at 6 weeks after pulpal CFA application, and these increase and duration were significantly attenuated by i.t. PD98059, a MEK1 inhibitor. These findings suggest that Vi/Vc and Vc neuronal excitation is involved in the facilitation of extraterritorial hyperalgesia for Mass primed with periapical periodontitis or acute pulpal-inflammation. Furthermore, phosphorylation of ERK in the Vi/Vc and Vc play pivotal roles in masseter hyperalgesia after pulpitis or periapical periodontitis.

Indexed as

AnimalsExtracellular Signal-Regulated MAP KinasesImmunohistochemistryMaleMasseter MusclePeriapical PeriodontitisPhosphorylationProto-Oncogene Proteins c-fosRatsRats, Sprague-DawleyTooth DiseasesExtracellular Signal-Regulated MAP KinasesProto-Oncogene Proteins c-fos

Identifiers

PMID25279551
PMCPMC4184877
OpenAlexW2062202403

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.