Evidence map›Paper›PMID 32300146›Full record

ArticleScientific reports2020

Mechanical allodynia in mice with tenascin-X deficiency associated with Ehlers-Danlos syndrome.

Emiko Okuda-Ashitaka, Yuka Kakuchi, Hiroaki Kakumoto, Shota Yamanishi, Hiroki Kamada, Takafumi Yoshidu, Satoshi Matsukawa, Naoya Ogura, Sadahito Uto, Toshiaki Minami and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. 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

12 authors at 3 institutions in 1 country.

Emiko Okuda-AshitakaDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan. emiko.ashitaka@oit.ac.jp.
Yuka KakuchiDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan.
Hiroaki KakumotoDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan.
Shota YamanishiDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan.
Hiroki KamadaDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan.
Takafumi YoshiduDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan.
Satoshi MatsukawaDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan.
Naoya OguraDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan.
Sadahito UtoDepartment of Biomedical Engineering, Osaka Institute of Technology, Osaka, 535-8585, Japan.
Toshiaki MinamiDepartment of Anesthesiology, Osaka Medical College, Takatsuki, 569-8686, Japan.
Seiji ItoDepartment of Anesthesiology, Osaka Medical College, Takatsuki, 569-8686, Japan.
Ken-Ichi MatsumotoDepartment of Biosignaling and Radioisotope Experiment, Interdisciplinary Center for Science Research, Organization for Research and Academic Information, Shimane University, Izumo, 693-8501, Japan.
Osaka Institute of Technology · JPOsaka Medical and Pharmaceutical University · JPShimane University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tenascin-X (TNX) is a member of the extracellular matrix glycoprotein tenascin family, and TNX deficiency leads to Ehlers-Danlos syndrome, a heritable human disorder characterized mostly by skin hyperextensibility, joint hypermobility, and easy bruising. TNX-deficient patients complain of chronic joint pain, myalgia, paresthesia, and axonal polyneuropathy. However, the molecular mechanisms by which TNX deficiency complicates pain are unknown. Here, we examined the nociceptive behavioral responses of TNX-deficient mice. Compared with wild-type mice, TNX-deficient mice exhibited mechanical allodynia but not thermal hyperalgesia. TNX deficiency also increased pain sensitivity to chemical stimuli and aggravated early inflammatory pain elicited by formalin. TNX-deficient mice were significantly hypersensitive to transcutaneous sine wave stimuli at frequencies of 250 Hz (Aδ fiber responses) and 2000 Hz (Aβ fiber responses), but not to stimuli at frequency of 5 Hz (C fiber responses). In addition, the phosphorylation levels of extracellular signal-related kinase, an active neuronal marker, and the activity of NADPH-diaphorase, a neuronal nitric oxide activation marker, were enhanced in the spinal dorsal horns of TNX-deficient mice. These results suggest that TNX deficiency contributes to the development of mechanical allodynia and hypersensitivity to chemical stimuli, and it induces hypersensitization of myelinated A fibers and activation of the spinal dorsal horn.

Indexed as

AnalgesicsAnimalsEhlers-Danlos SyndromeFormaldehydeHyperalgesiaMaleMice, Inbred C57BLPainRNA, MessengerSpinal Cord Dorsal HornTenascinAnalgesicsFormaldehydeRNA, MessengerTenascintenascin X

Identifiers

PMID32300146
PMCPMC7162960
OpenAlexW3017201668

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.