Evidence map›Paper›PMID 29887879›Full record

ReviewNeural plasticity2018

A Proposed Molecular Mechanism for Physical Analgesia in Chronic Pain.

Norio Saito, Rei Shima, Yurika Yamada, Masaru Nagaoka, Etsuro Ito, Tohru Yoshioka

Open access · goldAbstract readReview
In one paragraph

Review in Neural plasticity, 2018. 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
1.1field-weighted citation impact, top 23% 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, 16 citations in OpenAlex.

  1. Adhesive pyramidal thorn patches provide pain relief to athletes.The Kaohsiung journal of medical sciences · 2019
    Trial
  2. Article
  3. Revisiting oxytocin generation in keratinocytes.Biophysics and physicobiology · 2023
    Article
  4. Article
  5. Dorsolateral prefrontal cortex sensing analgesia.Biophysics and physicobiology · 2022
    Article
  6. Influence of gap junctions upon CaBiophysics and physicobiology · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. 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

6 authors at 2 institutions in 2 countries.

Norio SaitoResearch Institute for Elderly Health, Waseda University, 2-579-15 Mikashima, Tokorozawa, Saitama 359-1192, Japan.
Rei ShimaDepartment of Biology, Waseda University, 2-2 Wakamatsucho, Shinjuku, Tokyo 162-8480, Japan.
Yurika YamadaDepartment of Biology, Waseda University, 2-2 Wakamatsucho, Shinjuku, Tokyo 162-8480, Japan.
Masaru NagaokaDepartment of Biology, Waseda University, 2-2 Wakamatsucho, Shinjuku, Tokyo 162-8480, Japan.
Etsuro ItoDepartment of Biology, Waseda University, 2-2 Wakamatsucho, Shinjuku, Tokyo 162-8480, Japan.ORCID 0000-0002-1877-6566
Tohru YoshiokaGraduate Institute of Medicine, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Sanmin, Kaohsiung 80708, Taiwan.ORCID 0000-0003-2831-6421
Waseda University · JPKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although pain is indispensable for survival, chronic pain places a heavy burden on humans. As the efficacy of opioid treatment is limited, the development of alternative methods of pain relief without medication is desirable. Recently, we have developed a novel method of physical analgesia using an adhesive "pyramidal thorn patch." When we apply about 3 trials of these patches on the skin of a pain region, the pain region moves toward the spinal cord like a "cutaneous rabbit," and finally, the pain vanishes. In the present review, we propose a molecular mechanism for this analgesic method or pain relief following application of the pyramidal thorn patch where firstly the mechanoreceptors and their related nerves under the skin are activated in response to touch. Transient receptor potential (TRP) channels serve as mechanosensitive channels within these mechanoreceptors. We further propose that activation of the nerves connected with the mechanoreceptors releases oxytocin, which has an antinociceptive function and activates TRP channels to hyperpolarize the pain signal nerves. We believe that our system will pave the way for alternative pain treatment.

Indexed as

AnalgesiaAnimalsChronic PainHumansPain ManagementPain MeasurementTransient Receptor Potential ChannelsTransient Receptor Potential Channels

Identifiers

PMID29887879
PMCPMC5985137
OpenAlexW2804752573

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.