Evidence map›Paper›PMID 39314223›Full record

ArticleDermatology research and practice2024

Molecular Biological Verification of the Healing Effect of Biphasic Microcurrent Electrical Stimulation in Model Rats of Skin Abrasion.

Akira Sakaguchi, Yuzuru Sakaue, Shuhei Haraguchi, Daisuke Hasegawa, Rui Tsukagoshi, Kotaro Kawaguchi, Hideyuki Yamamoto

Abstract read
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Article in Dermatology research and practice, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Akira SakaguchiHyogo Medical University School of Rehabilitation Department of Physical Therapy, Kobe, Japan.ORCID https://orcid.org/0000-0002-5316-8750
Yuzuru SakaueJCHO Osaka Hospital, Osaka, Japan.
Shuhei HaraguchiPLAST Co., Ltd., Hyogo, Japan.
Daisuke HasegawaMedical Corporation Ikeikai Ando Surgery Orthopedics Clinic, Osaka, Japan.
Rui TsukagoshiHyogo Medical University School of Rehabilitation Department of Physical Therapy, Kobe, Japan.
Kotaro KawaguchiHyogo Medical University School of Rehabilitation Department of Physical Therapy, Kobe, Japan.
Hideyuki YamamotoHyogo Medical University School of Rehabilitation Department of Physical Therapy, Kobe, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we investigated the effect of biphasic microcurrent electrical stimulation (b-MES) on the epidermal healing process using a rat model of skin abrasion. We analyzed the expression levels of growth factors [fibroblast growth factor 2 (FGF2) and epidermal growth factor (EGF)] and keratin subtypes (K10) in both the b-MES and control groups at different time points after wounding. The b-MES group showed a significantly accelerated healing process of the epithelial tissue, resulting in more consistent healing as compared to the control group. A molecular biological analysis showed that the FGF2 mRNA expression level on Day 2 after wounding was significantly higher in the b-MES group, whereas the EGF mRNA expression level on Days 1, 2, and 4 after wounding was significantly lower in the b-MES group. Additionally, the K10 mRNA expression level on Days 1 and 2 after wounding was significantly higher in the b-MES group. Our study findings suggest that b-MES facilitates wound healing by regulating the growth factors. However, the precise mechanisms underlying these effects remain to be fully elucidated. Further research is needed to fully understand the therapeutic potential of b-MES and its applications in clinical setting. Clinically, m-MES requires shunting due to residual electrical charge at the application site. However, b-MES alternates polarity, leaving no charge at the site of application. Therefore, b-MES also has the advantage of being safer and allowing treatment for longer periods of time.

Identifiers

PMID39314223
PMCPMC11419832

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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.