Evidence map›Paper›PMID 41025999›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2025

Overuse-Induced Muscle Disorder: Establishing a Rat Model to Unravel the Role of Fibro-Adipogenic Progenitor Cells in Intramuscular Fibrosis.

Hiroyori Fusagawa, Tatsuya Sato, Azuma Naito, Nao Tokuda, Nao Yamauchi, Akiyoshi Uezumi, Madoka Uezumi, Yuki Saito, Minami Fusagawa, Hiroyuki Takashima and 8 more

Abstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Hiroyori FusagawaSan Francisco Veterans Affairs Health Care System, San Francisco, California, USA.ORCID 0000-0001-8322-463X
Tatsuya SatoDivision of Cellular Physiology and Signal Transduction, Department of Physiology, Sapporo Medical University School of Medicine, Sapporo, Japan.ORCID 0000-0001-7876-1772
Azuma NaitoGraduate School of Health Sciences, Sapporo Medical University, Hokkaido, Japan.
Nao TokudaGraduate School of Health Sciences, Sapporo Medical University, Hokkaido, Japan.
Nao YamauchiGraduate School of Health Sciences, Sapporo Medical University, Hokkaido, Japan.
Akiyoshi UezumiDivision of Cell Heterogeneity, Medical Research Center for High Depth Omics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Madoka UezumiDivision of Cell Heterogeneity, Medical Research Center for High Depth Omics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Yuki SaitoGraduate School of Health Sciences, Sapporo Medical University, Hokkaido, Japan.
Minami FusagawaDepartment of Pathology, Sapporo Medical University School of Medicine, Hokkaido, Japan.
Hiroyuki TakashimaDivision of Biomedical Science and Engineering, Faculty of Health Sciences, Biomedical Science and Engineering, Hokkaido University, Hokkaido, Japan.
Nobutoshi IchiseDivision of Cellular Physiology and Signal Transduction, Department of Physiology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Toshifumi OgawaDivision of Cellular Physiology and Signal Transduction, Department of Physiology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Takuro KaraushiDivision of Cellular Physiology and Signal Transduction, Department of Physiology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Noritsugu TohseDivision of Cellular Physiology and Signal Transduction, Department of Physiology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Brian FeeleySan Francisco Veterans Affairs Health Care System, San Francisco, California, USA.
Xuhui LiuSan Francisco Veterans Affairs Health Care System, San Francisco, California, USA.ORCID 0000-0002-2418-0291
Atsushi TeramotoDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, Hokkaido, Japan.
Takashi YamadaGraduate School of Health Sciences, Sapporo Medical University, Hokkaido, Japan.ORCID 0000-0003-1797-3880

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overuse-induced muscle disorders (OIMD) frequently occur in athletes due to excessive and improper use under high physical demand, often leading to muscle pain and weakness. Limited studies have shown intramuscular fibrosis in OIMD, with fibro-adipogenic progenitors (FAPs), also known as mesenchymal stromal cells (MSCs), playing a crucial role in this fibrosis. This study aimed to develop a rat OIMD model using neuromuscular electrical stimulation-induced isometric exercise (NMES-ISO) and to investigate mechanisms by which excessive exercise without adequate rest leads to OIMD. We hypothesize that daily NMES-ISO would cause muscle weakness and fibrogenesis mediated by FAP activation triggered by muscle fiber damage. Male Wistar rats received daily NMES-ISO loading on the plantar flexor muscles at a lengthened position. Two weeks of NMES-ISO led to decreased muscle torque without muscle mass reduction. Masson-Trichrome stain revealed collagen-rich fibrogenic lesions in the gastrocnemius muscles, while Evans blue stain detected no muscle fiber damage during the first 5 days. MRI showed increased T2*wi signals correlating with fibrogenic areas. Excessive NMES-ISO stimulated FAP proliferation. This study established a rat model of OIMD using NMES-ISO, characterized by muscle weakness and intramuscular fibrogenesis. Contrary to our hypothesis, FAP activation occurred without overt muscle injury, suggesting excessive mechanical loading may directly trigger FAP proliferation and fibrogenesis. It was cautioned that even relatively safe isometric contraction training could lead to FAP activation and intramuscular fibrosis without proper methods and recovery periods.

Indexed as

Cumulative Trauma DisordersMesenchymal Stem CellsMuscle, SkeletalMuscular DiseasesAnimalsDisease Models, AnimalFibrosisMalePhysical Conditioning, AnimalRatsRats, Wistarfibrosisisometric contractionMSCs/FAPsNMESoveruse

Identifiers

PMID41025999
PMCPMC12604459

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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.