Evidence map›Paper›PMID 35372342›Full record

ArticleFrontiers in cell and developmental biology2022

The Protective Effects of γ-Tocotrienol on Muscle Stem Cells Through Inhibiting Reactive Oxidative Stress Production.

Shuo Yang, Juan Yang, Huiwen Zhao, Rong Deng, Hancheng Fan, Jinfu Zhang, Zihao Yang, Huihong Zeng, Bohai Kuang, Lijian Shao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. 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
0.3field-weighted citation impact, top 49% 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, 3 citations in OpenAlex.

  1. PdgfrαGenes & diseases · 2025
    Review
  2. Potential Vitamin E Signaling Mediators in Skeletal Muscle.Antioxidants (Basel, Switzerland) · 2024
    Review
  3. Article
  4. 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

10 authors at 1 institution in 1 country.

Shuo YangDepartment of Occupational Health and Toxicology, School of Public Health, Nanchang University, Nanchang, China.
Juan YangDepartment of Occupational Health and Toxicology, School of Public Health, Nanchang University, Nanchang, China.
Huiwen ZhaoDepartment of Biological Genetics, School of Basic Medicine, Nanchang University, Nanchang, China.
Rong DengDepartment of Occupational Health and Toxicology, School of Public Health, Nanchang University, Nanchang, China.
Hancheng FanDepartment of Histology and Embryology, School of Basic Medicine, Nanchang University, Nanchang, China.
Jinfu ZhangDepartment of Occupational Health and Toxicology, School of Public Health, Nanchang University, Nanchang, China.
Zihao YangDepartment of Occupational Health and Toxicology, School of Public Health, Nanchang University, Nanchang, China.
Huihong ZengDepartment of Histology and Embryology, School of Basic Medicine, Nanchang University, Nanchang, China.
Bohai KuangDepartment of Biological Genetics, School of Basic Medicine, Nanchang University, Nanchang, China.
Lijian ShaoDepartment of Occupational Health and Toxicology, School of Public Health, Nanchang University, Nanchang, China.
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudotrophic muscular dystrophy is a common clinical skeletal muscle necrotic disease, among which Duchenne muscular dystrophy (DMD) is the predominant. For such diseases, there is no clinically effective treatment, which is only symptomatic or palliative treatment. Oxidative stress and chronic inflammation are common pathological features of DMD. In recent years, it has been found that the pathophysiological changes of skeletal muscle in DMD mice are related to muscle stem cell failure. In the present study, we established a DMD mice model and provided tocotrienol (γ-tocotrienol, GT3), an antioxidant compound, to explore the relationship between the physiological state of muscle stem cells and oxidative stress. The results showed that the application of GT3 can reduce ROS production and cellular proliferation in the muscle stem cells of DMD mice, which is beneficial to promote the recovery of muscle stem cell function in DMD mice. GT3 treatment improved the differentiation ability of muscle stem cells in DMD mice with increasing numbers of MyoD

Indexed as

cellular proliferationDuchenne muscular dystrophymuscle stem cellsoxidative stressγ-tocotrienol

Identifiers

PMID35372342
PMCPMC8965065
OpenAlexW4221027106

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.