Study record

MOTS-c mimics exercise to combat diabetic liver fibrosis by targeting Keap1-Nrf2-Smad2/3

Chen F, Li Z, Wang T et al. · Sci Rep · 2025

AnimalMOTS-c administeredEvidence tier CAlso: Cell study (in vitro)

What this study reported

Reported that administered MOTS-c, aerobic exercise, or their combination were each associated with less liver fibrosis in a rat model of type 2 diabetes. Found in cultured cells that MOTS-c overexpression or addition to the medium was associated with lower reactive oxygen species, higher Keap1-Nrf2 pathway mRNA and protein expression, and lower TGF-β1/Smad pathway gene expression.

Limitations

Male rats of a single strain and one chemically induced diabetes model; group sizes are not reported in the abstract; the cell work uses overexpression constructs rather than physiological exposure.

Study record

Annotated fields for this study
Study modelAnimal study (in vivo)
Substance studiedMOTS-c administeredSynthetic MOTS-c was given to cells, animals or people.
Speciesrat
System studiedMale Sprague-Dawley rat model of type 2 diabetes with liver fibrosis; cultured cells transfected with MOTS-c constructs
PopulationNot reported
DesignControlled animal experiment with parallel cell culture experiments
Sample size as reportednot reported
Control groupUntreated diabetic rats with liver fibrosis; untransfected and untreated cells
Route (data field only)Not reported
Endpoints measuredliver histology (HE and Masson staining); liver fibrosis scoring and immunohistochemistry; Keap1-Nrf2 pathway gene and protein expression; TGF-β1/Smad2/3/4 expression; reactive oxygen species levels; liver transcriptome
Pathways measuredNRF2 / antioxidant response · TGF-β / SMAD · Oxidative stress
Research areasLiver · Metabolic · Exercise · Mitochondrial biology
Evidence tierC — Animal in vivo
Publication typesJournal Article

Appraisal

Each dimension is recorded separately and never combined into a single score. A study can be well controlled and still tell you little about people.

Relevance to MOTS-c
Direct
Model applicability
Mammalian
Sample size
Not reported
Controls
Appropriate
Outcome validity
Surrogate
Support for its own conclusion
Moderate

Provenance

  • Bibliographic fields retrieved from PubMed E-utilities efetch (title, journal, date, authors, DOI) on 2026-11-11.
  • Annotated from the published abstract.
  • Editorial review: approved (2026-11-11).
  • Classification follows the site methodology; the record describes the study, not what MOTS-c does in people.