Study record

Β-GPA administration activates slow oxidative muscle signaling pathways and protects soleus muscle against the increased fatigue under 7-days of rat hindlimb suspension

Sharlo KA, Lvova ID, Sidorenko DA et al. · Arch Biochem Biophys · 2023

AnimalEndogenous MOTS-c measuredEvidence tier C

What this study reported

Measured slow-type muscle signalling in the unloaded rat soleus after hindlimb suspension with and without the creatine kinase inhibitor beta-guanidine propionic acid. Reported that the inhibitor preserved a slow-type signalling network including MOTS-C, AMPK, PGC-1alpha and microRNA-499, and that fatigue resistance, slow-type fibre percentage and mitochondrial DNA copy number were preserved in rats under muscle unloading.

Limitations

Small group size (8 per group); male rats only; single strain and a single 7-day unloading period; MOTS-C was one component of a signalling panel rather than the manipulated variable, so its contribution was not tested directly.

Study record

Annotated fields for this study
Study modelAnimal study (in vivo)
Substance studiedEndogenous MOTS-c measuredNaturally occurring MOTS-c was measured; nothing was given.
Speciesrat
System studiedMale Wistar rats undergoing 7-day hindlimb suspension, with or without beta-guanidine propionic acid; soleus muscle analysed
PopulationNot reported
DesignControlled animal experiment
Sample size as reported24 rats (8 per group: control, hindlimb suspension, hindlimb suspension plus beta-guanidine propionic acid)
Control groupvivarium control rats and untreated hindlimb-suspension rats
Route (data field only)Not reported
Endpoints measuredMOTS-C signalling in soleus muscle; AMPK and PGC-1alpha signalling; microRNA-499; soleus fatigue resistance; slow-type fibre percentage; mitochondrial DNA copy number
Pathways measuredAMPK signalling · SIRT1 / PGC-1α / biogenesis
Research areasSkeletal muscle · Mitochondrial biology
Evidence tierC — Animal in vivo
Publication typesJournal Article, Research Support, Non-U.S. Gov't

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
Indirect
Model applicability
Mammalian
Sample size
Small
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.