Study record

Mitohormesis in Hypothalamic POMC Neurons Mediates Regular Exercise-Induced High-Turnover Metabolism

Kang GM, Min SH, Lee CH et al. · Cell Metab · 2021

AnimalSeveralEvidence tier CAlso: Cell study (in vitro)

What this study reported

Reported that mild mitoribosomal stress in mouse POMC neurons raised hypothalamic MOTS-c and beta-endorphin expression and was associated with higher-turnover metabolism and resistance to obesity. Central administration of MOTS-c in mice reproduced the adipose thermogenic and unfolded-protein-response phenotype, and moderate running exercise was associated with higher hypothalamic MOTS-c expression.

Limitations

Single mouse strain and male mice only, with MOTS-c identified as a candidate mediator by phenocopying rather than by blocking its action; central delivery does not reflect endogenous hypothalamic exposure.

Study record

Annotated fields for this study
Study modelAnimal study (in vivo)
Substance studiedSeveralMore than one of these is central to the paper (common for reviews).
Speciesmouse
System studiedPOMC neuron-specific Crif1-deficient mice, exercising wild-type mice given central MOTS-c, and hypothalamic cell lines
PopulationNot reported
DesignControlled animal experiment with transgenic models
Sample size as reportedNot reported
Control groupwild-type and vehicle-infused mice
Route (data field only)intracerebroventricular
Endpoints measuredbody weight and adiposity; thermogenesis; adipose mitochondrial unfolded protein response; hypothalamic MOTS-c expression
Pathways measuredThermogenesis / brown fat · Other
Research areasMetabolic · Nervous system · Exercise · Mitochondrial biology
Evidence tierC — Animal in vivo
Publication typesJournal Article, Research Support, N.I.H., Extramural, 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
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.