Study record

MOTS‑c protects against placental injury via Nrf2 activation in hypoxia‑induced intrauterine growth restriction mice

Chen D, Zhao HM, Sun XL et al. · Int J Mol Med · 2026

AnimalSeveralEvidence tier CAlso: Cell study (in vitro)

What this study reported

Measured maternal serum and placental MOTS-c in mice with hypoxia-induced intrauterine growth restriction and reported that lower placental MOTS-c content correlated positively with lower fetal weight. Found that administered MOTS-c was associated with attenuated hypoxia-induced growth restriction, greater placental angiogenesis and less oxidative stress-related placental dysfunction in these mice. Reported that these associations were absent in Nrf2 knockout mice and in human umbilical vein endothelial cells pretreated with the Nrf2 inhibitor ML385.

Limitations

Single mouse strain and a single hypoxia model with group sizes not reported in the abstract, one human endothelial cell line used for the in vitro arm, and surrogate placental and expression endpoints rather than offspring outcomes beyond birth.

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, human
System studiedWild-type and Nrf2 knockout pregnant C57BL/6 mice under gestational hypoxia; human umbilical vein endothelial cells
PopulationNot reported
DesignControlled animal experiment with knockout comparison and cell culture experiments
Sample size as reportedNot reported
Control groupnormoxic pregnant mice and untreated hypoxia-exposed mice; Nrf2 knockout mice and ML385-pretreated cells
Route (data field only)Not reported
Endpoints measuredfetal weight; maternal serum and placental MOTS-c concentration; placental histology and angiogenesis markers; oxidative stress markers; Nrf2 pathway protein and transcript expression
Pathways measuredNRF2 / antioxidant response · Oxidative stress
Research areasPregnancy · Reproductive · 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.