Study record

The Mitochondrial-Derived Peptide (MOTS-c) Interacted with Nrf2 to Defend the Antioxidant System to Protect Dopaminergic Neurons Against Rotenone Exposure

Xiao J, Zhang Q, Shan Y et al. · Mol Neurobiol · 2023

AnimalSeveralEvidence tier CAlso: Cell study (in vitro)

What this study reported

Reported that rotenone altered MOTS-c expression and promoted its translocation from mitochondria to the nucleus in PC12 cells, where MOTS-c interacted with Nrf2 and regulated HO-1 and NQO1 expression. In rats and PC12 cells exposed to rotenone, reported that exogenous MOTS-c pretreatment was associated with less mitochondrial dysfunction and oxidative stress, smaller reductions in striatal TH, PSD95 and SYP protein, and attenuated changes in Nrf2, HO-1, NQO1 and Keap1 expression.

Limitations

Group sizes and animal sex not reported in the abstract; a single rat rotenone model and a single immortalised cell line (PC12); pretreatment design only, with no post-exposure comparison and no behavioural outcomes reported.

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).
Speciesrat
System studiedRats exposed to rotenone with striatum analysed; PC12 cells exposed to rotenone in culture
PopulationNot reported
DesignControlled animal experiment with cell culture experiments
Sample size as reportednot reported
Control grouprotenone-exposed animals and cells without MOTS-c pretreatment
Route (data field only)other
Endpoints measuredMOTS-c expression and subcellular localization; Nrf2, HO-1, NQO1 and Keap1 expression; mitochondrial function; oxidative stress markers; TH, PSD95 and SYP protein expression in striatum
Pathways measuredNRF2 / antioxidant response · Oxidative stress · Nuclear translocation
Research areasNervous system · 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.