Study record

The Mitochondrial-Derived Peptide MOTS-c Attenuates Oxidative Stress Injury and the Inflammatory Response of H9c2 Cells Through the Nrf2/ARE and NF-κB Pathways

Shen C, Wang J, Feng M et al. · Cardiovasc Eng Technol · 2022

CellsMOTS-c administeredEvidence tier D

What this study reported

Reported that hydrogen peroxide lowered viability and superoxide dismutase and raised reactive oxygen species, malondialdehyde and inflammatory cytokines in rat H9c2 cardiomyocytes, and that MOTS-c pretreatment reversed these changes. Knocking down Nrf2 or activating NF-κB reduced the effects of MOTS-c, pointing to the Nrf2/ARE and NF-κB pathways.

Limitations

Single immortalised rat cardiomyoblast line with an acute chemical oxidant challenge and no in vivo work; concentrations tested were supraphysiological relative to circulating levels.

Study record

Annotated fields for this study
Study modelCell study (in vitro)
Substance studiedMOTS-c administeredSynthetic MOTS-c was given to cells, animals or people.
Speciesrat
System studiedRat H9c2 cardiomyocytes pretreated with MOTS-c before hydrogen peroxide exposure, with Nrf2 knockdown and NF-κB activation models
PopulationNot reported
DesignCell culture experiments
Sample size as reportedNot reported
Control groupuntreated and hydrogen-peroxide-only cells, with sh-Nrf2 and PMA comparison conditions
Route (data field only)in-culture
Endpoints measuredcell viability; reactive oxygen species; malondialdehyde and superoxide dismutase; Nrf2, HO-1 and NQO-1 expression; NF-κB p65 phosphorylation; TNF-α, IL-6 and IL-1β
Pathways measuredNRF2 / antioxidant response · Inflammation · Oxidative stress
Research areasCardiovascular · Inflammation & immunity
Evidence tierD — Cell, tissue or analytical
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
Direct
Model applicability
Cellular
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.