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Mots-C

Mitochondrial open reading frame of the 12S rRNA-c, MT-RNR1, Mitochondrial-derived peptide MOTS-c

Quick Stats
Studies 137
Trials 5
Score 2
2021 pubmed 50 citations

The mitochondrial-derived peptide MOTS-c relieves hyperglycemia and insulin resistance in gestational diabetes mellitus.

Yin. Yadong Y; Pan. Yihui Y; He. Jin J; Zhong. Hong H; Wu. Yangyang Y; Ji. Chenbo C; Liu. Lan L; Cui. Xianwei X

Key Findings

  • MOTS‑c lowered hyperglycemia and improved insulin sensitivity in GDM mice
  • MOTS‑c enhanced glucose uptake in skeletal muscle and protected pancreatic β‑cells from damage
  • MOTS‑c reduced excessive birth weight and offspring mortality caused by GDM

Practical Outcomes

  • The results are promising but only in animal models, so it’s not ready for personal use. Biohackers should view MOTS‑c as a potential future therapy that needs human trials, dosing studies, and safety data before any self‑experimentation.

Summary

A study in pregnant mice with gestational diabetes showed that daily injections of the mitochondrial peptide MOTS‑c lowered blood sugar, improved insulin response, protected pancreatic cells, and led to healthier baby mice, suggesting it could one day help treat this condition.

Abstract

The most common complication during pregnancy, gestational diabetes mellitus (GDM), can cause adverse pregnancy outcomes and result in the mother and infant having a higher risk of developing type 2 diabetes after pregnancy. However, existing therapies for GDM remain scant, with the most common being lifestyle intervention and appropriate insulin treatment. MOTS-c, a mitochondrial-derived peptide, can target skeletal muscle and enhance glucose metabolism. Here, we demonstrate that MOTS-c can be an effective treatment for GDM. A GDM mouse model was established by short term high-fat diet combined with low-dose streptozotocin (STZ) treatment while MOTS-c was administrated daily during pregnancy. GDM symptoms such as blood glucose and insulin levels, glucose and insulin tolerance, as well as reproductive outcomes were investigated. MOTS-c significantly alleviated hyperglycemia, improved insulin sensitivity and glucose tolerance, and reduced birth weight and the death of offspring induced by GDM. Similar to a previous study, MOTS-c also could activate insulin sensitivity in the skeletal muscle of GDM mice and elevate glucose uptake in vitro. In addition, we found that MOTS-c protects pancreatic β-cell from STZ-mediated injury. Taken together, our findings demonstrate that MOTS-c could be a promising strategy for the treatment of GDM.

Study Information

Provider

pubmed

Year

2021

Date

2021-11-17T00:00:00.000Z

DOI

10.1016/j.phrs.2021.105987

Citations

50

References

35