Study summary · research use only
The mitochondrial-derived peptide MOTS-c relieves hyperglycemia and insulin resistance in gestational diabetes mellitus
Plain-language summary
Paraphrased from the published abstract below — not a verdict on whether anything works.
This study in a mouse model of gestational diabetes mellitus (GDM), induced by short-term high-fat diet combined with low-dose streptozotocin (STZ), administered the mitochondrial-derived peptide MOTS-c daily during pregnancy. The abstract reports MOTS-c was associated with reduced hyperglycemia, improved insulin sensitivity and glucose tolerance, and reduced birth weight and offspring death linked to GDM. MOTS-c also activated insulin sensitivity in skeletal muscle and increased glucose uptake in vitro in this study, and was reported to protect pancreatic β-cells from STZ-mediated injury.
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.
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