Serotonin reuptake inhibitors improve muscle stem cell function and muscle regeneration in male mice.
Mylène FefeuMichael BlatzerAnita KneppersDavid BriandPierre RocheteauAlexandre HarocheFabrice ChrétienMélanie Juchet-MartinAnne DanckaertFrançois CoudoréAbdulkarim TutakhailCorinne HuchetAude LafouxRémi MounierOlivier MirRaphaël GaillardFabrice ChrétienPublished in: Nature communications (2024)
Serotonin reuptake inhibitor antidepressants such as fluoxetine are widely used to treat mood disorders. The mechanisms of action include an increase in extracellular level of serotonin, neurogenesis, and growth of vessels in the brain. We investigated whether fluoxetine could have broader peripheral regenerative properties. Following prolonged administration of fluoxetine in male mice, we showed that fluoxetine increases the number of muscle stem cells and muscle angiogenesis, associated with positive changes in skeletal muscle function. Fluoxetine also improved skeletal muscle regeneration after single and multiples injuries with an increased muscle stem cells pool and vessel density associated with reduced fibrotic lesions and inflammation. Mice devoid of peripheral serotonin treated with fluoxetine did not exhibit beneficial effects during muscle regeneration. Specifically, pharmacological, and genetic inactivation of the 5-HT1B subtype serotonin receptor also abolished the enhanced regenerative process induced by fluoxetine. We highlight here a regenerative property of serotonin on skeletal muscle.
Keyphrases
- skeletal muscle
- stem cells
- insulin resistance
- cell therapy
- mesenchymal stem cells
- oxidative stress
- gene expression
- depressive symptoms
- adipose tissue
- systemic sclerosis
- metabolic syndrome
- bipolar disorder
- tissue engineering
- high resolution
- newly diagnosed
- genome wide
- multiple sclerosis
- white matter
- brain injury
- binding protein
- chemotherapy induced
- single molecule