GHU Paris Psychiatrie & Neurosciences, site Sainte Anne, Service Hospitalo-Universitaire de psychiatrie, Paris, France.
Institut Pasteur, Experimental Neuropathology Unit, Global Health Department, Paris, France.
Nat Commun. 2024 Jul 31;15(1):6457. doi: 10.1038/s41467-024-50220-4.
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.
选择性 5-羟色胺再摄取抑制剂类抗抑郁药,如氟西汀,被广泛用于治疗情绪障碍。其作用机制包括增加细胞外 5-羟色胺水平、神经发生和大脑血管生长。我们研究了氟西汀是否具有更广泛的外周再生特性。在雄性小鼠中长时间给予氟西汀后,我们发现氟西汀增加了肌肉干细胞的数量和肌肉血管生成,与骨骼肌功能的积极变化相关。氟西汀还可改善单次和多次损伤后的骨骼肌再生,增加肌肉干细胞池和血管密度,同时减少纤维性病变和炎症。用氟西汀治疗缺乏外周 5-羟色胺的小鼠在肌肉再生过程中并未表现出有益的效果。具体而言,5-HT1B 型血清素受体的药理学和基因失活也消除了氟西汀诱导的增强再生过程。我们在这里强调了 5-羟色胺对骨骼肌的再生特性。