PLoS ONE · 2014 · 19 citations · 54 references
MedicineNeurosciencePharmacologyDevelopmental NeuroscienceNeuropharmacologyPsychopharmacologyAntidepressant PharmacologyAntidepressant PharmacotherapyAppetite RegulationDevelopmental NeuroendocrinologyDevelopmental NeuropharmacologyFetal PhysiologyAntidepressant Use In PregnancyAppetite SuppressantsDifferentiationHypothalamic HormonesPrenatal NeuropharmacologySelective Serotonin Reuptake Inhibitor TreatmentSelective Serotonin Reuptake Inhibitor UseSerotonin Reuptake Inhibition
A significant number of children undergo maternal exposure to antidepressants and they often present low birth weight. Therefore, it is important to understand how selective serotonin reuptake inhibitors (SSRIs) affect the development of the hypothalamus, the key center for metabolism regulation. In this study we investigated the proliferative actions of fluoxetine in fetal hypothalamic neuroprogenitor cells and demonstrate that fluoxetine induces the proliferation of these cells, as shown by increased neurospheres size and number of proliferative cells (Ki-67+ cells). Moreover, fluoxetine inhibits the differentiation of hypothalamic neuroprogenitor cells, as demonstrated by decreased number of mature neurons (Neu-N+ cells) and increased number of undifferentiated cells (SOX-2+ cells). Additionally, fluoxetine-induced proliferation and maintenance of hypothalamic neuroprogenitor cells leads to changes in the mRNA levels of appetite regulator neuropeptides, including Neuropeptide Y (NPY) and Cocaine-and-Amphetamine-Regulated-Transcript (CART). This study provides the first evidence that SSRIs affect the development of hypothalamic neuroprogenitor cells in vitro with consequent alterations on appetite neuropeptides.
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Requirement of Hippocampal Neurogenesis for the Behavioral Effects of Antidepressants
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Chronic Antidepressant Treatment Increases Neurogenesis in Adult Rat Hippocampus
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