Department of Biosciences, Federal University of Sao Paulo/UNIFESP (Campus Baixada Santista), 11060-001 Santos, Brazil.
Neurosci Lett. 2010 Oct 15;483(3):179-83. doi: 10.1016/j.neulet.2010.08.003. Epub 2010 Aug 7.
The goal of the present study was to investigate morphological changes in the serotonergic neurons/terminals in the dorsal (DR) and median (MnR) raphe nuclei and on the hippocampal dentate gyrus (DG) in neonatal rats treated from the 1st to the 21st postnatal day with fluoxetine (10 mg/kg sc, daily) or drug vehicle (0.9% saline 1 ml/kg). The results show that postnatal chronic treatment with fluoxetine promoted: (1) a smaller body weight increase during the pre-weaning period; (2) smaller number of 5-HT neurons in the DR; (3) smaller 5-HT neuronal cell bodies (area, perimeter and diameter) in the DR and the MnR and (4) diminished serotonergic terminals in the DG. These data suggest that the development of the serotonergic system was impaired and that early exposure to fluoxetine damaged the morphology of 5-HT neurons in young adult rats. While these findings are consistent with other work, more studies are needed to better clarify the effects of postnatal chronic treatment with fluoxetine on the serotonergic system and, consequently, on the functions modulated by serotonin.
本研究的目的是探讨新生大鼠在第 1 至 21 天接受氟西汀(10mg/kg sc,每日)或药物载体(0.9%生理盐水 1ml/kg)治疗后,其背侧(DR)和中缝核(MnR)的 5-羟色胺能神经元/末梢以及海马齿状回(DG)的形态变化。结果表明,产后慢性氟西汀治疗可促进:(1)在断奶前体重增加减少;(2)DR 中 5-HT 神经元数量减少;(3)DR 和 MnR 中 5-HT 神经元细胞体(面积、周长和直径)变小;(4)DG 中的 5-羟色胺能末梢减少。这些数据表明,5-羟色胺能系统的发育受到损害,早期暴露于氟西汀会损害年轻成年大鼠 5-HT 神经元的形态。虽然这些发现与其他研究一致,但需要更多的研究来更好地阐明产后慢性氟西汀治疗对 5-羟色胺能系统的影响,以及对 5-羟色胺调节的功能的影响。