Universidade Federal de Pernambuco, Departamento de Clínica e Odontologia Preventiva - Recife/PE, Brazil.
Clinics (Sao Paulo). 2010;65(1):61-5. doi: 10.1590/S1807-59322010000100010.
Previous studies have evaluated the presence of serotonin in the dental epithelia and mesenchyme during odontogenesis, suggesting its participation in tooth development.
Here, we used fluoxetine, a selective serotonin re-uptake inhibitor, at a dose of 10 mg/kg, administered for 20 days during pregnancy in 12 Wistar rats to examine the influence of this drug on the development of the enamel organ of the upper first molars of rat fetuses at 17 days of intra-uterine life (i.u.l.), and at one, five and ten days postpartum. The pregnant rats were anesthetized with xylazine at 10 mg/kg and ketamine at 25 mg/kg. The fetuses were removed and beheaded; their jaws were removed, and the upper jaws were exposed. The tissues were fixed in Bouin's fixative, decalcified in 5% nitric acid for 4 - 12 h, conventionally processed for microscopy, and embedded in paraffin. Serial sections of approximately 5 mum were obtained and stained with hematoxylin and eosin, as well as periodic acid-Schiff.
Morphological analysis showed no structural changes in the experimental group compared to the controls, suggesting that, at the dose used, fluoxetine does not interfere with serotonin-mediated development of the enamel organ or the process of amelogenesis.
先前的研究已经评估了在牙发生过程中,牙上皮和间充质中 5-羟色胺的存在,表明其参与了牙齿发育。
在这里,我们使用氟西汀(一种选择性 5-羟色胺再摄取抑制剂),剂量为 10mg/kg,在妊娠期间连续 20 天给 12 只 Wistar 大鼠腹腔注射,以检查该药物对上 17 天宫内发育(I.U.L.)大鼠胎仔第一磨牙釉质器官发育的影响,以及产后 1、5 和 10 天。妊娠大鼠用 10mg/kg 的甲苯噻嗪和 25mg/kg 的氯胺酮麻醉。取出胎儿并断头;取出其颌骨,暴露上颌骨。组织用 Bouin 固定液固定,5%硝酸脱钙 4-12 小时,常规进行显微镜检查,并石蜡包埋。获得约 5 微米的连续切片,并用苏木精和曙红以及过碘酸希夫染色。
形态学分析显示实验组与对照组相比无结构变化,表明在使用的剂量下,氟西汀不会干扰 5-羟色胺介导的釉质器官发育或成釉过程。