Fadel R A, Sequeira R P, Abu-Hijleh M F, Obeidat M, Salem A H A
Department of Anatomy, College of Medicine and Medical Sciences, Arabian Gulf University, Manama, Bahrain.
Rom J Morphol Embryol. 2012;53(2):321-7.
There are few studies that have addressed the effects of prenatal exposure of topiramate on ossification of the bones derived from the paraxial mesoderm. This study aimed to evaluate skeletal ossification of ribs and vertebrae in 20-day-old rat fetuses after maternal exposure to two therapeutic doses of topiramate. Three groups of Sprague-Dawley pregnant rats were used: control, topiramate 50 mg/kg/day and topiramate 100 mg/kg/day treated groups. Topiramate was administered by gavage from day 6-19 of gestation. Fetuses were collected on day 20 by caesarean section. Fetal bones were stained with alizarin red and ossification was assessed. Results showed significant delayed ossification of ribs and vertebrae in topiramate-exposed fetuses at both doses and the effects were not dose dependent. In all examined groups, there was a direct correlation between the fetal weight and the number of complete ossified vertebral centers. Also, there were significant increases in skeletal abnormalities, particularly in ribs in both treated groups when compared to the control group. In conclusion, therapeutic doses of topiramate should be taken cautiously during pregnancy as they lead to fetal growth restriction and increases abnormalities of axial skeleton in rat fetuses.
很少有研究探讨产前接触托吡酯对源自轴旁中胚层的骨骼骨化的影响。本研究旨在评估母体接触两种治疗剂量的托吡酯后20日龄大鼠胎儿肋骨和椎骨的骨骼骨化情况。使用了三组斯普拉格-道利妊娠大鼠:对照组、托吡酯50 mg/kg/天和托吡酯100 mg/kg/天治疗组。从妊娠第6天至第19天通过灌胃给予托吡酯。在第20天通过剖腹产收集胎儿。用茜素红对胎儿骨骼进行染色并评估骨化情况。结果显示,两种剂量的托吡酯暴露胎儿的肋骨和椎骨骨化均显著延迟,且效果不依赖于剂量。在所有检查的组中,胎儿体重与完全骨化的椎体中心数量之间存在直接相关性。此外,与对照组相比,两个治疗组的骨骼异常显著增加,尤其是肋骨。总之,孕期应谨慎使用治疗剂量的托吡酯,因为它们会导致胎儿生长受限并增加大鼠胎儿轴向骨骼的异常。