Turgut U, Kazan S, Cakin H, Ozak A
Akdeniz University, B Block 2nd Floor, 07000, Antalya, Turkey.
Int J Dev Neurosci. 2019 Nov;78:45-48. doi: 10.1016/j.ijdevneu.2019.05.008. Epub 2019 Jul 31.
Neural tube defect is one of the most prevalent congenital malformations and it involves a variety of malformations ranging from anencephaly to spina bifida. Folic acid supplementation during pregnancy is known to reduce risk of neural tube defects. Antiepileptic drugs have been associated with neural tube defects, one of which is valproic acid. Protective effect of folic acid on congenital malformations in patients using valproic acid or other antiepileptic medicines during pregnancy has not clearly been delineated uniformly in previous clinical series. In this experimental animal study of early chick embryo model, we would like to determine if there is any dose-response relationship between VA and NTDs and if there is any protective effect of FA on this relationship in early chick embryo period.
One hundred twenty-two fertile leghorn type chicken eggs were used in this study. Six groups, each of which composed of 20 fertilized eggs, were categorized as: group A-control, group B- folic acid, group C-low-dose valproic acid, group D-high-dose valproic acid, group E-low-dose valproic acid + folic acid, group F-high-dose valproic acid + folic acid. Eggs were hatched for 24 h and injected with destined solutions and hatched till 72th hour.
No neural tube defect was observed in group A and B. High dose valproic acid led to significantly higher number of embryos with neural tube defects compared to low-dose valproic acid (p = 0.018). This significant difference was also present between low-dose and high dose valproic acid combined with folic acid (p = 0.031). When effect of folic acid was evaluated no significant difference observed between groups.
Even though number of embryos with neural tube defects decreased with concomitant folic acid administration, this difference could not reach a statistical level. More experimental animal and large-scaled prospective clinical studies are in need to detect folic acid mechanism in inhibiting antiepileptic drugs, if any present.
神经管缺陷是最常见的先天性畸形之一,它涉及从无脑儿到脊柱裂等多种畸形。已知孕期补充叶酸可降低神经管缺陷的风险。抗癫痫药物与神经管缺陷有关,丙戊酸就是其中之一。在先前的临床系列研究中,叶酸对孕期使用丙戊酸或其他抗癫痫药物的患者先天性畸形的保护作用尚未得到统一明确的界定。在这项关于早期鸡胚模型的实验动物研究中,我们想确定丙戊酸(VA)与神经管缺陷(NTDs)之间是否存在剂量反应关系,以及叶酸(FA)在鸡胚早期对这种关系是否有任何保护作用。
本研究使用了122枚来航鸡种蛋。将其分为六组,每组20枚受精卵,分别为:A组 - 对照组,B组 - 叶酸组,C组 - 低剂量丙戊酸组,D组 - 高剂量丙戊酸组,E组 - 低剂量丙戊酸 + 叶酸组,F组 - 高剂量丙戊酸 + 叶酸组。将种蛋孵化24小时后注射相应溶液,然后继续孵化至72小时。
A组和B组未观察到神经管缺陷。与低剂量丙戊酸相比,高剂量丙戊酸导致神经管缺陷胚胎数量显著增加(p = 0.018)。低剂量和高剂量丙戊酸联合叶酸组之间也存在显著差异(p = 0.031)。在评估叶酸的作用时,各实验组之间未观察到显著差异。
尽管同时给予叶酸时神经管缺陷胚胎数量有所减少,但这种差异未达到统计学水平。需要更多的实验动物和大规模前瞻性临床研究来检测叶酸抑制抗癫痫药物(若存在)的机制。