Wegner C, Drews E, Nau H
Children's Hospital Medical Center, Cincinnati, OH 45229.
Biol Trace Elem Res. 1990 Jun;25(3):211-7. doi: 10.1007/BF02990416.
The effect of a single teratogenic dose of the antiepileptic drug valproic acid and its nonteratogenic metabolite, 2-en-valproic acid, on zinc concentrations in mouse plasma, embryo, and decidua on d 9 of gestation was investigated. The substances were injected subcutaneously (sc) as their sodium salts. In this mouse model, valproic acid induced between 20% (400 mg/kg dose) and 60% (600 mg/kg dose) incidence of exencephaly in living fetuses; 2-en-valproic acid was not teratogenic at these dose levels. The zinc concentrations in plasma were significantly increased 1 and 2 h after administration of both substances. The embryonic zinc concentrations were increased 2 and 4 h after application of both substances. The concentrations of zinc in the decidua were not affected. The similarity of effects of valproic acid and its nonteratogenic analog on zinc concentrations in maternal plasma and embryo suggests that the teratogenicity of a single administration of valproic acid in the mouse is not owing to interference with the zinc metabolism in this species.
研究了致畸剂量的抗癫痫药物丙戊酸及其非致畸代谢物2-烯丙戊酸对妊娠第9天小鼠血浆、胚胎和蜕膜中锌浓度的影响。这些物质以钠盐形式皮下注射。在该小鼠模型中,丙戊酸导致活胎中无脑儿的发生率在20%(400mg/kg剂量)至60%(600mg/kg剂量)之间;在这些剂量水平下,2-烯丙戊酸无致畸性。两种物质给药后1小时和2小时,血浆中的锌浓度显著升高。两种物质应用后2小时和4小时,胚胎锌浓度升高。蜕膜中的锌浓度未受影响。丙戊酸及其非致畸类似物对母体血浆和胚胎中锌浓度的影响相似,这表明单次给予丙戊酸在小鼠中的致畸性并非由于干扰该物种的锌代谢。