Keen C L, Peters J M, Hurley L S
Department of Nutrition, University of California, Davis 95616.
J Nutr. 1989 Apr;119(4):607-11. doi: 10.1093/jn/119.4.607.
The effect of valproic acid on the distribution of gavaged 65Zn in maternal and embryonic tissue of Sprague-Dawley rats was examined 24 h after gavaging of the drug on d 13 of pregnancy. Valproic acid treatment resulted in a significantly higher retention of 65Zn in maternal liver and lower amounts in uterus, placenta and embryos than in controls. Compared to controls, gel chromatography of maternal liver from valproic acid-treated dams showed higher 65Zn counts associated with a protein peak of molecular weight of 6,500, the approximate molecular weight of the Zn-binding protein metallothionein. These results support the idea that the teratogenicity of valproic acid is in part due to an induction of embryonic Zn deficiency secondary to a drug-induced sequestering of Zn into maternal liver that results in a decrease in maternal plasma Zn and subsequent reduction in embryonic Zn uptake.
在妊娠第13天灌胃给予丙戊酸24小时后,检测了丙戊酸对灌胃给予的65Zn在Sprague-Dawley大鼠母体和胚胎组织中分布的影响。与对照组相比,丙戊酸处理导致母体肝脏中65Zn的潴留显著增加,而子宫、胎盘和胚胎中的含量则低于对照组。与对照组相比,对丙戊酸处理的母鼠的母体肝脏进行凝胶色谱分析显示,与分子量为6500的蛋白质峰相关的65Zn计数更高,该分子量约为锌结合蛋白金属硫蛋白的分子量。这些结果支持了这样一种观点,即丙戊酸的致畸性部分归因于药物诱导锌螯合到母体肝脏中,继而导致母体血浆锌减少以及随后胚胎锌摄取减少,从而引发胚胎锌缺乏。