Nagao Tetsuji, Kagawa Nao, Saito Yoshiaki, Komada Munekazu
Laboratory of Developmental Biology, Department of Life Science, Kinki University, Osaka, 577-8502, Japan.
J Appl Toxicol. 2013 Nov;33(11):1213-21. doi: 10.1002/jat.2766. Epub 2012 Jun 25.
Placental growth and function are of biological significance in that placental tissue promotes prenatal life and the maintenance of pregnancy. Exposure to synthetic estrogens causes embryonic mortality and placental growth restriction in mice. The aim of the present study was to examine the effects of diethylstilbestrol (DES) on placenta in mice. DES at 1, 5, 10 or 15 µg kg(-1) day(-1) , or 17β-estradiol (E2 ) at 50 µg kg(-1) day(-1) , was administered orally to ICR mice on days 4 through to 8 of gestation. Expression of ERα, ERβ, ERRβ or ERRγ mRNA in the junctional or labyrinth zone of the placentas on day 13 was assessed using RT-PCR, as well as the embrynic mortality, embryonic and placental weight, histological changes of labyrinth and ultrastructural changes of the trophoblast giant cells (TGCs). Embryo mortalities in the DES 10 and 15 µg kg(-1) day(-1) groups were markedly increased. No significant changes in embryonic and placental weight were observed in any DES- or E2 -exposed groups. Expression of ERα mRNA in the junctional zone with male embryos in the 5 µg kg(-1) day(-1) group was significantly higher than that in the control, whereas expression was not determined in the 15 µg kg(-1) day(-1) group. Histological observation revealed that the placentas exposed to DES at 10 µg kg(-1) day(-1) lacked the developing labyrinth. Ultrastructural observation of the TGCs showed poor rough-surfaced endoplasmic reticulum in the DES 10 µg kg(-1) day(-1) group. The present data suggest that developmental changes induced by DES may be related to interference with the nutrition and oxygen exchange between mother and embryo or decreased protein synthesis, resulting in a high frequency of embryo mortality.
胎盘的生长和功能具有生物学意义,因为胎盘组织促进胎儿期生命及维持妊娠。接触合成雌激素会导致小鼠胚胎死亡和胎盘生长受限。本研究的目的是检测己烯雌酚(DES)对小鼠胎盘的影响。在妊娠第4至8天,对ICR小鼠口服给予1、5、10或15 μg kg⁻¹ 天⁻¹ 的DES,或50 μg kg⁻¹ 天⁻¹ 的17β-雌二醇(E2)。使用逆转录聚合酶链反应(RT-PCR)评估妊娠第13天胎盘交界区或迷路区中雌激素受体α(ERα)、雌激素受体β(ERβ)、雌激素相关受体β(ERRβ)或雌激素相关受体γ(ERRγ)mRNA的表达,以及胚胎死亡率、胚胎和胎盘重量、迷路的组织学变化和滋养层巨细胞(TGCs)的超微结构变化。DES 10和15 μg kg⁻¹ 天⁻¹ 组的胚胎死亡率显著增加。在任何DES或E2暴露组中均未观察到胚胎和胎盘重量的显著变化。5 μg kg⁻¹ 天⁻¹ 组雄性胚胎交界区中ERα mRNA的表达显著高于对照组,而15 μg kg⁻¹ 天⁻¹ 组未检测到该表达。组织学观察显示,10 μg kg⁻¹ 天⁻¹ 的DES暴露组胎盘缺乏发育中的迷路。TGCs的超微结构观察显示,DES 10 μg kg⁻¹ 天⁻¹ 组粗面内质网较差。目前的数据表明,DES诱导的发育变化可能与干扰母体与胚胎之间的营养和氧气交换或蛋白质合成减少有关,从而导致胚胎死亡率较高。