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Maternal cadmium exposure reduces placental zinc transport and induces fetal growth restriction in mice

机译:母体接触镉会降低胎盘中锌的运输并诱发小鼠胎儿生长受限

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Cadmium (Cd) is linked with increased risk of fetal growth restriction (FGR). Nevertheless, the mechanism remains unknown. This study established a mouse model of Cd-induced FGR through two exposure methods. Pregnant mice were either administered with CdCl2 (5, 50 and 250 ppm) throughout pregnancy through drinking water or intraperitoneally injected with CdCl2 (4.5 mg/kg) on GD9. As expected, fetal weight and crown-rump length were reduced in a gender-independent manner. Interestingly, Mt1 and Mt2, two metallothionein genes, were up-regulated in maternal liver. Correspondingly, Cd accumulated mainly in maternal liver and kidney, and only trace amounts of Cd could pass from dam to placentas and fetuses. Further analysis showed that placental Zn concentration was elevated. Conversely, embryonic Zn concentration was reduced. Moreover, placental Znt1 and Znt2, two zinc transporters, were down regulated in Cd-exposed mice. These results suggest that maternal Cd exposure during pregnancy reduces placental Zn transport and induces fetal growth restriction. (C) 2016 Elsevier Inc. All rights reserved.
机译:镉(Cd)与胎儿生长受限(FGR)的风险增加有关。但是,该机制仍然未知。这项研究通过两种暴露方法建立了Cd诱导的FGR小鼠模型。在怀孕期间,通过饮用水给怀孕的小鼠施用CdCl2(5、50和250 ppm),或在GD9腹膜内注射CdCl2(4.5 mg / kg)。正如预期的那样,胎儿体重和冠臀长度以性别无关的方式减少。有趣的是,母体肝脏中的两个金属硫蛋白基因Mt1和Mt2被上调。相应地,镉主要在母体肝脏和肾脏中积累,只有微量的镉可以从大坝传到胎盘和胎儿。进一步分析表明胎盘中锌的浓度升高。相反,降低了胚胎锌的浓度。此外,在暴露于Cd的小鼠中胎盘Znt1和Znt2这两种锌转运蛋白被下调。这些结果表明,孕妇在怀孕期间接触Cd会减少胎盘中Zn的转运并引起胎儿生长受限。 (C)2016 Elsevier Inc.保留所有权利。

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