Fuentes Silvia, Colomina M Teresa, Rodriguez Judit, Vicens Paloma, Domingo José L
Department of Psychology, Psychobiology Unit, Rovira i Virgili University, Sescelades Campus, 43007 Tarragona, Spain.
Toxicol Lett. 2006 Jun 20;164(1):81-9. doi: 10.1016/j.toxlet.2005.11.013. Epub 2005 Dec 27.
The maternal and developmental toxicity of combined exposure to restraint stress and perfluorooctane sulfonate (PFOS) was assessed in mice. On gestation Days 6-18, four groups of plug-positive female mice were orally exposed to PFOS at 0, 1.5, 3 and 6 mg/kg/day. Four additional groups of plug-positive animals received the same PFOS doses being restrained during 30 min three times per day. A control group was also included. Cesarean sections were performed on Day 18 of gestation and fetuses were weighed and examined for external, internal and skeletal malformations and variations. Before sacrifice of the dams, blood was collected and serum samples were prepared for thyroid hormones (total and free T3 and T4) and corticosterone analyses. The results of the present study show that both PFOS and restraint stress induced maternal toxicity. In turn, PFOS-induced fetal toxicity was evidenced by increased prenatal mortality. The only effect of restraint on fetal toxicity was a reduction on body weight and an increased prenatal mortality in fetuses concurrently exposed to 1.5 mg/kg of PFOS and restraint. PFOS-induced adverse effects on maternal and fetal toxicity in mice were observed at lower doses than those previously reported.
在小鼠中评估了联合暴露于束缚应激和全氟辛烷磺酸(PFOS)的母体毒性和发育毒性。在妊娠第6至18天,四组确认受孕的雌性小鼠分别以0、1.5、3和6 mg/kg/天的剂量经口暴露于PFOS。另外四组确认受孕的动物接受相同剂量的PFOS,并每天三次进行30分钟的束缚。还设立了一个对照组。在妊娠第18天进行剖宫产,对胎儿称重,并检查其外部、内部和骨骼的畸形及变异情况。在处死母鼠前,采集血液并制备血清样本,用于分析甲状腺激素(总T3、游离T3、总T4、游离T4)和皮质酮。本研究结果表明,PFOS和束缚应激均会诱发母体毒性。反过来,产前死亡率增加证明了PFOS会诱发胎儿毒性。束缚对胎儿毒性的唯一影响是,在同时暴露于1.5 mg/kg PFOS和束缚的胎儿中,体重减轻且产前死亡率增加。在小鼠中,观察到PFOS诱发母体和胎儿毒性的剂量低于先前报告的剂量。