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双酚A(BPA)的代谢与药代动力学以及BPA和BPA - 单葡萄糖醛酸苷在三个妊娠阶段的CD斯普拉格 - 道利大鼠胚胎 - 胎儿中的分布情况。

Metabolism and pharmacokinetics of bisphenol A (BPA) and the embryo-fetal distribution of BPA and BPA-monoglucuronide in CD Sprague-Dawley rats at three gestational stages.

作者信息

Domoradzki J Y, Pottenger L H, Thornton C M, Hansen S C, Card T L, Markham D A, Dryzga M D, Shiotsuka R N, Waechter J M

机构信息

Toxicology & Environmental Research and Consulting, The Dow Chemical Company, Midland, Michigan 48674, USA.

出版信息

Toxicol Sci. 2003 Nov;76(1):21-34. doi: 10.1093/toxsci/kfg206. Epub 2003 Aug 12.

Abstract

The pharmacokinetics of bisphenol A (BPA), including the quantification of the major BPA metabolite BPA-monoglucuronide conjugate (BPA-glucuronide) was studied in Sprague-Dawley rats at different stages of gestation. 14C-BPA was administered orally at 10 mg BPA/kg body weight (0.2 mCi/rat) to nongravid rats and to other groups on gestation days (GD) 6, 14, and 17. GD 0 was when the vaginal smear was sperm positive or a copulatory plug was observed. Radioactivity derived from 14C-BPA was quantified in the maternal blood, selected tissues, and the embryo or fetus. BPA and BPA-glucuronide were quantified in maternal plasma and excreta. Additional rats were dosed orally at 10 mg 14C-BPA/kg (0.2 mCi/rat or 0.5 mCi/rat) on GD 11, 13, and 16 to further study the distribution of BPA and BPA-glucuronide to the embryo/fetal tissue. The tissue distribution, metabolism, or the rates or routes of excretion of BPA, or the plasma concentration-time profiles of BPA-glucuronide did not appear to be altered at any stage of gestation as compared to nonpregnant rats. In the GD 11 group, neither BPA nor BPA-glucuronide was detected in the yolk sacs or embryos, except for trace concentrations of BPA-glucuronide in the yolk sacs at 15 min postdosing. In the GD 13 group, both BPA and BPA-glucuronide were detected in the yolk sacs of the conceptus but not in the embryos/fetuses, except for BPA at 15 min. For the animals dosed with 0.2 mCi/rat on GD 16, both analytes were detected in the placentae at 15 min and 12 h, but not at 96 h. Traces of both analytes were detected in fetal tissue in two of five specimens at 15 min only. In rats dosed on GD 16 with 0.5 mCi/rat, the BPA-glucuronide and BPA concentrations in maternal plasma at 15 min were 1.7 and 0.06 mug equivalents (eq)/g plasma, respectively. At the same time postdosing in these animals, the placental BPA-glucuronide concentrations were lower (0.34 mug eq BPA [as glucuronide]/g), and the BPA concentrations were about equivalent (0.095 mug/g). Fetal BPA-glucuronide and BPA concentrations were markedly lower, 0.013 and 0.018 mug eq/g, respectively. Therefore, no selective affinity of either yolk sac/placenta or embryo/fetus for BPA or BPA metabolites relative to maternal plasma or tissues was observed in this study.

摘要

在不同妊娠阶段的斯普拉格-道利大鼠中研究了双酚A(BPA)的药代动力学,包括对主要BPA代谢物BPA-单葡萄糖醛酸结合物(BPA-葡萄糖醛酸)的定量分析。将14C-BPA以10 mg BPA/千克体重(0.2 mCi/只大鼠)的剂量口服给予未孕大鼠以及妊娠第6、14和17天的其他组大鼠。妊娠第0天是指阴道涂片精子呈阳性或观察到交配栓的日子。对母体血液、选定组织以及胚胎或胎儿中的14C-BPA衍生放射性进行了定量分析。对母体血浆和排泄物中的BPA和BPA-葡萄糖醛酸进行了定量分析。另外的大鼠在妊娠第11、13和16天以10 mg 14C-BPA/千克(0.2 mCi/只大鼠或0.5 mCi/只大鼠)的剂量口服给药,以进一步研究BPA和BPA-葡萄糖醛酸在胚胎/胎儿组织中的分布情况。与未孕大鼠相比,BPA的组织分布、代谢、排泄速率或途径,或BPA-葡萄糖醛酸的血浆浓度-时间曲线在妊娠的任何阶段似乎均未改变。在妊娠第11天的组中,除给药后15分钟卵黄囊中存在痕量的BPA-葡萄糖醛酸外,在卵黄囊或胚胎中均未检测到BPA或BPA-葡萄糖醛酸。在妊娠第13天的组中,在孕体的卵黄囊中检测到了BPA和BPA-葡萄糖醛酸,但在胚胎/胎儿中未检测到,给药后15分钟时除外。对于在妊娠第16天以0.2 mCi/只大鼠给药的动物,在15分钟和12小时时在胎盘中检测到了两种分析物,但在96小时时未检测到。仅在15分钟时,在五个标本中的两个标本的胎儿组织中检测到了痕量的两种分析物。在妊娠第16天以0.5 mCi/只大鼠给药的大鼠中,给药后15分钟时母体血浆中BPA-葡萄糖醛酸和BPA的浓度分别为1.7和0.06微克当量(eq)/克血浆。在这些动物给药后相同时间,胎盘BPA-葡萄糖醛酸浓度较低(0.34微克当量BPA[以葡萄糖醛酸形式计]/克),BPA浓度大致相当(0.095微克/克)。胎儿BPA-葡萄糖醛酸和BPA浓度明显较低,分别为0.013和0.018微克当量/克。因此,在本研究中未观察到卵黄囊/胎盘或胚胎/胎儿对BPA或BPA代谢物相对于母体血浆或组织有选择性亲和力。

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