Literature DB >> 12915710

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.

J Y Domoradzki1, L H Pottenger, C M Thornton, S C Hansen, T L Card, D A Markham, M D Dryzga, R N Shiotsuka, J M Waechter.   

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.

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Year:  2003        PMID: 12915710     DOI: 10.1093/toxsci/kfg206

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  17 in total

1.  In vivo and ex vivo percutaneous absorption of [14C]-bisphenol A in rats: a possible extrapolation to human absorption?

Authors:  Fabrice Marquet; Jean-Paul Payan; Dominique Beydon; Ludivine Wathier; Marie-Christine Grandclaude; Elisabeth Ferrari
Journal:  Arch Toxicol       Date:  2011-02-02       Impact factor: 5.153

2.  The Bisphenols Found in the Ejaculate of Men Does Not Pass through the Testes.

Authors:  Michal Ješeta; Kateřina Franzová; Simona Machynová; Jiří Kalina; Jiří Kohoutek; Lenka Mekiňová; Igor Crha; Bartosz Kempisty; Marek Kašík; Jana Žáková; Pavel Ventruba; Jana Navrátilová
Journal:  Toxics       Date:  2022-06-09

3.  Bisphenol A (BPA) pharmacokinetics with daily oral bolus or continuous exposure via silastic capsules in pregnant rhesus monkeys: Relevance for human exposures.

Authors:  Frederick S Vom Saal; Catherine A VandeVoort; Julia A Taylor; Wade V Welshons; Pierre-Louis Toutain; Patricia A Hunt
Journal:  Reprod Toxicol       Date:  2014-02-25       Impact factor: 3.143

4.  A Conflicted Tale of Two Novel AR Antagonists In Vitro and In Vivo: Pyrifluquinazon Versus Bisphenol C.

Authors:  Leon Earl Gray; Johnathan R Furr; Justin M Conley; Christy S Lambright; Nicola Evans; Mary C Cardon; Vickie S Wilson; Paul M Foster; Phillip C Hartig
Journal:  Toxicol Sci       Date:  2019-04-01       Impact factor: 4.849

5.  Developmental neurotoxicity study of dietary bisphenol A in Sprague-Dawley rats.

Authors:  Donald G Stump; Melissa J Beck; Ann Radovsky; Robert H Garman; Lester L Freshwater; Larry P Sheets; M Sue Marty; John M Waechter; Stephen S Dimond; John P Van Miller; Ronald N Shiotsuka; Dieter Beyer; Anne H Chappelle; Steven G Hentges
Journal:  Toxicol Sci       Date:  2010-02-17       Impact factor: 4.849

6.  Neither direct nor developmental exposure to bisphenol A alters the severity of experimental inflammatory colitis in mice.

Authors:  Anirban Roy; Alison Gaylo; Wenqing Cao; Lawrence J Saubermann; B Paige Lawrence
Journal:  J Immunotoxicol       Date:  2013-01-03       Impact factor: 3.000

7.  Placental transfer of conjugated bisphenol A and subsequent reactivation in the rat fetus.

Authors:  Miyu Nishikawa; Hidetomo Iwano; Risa Yanagisawa; Nanako Koike; Hiroki Inoue; Hiroshi Yokota
Journal:  Environ Health Perspect       Date:  2010-04-09       Impact factor: 9.031

8.  Does rapid metabolism ensure negligible risk from bisphenol A?

Authors:  Gary Ginsberg; Deborah C Rice
Journal:  Environ Health Perspect       Date:  2009-07-14       Impact factor: 9.031

9.  Basic exploratory research versus guideline-compliant studies used for hazard evaluation and risk assessment: bisphenol A as a case study.

Authors:  Rochelle W Tyl
Journal:  Environ Health Perspect       Date:  2009-06-29       Impact factor: 9.031

10.  Pregnancy-specific physiologically-based toxicokinetic models for bisphenol A and bisphenol S.

Authors:  Jeremy Gingrich; David Filipovic; Rory Conolly; Sudin Bhattacharya; Almudena Veiga-Lopez
Journal:  Environ Int       Date:  2020-12-22       Impact factor: 9.621

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