Similarity of bisphenol a pharmacokinetics in rhesus monkeys and Mice: Relevance for human exposure

Julia A. Taylor, Frederick S. vom Saal, Wade V. Welshons, Bertram Drury, George Rottinghaus, Patricia A. Hunt, Pierre Louis Toutain, Céline M. Laffont, Catherine A. Vande Voort

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186 Scopus citations

Abstract

Objective: Daily adult human exposure to bisphenol A (BPA) has been estimated at < 1 μg/kg, with virtually complete first-pass conjugation in the liver in primates but not in mice. We measured unconjugated and conjugated BPA levels in serum from adult female rhesus monkeys and adult female mice after oral administration of BPA and compared findings in mice and monkeys with prior published data in women. Methods: Eleven adult female rhesus macaques were fed 400 μg/kg deuterated BPA (dBPA) daily for 7 days. Levels of serum dBPA were analyzed by isotope-dilution liquid chromatography-mass spectrometry (0.2 ng/mL limit of quantitation) over 24 hr on day 1 and on day 7. The same dose of BPA was fed to adult female CD-1 mice; other female mice were administered 3H-BPA at doses ranging from 2 to 100,000 μg/kg. Results: In monkeys, the maximum unconjugated serum dBPA concentration of 4 ng/mL was reached 1 hr after feeding and declined to low levels by 24 hr, with no significant bioaccumulation after seven daily doses. Mice and monkeys cleared unconjugated serum BPA at virtually identical rates. We observed a linear (proportional) relationship between administered dose and serum BPA in mice. Conclusions: BPA pharmacokinetics in women, female monkeys, and mice is very similar. By comparison with approximately 2 ng/mL unconjugated serum BPA reported in multiple human studies, the average 24-hr unconjugated serum BPA concentration of 0.5 ng/mL in both monkeys and mice after a 400 μg/kg oral dose suggests that total daily human exposure is via multiple routes and is much higher than previously assumed.

Original languageEnglish (US)
Pages (from-to)422-430
Number of pages9
JournalEnvironmental Health Perspectives
Volume119
Issue number2
StatePublished - Feb 2011

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Keywords

  • Biomonitoring
  • Bisphenol A
  • Endocrine disruption
  • Pharmacokinetics
  • Xenobiotic metabolism

ASJC Scopus subject areas

  • Health, Toxicology and Mutagenesis
  • Public Health, Environmental and Occupational Health

Cite this

Taylor, J. A., vom Saal, F. S., Welshons, W. V., Drury, B., Rottinghaus, G., Hunt, P. A., Toutain, P. L., Laffont, C. M., & Vande Voort, C. A. (2011). Similarity of bisphenol a pharmacokinetics in rhesus monkeys and Mice: Relevance for human exposure. Environmental Health Perspectives, 119(2), 422-430.