Metabolism of the liver tumor promoter ethinyl estradiol by primary cultures of rat hepatocytes

Andrew M. Standeven, Yuenian E. Shi, Jacqueline F. Sinclair, Peter R. Sinclair, James D. Yager

Research output: Contribution to journalArticlepeer-review

10 Scopus citations


Previously, we reported that relatively high micromolar concentrations of the liver tumor promoter 17α-ethinyl estradiol (EE2) stimulated DNA synthesis and enhanced the DNA synthetic response to epidermal growth factor (EGF) in primary cultures of female rat hepatocytes [J. D. Yager, B. D. Roebuck, T. L. Paluszcyk, and V. A. Memoli, Carcinogenesis 7, 2007-2014 (1986); Y. E. Shi and J. D. Yager, Cancer Res. 49, 3574-3580 (1989)]. In this study, our goal was to examine the metabolism of EE2 in cultured hepatocytes. After 4, 24, and 48 hr of culture, hepatocytes maintained their ability to convert up to 95% of a 4 nm concentration of [3H]EE2 to polar conjugates within 4 hr. EE2 at 2 μm was also 95% metabolized within 4 hr. HPLC analysis of the metabolites confirmed the rapid disappearance of [3H]EE2 and the formation of polar conjugates as detected by organic extraction. HPLC separation of hydrolyzed conjugates indicated that the major aglycone was the parent compound, EE2. In general, the metabolites differed both qualitatively and quantitatively from those reported in vivo in the rat. The rapid metabolism of EE2 by hepatocytes in culture may, at least in part, explain the high concentrations of EE2 required to stimulate DNA synthesis in cultured hepatocytes and to potentiate the response to EGF.

Original languageEnglish (US)
Pages (from-to)486-496
Number of pages11
JournalToxicology and Applied Pharmacology
Issue number3
StatePublished - Mar 1 1990
Externally publishedYes

ASJC Scopus subject areas

  • Toxicology
  • Pharmacology


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