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Effect of bisphenol A on drug metabolising enzymes in rat hepatic microsomes and precision-cut rat liver slices

  • Toxicokinetics and Metabolism
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Abstract

In order to assess the effects of bisphenol A (BPA) on enzymes of phase I and II biotransformation, studies were conducted in hepatic microsomes and precision-cut liver slices from male Sprague-Dawley rats. A testosterone hydroxylation assay was used for probing the activity of cytochrome P450 (CYP) forms, and an appropriate HPLC method for the separation of testosterone metabolites was developed. BPA markedly inhibited the hydroxylation of testosterone at 2α and 16α but not at 6β or 7α, suggesting a differential inhibition of some CYP forms, in particular CYP2C11. This inhibitory effect was also observed when slices were first exposed to BPA and then incubated with testosterone in the absence of BPA, indicative of an irreversible inhibition of CYP. In liver slices, a differential conjugation of hydroxylated testosterone metabolites was observed, which was significantly decreased in the presence of BPA. BPA also inhibited the conjugation of the model compound umbelliferone. Pretreatment with BPA did not affect the conjugation of testosterone and umbelliferone. No hydroxylation, but extensive conjugation of BPA was observed upon incubation of liver slices with BPA alone or with testosterone or umbelliferone. The rapid and preferred conjugation, however, does not prevent the irreversible inhibition of some CYP forms by BPA. In conclusion, this study has shown that BPA causes a selective and irreversible inhibition of certain CYP forms and interferes with the conjugation of other drugs.

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Abbreviations

BPA :

Bisphenol A

CYP :

Cytochrome P450

DMSO :

Dimethylsulfoxide

LDH :

Lactate dehydrogenase

PCTS :

Precision-cut tissue slice

References

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  • Elsby R, Maggs JL, Ashby J, Park B K (2001) Comparison of the modulatory effects of human and rat liver microsomal metabolism on the estrogenicity of bisphenol A: implications for extrapolation to humans. J Pharmacol Exp Ther 297:103–113

    CAS  PubMed  Google Scholar 

  • Fisher R, Smith PF, Sipes IG, Gandolfi AJ, Krumdieck CL, Brendel K (1990) Toxicity of chlorobenzenes in cultured rat liver slices. In Vitro Toxicol 3:181–194

    CAS  Google Scholar 

  • Gonzales FJ (1990) Molecular genetics of the P-450 superfamily. Pharmacol Therap 45:1–38

    Article  Google Scholar 

  • Hanioka N, Jinno H, Nishimura T, Ando M (1998) Suppression of male-specific cytochrome P450 isoforms by bisphenol A in rat liver. Arch Toxicol 72:387–394

    Article  CAS  PubMed  Google Scholar 

  • Hanioka N, Jinno H, Tanaka-Kagawa T, Nishimura T, Ando M (2000) Interaction of bisphenol A with rat hepatic cytochrome P450 enzymes. Chemosphere 41:973–978

    Article  CAS  PubMed  Google Scholar 

  • Krishnan AV, Stathis P, Permuth SF, Tokes L, Feldman D (1993) Bisphenol-A: an estrogenic substance is released from polycarbonate flasks during autoclaving. Endocrinology 132:2279–2286

    CAS  PubMed  Google Scholar 

  • Lake BG (1987) Preparation and characterization of microsomal fractions for studies on xenobiotic metabolism. In: Snell K, Mullock B (eds) Biochemical toxicology. IRL Press, Oxford, pp 183–215

  • Markey CM, Michaelson CL, Sonnenschein C, Soto AM (2001) Alkylphenols and bisphenol A as environmental estrogens. In: Metzler M (ed) Endocrine disruptors, Part I. Springer, Berlin Heidelberg New York, pp 129–153

  • Niwa T, Tsutsui M, Kishimoto K Yabusaki Y, Ishibashi F, Katagiri M (2000) Inhibition of drug-metabolizing enzyme activity in human hepatic cytochrome P450 s by bisphenol A. Biol Pharm Bull 23:498–501

    CAS  PubMed  Google Scholar 

  • Omura T, Sato R (1964) The carbon monoxide-binding pigment of liver microsomes: I. Evidence for its hemoprotein nature. J Biol Chem 239:2370–2377

    CAS  Google Scholar 

  • Parrish AR, Gandolfi AJ, Brendel K (1995) Precision-cut tissue slices: applications in pharmacology and toxicology. Life Sci 57:1887–1901

    Article  CAS  PubMed  Google Scholar 

  • Pfeiffer E, Metzler M (1998) In vitro metabolism of bisphenol-A. Toxicologist 42:279

    Google Scholar 

  • Pfeiffer E, Rosenberg B, Deuschel S, Metzler M (1997) Interference with microtubules and induction of micronuclei in vitro by various bisphenols. Mutat Res 390:21–31

    Article  CAS  PubMed  Google Scholar 

  • Pottenger LH, Domoradzki JY, Markham DA, Hansen SC, Cagen SZ, Waechter JM Jr (2000) The relative bioavailability and metabolism of bisphenol A in rats is dependent upon the route of administration. Toxicol Sci 54:3–18

    CAS  PubMed  Google Scholar 

  • Reid EE, Wilson E (1944) The relation of estrogenic activity to structure in some 4,4’- dihydroxydiphenylmethanes. J Am Chem Soc 66:967–969

    CAS  Google Scholar 

  • Ryan DE, Levin W (1990) Purification and characterization of hepatic microsomal cytochrome P-450. Pharmacol Ther 45:153–239

    CAS  PubMed  Google Scholar 

  • Schenkman JB, Thummel KE, Favreau LV (1989) Physiological and pathophysiological alterations in rat hepatic cytochrome P-450. Drug Metab Rev 20:557–584

    CAS  PubMed  Google Scholar 

  • Snyder RW, Maness SC, Gaido KW, Welsch F, Sumner SC, Fennell TR (2000) Metabolism and disposition of bisphenol A in female rats. Toxicol Appl Pharmacol 168:225–234

    CAS  PubMed  Google Scholar 

  • Soucek P, Gut I (1992) Cytochromes P-450 in rats: structures, functions, properties and relevant human forms. Xenobiotica 22:83–103

    CAS  PubMed  Google Scholar 

  • Staples CA, Dorn PB, Klecka GM, O’Block ST, Harris LR (1998) A review of the environmental fate, effects, and exposures of bisphenol A. Chemosphere 36:2149–2173

    CAS  PubMed  Google Scholar 

  • Tsutsui T, Tamura Y, Suzuki A, Hirose Y, Kobayashi M, Nishimura H, Metzler M, Barrett JC (2000) Mammalian cell transformation and aneuploidy induced by five bisphenols. Int J Cancer 86:151–154

    Article  CAS  PubMed  Google Scholar 

  • Waxman DJ (1988) Interactions of hepatic cytochromes P-450 with steroid hormones. Regioselectivity and stereospecificity of steroid metabolism and hormonal regulation of rat P-450 enzyme expression. Biochem Pharmacol 37:71–84

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

The research reported in this study complies with the current laws of Germany, where the experiments were carried out.

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Correspondence to Manfred Metzler.

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Pfeiffer, E., Metzler, M. Effect of bisphenol A on drug metabolising enzymes in rat hepatic microsomes and precision-cut rat liver slices. Arch Toxicol 78, 369–377 (2004). https://doi.org/10.1007/s00204-004-0543-6

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  • DOI: https://doi.org/10.1007/s00204-004-0543-6

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