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Vol. 29, Issue 8, 1084-1087, August 2001
Department of Veterinary Physiology, School of Veterinary Medicine,
Rakuno Gakuen University, Hokkaido, Japan
The environmental estrogen bisphenol A, orally introduced
into the body, passes through the liver and modulates the endocrine system to elicit irreversible changes in the functioning of
reproduction. To elucidate the actual and dynamic metabolism of
bisphenol A in the liver before its arrival at target organs, this
study evaluated the metabolism and disposition of the compound within
the passage through the liver in Sprague-Dawley rats. On perfusion of
7.5 µmol of bisphenol A into the liver via the portal vein,
approximately 91% of the infused bisphenol A was absorbed by the liver
tissue, and about 65% of the absorbed bisphenol A was glucuronidated
within 60 min. Roughly 65% of the bisphenol A glucuronide that formed in the liver was excreted into the bile and about 35% into the hepatic
vein. On perfusion of 0.01, 0.05, and 0.1 mM bisphenol A solution into
the liver, free bisphenol A was excreted only into the vein at 5.6, 9.3, and 14.6%, respectively, of the total bisphenol A. These results
suggest that most bisphenol A absorbed by the intestine is probably
glucuronidated exclusively in the liver and the conjugate is excreted
mainly into the bile.
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