DMD Simcyp

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Inoue, H.
Right arrow Articles by Kato, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Inoue, H.
Right arrow Articles by Kato, S.

Vol. 29, Issue 8, 1084-1087, August 2001

Bisphenol A Glucuronide, a Major Metabolite in Rat Bile after Liver Perfusion

Hiroki Inoue, Hiroshi Yokota,1 Tsunehisa Makino,2 Akira Yuasa,1 and Seiyu Kato

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.


1 Present address: Department of Veterinary Biochemistry, School of Veterinary Medicine, Rakuno Gakuen University, Ebetsu, Hokkaido, 069-8501 Japan.

2 Present address: Department of Obstetrics and Gynecology, Tokai University School of Medicine, Bohseidai, Isehara, Kanagawa, 259-1153 Japan.


Copyright © 2001 by The American Society for Pharmacology and Experimental Therapeutics



This article has been cited by other articles:


Home page
Drug Metab. Dispos.Home page
R. K. Kuester and I. G. Sipes
Prediction of Metabolic Clearance of Bisphenol A (4,4 '-Dihydroxy-2,2-diphenylpropane) using Cryopreserved Human Hepatocytes
Drug Metab. Dispos., October 1, 2007; 35(10): 1910 - 1915.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
T. Daidoji, M. Ozawa, H. Sakamoto, T. Sako, H. Inoue, R. Kurihara, S. Hashimoto, and H. Yokota
SLOW ELIMINATION OF NONYLPHENOL FROM RAT INTESTINE
Drug Metab. Dispos., January 1, 2006; 34(1): 184 - 190.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
W. Volkel, N. Bittner, and W. Dekant
QUANTITATION OF BISPHENOL A AND BISPHENOL A GLUCURONIDE IN BIOLOGICAL SAMPLES BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY
Drug Metab. Dispos., November 1, 2005; 33(11): 1748 - 1757.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
J. G. Teeguarden, J. M. Waechter Jr., H. J. Clewell III, T. R. Covington, and H. A. Barton
Evaluation of Oral and Intravenous Route Pharmacokinetics, Plasma Protein Binding, and Uterine Tissue Dose Metrics of Bisphenol A: A Physiologically Based Pharmacokinetic Approach
Toxicol. Sci., June 1, 2005; 85(2): 823 - 838.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
H. Inoue, A. Tsuruta, S. Kudo, T. Ishii, Y. Fukushima, H. Iwano, H. Yokota, and S. Kato
BISPHENOL A GLUCURONIDATION AND EXCRETION IN LIVER OF PREGNANT AND NONPREGNANT FEMALE RATS
Drug Metab. Dispos., January 1, 2005; 33(1): 55 - 59.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
J. Y. Domoradzki, L. H. Pottenger, C. M. Thornton, S. C. Hansen, T. L. Card, D. A. Markham, M. D. Dryzga, R. N. Shiotsuka, and J. M. Waechter Jr.
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
Toxicol. Sci., November 1, 2003; 76(1): 21 - 34.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
T. Daidoji, H. Inoue, S. Kato, and H. Yokota
GLUCURONIDATION AND EXCRETION OF NONYLPHENOL IN PERFUSED RAT LIVER
Drug Metab. Dispos., August 1, 2003; 31(8): 993 - 998.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
H. Kurebayashi, H. Betsui, and Y. Ohno
Disposition of a Low Dose of 14C-Bisphenol A in Male Rats and Its Main Biliary Excretion as BPA Glucuronide
Toxicol. Sci., May 1, 2003; 73(1): 17 - 25.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
R. Thuillier, Y. Wang, and M. Culty
Prenatal Exposure to Estrogenic Compounds Alters the Expression Pattern of Platelet-Derived Growth Factor Receptors {alpha} and {beta} in Neonatal Rat Testis: Identification of Gonocytes as Targets of Estrogen Exposure
Biol Reprod, March 1, 2003; 68(3): 867 - 880.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
H. Inoue, G. Yuki, H. Yokota, and S. Kato
Bisphenol A Glucuronidation and Absorption in Rat Intestine
Drug Metab. Dispos., January 1, 2003; 31(1): 140 - 144.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
J. J. Pritchett, R. K. Kuester, and I. G. Sipes
Metabolism of Bisphenol A in Primary Cultured Hepatocytes from Mice, Rats, and Humans
Drug Metab. Dispos., November 1, 2002; 30(11): 1180 - 1185.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 2001 by the American Society for Pharmacology and Experimental Therapeutics.