FASEB J. Cell Migration Consortium
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
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
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Suchy, F. J.
Right arrow Articles by Ananthanarayanan, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Suchy, F. J.
Right arrow Articles by Ananthanarayanan, M.

The FASEB Journal, Vol 11, 199-205, Copyright © 1997 by The Federation of American Societies for Experimental Biology


REVIEWS

Bile acid transport across the hepatocyte canalicular membrane

FJ Suchy, CJ Sippel and M Ananthanarayanan
Department of Pediatrics and Cellular and Molecular Physiology, Yale University School of Medicine, New Heaven, Connecticut 06520, USA.

Transport of bile acids across the canalicular membrane of the hepatocyte provides the primary motive force for generation of bile flow and is rate limiting in the vectorial movement of bile acids from blood to bile. Several distinct carriers for bile acids have been defined based on physiological studies in isolated hepatocytes, membrane vesicles, hepatocyte couples, and the perfused rat liver including membrane potential-driven and ATP-dependent mechanisms. Several groups have isolated and functionally reconstituted a canalicular bile acid transport protein of M(r) approximately 110 kDa. The ATP-dependent mechanism for secretion of monovalent bile acids appears to be mediated by a yet to be identified protein of the ATP binding cassette family of transporters. However, it remains conjectural whether the ATP-dependent and membrane potential-driven components of canalicular bile acid transport are mediated by one or more transport proteins. Bile acid sulfates and glucuronides are substrates for the canalicular multispecific organic anion transporter whose activity has recently been associated with the multidrug resistance-associated protein.


This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
S. M. Post, M. Groenendijk, K. Solaas, P. C. N. Rensen, and H. M. G. Princen
Cholesterol 7{alpha}-Hydroxylase Deficiency in Mice on an APOE*3-Leiden Background Impairs Very-Low-Density Lipoprotein Production
Arterioscler. Thromb. Vasc. Biol., April 1, 2004; 24(4): 768 - 774.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
N. Mano, T. Goto, M. Uchida, K. Nishimura, M. Ando, N. Kobayashi, and J. Goto
Presence of protein-bound unconjugated bile acids in the cytoplasmic fraction of rat brain
J. Lipid Res., February 1, 2004; 45(2): 295 - 300.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
J. Y. L. Chiang
Bile Acid Regulation of Gene Expression: Roles of Nuclear Hormone Receptors
Endocr. Rev., August 1, 2002; 23(4): 443 - 463.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
K. J. Dix, D. P. Coleman, and A. R. Jeffcoat
Comparative Metabolism and Disposition of Gemfibrozil in Male and Female Sprague-Dawley Rats and Syrian golden Hamsters
Drug Metab. Dispos., January 1, 1999; 27(1): 138 - 146.
[Abstract] [Full Text]


Home page
Drug Metab. Dispos.Home page
A. Y. H. Lu
Drug-Metabolism Research Challenges in the New Millennium. Individual Variability in Drug Therapy and Drug Safety
Drug Metab. Dispos., December 1, 1998; 26(12): 1217 - 1222.
[Abstract] [Full Text]


Home page
Drug Metab. Dispos.Home page
J. A. Jackson, L. S. Birnbaum, and J. J. Diliberto
Effects of Age, Sex, and Pharmacologic Agents on the Biliary Elimination of 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) in F344 Rats
Drug Metab. Dispos., July 1, 1998; 26(7): 714 - 719.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
T. Gerloff, B. Stieger, B. Hagenbuch, J. Madon, L. Landmann, J. Roth, A. F. Hofmann, and P. J. Meier
The Sister of P-glycoprotein Represents the Canalicular Bile Salt Export Pump of Mammalian Liver
J. Biol. Chem., April 17, 1998; 273(16): 10046 - 10050.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Ananthanarayanan, N. Balasubramanian, M. Makishima, D. J. Mangelsdorf, and F. J. Suchy
Human Bile Salt Export Pump Promoter Is Transactivated by the Farnesoid X Receptor/Bile Acid Receptor
J. Biol. Chem., July 27, 2001; 276(31): 28857 - 28865.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1997 by The Federation of American Societies for Experimental Biology.