Literature DB >> 7846117

The role of the canalicular multispecific organic anion transporter in the disposal of endo- and xenobiotics.

R P Oude Elferink1, P L Jansen.   

Abstract

Bile is an important excretory route for the elimination of amphiphilic organic anions, and hepatocytes are the primary secretory units of bile formation. The hepatocytic basolateral and canalicular membranes are equipped with various carrier proteins. Transport across the canalicular membrane represents a major concentrative step. Various ATP-dependent transporters have been identified, such as a multispecific organic anion transporter (canalicular multispecific organic ion transporter, cMOAT), a bile acid transporter and several P-glycoproteins. TR- rats, which lack cMOAT activity, have been valuable in defining the substrate specificity of cMOAT. A wide range of glucuronide-, glutathione- and sulfate-conjugates are transported by this system.

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Year:  1994        PMID: 7846117     DOI: 10.1016/0163-7258(94)90034-5

Source DB:  PubMed          Journal:  Pharmacol Ther        ISSN: 0163-7258            Impact factor:   12.310


  17 in total

Review 1.  Modeling kinetics of subcellular disposition of chemicals.

Authors:  Stefan Balaz
Journal:  Chem Rev       Date:  2009-05       Impact factor: 60.622

2.  Induction of the multispecific organic anion transporter (cMoat/mrp2) gene and biliary glutathione secretion by the herbicide 2,4,5-trichlorophenoxyacetic acid in the mouse liver.

Authors:  A M Wielandt; V Vollrath; M Manzano; S Miranda; L Accatino; J Chianale
Journal:  Biochem J       Date:  1999-07-01       Impact factor: 3.857

3.  Biliary excretion of ciprofloxacin and piperacillin in the obstructed biliary tract.

Authors:  S J van den Hazel; X H de Vries; P Speelman; J Dankert; G N Tytgat; K Huibregtse; D J van Leeuwen
Journal:  Antimicrob Agents Chemother       Date:  1996-11       Impact factor: 5.191

4.  MOAT4, a novel multispecific organic-anion transporter for glucuronides and mercapturates in mouse L1210 cells and human erythrocytes.

Authors:  M Saxena; G B Henderson
Journal:  Biochem J       Date:  1996-11-15       Impact factor: 3.857

5.  Influence of mild liver impairment on the pharmacokinetics of tezosentan, a drug excreted unchanged into bile.

Authors:  Jasper Dingemanse; Paul L M van Giersbergen
Journal:  Br J Clin Pharmacol       Date:  2004-03       Impact factor: 4.335

6.  Basolateral and canalicular transport of xenobiotics in the hepatocyte: A review.

Authors:  G J Diaz
Journal:  Cytotechnology       Date:  2000-11       Impact factor: 2.058

7.  Intracellular nucleotide pools and ratios as tools for monitoring dedifferentiation of primary porcine hepatocytes in culture.

Authors:  Dirk Rocker; Friedemann Hesse; Augustinus Bader; Roland Wagner
Journal:  Cytotechnology       Date:  2006-11-21       Impact factor: 2.058

8.  Quantitative in vivo assessment of radiation injury of the liver using Gd-EOB-DTPA enhanced MRI: tolerance dose of small liver volumes.

Authors:  Max Seidensticker; Ricarda Seidensticker; Konrad Mohnike; Christian Wybranski; Thomas Kalinski; Sebastian Luess; Maciej Pech; Peter Wust; Jens Ricke
Journal:  Radiat Oncol       Date:  2011-04-17       Impact factor: 3.481

9.  Liver dysfunction and phosphatidylinositol-3-kinase signalling in early sepsis: experimental studies in rodent models of peritonitis.

Authors:  Peter Recknagel; Falk A Gonnert; Martin Westermann; Sandro Lambeck; Amelie Lupp; Alain Rudiger; Alex Dyson; Jane E Carré; Andreas Kortgen; Christoph Krafft; Jürgen Popp; Christoph Sponholz; Valentin Fuhrmann; Ingrid Hilger; Ralf A Claus; Niels C Riedemann; Reinhard Wetzker; Mervyn Singer; Michael Trauner; Michael Bauer
Journal:  PLoS Med       Date:  2012-11-13       Impact factor: 11.069

Review 10.  Molecular alterations of canalicular transport systems in experimental models of cholestasis: possible functional correlations.

Authors:  M Trauner
Journal:  Yale J Biol Med       Date:  1997 Jul-Aug
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