Role of Rat Multidrug Resistance Protein 2 in Plasma and Biliary Disposition of Dibromosulfophthalein after Microsomal Enzyme Induction

This publication has 16 references indexed in Scilit:

• Increase in Bile Flow and Biliary Excretion of Glutathione-Derived Sulfhydryls in Rats by Drug-Metabolizing Enzyme Inducers Is Mediated by Multidrug Resistance Protein 2
  Toxicological Sciences, 2002
• Oatp2 Mediates Bidirectional Organic Solute Transport: A Role for Intracellular Glutathione
  Molecular Pharmacology, 2000
• cDNA Cloning of the Hepatocyte Canalicular Isoform of the Multidrug Resistance Protein, cMrp, Reveals a Novel Conjugate Export Pump Deficient in Hyperbilirubinemic Mutant Rats
  Journal of Biological Chemistry, 1996
• The role of the canalicular multispecific organic anion transporter in the disposal of endo-and xenobiotics
  Pharmacology & Therapeutics, 1994
• Organic anion transport study in mutant rats with autosomal recessive conjugated hyperbilirubinemia
  Life Sciences, 1991
• Mechanistic aspects of uptake and sinusoidal efflux of dibromosulfophthalein in the isolated perfused rat liver
  Biochemical Pharmacology, 1991
• Selective hepatobiliary transport defect for organic anions and neutral steroids in mutant rats with hereditary-conjugated hyperbilirubinemia
  Hepatology, 1987
• Hereditary Chronic Conjugated Hyperbilirubinemia in Mutant Rats Caused by Defective Hepatic Anion Transport
  Hepatology, 1985
• Role of Glutathione and Hepatic Glutathione S‐transferase in the Biliary Excretion of Methyl Mercury, Cadmium and Zinc: A Study with Enzyme Inducers and Glutathione Depletors
  Acta Pharmacologica et Toxicologica, 1985
• Plasma disappearance and biliary excretion of sulfobromophthalein and phenol-3,6-dibromphthalein disulfonate after microsomal enzyme induction
  Biochemical Pharmacology, 1970