Effects of atorvastatin metabolites on induction of drug‐metabolizing enzymes and membrane transporters through human pregnane X receptor
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M Schwab | W. Thasler | A. Nussler | M. Schwab | T. Weiss | O. Burk | M. Schwab | E. Hoffart | E Hoffart | L Ghebreghiorghis | A K Nussler | W E Thasler | T S Weiss | O Burk | L. Ghebreghiorghis | W. Thasler | T. Weiß | AK Nussler
[1] J. Xu,et al. DIFFERENTIAL INTERACTION OF 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE INHIBITORS WITH ABCB1, ABCC2, AND OATP1B1 , 2005, Drug Metabolism and Disposition.
[2] J. Shyy,et al. Statins Activate AMP-Activated Protein Kinase In Vitro and In Vivo , 2006, Circulation.
[3] Julia Qiu,et al. Interactions of Human P-glycoprotein with Simvastatin, Simvastatin Acid, and Atorvastatin , 2004, Pharmaceutical Research.
[4] Ute Hofmann,et al. Profiling Induction of Cytochrome P450 Enzyme Activity by Statins Using a New Liquid Chromatography-Tandem Mass Spectrometry Cocktail Assay in Human Hepatocytes , 2010, Drug Metabolism and Disposition.
[5] D. Corella,et al. Apolipoprotein E genotype affects plasma lipid response to atorvastatin in a gender specific manner. , 2001, Atherosclerosis.
[6] Kaoru Kobayashi,et al. Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1*5, SLCO1B1*15 and SLCO1B1*15+C1007G, by using transient expression systems of HeLa and HEK293 cells , 2005, Pharmacogenetics and genomics.
[7] B. M. Forman,et al. The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux , 2001, Nature Medicine.
[8] H. Lennernäs. Clinical Pharmacokinetics of Atorvastatin , 2003, Clinical pharmacokinetics.
[9] Tao Chen,et al. Multi-species analyses of direct activators of the constitutive androstane receptor. , 2011, Toxicological sciences : an official journal of the Society of Toxicology.
[10] P. Neuvonen,et al. Different Effects of SLCO1B1 Polymorphism on the Pharmacokinetics of Atorvastatin and Rosuvastatin , 2007, Clinical pharmacology and therapeutics.
[11] D. Moore,et al. Dynamic stabilization of nuclear receptor ligand binding domains by hormone or corepressor binding. , 2000, Molecular cell.
[12] N. Plant,et al. The statin class of HMG-CoA reductase inhibitors demonstrate differential activation of the nuclear receptors PXR, CAR and FXR, as well as their downstream target genes , 2011, Xenobiotica; the fate of foreign compounds in biological systems.
[13] Thomas S Weiss,et al. Cellular damage to human hepatocytes through repeated application of 5-aminolevulinic acid. , 2003, Journal of hepatology.
[14] M. Hirata,et al. Statin regulation of CYP3A4 and CYP3A5 expression. , 2009, Pharmacogenomics.
[15] L. A. Lim,et al. Effects of SLCO1B1 and ABCB1 genotypes on the pharmacokinetics of atorvastatin and 2-hydroxyatorvastatin in healthy Korean subjects. , 2010, International journal of clinical pharmacology and therapeutics.
[16] D. Hardie,et al. AMP-activated Protein Kinase Mediates Phenobarbital Induction of CYP2B Gene Expression in Hepatocytes and a Newly Derived Human Hepatoma Cell Line* , 2005, Journal of Biological Chemistry.
[17] Oliver Burk,et al. Antimalarial Artemisinin Drugs Induce Cytochrome P450 and MDR1 Expression by Activation of Xenosensors Pregnane X Receptor and Constitutive Androstane Receptor , 2005, Molecular Pharmacology.
[18] V. Trezza,et al. Xenosensors CAR and PXR at work: impact on statin metabolism. , 2011, Current drug metabolism.
[19] B. Ma,et al. Glucuronidation of statins in animals and humans: a novel mechanism of statin lactonization. , 2002, Drug metabolism and disposition: the biological fate of chemicals.
[20] M. Eichelbaum,et al. Alternative splicing affects the function and tissue-specific expression of the human constitutive androstane receptor , 2004, Nuclear receptor.
[21] L. Benet,et al. Effect of OATP1B Transporter Inhibition on the Pharmacokinetics of Atorvastatin in Healthy Volunteers , 2007, Clinical pharmacology and therapeutics.
[22] P. Kollman,et al. Lactonization is the critical first step in the disposition of the 3-hydroxy-3-methylglutaryl-CoA reductase inhibitor atorvastatin. , 2000, Drug metabolism and disposition: the biological fate of chemicals.
[23] M. Stoner,et al. Rational quantitative structure-activity relationship (RQSAR) screen for PXR and CAR isoform-specific nuclear receptor ligands. , 2010, Chemico-biological interactions.
[24] A. Poli. Atorvastatin , 2012, Drugs.
[25] J. Pascussi,et al. Drug Interaction Potential of 2-((3,4-Dichlorophenethyl)(propyl)amino)-1-(pyridin-3-yl)ethanol (LK-935), the Novel Nonstatin-Type Cholesterol-Lowering Agent , 2009, Drug Metabolism and Disposition.
[26] P. Ascenzi,et al. Nuclear receptors CAR and PXR: Molecular, functional, and biomedical aspects. , 2009, Molecular aspects of medicine.
[27] T. Sakaeda,et al. Effects of Acid and Lactone Forms of Eight HMG-CoA Reductase Inhibitors on CYP-Mediated Metabolism and MDR1-Mediated Transport , 2005, Pharmaceutical Research.
[28] K. Kivistö,et al. Rhabdomyolysis in a patient receiving atorvastatin and fluconazole , 2005, European Journal of Clinical Pharmacology.
[29] Stephen P. H. Alexander,et al. Guide to Receptors and Channels (GRAC), 5th edition , 2011, British journal of pharmacology.
[30] M. Hirai,et al. Effects of acid and lactone forms of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors on the induction of MDR1 expression and function in LS180 cells. , 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[31] B. H. Stewart,et al. Atorvastatin Transport in the Caco-2 Cell Model: Contributions of P-Glycoprotein and the Proton-Monocarboxylic Acid Co-Transporter , 2000, Pharmaceutical Research.
[32] P. Neuvonen,et al. Effect of itraconazole on the pharmacokinetics of atorvastatin , 1998, Clinical pharmacology and therapeutics.
[33] Kosuke Saito,et al. Ligand-dependent assembly of pregnane X receptor, constitutive androstane receptor and liver X receptor is applicable to identify ligands. , 2010, Drug metabolism letters.
[34] Peter-Tobias Stoll,et al. Charitable State-Controlled Foundation Human Tissue and Cell Research: Ethic and Legal Aspects in the Supply of Surgically Removed Human Tissue For Research in the Academic and Commercial Sector in Germany , 2004, Cell and Tissue Banking.
[35] Yoshiro Saito,et al. Identification of novel alternative splice variants of human constitutive androstane receptor and characterization of their expression in the liver. , 2004, Molecular pharmacology.
[36] U. Brinkmann,et al. Natural protein variants of pregnane X receptor with altered transactivation activity toward CYP3A4. , 2001, Drug metabolism and disposition: the biological fate of chemicals.
[37] Oliver Burk,et al. Nuclear Receptor Response Elements Mediate Induction of Intestinal MDR1 by Rifampin* , 2001, The Journal of Biological Chemistry.
[38] Hongbing Wang,et al. Activation of xenobiotic receptors: driving into the nucleus , 2010, Expert opinion on drug metabolism & toxicology.
[39] M. Negishi,et al. IDENTIFICATION OF HMG-CoA REDUCTASE INHIBITORS AS ACTIVATORS FOR HUMAN, MOUSE AND RAT CONSTITUTIVE ANDROSTANE RECEPTOR , 2005, Drug Metabolism and Disposition.
[40] C. Bisgaier,et al. Atorvastatin and gemfibrozil metabolites, but not the parent drugs, are potent antioxidants against lipoprotein oxidation. , 1998, Atherosclerosis.
[41] M Schwab,et al. UDP‐Glucuronosyltransferase (UGT) Polymorphisms Affect Atorvastatin Lactonization In Vitro and In Vivo , 2010, Clinical pharmacology and therapeutics.
[42] H. Cai,et al. Regulation of CYP2B6 and CYP3A expression by hydroxymethylglutaryl coenzyme A inhibitors in primary cultured human hepatocytes. , 2002, Drug metabolism and disposition: the biological fate of chemicals.
[43] Jan G. Hengstler,et al. The Holy Grail of Hepatocyte Culturing and Therapeutic Use , 2009 .
[44] S. Numazawa,et al. A physiological role of AMP-activated protein kinase in phenobarbital-mediated constitutive androstane receptor activation and CYP2B induction. , 2007, The Biochemical journal.
[45] Rosario,et al. Statin regulation of CYP 3 A 4 and CYP 3 A 5 expression CYP 3 A 4 & CYP 3 A 5 : function & variants , 2009 .
[46] P. Neuvonen,et al. Drug interactions with lipid‐lowering drugs: Mechanisms and clinical relevance , 2006, Clinical pharmacology and therapeutics.
[47] H. Glaeser,et al. Molecular Mechanisms of Polymorphic CYP3A7 Expression in Adult Human Liver and Intestine* , 2002, The Journal of Biological Chemistry.
[48] P. Neuvonen,et al. Rifampin markedly decreases and gemfibrozil increases the plasma concentrations of atorvastatin and its metabolites , 2005, Clinical pharmacology and therapeutics.
[49] P. Neuvonen,et al. ABCB1 Haplotypes Differentially Affect the Pharmacokinetics of the Acid and Lactone Forms of Simvastatin and Atorvastatin , 2008, Clinical pharmacology and therapeutics.
[50] Joseph L Goldstein,et al. SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver. , 2002, The Journal of clinical investigation.