Nuclear receptors in drug metabolism

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245 1 0 |a Nuclear receptors in drug metabolism  |c ed. by Wen Xie 
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500 |a Includes bibliographical references and index 
650 4 |a Drugs  |x Metabolism 
650 4 |a Nuclear receptors (Biochemistry) 
650 4 |a Genetic regulation 
650 4 |a Receptors, Cytoplasmic and Nuclear  |x metabolism 
650 4 |a Drug Delivery Systems  |x methods 
650 4 |a Pharmaceutical Preparations  |x metabolism 
650 4 |a Receptors, Steroid  |x metabolism 
700 1 |a Xie, Wen  |e Sonstige  |4 oth 
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Datensatz im Suchindex

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adam_text CONTENTS Preface xiii Abbreviations xv Contributors xxi 1 Drug Metabolism: Significance and Challenges 1 Chandra Prakash and Alfin D. N. Vaz 1.1 Introduction 1 1.2 Phase I Drug-Metabolizing Enzymes 3 1.2.1 Cytochrome P450 4 1.2.2 Flavin Mono-Oxygenase (FMO) 8 1.2.3 Monoamine Oxidase 8 1.2.4 Molybdenum Hydroxylases 9 1.2.5 Epoxide Hydrolase 9 1.2.6 Esterase/Amidase 9 1.3 Phase II Conjugative Enzymes 10 1.3.1 Uridine Diphosphate Glucuronosyltransferase (UGT) 10 1.3.2 Sulfotransferase 10 1.3.3 Glutathione S-Transferase 11 1.3.4 N-Acetyltransferase 11 1.3.5 Methyl Transferase (MT) 11 1.4 Drug Efflux Transporters 12 1.4.1 ABCB1 (P-Glycoprotein, MDR1) 12 1.4.2 ABCC1 (Multidrug Resistance Related Protein 1, MRP 1) 13 v vi CONTENTS 1.4.3 ABCC2 (Multidrug Resistance Related Protein2, MRP2) 13 1.4.4 ABCG2 (Breast Cancer Resistance Protein, BCRP) 13 1.5 Drag Uptake Transporters 14 1.5.1 Organic Anion Transporter Polypeptides 14 1.5.2 Organic Cation Transporter 14 1.5.3 Organic Anion Transporter 14 1.5.4 Peptide Transporter 14 1.6 Challenges in Drug Metabolism 15 1.6.1 Prediction of Metabolism and Pharmacokinetics in Humans 15 1.6.2 Drag-Drag Interactions 17 1.6.3 Polymorphisms 22 1.7 Summary 26 References 27 2 Establishing Orphan Nuclear Receptors PXR and CAR as Xenobiotic Receptors 43 Tao Li, Junichiro Sonoda, and Ronald M. Evans 2.1 Introduction 43 2.2 Nuclear Receptor and Orphan Nuclear Receptor Superfamily 44 2.3 Orphan Nuclear Receptors as Xenobiotic Receptors and Their Implications in Phase I Enzyme Regulation 47 2.3.1 Cloning of PXR as a Xenobiotic Receptor and Its Regulation of P450s 47 2.3.2 Characterization of CAR as a Xenobiotic Receptor 51 2.4 Perspective 53 References 53 3 Nuclear Receptor-Mediated Regulation of Phase II Conjugating Enzymes 61 Olivier Barbier 3.1 Introduction 61 3.2 Phase II Drag Metabolizing Enzymes 62 3.2.1 Glucuronidation and UGTs 62 3.2.2 Sulfonation and SULTs 64 3.2.3 Sulfonation and Glucuronidation: Two Complementary Metabolic Pathways 67 3.2.4 Glutathione Conjugation and GSTs 68 3.2.5 Acetylation, Methylation, and EPHXs 69 3.3 The Xenosensors CAR and PXR: Two Master Regulators of Phase II Metabolism 70 3.3.1 General Considerations 70 3.3.2 Phase II XMEs Identified as PXR and/or CAR Target Genes 71 : CONTENTS vii 3.3.3 Physiological and Pharmacological Interests of Phase II Enzymes Regulation by PXR and/or CAR 73 3.3.4 Functional Mechanisms of Phase II Genes Regulation by PXR and CAR: Role of the Glucocorticoid Receptor 77 3.4 AhR and Nrf2, Two Important Regulators of Phase II Enzymes 78 3.4.1 AhR and Phase II XMEs Regulation 78 3.4.2 Nrf2 and Phase II XMEs Regulation 81 3.5 PPARs and Phase II XMEs Regulation 85 3.6 FXR/LXRa and Phase II XMEs Regulation 88 3.7 HNF and Phase II XMEs Regulation 89 3.8 Regulation of Phase II Conjugating Enzymes by Steroid and Thyroid Receptors 90 3.9 Concluding Remarks and Perspectives 91 References 92 4 Nuclear Receptor-Mediated Regulation of Drug Transporters 111 Oliver Burk 4.1 Introduction 111 4.2 Drug Transporters 112 4.2.1 ABC Efflux Transporters 113 4.2.2 SLCO/OATP Transporters 114 4.2.3 SLC22/Organic Ion Transporters 115 4.3 Induction of Drug Transporters by Activation of PXR and CAR 116 4.3.1 Induction in Liver and Intestine 117 4.3.2 Induction in Other Organs and Tissues 127 4.4 Induction of Drug Transporters by Activation of PPARa 128 4.5 Molecular Mechanism of PXR- and CAR-Dependent Drug Transporter Regulation 129 4.5.1 MDR1 (ABCB1) 130 4.5.2 Mrp2(Abcc2) 131 4.5.3 Mrp4(Abcc4) 132 4.5.4 Slcola4 132 4.5.5 SLCO1B1 133 4.6 Induction of Drug Transporter Expression and Drug Disposition 133 4.7 Conclusions and Future Perspectives 134 References 135 5 Structurejind Function of PXR and CAR 147 X. Edward Zhou and H. Eric Xu 5.1 Introduction 147 5.2 Structure and Function of PXR 148 5.2.1 Crystal Structures of Human PXR LBD/Ligand Complexes 148 viii CONTENTS 5.2.2 The Flexibility of the Ligand Binding Pocket of the PXR LBD 148 5.2.3 Coactivator Binding and Transcriptional Activity 152 5.2.4 Species Differences among LBD Sequences 152 5.2.5 Heterodimerization with RXR 154 5.3 Structure and Function of CAR 154 5.3.1 Crystal Structure of CAR 154 5.3.2 Ligand Binding and Activation of CAR 156 5.3.3 Cofactor Recruitment and Transcription Activation 162 5.3.4 Species Differences in CAR Ligand Binding and Activation 162 5.3.5 Heterodimerization with RXR 163 5.4 Concluding Remarks 163 References 164 6 Xenobiotic Receptor Cofactors and Coregulators 167 John Y. L. Chiang 6.1 Regulation of PXR and CAR Nuclear Translation 167 6.1.1 Activation and Nuclear Translocation of CAR 167 6.1.2 Nuclear Translocation of PXR 168 6.2 Nuclear Receptor Coregulators and Epigenetic Regulation of Gene Transcription 169 6.2.1 Ligand-Independent and Ligand-Dependent Recruitment of Nuclear Receptor Coactivators 169 6.2.2 Nuclear Receptor Corepressor in Xenobiotic Receptor Signaling 171 6.3 PXR and CAR Cross Talk With Other Nuclear Receptors and Transcription Factors 171 6.3.1 PXR and CAR Interact with Other Nuclear Receptors 171 6.3.2 PXR and CAR Interact with Other Transcription Factors 172 6.4 PXR and CAR Regulation of Lipid and Glucose Homeostasis 173 6.4.1 CAR and PXR Regulation of Fatty Acid Metabolism 173 6.4.2 PXR and CAR Regulation of Bile Acid Metabolism 173 6.4.3 PXR Regulation of Cholesterol Metabolism 175 6.4.4 CAR and PXR Regulation of Glucose and Energy Metabolism 176 6.5 Conclusion 176 References 177 7 Animal Models of Xenobiotic Nuclear Receptors and Their Utility in Drug Development 185 Haibiao Gong and Wen Xie 7.1 Introduction 185 I i CONTENTS ix ; 7.2 PXR and CAR Loss-of-Function (Knock-Out) Mouse Models 186 7.2.1 PXR Knock-Out Mice 186 7.2.2 Phenotype of the PXR Knock-Out Mice 188 7.2.3 Another Independently Developed PXR Null Mouse Line 188 7.2.4 CAR Knock-Out Mice 189 7.2.5 Another Independently Developed CAR Null Mouse Line 189 7.2.6 Combined Loss of PXR and CAR 190 7.3 PXR and CAR Gain-of-Function (Transgenic) Mouse Models 191 7.3.1 Albumin Promoter-Human PXR (Alb-hPXR) Transgenic Mice 191 7.3.2 Alb-VP-hPXR Transgenic Mice Expressing the Activated hPXR 192 7.3.3 Fatty Acid Binding Protein Promoter-Human PXR (FABP-hPXR) Transgenic Mice 194 7.3.4 FABP-VP-hPXR Transgenic Mice 194 7.3.5 Tetracycline-Inducible VP-CAR Transgenic Mice 196 7.4 Humanized Mouse Models 198 7.4.1 Humanized PXR Mice Carrying Human PXR cDNA 198 7.4.2 Humanized PXR Mice Carrying Human PXR Genomic DNA 199 7.4.3 Humanized CAR Mice 200 7.4.4 Humanized PPARa Mice 200 7.4.5 Humanized AhR Mice 201 7.4.6 Cytochrome P450 Humanized Mice 201 7.5 Utility of Xenobiotic Mouse Models in Pharmaceutical Development 202 7.6 Closing Remarks 203 References 204 8 Nuclear Receptors and Drug-Drug Interactions with Prescription and Herbal Medicines 211 Rommel G. Tirona and Richard B. Kim 8.1 Introduction 211 8.2 Prescription Drugs/Drug Classes Involved in Inductive Drug Interactions 213 8.2.1 Anticonvulsants 214 8.2.2 Rifamycin Antibiotics 214 8.2.3 HIV Protease Inhibitors (HIV-PI) 216 8.2.4 Non-Nucleoside Reverse Transcriptase Inhibitors 216 8.2.5 Bosentan 216 8.3 Herbal Medicines Involved in Inductive Drug Interactions 216 8.3.1 St. John s Wort 217 8.3.2 Other Herbal Medicines 218 x CONTENTS 8.4 Pharmacology of Induction 218 8.5 Clinical Aspects of Induction-Type Drug Interactions 222 8.5.1 Enzymes, Transporters, and Drugs Highly Sensitive to Induction 222 8.5.2 Therapeutic Implications of Induction-Type Drug Interactions 224 8.5.3 Time Course of Induction and Deinduction 225 8.6 Inhibition of Nuclear Receptors in Clinical Drug Interactions 226 8.7 Nuclear Receptor Mediated Drug Side Effects 226 8.8 Perspectives 227 References 227 9 Genetic Variants of Xenobiotic Receptors and Their Implications in Drug Metabolism and Pharmacogenetics 241 Jatinder Lamba and Erin G. Schuetz 9.1 PXR (Pregnane X Receptor) Background 241 9.2 PXR Gene Structure 243 9.3 PXR Alternative mRNAs 243 9.4 Genetic Variants in PXR s Exons and their Functional Consequences 246 9.5 Genetic Variants in Introns 2-8 and the 3 -UTR of PXR and their Functional Consequences 251 9.6 Resequencing Strategy for the PXR Promoter and Intron 1 251 9.7 Genetic Variation in the PXR Promoter and 5 -UTR and Its Functional Relevance 252 9.8 Genetic Variation in PXR s Intron 1 and Its Functional Relevance 253 9.9 In Silico Analysis for Functional Effect of SNPs in PXR s Promoter, 5 -UTR, and Intron 1 256 9.10 SNPs in PXR s Promoter and Intron 1 Affect Putative HNF Binding Sites 256 9.11 PXR SNPs Have Been Associated with Intestinal and Hepatic Inflammation and Diseases 257 9.12 PXR Structural Variation and Other Genomic Features 258 9.13 PXR Summary 259 9.14 CAR Background 259 9.15 CAR Gene Structure 260 9.16 CAR Alternatively Spliced mRNAs 261 9.17 CAR Genetic Variants (SNPs) and their Functional Consequences 264 9.18 CAR Summary 266 References 267 CONTENTS xi 10 Beyond PXR and CAR, Regulation of Xenobiotic Metabolism by Other Nuclear Receptors 275 Martin Wagner, Gernot Zollner, and Michael Trauner 10.1 Introduction 275 10.2 Farnesoid X Receptor 277 10.2.1 FXR-Dependent Regulation of Basolateral Drug and Bile Acid Uptake 277 10.2.2 FXR-Dependent Regulation of Phase I and II Metabolism 282 10.2.3 FXR-Dependent Regulation of Canalicular and Basolateral Drug and Bile Acid Excretion 282 10.2.4 FXR-Dependent Effects on Sterol and Lipid Metabolism 283 10.3 Hepatocyte Nuclear Factor 4a 284 10.4 Vitamin D Receptor 285 10.5 Glucocorticoid Receptor 286 10.6 Peroxisome Proliferator-Activated Receptors 286 10.7 Aryl Hydrocarbon Receptor (AhR) 287 10.8 Conclusions 288 References 288 11 Emerging Role of Retinoid-Related Orphan Receptor (ROR) and Its Cross Talk with LXR (Liver X Receptor) in the Regulation of Drug-Metabolizing Enzymes 301 Taira Wada and Wen Xie 11.1 Introduction 301 11.2 Orphan Nuclear Receptor RORct 303 11.3 A Potential Role of RORs in Xeno- and Endobiotic Gene Regulation 305 11.4 LXR and Its Regulation of Drug-Metabolizing Enzymes 307 11.5 A Functional Cross Talk Between RORa and LXR in the Regulation of Xeno- and Endobiotic Genes 308 11.6 Closing Remarks 310 References 312 Index 319
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spellingShingle Nuclear receptors in drug metabolism
Drugs Metabolism
Nuclear receptors (Biochemistry)
Genetic regulation
Receptors, Cytoplasmic and Nuclear metabolism
Drug Delivery Systems methods
Pharmaceutical Preparations metabolism
Receptors, Steroid metabolism
title Nuclear receptors in drug metabolism
title_auth Nuclear receptors in drug metabolism
title_exact_search Nuclear receptors in drug metabolism
title_full Nuclear receptors in drug metabolism ed. by Wen Xie
title_fullStr Nuclear receptors in drug metabolism ed. by Wen Xie
title_full_unstemmed Nuclear receptors in drug metabolism ed. by Wen Xie
title_short Nuclear receptors in drug metabolism
title_sort nuclear receptors in drug metabolism
topic Drugs Metabolism
Nuclear receptors (Biochemistry)
Genetic regulation
Receptors, Cytoplasmic and Nuclear metabolism
Drug Delivery Systems methods
Pharmaceutical Preparations metabolism
Receptors, Steroid metabolism
topic_facet Drugs Metabolism
Nuclear receptors (Biochemistry)
Genetic regulation
Receptors, Cytoplasmic and Nuclear metabolism
Drug Delivery Systems methods
Pharmaceutical Preparations metabolism
Receptors, Steroid metabolism
url http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=017385973&sequence=000004&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
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