Comparison of the induction profile for drug disposition proteins by typical nuclear receptor activators in human hepatic and intestinal cells. [electronic resource]
- British journal of pharmacology Feb 2008
- 805-19 p. digital
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
0007-1188
10.1038/sj.bjp.0707601 doi
ATP Binding Cassette Transporter, Subfamily B ATP Binding Cassette Transporter, Subfamily B, Member 1--biosynthesis ATP-Binding Cassette Transporters--biosynthesis Aryl Hydrocarbon Hydroxylases--biosynthesis Caco-2 Cells Cell Culture Techniques Cells, Cultured Chenodeoxycholic Acid--pharmacology Constitutive Androstane Receptor Cytochrome P-450 CYP2B6 Cytochrome P-450 CYP3A--biosynthesis Cytochrome P-450 Enzyme System--biosynthesis DNA-Binding Proteins--agonists Dexamethasone--pharmacology Dose-Response Relationship, Drug Enzyme Induction Epithelial Cells--drug effects Hepatocytes--drug effects Humans Intestinal Mucosa--drug effects Membrane Transport Proteins--biosynthesis Multidrug Resistance-Associated Protein 2 Multidrug Resistance-Associated Proteins--biosynthesis Oxidoreductases, N-Demethylating--biosynthesis Phenobarbital--pharmacology Pregnane X Receptor Pregnenolone Carbonitrile--pharmacology RNA, Messenger--biosynthesis Receptors, Cytoplasmic and Nuclear--agonists Receptors, Steroid--agonists Research Design Rifampin--pharmacology Transcription Factors--agonists Up-Regulation