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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-589075
- DOI to cite this document:
- 10.5283/epub.58907
Abstract
BACKGROUND AND PURPOSE Atorvastatin metabolites differ in their potential for drug interaction because of differential inhibition of drug-metabolizing enzymes and transporters. We here investigate whether they exert differential effects on the induction of these genes via activation of pregnane X receptor (PXR) and constitutive androstane receptor (CAR). EXPERIMENTAL APPROACH Ligand binding to ...

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