PT - JOURNAL ARTICLE AU - Denise G. Teotico AU - Jason J. Bischof AU - Li Peng AU - Steven A. Kliewer AU - Matthew R. Redinbo TI - Structural Basis of Human Pregnane X Receptor Activation by the Hops Constituent Colupulone AID - 10.1124/mol.108.050732 DP - 2008 Dec 01 TA - Molecular Pharmacology PG - 1512--1520 VI - 74 IP - 6 4099 - http://molpharm.aspetjournals.org/content/74/6/1512.short 4100 - http://molpharm.aspetjournals.org/content/74/6/1512.full SO - Mol Pharmacol2008 Dec 01; 74 AB - Hops extracts are used to alleviate menopausal symptoms and as an alternative to hormone replacement therapy, but they can produce potentially harmful drug-drug interactions. The nuclear xenobiotic receptor pregnane X receptor (PXR) is promiscuously activated by a range of structurally distinct chemicals. It has a key role in the transcriptional regulation of genes that encode xenobiotic metabolism enzymes. In this study, hops extracts are shown to induce the expression of numerous drug metabolism and excretion proteins. The β-bitter acid colupulone is demonstrated to be a bioactive component and direct activator of human PXR. The 2.8-Å resolution crystal structure of the ligand binding domain of human PXR in complex with colupulone was elucidated, and colupulone was observed to bind in a single orientation stabilized by both van der Waals and hydrogen bonding contacts. The crystal structure also indicates that related α- and β-bitter acids have the capacity to serve as PXR agonists as well. Taken together, these results reveal the structural basis for drug-drug interactions mediated by colupulone and related constituents of hops extracts. The American Society for Pharmacology and Experimental Therapeutics