Biochemical and Biophysical Research Communications, Vol.318, No.2, 428-434, 2004
Expression and induction of CYP3As in human fetal hepatocytes
CYP3A4 and CYP3A7 mRNA expression levels were markedly up-regulated by dexamethasone (DEX), but not by rifampicin (RIF). CYP3A5 mRNA level was not increased significantly by DEX, RIF, or phenobarbital. Testosterone 6 6beta-hydroxylase activity was induced to about 2-fold of control by DEX. However, concomitant treatment with RIF did not alter DEX-mediated induction of CYP3A mRNA expression and testosterone 6beta-hydroxylase activity. DEX-mediated induction of CYP3A mRNA was suppressed in a dose-dependent manner by RU486, a glucocorticoid receptor (GR) antagonist. At 5muM RU486, DEX-mediated induction of CYP3A4, CYP3A5, and CYP3A7 mRNA expression was inhibited almost completely. These results suggest that, in human fetal hepatocytes, PXR is not involved in DEX-mediated induction of CYP3A4 and CYP3A7, and that the induction is mediated directly by GR. (C) 2004 Elsevier Inc. All rights reserved.
Keywords:cytochrome P450;CYP3A4;C7YP3A7;human fetal hepatocytes;glucccorticoid receptor;pregnane X receptor;dexamethasone;rifampicin;induction;RU486