Aubrecht J, Hirsch-Ernst K I, Becker-Rabbenstein V, Kahl G F, Taniguchi H, Höhne M W
Institute of Pharmacology and Toxicology, University of Göttingen, Germany.
Biochem Pharmacol. 1995 Sep 7;50(6):781-5. doi: 10.1016/0006-2952(95)00200-j.
Phenobarbital-dependent induction of mouse cytochrome P-450 (Cyp) orthologous to rat CYP2B1 and its modulation by hepatotrophic growth factors were examined in primary hepatocyte cultures. Compared to rat hepatocytes, induction in mouse hepatocytes was more rapid and effective. Ligands of the EGF receptor, epidermal growth factor, and transforming growth factor alpha inhibited induction on the basis of protein expression and CYP2B-associated 7-pentoxyresorufin-O-depentylase activity. Furthermore, EGF led to repression of accumulation of corresponding mRNA under phenobarbital, an effect not blocked by inhibition of protein synthesis under cycloheximide. Ligands of the EGF receptor may contribute towards the decrease in hepatic CYP expression observed during (pre)neoplastic development and regeneration.