Acetone-dependent regulation of cytochrome P-450j (IIE1) and P-450b (IIB1) in rat liver

Xenobiotica. 1989 Oct;19(10):1161-5. doi: 10.3109/00498258909043168.

Abstract

1. Concomitant changes in the concentration of P450 IIB1 (P-450b) and the rate of O-depentylation of 7-pentoxyresorufin was observed in rat liver microsomes after a single intragastric dose of acetone. 2. In contrast the concentration of P450 IIE1 (P-450j) did not coincide with changes in the rate of P450 IIE1-dependent p-nitrophenol hydroxylation or metabolic activation of carbon tetrachloride. 3. Quantification of the proteins in lysosomes indicated that both P450 IIB1 and P450 IIE1 are degraded via an autophagosomal/autolysosomal pathway. 4. It is concluded that P450 IIE1 is catalytically inactivated in microsomes prior to the degradation of this protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetone / pharmacology*
  • Animals
  • Cytochrome P-450 Enzyme System / biosynthesis*
  • Enzyme Induction
  • Isoenzymes / biosynthesis*
  • Male
  • Microsomes, Liver / drug effects*
  • Mixed Function Oxygenases / biosynthesis*
  • Rats
  • Rats, Inbred Strains

Substances

  • Isoenzymes
  • Acetone
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases