Regulation of cytochrome P-4501A and cytochrome P-4502E induction in the rat during the production of interferon α/β

A. E. Cribb, E. Delaporte, S. G. Kim, R. F. Novak, K. W. Renton

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42 Citations (Scopus)

Abstract

The down regulation of constitutive hepatic microsomal cytochromes P-450 (P450) by interferons has been well described in experimental animals and humans, however the down regulation of induced forms of P450 has not been documented clearly. Differential down regulation of constitutive and induced P450 could alter the proportions of P450 enzymes and, hence, the relative bioactivation/detoxification of xenobiotics. We investigated the effects of polyinosinic acid-polycytidylic acid, a potent stimulator of interferon α/β production on CYP1A and CYP2E induction in the rat. Polyinosinic acid- polycytidylic acid down regulated the constitutive and pyridine-induced expression of CYP2E1 and the pyridine- and β-naphthoflavone-induced expression of CYP1A1 as demonstrated by metabolic activity and immunoblot analyses. Depression of CYP2E1 and CYP1A1 protein expression by polyinosinic acid-polycytidylic acid was accompanied by a corresponding decrease in mRNA encoding these proteins. Induction of CYP1A2 mRNA also was depressed. Therefore, interferon α/β down regulated induction of members of the CYP1A and CYP2E subfamilies at a pretranslational level independent of the mechanism of induction. Induction of the CYP1A and CYP2E subfamilies did not confer resistance to down regulation by interferon, although the magnitude of down regulation by interferon appeared to be influenced by the magnitude of P450 induction. The potential significance of down regulation of induced P450 in the clearance of certain therapeutic agents and in xenobiotic bioactivation and detoxification is discussed.

Original languageEnglish
Pages (from-to)487-494
Number of pages8
JournalJournal of Pharmacology and Experimental Therapeutics
Volume268
Issue number1
Publication statusPublished - 1994

ASJC Scopus Subject Areas

  • Molecular Medicine
  • Pharmacology

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