Nicotine metabolism by rat hepatic cytochrome P450s

Biochem Pharmacol. 1993 Jun 22;45(12):2554-6. doi: 10.1016/0006-2952(93)90238-r.

Abstract

Many kinds of cytochrome P450s were purified from rat hepatic microsomes, and their role in the metabolization of nicotine in a reconstituted system examined. Of four phenobarbital-inducible P450s, P450 2B1 had the highest nicotine oxidation activity and P450 2B2 showed a low rate of nicotine oxidation, whereas P450 2C6 and 3A2 had no detectable activity toward nicotine. Among eleven other purified cytochrome P450s tested, P450 2C11 had high nicotine oxidation activity and P450 1A2 and 2D1 showed low catalytic activity toward nicotine. The other cytochrome P450s, P450 1A1, 2A1, 2A2, 2C7, 2C12, 2C13, 2E1 and 4A1, had no detectable nicotine oxidation activity. Based on these results, participation of cytochrome P450s in nicotine metabolism in human and animal livers is discussed.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Cytochrome P-450 Enzyme System / isolation & purification
  • Cytochrome P-450 Enzyme System / metabolism*
  • Isoenzymes / isolation & purification
  • Isoenzymes / metabolism*
  • Male
  • Microsomes, Liver / enzymology*
  • Nicotine / metabolism*
  • Oxidation-Reduction
  • Phenobarbital
  • Rats
  • Rats, Wistar

Substances

  • Isoenzymes
  • Nicotine
  • Cytochrome P-450 Enzyme System
  • Phenobarbital