Influence of some anti-inflammatory drugs on the activity of aryl hydrocarbon hydroxylase and the cytochrome P450 content

Environ Res. 1990 Jun;52(1):77-82. doi: 10.1016/s0013-9351(05)80152-5.

Abstract

The metabolism of benzo[a]pyrene is mediated by the mixed function oxidase system including the cytochrome P450-dependent aryl hydrocarbon hydroxylase. The data of the present study revealed the ability of various commonly used anti-inflammatory drugs to alter the activity of this enzyme system, where all the tested drugs, namely phenyl butazone, ketoprofen, piroxicam, and acetaminophen, caused an increase in both the activity of aryl hydrocarbon hydroxylase and the cytochrome P450 content whether administered as a single dose or as a repeated dose for 6 consecutive days. The percentage of change for all drugs except phenyl butazone was proportional to the duration of drug administration. On the other hand, pyrazole which is chemically related to phenyl butazone, had no significant effect when administered as a single dose but caused a decrease in both studied parameters when administered as a repeated dose for 6 consecutive days. The mechanisms by which these commonly used drugs modify the aryl hydrocarbon hydroxylase activity and the cytochrome p450 content are discussed in the text.

MeSH terms

  • Acetaminophen / pharmacology
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Aryl Hydrocarbon Hydroxylases / metabolism*
  • Cytochrome P-450 Enzyme System / metabolism*
  • Injections, Intraperitoneal
  • Ketoprofen / pharmacology
  • Male
  • Mice
  • Microsomes, Liver / drug effects*
  • Microsomes, Liver / enzymology
  • Phenylbutazone / pharmacology
  • Piroxicam / pharmacology
  • Pyrazoles / pharmacology

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Pyrazoles
  • Piroxicam
  • Acetaminophen
  • pyrazole
  • Cytochrome P-450 Enzyme System
  • Ketoprofen
  • Aryl Hydrocarbon Hydroxylases
  • Phenylbutazone