The role of cytochrome P4502D6 in the metabolism of paroxetine by human liver microsomes

Br J Clin Pharmacol. 1992 May;33(5):521-3. doi: 10.1111/j.1365-2125.1992.tb04082.x.


Paroxetine is a selective serotonin reuptake inhibitor possessing anti-depressant activity. Demethylenation of the methylenedioxy phenyl group is the initial step in its metabolism, the liberated carbon appearing in vitro as formate. A radioassay involving [14C-methylenedioxy] paroxetine was developed and used to examine the role of cytochrome P4502D6 in paroxetine metabolism by human liver microsomes. The rate of formate production was much higher in microsomes from an extensive metaboliser of debrisoquine than from a poor metaboliser. Also, demethylenation of paroxetine was inhibited by the quinidine and quinine isomer pair in microsomes from the extensive metaboliser only. These observations strongly suggested that the process was catalysed by the enzyme cytochrome P4502D6. Metabolism could not be completely inhibited by quinidine, the residual activity representing the contribution of at least one other enzyme. The ability of microsomes from a poor metaboliser of debrisoquine to demethylenate paroxetine provided further evidence for the involvement of an enzyme distinct from P4502D6. This was confirmed by kinetic analysis of the process in microsomes from both poor and extensive metabolisers. It is concluded that, in man, the initial step of paroxetine metabolism is performed by at least two enzymes, one of which is cytochrome P4502D6.

MeSH terms

  • Antidepressive Agents / metabolism*
  • Carbon Radioisotopes
  • Cytochrome P-450 CYP2D6
  • Cytochrome P-450 Enzyme System / metabolism*
  • Formates / analysis
  • Humans
  • In Vitro Techniques
  • Microsomes, Liver / metabolism*
  • Mixed Function Oxygenases / metabolism*
  • Paroxetine
  • Piperidines / metabolism*
  • Serotonin Antagonists / metabolism*


  • Antidepressive Agents
  • Carbon Radioisotopes
  • Formates
  • Piperidines
  • Serotonin Antagonists
  • formic acid
  • Paroxetine
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • Cytochrome P-450 CYP2D6