The effect of carbamazepine (CBZ, 200 mg twice daily for 28 days) on t
he kinetics of a single oral. dose of desipramine (DMI, 100 mg) was in
vestigated in six healthy volunteers. Compared with a control session,
treatment with CBZ caused a marked increase in DMI apparent oral clea
rance (from 1.05 +/- 0.40 to 1.38 +/- 0.52 1 h per kg, means +/- SD, P
< 0.01) and a significant shortening in DMI half-life (from 22.1 +/-
3.5 to 17.8 +/- 3.5 h, P < 0.01). The amount of 2-hydroxydesipramine (
2-OH-DMI) excreted in urine over a 24-h period was significantly incre
ased during CBZ intake (from 75 +/- 15 to 92 +/- 16 mu mol, P < 0.01).
These findings suggest that CBZ induces the 2-hydroxylation of DMI, a
reaction primarily catalyzed by the polymorphic CYP2D6 isozyme. This
interaction may have considerable practical significance.