A kinetic and dynamic study of oral alprazolam with and without erythromycin in humans : In vivo evidence for the involvement of CYP3A4 in alprazolam metabolism

Objective To assess the possible involvement of CYP3A4 in the metabolism of alprazolam in vivo. Method Twelve healthy male volunteers were randomly allocated to one of the two different treatment sequences, placebo-erythromycin or erythromycin-placebo, with an at least 6-week washout period between the two trial phases. Each volunteer received 400 mg erythromycin or matched placebo given orally three times a day for 10 days and an oral dose (0.8 mg) of alprazolam on the posttreatment day 8. Plasma concentration of alprazolam was measured up to 48 hours after the administration, and psychomotor function was assessed at each time of blood samplings with use of the Digit Symbol Substitution Test, visual analog scale, and Udvalg for kliniske undersogelser side effect rating scale. Results Erythromycin significantly (p < 0.001) increased the area under the plasma concentration-time curves (200 ± 43 versus 322 ± 49 ng · hr/ml from 0 to 48 hours and 229 ± 52 versus 566 ± 161 ng · hr/ml from 0 hour to infinity), decreased the apparent oral clearance (1.02 ± 0.31 versus 0.41 ± 0.12 ml/min/kg), and prolonged the elimination half-life (16.0 ± 4.5 versus 40.3 ± 14.4 hours) of alprazolam. However, any psychomotor function variables did not differ significantly between the erythromycin and placebo trial phases. Conclusion This study suggests that erythromycin, an inhibitor of CYP3A4, inhibits the metabolism of alprazolam, providing an in vivo evidence for the involvement of CYP3A4 in its metabolism. However, the kinetic change of alprazolam by erythromycin does not result in the pharmacodynamic change of this triazolobenzodiazepine, at least after single dosing. Clinical Pharmacology & Therapeutics (1996) 59, 514–519; doi: