期刊
CLINICAL PHARMACOLOGY & THERAPEUTICS
卷 90, 期 2, 页码 296-302出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/clpt.2011.140
关键词
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资金
- Turku University Hospital, Turku, Finland [EVO 13821]
- Instrumentarium Research Foundation, Helsinki, Finland
- Sigrid Juselius Foundation, Helsinki, Finland
This study examined drug-drug interactions of oral S-ketamine with the cytochrome P450 (CYP) 2B6 inhibitor ticlopidine and the CYP3A inhibitor itraconazole. In this randomized, blinded, crossover study, 11 healthy volunteers ingested 0.2 mg/kg S-ketamine after pretreatments with oral ticlopidine (250 mg twice daily), itraconazole (200 mg once daily), or placebo in 6-day treatment periods at intervals of 4 weeks. Ticlopidine treatment increased the mean area under the plasma concentration-time curve extrapolated to infinity (AUC(0-infinity)) of oral ketamine by 2.4-fold (P < 0.001), whereas itraconazole treatment did not increase the exposure to S-ketamine. The ratio of norketamine AUC(0-infinity) to ketamine AUC(0-infinity) was significantly decreased in the ticlopidine (P < 0.001) and itraconazole phases (P = 0.006) as compared to placebo. In the ticlopidine and itraconazole phases, the areas under the effect-time curves (self-reported drowsiness and performance) were significantly higher than those in the placebo phase (P < 0.05). The findings suggest that the dosage of S-ketamine should be reduced in patients receiving ticlopidine.
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