Kondo T, Tanaka O, Otani K, Mihara K, Tokinaga N, Kaneko S, Chiba K, Ishizaki T
Department of Neuropsychiatry, Hirosaki University School of Medicine, Japan.
Psychopharmacology (Berl). 1996 Oct;127(4):311-4. doi: 10.1007/s002130050091.
Effects of smoking and cytochrome P450 2C19 (CYP2C19) status on the single dose kinetics of zotepine and pharmacokinetic interaction between zotepine and diazepam were investigated. In 14 healthy volunteers, the pharmacokinetics of zotepine after a single oral 25 mg dose were compared between eight smokers and six non-smokers, or between seven extensive metabolizers (EMs) and seven poor metabolizers (PMs) of S-mephenytoin. There was no significant difference in any pharmacokinetic parameters between smokers and non-smokers, or between the EM and PM groups. In 17 patients treated with zotepine 80-340 mg/day, intra-individual changes in plasma concentrations of zotepine caused by coadministration of diazepam 10 mg/day for 2 weeks were examined. Plasma concentrations of zotepine were significantly increased after coadministration of diazepam (P < 0.05). Consequently, it is suggested that neither smoking nor CYP2C19 status affects the metabolism of zotepine. The elevation in plasma concentrations of zotepine after coadministration of diazepam may be a result of competitive inhibition of zotepine metabolism by diazepam via other isoenzyme than CYP2C19, e.g., CYP3A4.
研究了吸烟和细胞色素P450 2C19(CYP2C19)状态对佐替平单剂量动力学的影响以及佐替平和地西泮之间的药代动力学相互作用。在14名健康志愿者中,比较了8名吸烟者和6名不吸烟者,或7名S-美芬妥因的广泛代谢者(EMs)和7名慢代谢者(PMs)单次口服25mg佐替平后的药代动力学。吸烟者与不吸烟者之间,或EM组与PM组之间的任何药代动力学参数均无显著差异。在17例每天服用80 - 340mg佐替平的患者中,研究了连续2周每天合用10mg地西泮引起的佐替平血浆浓度的个体内变化。合用后佐替平的血浆浓度显著升高(P < 0.05)。因此,提示吸烟和CYP2C19状态均不影响佐替平的代谢。合用后佐替平血浆浓度升高可能是地西泮通过CYP2C19以外的其他同工酶(如CYP3A4)对佐替平代谢的竞争性抑制所致。