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卡马西平对丙嗪药代动力学的影响。

Effect of carbamazepine on the pharmacokinetics of promazine.

作者信息

Syrek M, Wójcikowski J, Daniel W

机构信息

Department of Pharmacokinetics and Drug Metabolism, Polish Academy of Sciences, Kraków, Poland.

出版信息

Pol J Pharmacol. 1996 Nov-Dec;48(6):601-8.

PMID:9112700
Abstract

Combinations of neuroleptics and carbamazepine are administered to psychiatric patients in the therapy of mania, manic-depressive illness and schizophrenia. The present study was aimed at assessing the influence of carbamazepine on the pharmacokinetics of promazine. Male Wistar rats received promazine and/or carbamazepine twice daily for two weeks (promazine, 10 mg/kg ip; carbamazepine, 15 mg/kg ip during the 1st, and 20 mg/kg ip during the 2nd week of treatment). In a short time (1 h) after administration, carbamazepine had a tendency to increase the concentration of promazine in the blood plasma and brain. Lineweaver-Burk's analysis showed that carbamazepine added in vitro competitively inhibited the N-demethylation of promazine in liver microsomes, without affecting the sulphoxidation process. The effect was reflected in vivo (1 h) by an increased promazine/desmethylpromazine ratio. After a long time interval (6 h, 12 h), carbamazepine decreased the concentration of promazine and its metabolites. In vitro studies into the promazine metabolism, conducted on microsomes from rats treated with promazine and/or carbamazepine, did not show acceleration of its demethylation or sulphoxidation by carbamazepine. The obtained results suggest that induction of promazine metabolism by carbamazepine involves metabolic pathways other than N-demethylation or sulphoxidation. It has been concluded that when a phenothiazine neuroleptic, such as promazine, is administered jointly with carbamazepine, a slight increase in the neuroleptic concentration may be expected in a short time after administration, followed by its significant decrease.

摘要

在躁狂症、躁郁症和精神分裂症的治疗中,会将抗精神病药物与卡马西平联合用于精神病患者。本研究旨在评估卡马西平对丙嗪药代动力学的影响。雄性Wistar大鼠每天接受两次丙嗪和/或卡马西平,持续两周(丙嗪,腹腔注射10mg/kg;治疗第1周卡马西平腹腔注射15mg/kg,第2周腹腔注射20mg/kg)。给药后短时间内(1小时),卡马西平有使血浆和脑中丙嗪浓度升高的趋势。Lineweaver-Burk分析表明,体外添加卡马西平可竞争性抑制肝微粒体中丙嗪的N-去甲基化,而不影响硫氧化过程。该作用在体内(1小时)表现为丙嗪/去甲丙嗪比值升高。长时间间隔(6小时、12小时)后,卡马西平降低了丙嗪及其代谢产物的浓度。在用丙嗪和/或卡马西平处理的大鼠微粒体上进行的丙嗪代谢体外研究未显示卡马西平能加速其去甲基化或硫氧化。所得结果表明,卡马西平诱导丙嗪代谢涉及N-去甲基化或硫氧化以外的代谢途径。得出的结论是,当将吩噻嗪类抗精神病药物如丙嗪与卡马西平联合使用时,给药后短时间内可能预期抗精神病药物浓度略有升高,随后显著降低。

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引用本文的文献

1
Contribution of human cytochrome p-450 isoforms to the metabolism of the simplest phenothiazine neuroleptic promazine.人细胞色素P-450同工型对最简单的吩噻嗪类抗精神病药物丙嗪代谢的贡献。
Br J Pharmacol. 2003 Apr;138(8):1465-74. doi: 10.1038/sj.bjp.0705195.