补充美拉酮对难治性单极抑郁症患者丙咪嗪治疗的影响。

Polish journal of pharmacology Pub Date : 2004-11-01
Zofia Rogóz, Grazyna Skuza, Jacek Wójcikowski, Władysława A Daniel, Andrzej Wróbel, Dominika Dudek, Andrzej Zieba
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引用次数: 0

摘要

本文描述了在满足DSM IV重度抑郁症标准的患者(治疗难治性单极抑郁症)中,补充美拉酮对丙咪嗪治疗的影响。9名患者根据他们的病史和治疗方法被纳入研究。洗脱期2周后,患者给予丙咪嗪每日2次(100 mg/天)治疗6周,然后引入美替拉酮(每日2次,500 mg/天),并与丙咪嗪联合用药6周。采用汉密尔顿抑郁评定量表(HDRS)和贝克抑郁量表(BDI)评估抗抑郁治疗的疗效。与基线(治疗前)相比,治疗6周后丙咪嗪未改变HDRS和BDI评分。补充Metyrapone显著降低了6周后的HDRS和BDI评分。此外,药代动力学数据显示,在美替拉酮与丙咪嗪联合治疗期间,甲替拉酮对患者血浆丙咪嗪及其代谢物地西帕明的浓度没有显著影响,提示其缺乏药代动力学相互作用。本初步研究首次证实了补充美拉酮对丙咪嗪治疗难治性单极抑郁症的益处,并提示抑郁症中受到干扰的神经递质、激素和免疫参数水平的变化可能参与了该药物的作用机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of metyrapone supplementation on imipramine therapy in patients with treatment-resistant unipolar depression.

The paper describes the effect of metyrapone supplementation on imipramine therapy in patients (with treatment-resistant unipolar depression) who fulfilled DSM IV criteria for major depression. Nine patients were enrolled to the study on the basis of history of their illness and therapy. Following 2 weeks of washout period, the patients were treated with imipramine twice daily (100 mg/day) for 6 weeks, and then metyrapone was introduced (twice daily, 500 mg/day), and administered jointly with imipramine for further 6 weeks. Hamilton Depression Rating Scale (HDRS) and Beck Depression Inventory (BDI) were used to assess efficacy of antidepressant therapy. Imipramine changed neither HDRS nor BDI score after 6 weeks of treatment when compared with baseline (before treatment). Metyrapone supplementation significantly reduced both HDRS and BDI scores after 6-week supplementation. Moreover, pharmacokinetic data indicate that metyrapone did not influence significantly the plasma concentration of imipramine and its metabolite, desipramine in the patients during joint treatment with metyrapone and imipramine, what suggests the lack of pharmacokinetic interaction. This preliminary study is the first demonstration of the benefit of metyrapone supplementation in imipramine therapy of treatment-resistant unipolar depression and suggests that a change in the level of neurotransmitters, hormones and immunological parameters, which are disturbed in depression, may contribute to the mechanism of the action of this drug.

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