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健康志愿者单次及重复给药后利托西汀的脑电图特征。

EEG profile of litoxetine after single and repeated administration in healthy volunteers.

作者信息

Patat A, Trocherie S, Thébault J J, Rosenzweig P, Dubruc C, Bianchetti G, Morselli P L, Court L A

机构信息

Synthélabo Recherche (L.E.R.S.), Bagneux, France.

出版信息

Br J Clin Pharmacol. 1994 Feb;37(2):157-63. doi: 10.1111/j.1365-2125.1994.tb04255.x.

Abstract
  1. Litoxetine is a selective serotonin reuptake inhibitor with antidepressant activity in animal models and in depressed patients. 2. This double-blind, cross-over, placebo-controlled study was carried out in 12 healthy young male volunteers. The aim was to assess the EEG profile of litoxetine in parallel with its pharmacokinetics after a single dose or multiple administrations for 4 days (6 doses) of two dosages (10 mg and 25 mg). Spectral analysis of four EEG leads (F4-T4, F3-T3, T4-02 and T3-01) was done up to 12 h post-dose. 3. In single or multiple doses, litoxetine induced EEG changes characterised by a dose-related increase in fast beta energies, mainly beta 2, without any changes in slow waves (delta and theta). A slight reduction in alpha activity occurred only after repeated doses. 4. EEG changes occurred after a single oral administration and lasted at least 12 h with litoxetine blood concentrations ranging from 4 to 10 ng ml-1. With repeated administrations, the pharmacodynamic steady-state was achieved as the increase in beta 2 energies was the same before and 12 h post-dose. These effects occurred with litoxetine blood concentrations ranging from 3 to 7 ng ml-1 with the 10 mg dosage and from 8 to 18 ng ml-1 with the 25 mg dosage. The EEG profile did not change after 4 days of repeated administration, indicating that tolerance did not develop. 5. Cmax and AUC showed proportionality between the administered dosages of 10 and 25 mg.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 利托西汀是一种选择性5-羟色胺再摄取抑制剂,在动物模型和抑郁症患者中具有抗抑郁活性。2. 这项双盲、交叉、安慰剂对照研究在12名健康年轻男性志愿者中进行。目的是评估单次给药或连续4天(6次剂量)给予两种剂量(10毫克和25毫克)利托西汀后,其脑电图特征及其药代动力学。给药后12小时内对四个脑电图导联(F4-T4、F3-T3、T4-O2和T3-O1)进行频谱分析。3. 单次或多次给药时,利托西汀引起脑电图变化,其特征为快速β波能量(主要是β2)呈剂量相关增加,慢波(δ波和θ波)无任何变化。仅在重复给药后α波活动略有减少。4. 单次口服利托西汀后即出现脑电图变化,持续至少12小时,此时利托西汀血药浓度为4至10纳克/毫升。重复给药时,达到药效学稳态,因为给药前和给药后12小时β2能量增加相同。这些效应在10毫克剂量组利托西汀血药浓度为3至7纳克/毫升时出现,在25毫克剂量组血药浓度为8至18纳克/毫升时出现。重复给药4天后脑电图特征未改变,表明未产生耐受性。5. Cmax和AUC显示10毫克和25毫克给药剂量之间呈比例关系。(摘要截选至250字)

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