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抗抑郁药的药物脑电图图谱。氟伏沙明的药效学研究。

Pharmaco-EEG profiles of antidepressants. Pharmacodynamic studies with fluvoxamine.

作者信息

Saletu B, Grünberger J, Rajna P

出版信息

Br J Clin Pharmacol. 1983;15 Suppl 3(Suppl 3):369S-383S. doi: 10.1111/j.1365-2125.1983.tb02128.x.

Abstract

1 Antidepressant drugs produce significant changes in human brain function as reflected in the quantitatively analysed EEG. Two main types of pharmaco-EEG profiles may be differentiated: a thymeretic (desipramine-like) profile characterised mainly by an alpha increase suggesting activating properties and a thymoleptic (imipramine- or amitriptyline-like) profile showing a concomitant increase of slow and fast activities and a decrease in alpha activity indicating also sedative qualities. A small number of compounds exhibit still different profiles. 2 Aside from determining the type of EEG changes, the pharmaco-EEG method seems to be of value in determining time and dose efficacy relations at the target organ, the human brain. Moreover, the relationships between pharmacodynamics and pharmacokinetics may be determined. 3 Fluvoxamine, a selective 5-hydroxytryptamine (5-HT) re-uptake inhibitor from the new class of 2-aminoethyloximethers of aralkylketones, produced a typical thymoleptic pharmaco-EEG profile after oral doses of 75 mg in a double-blind placebo-controlled study involving 10 healthy volunteers. Fluvoxamine (75 mg) induced less augmentation of slow activity than 75 mg imipramine, indicating less sedative properties of fluvoxamine than imipramine. 4 After 75 mg fluvoxamine psychometric tests demonstrated a tendency towards an improvement in attention, concentration, psychomotor activity, after-effect and mood and a significant increase in critical flicker fusion frequency as compared with placebo. Comparison with the reference drug, 75 mg imipramine, revealed a significant superiority of fluvoxamine regarding concentration, psychomotor activity, tapping, reaction time, mood and affectivity. 5 Side-effects (mostly tiredness) were seen in five out of 10 subjects after 75 mg fluvoxamine and in eight out of 10 subjects after 75 mg imipramine. There were no clinically relevant changes in pulse, systolic and diastolic blood pressure.

摘要
  1. 抗抑郁药物会使人类大脑功能产生显著变化,这在定量分析脑电图(EEG)中得到体现。可区分出两种主要的药物脑电图特征类型:一种是兴奋型(地昔帕明样)特征,主要表现为α波增加,提示具有激活特性;另一种是镇静型(丙咪嗪或阿米替林样)特征,显示慢波和快波活动同时增加,α波活动减少,也表明具有镇静作用。少数化合物表现出不同的特征。2. 除了确定脑电图变化的类型外,药物脑电图方法似乎在确定对目标器官——人类大脑的时间和剂量疗效关系方面具有价值。此外,还可以确定药效学和药代动力学之间的关系。3. 氟伏沙明是一种新型的芳烷基酮2-氨基乙氧基醚类选择性5-羟色胺(5-HT)再摄取抑制剂,在一项涉及10名健康志愿者的双盲安慰剂对照研究中,口服75毫克后产生了典型的镇静型药物脑电图特征。氟伏沙明(75毫克)引起的慢波活动增强比75毫克丙咪嗪少,表明氟伏沙明的镇静作用比丙咪嗪弱。4. 服用75毫克氟伏沙明后,心理测试表明与安慰剂相比注意力、专注力、精神运动活动、后效应和情绪有改善趋势,临界闪烁融合频率显著增加。与对照药物75毫克丙咪嗪相比,氟伏沙明在专注力、精神运动活动、敲击、反应时间、情绪和情感方面具有显著优势。5. 10名受试者中有5名在服用75毫克氟伏沙明后出现副作用(主要是疲劳),10名受试者中有8名在服用75毫克丙咪嗪后出现副作用。脉搏、收缩压和舒张压没有临床相关变化。

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