Suppr超能文献

正常受试者中诺米芬辛与阿米替林药效学特征的比较。

A comparison of the pharmacodynamic profiles of nomifensine and amitriptyline in normal subjects.

作者信息

Chan M Y, Ehsanullah R, Wadsworth J, McEwen J

出版信息

Br J Clin Pharmacol. 1980 Mar;9(3):247-53. doi: 10.1111/j.1365-2125.1980.tb04834.x.

Abstract

1 Six healthy male volunteers participated in a double-blind placebo crossover comparison of the pharmacodynamic profiles of single oral doses of 75 mg nomifensine and 50 mg amitriptyline. 2 Nomifensine treatment did not influence salivary flow and did not significantly affect psychomotor performance (critical flicker fusion, pursuit rotor and reaction time): in addition nomifensine had no significant effect on subjective measurements of sedation and concentration. 3 By contrast, amitriptyline treatment significantly reduced salivary flow and was associated with significant sedation and reduced concentration: significant changes in psychomotor performance were also noted. 4 Plasma concentrations of amitriptyline and nomifensine were measured at 2 h. The respective median concentration values were 55.0 ng/ml and 52.0 ng/ml. 5 Ex vivo platelet amine uptake of dopamine (DA) and 5-hydroxytryptamine (5HT) was measured 2 h after each treatment. Both nomifensine and amitriptyline treatment significantly inhibited DA uptake to a similar extent. Amitriptyline treatment additionally inhibited 5-HT uptake.

摘要
  1. 六名健康男性志愿者参与了一项双盲安慰剂交叉对照试验,比较单次口服75毫克诺米芬辛和50毫克阿米替林的药效学特征。2. 诺米芬辛治疗不影响唾液分泌,对精神运动性能(临界闪烁融合、追踪转子和反应时间)也无显著影响:此外,诺米芬辛对镇静和注意力的主观测量无显著影响。3. 相比之下,阿米替林治疗显著减少唾液分泌,伴有显著的镇静作用和注意力下降:精神运动性能也有显著变化。4. 在2小时时测量了阿米替林和诺米芬辛的血浆浓度。各自的中位数浓度值分别为55.0纳克/毫升和52.0纳克/毫升。5. 在每次治疗后2小时测量体外血小板对多巴胺(DA)和5-羟色胺(5HT)的胺摄取。诺米芬辛和阿米替林治疗均显著抑制DA摄取,且程度相似。阿米替林治疗还额外抑制5-HT摄取。

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本文引用的文献

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Critical flicker frequency and centrally-acting drugs.临界闪烁频率与中枢作用药物。
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