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单剂量三唑仑的药代动力学和药效学:脑电图与数字符号替换测验的比较

Pharmocokinetics and pharmacodynamics of single-dose triazolam: electroencephalography compared with the Digit-Symbol Substitution Test.

作者信息

Greenblatt David J, Gan Lu, Harmatz Jerold S, Shader Richard I

机构信息

Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine and Tufts-New England Medical Center, Boston, MA 02111, USA.

出版信息

Br J Clin Pharmacol. 2005 Sep;60(3):244-8. doi: 10.1111/j.1365-2125.2005.02409.x.

Abstract

AIMS

To investigate whether the electroencephalogram (EEG) directly reflects the CNS effects of benzodiazepines by evaluating the relation of the EEG to plasma drug concentrations and to Digit-Symbol Substitution Test (DSST) scores after a single dose of triazolam, a representative benzodiazepine agonist.

METHODS

Thirteen healthy male subjects were given 0.375 mg triazolam or placebo in a double-blind crossover study. Plasma samples were collected during 8 h after dosage. Pharmacodynamic effects were measured by DSST and EEG at corresponding times.

RESULTS

Pharmacokinetic parameters for triazolam were consistent with established values. Compared with placebo, triazolam significantly impaired psychomotor performance on the DSST (P < 0.001) and increased beta amplitude on the EEG (P < 0.002). DSST and EEG changes both closely tracked changes in plasma concentrations over time. The changes for the two measures were highly correlated with each other (r =-0.94, P < 0.001) based on aggregate values at individual time points. However, the variations in area under the curve of pharmacodynamic effect vs. time (AUCeffect) measured by either method did not reflect the variations in plasma AUC across individuals. The individual variability in AUCeffect from the EEG was similar to that measured by the DSST.

CONCLUSIONS

Both the EEG and the DSST reflect the central benzodiazepine agonist effects of triazolam. Intrinsic variability in both measures is similar.

摘要

目的

通过评估脑电图(EEG)与血浆药物浓度的关系以及单次服用代表性苯二氮䓬激动剂三唑仑后与数字符号替换测验(DSST)分数的关系,研究脑电图是否直接反映苯二氮䓬对中枢神经系统的作用。

方法

在一项双盲交叉研究中,13名健康男性受试者服用0.375mg三唑仑或安慰剂。给药后8小时内采集血浆样本。在相应时间通过DSST和EEG测量药效学效应。

结果

三唑仑的药代动力学参数与既定值一致。与安慰剂相比,三唑仑显著损害了DSST上的精神运动表现(P<0.001),并增加了EEG上的β波幅(P<0.002)。DSST和EEG的变化都随时间密切跟踪血浆浓度的变化。基于各个时间点的汇总值,这两种测量方法的变化彼此高度相关(r=-0.94,P<0.001)。然而,通过任何一种方法测量的药效学效应-时间曲线下面积(AUCeffect)的变化并未反映个体间血浆AUC 的变化。EEG测量的AUCeffect个体变异性与DSST测量的相似。

结论

EEG和DSST都反映了三唑仑的中枢苯二氮䓬激动剂作用。两种测量方法的内在变异性相似。

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本文引用的文献

2
Pharmacokinetic-pharmacodynamic relationships for benzodiazepines.
Clin Pharmacokinet. 1996 Jan;30(1):52-76. doi: 10.2165/00003088-199630010-00004.
4
Kinetic-dynamic modeling in clinical psychopharmacology.
J Clin Psychopharmacol. 1993 Aug;13(4):231-4.
5
Use of benzodiazepines in anxiety disorders.
N Engl J Med. 1993 May 13;328(19):1398-405. doi: 10.1056/NEJM199305133281907.
6
Clinical uses of benzodiazepines.
J Clin Psychopharmacol. 1993 Dec;13(6 Suppl 1):1S-169S.
7
Sedative-hypnotics and human performance.
Psychopharmacology (Berl). 1982;76(2):101-13. doi: 10.1007/BF00435262.
8
Pencil and paper tests--sensitivity to psychotropic drugs.
Br J Clin Pharmacol. 1984;18 Suppl 1(Suppl 1):15S-20S. doi: 10.1111/j.1365-2125.1984.tb02578.x.
9
Drug therapy. Current status of benzodiazepines.
N Engl J Med. 1983 Aug 11;309(6):354-8. doi: 10.1056/NEJM198308113090607.
10
A simplex procedure for fitting nonlinear pharmacokinetic models.
Comput Biol Med. 1987;17(3):199-208. doi: 10.1016/0010-4825(87)90044-8.

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