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氟马西尼与猴辨别咪达唑仑中咪达唑仑相互作用的定量药理学分析:氟马西尼功能半衰期的测定。

Quantitative pharmacological analyses of the interaction between flumazenil and midazolam in monkeys discriminating midazolam: Determination of the functional half life of flumazenil.

机构信息

Department of Pharmacology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr.-mail code 7764, San Antonio, TX 78229-3900, USA.

Department of Pharmacology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr.-mail code 7764, San Antonio, TX 78229-3900, USA.

出版信息

Eur J Pharmacol. 2014 Jan 15;723:405-9. doi: 10.1016/j.ejphar.2013.10.065. Epub 2013 Nov 8.

Abstract

The duration of action of a drug is commonly estimated using plasma concentration, which is not always practical to obtain or an accurate estimate of functional half life. For example, flumazenil is used clinically to reverse the effects of benzodiazepines like midazolam; however, its elimination can be altered by other drugs, including some benzodiazepines, thereby altering its half life. This study used Schild analyses to characterize antagonism of midazolam by flumazenil and determine the functional half life of flumazenil. Four monkeys discriminated 0.178mg/kg midazolam while responding under a fixed-ratio 10 schedule of stimulus-shock termination; flumazenil was given at various times before determination of a midazolam dose-effect curve. There was a time-related decrease in the magnitude of shift of the midazolam dose-effect curve as the interval between flumazenil and midazolam increased. The potency of flumazenil, estimated by apparent pA2 values (95% CI), was 7.30 (7.12, 7.49), 7.17 (7.03, 7.31), 6.91 (6.72, 7.10) and 6.80 (6.67, 6.92) at 15, 30, 60 and 120min after flumazenil administration, respectively. The functional half life of flumazenil, derived from potency estimates, was 57±13min. Thus, increasing the interval between flumazenil and midazolam causes orderly decreases in flumazenil potency; however, across a broad range of conditions, the qualitative nature of the interaction does not change, as indicated by slopes of Schild plots at all time points that are not different from unity. Differences in potency of flumazenil are therefore due to elimination of flumazenil and not due to pharmacodynamic changes over time.

摘要

药物的作用持续时间通常使用血浆浓度来估计,但获得或准确估计功能半衰期并不总是可行的。例如,氟马西尼临床上用于逆转苯二氮䓬类药物(如咪达唑仑)的作用;然而,其消除可能会被其他药物改变,包括一些苯二氮䓬类药物,从而改变其半衰期。本研究使用 Schild 分析来描述氟马西尼对咪达唑仑的拮抗作用,并确定氟马西尼的功能半衰期。四只猴子在固定比例 10 的刺激-终止方案下辨别 0.178mg/kg 的咪达唑仑;在确定咪达唑仑剂量-效应曲线之前,氟马西尼在不同时间给药。随着氟马西尼和咪达唑仑之间的间隔增加,咪达唑仑剂量-效应曲线的偏移幅度呈时间相关下降。氟马西尼的效价,由表观 pA2 值(95%CI)估计,分别为 15、30、60 和 120min 后 7.30(7.12,7.49)、7.17(7.03,7.31)、6.91(6.72,7.10)和 6.80(6.67,6.92)。氟马西尼的功能半衰期,源自效价估计,为 57±13min。因此,增加氟马西尼和咪达唑仑之间的间隔会导致氟马西尼效价有序下降;然而,在广泛的条件下,Schild 图斜率在所有时间点都不不同于 1,表明相互作用的定性性质不会改变。因此,氟马西尼效价的差异是由于氟马西尼的消除,而不是由于随时间推移的药效变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845b/4118463/9002bb378eab/nihms541036f1.jpg

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