Simpao A, Sun L, Falk J L, Lau C E
Department of Psychology, Rutgers, The State University of New Jersey, Piscataway 08854-8020, USA.
Psychopharmacology (Berl). 2001 May;155(3):269-77. doi: 10.1007/s002130100707.
Environmental factors affect serum drug concentration-effect relations. For example, after midazolam administration, longer pre-session delays imposed in experimental chambers produced differential concentration-effect relations compared to those of shorter delays.
To evaluate the extent to which serum concentrations determine alprazolam's effects on spontaneous activity in the presence and absence of a differential reinforcement of low rate (DRL 45-s) contingency using pharmacokinetic-pharmacodynamic analysis. Serum concentrations reported here were simulated from our published pharmacokinetic parameters for alprazolam.
One group (n=8) was used to investigate alprazolam's effects on spontaneous activity within the DRL contingency by placing an activity platform beneath each operant chamber to monitor concurrently both spontaneous activity (large and small movements) and DRL performance (shorter-response and reinforcement rates) in 3-h sessions; a parallel group (n=7) was used without the operant context. The concentration-effect relation of the reinforcement rate was compared and contrasted with those of spontaneous activity.
Alprazolam decreased large and small movements within the DRL contingency, which corresponded to that of reinforcement rates under the DRL 45-s schedule. In contrast, without the DRL contingency, alprazolam's effects on small movements were short-lived (i.e., 30 min) and no effects on large movements were detected. Hence, the predicted concentration-effect relations for the reinforcement rate function described those of spontaneous activity well within the operant context, but not those without the operant context. Furthermore, the latter showed no correlation between serum alprazolam concentration and large movements; a significant, but low negative correlation for small movements was observed.
The duration of alprazolam's action was dependent on not only dose size but also the behavioral measure examined. By imposing the DRL contingency, spontaneous activity behaves as an ideal pharmacodynamic measure (i.e., continuous, sensitive, and objective).
环境因素会影响血清药物浓度-效应关系。例如,给予咪达唑仑后,与较短延迟相比,实验室内较长的给药前延迟会产生不同的浓度-效应关系。
使用药代动力学-药效学分析,评估在存在和不存在低速率差异强化(DRL 45秒)意外情况时,血清浓度对阿普唑仑自发活动影响的程度。此处报告的血清浓度是根据我们已发表的阿普唑仑药代动力学参数模拟得出的。
一组(n = 8)通过在每个操作箱下方放置一个活动平台,以在3小时的实验时段内同时监测自发活动(大动作和小动作)和DRL表现(较短反应和强化率),来研究阿普唑仑在DRL意外情况下对自发活动的影响;另一平行组(n = 7)在没有操作背景的情况下进行研究。将强化率的浓度-效应关系与自发活动的浓度-效应关系进行比较和对比。
阿普唑仑在DRL意外情况下减少了大动作和小动作,这与DRL 45秒时间表下的强化率相对应。相比之下,在没有DRL意外情况时,阿普唑仑对小动作的影响是短暂的(即30分钟),且未检测到对大动作有影响。因此,强化率函数的预测浓度-效应关系在操作背景下能很好地描述自发活动的关系,但在没有操作背景时则不然。此外,后者显示血清阿普唑仑浓度与大动作之间无相关性;而对于小动作,观察到显著但较低的负相关性。
阿普唑仑的作用持续时间不仅取决于剂量大小,还取决于所检测的行为指标。通过施加DRL意外情况,自发活动表现为一种理想的药效学指标(即连续、敏感且客观)。