Relative reinforcing strength of three N-methyl-D-aspartate antagonists with different onsets of action

被引:67
作者
Winger, G
Hursh, SR
Casey, KL
Woods, JH
机构
[1] Univ Michigan, Dept Pharmacol & Psychol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Physiol & Neurol, Ann Arbor, MI 48109 USA
[3] Sci Applicat Int Corp, Joppa, MD USA
[4] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
关键词
D O I
10.1124/jpet.301.2.690
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The potential contribution of onset and duration of pharmacological action to the reinforcing strength of three intravenously delivered N-methyl-D-aspartate antagonists was evaluated in this study. The onsets and durations of action of ketamine, phencyclidine, and dizocilpine were evaluated by observation and tabulation of their behavioral effects in rhesus monkeys after i.v. administration. The reinforcing effects of each drug were tested in a paradigm in which the fixed ratio requirements for i.v. drug injection were increased systematically. The peak observable effect of ketamine occurred immediately after its administration. There were some immediately observable effects of phencyclidine, although the peak effect of phencyclidine was delayed for 3 to 10 min. Dizocilpine had few immediate effects and a peak effect 32 min after administration. Ketamine had the shortest duration of action, followed by phencyclidine and dizocilpine. Analysis of demand curves and response output curves that were normalized to account for potency differences among the drugs revealed that ketamine and phencyclidine were equally effective as reinforcers, and they were both much stronger reinforcers than was dizocilpine. The data therefore suggest that a fast onset of action increases the reinforcing strength of drugs, although duration of action may play a role as well.
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页码:690 / 697
页数:8
相关论文
共 35 条
[1]   Effect of intravenous injection speed on responses to cocaine and hydromorphone in humans [J].
Abreu, ME ;
Bigelow, GE ;
Fleisher, L ;
Walsh, SL .
PSYCHOPHARMACOLOGY, 2001, 154 (01) :76-84
[2]   THE DISSOCIATIVE ANESTHETICS, KETAMINE AND PHENCYCLIDINE, SELECTIVELY REDUCE EXCITATION OF CENTRAL MAMMALIAN NEURONS BY N-METHYL-ASPARTATE [J].
ANIS, NA ;
BERRY, SC ;
BURTON, NR ;
LODGE, D .
BRITISH JOURNAL OF PHARMACOLOGY, 1983, 79 (02) :565-575
[3]   FIXED-INTERVAL SCHEDULE OF COCAINE REINFORCEMENT - EFFECT OF DOSE AND INFUSION DURATION [J].
BALSTER, RL ;
SCHUSTER, CR .
JOURNAL OF THE EXPERIMENTAL ANALYSIS OF BEHAVIOR, 1973, 20 (01) :119-129
[4]  
BALSTER RL, 1973, PHARM BIOCH BEHAV, V1, P169
[5]   Substitution and caloric regulation in a closed economy [J].
Bauman, RA ;
Raslear, TG ;
Hursh, SR ;
Shurtleff, D ;
Simmons, L .
JOURNAL OF THE EXPERIMENTAL ANALYSIS OF BEHAVIOR, 1996, 65 (02) :401-422
[6]  
BEARDSLEY PM, 1990, J PHARMACOL EXP THER, V252, P953
[7]   THE EFFECTS OF DELAY OF REINFORCEMENT AND DOSE ON THE SELF-ADMINISTRATION OF COCAINE AND PROCAINE IN RHESUS-MONKEYS [J].
BEARDSLEY, PM ;
BALSTER, RL .
DRUG AND ALCOHOL DEPENDENCE, 1993, 34 (01) :37-43
[8]   Deconstructing relative reinforcing efficacy and situating the measures of pharmacological reinforcement with behavioral economics: a theoretical proposal [J].
Bickel, WK ;
Marsch, LA ;
Carroll, ME .
PSYCHOPHARMACOLOGY, 2000, 153 (01) :44-56
[9]   THE BEHAVIORAL ECONOMICS OF CONCURRENT DRUG REINFORCERS - A REVIEW AND REANALYSIS OF DRUG SELF-ADMINISTRATION RESEARCH [J].
BICKEL, WK ;
DEGRANDPRE, RJ ;
HIGGINS, ST .
PSYCHOPHARMACOLOGY, 1995, 118 (03) :250-259
[10]  
CHEN G M, 1960, Anesth Analg, V39, P132