Repeated administration of flumazenil does not alter its potency in modifying schedule-controlled behavior in chlordiazepoxide-treated rhesus monkeys

被引:8
作者
Gerak, LR [1 ]
France, CP [1 ]
机构
[1] LOUISIANA STATE UNIV,MED CTR,DEPT PHARMACOL,NEW ORLEANS,LA 70119
关键词
chlordiazepoxide; flumazenil; benzodiazepine; dependence; rhesus monkeys; schedule-controlled behavior;
D O I
10.1007/s002130050266
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous reports have suggested that the effects of the benzodiazepine antagonist flumazenil diminish over repeated exposure in subjects treated chronically with a benzodiazepine agonist. The current study examined whether the frequency of exposure to flumazenil altered its potency in decreasing rates of responding in monkeys treated with chlordiazepoxide (CDP). Three monkeys responded under a multiple fixed ratio (FR10:FR10) schedule of food presentation and stimulus-shock termination (SST). In untreated monkeys, flumazenil (0.1-3.2 mg/kg) had no effect in either component. After 2 weeks of treatment with 32.0 mg/kg per day of CDP, flumazenil decreased response rates in the food component, with a dose of 3.2 mg/kg decreasing rates to 10% of control; rates in the SST component were not altered by flumazenil. When flumazenil dose-effect curves were redetermined at 28-, 14-, 7-, 4-, 2- or 1-day intervals, then was no further change in the potency of flumazenil in decreasing food-maintained responding. When CDP treatment was terminated, the potency of flumazenil recovered to pre-CDP values within 23 days. These results suggest that dependence develops to CDP, since changes in the potency of flumazenil co-varied with CDP treatment. Moreover, it does not appear as though results from previous reports, that showed a diminished response to frequently-administered flumazenil, can be generalized to all conditions.
引用
收藏
页码:64 / 70
页数:7
相关论文
共 29 条
[11]  
GELLERT VF, 1978, J PHARMACOL EXP THER, V205, P536
[12]  
Gerak L. R., 1996, Society for Neuroscience Abstracts, V22, P2075
[13]  
GIUSTI P, 1993, J PHARMACOL EXP THER, V266, P1018
[14]   WITHDRAWAL REACTIONS FROM CHLORDIAZEPOXIDE (LIBRIUM) [J].
HOLLISTER, LE ;
MOTZENBECKER, FP ;
DEGAN, RO .
PSYCHOPHARMACOLOGIA, 1961, 2 (01) :63-68
[15]  
JACOB JJC, 1974, ADV BIOCHEM PSYCHOPH, V8, P299
[16]   ETHANOL, PENTOBARBITAL, AND CHLORDIAZEPOXIDE EFFECTS IN SQUIRREL-MONKEYS RESPONDING UNDER FIXED-RATIO FOOD PRESENTATION AND STIMULUS-SHOCK TERMINATION SCHEDULES [J].
KATZ, JL ;
BARRETT, JE .
PSYCHOPHARMACOLOGY, 1978, 56 (02) :153-155
[17]   EFFECTS OF REPEATED RO 15-1788 ADMINISTRATION IN BENZODIAZEPINE-DEPENDENT BABOONS [J].
LAMB, RJ ;
GRIFFITHS, RR .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1985, 110 (02) :257-261
[18]   PRECIPITATED DIAZEPAM WITHDRAWAL IN BABOONS - EFFECTS OF DOSE AND DURATION OF DIAZEPAM EXPOSURE [J].
LUKAS, SE ;
GRIFFITHS, RR .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1984, 100 (02) :163-171
[19]   WITHDRAWAL FROM LONG-TERM BENZODIAZEPINE TREATMENT [J].
PETURSSON, H ;
LADER, MH .
BRITISH MEDICAL JOURNAL, 1981, 283 (6292) :643-645
[20]  
RICKELS K, 1990, ARCH GEN PSYCHIAT, V47, P899