Effects of acamprosate on sensitization to the locomotor-stimulant effects of alcohol in mice selectively bred for high and low alcohol preference

被引:16
作者
Chester, JA [1 ]
Grahame, NJ [1 ]
Li, TK [1 ]
Lumeng, L [1 ]
Froehlich, JC [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46202 USA
来源
BEHAVIOURAL PHARMACOLOGY | 2001年 / 12卷 / 6-7期
关键词
acamprosate; alcohol preference; relapse; craving; locomotor activity; sensitization; strain difference; mouse;
D O I
10.1097/00008877-200111000-00015
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Sensitization to the locomotor-stimulant effects of drugs is thought to play an important role in the development of drug-seeking behaviour. We hypothesized that the ability of acamprosate to reduce alcohol relapse rates in recovering alcoholics, and alcohol consumption in rodents, may be related to its ability to reduce sensitization to the locomotor-stimulant effects of alcohol. The purpose of the present study was to determine whether acamprosate reduces the expression of sensitization to the locomotor-stimulant effects of alcohol in lines of mice selectively bred for high (HAP) and low (LAP) alcohol preference. Mice were given six intraperitoneal (i.p.) injections of alcohol (3 g/kg) or saline at 48 h intervals. The test for sensitization to the locomotor-stimulant effects of alcohol consisted of a challenge dose of 2 g/kg i.p. alcohol followed immediately by assessment of locomotor activity for 20 min. Mice were pretreated with either saline or acamprosate (400 mg/kg) at 14 h and again at 2 h before the alcohol challenge. Both HAP and LAP mice showed sensitization to the locomotor-stimulant effects of alcohol. Acamprosate reduced the expression of sensitization to the locomotor-stimulant effects of alcohol in HAP but not LAP mice. These data suggest complex effects of acamprosate on alcohol-stimulated locomotor activity that depend on genotype. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:535 / 543
页数:9
相关论文
共 50 条
[1]  
BALDO BA, 1995, NEUR ABSTR, V21, P1701
[2]   A HOMOTAURINE DERIVATIVE REDUCES THE VOLUNTARY INTAKE OF ETHANOL BY RATS - ARE CEREBRAL GABA RECEPTORS INVOLVED [J].
BOISMARE, F ;
DAOUST, M ;
MOORE, N ;
SALIGAUT, C ;
LHUINTRE, JP ;
CHRETIEN, P ;
DURLACH, J .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1984, 21 (05) :787-789
[3]   Dizocilpine (MK-801) prevents the development of sensitization to ethanol in DBA/2J mice [J].
Broadbent, J ;
Weitemier, AZ .
ALCOHOL AND ALCOHOLISM, 1999, 34 (03) :283-288
[4]   PROLONGED TREATMENT WITH CARBAMAZEPINE INCREASES THE STIMULATORY EFFECTS OF ETHANOL IN MICE [J].
CAMARINI, R ;
ANDREATINI, R ;
MONTEIRO, MG .
ALCOHOL, 1995, 12 (04) :305-308
[5]   MK-801 blocks the development of behavioral sensitization to ethanol [J].
Camarini, R ;
Frussa, R ;
Monteiro, MG ;
Calil, HM .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2000, 24 (03) :285-290
[6]   Modulation of corticosterone does not affect the acquisition or expression of ethanol-induced conditioned place preference in DBA/2J mice [J].
Chester, JA ;
Cunningham, CL .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1998, 59 (01) :67-75
[7]   United Kingdom multicentre acamprosate study (UKMAS): A 6-month prospective study of acamprosate versus placebo in preventing relapse after withdrawal from alcohol [J].
Chick, J ;
Howlett, H ;
Morgan, MY ;
Ritson, B .
ALCOHOL AND ALCOHOLISM, 2000, 35 (02) :176-187
[8]   Acamprosate, but not naltrexone, inhibits conditioned abstinence behaviour associated with repeated ethanol administration and exposure to a plus-maze [J].
Cole, JC ;
Littleton, JM ;
Little, HJ .
PSYCHOPHARMACOLOGY, 2000, 147 (04) :403-411
[9]   LOCALIZATION OF GENES INFLUENCING ETHANOL-INDUCED CONDITIONED PLACE PREFERENCE AND LOCOMOTOR-ACTIVITY IN BXD RECOMBINANT INBRED MICE [J].
CUNNINGHAM, CL .
PSYCHOPHARMACOLOGY, 1995, 120 (01) :28-41
[10]   CONDITIONED ACTIVATION INDUCED BY ETHANOL - ROLE IN SENSITIZATION AND CONDITIONED PLACE PREFERENCE [J].
CUNNINGHAM, CL ;
NOBLE, D .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1992, 43 (01) :307-313