Time course of acamprosate action on operant ethanol self-administration after ethanol deprivation

被引:72
作者
Holter, SM
Landgraf, R
Zieglgansberger, W
Spanagel, R
机构
[1] Max Planck Institute of Psychiatry, Clinical Institute, Munich
[2] Max Planck Institute of Psychiatry, D-80804 Munich
关键词
acamprosate; alcohol deprivation effect (ADE); craving; ethanol; operant self-administration;
D O I
10.1111/j.1530-0277.1997.tb03850.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
The effects of the new alcohol anticraving compound acamprosate on the alcohol deprivation effect were tested in an operant two-lever free choice paradigm with concurrent water. Two groups of rats were tested alter long-term voluntary ethanol self-administration: the ''continuous access'' group consisting of animals that had continuous access to ethanol before operant testing; and the ''limited access'' group that was tested only after ethanol deprivation. The limited access group exhibited a strong alcohol deprivation effect with immediate high ethanol consumption and preference. Acamprosate (100, 200, or 400 mg/kg) dose-dependently reduced lever pressing for ethanol and, accordingly, ethanol consumption in both groups in a 23-hr session. The consumption-reducing effect was still evident at the end of the session. Ethanol preference was dose-dependently reduced during the first hour of the session, but returned to basal levels before the end of the 23-hr session in both groups. Thus, the time course of preference reduction was not identical with that of the reduction of ethanol consumption. Surprisingly, preference reduction was observed only after a considerable amount of ethanol had been consumed. These results suggest that the specific effect of preference reduction depended on the simultaneous presence of sufficient levels of acamprosate and ethanol, and that the longer-lasting reduction of ethanol consumption was the consequence of this experience.
引用
收藏
页码:862 / 868
页数:7
相关论文
共 23 条
[1]   ACAMPROSATE MODULATES SYNAPTOSOMAL GABA TRANSMISSION IN CHRONICALLY ALCOHOLIZED RATS [J].
DAOUST, M ;
LEGRAND, E ;
GEWISS, M ;
HEIDBREDER, C ;
DEWITTE, P ;
TRAN, G ;
DURBIN, P .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1992, 41 (04) :669-674
[2]  
DURBIN P, 1995, ALCOHOL ALCOHOLISM, V30, P548
[3]   ACAMPROSATE AND DIAZEPAM DIFFERENTIALLY MODULATE ALCOHOL-INDUCED BEHAVIORAL AND CORTICAL ALTERATIONS IN RATS FOLLOWING CHRONIC INHALATION OF ETHANOL VAPOR [J].
GEWISS, M ;
HEIDBREDER, C ;
OPSOMER, L ;
DURBIN, P ;
DEWITTE, P .
ALCOHOL AND ALCOHOLISM, 1991, 26 (02) :129-137
[4]   REINFORCING AND DISCRIMINATIVE STIMULUS EFFECTS OF CA-ACETYL HOMOTAURINE IN ANIMALS [J].
GRANT, KA ;
WOOLVERTON, WL .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1989, 32 (03) :607-611
[5]  
HEYSER CJ, 1996, ALCOHOL CLIN EXP RES, V20, pA15
[6]   EFFECT OF NALTREXONE ON ALCOHOL-CONSUMPTION DURING CHRONIC ALCOHOL DRINKING AND AFTER A PERIOD OF IMPOSED ABSTINENCE IN FREE-CHOICE DRINKING RHESUS-MONKEYS [J].
KORNET, M ;
GOOSEN, C ;
VANREE, JM .
PSYCHOPHARMACOLOGY, 1991, 104 (03) :367-376
[7]   DOSE-DEPENDENT SUPPRESSION OF THE HIGH ALCOHOL INTAKE OF CHRONICALLY INTOXICATED RATS BY CA-ACETYL HOMOTAURINATE [J].
LEMAGNEN, J ;
TRAN, G ;
DURLACH, J ;
MARTIN, C .
ALCOHOL, 1987, 4 (02) :97-102
[8]   LACK OF EFFECTS OF CA-ACETYL HOMOTAURINATE ON CHRONIC AND ACUTE TOXICITIES OF ETHANOL IN RATS [J].
LEMAGNEN, J ;
TRAN, G ;
DURLACH, J .
ALCOHOL, 1987, 4 (02) :103-108
[9]   ACAMPROSATE APPEARS TO DECREASE ALCOHOL INTAKE IN WEANED ALCOHOLICS [J].
LHUINTRE, JP ;
MOORE, N ;
TRAN, G ;
STERU, L ;
LANGRENON, S ;
DAOUST, M ;
PAROT, P ;
LADURE, P ;
LIBERT, C ;
BOISMARE, F ;
HILLEMAND, B .
ALCOHOL AND ALCOHOLISM, 1990, 25 (06) :613-622
[10]   ABILITY OF CALCIUM BIS ACETYL HOMOTAURINE, A GABA AGONIST, TO PREVENT RELAPSE IN WEANED ALCOHOLICS [J].
LHUINTRE, JP ;
MOORE, ND ;
SALIGAUT, C ;
BOISMARE, F ;
DAOUST, M ;
CHRETIEN, P ;
TRAN, G ;
HILLEMAND, B .
LANCET, 1985, 1 (8436) :1014-1016