EFFECTS OF D1 AND D2 DOPAMINE RECEPTOR AGENTS ON ETHANOL-CONSUMPTION IN THE HIGH-ALCOHOL-DRINKING (HAD) LINE OF RATS

被引:136
作者
DYR, W
MCBRIDE, WJ
LUMENG, L
LI, TK
MURPHY, JM
机构
[1] IUPUI,PURDUE SCH SCI,DEPT PSYCHOL,LD-3124,402 N BLACKFORD ST,INDIANAPOLIS,IN 46202
[2] INDIANA UNIV,SCH MED,INST PSYCHIAT RES,DEPT PSYCHIAT,INDIANAPOLIS,IN 46202
[3] INDIANA UNIV,SCH MED,INST PSYCHIAT RES,DEPT MED & BIOCHEM,INDIANAPOLIS,IN 46202
[4] INDIANA UNIV,SCH MED,INST REGENSTRIEF,INDIANAPOLIS,IN 46202
[5] RICHARD L ROUDEBUSH VET ADM MED CTR,INDIANAPOLIS,IN 46202
[6] INST PSYCHIAT & NEUROL,DEPT PHARMACOL & PHYSIOL NERVOUS SYST,PL-02957 WARSAW,POLAND
关键词
HIGH-ALCOHOL-DRINKING (HAD) RATS; ETHANOL REINFORCEMENT; DOPAMINE AGONISTS; DOPAMINE ANTAGONISTS; SKF-38393; SCH-23390; QUINPIROLE; SPIPERONE;
D O I
10.1016/0741-8329(93)90037-O
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
Dopamine receptor agonists and antagonists were tested for effects on alcohol drinking in female HAD rats (n = 10) given limited access (4 h/day) to a 10% (v/v) ethanol solution. Food and water were available ad libitum. Subcutaneous drug injections were given 30-60 min before the ethanol access periods. The D2 agonist quinpirole (0.04-2.0 mg/kg) caused a dose-dependent decrease in alcohol drinking throughout the 4-h period. Spiperone, a D2 antagonist, had no effect during the initial part of the session, but by the fourth hour, the 10 mug/kg dose tended to increase alcohol intake and the 30 mug/kg dose reduced intake. The D1 antagonist SCH-23390 (3-30 mug/kg) dose-dependently decreased ethanol drinking during the first hour of access. The D1 agonist SKF-38393 (2-6 mg/kg) also decreased alcohol intake, but it was less effective than SCH-23390. The findings implicate both D1 and D2 receptors in the reinforcing effects of alcohol drinking by the HAD line of rats.
引用
收藏
页码:207 / 212
页数:6
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