Studies on the role of 5-HT3 receptors in the mediation of the ethanol interoceptive cue

被引:23
作者
Stefanski, R
Bienkowski, P
Kostowski, W
机构
[1] INST PSYCHIAT & NEUROL,DEPT PHARMACOL & PHYSIOL NERVOUS SYST,PL-02957 WARSAW,POLAND
[2] MED HIGH SCH,DEPT EXPT & CLIN PHARMACOL,PL-00527 WARSAW,POLAND
关键词
discriminative stimulus; ethanol; 5-HT3 receptor agonist; 5-HT3 receptor antagonist;
D O I
10.1016/0014-2999(96)00345-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The drug discrimination test was used to evaluate the role of 5-HT3 receptors in the mediation of the stimulus properties of ethanol in rats trained to discriminate between ethanol (1.0 g/kg, 10% v/v, i.p.) and saline vehicle. Rats trained to discriminate between a lower dose of ethanol (0.5 g/kg i.p.) failed to attain discrimination criteria after 20 weeks (100 sessions) of training. None of the doses of 5-HT, receptor antagonists (0.001, 0.01, 0.1, 1.O, 10.0 mg/kg of tropisetron or ondansetron) administered i.p. 30 min before ethanol, antagonized the discriminative stimulus properties of ethanol. Furthermore, none of the centrally (1, 10, 35 mu g per rat) or i.p. (0.1, 1.0, 2.5, 5.0, 10.0 mg/kg) administered doses of 5-HT3 receptor agonist, 1-(m-chlorophenyl)-biguanide, could replace the ethanol discriminative cue. These results suggest that 5-HT3 receptors are not primarily involved in the mediation of the stimulus properties of ethanol.
引用
收藏
页码:141 / 147
页数:7
相关论文
共 47 条
[1]   FAILURE TO ESTABLISH A CONDITIONED PLACE PREFERENCE WITH ETHANOL IN RATS [J].
ASIN, KE ;
WIRTSHAFTER, D ;
TABAKOFF, B .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1985, 22 (02) :169-173
[2]  
BOCKAERT J, 1990, MOL PHARMACOL, V37, P408
[3]   RAT STRAIN DIFFERENCES IN ETHANOL SELF-ADMINISTRATION AND TASTE-AVERSION LEARNING [J].
CANNON, DS ;
CARRELL, LE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1987, 28 (01) :57-63
[4]   5HT3 RECEPTOR ANTAGONISTS BLOCK MORPHINE-INDUCED AND NICOTINE-INDUCED BUT NOT AMPHETAMINE-INDUCED REWARD [J].
CARBONI, E ;
ACQUAS, E ;
LEONE, P ;
DICHIARA, G .
PSYCHOPHARMACOLOGY, 1989, 97 (02) :175-178
[5]   DIFFERENTIAL INHIBITORY EFFECTS OF A 5-HT3 ANTAGONIST ON DRUG-INDUCED STIMULATION OF DOPAMINE RELEASE [J].
CARBONI, E ;
ACQUAS, E ;
FRAU, R ;
DICHIARA, G .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1989, 164 (03) :515-519
[6]   BLOCKADE OF ETHANOL DISCRIMINATION BY ISRADIPINE [J].
COLOMBO, G ;
AGABIO, R ;
LOBINA, C ;
REALI, R ;
FADDA, F ;
GESSA, GL .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 265 (03) :167-170
[7]  
COLOMBO G, 1995, ALCOHOL ALCOHOLISM, V30, P493
[8]  
COLPAERT FC, 1986, BEHAV ANAL DRUG DEPE, P161
[9]   THE GASTROINTESTINAL PROKINETIC BENZAMIDE DERIVATIVES ARE AGONISTS AT THE NON-CLASSICAL 5-HT RECEPTOR (5-HT4) POSITIVELY COUPLED TO ADENYLATE-CYCLASE IN NEURONS [J].
DUMUIS, A ;
SEBBEN, M ;
BOCKAERT, J .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1989, 340 (04) :403-410
[10]   MDL 72222, A SELECTIVE 5-HT3 RECEPTOR ANTAGONIST, SUPPRESSES VOLUNTARY ETHANOL-CONSUMPTION IN ALCOHOL-PREFERRING RATS [J].
FADDA, F ;
GARAU, B ;
MARCHEI, F ;
COLOMBO, G ;
GESSA, GL .
ALCOHOL AND ALCOHOLISM, 1991, 26 (02) :107-110