DIFFERENTIAL INTERACTIONS BETWEEN ETHANOL AND RO-15-4513 ON 2 ANXIETY TESTS IN RATS

被引:16
|
作者
PRUNELL, M [1 ]
ESCORIHUELA, RM [1 ]
FERNANDEZTERUEL, A [1 ]
NUNEZ, JF [1 ]
TOBENA, A [1 ]
机构
[1] UNIV AUTONOMA BARCELONA,FAC MED,DEPT FARMACOL & PSIQUIATRIA,UNITAT PSICOL MED,E-08193 BARCELONA,SPAIN
关键词
ETHANOL; RO; 15-4513; GABA/BZ RECEPTOR; ELEVATED PLUS-MAZE; SHUTTLEBOX AVOIDANCE; RATS;
D O I
10.1016/0091-3057(94)90124-4
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
The effects of low (2 g/kg) and high (4 g/kg) doses of ethanol and their interaction with the imidazobenzodiazepine Ro 15-4513 (a partial inverse agonist of the benzodiazepine receptor) were studied in two different models of anxiety in rats: the ''elevated plus-maze'' test and the early acquisition of two-way (shuttlebox) avoidance. In the elevated plus-maze, ethanol (2 g/kg) increased the percentage of entries into the open arms (%EOA) and both ethanol doses increased the percentage of time spent into the open arms (%TOA), thus indicating an anxiolytic action which was reversed by Ro 15-4513 (5 mg/kg). By contrast, Ro 15-4513 did not counteract the anxiolytic effect of the low dose of ethanol in the acquisition of shuttlebox avoidance. Thus, the treatment with 2 g/kg of ethanol (plus either vehicle or Ro 15-4513) significantly increased the total number of avoidances. Conversely, animals treated with 4 g/kg of ethanol showed impaired shuttlebox avoidance acquisition, and this effect was completely reversed by Ro 15-4513. Ro 15-4513 was without effect on its own in any of the anxiety-related parameters (i.e., %EOA, %TOA, and avoidance acquisition). The results indicate a different pattern of ethanol effects and Ethanol x Ro 15-4513 interactions depending upon the task used.
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页码:147 / 151
页数:5
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