Influence of 5-HT1A receptor antagonism on plus-maze behaviour in mice .2. WAY 100635, SDZ 216-525 and NAN-190

被引:58
作者
Cao, BJ [1 ]
Rodgers, RJ [1 ]
机构
[1] UNIV LEEDS, DEPT PSYCHOL, ETHOPHARMACOL LAB, LEEDS LS2 9JT, W YORKSHIRE, ENGLAND
基金
英国惠康基金;
关键词
anxiety elevated plus-maze; 5-HT1A receptors; alpha(1)-adrenoceptors; WAY; 100635; SDZ; 216-525; NAN-190; prazosin; mice;
D O I
10.1016/S0091-3057(97)00279-7
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
To understand further the role of 5-hydroxytryptamine receptor subtype 1A (5-HT1A) mechanisms in anxiety, the behavioural effects of 5-HT1A receptor antagonists with different selectivity and intrinsic activity were examined using an ethological version of the murine elevated plus-maze test. WAY 100635 (0.03-9.0 mg/kg) produced a behavioural profile indicative of an anxiolyticlike effect, with an apparent bell-shaped dose-response relationship and increases in nonexploratory behaviours at the largest dose tested. SDZ 216-525 exerted a dose-dependent antianxiety action at doses of 0.05-0.8 mg/kg, with some loss of activity at 3.2 mg/kg. In contrast, smaller doses of NAN-190 had a significant effect, whereas higher doses (2.5-10.0 mg/kg) decreased locomotor activity and other active behaviours, a profile similar to that produced by the alpha(1)-adrenoceptor antagonist prazosin (2.5 mg/kg), which also inhibited open arm activity. Findings are discussed in relation to 5-HT1A receptor and alpha(1)-adrenoceptor antagonism and corresponding neurochemical changes. The results of the present series support the view that 5-HT1A receptor antagonists have therapeutic potential in the management of anxiety. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:593 / 603
页数:11
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