Effects of endomorphins-1 and-2, endogenous μ-opioid receptor agonists, on spontaneous alternation performance in mice

被引:37
|
作者
Ukai, M [1 ]
Watanabe, Y [1 ]
Kameyama, T [1 ]
机构
[1] Meijo Univ, Fac Pharmaceut Sci, Dept Chem Pharmacol, Nagoya, Aichi 4688503, Japan
关键词
endomorphin-1; endomorphin-2; mu-opioid receptor; spontaneous alternation performance; (mouse);
D O I
10.1016/S0014-2999(00)00179-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects of intracerebroventricular (i.c.v.) administration of endomorphins-1 and -2, endogenous mu-opioid receptor agonists, on the spontaneous alternation performance associated with spatial working memory were investigated in mice. Endomorphin-1 (10 and 17.5 mu g) and endomorphin-2 (10 mu g) produced a significant decrease in percent alternation without affecting total arm entries. beta-Funaltrexamine (5 mu g) almost completely reversed the endomorphin-1 (10 mu g) and endomorphin-2 (10 mu g)-induced decrease in percent alternation, although neither naltrindole (4 ng) nor nor-binaltorphimine (4 mu g) produced any significant effects on alternation performance. These results suggest that endomorphins impair spatial working memory through the mediation of mu-opioid receptors. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:211 / 215
页数:5
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