DOPAMINE RECEPTOR OCCUPANCY INVIVO - BEHAVIORAL-CORRELATES USING NNC-112, NNC-687 AND NNC-756, NEW SELECTIVE DOPAMINE D1 RECEPTOR ANTAGONISTS

被引:38
作者
NIELSEN, EB [1 ]
ANDERSEN, PH [1 ]
机构
[1] NOVO NORDISK AS,DEPT MOLEC PHARMACOL BIOSCI,DK-2880 BOGSVAERD,DENMARK
关键词
DOPAMINE D1 RECEPTORS; DOPAMINE D2 RECEPTORS; BINDING (INVIVO); BEHAVIOR; (RAT);
D O I
10.1016/0014-2999(92)90577-Q
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ability of dopamine D2, mixed D1/D2 and selective D1 receptor antagonists, including NNC-112, NNC-687, NNC-756, to inhibit the in vivo binding of [H-3]SCH 23390 or [H-3]raclopride to dopamine receptors was studied in mice and rats. Furthermore, the dopamine-antagonistic effects of these drugs were also studied in various behavioral models. Significant levels of in vivo receptor blockade were required for antagonism of typical dopamine agonist-mediated behaviors. However, fewer D1 than D2 receptors had to be blocked to produce similar antagonistic effects. Thus, there may be a greater receptor reserve for D2 receptors than for D1 receptors.
引用
收藏
页码:35 / 44
页数:10
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