The dopamine D3 receptor partial agonist, BP 897, is an antagonist at human dopamine D3 receptors and at rat somatodendritic dopamine D3 receptors

被引:67
作者
Wicke, K
Garcia-Ladona, J
机构
[1] Knoll AG, Dept Mol Biol, D-67008 Ludwigshafen, Germany
[2] Knoll AG, Dept Pharmacol, D-67008 Ludwigshafen, Germany
关键词
BP; 897; dopamine; dopamine D3 receptor; functional assay; electrophysiology; drug dependence;
D O I
10.1016/S0014-2999(01)01054-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recent studies have fueled the interest in dopamine D3 receptor antagonists and partial agonist for the treatment of psychosis and drug abuse, respectively. N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]naphthalene-2-carboxamide (BP 897) is a dopamine D3 receptor selective ligand recently described as partial agonist with potential effects on drug-dependence. The aim of the present study was to determine both the functional activity of BP 897 at human dopamine D3 receptors expressed in Chinese hamster ovary (CHO) cells and in an electrophysiological in vivo model of dopaminergic activity. BP 897 failed to stimulate the human dopamine D3 receptor and showed antagonistic effects (cpIC(50) = 9.51) in a [S-35]GTP gammaS binding assay in cells expressing the human dopamine D3 receptor. In vivo, BP 897 up to 8.2 mg/kg, i.v., had no agonistic effects on firing rate of substantia nigra dopaminergic neurons and antagonized the quinpirole-induced inhibition of firing (DID50 = 1.1 mg/kg). Our data demonstrate that BP 897 acts, in vivo and in vitro, as a dopamine D3 receptor antagonist. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:85 / 90
页数:6
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