Compounds selective for dopamine receptor subtypes

被引:54
作者
Kebabian, JW
Tarazi, FI
Kula, NS
Baldessarini, RJ
机构
[1] MASSACHUSETTS GEN HOSP, MCLEAN DIV, MAILMAN RES CTR, BELMONT, MA 02178 USA
[2] HARVARD UNIV, SCH MED, DEPT PSYCHIAT, BELMONT, MA 02178 USA
[3] HARVARD UNIV, SCH MED, NEUROSCI PROGRAM, BELMONT, MA 02178 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1359-6446(97)01075-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Novel dopamine (DA) receptor proteins of relatively low natural abundance and uncertain physiology can be expressed selectively in genetically transfected cultured cells to facilitate screening of novel DA receptor ligands. Selective agonists or antagonists for most of the five major DA receptor types are emerging, but better D-4 and D-5 agonists, D-3 and D-5 antagonists, and more selective D-2 antagonists are needed. Clinical development of such compounds as diagnostic neuroradiopharmaceuticals or neuropsychiatric drugs remains empirical and somewhat unpredictable. The search for novel receptor-selective agents can be enhanced by better understanding of the physiology and pharmacology of DA neuroreceptors.
引用
收藏
页码:333 / 340
页数:8
相关论文
共 93 条
[91]   EFFECT OF A STEREOSPECIFIC D2-DOPAMINE AGONIST ON ACETYLCHOLINE CONCENTRATION IN CORPUS-STRIATUM OF RAT-BRAIN [J].
WONG, DT ;
BYMASTER, FP ;
REID, LR ;
FULLER, RW ;
PERRY, KW ;
KORNFELD, EC .
JOURNAL OF NEURAL TRANSMISSION, 1983, 58 (1-2) :55-67
[92]   CLONING AND EXPRESSION OF HUMAN AND RAT D1 DOPAMINE-RECEPTORS [J].
ZHOU, QY ;
GRANDY, DK ;
THAMBI, L ;
KUSHNER, JA ;
VANTOL, HHM ;
CONE, R ;
PRIBNOW, D ;
SALON, J ;
BUNZOW, JR ;
CIVELLI, O .
NATURE, 1990, 347 (6288) :76-80
[93]  
Zorn S. H., 1996, Society for Neuroscience Abstracts, V22, P1771