The dopamine D4 receptor:: one decade of research

被引:344
|
作者
Oak, JN
Oldenhof, J
Van Tol, HHM
机构
[1] Ctr Addict & Mental Hlth, Mol Neurobiol Lab, Clarke Div, Toronto, ON M5T 1R8, Canada
[2] Univ Toronto, Dept Pharmacol, Toronto, ON, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
[4] Univ Toronto, Dept Psychiat, Toronto, ON M5S 1A1, Canada
关键词
dopamine D-4 receptor; G protein-coupled receptor; structure; pharmacology; signaling; physiology; genetics;
D O I
10.1016/S0014-2999(00)00562-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dopamine is an important neurotransmitter involved in motor control, endocrine function, reward, cognition and emotion. Dopamine receptors belong to the superfamily of G protein-coupled receptors and play a crucial role in mediating the diverse effects of dopamine in the central nervous system (CNS). The dopaminergic system is implicated in disorders such as Parkinson's disease and addiction, and is the major target for antipsychotic medication in the treatment of schizophrenia. Molecular cloning studies a decade ago revealed the existence of five different dopamine receptor subtypes in mammalian species. While the presence of the abundantly expressed dopamine D-1 and D-2 receptors was predicted from biochemical and pharmacological work, the cloning of the less abundant dopamine D-3, D-4 and D-5 receptors was not anticipated. The identification of these novel dopamine receptor family members posed a challenge with respect to determining their precise physiological roles and identifying their potential as therapeutic targets for dopamine-related disorders. This review is focused on the accomplishments of one decade of research on the dopamine D-4 receptor. New insights into the biochemistry of the dopamine D-4 receptor include the discovery that this G protein-coupled receptor can directly interact with SH3 domains. At the physiological level, converging evidence from transgenic mouse work and human genetic studies suggests that this receptor has a role in exploratory behavior and as a genetic susceptibility factor for attention deficit hyperactivity disorder. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:303 / 327
页数:25
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