Dopamine and N-methyl-D-aspartate receptor interactions in the neostriatum

被引:269
|
作者
Cepeda, C [1 ]
Levine, MS [1 ]
机构
[1] Univ Calif Los Angeles, Mental Retardat Res Ctr, Los Angeles, CA 90024 USA
关键词
dopamine; electrophysiology; neostriatum; N-methyl-D-aspartate; receptor interactions;
D O I
10.1159/000017294
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
This review examines dopamine (DA) and glutamate receptor interactions in the neostriatum (NS) primarily from a neurophysiological perspective. Historically, a clear understanding of the function of DA. in the NS has been difficult because it was considered a classical neurotransmitter with either excitatory or inhibitory actions and because many of the data were obtained by use of varying methodologies. When DA is considered a neuromodulator whose role is to alter how NS cells respond to glutamatergic inputs, many of its actions can be accounted for and predicted with great accuracy within a model of receptor subtype. In this model, DA via activation of D1 receptors potentiates responses mediated by activation of N-methyl-D-aspartate (NMDA) receptors. DA via activation of D2 receptors attenuates responses mediated by activation of non-NMDA receptors. Outcomes of combinations of NMDA and D2 and non-NMDA and DI receptors are not as predictable. The mechanisms underlying the D1-NMDA receptor interactions appear to involve alterations in cell excitability mediated by activation of Ca2+ conductances and/or phosphorylation of NMDA receptors. Less is known about mechanisms underlying the D2-non-NMDA receptor interaction. The functional implications of this model in setting membrane potentials, signal-to-noise ratio, plasticity and excitotoxicity are discussed.
引用
收藏
页码:1 / 18
页数:18
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