Metabotropic glutamate receptors and the generation of locomotor activity: Interactions with midbrain dopamine

被引:98
作者
Vezina, P [1 ]
Kim, JH [1 ]
机构
[1] Univ Chicago, Dept Psychiat, Chicago, IL 60637 USA
关键词
metabotropic and ionotropic glutamate receptors; excitatory amino acids; glutamate; dopamine; basal ganglia; ventral tegmental area; nucleus accumbens; striatum; locomotion; rotation; locomotor sensitization; psychomotor stimulants;
D O I
10.1016/S0149-7634(98)00055-4
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Interactions between excitatory amino acid (EAA) and dopamine (DA) pathways in the basal ganglia have been known for some time to contribute importantly to the generation of motor behaviors. In particular, the role played by ionotropic glutamate receptors (iGluRs) in such interactions and in the production of locomotion has received considerable attention, particularly in brain areas such as the ventral tegmental area (VTA) where EAA afferants are known to modulate the activity of DA neurons and the nucleus accumbens (NAcc) where descending EAA projections and ascending DA mesencephalic projections come in close apposition to each other and co-innervate intrinsic neurons projecting to motor output regions. Recently, the growing importance of the metabotropic glutamate receptor (mGluR) in the generation of motor behaviors and various forms of plasticity has begun to emerge. The known coupling of the mGluR to second messenger systems and its demonstrated role in the long-term modulation of synaptic transmission make it a logical candidate not only for the generation of locomotion involving EAA-DA interactions, but also for the induction and expression of locomotor plasticity involving these neurotransmitters. In this review, we examine the evidence supporting a role for mGluRs in the generation of DA-dependent locomotion as well as in one form of locomotor plasticity: the sensitization of locomotor activity by psychomotor stimulant drugs. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:577 / 589
页数:13
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