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P2 受体参与了与动机相关行为的调节。

P2 receptors are involved in the mediation of motivation-related behavior.

机构信息

Rudolf-Boehm-Institute of Pharmacology and Toxicology, University of Leipzig, Leipzig, Germany,

出版信息

Purinergic Signal. 2004 Dec;1(1):21-9. doi: 10.1007/s11302-004-4745-4.

Abstract

The importance of purinergic signaling in the intact mesolimbic-mesocortical circuit of the brain of freely moving rats is reviewed. In the rat, an endogenous ADP/ATPergic tone reinforces the release of dopamine from the axon terminals in the nucleus accumbens as well as from the somatodendritic region of these neurons in the ventral tegmental area, as well as the release of glutamate, probably via P2Y(1) receptor stimulation. Similar mechanisms may regulate the release of glutamate in both areas of the brain. Dopamine and glutamate determine in concert the activity of the accumbal GABAergic, medium-size spiny neurons thought to act as an interface between the limbic cortex and the extrapyramidal motor system. These neurons project to the pallidal and mesencephalic areas, thereby mediating the behavioral reaction of the animal in response to a motivation-related stimulus. There is evidence that extracellular ADP/ATP promotes goal-directed behavior, e.g., intention and feeding, via dopamine, probably via P2Y(1) receptor stimulation. Accumbal P2 receptor-mediated glutamatergic mechanisms seem to counteract the dopaminergic effects on behavior. Furthermore, adaptive changes of motivation-related behavior, e.g., by chronic succession of starvation and feeding or by repeated amphetamine administration, are accompanied by changes in the expression of the P2Y(1) receptor, thought to modulate the sensitivity of the animal to respond to certain stimuli.

摘要

本文回顾了嘌呤能信号在自由活动大鼠完整中脑边缘-中皮层回路中的重要作用。在大鼠中,内源性 ADP/ATP 能通过刺激 P2Y(1)受体增强伏隔核(NAc)轴突末梢和腹侧被盖区(VTA)这些神经元的胞体树突区多巴胺的释放,以及谷氨酸的释放。类似的机制可能调节大脑这两个区域的谷氨酸释放。多巴胺和谷氨酸共同决定了中脑边缘 GABA 能中型棘突神经元的活性,这些神经元被认为是边缘皮层和锥体外系运动系统之间的接口。这些神经元投射到苍白球和中脑区域,从而介导动物对与动机相关刺激的行为反应。有证据表明,细胞外 ADP/ATP 通过多巴胺促进目标导向行为,例如意图和进食,可能通过刺激 P2Y(1)受体。伏隔核 P2 受体介导的谷氨酸能机制似乎抵消了多巴胺对行为的影响。此外,与动机相关的行为的适应性变化,例如通过饥饿和进食的慢性交替或通过重复安非他命给药,伴随着 P2Y(1)受体表达的变化,被认为调节动物对某些刺激的反应敏感性。

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