Sahlholm Kristoffer, Nilsson Johanna, Marcellino Daniel, Fuxe Kjell, Arhem Peter
Department of Neuroscience, Karolinska Institutet, SE-117 77 Stockholm, Sweden.
Synapse. 2008 Jun;62(6):476-80. doi: 10.1002/syn.20509.
The dopamine D2 receptor plays a critical role in activity-dependent synaptic plasticity in the striatum, and regulates the transitions between different states of electrical activity. The D2 receptor is the main target for antipsychotics, and its affinity towards dopamine has been shown to be increased in psychotic patients. Recently, voltage-sensitivity has been reported for the ligand binding and G protein-coupling properties of some neurotransmitter receptors, raising the question whether the D2 receptor is also regulated by voltage. Our present electrophysiology data from Xenopus oocytes indicate that the D2 receptor is indeed voltage-sensitive. Comparing concentration-response relationships for the activation of G protein-coupled inward rectifier potassium (GIRK) channels via D2 receptor stimulation by quinpirole or dopamine at -80 and at +40 mV revealed rightward shifts upon depolarisation of nearly tenfold, for both agonists. Our results are likely to bear relevance to the function of the D2 receptor in gating synaptic input and in regulating plasticity.
多巴胺D2受体在纹状体中依赖活动的突触可塑性中起关键作用,并调节不同电活动状态之间的转换。D2受体是抗精神病药物的主要靶点,并且已证明其对多巴胺的亲和力在精神病患者中会增加。最近,已报道某些神经递质受体的配体结合和G蛋白偶联特性具有电压敏感性,这就提出了D2受体是否也受电压调节的问题。我们目前来自非洲爪蟾卵母细胞的电生理学数据表明,D2受体确实具有电压敏感性。比较在-80 mV和+40 mV下通过喹吡罗或多巴胺刺激D2受体激活G蛋白偶联内向整流钾(GIRK)通道的浓度-反应关系,发现两种激动剂在去极化时浓度-反应关系均向右移动近十倍。我们的结果可能与D2受体在控制突触输入和调节可塑性方面的功能有关。