Hsu K S, Huang C C, Yang C H, Gean P W
Department of Pharmacology, College of Medicine, National Cheng-Kung University, Tainan, Taiwan.
Brain Res. 1995 Sep 4;690(2):264-8. doi: 10.1016/0006-8993(95)00734-8.
The effect of dopamine (DA) on excitatory synaptic transmission was studied in rat neostriatal neurons using intracellular- and whole-cell voltage clamp-recording methods. Depolarizing excitatory postsynaptic potentials (EPSPs) were evoked by cortical stimulation. Superfusion of DA (0.01-10 microM) reversibly decreases EPSP in a concentration-dependent manner and with a estimated IC50 of 0.3 microM. In addition, the inhibitory effect induced by DA at a low concentration (0.1 microM) was antagonized by sulpiride (1-10 nM), a selective D2 dopaminergic receptor antagonist. However, D1 dopaminergic receptor antagonist SKF-83566 (1-5 microM) did not affect the blocking effect by DA 0.1 microM. Based on these findings, we conclude that DA at a low concentration (< or = 0.1 microM) reduced the excitatory response of neostriatal neurons following cortical stimulation via the activation of D2, but not D1 dopaminergic receptors, located on the terminals of corticostriatal neurons.
利用细胞内和全细胞电压钳记录方法,在大鼠新纹状体神经元中研究了多巴胺(DA)对兴奋性突触传递的影响。通过皮层刺激诱发去极化兴奋性突触后电位(EPSP)。DA(0.01 - 10微摩尔)的灌流以浓度依赖的方式可逆地降低EPSP,估计IC50为0.3微摩尔。此外,低浓度(0.1微摩尔)的DA所诱导的抑制作用被选择性D2多巴胺能受体拮抗剂舒必利(1 - 10纳摩尔)拮抗。然而,D1多巴胺能受体拮抗剂SKF - 83566(1 - 5微摩尔)并不影响0.1微摩尔DA的阻断作用。基于这些发现,我们得出结论:低浓度(≤0.1微摩尔)的DA通过激活位于皮质纹状体神经元终末的D2而非D1多巴胺能受体,降低了皮层刺激后新纹状体神经元的兴奋性反应。