Price C J, Pittman Q J
Neuroscience Research Group, Department of Physiology and Biophysics, University of Calgary, 3330 Hospital Dr., Calgary, Alberta T2N 4N1, Canada.
J Neurophysiol. 2001 Sep;86(3):1149-55. doi: 10.1152/jn.2001.86.3.1149.
Oxytocin and vasopressin release from magnocellular neurons of the supraoptic nucleus is under the control of glutamate-dependent excitation. The supraoptic nucleus also receives a generalized dopaminergic input from hypothalamic sources. To determine if dopamine can influence this excitatory drive onto the magnocellular neurons, we used whole-cell patch clamp to record the effect of dopamine on evoked and miniature excitatory postsynaptic currents in rat hypothalamic slices. Dopamine exposure (30 microM to 1 mM) induced a large and reversible reduction in the amplitude of evoked excitatory postsynaptic current in nearly all magnocellular cells tested. D4 receptors appeared to mediate dopamine's activity, based on inhibition of the response with 50 microM clozapine, but not by SCH 23390 or sulpiride, and mimicry of dopamine's action with the D4 specific agonist, PD 168077. Analysis of paired-pulse experiments and miniature postsynaptic currents indicated that dopamine's action involved a presynaptic mechanism, since the frequency of miniature postsynaptic currents was reduced with dopamine exposure without any change in current kinetics or amplitude, while the paired-pulse ratio increased. We therefore have demonstrated for the first time a role for dopamine D4 receptors in the supraoptic nucleus in the presynaptic inhibition of glutamatergic neurotransmission onto magnocellular neurons.
视上核大细胞神经元释放的催产素和加压素受谷氨酸依赖性兴奋的控制。视上核还接受来自下丘脑的广泛多巴胺能输入。为了确定多巴胺是否能影响对大细胞神经元的这种兴奋性驱动,我们使用全细胞膜片钳记录多巴胺对大鼠下丘脑切片中诱发的和微小兴奋性突触后电流的影响。多巴胺暴露(30微摩尔至1毫摩尔)在几乎所有测试的大细胞中诱导诱发的兴奋性突触后电流幅度出现大幅且可逆的降低。基于用50微摩尔氯氮平抑制反应,但不是用SCH 23390或舒必利,以及用D4特异性激动剂PD 168077模拟多巴胺的作用,D4受体似乎介导了多巴胺的活性。对双脉冲实验和微小突触后电流的分析表明,多巴胺的作用涉及一种突触前机制,因为多巴胺暴露时微小突触后电流的频率降低,而电流动力学或幅度没有任何变化,同时双脉冲比率增加。因此,我们首次证明了多巴胺D4受体在视上核中对大细胞神经元谷氨酸能神经传递的突触前抑制作用。