Stoof J C, De Boer T, Sminia P, Mulder A H
Eur J Pharmacol. 1982 Oct 22;84(3-4):211-4. doi: 10.1016/0014-2999(82)90204-7.
D1-dopamine receptor stimulation did not affect the K+-induced release of [3H]GABA, [3H]glutamate, [3H]serotonin, [3H]dopamine and [14C]acetylcholine from slices of rat neostriatum. D2-dopamine receptor stimulation did not change the release of [3H]GABA, [3H]glutamate and [3H]serotonin, but inhibited the release of both [3H]dopamine and [14C]acetylcholine; this inhibition was antagonized by (-)-sulpiride. The release-inhibiting dopamine autoreceptors and the post synaptic dopamine receptors mediating the inhibition of acetylcholine release appear to be pharmacologically similar and can be classified as D2-receptors.
D1-多巴胺受体刺激不影响钾离子诱导的大鼠新纹状体切片中[3H]GABA、[3H]谷氨酸、[3H]5-羟色胺、[3H]多巴胺和[14C]乙酰胆碱的释放。D2-多巴胺受体刺激不改变[3H]GABA、[3H]谷氨酸和[3H]5-羟色胺的释放,但抑制[3H]多巴胺和[14C]乙酰胆碱的释放;这种抑制作用被(-)-舒必利拮抗。释放抑制性多巴胺自身受体和介导乙酰胆碱释放抑制的突触后多巴胺受体在药理学上似乎相似,可归类为D2-受体。