Hetey L, Drescher K
Neuropharmacology. 1986 Oct;25(10):1103-9. doi: 10.1016/0028-3908(86)90157-7.
The release of preloaded [3H]dopamine (DA) from superfused synaptosomes stimulated by 30 mM K+ was investigated in the nucleus accumbens of rats. Under conditions preventing the uptake of DA (presence of 40 microM cocaine) release of [3H]DA was inhibited by DA and apomorphine in a concentration-dependent manner (IC50s 0.65 and 0.3 microM, respectively). The maximal inhibitory effects of DA, as well as of apomorphine, were about 50% of the controls. The DA-induced inhibition was antagonized by antipsychotics completely; the rank order of antagonistic potencies was haloperidol greater than clozapine greater than sulpiride; methiothepine was ineffective. Furthermore, the K+-stimulated release of [3H]DA was inhibited by serotonin in a concentration-dependent manner (IC50 = 0.9 microM). This inhibitory effect was antagonized by methiothepine with a high efficiency, by clozapine and methysergide with moderate efficiencies; haloperidol and sulpiride were ineffective. The experimental system demonstrated appears to be suitable for characterizing the DA- and serotonin-antagonistic potencies of antipsychotics and other drugs on presynaptic autoreceptors as well as receptors modulating release of DA in the nucleus accumbens.
研究了在大鼠伏隔核中,30 mM K⁺刺激下预加载的[³H]多巴胺(DA)从超融合突触体中的释放情况。在阻止DA摄取的条件下(存在40 μM可卡因),[³H]DA的释放受到DA和阿扑吗啡的浓度依赖性抑制(IC50分别为0.65和0.3 μM)。DA以及阿扑吗啡的最大抑制作用约为对照的50%。DA诱导的抑制作用被抗精神病药物完全拮抗;拮抗效力的顺序为氟哌啶醇大于氯氮平大于舒必利;甲硫哒嗪无效。此外,[³H]DA的K⁺刺激释放受到5-羟色胺的浓度依赖性抑制(IC50 = 0.9 μM)。这种抑制作用被甲硫哒嗪高效拮抗,被氯氮平和甲基麦角新碱中度拮抗;氟哌啶醇和舒必利无效。所展示的实验系统似乎适用于表征抗精神病药物和其他药物对突触前自身受体以及调节伏隔核中DA释放的受体的DA和5-羟色胺拮抗效力。