Edvinsson L, Hardebo J E, McCulloch J, Owman C
Acta Physiol Scand. 1978 Nov;104(3):349-59. doi: 10.1111/j.1748-1716.1978.tb06286.x.
The vasomotor response of dopamine and dopaminergic agonists was studied in vitro on middle cerebral arteries from cat and pial arteries from humans. The action of various inhibitors was tested in order to define the receptors involved. A contractile response could be obtained by epinine, apomorphine and dopamine in the mentioned order of potency. The effect was blocked by alpha-receptor as well as serotonin receptor antagonists. The mode of inhibition suggested that serotonin receptors rather than alpha-adrenoceptors mediated the dopamine-induced contraction. A dose-dependent dilatation could be evoked by the dopaminergic agonists on actively contracted pial arteries. The relative potency was epinine greater than dopamine greater than apomorphine. The order of potency for the agonists, together with blocking experiments (including a parallel shift in the log dose-response curve induced by bulbocapnine), indicated that the vasodilatation is mediated by specific dopamine receptors.
在体外研究了多巴胺和多巴胺能激动剂对猫大脑中动脉和人软脑膜动脉的血管舒缩反应。测试了各种抑制剂的作用,以确定所涉及的受体。依匹宁、阿扑吗啡和多巴胺可按上述效力顺序引起收缩反应。该效应被α受体以及5-羟色胺受体拮抗剂阻断。抑制模式表明,5-羟色胺受体而非α肾上腺素受体介导了多巴胺诱导的收缩。多巴胺能激动剂可在主动收缩的软脑膜动脉上引起剂量依赖性扩张。相对效力为依匹宁大于多巴胺大于阿扑吗啡。激动剂的效力顺序以及阻断实验(包括荷包牡丹碱诱导的对数剂量-反应曲线的平行位移)表明,血管舒张是由特定的多巴胺受体介导的。