Bell C, Gillespie J S, Macrae I M
Br J Pharmacol. 1984 Mar;81(3):563-9. doi: 10.1111/j.1476-5381.1984.tb10110.x.
Spontaneous and nerve stimulated release of noradrenaline and dopamine from rat and guinea-pig vas deferens have been measured electrochemically after separation by high performance liquid chromatography (h.p.l.c.). In the absence of nerve stimulation both noradrenaline (NA) and dopamine were released into the bathing fluid in the rat but in the guinea-pig only noradrenaline could be detected. Drugs which block neuronal and extraneuronal uptake of catecholamines had little effect on spontaneous overflow but both tetraethylammonium and phenoxybenzamine increased overflow. Transmural nerve stimulation (5-10 Hz) increased catecholamine overflow in both species and dopamine release was now measurable from the guinea-pig vas. In the rat, the proportion of dopamine to NA was unchanged from that released spontaneously. The release of both amines was little affected by drugs that block neuronal and extraneuronal uptake and a monoamine oxidase inhibitor, but was inhibited by tetrodotoxin 0.2 microgram ml-1. In the guinea-pig tetraethylammonium 10 mM doubled overflow and phenoxybenzamine 10(-5)M increased it by five times but the dopamine percentage remained constant and equal to the control. Following nerve stimulation the amount of dopamine released expressed as a percentage of total catecholamine release was 6% for the rat and 1.3% for the guinea-pig. These values were considerably higher than the comparable figures for dopamine: NA content of the two tissues (2% and 0.5% respectively). Repeated periods of stimulation depleted these tissue stores and the depletion of dopamine was significantly greater than that of NA. 6 Our interpretation of these results is that both dopamine and NA are released from a common store during normal noradrenergic transmission. While all or most of the axonal dopamine is contained in this releasable pool, most of the axonal NA lies in a second, less readily released pool.
通过高效液相色谱(h.p.l.c.)分离后,用电化学方法测定了大鼠和豚鼠输精管中去甲肾上腺素和多巴胺的自发释放及神经刺激释放。在无神经刺激的情况下,大鼠输精管中的去甲肾上腺素(NA)和多巴胺均释放到浴液中,但豚鼠输精管中仅能检测到去甲肾上腺素。阻断儿茶酚胺神经元和非神经元摄取的药物对自发溢出影响不大,但四乙铵和酚苄明均可增加溢出量。跨膜神经刺激(5 - 10 Hz)可增加两种动物的儿茶酚胺溢出量,此时豚鼠输精管中可检测到多巴胺释放。在大鼠中,多巴胺与NA的释放比例与自发释放时相同。两种胺类的释放受阻断神经元和非神经元摄取的药物及单胺氧化酶抑制剂影响较小,但受0.2微克/毫升河豚毒素抑制。在豚鼠中,10 mM四乙铵使溢出量加倍,10⁻⁵ M酚苄明使其增加5倍,但多巴胺百分比保持恒定且与对照组相同。神经刺激后,大鼠多巴胺释放量占总儿茶酚胺释放量的百分比为6%,豚鼠为1.3%。这些值显著高于两种组织中多巴胺与NA的含量比例(分别为2%和0.5%)。重复刺激会耗尽这些组织中的储存物,多巴胺的耗竭明显大于NA。我们对这些结果的解释是,在正常的去甲肾上腺素能传递过程中,多巴胺和NA均从共同储存池中释放。虽然所有或大部分轴突多巴胺都包含在这个可释放池中,但大部分轴突NA位于第二个较难释放的池中。