Andén N E, Leander S
J Neural Transm. 1979;44(1-2):1-12. doi: 10.1007/BF01252697.
The effects of 4-aminopyridine (4-AP) on the turnovers of 5-hydroxytryptamine, dopamine and noradrenaline in the central nervous system of rats were studied by means of amine disappearance following inhibition of tryptophan or tyrosin hydroxylase. 4-AP (3 mg/kg i.p.) did not change the utilizations of 5-hydroxytryptamine or dopamine but it markedly accelerated that of noradrenaline in the brain and in the spinal cord. This stimulatory effect of 4-AP was completely dependent on nerve impulses since no effect was observed following an acute section of the noradrenaline nerves to the spinal cord. The effect of 4-AP was blocked by the alpha-adrenoreceptor stimulating agent clonidine. Pentylenetetrazole, at a dose producing similar behavioural changes as 4-AP, caused only a slight stimulation of the noradrenaline turnover. 4-AP might enhance the flux of calcium ions into nerve terminals during depolarization, and thus increase the release of noradrenaline, whereas this process might be of less importance in the dopamine and the 5-hydroxytryptamine nerves.
通过抑制色氨酸或酪氨酸羟化酶后胺类物质的消失,研究了4-氨基吡啶(4-AP)对大鼠中枢神经系统中5-羟色胺、多巴胺和去甲肾上腺素周转的影响。腹腔注射4-AP(3毫克/千克)不会改变5-羟色胺或多巴胺的利用情况,但会显著加速大脑和脊髓中去甲肾上腺素的利用。4-AP的这种刺激作用完全依赖于神经冲动,因为在对脊髓的去甲肾上腺素神经进行急性切断后未观察到任何作用。4-AP的作用被α-肾上腺素能受体激动剂可乐定阻断。戊四氮在产生与4-AP相似行为变化的剂量下,仅对去甲肾上腺素周转有轻微刺激作用。4-AP可能在去极化过程中增强钙离子流入神经末梢,从而增加去甲肾上腺素的释放,而这一过程在多巴胺和5-羟色胺神经中可能不太重要。