Paton D M
J Auton Pharmacol. 1980 Nov;1(1):67-71. doi: 10.1111/j.1474-8673.1980.tb00443.x.
1 In the rabbit portal veins, cocaine potentiated responses to (-)-noradrenaline, and prolonged relaxation following transmural stimulation. Neither process was altered by hydrocortisone and U-0521, oxytetracycline or 4-aminopyridine alone or in combination with cocaine. These findings indicated that neuronal uptake was principally responsible for the inactivation of noradrenaline in this tissue. 2 In the rabbit pulmonary artery, the rate of relaxation following transmural stimulation was prolonged by cocaine and by hydrocortisone and U-0521, and further prolonged by the combination of all three drugs. These findings suggest that both neuronal and extra-neuronal uptake are responsible for the inactivation of noradrenaline in this tissue. 3 4-Aminopyridine potentiated responses to (-)-noradrenaline and prolonged relaxation after transmural stimulation in pulmonary artery possibly as a consequence of a postjunctional action in this tissue. 4 The rabbit portal vein was less sensitive to (-)-noradrenaline and relaxed more after transmural stimulation than the pulmonary artery. It is suggested that this reflects the denser noradrenergic innervation and smaller neuromuscular distance present in the portal vein.
在兔门静脉中,可卡因增强了对(-)-去甲肾上腺素的反应,并延长了跨壁刺激后的舒张时间。单独使用氢化可的松、U-0521、土霉素或4-氨基吡啶,或与可卡因联合使用,均未改变这两个过程。这些发现表明,神经元摄取是该组织中去甲肾上腺素失活的主要原因。
在兔肺动脉中,跨壁刺激后的舒张速率因可卡因、氢化可的松和U-0521而延长,三种药物联合使用时延长更明显。这些发现表明,神经元摄取和非神经元摄取均参与该组织中去甲肾上腺素的失活。
4-氨基吡啶增强了对(-)-去甲肾上腺素的反应,并延长了肺动脉跨壁刺激后的舒张时间,这可能是由于该组织中的节后作用。
兔门静脉对(-)-去甲肾上腺素的敏感性低于肺动脉,且跨壁刺激后的舒张程度更大。这表明这反映了门静脉中去甲肾上腺素能神经支配更密集且神经肌肉距离更小。