Lokhandwala M F, Coats J T, Buckley J P
Eur J Pharmacol. 1977 Apr 7;42(3):257-65. doi: 10.1016/0014-2999(77)90292-8.
Effects of several alpha-adrenoceptor agonists on presynaptic alpha-adrenoceptors were evaluated by studying chronotropic responses to cardioaccelerator nerve stimulation in anesthetized dogs. I.v. infusions of norepinephrine (NE), methylnorepinephrine (MNE), epinephrine (E) or phenylephrine (PHE) in desipramine-treated dogs caused significant attenuation of nerve stimulation responses. The inhibitory influence of all these agents could be prevented by prior treatment with phentolamine, but not with haloperidol. Comparisons of relative pressor and presynaptic inhibitory actions of these compounds revealed that in equipressor doses, MNE caused a significantly greater attenuation of nerve stimmulation responses than NE, while PHE had similar pressor and presynaptic inhibitory activity to that of NE. The inhibition of chronotropic responses to nerve stimulation observed following E was significantly greater compared to its relative pressor effect. These results demonstrate the existence of a presynaptic alpha-adrenoceptor mechanism modulating cardiac rate in intact dogs and indicate that the false transmitter MNE may be more potent than NE in imparing neuronal transmission by an action on presynaptic alpha-adrenoceptors.
通过研究麻醉犬对心脏加速神经刺激的变时反应,评估了几种α-肾上腺素能受体激动剂对突触前α-肾上腺素能受体的作用。在接受地昔帕明治疗的犬中静脉输注去甲肾上腺素(NE)、甲基去甲肾上腺素(MNE)、肾上腺素(E)或去氧肾上腺素(PHE),可导致神经刺激反应显著减弱。酚妥拉明预先处理可防止所有这些药物的抑制作用,但氟哌啶醇则不能。比较这些化合物的相对升压和突触前抑制作用发现,在等升压剂量下,MNE引起的神经刺激反应减弱程度明显大于NE,而PHE的升压和突触前抑制活性与NE相似。与E的相对升压作用相比,观察到E后对神经刺激的变时反应抑制作用明显更大。这些结果证明了完整犬中存在调节心率的突触前α-肾上腺素能受体机制,并表明假递质MNE可能比NE更有效地通过作用于突触前α-肾上腺素能受体来损害神经元传递。