Rodrigues-Pereira E
Arch Int Pharmacodyn Ther. 1977 Sep;229(1):105-15.
The aim of these study was to investigate peripheral vascular actions of alpha-methyldopa. The following experimental procedures were used: hind-limb of the dog perfused with the animals own blood or with Krebs solution; nictitating membrane of the dog; isolated and perfused segments of the saphenous vein of the dog; superfused strips of the saphenous vein of the dog. In these preparations, effects of alpha-methyldopa on responses elicited by electrical stimulation and on release of 3H-noradrenaline were studied. In dogs pretreated with alpha-methyldopa (200 mg/kg, i.v., 36, 24 and 4 hr before the experiment) contractions of the nictitating membrane caused by cervical sympathetic electrical stimulation were markedly reduced: however, the frequency--response curve to stimulation in the hind-limb and responsiveness to noradrenaline were not significantly different of controls. Perfusion of the hind-limb with Krebs containing alpha-methyldopa (2.2 mM) resulted in a significant reduction of perfusion pressure responses to lumbar sympathetic electrical stimulation with augmented responsiveness to exogenous noradrenaline. Similar results were obtained in in vitro experiments. Effects of alpha-methyldopa were not prevented by cocaine nor by inhibition of decarboxylase by Ro 4-4602 (D,L-serine,2-(2,3,4-,trihydroxybenzyl) hydrazine hydrochloride). Alpha-methyldopa depresses the release of tritiated compounds evoked by electrical stimulation, in saphenous vein strips. This suggests that inhibition of transmitter release could be an important factor to understand peripheral actions of alpha-methyldopa.
这些研究的目的是探究α-甲基多巴的外周血管作用。采用了以下实验程序:用动物自身血液或 Krebs 溶液灌注狗的后肢;狗的瞬膜;狗的隐静脉分离并灌注段;狗的隐静脉超融合条。在这些制备物中,研究了α-甲基多巴对电刺激引发的反应以及对 3H-去甲肾上腺素释放的影响。在用α-甲基多巴预处理的狗(实验前 36、24 和 4 小时静脉注射 200mg/kg)中,颈交感神经电刺激引起的瞬膜收缩明显减少:然而,后肢对刺激的频率-反应曲线以及对去甲肾上腺素的反应性与对照组无显著差异。用含α-甲基多巴(2.2mM)的 Krebs 溶液灌注后肢,导致对腰交感神经电刺激的灌注压力反应显著降低,对外源性去甲肾上腺素的反应性增强。在体外实验中也获得了类似结果。可卡因或 Ro 4-4602(D,L-丝氨酸,2-(2,3,4-三羟基苄基)盐酸肼)抑制脱羧酶均不能阻止α-甲基多巴的作用。α-甲基多巴抑制隐静脉条中电刺激诱发的氚标记化合物的释放。这表明抑制递质释放可能是理解α-甲基多巴外周作用的一个重要因素。