Márquez M T, De Mikulic L E, Aramendía P
Acta Physiol Lat Am. 1977;27(2):59-64.
Ethylephrine, assayed in isolated rat atria, as a dose-chronotropic response curve showed a typical bell-dome shape of the sympathomimetic amines. Yet, on the same basis, it was less powerful than epinephrine, norepinephrine or isoproterenol. Pretreatment with reserpine provoked supersensitivity and increase in the maximum. As well, previous administration of pargyline to the animals resulted in augmented accelerating effects, either in normal or reserpinized preparations. Cocaine or phentolamine shifted the dose-response curve to the left. On the contrary, propranolol, produced a marked action, decelerating the effects of ethylephrine and also decreased the maxima with higher doses. It is concluded that ethylephrine: a) is a direct-acting sympathomimetic amine; b) it brings beta-receptor stimulation; c) a certain degree of alpha-receptor decelerating effect is also involved; d) it is a good substrate of monoaminoxidase.
在离体大鼠心房中测定的乙基肾上腺素,其剂量-变时反应曲线呈现出拟交感神经胺典型的钟形。然而,基于同样的标准,它的效力比肾上腺素、去甲肾上腺素或异丙肾上腺素弱。用利血平预处理会引发超敏反应并使最大值增加。同样,预先给动物施用帕吉林会增强加速作用,无论是在正常制剂还是利血平化制剂中。可卡因或酚妥拉明使剂量-反应曲线左移。相反,普萘洛尔产生显著作用,减慢乙基肾上腺素的作用,并且在高剂量时也降低最大值。结论是乙基肾上腺素:a)是一种直接作用的拟交感神经胺;b)它能刺激β受体;c)也涉及一定程度的α受体减慢效应;d)它是单胺氧化酶的良好底物。