Morad M, Weiss J, Cleemann L
Eur J Cardiol. 1978 Jun;7 Suppl:53-62.
Adrenaline has been shown to increase twitch tension and enhance relaxation in cardiac muscle. In mammalian myocardium, a unitary mechanism, namely facilitated uptake of calcium by the sarcoplasmic reticulum, is proposed to increase the internal recirculating store of calcium (thereby potentiating twitch tension) and simultaneously enhance relaxation. In frog ventricular myocardium, where tension is directly controlled by membrane potential, adrenaline seems to produce its positive inotropic effect by increasing the duration and amplitude of cardiac action potential plateau. If adrenaline is prevented from changing the action potential, either by electrical or pharmacologic means, the relaxant effect of the drug is unmasked. The results suggest that in frog ventricle, unlike mammalian myocardium, adrenaline may not have a 'true' positive inotropic effect independent of membrane potential. The findings in frog ventricle, where there is little or no internal recirculation of calcium, are consistent with the model proposed for the mammalian myocardium.
肾上腺素已被证明可增加心肌的抽搐张力并增强舒张功能。在哺乳动物心肌中,提出了一种单一机制,即肌浆网对钙的易化摄取,以增加钙的内部再循环储备(从而增强抽搐张力)并同时增强舒张功能。在青蛙心室肌中,张力直接受膜电位控制,肾上腺素似乎通过增加心脏动作电位平台期的持续时间和幅度来产生其正性肌力作用。如果通过电或药理学方法阻止肾上腺素改变动作电位,该药物的舒张作用就会显现出来。结果表明,在青蛙心室中,与哺乳动物心肌不同,肾上腺素可能没有独立于膜电位的“真正”正性肌力作用。在青蛙心室中,钙的内部再循环很少或没有,这一发现与为哺乳动物心肌提出的模型一致。