Riccioppo Neto F
Br J Pharmacol. 1983 Oct;80(2):335-41. doi: 10.1111/j.1476-5381.1983.tb10038.x.
The effects of cyproheptadine were studied on cardiac Purkinje and ventricular muscle fibres of the dog and on cells of the sinoatrial (SA) node region of rabbit hearts, by means of electrophysiological techniques. Cyproheptadine (2-8 microM) decreased, in a dose-dependent manner, the plateau amplitude and the action potential duration to 50% repolarization of Purkinje and ventricular muscle cells. Higher concentrations also depressed the action potential amplitude, the overshoot and the maximum rate of rise of the upstroke. These effects were only partially reversed on washing. A four fold increase in Ca concentration of the standard Tyrode solution antagonized the effects of cyproheptadine on the action potential characteristics. The 'slow response' obtained in K-depolarized isoprenaline-treated fibres was blocked by cyproheptadine (4 microM). Cyproheptadine (10 microM) depolarized and suppressed the automaticity of spontaneously beating Purkinje fibres. The frequency of discharge of the SA node cells was slowed or abolished by cyproheptadine (2-4 microM). Atropine (2.6 microM) did not affect the negative chronotropic effect, whereas adrenaline (5 microM) reversed it. It is suggested that cyproheptadine depresses the slow inward current in all types of myocardial fibres studied. Higher concentrations might also affect the fast inward sodium current system.
采用电生理技术,研究了赛庚啶对犬心脏浦肯野纤维和心室肌纤维以及兔心脏窦房结区细胞的作用。赛庚啶(2 - 8微摩尔)以剂量依赖的方式降低了浦肯野纤维和心室肌细胞的平台期振幅以及动作电位持续时间至复极化50%时的值。更高浓度还会抑制动作电位振幅、超射值和上升支的最大上升速率。这些作用在冲洗后仅部分逆转。标准台氏液中钙浓度增加四倍可拮抗赛庚啶对动作电位特征的影响。在钾去极化并用异丙肾上腺素处理的纤维中获得的“慢反应”被赛庚啶(4微摩尔)阻断。赛庚啶(10微摩尔)使自发搏动的浦肯野纤维去极化并抑制其自律性。赛庚啶(2 - 4微摩尔)可减慢或消除窦房结细胞的放电频率。阿托品(2.6微摩尔)不影响负性变时作用,而肾上腺素(5微摩尔)可逆转该作用。提示赛庚啶抑制了所研究的所有类型心肌纤维中的慢内向电流。更高浓度可能还会影响快内向钠电流系统。