Dukes I D, Vaughan Williams E M
Br J Pharmacol. 1984 Oct;83(2):419-26. doi: 10.1111/j.1476-5381.1984.tb16502.x.
The effects of prazosin, labetalol, and medroxalol were studied in the rabbit sino-atrial node, Purkinje cells and papillary muscles. At concentrations producing similar bradycardia, labetalol and medroxalol reduced the maximum rate of depolarization (Vmax) and overshoot potential in the sinus node. Prazosin had no such effects. These large and highly significant reductions in Vmax and overshoot in sinus node cells were observed at concentrations of medroxalol and labetalol which had no negative inotropic effect. If depolarization in the sinus node was due to the second inward current, this would imply that such currents in the sinus node and contracting cardiac muscle are pharmacologically distinct. All three drugs prolonged action potential duration in the sinus node, Purkinje cells and papillary muscles in a dose-related manner. Recovery after 1 h in drug-free solution from the effects of medroxalol and labetalol was only partial in the sinus node, but almost complete in Purkinje cells and papillary muscle. Recovery from prazosin was complete in all tissues. All three drugs depressed Vmax in Purkinje cells and papillary muscles in a dose-related manner, and recovery was complete. It is concluded that all three drugs had class 1 and class 3 antiarrhythmic actions, which could contribute to their protective effects in ischaemia and reperfusion independently of blockade of myocardial alpha-adrenoceptors.
在兔窦房结、浦肯野细胞和乳头肌中研究了哌唑嗪、拉贝洛尔和美多心安的作用。在产生相似心动过缓的浓度下,拉贝洛尔和美多心安降低了窦房结的最大去极化速率(Vmax)和超射电位。哌唑嗪无此作用。在美多心安和拉贝洛尔浓度下观察到窦房结细胞Vmax和超射的大幅且高度显著降低,而这些浓度并无负性肌力作用。如果窦房结的去极化是由于第二内向电流,这将意味着窦房结和收缩心肌中的此类电流在药理学上是不同的。所有三种药物均以剂量相关方式延长了窦房结、浦肯野细胞和乳头肌的动作电位持续时间。在无药溶液中1小时后,美多心安和拉贝洛尔对窦房结的作用仅部分恢复,但在浦肯野细胞和乳头肌中几乎完全恢复。哌唑嗪在所有组织中的恢复均为完全恢复。所有三种药物均以剂量相关方式降低浦肯野细胞和乳头肌的Vmax,且恢复完全。结论是,所有三种药物均具有Ⅰ类和Ⅲ类抗心律失常作用,这可能独立于心肌α-肾上腺素能受体阻断作用而有助于它们在缺血和再灌注中的保护作用。