Bao R D, Li C Z, Liu Y M, Xu Y Q
Shanghai Second Medical University.
Sheng Li Xue Bao. 1994 Apr;46(2):181-6.
By using acetyl strophanthidin (AS) 0.2 mumol/L, the delayed after-depolarization (DAD) was induced in sheep cardiac Purkinje fibers and recorded with intra-cellular microelectrode. When beta-adrenoceptor was blocked by propranolol 1.0 mumol/L, phenylephrine 1.0 mumol/L increased the amplitude of DAD from 8.1 +/- 2.2 mV to 9.5 +/- 2.8 mV, prolonged the duration of DAD from 240 +/- 47 ms to 273 +/- 47 ms (n = 13, P < 0.01) and increased the up rising velocity of DAD from 0.039 +/- 0.023 V/s to 0.051 +/- 0.026 V/s (n = 13, P < 0.05). The DAD occurred earlier for 30 +/- 47 ms to preceding action potential (n = 13, P < 0.05). When triggered action potentials were induced by norepinephrine 1.0 mumol/L on the basis of DAD, propranolol 1.0 mumol/L could suppress the triggered beats while phentolamine 1.8 mumol/L showed little effect. The above results indicate that excitation of alpha-receptor had only slight augmentation effect on DAD. However, for the triggered activity induced by DAD, the inhibitory effect of beta-blockers are stronger than that of alpha-blockers.
应用0.2μmol/L的乙酰毒毛花苷(AS)诱发绵羊心脏浦肯野纤维延迟后除极(DAD),并用细胞内微电极记录。当用1.0μmol/L普萘洛尔阻断β肾上腺素能受体后,1.0μmol/L去氧肾上腺素使DAD的幅度从8.1±2.2mV增加到9.5±2.8mV,DAD的时程从240±47ms延长到273±47ms(n = 13,P < 0.01),DAD的上升速度从0.039±0.023V/s增加到0.051±0.026V/s(n = 13,P < 0.05)。DAD较前一个动作电位提前30±47ms出现(n = 13,P < 0.05)。当在DAD基础上用1.0μmol/L去甲肾上腺素诱发触发动作电位时,1.0μmol/L普萘洛尔可抑制触发搏动,而1.8μmol/L酚妥拉明作用不明显。上述结果表明,α受体兴奋对DAD仅有轻微增强作用。然而,对于由DAD诱发的触发活动,β受体阻滞剂的抑制作用强于α受体阻滞剂。