Cukierman S
Braz J Med Biol Res. 1986;19(1):119-22.
Slow responses were induced in isolated rabbit left atrial trabeculae in a medium containing 20 mM K+ and 1.8 microM epinephrine. Under these conditions, the Na+-dependent upstroke of the cardiac action potential is absent but it is possible to obtain tetrodotoxin-resistant Ca2+-action potentials (slow responses). Conventional electrophysiological techniques were employed for stimulating the preparation and measuring transmembrane potentials. Under these experimental conditions, slow responses exhibit frequency-dependent excitability changes. The excitability of epinephrine-induced slow responses increases with increasing stimulation frequency. This increase is manifested by a decrease in the latency of the slow response and also by a decrease in the stimuli requirements. In this respect, slow responses induced by epinephrine are similar to barium-induced slow responses. These observations provide further support for the hypothesis that the Ca2+-inflow during slow response electrogenesis promotes an increase in slow response excitability. These results are discussed in relation to the propagation of the slow response through the atrioventricular node under physiological conditions.
在含有20 mM钾离子和1.8 microM肾上腺素的培养基中,分离的兔左心房小梁诱导出缓慢反应。在这些条件下,心脏动作电位依赖钠离子的上升支不存在,但有可能获得对河豚毒素耐药的钙离子动作电位(缓慢反应)。采用传统的电生理技术刺激标本并测量跨膜电位。在这些实验条件下,缓慢反应表现出频率依赖性的兴奋性变化。肾上腺素诱导的缓慢反应的兴奋性随着刺激频率的增加而增加。这种增加表现为缓慢反应潜伏期的缩短以及刺激阈值的降低。在这方面,肾上腺素诱导的缓慢反应与钡诱导的缓慢反应相似。这些观察结果进一步支持了这样的假设,即在缓慢反应电活动期间钙离子内流促进了缓慢反应兴奋性的增加。结合生理条件下缓慢反应通过房室结的传播对这些结果进行了讨论。