Gintant G A, Liu D W
Masonic Medical Research Laboratory, Utica, N.Y. 13501.
Circ Res. 1992 Apr;70(4):844-50. doi: 10.1161/01.res.70.4.844.
Reports have suggested that the fast inward sodium current (INa) in cardiac tissues may be modulated by beta-adrenergic stimulation and that such modulation may affect conduction in the setting of myocardial ischemia and infarction. However, many of these studies have used dissociated myocytes or broken cell preparations, whose responses need not necessarily reflect those of syncytial preparations. To investigate further the possibility that beta-adrenergic stimulation of INa may differ in various preparations, we compared the effects of the beta-agonist isoproterenol (ISO) on syncytial canine Purkinje fibers and ventricular muscle preparations, as well as isolated ventricular myocytes. Alterations of the maximum rate of rise of the action potential upstroke (Vmax) were used as an index of changes of INa. ISO (1 microM) had no effect on Vmax of upstrokes of normally polarized (fast responses) or partially depolarized (elevated [K+]o, depressed fast responses) syncytial ventricular muscle preparations or Purkinje fibers. In contrast, lower concentrations of ISO (0.5-1.0 microM) modulated Vmax of isolated ventricular myocytes, depending on the technique used to monitor transmembrane potential. When 2.7 M KCl-filled microelectrodes were used, ISO reduced Vmax of partially depolarized myocytes without affecting Vmax of normally polarized myocytes. However, when myocytes were dialyzed using patch pipettes, ISO reduced Vmax of partially depolarized myocytes and increased Vmax of normally polarized myocytes, effecting a hyperpolarized shift of the normalized inactivation curve relating Vmax to resting membrane potential. The different beta-adrenergic responses of syncytial preparations and nondialyzed and dialyzed myocytes suggest that differences in the ionic or metabolic condition of the preparations likely alter cAMP-dependent responses and channel phosphorylation.(ABSTRACT TRUNCATED AT 250 WORDS)
有报道称,心脏组织中的快速内向钠电流(INa)可能受β-肾上腺素能刺激调节,且这种调节可能在心肌缺血和梗死情况下影响传导。然而,这些研究中有许多使用的是分离的心肌细胞或破碎的细胞制剂,其反应不一定反映合胞体制剂的反应。为了进一步研究β-肾上腺素能刺激INa在不同制剂中可能存在差异的可能性,我们比较了β-激动剂异丙肾上腺素(ISO)对犬合胞体浦肯野纤维、心室肌制剂以及分离的心室肌细胞的影响。动作电位上升的最大速率(Vmax)的变化被用作INa变化的指标。ISO(1微摩尔)对正常极化(快速反应)或部分去极化(细胞外钾离子浓度升高,快速反应受抑制)的合胞体心室肌制剂或浦肯野纤维的动作电位上升Vmax没有影响。相比之下,较低浓度的ISO(0.5 - 1.0微摩尔)可调节分离的心室肌细胞的Vmax,这取决于监测跨膜电位所使用的技术。当使用充满2.7 M氯化钾的微电极时,ISO降低了部分去极化心肌细胞的Vmax,但不影响正常极化心肌细胞的Vmax。然而,当使用膜片钳微量移液器对心肌细胞进行透析时,ISO降低了部分去极化心肌细胞的Vmax,并增加了正常极化心肌细胞的Vmax,使将Vmax与静息膜电位相关的标准化失活曲线发生超极化偏移。合胞体制剂、未透析和透析的心肌细胞对β-肾上腺素能的不同反应表明,制剂离子或代谢状况的差异可能改变环磷酸腺苷(cAMP)依赖性反应和通道磷酸化。(摘要截断于250字)