Refsum H, Landmark K
Acta Pharmacol Toxicol (Copenh). 1977 Feb;40(2):259-66. doi: 10.1111/j.1600-0773.1977.tb02076.x.
The effects of ouabain 5 x 10-5 M, noradrenaline 10-7 M and nifedipine 100 mug/1 on the contractile force of the isolated rat left atrium were tested and compared at varying concentrations of calcium in the Ringer solution. The effect of ouabain was small, developed slowly and almost independently of the calcium concentration. Noradrenaline, which increases Ca++ influx during excitation, caused an increase in the contractile force which was complete within 2 min. The percentage as well as the absolute increase in contractile force was pronounced at lower, but small at higher calcium concentrations. Nifedipine, which reduces Ca++ influx during excitation, caused a decrease in contractile force which was complete within 2-4 min. The nifedipine-induced depression in contractile force decreased with a rise in the calcium concentration. It is assumed that the ouabain-induced increase in contractile force in the rat, is not mediated by an increase in the magnitude of the inward calcium current, and other modes of action for the inotropic effect of glycosides are discussed.
在林格溶液中钙浓度不同的情况下,测试并比较了5×10⁻⁵M哇巴因、10⁻⁷M去甲肾上腺素和100μg/1硝苯地平对离体大鼠左心房收缩力的影响。哇巴因的作用较小,起效缓慢,且几乎与钙浓度无关。去甲肾上腺素在兴奋时增加Ca²⁺内流,导致收缩力在2分钟内完全增加。收缩力的百分比增加以及绝对增加在较低钙浓度时明显,但在较高钙浓度时较小。硝苯地平在兴奋时减少Ca²⁺内流,导致收缩力在2 - 4分钟内完全下降。硝苯地平引起的收缩力降低随着钙浓度的升高而减小。据推测,哇巴因引起的大鼠收缩力增加不是由内向钙电流幅度增加介导的,并讨论了糖苷类正性肌力作用的其他作用方式。