Wakisaka C, Kitamura N, Ohta T, Kai T, Nakazato Y, Ito S
Laboratory of Pharmacology, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Fundam Clin Pharmacol. 2000 Jul-Aug;14(4):379-85. doi: 10.1111/j.1472-8206.2000.tb00419.x.
Effects of a new cardiotonic agent, pimobendan, on contraction were investigated in single intact skeletal muscle fibres of the frog. Pimobendan increased twitch tension in a concentration-dependent manner regardless of the presence or absence of Ca2+ without any effect on tetanic tension, the resting membrane potential and the shape of the action potential. Pimobendan caused a further increase in twitch tension potentiated by caffeine (1 mM). Adenine, an inhibitor of Ca2+-induced Ca2+ release from the sarcoplasmic reticulum, inhibited twitch tension potentiated by caffeine but not by pimobendan, suggesting that twitch potentiation by pimobendan is not attributed to increases in Ca2+-induced Ca2+ release. Pimobendan failed to increase cAMP levels in the skeletal muscle, though forskolin significantly increased it without any effect on twitch tension. Contractile responses to high concentrations of caffeine and K+ were also potentiated by pimobendan. These results suggest that the potentiating effect of pimobendan on skeletal muscle contraction is mainly due to the increase in Ca2+ sensitivity to the contractile apparatus.
在青蛙的单个完整骨骼肌纤维中研究了一种新型强心剂匹莫苯丹对收缩的影响。无论有无Ca2+,匹莫苯丹均以浓度依赖性方式增加单收缩张力,而对强直张力、静息膜电位和动作电位的形状均无影响。匹莫苯丹使咖啡因(1 mM)增强的单收缩张力进一步增加。腺嘌呤是肌浆网中Ca2+诱导的Ca2+释放的抑制剂,它抑制咖啡因增强的单收缩张力,但不抑制匹莫苯丹增强的单收缩张力,这表明匹莫苯丹引起的单收缩增强并非归因于Ca2+诱导的Ca2+释放增加。尽管福斯高林能显著增加骨骼肌中的cAMP水平且对单收缩张力无影响,但匹莫苯丹未能增加骨骼肌中的cAMP水平。匹莫苯丹还增强了对高浓度咖啡因和K+的收缩反应。这些结果表明,匹莫苯丹对骨骼肌收缩的增强作用主要是由于Ca2+对收缩装置的敏感性增加。