Godfraind T
J Pharmacol Exp Ther. 1983 Feb;224(2):443-50.
Experiments were performed on isolated rat aorta and superior mesenteric artery in order to study the action of nifedipine on norepinephrine and K-depolarization-evoked contractions and transmembrane calcium fluxes. Concentration-dependent contractions were obtained with norepinephrine in physiological solution and with Ca++ in K-depolarizing solution. Nifedipine caused a concentration-dependent depression of the maximum response. When aorta was depolarized by 40 mM KCI (instead of usual 100 mM KCI concentration), high concentrations of Ca++ evoked a relaxation that was also blocked by nifedipine. The action of nifedipine has been examined on Ca influx and efflux in arteries stimulated by norepinephrine and K-depolarization. Norepinephrine-evoked Ca influx, but not Ca efflux, was reduced by nifedipine. Concentration inhibitory curves for Ca influx and contraction could be superimposed. K-depolarization-dependent Ca entry and Ca efflux were blocked by nifedipine at concentrations lower than those required to antagonize norepinephrine actions. The results suggest that the action of nifedipine on artery contractility can be related to blockade of calcium entry through channels opened during depolarization or receptor-response coupling.
为了研究硝苯地平对去甲肾上腺素和钾离子去极化诱发的收缩以及跨膜钙通量的作用,在离体大鼠主动脉和肠系膜上动脉上进行了实验。在生理溶液中用去甲肾上腺素以及在钾离子去极化溶液中用钙离子可获得浓度依赖性收缩。硝苯地平引起最大反应的浓度依赖性抑制。当主动脉用40 mM氯化钾去极化(而不是通常的100 mM氯化钾浓度)时,高浓度的钙离子引起的舒张也被硝苯地平阻断。已经研究了硝苯地平对去甲肾上腺素和钾离子去极化刺激的动脉中钙内流和外流的作用。硝苯地平降低了去甲肾上腺素诱发的钙内流,但不影响钙外流。钙内流和收缩的浓度抑制曲线可以叠加。硝苯地平在低于拮抗去甲肾上腺素作用所需浓度时,可阻断钾离子去极化依赖性钙内流和钙外流。结果表明,硝苯地平对动脉收缩性的作用可能与通过去极化或受体反应偶联过程中开放的通道阻断钙内流有关。