Oz M, Frank G B
Can J Physiol Pharmacol. 1994 Oct;72(10):1220-5. doi: 10.1139/y94-173.
The effects of Bay K8644, a Ca2+ channel agonist, on the mechanical and electrical properties of frog skeletal muscle fibers were investigated. At relatively low concentrations, such as 10(-6) and 10(-5) M, Bay K8644 significantly potentiated the maximum amplitudes of twitch responses, and this effect was not reversed in the presence of the calcium channel antagonist nitrendipine. At higher concentrations, such as 10(-4) M, Bay K8644 depressed the amplitudes of twitch responses, and nitrendipine did not change this effect. At all concentrations, Bay K8644 greatly reduced the area under the tetanic force versus time curve, and this effect was not modified by the concomitant application of Bay K8644 and nitrendipine. Intracellular recordings revealed that the depressing effect of Bay K8644 on tetanic contractions was due to the blockade of sodium action potentials. In conclusion, the present results suggest that the modulation of twitch responses by calcium channel agonist and antagonists, at the concentration range used, is not related to the expected modulation of voltage-sensitive slow calcium channels in frog skeletal muscle fibers, and tetanic contractions are depressed by the calcium channel agonist Bay K8644 through its effect on sodium channels.
研究了钙离子通道激动剂Bay K8644对青蛙骨骼肌纤维力学和电学特性的影响。在相对较低的浓度下,如10(-6)和10(-5)M,Bay K8644显著增强了单收缩反应的最大幅度,并且在存在钙通道拮抗剂尼群地平的情况下这种效应并未逆转。在较高浓度下,如10(-4)M,Bay K8644降低了单收缩反应的幅度,而尼群地平并未改变这种效应。在所有浓度下,Bay K8644都极大地减小了强直收缩力随时间变化曲线下的面积,并且同时应用Bay K8644和尼群地平并未改变这种效应。细胞内记录显示,Bay K8644对强直收缩的抑制作用是由于钠动作电位的阻断。总之,目前的结果表明,在所使用的浓度范围内,钙通道激动剂和拮抗剂对单收缩反应的调节与青蛙骨骼肌纤维中电压敏感性慢钙通道的预期调节无关,并且钙通道激动剂Bay K8644通过其对钠通道的作用抑制强直收缩。