Karaki H, Nagase H, Ozaki H, Urakawa N, Weiss G B
Br J Pharmacol. 1986 Oct;89(2):423-9. doi: 10.1111/j.1476-5381.1986.tb10276.x.
Effects of a Ca2+ channel facilitator, CGP 28,392, on smooth muscle contractions were examined in order to delineate characteristics of Ca2+ channels in rabbit and rat aortae and guinea-pig taenia caeci. Application of increasing concentrations of KCl induced contractile responses in these smooth muscles and CGP 28,392 shifted the concentration-response curve for KCl to the left. The maximum response was also increased in rat aorta and guinea-pig taenia. CGP 28,392 also shifted the concentration-response curves for noradrenaline in rat aorta and for histamine in taenia to the left and increased the maximum response in rat aorta. However, the corresponding curve for noradrenaline in rabbit aorta was not affected by CGP 28,392. The sustained contractions induced by KCl were inhibited by cumulative application of verapamil in these smooth muscles. Pretreatment of the muscle with CGP 28,392 decreased the inhibitory effect of verapamil. The noradrenaline-induced contraction in rat aorta and the histamine-induced contraction in taenia were also inhibited by verapamil, and CGP 28,392 antagonized the effect of verapamil. The noradrenaline-induced contraction in rabbit aorta was only slightly inhibited by verapamil, and CGP 28,392 did not modify the effect of verapamil. In these smooth muscles, cumulative application of Ca2+ to the Ca2+-depleted, KCl-treated muscle induced contraction, and the concentration-response curve for Ca2+ was shifted to the left by CGP 28,392 and to the right by verapamil. The concentration-response curves for Ca2+ in Ca2+-depleted, noradrenaline-treated rabbit and rat aortae and in Ca2+-depleted, histamine-treated taenia were also shifted to the left by CGP 28,392 and to the right by verapamil. In some contractions, CGP 28,392 increased and verapamil decreased the maximum responses. CGP 28,392 antagonized the inhibitory effect of verapamil. 5 These results suggest that the Ca2 channel facilitator, CGP 28,392, has a relatively selective activating effect on voltage-dependent Ca2+ channels in rabbit aorta. However, it also activates receptor-linked Ca2+ channels in rabbit aorta when Ca2+ concentrations are low. In rat aorta and guinea-pig taenia this facilitator activates both types of Ca2+ channels.
为了阐明兔和大鼠主动脉以及豚鼠结肠带中Ca2+通道的特性,研究了Ca2+通道促进剂CGP 28392对平滑肌收缩的影响。增加氯化钾浓度可诱导这些平滑肌产生收缩反应,CGP 28392使氯化钾的浓度-反应曲线左移。在大鼠主动脉和豚鼠结肠带中,最大反应也增强。CGP 28392还使大鼠主动脉中去甲肾上腺素的浓度-反应曲线以及结肠带中组胺的浓度-反应曲线左移,并增加了大鼠主动脉中的最大反应。然而,CGP 28392对兔主动脉中去甲肾上腺素的相应曲线没有影响。在这些平滑肌中,氯化钾诱导的持续性收缩可被维拉帕米的累积应用所抑制。用CGP 28392预处理肌肉可降低维拉帕米的抑制作用。维拉帕米也可抑制大鼠主动脉中去甲肾上腺素诱导的收缩以及结肠带中组胺诱导的收缩,CGP 28392可拮抗维拉帕米的作用。维拉帕米仅轻微抑制兔主动脉中去甲肾上腺素诱导的收缩,CGP 28392不改变维拉帕米的作用。在这些平滑肌中,向用氯化钾处理过的、Ca2+耗尽的肌肉累积应用Ca2+可诱导收缩,CGP 28392使Ca2+的浓度-反应曲线左移,维拉帕米使其右移。在Ca2+耗尽的、用去甲肾上腺素处理过的兔和大鼠主动脉以及Ca2+耗尽的、用组胺处理过的结肠带中,Ca2+的浓度-反应曲线也被CGP 28392左移,被维拉帕米右移。在某些收缩中,CGP 28392增强而维拉帕米降低最大反应。CGP 28392拮抗维拉帕米的抑制作用。这些结果表明,Ca2+通道促进剂CGP 28392对兔主动脉中电压依赖性Ca2+通道具有相对选择性的激活作用。然而,当Ca2+浓度较低时,它也可激活兔主动脉中受体偶联的Ca2+通道。在大鼠主动脉和豚鼠结肠带中,这种促进剂可激活两种类型的Ca2+通道。