Satoh H, Hashimoto K
Naunyn Schmiedebergs Arch Pharmacol. 1986 May;333(1):83-90. doi: 10.1007/BF00569665.
Effects of amiloride were studied on canine and rabbit sino-atrial node cells and the canine ventricular cells. In the canine sino-atrial node selectively perfused with Tyrode solution through the sinus node artery, amiloride (4.4 X 10(-4)-1.3 X 10(-2)mol/l) induced a negative chronotropic and a positive inotropic effect in a concentration-dependent manner. In canine ventricular muscle, the amplitude of the action potential and the resting membrane potential were decreased in the presence of amiloride (4.4 X 10(-6)-8.7 X 10(-4) mol/l). The maximum rate of rise was also depressed in a use-dependent manner as well as a concentration-dependent manner. Simultaneously the action potential duration was markedly prolonged. Low concentrations of amiloride decreased the contractile force, but higher concentrations (over 8.7 X 10(-5) mol/l) enhanced it. In the spontaneously beating rabbit sino-atrial node, amiloride (8.7 X 10(-5)-2.2 X 10(-3) mol/l) lengthened the action potential duration and the cycle length accompanied with the decreases in the amplitude and the maximum rate of rise of the action potential. The maximum diastolic potential was slightly depolarized. In voltage clamp experiments of the rabbit sino-atrial node, amiloride (4.4 X 10(-4)-1.3 X 10(-3) mol/l) suppressed the slow inward current (Isi) and the outward current (Ik) concentration-dependently, without altering steady-state inactivation of Isi (f infinity) and the activation of Ik (p infinity). The hyperpolarization-activated inward current (Ih) was also reduced. These results suggest that amiloride decreased Isi, Ik and Ih by a reduction in the conductance of these current systems.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了氨氯吡咪对犬和兔窦房结细胞以及犬心室细胞的作用。在通过窦房结动脉选择性地用台氏液灌注的犬窦房结中,氨氯吡咪(4.4×10⁻⁴ - 1.3×10⁻²mol/L)以浓度依赖的方式诱导负性变时作用和正性变力作用。在犬心室肌中,在存在氨氯吡咪(4.4×10⁻⁶ - 8.7×10⁻⁴mol/L)的情况下,动作电位的幅度和静息膜电位降低。最大上升速率也以使用依赖和浓度依赖的方式受到抑制。同时,动作电位持续时间明显延长。低浓度的氨氯吡咪降低收缩力,但较高浓度(超过8.7×10⁻⁵mol/L)则增强收缩力。在自发搏动的兔窦房结中,氨氯吡咪(8.7×10⁻⁵ - 2.2×10⁻³mol/L)延长动作电位持续时间和周期长度,同时伴有动作电位幅度和最大上升速率的降低。最大舒张电位略有去极化。在兔窦房结的电压钳实验中,氨氯吡咪(4.4×10⁻⁴ - 1.3×10⁻³mol/L)浓度依赖性地抑制慢内向电流(Isi)和外向电流(Ik),而不改变Isi的稳态失活(f∞)和Ik的激活(p∞)。超极化激活的内向电流(Ih)也降低。这些结果表明,氨氯吡咪通过降低这些电流系统的电导来降低Isi、Ik和Ih。(摘要截断于250字)