Towart R
J Cardiovasc Pharmacol. 1982 Nov-Dec;4(6):895-902.
The effects of nitrendipine, a new antihypertensive agent, have been examined using the isolated rabbit aortic strip stimulated with either noradrenaline (1.7 X 10(-8) - 1.7 X 10(-5) mol/L) or potassium (22.7-52.7 mmol/L). Nifedipine, verapamil, phentolamine, papaverine, and minoxidil were used as reference compounds. Nitrendipine and nifedipine had little effect on the contractions of the aortic strip induced by noradrenaline, but concentration-dependently inhibited contractions induced by potassium depolarisation (IC50) (3.1 X 10(-9) and 8.1 X 10(-9) mol/L, respectively). Verapamil had little effect on contractions induced by the highest concentration of noradrenaline (1.7 X 10(-5) mol/L) but inhibited contractions induced by lower concentrations of noradrenaline. Potassium-induced contractions were inhibited with an IC50 of 1.4 X 10(-7) mol/L. Phentolamine competitively inhibited noradrenaline-induced contractions, but had no effect on those induced by potassium. Papaverine inhibited both noradrenaline- and potassium-induced contractions with an IC50 of 2.5 X 10(-5) and 3 X 10(-5) mol/L, respectively. Minoxidil also inhibited both types of contractions, but only at very high concentrations (IC50 1.3 X 10(-3) and 1.8 X 10(-3) mol/L). I conclude that nitrendipine, like nifedipine, acts by inhibiting the depolarisation-induced influx of calcium ions into the vascular smooth muscle. There is no evidence for alpha-adrenoceptor-blocking activity, nor for papaverine-like vasodilator activity. Verapamil also appears to act by a calcium antagonistic action; but may, in addition, possess some alpha-adrenoceptor-blocking activity.
使用去甲肾上腺素(1.7×10⁻⁸ - 1.7×10⁻⁵mol/L)或钾(22.7 - 52.7mmol/L)刺激离体兔主动脉条,研究了新型抗高血压药物尼群地平的作用。硝苯地平、维拉帕米、酚妥拉明、罂粟碱和米诺地尔用作参考化合物。尼群地平和硝苯地平对去甲肾上腺素诱导的主动脉条收缩作用很小,但浓度依赖性地抑制钾去极化诱导的收缩(IC50)(分别为3.1×10⁻⁹和8.1×10⁻⁹mol/L)。维拉帕米对最高浓度去甲肾上腺素(1.7×10⁻⁵mol/L)诱导的收缩作用很小,但抑制较低浓度去甲肾上腺素诱导的收缩。钾诱导的收缩被抑制,IC50为1.4×10⁻⁷mol/L。酚妥拉明竞争性抑制去甲肾上腺素诱导的收缩,但对钾诱导的收缩无作用。罂粟碱抑制去甲肾上腺素和钾诱导的收缩,IC50分别为2.5×10⁻⁵和3×10⁻⁵mol/L。米诺地尔也抑制两种类型的收缩,但仅在非常高的浓度下(IC50为1.3×10⁻³和1.8×10⁻³mol/L)。我得出结论,尼群地平与硝苯地平一样,通过抑制去极化诱导的钙离子流入血管平滑肌起作用。没有证据表明其具有α-肾上腺素能受体阻断活性,也没有罂粟碱样血管舒张活性。维拉帕米似乎也通过钙拮抗作用起作用;但此外,可能还具有一些α-肾上腺素能受体阻断活性。