Post J M, Smith J M, Jones A W
Department of Physiology, University of Missouri School of Medicine, Columbia.
J Pharmacol Exp Ther. 1989 Aug;250(2):591-7.
BRL 34915 (Cromakalim) is a novel benzopyran that has anti-hypertensive actions. Contractile and 42K efflux responses to BRL 34915 were measured in blood vessels from the rabbit to determine whether Ca-dependent K-channels [K(Ca)] were involved. BRL 34915 increased 42K efflux from all blood vessels tested with an EC50 of 0.2 to 0.7 microM in the superior mesenteric artery (SMA). BRL 34915 also inhibited norepinephrine (NE)-stimulated 42K efflux (96%) and contraction (50%) in SMA with IC50 values (0.2-0.3 microM) which were similar to the EC50. Comparison of two vascular sites showed that the portal mesenteric vein required 10-fold higher BRL 34915 to achieve a 42K response equivalent to the maximal effect on SMA, yet the maximum response to NE was 4-fold greater in portal vein than SMA. The 42K efflux stimulated by BRL 34915 exhibited a significant decrement with time. Ca-removal increased the magnitude and stability of the BRL 34915 response in SMA and femoral arteries, whereas reapplication of Ca in the presence of BRL 34915 caused the 42K efflux to decrease rapidly. These effects of Ca were not altered by nisoldipine (NIS). The 42K efflux stimulated by BRL 34915 and by K-depolarization was additive when applied in combination in SMA. BRL 34915 had no effect on the NIS-inhibited 42K efflux (a Ca-dependent component) during K-depolarization. It is concluded that BRL 34915 acts on K-channels which differ significantly from the known properties of K(Ca)-channels and that BRL 34915 indirectly inhibits NE stimulation of contraction and K(Ca)-channels by hyperpolarizing the smooth muscle membrane.
BRL 34915(克罗卡林)是一种具有抗高血压作用的新型苯并吡喃。在兔血管中测量对BRL 34915的收缩反应和42K外流反应,以确定是否涉及钙依赖性钾通道[K(Ca)]。BRL 34915使所有受试血管的42K外流增加,在肠系膜上动脉(SMA)中其半数有效浓度(EC50)为0.2至0.7微摩尔。BRL 34915还抑制SMA中去甲肾上腺素(NE)刺激的42K外流(96%)和收缩(50%),其半数抑制浓度(IC50)值(0.2 - 0.3微摩尔)与EC50相似。对两个血管部位的比较表明,门静脉肠系膜静脉需要比BRL 34915高10倍的浓度才能产生与对SMA的最大效应相当的42K反应,然而门静脉对NE的最大反应比对SMA大4倍。BRL 34915刺激的42K外流随时间显著减少。去除钙增加了SMA和股动脉中BRL 34915反应的幅度和稳定性,而在存在BRL 34915的情况下重新加入钙会使42K外流迅速减少。钙的这些作用不受尼索地平(NIS)的影响。当在SMA中联合应用时,BRL 34915刺激的42K外流和钾去极化刺激的42K外流具有相加性。在钾去极化期间,BRL 34915对尼索地平抑制的42K外流(一种钙依赖性成分)没有影响。得出的结论是,BRL 34915作用于与已知K(Ca)通道特性有显著差异的钾通道,并且BRL 34915通过使平滑肌膜超极化间接抑制NE对收缩和K(Ca)通道的刺激。