Albus U, Linz W, Wiemer G, Knolle J, Breipohl G, Schölkens B A
Hoechst Aktiengesellschaft, Frankfurt/Main, Fed. Rep. of Germany.
Arzneimittelforschung. 1989 Sep;39(9):1096-9.
Amiloride has previously been shown to facilitate receptor binding of atrial natriuretic factor (ANF) to membranes of adrenal cortex and to enhance ANF induced inhibition of steroid secretion in vitro. This interaction of amiloride and ANF also holds true for the cardiovascular system. In precontracted rabbit aortic strips the relaxing effect induced by the combination of ANF (10(-10) mol/l) and amiloride (10(-5) mol/l) was overadditional. The production of cyclic guanosine monophosphate (cGMP), which parallels ANF induced relaxations of vascular strips, was not affected by amiloride alone up to 10(-3) mol/l, but was concentration-dependently increased in the presence of ANF (10(-8) mol/l). In spontaneously hypertensive rats ANF-induced decreases in blood pressure were potentiated by amiloride. Post ischemia reperfusion arrhythmias in isolated rat hearts were reduced by ANF. Amiloride increased this effect. The binding experiments revealed an interaction of amiloride and ANF on the receptor level. Binding of labeled ANF to aortic tissue was concentration-dependently increased by amiloride. Addition of ATP had the opposite effect. Therefore it can be suggested that amiloride and ATP interfere with a mechanism regulating the sensitivity of the vascular ANF-receptor for its ligand regarding binding and signal transforming presumably by a kinase mediated phosphorylation/dephosphorylation process.
氨氯地平此前已被证明可促进心房利钠因子(ANF)与肾上腺皮质膜的受体结合,并增强ANF在体外诱导的类固醇分泌抑制作用。氨氯地平和ANF的这种相互作用在心血管系统中也成立。在预先收缩的兔主动脉条中,ANF(10^-10摩尔/升)和氨氯地平(10^-5摩尔/升)联合诱导的舒张作用是额外的。与ANF诱导的血管条舒张平行的环磷酸鸟苷(cGMP)生成,在高达10^-3摩尔/升的氨氯地平单独存在时不受影响,但在ANF(10^-8摩尔/升)存在下呈浓度依赖性增加。在自发性高血压大鼠中,氨氯地平增强了ANF诱导的血压降低。ANF可减少离体大鼠心脏缺血再灌注后的心律失常。氨氯地平增强了这种作用。结合实验揭示了氨氯地平和ANF在受体水平上的相互作用。氨氯地平使标记的ANF与主动脉组织的结合呈浓度依赖性增加。添加ATP则有相反的效果。因此,可以推测氨氯地平和ATP可能通过激酶介导的磷酸化/去磷酸化过程,干扰了一种调节血管ANF受体对其配体结合和信号转换敏感性的机制。