Delbono O, Kotsias B A
Instituto de Investigaciones Médicas A. Lanari, Buenos Aires, Argentina.
J Appl Physiol (1985). 1993 Jun;74(6):2745-9. doi: 10.1152/jappl.1993.74.6.2745.
We studied the antagonism between aminophylline and two calcium channel blockers, nifedipine and verapamil, and its effect on the resting membrane potential of rat diaphragm fibers in vitro at 25 degrees C. Aminophylline hyperpolarizes the fibers in a dose-dependent manner, and the maximum effect is reached with 1 mM of the drug, approximately 9 mV compared with normal values. Both nifedipine and verapamil (1-5 microM) decreased the amount of hyperpolarization induced by aminophylline, and this is partially reversed when the xanthine concentration in the bath is increased. From the Hill equation we obtained a value of 2 for the slope, suggesting that two molecules of aminophylline bind to the receptor. Nifedipine modifies the affinity and the intrinsic activity of aminophylline, whereas verapamil reduces its intrinsic activity. The effect of nifedipine and verapamil is explained on the basis of the changed action of aminophylline on its site as a result of the interaction of the calcium channel blockers with their interdependent receptors.
我们研究了氨茶碱与两种钙通道阻滞剂硝苯地平和维拉帕米之间的拮抗作用,以及在25摄氏度下其对体外大鼠膈肌纤维静息膜电位的影响。氨茶碱以剂量依赖性方式使纤维超极化,当药物浓度达到1 mM时达到最大效应,与正常值相比约为9 mV。硝苯地平和维拉帕米(1 - 5 microM)均降低了氨茶碱诱导的超极化程度,当浴液中黄嘌呤浓度增加时,这种作用部分逆转。根据希尔方程,我们得到斜率值为2,表明有两个氨茶碱分子与受体结合。硝苯地平改变了氨茶碱的亲和力和内在活性,而维拉帕米降低了其内在活性。硝苯地平和维拉帕米的作用是基于钙通道阻滞剂与其相互依赖的受体相互作用导致氨茶碱对其作用位点的作用改变来解释的。