Kaumann A J, McInerny T K, Gilmour D P, Blinks J R
Naunyn Schmiedebergs Arch Pharmacol. 1980 Apr;311(3):219-36. doi: 10.1007/BF00569402.
The pattern of antagonism between isoproterenol and various beta-adrenoceptor blocking agents was explored in spontaneously beating right atria and in driven left atrial strips from kittens and guinea pigs. The onset of beta-adrenoceptor blockade is usually very slow in such preparations; incubation periods of up to an hour may be required for equilibrium conditions. The speed of onset of the blocking action is directly related to the concentration of the antagonist, and therefore, for a given degree of blockade, inversely related to its potency. beta-Adrenoceptor blocking agents were found to interact with isoproterenol in a manner consistent with a simple competitive antagonism provided that (1) the antagonist had little intrinsic stimulant action on the preparation under study, (2) the concentrations of antagonist used had no direct depressant action on the preparation, (3) precautions were taken to assure that the pattern of antagonism was not distorted by loss of agonist into tissue sinks, and (4) dose-response curves were normalized for changes in the baseline frequency or force in successive curves. Corrections for desensitization were necessary only in inotropic dose-response curves. Estimates of the equilibrium dissociation constants (KB) derived from the antagonism of the chronotropic and inotropic effects of isoproterenol were determined for fifteen beta-adrenoceptor blocking agents of widely differing potency. In no case was there a substantial difference between the inotropic and chronotropic values. Published estimates of binding constants for beta-blockers determined on cardiac membrane particles are more variable than those determined on intact tissues, and tend to be slightly (adenylyl cyclase measurements) or considerably (radioligand binding studies) lower than the values obtained in intact tissues. These differences raise the possibility that the properties of the beta-adrenoceptor may sometimes be altered during the isolation and partial purification of membrane fragments.
在自发搏动的右心房以及来自小猫和豚鼠的驱动左心房肌条中,研究了异丙肾上腺素与各种β-肾上腺素能受体阻滞剂之间的拮抗模式。在此类制剂中,β-肾上腺素能受体阻滞的起效通常非常缓慢;达到平衡状态可能需要长达一小时的孵育期。阻滞作用的起效速度与拮抗剂的浓度直接相关,因此,对于给定程度的阻滞,与拮抗剂的效能呈反比。发现β-肾上腺素能受体阻滞剂与异丙肾上腺素相互作用的方式符合简单的竞争性拮抗作用,前提是:(1)拮抗剂对所研究的制剂几乎没有内在刺激作用;(2)所用拮抗剂的浓度对制剂没有直接的抑制作用;(3)采取了预防措施以确保拮抗模式不会因激动剂向组织池的丢失而扭曲;(4)对连续曲线中基线频率或张力的变化进行了剂量反应曲线的标准化。仅在变力性剂量反应曲线中需要对脱敏进行校正。针对十五种效能差异很大的β-肾上腺素能受体阻滞剂,测定了由异丙肾上腺素的变时性和变力性作用的拮抗作用得出的平衡解离常数(KB)。在任何情况下,变力性和变时性值之间都没有实质性差异。已发表的关于在心脏膜颗粒上测定的β受体阻滞剂结合常数的估计值比在完整组织上测定的更具变异性,并且往往略低于(腺苷酸环化酶测量)或显著低于(放射性配体结合研究)在完整组织中获得的值。这些差异增加了在膜片段的分离和部分纯化过程中β-肾上腺素能受体的特性有时可能会改变的可能性。