Kaumann A J, Lemoine H
Naunyn Schmiedebergs Arch Pharmacol. 1985 Oct;331(1):27-39. doi: 10.1007/BF00498849.
A radioligand that selectively labels beta 1-adrenoceptors, 3H-(-)-bisoprolol (3H-BIS), is introduced. The binding properties of 3H-BIS to membrane particles of kitten heart are compared with the blocking properties of (-)-bisoprolol against stimulant effects of (-)-adrenaline and (-)-noradrenaline in heart preparations of kitten and guinea pig. 1. On kitten heart tissues (-)-bisoprolol antagonized the positive chronotropic and inotropic effects of catecholamines competitively. The effects of (-)-adrenaline were antagonized considerably less by (-)-bisoprolol than the corresponding effects of (-)-noradrenaline on sinoatrial pacemakers. The antagonism was nearly the same against both (-)-adrenaline and (-)-noradrenaline in left atria and papillary muscles. The data were analyzed with a model for 2-receptor subtypes by non-linear regression. Equilibrium dissociation constants KB (mol/l; -log KB = pKB) for a high-affinity beta 1-adrenoceptor of 8.8 and for a low-affinity beta 2-adrenoceptor of 7.0 were estimated in the three classes of tissues. In kitten sinoatrial pacemaker beta 1-adrenoceptors contribute 76% to the stimulus induced by (-)-adrenaline and 97% to the stimulus induced by (-)-noradrenaline. In ventricle and left atrium beta 1-adrenoceptors contribute 97-99% and 100% to the stimulus caused by (-)-adrenaline and (-)-noradrenaline, respectively. 2. Both 3H-BIS and unlabelled (-)-bisoprolol caused competitive blockade of the positive chronotropic effects of (-)-noradrenaline in guinea-pig right atria. pKB-values of 8.7 were estimated for both unlabelled and tritiated (-)-bisoprolol. The positive chronotropic effects of (-)-adrenaline were antagonized considerably less by (-)-bisoprolol than those of (-)-noradrenaline in guinea-pig atria. In the presence of low concentrations of beta 2-selective ICI 118,551, which did not antagonize beta 1-adrenoceptor mediated effects, (-)-bisoprolol antagonized positive chronotropic effects of (-)-adrenaline to the same extent as those of (-)-noradrenaline. The results are consistent with the concept of a significant role of sinoatrial beta 2-adrenoceptors of guinea pig for the effects of (-)-adrenaline but not for those of (-)-noradrenaline. 3. 3H-BIS associated and dissociated quickly with and from ventricular beta 1-adrenoceptors. A koff of 1.0 min-1 was estimated. An equilibrium dissociation constant pKL* of 8.2 for 3H-BIS was estimated from saturation binding.(ABSTRACT TRUNCATED AT 400 WORDS)
一种选择性标记β1 -肾上腺素能受体的放射性配体3H -(-)-比索洛尔(3H - BIS)被引入。将3H - BIS与小猫心脏膜颗粒的结合特性,与(-)-比索洛尔对小猫和豚鼠心脏制剂中(-)-肾上腺素和(-)-去甲肾上腺素刺激作用的阻断特性进行了比较。1. 在小猫心脏组织中,(-)-比索洛尔竞争性地拮抗儿茶酚胺的正性变时和变力作用。(-)-比索洛尔对(-)-肾上腺素作用的拮抗作用比对(-)-去甲肾上腺素对窦房结起搏器相应作用的拮抗作用小得多。在左心房和乳头肌中,(-)-比索洛尔对(-)-肾上腺素和(-)-去甲肾上腺素的拮抗作用几乎相同。用双受体亚型模型通过非线性回归分析数据。在三类组织中估计出高亲和力β1 -肾上腺素能受体的平衡解离常数KB(mol/L;-log KB = pKB)为8.8,低亲和力β2 -肾上腺素能受体的平衡解离常数KB为7.0。在小猫窦房结起搏器中,β1 -肾上腺素能受体对(-)-肾上腺素诱导的刺激作用贡献76%,对(-)-去甲肾上腺素诱导的刺激作用贡献97%。在心室和左心房中,β1 -肾上腺素能受体分别对(-)-肾上腺素和(-)-去甲肾上腺素引起的刺激作用贡献97 - 99%和100%。2. 3H - BIS和未标记的(-)-比索洛尔均对豚鼠右心房中(-)-去甲肾上腺素的正性变时作用产生竞争性阻断。未标记的和氚化的(-)-比索洛尔的pKB值估计均为8.7。在豚鼠心房中,(-)-比索洛尔对(-)-肾上腺素正性变时作用的拮抗作用比对(-)-去甲肾上腺素的拮抗作用小得多。在存在低浓度的β2选择性ICI 118,551(其不拮抗β1 -肾上腺素能受体介导的作用)的情况下,(-)-比索洛尔对(-)-肾上腺素正性变时作用的拮抗作用与对(-)-去甲肾上腺素的拮抗作用程度相同。结果与豚鼠窦房结β2 -肾上腺素能受体对(-)-肾上腺素的作用起重要作用但对(-)-去甲肾上腺素的作用不起重要作用这一概念一致。3. 3H - BIS与心室β1 -肾上腺素能受体的结合和解离迅速。估计解离常数koff为1.0 min-1。通过饱和结合估计3H - BIS的平衡解离常数pKL*为8.2。(摘要截断于400字)