Besse J C, Furchgott R F
J Pharmacol Exp Ther. 1976 Apr;197(1):66-78.
The dissociation constants (KA values) of l-norepinephrine (l-NE) and seven other agonists acting on alpha adrenergic receptors in rabbit aorta strips were determined by analysis of concentration-response data before and after fractional inactivation of receptors with Dibenamine. In experiments to determine KA values, propranolol was added to block activation of beta receptors and cocaine to block the neuronal uptake mechanism. The KA of l-NE and the KA of a second agonist, when determined on paired strips from the same aorta, were used to calculate the relative affinity and the relative efficacy (er) of the second agonist as compared to l-NE. The validity of the method used for determining KA and er values was supported by the following findings. 1) The dissociation constant (KB) of the competitive antagonist, phentolamine, determined with each of the agonists, was the same as that determined with l-NE. 2) The KA determined for l-NE was independent of the fraction of active receptors remaining (q) after pretreatment with different concentrations of Dibenamine. 3) The KB of phentolamine determined with l-NE as the agonist was the same before and after fractional inactivation of receptors. 4) After inactivation in paired strips by equal exposures to Dibenamine, the q value determined with each agonist was the same as that determined with l-NE. The mean KA value for l-NE was 3.39 +/- 0.15 X 10(-7) M. The mean relative affinities of the agonists for the alpha receptor were: l-NE, 1;L-EPINEPHRINE, 1.25; L-PHENYLEPHRINE, 0.200; L-norphenylephrine, 0.217; epinine, 0.136; dopamine, 0.0055; l-alpha-methylnorepinephrine, 0.095; dl-alpha-ethylnorepinephrine, 0.0048. The mean er of each agonist was not significantly different from that of l-NE, except for l-norphenylephrine with an e of 0.71, and dl-alpha-ethylnorepinephrine with an er of 0.41. The results are discussed from the standpoint of structure-activity relationships.
通过分析在用双苄胺对受体进行部分失活前后的浓度-反应数据,测定了去甲肾上腺素(l-NE)以及其他七种作用于兔主动脉条α肾上腺素能受体的激动剂的解离常数(KA值)。在测定KA值的实验中,加入普萘洛尔以阻断β受体的激活,并加入可卡因以阻断神经元摄取机制。当在来自同一主动脉的配对条带上测定l-NE的KA值和第二种激动剂的KA值时,用于计算第二种激动剂相对于l-NE的相对亲和力和相对效能(er)。用于测定KA和er值的方法的有效性得到以下发现的支持。1)用每种激动剂测定的竞争性拮抗剂酚妥拉明的解离常数(KB)与用l-NE测定的相同。2)用不同浓度的双苄胺预处理后,测定的l-NE的KA值与剩余活性受体的分数(q)无关。3)在用l-NE作为激动剂测定时,酚妥拉明的KB在受体部分失活前后相同。4)在配对条带中通过等量暴露于双苄胺使其失活后,用每种激动剂测定的q值与用l-NE测定的相同。l-NE的平均KA值为3.39±0.15×10⁻⁷M。这些激动剂对α受体的平均相对亲和力为:l-NE,1;肾上腺素,1.25;去氧肾上腺素,0.200;去甲去氧肾上腺素,0.217;依匹宁,0.136;多巴胺,0.0055;l-α-甲基去甲肾上腺素,0.095;dl-α-乙基去甲肾上腺素,0.0048。除了去甲去氧肾上腺素的er为0.71和dl-α-乙基去甲肾上腺素的er为0.41外,每种激动剂的平均er与l-NE的平均er没有显著差异。从构效关系的角度对结果进行了讨论。