Adams A, Jarrott B, Denny W A, Wakelin L P
Eur J Pharmacol. 1986 Aug 7;127(1-2):27-35. doi: 10.1016/0014-2999(86)90202-5.
We have used two homologous series of binuclear ligands, diacridines and diquinolines, and the radioligand receptor assay to compare the topology of alpha 1- and alpha 2-adrenoceptors in rat cerebral cortex and kidney membranes. While the chain length-dependence of affinity of the diacridines, as well as that of the diquinolines, for the alpha 1-adrenoceptors of these central and peripheral tissues are similar, we find marked differences in affinity profiles for interaction with central and peripheral alpha 2-adrenoceptors. In the context of our previously proposed model for the binding of diacridines and diquinolines to alpha-adrenoceptors the results suggest that the surface features of central and peripheral alpha 2-adrenoceptors differ in the area surrounding the noradrenaline binding site. This difference may prove to be of therapeutic relevance.
我们使用了两个同系双核配体系列,即二吖啶和二喹啉,并采用放射性配体受体分析法,比较大鼠大脑皮层和肾膜中α1和α2肾上腺素能受体的拓扑结构。虽然二吖啶以及二喹啉对这些中枢和外周组织的α1肾上腺素能受体的亲和力的链长依赖性相似,但我们发现与中枢和外周α2肾上腺素能受体相互作用的亲和力谱存在显著差异。根据我们之前提出的二吖啶和二喹啉与α肾上腺素能受体结合的模型,结果表明中枢和外周α2肾上腺素能受体的表面特征在去甲肾上腺素结合位点周围区域有所不同。这种差异可能具有治疗意义。