Herz A, Höllt V
Arzneimittelforschung. 1977;27(96):1865-7.
The availability of highly radioactively labelled opiates with high receptor affinity has made it possible to identify and characterize opiate receptors in vitro as well as in vivo. These investigations revealed that the affinity of the compounds to the receptor decides about the pharmacological potency of the compounds. The differing action of opiate agonists and antagonists are explained by an allosteric receptor model. In vivo experiments showed that the dose range at which opiates induce specific pharmacological actions is identical with those doses at which increasing and finally complete receptor occupancy is obtained. Toxicological aspects of receptor occupation are discussed.
具有高受体亲和力的高放射性标记阿片类药物的可得性,使得在体外以及体内识别和表征阿片受体成为可能。这些研究表明,化合物与受体的亲和力决定了化合物的药理效力。阿片激动剂和拮抗剂的不同作用可以用变构受体模型来解释。体内实验表明,阿片类药物诱导特定药理作用的剂量范围与获得逐渐增加并最终完全占据受体的剂量相同。文中讨论了受体占据的毒理学方面。