A REVIEW OF RECENTLY-DEVELOPED LIGANDS FOR NEURONAL BENZODIAZEPINE RECEPTORS AND THEIR PHARMACOLOGICAL ACTIVITIES

被引:25
作者
GARDNER, CR
机构
[1] Drug Development Research, Roussel Laboratories, Covingham Swindon, Wiltshire England
关键词
BENZODIAZEPINE RECEPTORS; INVERSE AGONISM; LIGANDS; PHARMACOPHORE; PARTIAL AGONISM;
D O I
10.1016/0278-5846(92)90099-Z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
1. There has recently been a large increase in the number of new benzodiazepine receptor ligands, some with benzodiazepine structures, but many with other chemical structures. 2. The pharmacological activities of these ligands have been interpreted on the basis of a continuum of efficacy ranging from full agonist through different degrees of partial agonism to antagonist and through partial to full inverse agonists. 3. Inconsistencies with this hypothesis are considered in terms of alternative hypotheses, particularly the existence of functionally separable receptor subtypes. 4. The potential of partial agonists as non-sedative anxiolytic agents with reduced potential of dependence and of weak partial inverse agonists as pro-cognitive agents is discussed. 5. A pharmacophore for benzodiazepine receptors is proposed and supporting evidence presented.
引用
收藏
页码:755 / 781
页数:27
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