Affinity and efficacy of selective agonists and antagonists for vasopressin and oxytocin receptors: an "easy guide'' to receptor pharmacology

被引:45
作者
Chini, Bice [1 ]
Manning, Maurice [2 ]
Guillon, Gilles [3 ,4 ]
机构
[1] CNR Inst Neurosci, Milan, Italy
[2] Univ Toledo, Coll Med, Toledo, OH 43606 USA
[3] Univ Montpellier 1, Inst Genom Fonct, CNRS,INSERM, UMR5203,U661, Montpellier, France
[4] Univ Montpellier 2, Inst Genom Fonct, CNRS,INSERM, UMR5203,U661, Montpellier, France
来源
ADVANCES IN VASOPRESSIN AND OXYTOCIN: FROM GENES TO BEHAVIOUR TO DISEASE | 2008年 / 170卷
关键词
vasopressin; oxytocin; agonist; antagonist; selectivity; species difference;
D O I
10.1016/S0079-6123(08)00438-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The development of "selective'' drugs targeting oxytocin/vasopressin receptors has enormously progressed since the original synthesis of oxytocin more than 50 years ago. However, several factors still hamper the availability of a rich and complete range of selective agonists and antagonists acting at the different oxytocin/vasopressin receptor subtypes, making the use of these drugs still a daunting task. In this paper we will briefly review the major problems encountered when dealing with oxytocin/vasopressin selective ligands, proving few rules for their correct pharmacological use, in order to avoid common pitfalls. Finally, we will glimpse at new challenges, such us the discovery of coupling selective ligands, which foster the search for new classes of selective compounds.
引用
收藏
页码:513 / 517
页数:5
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