Molecular pharmacology of the mouse melatonin receptors MT1 and MT2

被引:19
作者
Devavry, Severine [1 ,2 ,3 ,4 ,5 ]
Legros, Celine
Brasseur, Chantal
Cohen, William
Guenin, Sophie-Penelope
Delagrange, Philippe [6 ]
Malpaux, Benoit [1 ,2 ,3 ,4 ,5 ]
Ouvry, Christine
Coge, Francis
Nosjean, Olivier
Boutin, Jean A.
机构
[1] INRA, UMR Physiol Reprod & Comportements 85, F-37380 Nouzilly, France
[2] CNRS, UMR6175, F-37380 Nouzilly, France
[3] Univ Tours, F-37041 Tours, France
[4] Haras Nationaux, F-37380 Nouzilly, France
[5] IFR135 Imagerie Fonct, F-37044 Tours, France
[6] Inst Rech Servier, Unite Rech & Decouvertes Neurosci, F-78290 Croissy Sur Seine, France
关键词
Melatonin; Molecular pharmacology; Mouse melatonin receptor; Agonist; Binding; SIGNAL-TRANSDUCTION; CLONING; DISCOVERY; LIGANDS; EXPRESSION; PATHWAYS; AGONISTS; CELLS; MICE;
D O I
10.1016/j.ejphar.2011.12.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The main melatonin receptors are two G-protein coupled receptors named MT1 and MT2. Having described the molecular pharmacology of the human versions of these receptors, we turned to two of the three species most useful in studying melatonin physiology: rat and sheep (a diurnal species used to understand the relationship between circadian rhythm and depression). We also employed previously used compounds to describe the mouse melatonin receptors; despite the early cloning of mouse receptors, few molecular pharmacology studies on these receptors exist. To our surprise, we detected no major differences between the data obtained from mice and those from other species. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:15 / 21
页数:7
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