Identification and pharmacological properties of E339-3D6, the first nonpeptidic apelin receptor agonist

被引:94
作者
Iturrioz, Xavier [1 ]
Alvear-Perez, Rodrigo [1 ]
De Mota, Nadia [1 ]
Franchet, Christel [2 ,3 ]
Guillier, Fabrice [2 ,3 ]
Leroux, Vincent [4 ]
Dabire, Hubert [5 ]
Le Jouan, Melissande [1 ]
Chabane, Hadjila [2 ,3 ]
Gerbier, Romain [1 ]
Bonnet, Dominique [2 ,3 ]
Berdeaux, Alain [5 ]
Maigret, Bernard [4 ]
Galzi, Jean-Luc [2 ,3 ]
Hibert, Marcel [2 ,3 ]
Llorens-Cortes, Catherine [1 ]
机构
[1] Univ Paris 06, INSERM, U691, Coll France, F-75005 Paris, France
[2] Univ Strasbourg 1, CNRS, Fac Pharm, UMR 7175,LC1, Illkirch Graffenstaden, France
[3] Ecole Biotechnol, Illkirch Graffenstaden, France
[4] H Poincare Univ, Fac 7503, CNRS, Unite Mixte Rech,Orpailleur Grp,Lab Lorrain Rech, Nancy, France
[5] Univ Paris, Fac Med, INSERM, U955, Creteil, France
关键词
NITRIC-OXIDE; ENDOGENOUS LIGAND; BIASED AGONISM; BLOOD-PRESSURE; APJ RECEPTOR; CORECEPTOR; PEPTIDE; VASOPRESSIN; INHIBITION; IMMUNOREACTIVITY;
D O I
10.1096/fj.09-140715
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apelin plays a prominent role in body fluid and cardiovascular homeostasis. To explore further upstream the role played by this peptide, nonpeptidic agonists and antagonists of the apelin receptor are required. To identify such compounds that do not exist to date, we used an original fluorescence resonance energy transfer-based assay to screen a G-protein-coupled receptor-focused library of fluorescent compounds on the human EGFP-tagged apelin receptor. This led to isolated E339-3D6 that displayed a 90 nM affinity and behaved as a partial agonist with regard to cAMP production and as a full agonist with regard to apelin receptor internalization. Finally, E339-3D6 induced vasorelaxation of rat aorta precontracted with noradrenaline and potently inhibited systemic vasopressin release in water-deprived mice when intracerebroventricularly injected. This compound represents the first nonpeptidic agonist of the apelin receptor, the optimization of which will allow development of a new generation of vasodilator and aquaretic agents.-Iturrioz, X., Alvear-Perez, R., De Mota, N., Franchet, C., Guillier, F., Leroux, V., Dabire, H., Le Jouan, M., Chabane, H., Gerbier, R., Bonnet, D., Berdeaux, A., Maigret, B., Galzi J.-L., Hibert, M., Llorens-Cortes, C. Identification and pharmacological properties of E339-3D6, FASEB J. 24, 1506-1517 (2010). www.fasebj.org
引用
收藏
页码:1506 / 1517
页数:12
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