Salusin β is a surrogate ligand of the mas-like G protein-coupled receptor MrgA1

被引:37
作者
Wang, Zhiwei
Takahashi, Toshio
Saito, Yumiko
Nagasaki, Hiroshi
Ly, Nga Kim
Nothacker, Hans-Peter
Reinscheid, Rainer K.
Yang, Jun
Chang, Jaw Kang
Shichiri, Masayoshi
Civelli, Olivier
机构
[1] Univ Calif Irvine, Dept Pharmacol, Irvine, CA 92697 USA
[2] Suntory Inst Bioorgan Res, Osaka 6188503, Japan
[3] Saitama Med Sch, Dept Pharmacol, Morohongo, Saitama 3500495, Japan
[4] Nagoya Univ, Sch Med, Nagoya, Aichi 4668550, Japan
[5] Phoenix Pharmaceut Inc, Belmont, CA 94002 USA
[6] Tokyo Med & Dent Univ, Hosp Med, Bunkyo Ku, Tokyo 1138519, Japan
关键词
mas-like G protein-couple receptor; salusin; pain;
D O I
10.1016/j.ejphar.2006.03.064
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The mas-like G protein-coupled receptors form a subfamily of G protein-coupled receptors that includes variable member numbers across different species and that have been shown to bind a wide variety of ligands from peptides to amino acid derivatives. While screening a library of peptides against different orphan G protein-coupled receptors, we found that human salusin beta activates the mouse mas-like G protein-coupled receptor, mMrgA1 with an EC50 of about 300 nM. Salusin beta is a bioactive peptide recently discovered through bioinformatics analysis which stimulates arginine-vasopressin release from rat pituitary and causes rapid and profound hypotension and bradycardia. However, when we further analyzed the generality of the mMrgA1 activation, we found that human salusin does not activate corresponding human mas-like G protein-coupled receptors. Our results show that human salusin beta is a surrogate ligand of the mouse MrgA1 and raises a cautionary flag for experiments that analyze the pharmacological profiles of mas-like G protein-coupled receptors from different species. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:145 / 150
页数:6
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