Medical Journals

Salusin Beta is a Surrogate Ligand of the Mas-like G Protein-coupled Receptor Mrga1.

Authors:
  • 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

From: Department of Pharmacology, University of California, Irvine, CA 92697, USA.

European journal of pharmacology

  • Publish Date: Jun 2006
  • ISSN: 0014-2999
  • Volume: 539
  • Issue: 3
  • Pages: 145-50
  • Medium: Print
  • Language: English
  • Citation (JAMA): Wang Zhiwei, Takahashi Toshio, Saito Yumiko, et al. Salusin Beta is a Surrogate Ligand of the Mas-like G Protein-coupled Receptor Mrga1.. Eur. J. Pharmacol. Jun 2006;539:145-50

Abstract

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 EC(50) 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 beta 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.

Mesh Headings (Keywords): Adenosine Triphosphatases, Amino Acid Sequence, Animals, Cell Line, Dose-Response Relationship, Drug, Humans, Intercellular Signaling Peptides and Proteins, Ligands, Mice, Molecular Sequence Data, Rats, Receptors, G-Protein-Coupled


Check for Full Text / PubMed Unique Identifier (PMID): 16697365


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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