Document Detail

Pharmacology and Signaling of MAS-Related G Protein-Coupled Receptors.
MedLine Citation:
PMID:  24867890     Owner:  NLM     Status:  Publisher    
Signaling by heptahelical G protein-coupled receptors (GPCR) regulates many vital body functions. Consequently, dysfunction of GPCR signaling leads to pathologic states, and approximately 30% of all modern clinical drugs target GPCR. One decade ago, an entire new GPCR family was discovered, which was recently named MAS-related G protein-coupled receptors (MRGPR) by the HUGO Gene Nomenclature Committee. The MRGPR family consists of ∼40 members that are grouped into nine distinct subfamilies (MRGPRA to -H and -X) and are predominantly expressed in primary sensory neurons and mast cells. All members are formally still considered "orphan" by the Committee on Receptor Nomenclature and Drug Classification of the International Union of Basic and Clinical Pharmacology. However, several distinct peptides and amino acids are discussed as potential ligands, including β-alanine, angiotensin-(1-7), alamandine, GABA, cortistatin-14, and cleavage products of proenkephalin, pro-opiomelanocortin, prodynorphin, or proneuropeptide-FF-A. The full spectrum of biologic roles of all MRGPR is still ill-defined, but there is evidence pointing to a role of distinct MRGPR subtypes in nociception, pruritus, sleep, cell proliferation, circulation, and mast cell degranulation. This review article summarizes findings published in the last 10 years on the phylogenetic relationships, pharmacology, signaling, physiology, and agonist-promoted regulation of all MRGPR subfamilies. Furthermore, we highlight interactions between MRGPR and other hormonal systems, paying particular attention to receptor multimerization and morphine tolerance. Finally, we discuss the challenges the field faces presently and emphasize future directions of research.
Hans Jürgen Solinski; Thomas Gudermann; Andreas Breit
Publication Detail:
Type:  REVIEW    
Journal Detail:
Title:  Pharmacological reviews     Volume:  66     ISSN:  1521-0081     ISO Abbreviation:  Pharmacol. Rev.     Publication Date:  2014 Jul 
Date Detail:
Created Date:  2014-5-28     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0421737     Medline TA:  Pharmacol Rev     Country:  -    
Other Details:
Languages:  ENG     Pagination:  570-597     Citation Subset:  -    
Copyright Information:
Copyright © 2014 by The American Society for Pharmacology and Experimental Therapeutics.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  sAPP modulates iron efflux from brain microvascular endothelial cells by stabilizing the ferrous iro...
Next Document:  Optimization in Stent Implantation by Manual Thrombus Aspiration in ST-Segment-Elevation Myocardial ...