Do N-arachidonyl-glycine (NA-glycine) and 2-arachidonoyl glycerol (2-AG) share mode of action and the binding site on the β2subunit of GABAAreceptors?
Author(s) -
Roland Baur,
Jürg Gertsch,
Erwin Sigel
Publication year - 2013
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.149
Subject(s) - gpr18 , glycine receptor , glycine , gabaa receptor , endocannabinoid system , cannabinoid receptor , receptor , chemistry , anandamide , cannabinoid , class c gpcr , gabaa rho receptor , biochemistry , biophysics , agonist , amino acid , biology , metabotropic receptor
NA-glycine is an endogenous lipid molecule with analgesic properties, which is structurally similar to the endocannabinoids 2-AG and anandamide but does not interact with cannabinoid receptors. NA-glycine has been suggested to act at the G-protein coupled receptors GPR18 and GPR92. Recently, we have described that NA-glycine can also modulate recombinant α 1 β 2 γ 2 GABA A receptors. Here we characterize in more detail this modulation and investigate the relationship of its binding site with that of the endocannabinoid 2-AG.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom