Cargando…

Advances in Neurobiology and Pharmacology of GPR12

GPR12 is a G protein-coupled orphan receptor genetically related to type 1 and type 2 cannabinoid receptors (CB(1) and CB(2)) which are ancient proteins expressed all over the body. Both cannabinoid receptors, but especially CB(1), are involved in neurodevelopment and cognitive processes such as lea...

Descripción completa

Detalles Bibliográficos
Autores principales: Allende, Gonzalo, Chávez-Reyes, Jesús, Guerrero-Alba, Raquel, Vázquez-León, Priscila, Marichal-Cancino, Bruno A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226366/
https://www.ncbi.nlm.nih.gov/pubmed/32457622
http://dx.doi.org/10.3389/fphar.2020.00628
_version_ 1783534270516559872
author Allende, Gonzalo
Chávez-Reyes, Jesús
Guerrero-Alba, Raquel
Vázquez-León, Priscila
Marichal-Cancino, Bruno A.
author_facet Allende, Gonzalo
Chávez-Reyes, Jesús
Guerrero-Alba, Raquel
Vázquez-León, Priscila
Marichal-Cancino, Bruno A.
author_sort Allende, Gonzalo
collection PubMed
description GPR12 is a G protein-coupled orphan receptor genetically related to type 1 and type 2 cannabinoid receptors (CB(1) and CB(2)) which are ancient proteins expressed all over the body. Both cannabinoid receptors, but especially CB(1), are involved in neurodevelopment and cognitive processes such as learning, memory, brain reward, coordination, etc. GPR12 shares with CB(1) that both are mainly expressed into the brain. Regrettably, very little is known about physiology of GPR12. Concerning its pharmacology, GPR12 seems to be endogenously activated by the lysophospholipids sphingosine-1-phosphate (S1P) and sphingosyl-phosphorylcholine (SPC). Exogenously, GPR12 is a target for the phytocannabinoid cannabidiol (CBD). Functionally, GPR12 seems to be related to neurogenesis and neural inflammation, but its relationship with cognitive functions remains to be characterized. Although GPR12 was initially suggested to be a cannabinoid receptor, it does not meet the five criteria proposed in 2010 by the International Union of Basic and Clinical Pharmacology (IUPHAR). In this review, we analyze all the direct available information in PubMed database about expression, function, and pharmacology of this receptor in central nervous system (CNS) trying to provide a broad overview of its current and prospective neurophysiology. Moreover, in this mini-review we highlight the need to produce more relevant data about the functions of GPR12 in CNS. Hence, this work should motivate further research in this field.
format Online
Article
Text
id pubmed-7226366
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-72263662020-05-25 Advances in Neurobiology and Pharmacology of GPR12 Allende, Gonzalo Chávez-Reyes, Jesús Guerrero-Alba, Raquel Vázquez-León, Priscila Marichal-Cancino, Bruno A. Front Pharmacol Pharmacology GPR12 is a G protein-coupled orphan receptor genetically related to type 1 and type 2 cannabinoid receptors (CB(1) and CB(2)) which are ancient proteins expressed all over the body. Both cannabinoid receptors, but especially CB(1), are involved in neurodevelopment and cognitive processes such as learning, memory, brain reward, coordination, etc. GPR12 shares with CB(1) that both are mainly expressed into the brain. Regrettably, very little is known about physiology of GPR12. Concerning its pharmacology, GPR12 seems to be endogenously activated by the lysophospholipids sphingosine-1-phosphate (S1P) and sphingosyl-phosphorylcholine (SPC). Exogenously, GPR12 is a target for the phytocannabinoid cannabidiol (CBD). Functionally, GPR12 seems to be related to neurogenesis and neural inflammation, but its relationship with cognitive functions remains to be characterized. Although GPR12 was initially suggested to be a cannabinoid receptor, it does not meet the five criteria proposed in 2010 by the International Union of Basic and Clinical Pharmacology (IUPHAR). In this review, we analyze all the direct available information in PubMed database about expression, function, and pharmacology of this receptor in central nervous system (CNS) trying to provide a broad overview of its current and prospective neurophysiology. Moreover, in this mini-review we highlight the need to produce more relevant data about the functions of GPR12 in CNS. Hence, this work should motivate further research in this field. Frontiers Media S.A. 2020-05-08 /pmc/articles/PMC7226366/ /pubmed/32457622 http://dx.doi.org/10.3389/fphar.2020.00628 Text en Copyright © 2020 Allende, Chávez-Reyes, Guerrero-Alba, Vázquez-León and Marichal-Cancino http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Allende, Gonzalo
Chávez-Reyes, Jesús
Guerrero-Alba, Raquel
Vázquez-León, Priscila
Marichal-Cancino, Bruno A.
Advances in Neurobiology and Pharmacology of GPR12
title Advances in Neurobiology and Pharmacology of GPR12
title_full Advances in Neurobiology and Pharmacology of GPR12
title_fullStr Advances in Neurobiology and Pharmacology of GPR12
title_full_unstemmed Advances in Neurobiology and Pharmacology of GPR12
title_short Advances in Neurobiology and Pharmacology of GPR12
title_sort advances in neurobiology and pharmacology of gpr12
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226366/
https://www.ncbi.nlm.nih.gov/pubmed/32457622
http://dx.doi.org/10.3389/fphar.2020.00628
work_keys_str_mv AT allendegonzalo advancesinneurobiologyandpharmacologyofgpr12
AT chavezreyesjesus advancesinneurobiologyandpharmacologyofgpr12
AT guerreroalbaraquel advancesinneurobiologyandpharmacologyofgpr12
AT vazquezleonpriscila advancesinneurobiologyandpharmacologyofgpr12
AT marichalcancinobrunoa advancesinneurobiologyandpharmacologyofgpr12