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 (CB1 and CB2) which are ancient proteins expressed all over the body. Both cannabinoid receptors, but especially CB1, are involved in neurodevelopment and cognitive processes such as learning,...

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Main Authors: Gonzalo Allende, Jesús Chávez-Reyes, Raquel Guerrero-Alba, Priscila Vázquez-León, Bruno A. Marichal-Cancino
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-05-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphar.2020.00628/full
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author Gonzalo Allende
Jesús Chávez-Reyes
Raquel Guerrero-Alba
Priscila Vázquez-León
Bruno A. Marichal-Cancino
author_facet Gonzalo Allende
Jesús Chávez-Reyes
Raquel Guerrero-Alba
Priscila Vázquez-León
Bruno A. Marichal-Cancino
author_sort Gonzalo Allende
collection DOAJ
description GPR12 is a G protein-coupled orphan receptor genetically related to type 1 and type 2 cannabinoid receptors (CB1 and CB2) which are ancient proteins expressed all over the body. Both cannabinoid receptors, but especially CB1, are involved in neurodevelopment and cognitive processes such as learning, memory, brain reward, coordination, etc. GPR12 shares with CB1 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.
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spelling doaj.art-9961efeba846401281cdde1e49c431632022-12-22T00:44:47ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122020-05-011110.3389/fphar.2020.00628528446Advances in Neurobiology and Pharmacology of GPR12Gonzalo AllendeJesús Chávez-ReyesRaquel Guerrero-AlbaPriscila Vázquez-LeónBruno A. Marichal-CancinoGPR12 is a G protein-coupled orphan receptor genetically related to type 1 and type 2 cannabinoid receptors (CB1 and CB2) which are ancient proteins expressed all over the body. Both cannabinoid receptors, but especially CB1, are involved in neurodevelopment and cognitive processes such as learning, memory, brain reward, coordination, etc. GPR12 shares with CB1 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.https://www.frontiersin.org/article/10.3389/fphar.2020.00628/fullGPR12cannabinoid receptorssphingosyl-phosphorylcholinesphingosine-1-phosphatecannabidiol
spellingShingle Gonzalo Allende
Jesús Chávez-Reyes
Raquel Guerrero-Alba
Priscila Vázquez-León
Bruno A. Marichal-Cancino
Advances in Neurobiology and Pharmacology of GPR12
Frontiers in Pharmacology
GPR12
cannabinoid receptors
sphingosyl-phosphorylcholine
sphingosine-1-phosphate
cannabidiol
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 GPR12
cannabinoid receptors
sphingosyl-phosphorylcholine
sphingosine-1-phosphate
cannabidiol
url https://www.frontiersin.org/article/10.3389/fphar.2020.00628/full
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