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Some Prospective Alternatives for Treating Pain: The Endocannabinoid System and Its Putative Receptors GPR18 and GPR55

Background: Marijuana extracts (cannabinoids) have been used for several millennia for pain treatment. Regarding the site of action, cannabinoids are highly promiscuous molecules, but only two cannabinoid receptors (CB(1) and CB(2)) have been deeply studied and classified. Thus, therapeutic actions,...

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Autores principales: Guerrero-Alba, Raquel, Barragán-Iglesias, Paulino, González-Hernández, Abimael, Valdez-Moráles, Eduardo E., Granados-Soto, Vinicio, Condés-Lara, Miguel, Rodríguez, Martín G., Marichal-Cancino, Bruno A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331465/
https://www.ncbi.nlm.nih.gov/pubmed/30670965
http://dx.doi.org/10.3389/fphar.2018.01496
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author Guerrero-Alba, Raquel
Barragán-Iglesias, Paulino
González-Hernández, Abimael
Valdez-Moráles, Eduardo E.
Granados-Soto, Vinicio
Condés-Lara, Miguel
Rodríguez, Martín G.
Marichal-Cancino, Bruno A.
author_facet Guerrero-Alba, Raquel
Barragán-Iglesias, Paulino
González-Hernández, Abimael
Valdez-Moráles, Eduardo E.
Granados-Soto, Vinicio
Condés-Lara, Miguel
Rodríguez, Martín G.
Marichal-Cancino, Bruno A.
author_sort Guerrero-Alba, Raquel
collection PubMed
description Background: Marijuana extracts (cannabinoids) have been used for several millennia for pain treatment. Regarding the site of action, cannabinoids are highly promiscuous molecules, but only two cannabinoid receptors (CB(1) and CB(2)) have been deeply studied and classified. Thus, therapeutic actions, side effects and pharmacological targets for cannabinoids have been explained based on the pharmacology of cannabinoid CB(1)/CB(2) receptors. However, the accumulation of confusing and sometimes contradictory results suggests the existence of other cannabinoid receptors. Different orphan proteins (e.g., GPR18, GPR55, GPR119, etc.) have been proposed as putative cannabinoid receptors. According to their expression, GPR18 and GPR55 could be involved in sensory transmission and pain integration. Methods: This article reviews select relevant information about the potential role of GPR18 and GPR55 in the pathophysiology of pain. Results: This work summarized novel data supporting that, besides cannabinoid CB(1) and CB(2) receptors, GPR18 and GPR55 may be useful for pain treatment. Conclusion: There is evidence to support an antinociceptive role for GPR18 and GPR55.
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spelling pubmed-63314652019-01-22 Some Prospective Alternatives for Treating Pain: The Endocannabinoid System and Its Putative Receptors GPR18 and GPR55 Guerrero-Alba, Raquel Barragán-Iglesias, Paulino González-Hernández, Abimael Valdez-Moráles, Eduardo E. Granados-Soto, Vinicio Condés-Lara, Miguel Rodríguez, Martín G. Marichal-Cancino, Bruno A. Front Pharmacol Pharmacology Background: Marijuana extracts (cannabinoids) have been used for several millennia for pain treatment. Regarding the site of action, cannabinoids are highly promiscuous molecules, but only two cannabinoid receptors (CB(1) and CB(2)) have been deeply studied and classified. Thus, therapeutic actions, side effects and pharmacological targets for cannabinoids have been explained based on the pharmacology of cannabinoid CB(1)/CB(2) receptors. However, the accumulation of confusing and sometimes contradictory results suggests the existence of other cannabinoid receptors. Different orphan proteins (e.g., GPR18, GPR55, GPR119, etc.) have been proposed as putative cannabinoid receptors. According to their expression, GPR18 and GPR55 could be involved in sensory transmission and pain integration. Methods: This article reviews select relevant information about the potential role of GPR18 and GPR55 in the pathophysiology of pain. Results: This work summarized novel data supporting that, besides cannabinoid CB(1) and CB(2) receptors, GPR18 and GPR55 may be useful for pain treatment. Conclusion: There is evidence to support an antinociceptive role for GPR18 and GPR55. Frontiers Media S.A. 2019-01-08 /pmc/articles/PMC6331465/ /pubmed/30670965 http://dx.doi.org/10.3389/fphar.2018.01496 Text en Copyright © 2019 Guerrero-Alba, Barragán-Iglesias, González-Hernández, Valdez-Moráles, Granados-Soto, Condés-Lara, Rodríguez 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
Guerrero-Alba, Raquel
Barragán-Iglesias, Paulino
González-Hernández, Abimael
Valdez-Moráles, Eduardo E.
Granados-Soto, Vinicio
Condés-Lara, Miguel
Rodríguez, Martín G.
Marichal-Cancino, Bruno A.
Some Prospective Alternatives for Treating Pain: The Endocannabinoid System and Its Putative Receptors GPR18 and GPR55
title Some Prospective Alternatives for Treating Pain: The Endocannabinoid System and Its Putative Receptors GPR18 and GPR55
title_full Some Prospective Alternatives for Treating Pain: The Endocannabinoid System and Its Putative Receptors GPR18 and GPR55
title_fullStr Some Prospective Alternatives for Treating Pain: The Endocannabinoid System and Its Putative Receptors GPR18 and GPR55
title_full_unstemmed Some Prospective Alternatives for Treating Pain: The Endocannabinoid System and Its Putative Receptors GPR18 and GPR55
title_short Some Prospective Alternatives for Treating Pain: The Endocannabinoid System and Its Putative Receptors GPR18 and GPR55
title_sort some prospective alternatives for treating pain: the endocannabinoid system and its putative receptors gpr18 and gpr55
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331465/
https://www.ncbi.nlm.nih.gov/pubmed/30670965
http://dx.doi.org/10.3389/fphar.2018.01496
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