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Role of Sigma Receptors in Alcohol Addiction

Pharmacological treatments for alcohol use disorder (AUD) are few in number and often ineffective, despite the significant research carried out so far to better comprehend the neurochemical underpinnings of the disease. Hence, research has been directed towards the discovery of novel therapeutic tar...

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Detalles Bibliográficos
Autores principales: Quadir, Sema G., Cottone, Pietro, Sabino, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586921/
https://www.ncbi.nlm.nih.gov/pubmed/31258483
http://dx.doi.org/10.3389/fphar.2019.00687
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author Quadir, Sema G.
Cottone, Pietro
Sabino, Valentina
author_facet Quadir, Sema G.
Cottone, Pietro
Sabino, Valentina
author_sort Quadir, Sema G.
collection PubMed
description Pharmacological treatments for alcohol use disorder (AUD) are few in number and often ineffective, despite the significant research carried out so far to better comprehend the neurochemical underpinnings of the disease. Hence, research has been directed towards the discovery of novel therapeutic targets for the treatment of AUD. In the last decade, the sigma receptor system has been proposed as a potential mediator of alcohol reward and reinforcement. Preclinical studies have shown that the motivational effects of alcohol and excessive ethanol consumption involve the recruitment of the sigma receptor system. Furthermore, sigma receptor antagonism has been shown to be sufficient to inhibit many behaviors related to AUDs. This paper will review the most current evidence in support of this receptor system as a potential target for the development of pharmacological agents for the treatment of alcohol addiction.
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spelling pubmed-65869212019-06-28 Role of Sigma Receptors in Alcohol Addiction Quadir, Sema G. Cottone, Pietro Sabino, Valentina Front Pharmacol Pharmacology Pharmacological treatments for alcohol use disorder (AUD) are few in number and often ineffective, despite the significant research carried out so far to better comprehend the neurochemical underpinnings of the disease. Hence, research has been directed towards the discovery of novel therapeutic targets for the treatment of AUD. In the last decade, the sigma receptor system has been proposed as a potential mediator of alcohol reward and reinforcement. Preclinical studies have shown that the motivational effects of alcohol and excessive ethanol consumption involve the recruitment of the sigma receptor system. Furthermore, sigma receptor antagonism has been shown to be sufficient to inhibit many behaviors related to AUDs. This paper will review the most current evidence in support of this receptor system as a potential target for the development of pharmacological agents for the treatment of alcohol addiction. Frontiers Media S.A. 2019-06-14 /pmc/articles/PMC6586921/ /pubmed/31258483 http://dx.doi.org/10.3389/fphar.2019.00687 Text en Copyright © 2019 Quadir, Cottone and Sabino 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
Quadir, Sema G.
Cottone, Pietro
Sabino, Valentina
Role of Sigma Receptors in Alcohol Addiction
title Role of Sigma Receptors in Alcohol Addiction
title_full Role of Sigma Receptors in Alcohol Addiction
title_fullStr Role of Sigma Receptors in Alcohol Addiction
title_full_unstemmed Role of Sigma Receptors in Alcohol Addiction
title_short Role of Sigma Receptors in Alcohol Addiction
title_sort role of sigma receptors in alcohol addiction
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586921/
https://www.ncbi.nlm.nih.gov/pubmed/31258483
http://dx.doi.org/10.3389/fphar.2019.00687
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