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The 5-HT7 receptor as a potential target for treating drug and alcohol abuse

Alcohol and drug abuse take a large toll on society and affected individuals. However, very few effective treatments are currently available to treat alcohol and drug addiction. Basic and clinical research has begun to provide some insights into the underlying neurobiological systems involved in the...

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Autores principales: Hauser, Sheketha R., Hedlund, Peter B., Roberts, Amanda J., Sari, Youssef, Bell, Richard L., Engleman, Eric A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4292232/
https://www.ncbi.nlm.nih.gov/pubmed/25628528
http://dx.doi.org/10.3389/fnins.2014.00448
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author Hauser, Sheketha R.
Hedlund, Peter B.
Roberts, Amanda J.
Sari, Youssef
Bell, Richard L.
Engleman, Eric A.
author_facet Hauser, Sheketha R.
Hedlund, Peter B.
Roberts, Amanda J.
Sari, Youssef
Bell, Richard L.
Engleman, Eric A.
author_sort Hauser, Sheketha R.
collection PubMed
description Alcohol and drug abuse take a large toll on society and affected individuals. However, very few effective treatments are currently available to treat alcohol and drug addiction. Basic and clinical research has begun to provide some insights into the underlying neurobiological systems involved in the addiction process. Several neurotransmitter pathways have been implicated and distinct reward neurocircuitry have been proposed—including the mesocorticolimbic dopamine (MCL-DA) system and the extended amygdala. The serotonin (5-HT) neurotransmitter system is of particular interest and multiple 5-HT receptors are thought to play significant roles in alcohol and drug self-administration and the development of drug dependence. Among the 5-HT receptors, the 5-HT7 receptor is currently undergoing characterization as a potential target for the treatment of several psychiatric disorders. Although this receptor has received only limited research regarding addictive behaviors, aspects of its neuroanatomical, biochemical, physiological, pharmacological, and behavioral profiles suggest that it could play a key role in the addiction process. For instance, genomic studies in humans have suggested a link between variants in the gene encoding the 5-HT7 receptor and alcoholism. Recent behavioral testing using high-affinity antagonists in mice and preliminary tests with alcohol-preferring rats suggest that this receptor could mediate alcohol consumption and/or reinforcement and play a role in seeking/craving behavior. Interest in the development of new and more selective pharmacological agents for this receptor will aid in examining the 5-HT7 receptor as a novel target for treating addiction.
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spelling pubmed-42922322015-01-27 The 5-HT7 receptor as a potential target for treating drug and alcohol abuse Hauser, Sheketha R. Hedlund, Peter B. Roberts, Amanda J. Sari, Youssef Bell, Richard L. Engleman, Eric A. Front Neurosci Pharmacology Alcohol and drug abuse take a large toll on society and affected individuals. However, very few effective treatments are currently available to treat alcohol and drug addiction. Basic and clinical research has begun to provide some insights into the underlying neurobiological systems involved in the addiction process. Several neurotransmitter pathways have been implicated and distinct reward neurocircuitry have been proposed—including the mesocorticolimbic dopamine (MCL-DA) system and the extended amygdala. The serotonin (5-HT) neurotransmitter system is of particular interest and multiple 5-HT receptors are thought to play significant roles in alcohol and drug self-administration and the development of drug dependence. Among the 5-HT receptors, the 5-HT7 receptor is currently undergoing characterization as a potential target for the treatment of several psychiatric disorders. Although this receptor has received only limited research regarding addictive behaviors, aspects of its neuroanatomical, biochemical, physiological, pharmacological, and behavioral profiles suggest that it could play a key role in the addiction process. For instance, genomic studies in humans have suggested a link between variants in the gene encoding the 5-HT7 receptor and alcoholism. Recent behavioral testing using high-affinity antagonists in mice and preliminary tests with alcohol-preferring rats suggest that this receptor could mediate alcohol consumption and/or reinforcement and play a role in seeking/craving behavior. Interest in the development of new and more selective pharmacological agents for this receptor will aid in examining the 5-HT7 receptor as a novel target for treating addiction. Frontiers Media S.A. 2015-01-13 /pmc/articles/PMC4292232/ /pubmed/25628528 http://dx.doi.org/10.3389/fnins.2014.00448 Text en Copyright © 2015 Hauser, Hedlund, Roberts, Sari, Bell and Engleman. 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) or licensor 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
Hauser, Sheketha R.
Hedlund, Peter B.
Roberts, Amanda J.
Sari, Youssef
Bell, Richard L.
Engleman, Eric A.
The 5-HT7 receptor as a potential target for treating drug and alcohol abuse
title The 5-HT7 receptor as a potential target for treating drug and alcohol abuse
title_full The 5-HT7 receptor as a potential target for treating drug and alcohol abuse
title_fullStr The 5-HT7 receptor as a potential target for treating drug and alcohol abuse
title_full_unstemmed The 5-HT7 receptor as a potential target for treating drug and alcohol abuse
title_short The 5-HT7 receptor as a potential target for treating drug and alcohol abuse
title_sort 5-ht7 receptor as a potential target for treating drug and alcohol abuse
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4292232/
https://www.ncbi.nlm.nih.gov/pubmed/25628528
http://dx.doi.org/10.3389/fnins.2014.00448
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