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A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: Lessons learned from a human laboratory investigation
Previous studies suggest that GABA-B receptor agonism may represent an effective pharmacological approach to treat addictive disorders. Baclofen is a selective GABA-B receptor agonist which has been investigated as a potential treatment for alcohol use disorder. However, research is needed to unders...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494745/ https://www.ncbi.nlm.nih.gov/pubmed/30382188 http://dx.doi.org/10.1038/s41380-018-0287-y |
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author | Farokhnia, Mehdi Deschaine, Sara L. Sadighi, Armin Farinelli, Lisa A. Lee, Mary R. Akhlaghi, Fatemeh Leggio, Lorenzo |
author_facet | Farokhnia, Mehdi Deschaine, Sara L. Sadighi, Armin Farinelli, Lisa A. Lee, Mary R. Akhlaghi, Fatemeh Leggio, Lorenzo |
author_sort | Farokhnia, Mehdi |
collection | PubMed |
description | Previous studies suggest that GABA-B receptor agonism may represent an effective pharmacological approach to treat addictive disorders. Baclofen is a selective GABA-B receptor agonist which has been investigated as a potential treatment for alcohol use disorder. However, research is needed to understand the biobehavioral mechanisms underlying baclofen’s effect on alcohol use. In the present randomized, double-blind, placebo-controlled study, thirty-four alcohol-dependent individuals were randomized to receive baclofen (30 mg/d) or placebo for a week, and then participated in a laboratory experiment consisting of three procedures: alcohol cue-reactivity, priming, and self-administration. During the experiment, craving and other subjective responses to alcohol were assessed, and blood samples were collected for pharmacokinetic measurements. The effects of baclofen on the relationships between different alcohol-related laboratory parameters were investigated. Baclofen pharmacokinetic parameters and their correlations with behavioral measures were also examined. Results showed that baclofen disrupted the link between alcohol priming and self-administration, as indicated by significant interaction effects between drug condition (baclofen versus placebo) and some of the priming variables (alcohol craving: F(3,9)=6.03, p=0.01; alcohol sedation: F(3,6)=7.16, p=0.01) on the total amount of alcohol self-administered. Considerable inter-individual variability in baclofen pharmacokinetic parameters was observed. Maximum plasma concentrations of baclofen negatively correlated with cue-induced alcohol craving (r=−0.57, p=0.03) and priming-induced ratings of ‘like more’ (r=−0.59, p=0.02). In conclusion, baclofen may work by dissociating the link between an initial drink (priming) and subsequent alcohol consumption (self-administration). Considerable pharmacokinetic variability is an important factor to take into account when employing baclofen as a treatment for alcohol use disorder. |
format | Online Article Text |
id | pubmed-6494745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-64947452019-05-02 A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: Lessons learned from a human laboratory investigation Farokhnia, Mehdi Deschaine, Sara L. Sadighi, Armin Farinelli, Lisa A. Lee, Mary R. Akhlaghi, Fatemeh Leggio, Lorenzo Mol Psychiatry Article Previous studies suggest that GABA-B receptor agonism may represent an effective pharmacological approach to treat addictive disorders. Baclofen is a selective GABA-B receptor agonist which has been investigated as a potential treatment for alcohol use disorder. However, research is needed to understand the biobehavioral mechanisms underlying baclofen’s effect on alcohol use. In the present randomized, double-blind, placebo-controlled study, thirty-four alcohol-dependent individuals were randomized to receive baclofen (30 mg/d) or placebo for a week, and then participated in a laboratory experiment consisting of three procedures: alcohol cue-reactivity, priming, and self-administration. During the experiment, craving and other subjective responses to alcohol were assessed, and blood samples were collected for pharmacokinetic measurements. The effects of baclofen on the relationships between different alcohol-related laboratory parameters were investigated. Baclofen pharmacokinetic parameters and their correlations with behavioral measures were also examined. Results showed that baclofen disrupted the link between alcohol priming and self-administration, as indicated by significant interaction effects between drug condition (baclofen versus placebo) and some of the priming variables (alcohol craving: F(3,9)=6.03, p=0.01; alcohol sedation: F(3,6)=7.16, p=0.01) on the total amount of alcohol self-administered. Considerable inter-individual variability in baclofen pharmacokinetic parameters was observed. Maximum plasma concentrations of baclofen negatively correlated with cue-induced alcohol craving (r=−0.57, p=0.03) and priming-induced ratings of ‘like more’ (r=−0.59, p=0.02). In conclusion, baclofen may work by dissociating the link between an initial drink (priming) and subsequent alcohol consumption (self-administration). Considerable pharmacokinetic variability is an important factor to take into account when employing baclofen as a treatment for alcohol use disorder. 2018-10-31 2021-02 /pmc/articles/PMC6494745/ /pubmed/30382188 http://dx.doi.org/10.1038/s41380-018-0287-y Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Farokhnia, Mehdi Deschaine, Sara L. Sadighi, Armin Farinelli, Lisa A. Lee, Mary R. Akhlaghi, Fatemeh Leggio, Lorenzo A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: Lessons learned from a human laboratory investigation |
title | A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: Lessons learned from a human laboratory investigation |
title_full | A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: Lessons learned from a human laboratory investigation |
title_fullStr | A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: Lessons learned from a human laboratory investigation |
title_full_unstemmed | A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: Lessons learned from a human laboratory investigation |
title_short | A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: Lessons learned from a human laboratory investigation |
title_sort | deeper insight into how gaba-b receptor agonism via baclofen may affect alcohol seeking and consumption: lessons learned from a human laboratory investigation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494745/ https://www.ncbi.nlm.nih.gov/pubmed/30382188 http://dx.doi.org/10.1038/s41380-018-0287-y |
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