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Regional Influence of Cannabinoid CB(1) Receptors in the Regulation of Ethanol Self-Administration by Wistar Rats

Substantial evidence suggests a facilitatory influence of cannabinoid CB(1) receptors in the modulation of ethanol consumption by rodents. Studies performed in rats selectively bred for high alcohol preference point to an involvement of CB(1) receptors in the nucleus accumbens (NAC), ventral tegment...

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Autores principales: Alvarez-Jaimes, Lily, Polis, Ilham, Parsons, Loren H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5152943/
https://www.ncbi.nlm.nih.gov/pubmed/27974944
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author Alvarez-Jaimes, Lily
Polis, Ilham
Parsons, Loren H.
author_facet Alvarez-Jaimes, Lily
Polis, Ilham
Parsons, Loren H.
author_sort Alvarez-Jaimes, Lily
collection PubMed
description Substantial evidence suggests a facilitatory influence of cannabinoid CB(1) receptors in the modulation of ethanol consumption by rodents. Studies performed in rats selectively bred for high alcohol preference point to an involvement of CB(1) receptors in the nucleus accumbens (NAC), ventral tegmental area (VTA) and medial prefrontal cortex (mPFC) in the modulation ethanol self-administration. However, the neural mechanisms through which CB(1) receptors regulate ethanol intake in out-bred Wistar rats have not been investigated. The present study evaluated alterations in ethanol self-administration induced by localized infusions of the CB(1) receptor antagonist SR141716A (0, 1 and 3 μg/side) into the NAC, anterior and posterior VTA and mPFC. Separate groups of Wistar rats were trained to operantly respond for an oral ethanol solution and prepared with bilateral injection cannulae aimed at each brain region. Results revealed significant decreases in ethanol intake following intra-NAC SR141716A administration, consistent with our prior observation of ethanol-induced increases extracellular 2-arachidonoyl glycerol (2-AG) in this brain region. We also observed a significant dose-dependent reduction in ethanol intake following SR141716A administration into the posterior, but not anterior VTA, consistent with evidence of a specific involvement of the posterior VTA in the regulation of ethanol intake. Ethanol consumption was unaltered following intra-mPFC SR141716A administration and ethanol self-administration did not induce robust changes in anandamide or 2-AG levels in mPFC microdialysates. These findings implicate an involvement of CB(1) receptors in the NAC and posterior VTA, but not anterior VTA and mPFC in the regulation of ethanol self-administration behavior by outbred Wistar rats.
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spelling pubmed-51529432016-12-12 Regional Influence of Cannabinoid CB(1) Receptors in the Regulation of Ethanol Self-Administration by Wistar Rats Alvarez-Jaimes, Lily Polis, Ilham Parsons, Loren H. Open Neuropsychopharmacol J Article Substantial evidence suggests a facilitatory influence of cannabinoid CB(1) receptors in the modulation of ethanol consumption by rodents. Studies performed in rats selectively bred for high alcohol preference point to an involvement of CB(1) receptors in the nucleus accumbens (NAC), ventral tegmental area (VTA) and medial prefrontal cortex (mPFC) in the modulation ethanol self-administration. However, the neural mechanisms through which CB(1) receptors regulate ethanol intake in out-bred Wistar rats have not been investigated. The present study evaluated alterations in ethanol self-administration induced by localized infusions of the CB(1) receptor antagonist SR141716A (0, 1 and 3 μg/side) into the NAC, anterior and posterior VTA and mPFC. Separate groups of Wistar rats were trained to operantly respond for an oral ethanol solution and prepared with bilateral injection cannulae aimed at each brain region. Results revealed significant decreases in ethanol intake following intra-NAC SR141716A administration, consistent with our prior observation of ethanol-induced increases extracellular 2-arachidonoyl glycerol (2-AG) in this brain region. We also observed a significant dose-dependent reduction in ethanol intake following SR141716A administration into the posterior, but not anterior VTA, consistent with evidence of a specific involvement of the posterior VTA in the regulation of ethanol intake. Ethanol consumption was unaltered following intra-mPFC SR141716A administration and ethanol self-administration did not induce robust changes in anandamide or 2-AG levels in mPFC microdialysates. These findings implicate an involvement of CB(1) receptors in the NAC and posterior VTA, but not anterior VTA and mPFC in the regulation of ethanol self-administration behavior by outbred Wistar rats. 2009 /pmc/articles/PMC5152943/ /pubmed/27974944 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Alvarez-Jaimes, Lily
Polis, Ilham
Parsons, Loren H.
Regional Influence of Cannabinoid CB(1) Receptors in the Regulation of Ethanol Self-Administration by Wistar Rats
title Regional Influence of Cannabinoid CB(1) Receptors in the Regulation of Ethanol Self-Administration by Wistar Rats
title_full Regional Influence of Cannabinoid CB(1) Receptors in the Regulation of Ethanol Self-Administration by Wistar Rats
title_fullStr Regional Influence of Cannabinoid CB(1) Receptors in the Regulation of Ethanol Self-Administration by Wistar Rats
title_full_unstemmed Regional Influence of Cannabinoid CB(1) Receptors in the Regulation of Ethanol Self-Administration by Wistar Rats
title_short Regional Influence of Cannabinoid CB(1) Receptors in the Regulation of Ethanol Self-Administration by Wistar Rats
title_sort regional influence of cannabinoid cb(1) receptors in the regulation of ethanol self-administration by wistar rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5152943/
https://www.ncbi.nlm.nih.gov/pubmed/27974944
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