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Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms

Emerging evidence indicates that the endogenous cannabinoid system modulates the behavioral and physiological effects of nicotine. Fatty acid-binding proteins (FABPs) are among the primary intracellular trafficking mechanisms of endogenous cannabinoids, such as anandamide. To this end, changes in FA...

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Autores principales: Roeder, Nicole, Richardson, Brittany, Mihalkovic, Abrianna, Penman, Samantha, White, Olivia, Hamilton, John, Gupta, Ashim, Blum, Kenneth, Gold, Mark S., Thanos, Panayotis K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969817/
https://www.ncbi.nlm.nih.gov/pubmed/36864947
http://dx.doi.org/10.3390/futurepharmacol3010007
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author Roeder, Nicole
Richardson, Brittany
Mihalkovic, Abrianna
Penman, Samantha
White, Olivia
Hamilton, John
Gupta, Ashim
Blum, Kenneth
Gold, Mark S.
Thanos, Panayotis K.
author_facet Roeder, Nicole
Richardson, Brittany
Mihalkovic, Abrianna
Penman, Samantha
White, Olivia
Hamilton, John
Gupta, Ashim
Blum, Kenneth
Gold, Mark S.
Thanos, Panayotis K.
author_sort Roeder, Nicole
collection PubMed
description Emerging evidence indicates that the endogenous cannabinoid system modulates the behavioral and physiological effects of nicotine. Fatty acid-binding proteins (FABPs) are among the primary intracellular trafficking mechanisms of endogenous cannabinoids, such as anandamide. To this end, changes in FABP expression may similarly impact the behavioral manifestations associated with nicotine, particularly its addictive properties. FABP5(+/+) and FABP5(−/−) mice were tested for nicotine-conditioned place preference (CPP) at two different doses (0.1 or 0.5 mg/kg). The nicotine-paired chamber was assigned as their least preferred chamber during preconditioning. Following 8 days of conditioning, the mice were injected with either nicotine or saline. The mice were allowed to access to all the chambers on the test day, and their times spent in the drug chamber on the preconditioning versus the test days were used to examine the drug preference score. The CPP results showed that the FABP5(−/−) mice displayed a higher place preference for 0.1 mg/kg nicotine than the FABP5(+/+) mice, while no CPP difference was observed for 0.5 mg/kg nicotine between the genotypes. In conclusion, FABP5 plays an important role in regulating nicotine place preference. Further research is warranted to identify the precise mechanisms. The results suggest that dysregulated cannabinoid signaling may impact nicotine-seeking behavior.
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spelling pubmed-99698172023-03-01 Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms Roeder, Nicole Richardson, Brittany Mihalkovic, Abrianna Penman, Samantha White, Olivia Hamilton, John Gupta, Ashim Blum, Kenneth Gold, Mark S. Thanos, Panayotis K. Future Pharmacol Article Emerging evidence indicates that the endogenous cannabinoid system modulates the behavioral and physiological effects of nicotine. Fatty acid-binding proteins (FABPs) are among the primary intracellular trafficking mechanisms of endogenous cannabinoids, such as anandamide. To this end, changes in FABP expression may similarly impact the behavioral manifestations associated with nicotine, particularly its addictive properties. FABP5(+/+) and FABP5(−/−) mice were tested for nicotine-conditioned place preference (CPP) at two different doses (0.1 or 0.5 mg/kg). The nicotine-paired chamber was assigned as their least preferred chamber during preconditioning. Following 8 days of conditioning, the mice were injected with either nicotine or saline. The mice were allowed to access to all the chambers on the test day, and their times spent in the drug chamber on the preconditioning versus the test days were used to examine the drug preference score. The CPP results showed that the FABP5(−/−) mice displayed a higher place preference for 0.1 mg/kg nicotine than the FABP5(+/+) mice, while no CPP difference was observed for 0.5 mg/kg nicotine between the genotypes. In conclusion, FABP5 plays an important role in regulating nicotine place preference. Further research is warranted to identify the precise mechanisms. The results suggest that dysregulated cannabinoid signaling may impact nicotine-seeking behavior. 2023-03 2023-01-09 /pmc/articles/PMC9969817/ /pubmed/36864947 http://dx.doi.org/10.3390/futurepharmacol3010007 Text en https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Roeder, Nicole
Richardson, Brittany
Mihalkovic, Abrianna
Penman, Samantha
White, Olivia
Hamilton, John
Gupta, Ashim
Blum, Kenneth
Gold, Mark S.
Thanos, Panayotis K.
Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms
title Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms
title_full Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms
title_fullStr Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms
title_full_unstemmed Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms
title_short Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms
title_sort fatty acid-binding protein 5 gene deletion enhances nicotine-conditioned place preference: illuminating the putative gateway mechanisms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969817/
https://www.ncbi.nlm.nih.gov/pubmed/36864947
http://dx.doi.org/10.3390/futurepharmacol3010007
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