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A male mouse model of WIN 55,212–2 self-administration to study cannabinoid addiction

We have established for the first time a mouse model of cannabinoid addiction using WIN 55,212–2 intravenous self-administration (0.0125 mg/kg/infusion) in C57Bl/6J mice. This model allows to evaluate the addiction criteria by grouping them into 1) persistence of response during a period of non-avai...

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Autores principales: Cajiao-Manrique, María del Mar, Maldonado, Rafael, Martín-García, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083303/
https://www.ncbi.nlm.nih.gov/pubmed/37050910
http://dx.doi.org/10.3389/fphar.2023.1143365
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author Cajiao-Manrique, María del Mar
Maldonado, Rafael
Martín-García, Elena
author_facet Cajiao-Manrique, María del Mar
Maldonado, Rafael
Martín-García, Elena
author_sort Cajiao-Manrique, María del Mar
collection PubMed
description We have established for the first time a mouse model of cannabinoid addiction using WIN 55,212–2 intravenous self-administration (0.0125 mg/kg/infusion) in C57Bl/6J mice. This model allows to evaluate the addiction criteria by grouping them into 1) persistence of response during a period of non-availability of the drug, 2) motivation for WIN 55,212–2 with a progressive ratio, and 3) compulsivity when the reward is associated with a punishment such as an electric foot-shock, in agreement with the Diagnostic and Statistical Manual of Mental Disorders 5th edition (DSM-5). This model also allows to measure two parameters that have been related with the DSM-5 diagnostic criteria of craving, resistance to extinction and reinstatement, and two phenotypic traits suggested as predisposing factors, impulsivity and sensitivity to reward. We found that 35.6% of mice developed the criteria of cannabinoid addiction, allowing to differentiate between resilient and vulnerable mice. Therefore, we have established a novel and reliable model to study the neurobiological correlates underlying the resilience or vulnerability to develop cannabinoid addiction. This model included the chemogenetic inhibition of neuronal activity in the medial prefrontal cortex to the nucleus accumbens pathway to assess the neurobiological substrate of cannabinoid addiction. This model will shed light on the neurobiological substrate underlying cannabinoid addiction.
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spelling pubmed-100833032023-04-11 A male mouse model of WIN 55,212–2 self-administration to study cannabinoid addiction Cajiao-Manrique, María del Mar Maldonado, Rafael Martín-García, Elena Front Pharmacol Pharmacology We have established for the first time a mouse model of cannabinoid addiction using WIN 55,212–2 intravenous self-administration (0.0125 mg/kg/infusion) in C57Bl/6J mice. This model allows to evaluate the addiction criteria by grouping them into 1) persistence of response during a period of non-availability of the drug, 2) motivation for WIN 55,212–2 with a progressive ratio, and 3) compulsivity when the reward is associated with a punishment such as an electric foot-shock, in agreement with the Diagnostic and Statistical Manual of Mental Disorders 5th edition (DSM-5). This model also allows to measure two parameters that have been related with the DSM-5 diagnostic criteria of craving, resistance to extinction and reinstatement, and two phenotypic traits suggested as predisposing factors, impulsivity and sensitivity to reward. We found that 35.6% of mice developed the criteria of cannabinoid addiction, allowing to differentiate between resilient and vulnerable mice. Therefore, we have established a novel and reliable model to study the neurobiological correlates underlying the resilience or vulnerability to develop cannabinoid addiction. This model included the chemogenetic inhibition of neuronal activity in the medial prefrontal cortex to the nucleus accumbens pathway to assess the neurobiological substrate of cannabinoid addiction. This model will shed light on the neurobiological substrate underlying cannabinoid addiction. Frontiers Media S.A. 2023-03-27 /pmc/articles/PMC10083303/ /pubmed/37050910 http://dx.doi.org/10.3389/fphar.2023.1143365 Text en Copyright © 2023 Cajiao-Manrique, Maldonado and Martín-García. https://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
Cajiao-Manrique, María del Mar
Maldonado, Rafael
Martín-García, Elena
A male mouse model of WIN 55,212–2 self-administration to study cannabinoid addiction
title A male mouse model of WIN 55,212–2 self-administration to study cannabinoid addiction
title_full A male mouse model of WIN 55,212–2 self-administration to study cannabinoid addiction
title_fullStr A male mouse model of WIN 55,212–2 self-administration to study cannabinoid addiction
title_full_unstemmed A male mouse model of WIN 55,212–2 self-administration to study cannabinoid addiction
title_short A male mouse model of WIN 55,212–2 self-administration to study cannabinoid addiction
title_sort male mouse model of win 55,212–2 self-administration to study cannabinoid addiction
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083303/
https://www.ncbi.nlm.nih.gov/pubmed/37050910
http://dx.doi.org/10.3389/fphar.2023.1143365
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