Face validity of a pre‐clinical model of operant binge drinking: just a question of speed

Binge drinking (BD) is often defined as a large amount of alcohol consumed in a ‘short’ period of time or ‘per occasion’. In clinical research, few researchers have included the notion of ‘speed of drinking’ in the definition of BD. Here, we aimed to describe a novel pre‐clinical model based on volu...

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Veröffentlicht in:Addiction biology 2019-07, Vol.24 (4), p.664-675
Hauptverfasser: Jeanblanc, Jérôme, Sauton, Pierre, Jeanblanc, Virginie, Legastelois, Rémi, Echeverry‐Alzate, Victor, Lebourgeois, Sophie, Gonzalez‐Marin, Maria, Naassila, Mickaël
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container_end_page 675
container_issue 4
container_start_page 664
container_title Addiction biology
container_volume 24
creator Jeanblanc, Jérôme
Sauton, Pierre
Jeanblanc, Virginie
Legastelois, Rémi
Echeverry‐Alzate, Victor
Lebourgeois, Sophie
Gonzalez‐Marin, Maria
Naassila, Mickaël
description Binge drinking (BD) is often defined as a large amount of alcohol consumed in a ‘short’ period of time or ‘per occasion’. In clinical research, few researchers have included the notion of ‘speed of drinking’ in the definition of BD. Here, we aimed to describe a novel pre‐clinical model based on voluntary operant BD, which included both the quantity of alcohol and the rapidity of consumption. In adult Long–Evans male rats, we induced BD by regularly decreasing the duration of ethanol self‐administration from 1‐hour to 15‐minute sessions. We compared the behavioral consequences of BD with the behaviors of rats subjected to moderate drinking or heavy drinking (HD). We found that, despite high ethanol consumption levels (1.2 g/kg/15 minutes), the total amounts consumed were insufficient to differentiate HD from BD. However, consumption speed could distinguish between these groups. The motivation to consume was higher in BD than in HD rats. After BD, we observed alterations in locomotor coordination in rats that consumed greater than 0.8 g/kg, which was rarely observed in HD rats. Finally, chronic BD led to worse performance in a decision‐making task, and as expected, we observed a lower stimulated dopaminergic release within nucleus accumbens slices in poor decision makers. Our BD model exhibited good face validity and can now provide animals voluntarily consuming very rapidly enough alcohol to achieve intoxication levels and thus allowing the study of the complex interaction between individual and environmental factors underlying BD behavior. We developed an animal model of binge drinking behavior using an operant paradigm in which rats consume voluntarily more than 1 g/kg of pure ethanol in 15 min sessions. We demonstrated that the speed of consumption is, in addition to the quantity, the key factor leading to physical signs of intoxication. We also demonstrated the face validity of this model by showing that chronic operant binge drinking induces cognitive functions deficits such as decision making processes.
doi_str_mv 10.1111/adb.12631
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In clinical research, few researchers have included the notion of ‘speed of drinking’ in the definition of BD. Here, we aimed to describe a novel pre‐clinical model based on voluntary operant BD, which included both the quantity of alcohol and the rapidity of consumption. In adult Long–Evans male rats, we induced BD by regularly decreasing the duration of ethanol self‐administration from 1‐hour to 15‐minute sessions. We compared the behavioral consequences of BD with the behaviors of rats subjected to moderate drinking or heavy drinking (HD). We found that, despite high ethanol consumption levels (1.2 g/kg/15 minutes), the total amounts consumed were insufficient to differentiate HD from BD. However, consumption speed could distinguish between these groups. The motivation to consume was higher in BD than in HD rats. After BD, we observed alterations in locomotor coordination in rats that consumed greater than 0.8 g/kg, which was rarely observed in HD rats. Finally, chronic BD led to worse performance in a decision‐making task, and as expected, we observed a lower stimulated dopaminergic release within nucleus accumbens slices in poor decision makers. Our BD model exhibited good face validity and can now provide animals voluntarily consuming very rapidly enough alcohol to achieve intoxication levels and thus allowing the study of the complex interaction between individual and environmental factors underlying BD behavior. We developed an animal model of binge drinking behavior using an operant paradigm in which rats consume voluntarily more than 1 g/kg of pure ethanol in 15 min sessions. We demonstrated that the speed of consumption is, in addition to the quantity, the key factor leading to physical signs of intoxication. 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Finally, chronic BD led to worse performance in a decision‐making task, and as expected, we observed a lower stimulated dopaminergic release within nucleus accumbens slices in poor decision makers. Our BD model exhibited good face validity and can now provide animals voluntarily consuming very rapidly enough alcohol to achieve intoxication levels and thus allowing the study of the complex interaction between individual and environmental factors underlying BD behavior. We developed an animal model of binge drinking behavior using an operant paradigm in which rats consume voluntarily more than 1 g/kg of pure ethanol in 15 min sessions. We demonstrated that the speed of consumption is, in addition to the quantity, the key factor leading to physical signs of intoxication. 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subjects Alcohol
animal model
binge drinking
Decision making
Dopamine receptors
Drinking behavior
Environmental factors
Ethanol
fast cyclic voltammetry
Intoxication
Life Sciences
Mental task performance
Motivation
Nucleus accumbens
Operant conditioning
operant self‐administration
title Face validity of a pre‐clinical model of operant binge drinking: just a question of speed
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