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Reinforcement History Dependent Effects of Low Dose Ethanol on Reward Motivation in Male and Female Mice

Alcohol use disorders (AUDs) are more prevalent in men than in women, though AUD diagnoses in women are growing rapidly, making an understanding of sex differences in alcohol-related behaviors increasingly important. The development of AUDs involves the transition from casual, low levels of alcohol...

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Autores principales: Bryant, Kathleen G., Singh, Binay, Barker, Jacqueline M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036521/
https://www.ncbi.nlm.nih.gov/pubmed/35481242
http://dx.doi.org/10.3389/fnbeh.2022.875890
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author Bryant, Kathleen G.
Singh, Binay
Barker, Jacqueline M.
author_facet Bryant, Kathleen G.
Singh, Binay
Barker, Jacqueline M.
author_sort Bryant, Kathleen G.
collection PubMed
description Alcohol use disorders (AUDs) are more prevalent in men than in women, though AUD diagnoses in women are growing rapidly, making an understanding of sex differences in alcohol-related behaviors increasingly important. The development of AUDs involves the transition from casual, low levels of alcohol drinking to higher, maladaptive levels. The ability of low dose alcohol to drive reward and drug seeking may differ in males and females, and this could underlie differences in susceptibility to AUD. In this study we sought to determine whether a history of chronic, low dose ethanol exposure (0.5 g/kg; i.p.) could drive sucrose reward seeking and motivation, and whether this differed between male and female mice. Adult mice were trained to lever press for a liquid sucrose reward on two reinforcement schedules: a random interval (RI) schedule and a variable ratio (VR) schedule. After training, mice were tested on each of these levers for reward motivation using a progressive ratio test. We found that a history of low dose ethanol exposure increased sucrose reward motivation in male mice, but only on the RI lever and only when exposure occurred proximal to learning. Female mice were more motivated for sucrose on the RI lever than the VR lever regardless of ethanol exposure condition. These findings indicate that training on different reinforcement schedules affects reward motivation. Further, we show that males are more susceptible to the effects of low dose ethanol on sucrose reward motivation than females. These data broaden our understanding of sex differences in reward seeking as a result of ethanol exposure.
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spelling pubmed-90365212022-04-26 Reinforcement History Dependent Effects of Low Dose Ethanol on Reward Motivation in Male and Female Mice Bryant, Kathleen G. Singh, Binay Barker, Jacqueline M. Front Behav Neurosci Neuroscience Alcohol use disorders (AUDs) are more prevalent in men than in women, though AUD diagnoses in women are growing rapidly, making an understanding of sex differences in alcohol-related behaviors increasingly important. The development of AUDs involves the transition from casual, low levels of alcohol drinking to higher, maladaptive levels. The ability of low dose alcohol to drive reward and drug seeking may differ in males and females, and this could underlie differences in susceptibility to AUD. In this study we sought to determine whether a history of chronic, low dose ethanol exposure (0.5 g/kg; i.p.) could drive sucrose reward seeking and motivation, and whether this differed between male and female mice. Adult mice were trained to lever press for a liquid sucrose reward on two reinforcement schedules: a random interval (RI) schedule and a variable ratio (VR) schedule. After training, mice were tested on each of these levers for reward motivation using a progressive ratio test. We found that a history of low dose ethanol exposure increased sucrose reward motivation in male mice, but only on the RI lever and only when exposure occurred proximal to learning. Female mice were more motivated for sucrose on the RI lever than the VR lever regardless of ethanol exposure condition. These findings indicate that training on different reinforcement schedules affects reward motivation. Further, we show that males are more susceptible to the effects of low dose ethanol on sucrose reward motivation than females. These data broaden our understanding of sex differences in reward seeking as a result of ethanol exposure. Frontiers Media S.A. 2022-04-11 /pmc/articles/PMC9036521/ /pubmed/35481242 http://dx.doi.org/10.3389/fnbeh.2022.875890 Text en Copyright © 2022 Bryant, Singh and Barker. 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 Neuroscience
Bryant, Kathleen G.
Singh, Binay
Barker, Jacqueline M.
Reinforcement History Dependent Effects of Low Dose Ethanol on Reward Motivation in Male and Female Mice
title Reinforcement History Dependent Effects of Low Dose Ethanol on Reward Motivation in Male and Female Mice
title_full Reinforcement History Dependent Effects of Low Dose Ethanol on Reward Motivation in Male and Female Mice
title_fullStr Reinforcement History Dependent Effects of Low Dose Ethanol on Reward Motivation in Male and Female Mice
title_full_unstemmed Reinforcement History Dependent Effects of Low Dose Ethanol on Reward Motivation in Male and Female Mice
title_short Reinforcement History Dependent Effects of Low Dose Ethanol on Reward Motivation in Male and Female Mice
title_sort reinforcement history dependent effects of low dose ethanol on reward motivation in male and female mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036521/
https://www.ncbi.nlm.nih.gov/pubmed/35481242
http://dx.doi.org/10.3389/fnbeh.2022.875890
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