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Female mice are more prone to develop an addictive-like phenotype for sugar consumption

The concept of “sugar addiction” is gaining increasing attention in both the lay media and scientific literature. However, the concept of sugar addiction is controversial and only a few studies to date have attempted to determine the “addictive” properties of sugar using rigorous scientific criteria...

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Autores principales: Wei, Shoupeng, Hertle, Sarah, Spanagel, Rainer, Bilbao, Ainhoa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016940/
https://www.ncbi.nlm.nih.gov/pubmed/33795734
http://dx.doi.org/10.1038/s41598-021-86797-9
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author Wei, Shoupeng
Hertle, Sarah
Spanagel, Rainer
Bilbao, Ainhoa
author_facet Wei, Shoupeng
Hertle, Sarah
Spanagel, Rainer
Bilbao, Ainhoa
author_sort Wei, Shoupeng
collection PubMed
description The concept of “sugar addiction” is gaining increasing attention in both the lay media and scientific literature. However, the concept of sugar addiction is controversial and only a few studies to date have attempted to determine the “addictive” properties of sugar using rigorous scientific criteria. Here we set out to systematically test the addictive properties of sugar in male and female mice using established paradigms and models from the drug addiction field. Male and female C57BL/6N (8–10 weeks old) were evaluated in 4 experimental procedures to study the addictive properties of sugar: (i) a drinking in the dark (DID) procedure to model sugar binging; (ii) a long-term free choice home cage drinking procedure measuring the sugar deprivation effect (SDE) following an abstinence phase; (iii) a long-term operant sugar self-administration with persistence, motivation and compulsivity measures and (iv) intracranial self-stimulation (ICSS). Female mice were more vulnerable to the addictive properties of sugar than male mice, showing higher binge and long-term, excessive drinking, a more pronounced relapse-like drinking following deprivation, and higher persistence and motivation for sugar. No sex differences were seen in a compulsivity test or reward sensitivity measured using ICSS following extended sugar consumption. This study demonstrates the occurrence of an addictive-like phenotype for sugar in male and female mice, similar to drugs of abuse, and suggests sex-dependent differences in the development of sugar addiction.
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spelling pubmed-80169402021-04-05 Female mice are more prone to develop an addictive-like phenotype for sugar consumption Wei, Shoupeng Hertle, Sarah Spanagel, Rainer Bilbao, Ainhoa Sci Rep Article The concept of “sugar addiction” is gaining increasing attention in both the lay media and scientific literature. However, the concept of sugar addiction is controversial and only a few studies to date have attempted to determine the “addictive” properties of sugar using rigorous scientific criteria. Here we set out to systematically test the addictive properties of sugar in male and female mice using established paradigms and models from the drug addiction field. Male and female C57BL/6N (8–10 weeks old) were evaluated in 4 experimental procedures to study the addictive properties of sugar: (i) a drinking in the dark (DID) procedure to model sugar binging; (ii) a long-term free choice home cage drinking procedure measuring the sugar deprivation effect (SDE) following an abstinence phase; (iii) a long-term operant sugar self-administration with persistence, motivation and compulsivity measures and (iv) intracranial self-stimulation (ICSS). Female mice were more vulnerable to the addictive properties of sugar than male mice, showing higher binge and long-term, excessive drinking, a more pronounced relapse-like drinking following deprivation, and higher persistence and motivation for sugar. No sex differences were seen in a compulsivity test or reward sensitivity measured using ICSS following extended sugar consumption. This study demonstrates the occurrence of an addictive-like phenotype for sugar in male and female mice, similar to drugs of abuse, and suggests sex-dependent differences in the development of sugar addiction. Nature Publishing Group UK 2021-04-01 /pmc/articles/PMC8016940/ /pubmed/33795734 http://dx.doi.org/10.1038/s41598-021-86797-9 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wei, Shoupeng
Hertle, Sarah
Spanagel, Rainer
Bilbao, Ainhoa
Female mice are more prone to develop an addictive-like phenotype for sugar consumption
title Female mice are more prone to develop an addictive-like phenotype for sugar consumption
title_full Female mice are more prone to develop an addictive-like phenotype for sugar consumption
title_fullStr Female mice are more prone to develop an addictive-like phenotype for sugar consumption
title_full_unstemmed Female mice are more prone to develop an addictive-like phenotype for sugar consumption
title_short Female mice are more prone to develop an addictive-like phenotype for sugar consumption
title_sort female mice are more prone to develop an addictive-like phenotype for sugar consumption
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016940/
https://www.ncbi.nlm.nih.gov/pubmed/33795734
http://dx.doi.org/10.1038/s41598-021-86797-9
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