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Breaking It Down: Investigation of Binge Eating Components in Animal Models to Enhance Translation
Binge eating (BE) is a core eating disorder behavior that is present across nearly all eating disorder diagnoses (e. g., bulimia nervosa, binge eating disorder, anorexia nervosa binge/purge subtype), and is also widely present in the general population. Despite the prevalence of BE, limited treatmen...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414642/ https://www.ncbi.nlm.nih.gov/pubmed/34484010 http://dx.doi.org/10.3389/fpsyt.2021.728535 |
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author | Hildebrandt, Britny A. Ahmari, Susanne E. |
author_facet | Hildebrandt, Britny A. Ahmari, Susanne E. |
author_sort | Hildebrandt, Britny A. |
collection | PubMed |
description | Binge eating (BE) is a core eating disorder behavior that is present across nearly all eating disorder diagnoses (e. g., bulimia nervosa, binge eating disorder, anorexia nervosa binge/purge subtype), and is also widely present in the general population. Despite the prevalence of BE, limited treatment options exist and there are often high rates of relapse after treatment. There is evidence showing that genetic factors contribute to the heritability of BE and support for biological contributions to BE. However, more work is needed to fully understand neurobiological mechanisms underlying BE. One approach to target this problem is to separate BE into its distinct clinical components that can be more easily modeled using pre-clinical approaches. To date, a variety of animal models for BE have been used in pre-clinical studies; but there have been challenges translating this work to human BE. Here, we review these pre-clinical approaches by breaking them down into three clinically-significant component parts (1) consumption of a large amount of food; (2) food consumption within a short period of time; and (3) loss of control over eating. We propose that this rubric identifies the most frequently used and effective ways to model components of BE behavior using pre-clinical approaches with the strongest clinical relevance. Finally, we discuss how current pre-clinical models have been integrated with techniques using targeted neurobiological approaches and propose ways to improve translation of pre-clinical work to human investigations of BE that could enhance our understanding of BE behavior. |
format | Online Article Text |
id | pubmed-8414642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84146422021-09-04 Breaking It Down: Investigation of Binge Eating Components in Animal Models to Enhance Translation Hildebrandt, Britny A. Ahmari, Susanne E. Front Psychiatry Psychiatry Binge eating (BE) is a core eating disorder behavior that is present across nearly all eating disorder diagnoses (e. g., bulimia nervosa, binge eating disorder, anorexia nervosa binge/purge subtype), and is also widely present in the general population. Despite the prevalence of BE, limited treatment options exist and there are often high rates of relapse after treatment. There is evidence showing that genetic factors contribute to the heritability of BE and support for biological contributions to BE. However, more work is needed to fully understand neurobiological mechanisms underlying BE. One approach to target this problem is to separate BE into its distinct clinical components that can be more easily modeled using pre-clinical approaches. To date, a variety of animal models for BE have been used in pre-clinical studies; but there have been challenges translating this work to human BE. Here, we review these pre-clinical approaches by breaking them down into three clinically-significant component parts (1) consumption of a large amount of food; (2) food consumption within a short period of time; and (3) loss of control over eating. We propose that this rubric identifies the most frequently used and effective ways to model components of BE behavior using pre-clinical approaches with the strongest clinical relevance. Finally, we discuss how current pre-clinical models have been integrated with techniques using targeted neurobiological approaches and propose ways to improve translation of pre-clinical work to human investigations of BE that could enhance our understanding of BE behavior. Frontiers Media S.A. 2021-08-13 /pmc/articles/PMC8414642/ /pubmed/34484010 http://dx.doi.org/10.3389/fpsyt.2021.728535 Text en Copyright © 2021 Hildebrandt and Ahmari. 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 | Psychiatry Hildebrandt, Britny A. Ahmari, Susanne E. Breaking It Down: Investigation of Binge Eating Components in Animal Models to Enhance Translation |
title | Breaking It Down: Investigation of Binge Eating Components in Animal Models to Enhance Translation |
title_full | Breaking It Down: Investigation of Binge Eating Components in Animal Models to Enhance Translation |
title_fullStr | Breaking It Down: Investigation of Binge Eating Components in Animal Models to Enhance Translation |
title_full_unstemmed | Breaking It Down: Investigation of Binge Eating Components in Animal Models to Enhance Translation |
title_short | Breaking It Down: Investigation of Binge Eating Components in Animal Models to Enhance Translation |
title_sort | breaking it down: investigation of binge eating components in animal models to enhance translation |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414642/ https://www.ncbi.nlm.nih.gov/pubmed/34484010 http://dx.doi.org/10.3389/fpsyt.2021.728535 |
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