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Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food

Contemporary environments are saturated with food cues that stimulate appetites in the absence of hunger, which leads to maladaptive eating. These settings can induce persistent drive to eat, as learned behaviors can reappear after extinction. Behavioral paradigms of responding renewal provide a val...

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Autores principales: Anderson, Lauren C., Petrovich, Gorica D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797070/
https://www.ncbi.nlm.nih.gov/pubmed/29396448
http://dx.doi.org/10.1038/s41598-018-20553-4
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author Anderson, Lauren C.
Petrovich, Gorica D.
author_facet Anderson, Lauren C.
Petrovich, Gorica D.
author_sort Anderson, Lauren C.
collection PubMed
description Contemporary environments are saturated with food cues that stimulate appetites in the absence of hunger, which leads to maladaptive eating. These settings can induce persistent drive to eat, as learned behaviors can reappear after extinction. Behavioral paradigms of responding renewal provide a valuable framework to study how food cues contribute to the inability to resist palatable foods and change maladaptive eating habits. Using a rat model for this persistent food motivation, we determined sex differences in the causal function for the ventromedial prefrontal cortex (vmPFC) during context-mediated renewal of responding to food cues. Previously, we found behavioral sex differences (only males exhibited renewal) and differential recruitment within the vmPFC (increased Fos induction in males but decreased in females). Here, we used DREADDs (Designer Receptors Exclusively Activated by Designer Drugs) to silence vmPFC neurons in males and to stimulate vmPFC neurons in females specifically during renewal. Silencing vmPFC neurons in males disrupted renewal of responding to a food cue, while stimulating vmPFC neurons in females induced this behavior. These findings demonstrate sex differences in the vmPFC function in a model of food seeking relevant to environmentally driven appetites contributing to obesity and eating disorders.
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spelling pubmed-57970702018-02-12 Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food Anderson, Lauren C. Petrovich, Gorica D. Sci Rep Article Contemporary environments are saturated with food cues that stimulate appetites in the absence of hunger, which leads to maladaptive eating. These settings can induce persistent drive to eat, as learned behaviors can reappear after extinction. Behavioral paradigms of responding renewal provide a valuable framework to study how food cues contribute to the inability to resist palatable foods and change maladaptive eating habits. Using a rat model for this persistent food motivation, we determined sex differences in the causal function for the ventromedial prefrontal cortex (vmPFC) during context-mediated renewal of responding to food cues. Previously, we found behavioral sex differences (only males exhibited renewal) and differential recruitment within the vmPFC (increased Fos induction in males but decreased in females). Here, we used DREADDs (Designer Receptors Exclusively Activated by Designer Drugs) to silence vmPFC neurons in males and to stimulate vmPFC neurons in females specifically during renewal. Silencing vmPFC neurons in males disrupted renewal of responding to a food cue, while stimulating vmPFC neurons in females induced this behavior. These findings demonstrate sex differences in the vmPFC function in a model of food seeking relevant to environmentally driven appetites contributing to obesity and eating disorders. Nature Publishing Group UK 2018-02-02 /pmc/articles/PMC5797070/ /pubmed/29396448 http://dx.doi.org/10.1038/s41598-018-20553-4 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Anderson, Lauren C.
Petrovich, Gorica D.
Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food
title Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food
title_full Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food
title_fullStr Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food
title_full_unstemmed Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food
title_short Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food
title_sort ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797070/
https://www.ncbi.nlm.nih.gov/pubmed/29396448
http://dx.doi.org/10.1038/s41598-018-20553-4
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