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Sex Differences in Demand for Highly Palatable Foods: Role of the Orexin System

BACKGROUND: The prevalence of eating disorders, including binge eating disorder, is significantly higher in women. These findings are mirrored by preclinical studies, which indicate that female rats have a higher preference for palatable food and show greater binge-like eating compared with male rat...

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Autores principales: Freeman, Linnea R, Bentzley, Brandon S, James, Morgan H, Aston-Jones, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816693/
https://www.ncbi.nlm.nih.gov/pubmed/32496559
http://dx.doi.org/10.1093/ijnp/pyaa040
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author Freeman, Linnea R
Bentzley, Brandon S
James, Morgan H
Aston-Jones, Gary
author_facet Freeman, Linnea R
Bentzley, Brandon S
James, Morgan H
Aston-Jones, Gary
author_sort Freeman, Linnea R
collection PubMed
description BACKGROUND: The prevalence of eating disorders, including binge eating disorder, is significantly higher in women. These findings are mirrored by preclinical studies, which indicate that female rats have a higher preference for palatable food and show greater binge-like eating compared with male rats. METHODS: Here, we describe a novel within-session behavioral-economic paradigm that allows for the simultaneous measurement of the intake at null cost (Q(0)) and normalized demand elasticity (α) of 3 types of palatable food (low fat, high fat, and chocolate sucrose pellets) via demand curve analysis. In light of evidence that the orexin (hypocretin) system is critically involved in reward and feeding behaviors, we also examined the role of orexin function in sex differences of economic demand for palatable foods. RESULTS: The novel within-session behavioral-economic approach revealed that female rats have higher intake (demand) than males for all palatable foods at low cost (normalized to body weight) but no difference in intake at higher prices, indicating sex-dependent differences in the hedonic, but not motivational, aspects of palatable food. Immediately following behavioral-economic testing, we observed more orexin-expressing neurons and Fos expression (measure of recent neural activation) in these neurons in female rats compared with male rats. Moreover, the orexin-1 receptor antagonist SB334867 reduced both low- and high-cost intake for palatable food in both male and female rats. CONCLUSIONS: These findings provide evidence of higher demand at low prices for palatable food in females and indicate that these behavioral differences may be associated with sexual dimorphism in orexin system function.
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spelling pubmed-78166932021-01-26 Sex Differences in Demand for Highly Palatable Foods: Role of the Orexin System Freeman, Linnea R Bentzley, Brandon S James, Morgan H Aston-Jones, Gary Int J Neuropsychopharmacol Regular Research Articles BACKGROUND: The prevalence of eating disorders, including binge eating disorder, is significantly higher in women. These findings are mirrored by preclinical studies, which indicate that female rats have a higher preference for palatable food and show greater binge-like eating compared with male rats. METHODS: Here, we describe a novel within-session behavioral-economic paradigm that allows for the simultaneous measurement of the intake at null cost (Q(0)) and normalized demand elasticity (α) of 3 types of palatable food (low fat, high fat, and chocolate sucrose pellets) via demand curve analysis. In light of evidence that the orexin (hypocretin) system is critically involved in reward and feeding behaviors, we also examined the role of orexin function in sex differences of economic demand for palatable foods. RESULTS: The novel within-session behavioral-economic approach revealed that female rats have higher intake (demand) than males for all palatable foods at low cost (normalized to body weight) but no difference in intake at higher prices, indicating sex-dependent differences in the hedonic, but not motivational, aspects of palatable food. Immediately following behavioral-economic testing, we observed more orexin-expressing neurons and Fos expression (measure of recent neural activation) in these neurons in female rats compared with male rats. Moreover, the orexin-1 receptor antagonist SB334867 reduced both low- and high-cost intake for palatable food in both male and female rats. CONCLUSIONS: These findings provide evidence of higher demand at low prices for palatable food in females and indicate that these behavioral differences may be associated with sexual dimorphism in orexin system function. Oxford University Press 2020-06-04 /pmc/articles/PMC7816693/ /pubmed/32496559 http://dx.doi.org/10.1093/ijnp/pyaa040 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Research Articles
Freeman, Linnea R
Bentzley, Brandon S
James, Morgan H
Aston-Jones, Gary
Sex Differences in Demand for Highly Palatable Foods: Role of the Orexin System
title Sex Differences in Demand for Highly Palatable Foods: Role of the Orexin System
title_full Sex Differences in Demand for Highly Palatable Foods: Role of the Orexin System
title_fullStr Sex Differences in Demand for Highly Palatable Foods: Role of the Orexin System
title_full_unstemmed Sex Differences in Demand for Highly Palatable Foods: Role of the Orexin System
title_short Sex Differences in Demand for Highly Palatable Foods: Role of the Orexin System
title_sort sex differences in demand for highly palatable foods: role of the orexin system
topic Regular Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816693/
https://www.ncbi.nlm.nih.gov/pubmed/32496559
http://dx.doi.org/10.1093/ijnp/pyaa040
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