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Sex and estrogens alter the action of glucagon-like peptide-1 on reward
BACKGROUND: Feeding behavior is regulated through an intricate array of anorexic and orexigenic hormones acting on the central nervous system (CNS). Some of these hormones may have differential effects in males and females, effects potentially attributed to actions of gonadal steroids, especially es...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715328/ https://www.ncbi.nlm.nih.gov/pubmed/26779332 http://dx.doi.org/10.1186/s13293-016-0059-9 |
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author | Richard, Jennifer E. Anderberg, Rozita H. López-Ferreras, Lorena Olandersson, Kajsa Skibicka, Karolina P. |
author_facet | Richard, Jennifer E. Anderberg, Rozita H. López-Ferreras, Lorena Olandersson, Kajsa Skibicka, Karolina P. |
author_sort | Richard, Jennifer E. |
collection | PubMed |
description | BACKGROUND: Feeding behavior is regulated through an intricate array of anorexic and orexigenic hormones acting on the central nervous system (CNS). Some of these hormones may have differential effects in males and females, effects potentially attributed to actions of gonadal steroids, especially estrogens. Central stimulation of the glucagon-like peptide-1 (GLP-1) receptors reduces feeding and food-reward behavior by acting on CNS regions important for the anorexic actions of estrogens. Thus, we propose that the action of GLP-1 on food intake and reward may differ between sexes. METHODS: Male and female rats were centrally injected with the GLP-1 analog exendin-4 (Ex4) in a non-deprived or food-restricted state; reward behavior was measured in a progressive ratio operant conditioning task. Intake of chow and palatable food were also measured. To determine if sex differences in the actions of Ex4 are due to interactions with estrogens, Ex4 treatment was preceded by treatment with a nonselective estrogen receptor-α (ERα) and ERβ or ERα-selective antagonist. RESULTS: Central injection of Ex4 revealed increased reward behavior suppression in females, compared to males, in the operant conditioning task. This increase was present in both non-deprived and food-restricted animals with larger differences in the fed state. Intake of chow and palatable food, after Ex4, were similar in males and females. Food reward, but not food intake, effect of Ex4 was attenuated by pretreatment with ER antagonist in both sexes, suggesting that estrogens may modulate effects of Ex4 in both sexes. Furthermore, central pretreatment with ERα-selective antagonist was sufficient to attenuate effects of Ex4 on reward. CONCLUSIONS: Collectively, these data reveal that females display much higher sensitivity to the food reward impact of central GLP-1 receptor activation. Surprisingly, they also demonstrate that central ERα signaling is necessary for the actions of GLP-1 on food-reward behavior in both sexes. |
format | Online Article Text |
id | pubmed-4715328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47153282016-01-17 Sex and estrogens alter the action of glucagon-like peptide-1 on reward Richard, Jennifer E. Anderberg, Rozita H. López-Ferreras, Lorena Olandersson, Kajsa Skibicka, Karolina P. Biol Sex Differ Research BACKGROUND: Feeding behavior is regulated through an intricate array of anorexic and orexigenic hormones acting on the central nervous system (CNS). Some of these hormones may have differential effects in males and females, effects potentially attributed to actions of gonadal steroids, especially estrogens. Central stimulation of the glucagon-like peptide-1 (GLP-1) receptors reduces feeding and food-reward behavior by acting on CNS regions important for the anorexic actions of estrogens. Thus, we propose that the action of GLP-1 on food intake and reward may differ between sexes. METHODS: Male and female rats were centrally injected with the GLP-1 analog exendin-4 (Ex4) in a non-deprived or food-restricted state; reward behavior was measured in a progressive ratio operant conditioning task. Intake of chow and palatable food were also measured. To determine if sex differences in the actions of Ex4 are due to interactions with estrogens, Ex4 treatment was preceded by treatment with a nonselective estrogen receptor-α (ERα) and ERβ or ERα-selective antagonist. RESULTS: Central injection of Ex4 revealed increased reward behavior suppression in females, compared to males, in the operant conditioning task. This increase was present in both non-deprived and food-restricted animals with larger differences in the fed state. Intake of chow and palatable food, after Ex4, were similar in males and females. Food reward, but not food intake, effect of Ex4 was attenuated by pretreatment with ER antagonist in both sexes, suggesting that estrogens may modulate effects of Ex4 in both sexes. Furthermore, central pretreatment with ERα-selective antagonist was sufficient to attenuate effects of Ex4 on reward. CONCLUSIONS: Collectively, these data reveal that females display much higher sensitivity to the food reward impact of central GLP-1 receptor activation. Surprisingly, they also demonstrate that central ERα signaling is necessary for the actions of GLP-1 on food-reward behavior in both sexes. BioMed Central 2016-01-16 /pmc/articles/PMC4715328/ /pubmed/26779332 http://dx.doi.org/10.1186/s13293-016-0059-9 Text en © Richard et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Richard, Jennifer E. Anderberg, Rozita H. López-Ferreras, Lorena Olandersson, Kajsa Skibicka, Karolina P. Sex and estrogens alter the action of glucagon-like peptide-1 on reward |
title | Sex and estrogens alter the action of glucagon-like peptide-1 on reward |
title_full | Sex and estrogens alter the action of glucagon-like peptide-1 on reward |
title_fullStr | Sex and estrogens alter the action of glucagon-like peptide-1 on reward |
title_full_unstemmed | Sex and estrogens alter the action of glucagon-like peptide-1 on reward |
title_short | Sex and estrogens alter the action of glucagon-like peptide-1 on reward |
title_sort | sex and estrogens alter the action of glucagon-like peptide-1 on reward |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715328/ https://www.ncbi.nlm.nih.gov/pubmed/26779332 http://dx.doi.org/10.1186/s13293-016-0059-9 |
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