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Sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus

There is general agreement that the central nervous system in rodents differs between sexes due to the presence of gonadal steroid hormone during differentiation. Sex differences in feeding seem to occur among species, and responses to fasting (i.e., starvation), gonadal steroids (i.e., testosterone...

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Autores principales: Fukushima, Atsushi, Hagiwara, Hiroko, Fujioka, Hitomi, Kimura, Fukuko, Akema, Tatsuo, Funabashi, Toshiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378303/
https://www.ncbi.nlm.nih.gov/pubmed/25870535
http://dx.doi.org/10.3389/fnins.2015.00088
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author Fukushima, Atsushi
Hagiwara, Hiroko
Fujioka, Hitomi
Kimura, Fukuko
Akema, Tatsuo
Funabashi, Toshiya
author_facet Fukushima, Atsushi
Hagiwara, Hiroko
Fujioka, Hitomi
Kimura, Fukuko
Akema, Tatsuo
Funabashi, Toshiya
author_sort Fukushima, Atsushi
collection PubMed
description There is general agreement that the central nervous system in rodents differs between sexes due to the presence of gonadal steroid hormone during differentiation. Sex differences in feeding seem to occur among species, and responses to fasting (i.e., starvation), gonadal steroids (i.e., testosterone and estradiol), and diet (i.e., western-style diet) vary significantly between sexes. The hypothalamus is the center for controlling feeding behavior. We examined the activation of feeding-related peptides in neurons in the hypothalamus. Phosphorylation of cyclic AMP response element-binding protein (CREB) is a good marker for neural activation, as is the Fos antigen. Therefore, we predicted that sex differences in the activity of melanin-concentrating hormone (MCH) neurons would be associated with feeding behavior. We determined the response of MCH neurons to glucose in the lateral hypothalamic area (LHA) and our results suggested MCH neurons play an important role in sex differences in feeding behavior. In addition, fasting increased the number of orexin neurons harboring phosphorylated CREB in female rats (regardless of the estrous day), but not male rats. Glucose injection decreased the number of these neurons with phosphorylated CREB in fasted female rats. Finally, under normal spontaneous food intake, MCH neurons, but not orexin neurons, expressed phosphorylated CREB. These sex differences in response to fasting and glucose, as well as under normal conditions, suggest a vulnerability to metabolic challenges in females.
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spelling pubmed-43783032015-04-13 Sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus Fukushima, Atsushi Hagiwara, Hiroko Fujioka, Hitomi Kimura, Fukuko Akema, Tatsuo Funabashi, Toshiya Front Neurosci Endocrinology There is general agreement that the central nervous system in rodents differs between sexes due to the presence of gonadal steroid hormone during differentiation. Sex differences in feeding seem to occur among species, and responses to fasting (i.e., starvation), gonadal steroids (i.e., testosterone and estradiol), and diet (i.e., western-style diet) vary significantly between sexes. The hypothalamus is the center for controlling feeding behavior. We examined the activation of feeding-related peptides in neurons in the hypothalamus. Phosphorylation of cyclic AMP response element-binding protein (CREB) is a good marker for neural activation, as is the Fos antigen. Therefore, we predicted that sex differences in the activity of melanin-concentrating hormone (MCH) neurons would be associated with feeding behavior. We determined the response of MCH neurons to glucose in the lateral hypothalamic area (LHA) and our results suggested MCH neurons play an important role in sex differences in feeding behavior. In addition, fasting increased the number of orexin neurons harboring phosphorylated CREB in female rats (regardless of the estrous day), but not male rats. Glucose injection decreased the number of these neurons with phosphorylated CREB in fasted female rats. Finally, under normal spontaneous food intake, MCH neurons, but not orexin neurons, expressed phosphorylated CREB. These sex differences in response to fasting and glucose, as well as under normal conditions, suggest a vulnerability to metabolic challenges in females. Frontiers Media S.A. 2015-03-30 /pmc/articles/PMC4378303/ /pubmed/25870535 http://dx.doi.org/10.3389/fnins.2015.00088 Text en Copyright © 2015 Fukushima, Hagiwara, Fujioka, Kimura, Akema and Funabashi. http://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) or licensor 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 Endocrinology
Fukushima, Atsushi
Hagiwara, Hiroko
Fujioka, Hitomi
Kimura, Fukuko
Akema, Tatsuo
Funabashi, Toshiya
Sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus
title Sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus
title_full Sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus
title_fullStr Sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus
title_full_unstemmed Sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus
title_short Sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus
title_sort sex differences in feeding behavior in rats: the relationship with neuronal activation in the hypothalamus
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378303/
https://www.ncbi.nlm.nih.gov/pubmed/25870535
http://dx.doi.org/10.3389/fnins.2015.00088
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