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Insulin-like Growth Factor I Couples Metabolism with Circadian Activity through Hypothalamic Orexin Neurons

Uncoupling of metabolism and circadian activity is associated with an increased risk of a wide spectrum of pathologies. Recently, insulin and the closely related insulin-like growth factor I (IGF-I) were shown to entrain feeding patterns with circadian rhythms. Both hormones act centrally to modulat...

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Autores principales: Pignatelli, Jaime, de Sevilla, M. Estrella Fernandez, Sperber, Jacob, Horrillo, Daniel, Medina-Gomez, Gema, Aleman, Ignacio Torres
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101627/
https://www.ncbi.nlm.nih.gov/pubmed/35563069
http://dx.doi.org/10.3390/ijms23094679
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author Pignatelli, Jaime
de Sevilla, M. Estrella Fernandez
Sperber, Jacob
Horrillo, Daniel
Medina-Gomez, Gema
Aleman, Ignacio Torres
author_facet Pignatelli, Jaime
de Sevilla, M. Estrella Fernandez
Sperber, Jacob
Horrillo, Daniel
Medina-Gomez, Gema
Aleman, Ignacio Torres
author_sort Pignatelli, Jaime
collection PubMed
description Uncoupling of metabolism and circadian activity is associated with an increased risk of a wide spectrum of pathologies. Recently, insulin and the closely related insulin-like growth factor I (IGF-I) were shown to entrain feeding patterns with circadian rhythms. Both hormones act centrally to modulate peripheral glucose metabolism; however, whereas central targets of insulin actions are intensely scrutinized, those mediating the actions of IGF-I remain less defined. We recently showed that IGF-I targets orexin neurons in the lateral hypothalamus, and now we evaluated whether IGF-I modulates orexin neurons to align circadian rhythms with metabolism. Mice with disrupted IGF-IR activity in orexin neurons (Firoc mice) showed sexually dimorphic alterations in daily glucose rhythms and feeding activity patterns which preceded the appearance of metabolic disturbances. Thus, Firoc males developed hyperglycemia and glucose intolerance, while females developed obesity. Since IGF-I directly modulates orexin levels and hepatic expression of KLF genes involved in circadian and metabolic entrainment in an orexin-dependent manner, it seems that IGF-I entrains metabolism and circadian rhythms by modulating the activity of orexin neurons.
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spelling pubmed-91016272022-05-14 Insulin-like Growth Factor I Couples Metabolism with Circadian Activity through Hypothalamic Orexin Neurons Pignatelli, Jaime de Sevilla, M. Estrella Fernandez Sperber, Jacob Horrillo, Daniel Medina-Gomez, Gema Aleman, Ignacio Torres Int J Mol Sci Article Uncoupling of metabolism and circadian activity is associated with an increased risk of a wide spectrum of pathologies. Recently, insulin and the closely related insulin-like growth factor I (IGF-I) were shown to entrain feeding patterns with circadian rhythms. Both hormones act centrally to modulate peripheral glucose metabolism; however, whereas central targets of insulin actions are intensely scrutinized, those mediating the actions of IGF-I remain less defined. We recently showed that IGF-I targets orexin neurons in the lateral hypothalamus, and now we evaluated whether IGF-I modulates orexin neurons to align circadian rhythms with metabolism. Mice with disrupted IGF-IR activity in orexin neurons (Firoc mice) showed sexually dimorphic alterations in daily glucose rhythms and feeding activity patterns which preceded the appearance of metabolic disturbances. Thus, Firoc males developed hyperglycemia and glucose intolerance, while females developed obesity. Since IGF-I directly modulates orexin levels and hepatic expression of KLF genes involved in circadian and metabolic entrainment in an orexin-dependent manner, it seems that IGF-I entrains metabolism and circadian rhythms by modulating the activity of orexin neurons. MDPI 2022-04-23 /pmc/articles/PMC9101627/ /pubmed/35563069 http://dx.doi.org/10.3390/ijms23094679 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pignatelli, Jaime
de Sevilla, M. Estrella Fernandez
Sperber, Jacob
Horrillo, Daniel
Medina-Gomez, Gema
Aleman, Ignacio Torres
Insulin-like Growth Factor I Couples Metabolism with Circadian Activity through Hypothalamic Orexin Neurons
title Insulin-like Growth Factor I Couples Metabolism with Circadian Activity through Hypothalamic Orexin Neurons
title_full Insulin-like Growth Factor I Couples Metabolism with Circadian Activity through Hypothalamic Orexin Neurons
title_fullStr Insulin-like Growth Factor I Couples Metabolism with Circadian Activity through Hypothalamic Orexin Neurons
title_full_unstemmed Insulin-like Growth Factor I Couples Metabolism with Circadian Activity through Hypothalamic Orexin Neurons
title_short Insulin-like Growth Factor I Couples Metabolism with Circadian Activity through Hypothalamic Orexin Neurons
title_sort insulin-like growth factor i couples metabolism with circadian activity through hypothalamic orexin neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101627/
https://www.ncbi.nlm.nih.gov/pubmed/35563069
http://dx.doi.org/10.3390/ijms23094679
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