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


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
23 Apr 2022
Historique:
received: 31 03 2022
revised: 20 04 2022
accepted: 21 04 2022
entrez: 14 5 2022
pubmed: 15 5 2022
medline: 18 5 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 35563069
pii: ijms23094679
doi: 10.3390/ijms23094679
pmc: PMC9101627
pii:
doi:

Substances chimiques

Insulin 0
Orexins 0
Insulin-Like Growth Factor I 67763-96-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Biomedical Research Networking Center on Neurodegenerative Diseases
ID : PIE14/00061
Organisme : Ministerio de ciencia e innovación. Agencia estatal de investigación
ID : PID2019-104376RB-I00
Organisme : Comunidad de Madrid
ID : B2017/BMD-3700

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Auteurs

Jaime Pignatelli (J)

Cajal Institute-CSIC, 28002 Madrid, Spain.
CIBERNED, 28029 Madrid, Spain.

M Estrella Fernandez de Sevilla (MEF)

Cajal Institute-CSIC, 28002 Madrid, Spain.
CIBERNED, 28029 Madrid, Spain.
Medicine Faculty, Autonoma University, 28049 Madrid, Spain.

Jacob Sperber (J)

Cajal Institute-CSIC, 28002 Madrid, Spain.

Daniel Horrillo (D)

Department of Basic Sciences of Health, Area of Biochemistry and Molecular Biology, LAFEMEX Lab, University Rey Juan Carlos, 28933 Madrid, Spain.

Gema Medina-Gomez (G)

Department of Basic Sciences of Health, Area of Biochemistry and Molecular Biology, LAFEMEX Lab, University Rey Juan Carlos, 28933 Madrid, Spain.

Ignacio Torres Aleman (IT)

CIBERNED, 28029 Madrid, Spain.
Achucarro Basque Neuroscience Center, 48940 Leioa, Spain.
Ikerbasque Foundation for Science, 48009 Bilbao, Spain.

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Classifications MeSH