Effects of sex and fasting/refeeding on hepatic AMPK signaling in chickens (Gallus gallus).


Journal

Comparative biochemistry and physiology. Part A, Molecular & integrative physiology
ISSN: 1531-4332
Titre abrégé: Comp Biochem Physiol A Mol Integr Physiol
Pays: United States
ID NLM: 9806096

Informations de publication

Date de publication:
02 2020
Historique:
received: 30 07 2019
revised: 10 10 2019
accepted: 18 10 2019
pubmed: 5 11 2019
medline: 3 2 2021
entrez: 3 11 2019
Statut: ppublish

Résumé

The alpha-1 isoform of chicken AMPK situates on the Z-chromosome, in contrast, the other isoforms in birds and the mammalian AMPKα1 are located on the autosomes. The present study aimed to investigate the role of hepatic AMPK signaling in adaptation to nutritional status and the potential sex-specific response in chickens. Hepatic genes and proteins were compared between the two sexes immediately after hatching. From 20d of age, chicks from each sex received feed treatments: Control was fed ad libitum; Fasted was starved for 24 h; Refed was fed for 4 h after a 24 h fasting. As a result, hepatic AMPKα1 mRNA level in males was significantly higher at both ages compared to females, due to the presence of Z-chromosomes. However, this did not make this kinase "male-bias" as it was eventually compensated at a translational level, which was not reported in previous studies. The protein levels and activation of AMPKα were even lower in newly-hatched male compared to female chicks, accompanied with a higher FAS and SREBP-1 gene expressions. Accordingly, hepatic G6PC2 mRNA levels in males were significantly lower associated with lower plasma glucose levels after hatching. Fasting activated hepatic AMPK, which in turn inhibited gene expression of GS, FAS and SREBP-1, and stimulated the downstream G6PC2 in both sexes. These changes recovered after refeeding. In conclusion, AMPK plays a role in adaptation to nutritional environment for both sexes. The Z-linked AMPK did not exert a sex-specific signaling, due to a "translational compensation" of AMPKα1.

Identifiants

pubmed: 31676410
pii: S1095-6433(19)30370-8
doi: 10.1016/j.cbpa.2019.110606
pii:
doi:

Substances chimiques

AMP-Activated Protein Kinases EC 2.7.11.31

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

110606

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Yufeng Wang (Y)

Laboratory of Livestock Physiology, Department of Biosystems, KU Leuven, Kasteelpark Arenberg 30, 3001 Leuven, Belgium.

Johan Buyse (J)

Laboratory of Livestock Physiology, Department of Biosystems, KU Leuven, Kasteelpark Arenberg 30, 3001 Leuven, Belgium. Electronic address: johan.buyse@kuleuven.be.

Nathalie Courousse (N)

BOA, INRA, Université de Tours, 37380 Nouzilly, France.

Sophie Tesseraud (S)

BOA, INRA, Université de Tours, 37380 Nouzilly, France.

Sonia Métayer-Coustard (S)

BOA, INRA, Université de Tours, 37380 Nouzilly, France.

Cécile Berri (C)

BOA, INRA, Université de Tours, 37380 Nouzilly, France.

Seline Schallier (S)

Laboratory of Livestock Physiology, Department of Biosystems, KU Leuven, Kasteelpark Arenberg 30, 3001 Leuven, Belgium.

Nadia Everaert (N)

Livestock and Nutrition Unit, Gembloux Agro-Bio Tech, TERRA Teaching and Research Centre, University of Liège, Passage des Déportés 2, 5030 Gembloux, Belgium.

Anne Collin (A)

BOA, INRA, Université de Tours, 37380 Nouzilly, France.

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Classifications MeSH