Maternal high fat diet induces circadian clock-independent endocrine alterations impacting the metabolism of the offspring.
behavioral neuroscience
molecular neuroscience
neuroscience
omics
transcriptomics
Journal
iScience
ISSN: 2589-0042
Titre abrégé: iScience
Pays: United States
ID NLM: 101724038
Informations de publication
Date de publication:
19 Jul 2024
19 Jul 2024
Historique:
received:
24
11
2023
revised:
02
05
2024
accepted:
19
06
2024
medline:
24
7
2024
pubmed:
24
7
2024
entrez:
24
7
2024
Statut:
epublish
Résumé
Maternal obesity has long-term effects on offspring metabolic health. Among the potential mechanisms, prior research has indicated potential disruptions in circadian rhythms and gut microbiota in the offspring. To challenge this hypothesis, we implemented a maternal high fat diet regimen before and during pregnancy, followed by a standard diet after birth. Our findings confirm that maternal obesity impacts offspring birth weight and glucose and lipid metabolisms. However, we found minimal impact on circadian rhythms and microbiota that are predominantly driven by the feeding/fasting cycle. Notably, maternal obesity altered rhythmic liver gene expression, affecting mitochondrial function and inflammatory response without disrupting the hepatic circadian clock. These changes could be explained by a masculinization of liver gene expression similar to the changes observed in polycystic ovarian syndrome. Intriguingly, such alterations seem to provide the first-generation offspring with a degree of protection against obesity when exposed to a high fat diet.
Identifiants
pubmed: 39045103
doi: 10.1016/j.isci.2024.110343
pii: S2589-0042(24)01568-2
pmc: PMC11263959
doi:
Types de publication
Journal Article
Langues
eng
Pagination
110343Informations de copyright
© 2024 The Author(s).
Déclaration de conflit d'intérêts
Mark Morisson has received consultancy fees from Bayer Steigerwald Arzneimittelwerk (Bayer Consumer Health), Sanofi Australia, and Danone-Nutricia Australia, and serves on the science advisory board (non-remunerated) for GenieBiome, Hong Kong SAR. All other authors report no potential conflicts of interest.