Maternal dietary patterns are associated with susceptibility to a depressive-like phenotype in rat offspring.


Journal

Developmental cognitive neuroscience
ISSN: 1878-9307
Titre abrégé: Dev Cogn Neurosci
Pays: Netherlands
ID NLM: 101541838

Informations de publication

Date de publication:
02 2021
Historique:
received: 27 05 2020
revised: 21 10 2020
accepted: 06 11 2020
pubmed: 25 11 2020
medline: 14 10 2021
entrez: 24 11 2020
Statut: ppublish

Résumé

Environmental factors such as maternal diet, determine the pathologies that appear early in life and can persist in adulthood. Maternally modified diets provided through pregnancy and lactation increase the predisposition of offspring to the development of many diseases, including obesity, diabetes, and neurodevelopmental and mental disorders such as depression. Fetal and early postnatal development are sensitive periods in the offspring's life in which maternal nutrition influences epigenetic modifications, which results in changes in gene expression and affects molecular phenotype. This study aimed to evaluate the impact of maternal modified types of diet, including a high-fat diet (HFD), high-carbohydrate diet (HCD) and mixed diet (MD) during pregnancy and lactation on phenotypic changes in rat offspring with respect to anhedonia, depressive- and anxiety-like behavior, memory impairment, and gene expression profile in the frontal cortex. Behavioral results indicate that maternal HFD provokes depressive-like behavior and molecular findings showed that HFD leads to persistent transcriptomics alterations. Moreover, a HFD significantly influences the expression of neuronal markers specific to excitatory and inhibitory cortical neurons. Collectively, these experiments highlight the complexity of the impact of maternal modified diet during fetal programming. Undoubtedly, maternal HFD affects brain development and our findings suggest that nutrition exerts significant changes in brain function that may be associated with depression.

Identifiants

pubmed: 33232913
pii: S1878-9293(20)30129-8
doi: 10.1016/j.dcn.2020.100879
pmc: PMC7691544
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

100879

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Kinga Gawlińska (K)

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Drug Addiction Pharmacology, 31-343, Kraków, Smętna Street 12, Poland.

Dawid Gawliński (D)

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Drug Addiction Pharmacology, 31-343, Kraków, Smętna Street 12, Poland.

Michał Korostyński (M)

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Molecular Neuropharmacology, 31-343, Kraków, Smętna Street 12, Poland.

Małgorzata Borczyk (M)

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Molecular Neuropharmacology, 31-343, Kraków, Smętna Street 12, Poland.

Małgorzata Frankowska (M)

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Drug Addiction Pharmacology, 31-343, Kraków, Smętna Street 12, Poland.

Marcin Piechota (M)

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Molecular Neuropharmacology, 31-343, Kraków, Smętna Street 12, Poland.

Małgorzata Filip (M)

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Drug Addiction Pharmacology, 31-343, Kraków, Smętna Street 12, Poland. Electronic address: mal.fil@if-pan.krakow.pl.

Edmund Przegaliński (E)

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Drug Addiction Pharmacology, 31-343, Kraków, Smętna Street 12, Poland.

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Classifications MeSH