Impacts of the late adulthood diet-induced obesity onset on behavior, immune function, redox state and life span of male and female mice.


Journal

Brain, behavior, and immunity
ISSN: 1090-2139
Titre abrégé: Brain Behav Immun
Pays: Netherlands
ID NLM: 8800478

Informations de publication

Date de publication:
05 2019
Historique:
received: 15 08 2018
revised: 14 01 2019
accepted: 14 01 2019
pubmed: 20 1 2019
medline: 14 4 2020
entrez: 20 1 2019
Statut: ppublish

Résumé

The aim of the present study was to investigate whether the late onset of diet-induced obesity (DIO) in middle-aged mice affected behavioral, immunological and oxidative stress parameters as well as life span of male and female mice. Also, it was analyzed whether the late DIO onset aggravated immunosenescence in old female mice. Late-adult male and female ICR/CD1 mice (28 weeks old) were fed either a high-fat diet or a standard diet during 14 weeks. After that, in these middle-aged (42 weeks old) diet-induced obese (DIO) and non-DIO controls, behavior as well as functions and redox state of peritoneal leukocytes were evaluated. These same parameters (excepting behavioral tests) were repeated when female mice were old (72 weeks old). The results showed lower exploratory activity and higher anxiety-like behavior in middle-aged male and female DIO than in controls. Moreover, these DIO animals from both sexes exhibited statistically significant impaired immune cell functions, such as chemotaxis of macrophages and lymphocytes, phagocytosis of macrophages, natural killer activity and lymphoproliferation in response to ConA and LPS, as well as an oxidative stress state in comparison with controls. Male DIO mice exhibited higher impairments in a variety of the evaluated parameters and a shorter life span than their female counterparts. In addition, female DIO mice, at old age, showed aggravated immunosenescence. In conclusion, the late DIO onset leads to impairments in behavior as well as in immune system functions of middle-aged male and female mice, males being significantly more affected than females.

Identifiants

pubmed: 30659939
pii: S0889-1591(18)30459-8
doi: 10.1016/j.bbi.2019.01.010
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

65-77

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Caroline Hunsche (C)

Department of Genetics, Physiology and Microbiology, Faculty of Biology, Complutense University of Madrid and Research Institute of Hospital 12 de Octubre (i+12), Spain.

Irene Martínez de Toda (IM)

Department of Genetics, Physiology and Microbiology, Faculty of Biology, Complutense University of Madrid and Research Institute of Hospital 12 de Octubre (i+12), Spain.

Mónica De la Fuente (M)

Department of Genetics, Physiology and Microbiology, Faculty of Biology, Complutense University of Madrid and Research Institute of Hospital 12 de Octubre (i+12), Spain. Electronic address: mondelaf@bio.ucm.es.

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Classifications MeSH