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Licensed Unlicensed Requires Authentication Published by De Gruyter May 14, 2013

Role of maternal nutrition in programming adiposity in the offspring: potential implications of glucocorticoids

  • Christophe Breton EMAIL logo

Abstract

The epidemiological studies initially indicated that maternal undernutrition leading to a low birth weight may predispose to the long-lasting energy balance disorders. A high birth weight due to maternal obesity or diabetes, inappropriate early postnatal nutrition, and rapid catch-up growth, may also sensitize to an increased risk of obesity. As stated by the developmental origin of health and disease concept, the perinatal perturbation of the fetus/neonate nutrient supply might be a crucial determinant of the individual programming of the body weight set point. The adipose tissue is considered as the main fuel storage unit involved in the maintenance of the energy homeostasis. Several models have demonstrated that this tissue is a prime target of the developmental programming in a gender- and depot-specific manner. In the rodents, the perinatal period of life corresponds largely to the period of adipogenesis. In contrast, this phenomenon essentially takes place before birth in bigger mammals. Despite these different developmental time windows, the altricial and precocial species share several common offspring programming mechanisms. Thus, the adipose tissue of the offspring from malnourished dams exhibited impaired glucose uptake and leptin/insulin resistance with increased proinflammatory markers. It also displayed a modified sympathetic activity, circadian rhythm, fatty acid composition, and thermogenesis. This might lead to the reprogrammed metabolism and distribution of the adipose tissue with enhanced adipogenesis and fat accumulation predisposing to adiposity. The inappropriate glucocorticoid (GC) levels and modified tissue sensitivity might be key actors of perinatal programming and long-lasting altered adipose tissue activity in the offspring. Following maternal malnutrition, the epigenetic mechanisms might also be responsible for the adipose tissue programming.


Corresponding author: Professor Christophe Breton, Unité Environnement Périnatal et Croissance, UPRES EA 4489, Equipe Dénutritions Maternelles Périnatales, Université Lille-Nord de France, Villeneuve d’Ascq, France, Phone: +33 3 20 43 65 32, Fax: +33 3 20 33 63 49

Conflict of interest statement

Declaration of interest: The author declares that he has no conflict of interest that could be perceived as prejudicing the impartiality of the research reported.

Funding: This study was supported by the grants from the French Ministry of Education and the grants of the Conseil Régional du Nord-Pas de Calais.

Disclosure statement: The author has nothing to declare and has no conflict of interest.

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Received: 2013-4-11
Accepted: 2013-4-18
Published Online: 2013-05-14
Published in Print: 2013-08-01

©2013 by Walter de Gruyter Berlin Boston

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