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World J Diabetes. Sep 15, 2011; 2(9): 149-157
Published online Sep 15, 2011. doi: 10.4239/wjd.v2.i9.149
Alteration of mitochondrial function in adult rat offspring of malnourished dams
Brigitte Reusens, Nicolas Theys, Claude Remacle
Brigitte Reusens, Nicolas Theys, Claude Remacle, Laboratory of Cell Biology, Institute of Life Science, Université Catholique de Louvain, 1348 Louvain-la-Neuve, Belgium
Author contributions: Reusens B and Theys N wrote this manuscript; Remacle C reviewed this manuscript.
Supported by the European Commission (FOOD-CT-2005-007036); the Parthenon Trust (London, UK); the Belgian Fonds National de la Recherche Scientifique; the Belgian Fonds pour la Recherche dans l’Industrie et l’Agriculture
Correspondence to: Brigitte Reusens, Dr., Laboratory of Cell Biology, Institute of Life Science, Université Catholique de Louvain, 5 Place Croix du Sud, 1348 Louvain-la-Neuve, Belgium. brigitte.reusens@uclouvain.be
Telephone: +32-10-474003 Fax: +32-10-473515
Received: March 2, 2011
Revised: August 16, 2011
Accepted: August 21, 2011
Published online: September 15, 2011
Abstract

Under-nutrition as well as over-nutrition during pregnancy has been associated with the development of adult diseases such as diabetes and obesity. Both epigenetic modifications and programming of the mitochondrial function have been recently proposed to explain how altered intrauterine metabolic environment may produce such a phenotype. This review aims to report data reported in several animal models of fetal malnutrition due to maternal low protein or low calorie diet, high fat diet as well as reduction in placental blood flow. We focus our overview on the β cell. We highlight that, notwithstanding early nutritional events, mitochondrial dysfunctions resulting from different alteration by diet or gender are programmed. This may explain the higher propensity to develop obesity and diabetes in later life.

Keywords: Fetal programming; β cells; Mitochondria; Maternal malnutrition; Rats