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Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model
Authors:Anne Tarrade  Delphine Rousseau-Ralliard  Marie-Christine Aubrière  Nathalie Peynot  Michèle Dahirel  Justine Bertrand-Michel  Tiphaine Aguirre-Lavin  Olivier Morel  Nathalie Beaujean  Véronique Duranthon  Pascale Chavatte-Palmer
Affiliation:1. INRA, UMR1198 Biologie du Développement et Reproduction, Jouy-en-Josas, France.; 2. ENVA, Maisons Alfort, France.; 3. PremUp Foundation, Paris, France.; 4. INSERM, UMR 1048- Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France.; Otto-von-Guericke University Magdeburg, Germany,
Abstract:Maternal environment during early developmental stages plays a seminal role in the establishment of adult phenotype. Using a rabbit model, we previously showed that feeding dams with a diet supplemented with 8% fat and 0.2% cholesterol (HH diet) from the prepubertal period and throughout gestation induced metabolic syndrome in adult offspring. Here, we examined the effects of the HH diet on feto-placental phenotype at 28 days post-coïtum (term = 31days) in relation to earlier effects in the blastocyst (Day 6). At 28 days, both male and female HH fetuses were intrauterine growth retarded and dyslipidemic, with males more affected than females. Lipid droplets accumulated in the HH placentas’ trophoblast, consistent with the increased concentrations in cholesteryl esters (3.2-fold), triacylglycerol (2.5-fold) and stored FA (2.12-fold). Stored FA concentrations were significantly higher in female compared to male HH placentas (2.18-fold, p<0.01), whereas triacylglycerol was increased only in HH males. Trophoblastic lipid droplet accumulation was also observed at the blastocyst stage. The expression of numerous genes involved in lipid pathways differed significantly according to diet both in term placenta and at the blastocyst stage. Among them, the expression of LXR-α in HH placentas was reduced in HH males but not females. These data demonstrate that maternal HH diet affects the blastocyst and induces sex-dependent metabolic adaptations in the placenta, which appears to protect female fetuses from developing severe dyslipidemia.
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