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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
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 i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873307/ https://www.ncbi.nlm.nih.gov/pubmed/24386205 http://dx.doi.org/10.1371/journal.pone.0083458 |
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author | Tarrade, Anne Rousseau-Ralliard, Delphine Aubrière, Marie-Christine Peynot, Nathalie Dahirel, Michèle Bertrand-Michel, Justine Aguirre-Lavin, Tiphaine Morel, Olivier Beaujean, Nathalie Duranthon, Véronique Chavatte-Palmer, Pascale |
author_facet | Tarrade, Anne Rousseau-Ralliard, Delphine Aubrière, Marie-Christine Peynot, Nathalie Dahirel, Michèle Bertrand-Michel, Justine Aguirre-Lavin, Tiphaine Morel, Olivier Beaujean, Nathalie Duranthon, Véronique Chavatte-Palmer, Pascale |
author_sort | Tarrade, Anne |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3873307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38733072014-01-02 Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model Tarrade, Anne Rousseau-Ralliard, Delphine Aubrière, Marie-Christine Peynot, Nathalie Dahirel, Michèle Bertrand-Michel, Justine Aguirre-Lavin, Tiphaine Morel, Olivier Beaujean, Nathalie Duranthon, Véronique Chavatte-Palmer, Pascale PLoS One Research Article 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. Public Library of Science 2013-12-26 /pmc/articles/PMC3873307/ /pubmed/24386205 http://dx.doi.org/10.1371/journal.pone.0083458 Text en © 2013 Tarrade et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tarrade, Anne Rousseau-Ralliard, Delphine Aubrière, Marie-Christine Peynot, Nathalie Dahirel, Michèle Bertrand-Michel, Justine Aguirre-Lavin, Tiphaine Morel, Olivier Beaujean, Nathalie Duranthon, Véronique Chavatte-Palmer, Pascale Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model |
title | Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model |
title_full | Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model |
title_fullStr | Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model |
title_full_unstemmed | Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model |
title_short | Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model |
title_sort | sexual dimorphism of the feto-placental phenotype in response to a high fat and control maternal diets in a rabbit model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873307/ https://www.ncbi.nlm.nih.gov/pubmed/24386205 http://dx.doi.org/10.1371/journal.pone.0083458 |
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