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Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner

Male and female offspring of obese mothers are known to differ extensively in their metabolic adaptation and later development of complications. We investigate the sex-dependent responses in obese offspring mice with maternal obesity, focusing on changes in liver glucose and lipid metabolism. Here w...

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Autores principales: Savva, Christina, Helguero, Luisa A., González-Granillo, Marcela, Melo, Tânia, Couto, Daniela, Angelin, Bo, Domingues, Maria Rosário, Li, Xidan, Kutter, Claudia, Korach-André, Marion
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532402/
https://www.ncbi.nlm.nih.gov/pubmed/36195702
http://dx.doi.org/10.1038/s42003-022-04022-3
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author Savva, Christina
Helguero, Luisa A.
González-Granillo, Marcela
Melo, Tânia
Couto, Daniela
Angelin, Bo
Domingues, Maria Rosário
Li, Xidan
Kutter, Claudia
Korach-André, Marion
author_facet Savva, Christina
Helguero, Luisa A.
González-Granillo, Marcela
Melo, Tânia
Couto, Daniela
Angelin, Bo
Domingues, Maria Rosário
Li, Xidan
Kutter, Claudia
Korach-André, Marion
author_sort Savva, Christina
collection PubMed
description Male and female offspring of obese mothers are known to differ extensively in their metabolic adaptation and later development of complications. We investigate the sex-dependent responses in obese offspring mice with maternal obesity, focusing on changes in liver glucose and lipid metabolism. Here we show that maternal obesity prior to and during gestation leads to hepatic steatosis and inflammation in male offspring, while female offspring are protected. Females from obese mothers display important changes in hepatic transcriptional activity and triglycerides profile which may prevent the damaging effects of maternal obesity compared to males. These differences are sustained later in life, resulting in a better metabolic balance in female offspring. In conclusion, sex and maternal obesity drive differently transcriptional and posttranscriptional regulation of major metabolic processes in offspring liver, explaining the sexual dimorphism in obesity-associated metabolic risk.
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spelling pubmed-95324022022-10-06 Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner Savva, Christina Helguero, Luisa A. González-Granillo, Marcela Melo, Tânia Couto, Daniela Angelin, Bo Domingues, Maria Rosário Li, Xidan Kutter, Claudia Korach-André, Marion Commun Biol Article Male and female offspring of obese mothers are known to differ extensively in their metabolic adaptation and later development of complications. We investigate the sex-dependent responses in obese offspring mice with maternal obesity, focusing on changes in liver glucose and lipid metabolism. Here we show that maternal obesity prior to and during gestation leads to hepatic steatosis and inflammation in male offspring, while female offspring are protected. Females from obese mothers display important changes in hepatic transcriptional activity and triglycerides profile which may prevent the damaging effects of maternal obesity compared to males. These differences are sustained later in life, resulting in a better metabolic balance in female offspring. In conclusion, sex and maternal obesity drive differently transcriptional and posttranscriptional regulation of major metabolic processes in offspring liver, explaining the sexual dimorphism in obesity-associated metabolic risk. Nature Publishing Group UK 2022-10-04 /pmc/articles/PMC9532402/ /pubmed/36195702 http://dx.doi.org/10.1038/s42003-022-04022-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Savva, Christina
Helguero, Luisa A.
González-Granillo, Marcela
Melo, Tânia
Couto, Daniela
Angelin, Bo
Domingues, Maria Rosário
Li, Xidan
Kutter, Claudia
Korach-André, Marion
Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner
title Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner
title_full Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner
title_fullStr Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner
title_full_unstemmed Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner
title_short Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner
title_sort molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532402/
https://www.ncbi.nlm.nih.gov/pubmed/36195702
http://dx.doi.org/10.1038/s42003-022-04022-3
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