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Brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice

During pregnancy several maternal adaptations occur in order to support the growing fetus which are further exacerbated by gestational diabetes mellitus (GDM). Previously we developed a mouse model of GDM, however we did not evaluate alterations to energy and fat metabolism. We have also shown that...

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Autores principales: Pennington, Kathleen A., Dong, Yuanlin, Ruano, Simone Hernandez, van der Walt, Nicola, Sangi-Haghpeykar, Haleh, Yallampalli, Chandrasekhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705687/
https://www.ncbi.nlm.nih.gov/pubmed/33257770
http://dx.doi.org/10.1038/s41598-020-77529-6
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author Pennington, Kathleen A.
Dong, Yuanlin
Ruano, Simone Hernandez
van der Walt, Nicola
Sangi-Haghpeykar, Haleh
Yallampalli, Chandrasekhar
author_facet Pennington, Kathleen A.
Dong, Yuanlin
Ruano, Simone Hernandez
van der Walt, Nicola
Sangi-Haghpeykar, Haleh
Yallampalli, Chandrasekhar
author_sort Pennington, Kathleen A.
collection PubMed
description During pregnancy several maternal adaptations occur in order to support the growing fetus which are further exacerbated by gestational diabetes mellitus (GDM). Previously we developed a mouse model of GDM, however we did not evaluate alterations to energy and fat metabolism. We have also shown that alterations in lipid metabolism are mediated by adrenomedullin (ADM) in normal and GDM pregnancies. Our objectives were: (1) evaluate energy and fat homeostasis in our GDM mouse model and (2) determine if ADM may play a role in these changes. Female mice were placed on either control (P-CD) or high fat, high sucrose diet (P-HFHS) 1 week prior to and throughout pregnancy. Mice were placed into comprehensive lab animal monitoring system (CLAMS) chambers throughout pregnancy. Visceral adipose tissue (VAT) was collected at d17.5 of pregnancy for analysis. Energy Expenditure was significantly increased (p < 0.05) in P-HFHS dams compared to all other groups. VAT ex-vivo lipolysis was increased (p < 0.05) in P-HFHS compared to P-CD dams. VAT gene expression of ADM receptors Crlr, Ramp2, and Ramp3 was increased (p < 0.05) in P-HFHS dams. ADM dose dependently increased ex vivo lipolysis. This data further validates our animal model of GDM and is usefulness in investigating the pathophysiology of GDM.
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spelling pubmed-77056872020-12-02 Brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice Pennington, Kathleen A. Dong, Yuanlin Ruano, Simone Hernandez van der Walt, Nicola Sangi-Haghpeykar, Haleh Yallampalli, Chandrasekhar Sci Rep Article During pregnancy several maternal adaptations occur in order to support the growing fetus which are further exacerbated by gestational diabetes mellitus (GDM). Previously we developed a mouse model of GDM, however we did not evaluate alterations to energy and fat metabolism. We have also shown that alterations in lipid metabolism are mediated by adrenomedullin (ADM) in normal and GDM pregnancies. Our objectives were: (1) evaluate energy and fat homeostasis in our GDM mouse model and (2) determine if ADM may play a role in these changes. Female mice were placed on either control (P-CD) or high fat, high sucrose diet (P-HFHS) 1 week prior to and throughout pregnancy. Mice were placed into comprehensive lab animal monitoring system (CLAMS) chambers throughout pregnancy. Visceral adipose tissue (VAT) was collected at d17.5 of pregnancy for analysis. Energy Expenditure was significantly increased (p < 0.05) in P-HFHS dams compared to all other groups. VAT ex-vivo lipolysis was increased (p < 0.05) in P-HFHS compared to P-CD dams. VAT gene expression of ADM receptors Crlr, Ramp2, and Ramp3 was increased (p < 0.05) in P-HFHS dams. ADM dose dependently increased ex vivo lipolysis. This data further validates our animal model of GDM and is usefulness in investigating the pathophysiology of GDM. Nature Publishing Group UK 2020-11-30 /pmc/articles/PMC7705687/ /pubmed/33257770 http://dx.doi.org/10.1038/s41598-020-77529-6 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pennington, Kathleen A.
Dong, Yuanlin
Ruano, Simone Hernandez
van der Walt, Nicola
Sangi-Haghpeykar, Haleh
Yallampalli, Chandrasekhar
Brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice
title Brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice
title_full Brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice
title_fullStr Brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice
title_full_unstemmed Brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice
title_short Brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice
title_sort brief high fat high sugar diet results in altered energy and fat metabolism during pregnancy in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705687/
https://www.ncbi.nlm.nih.gov/pubmed/33257770
http://dx.doi.org/10.1038/s41598-020-77529-6
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