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Maternal high-fat diet impacts endothelial function in nonhuman primate offspring
OBJECTIVE: The link between maternal under-nutrition and cardiovascular disease (CVD) in the offspring later in life is well recognized, but the impact of maternal over-nutrition on the offspring's cardiovascular function and subsequent risk for CVD later in life remains unclear. Here, we inves...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3468685/ https://www.ncbi.nlm.nih.gov/pubmed/22450853 http://dx.doi.org/10.1038/ijo.2012.42 |
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author | Fan, L Lindsley, S R Comstock, S M Takahashi, D L Evans, A E He, G-W Thornburg, K L Grove, K L |
author_facet | Fan, L Lindsley, S R Comstock, S M Takahashi, D L Evans, A E He, G-W Thornburg, K L Grove, K L |
author_sort | Fan, L |
collection | PubMed |
description | OBJECTIVE: The link between maternal under-nutrition and cardiovascular disease (CVD) in the offspring later in life is well recognized, but the impact of maternal over-nutrition on the offspring's cardiovascular function and subsequent risk for CVD later in life remains unclear. Here, we investigated the impact of maternal exposure to a high-fat/calorie diet (HFD) during pregnancy and early postnatal period on endothelial function of the offspring in a nonhuman primate model. METHODS: Offspring, naturally born to either a control (CTR) diet (14% fat calories) or a HFD (36% fat calories) consumption dam, were breast-fed until weaning at about 8 months of age. After weaning, the offspring were either maintained on the same diet (CTR/CTR, HFD/HFD), or underwent a diet switch (CTR/HFD, HFD/CTR). Blood samples and arterial tissues were collected at necropsy when the animals were about 13 months of age. RESULTS: HFD/HFD juveniles displayed an increased plasma insulin level and glucose-stimulated insulin secretion in comparison with CTR/CTR. In abdominal aorta, but not the renal artery, acetylcholine-induced vasorelaxation was decreased remarkably for HFD/HFD juveniles compared with CTR/CTR. HFD/HFD animals also showed a thicker intima wall and an abnormal vascular-morphology, concurrent with elevated expression levels of several markers related to vascular inflammation and fibrinolytic function. Diet-switching animals (HFD/CTR and CTR/HFD) displayed modest damage on the abdominal vessel. CONCLUSION: Our data indicate that maternal HFD exposure impairs offspring's endothelial function. Both early programming events and postweaning diet contribute to the abnormalities that could be reversed partially by diet intervention. |
format | Online Article Text |
id | pubmed-3468685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34686852013-02-13 Maternal high-fat diet impacts endothelial function in nonhuman primate offspring Fan, L Lindsley, S R Comstock, S M Takahashi, D L Evans, A E He, G-W Thornburg, K L Grove, K L Int J Obes (Lond) Original Article OBJECTIVE: The link between maternal under-nutrition and cardiovascular disease (CVD) in the offspring later in life is well recognized, but the impact of maternal over-nutrition on the offspring's cardiovascular function and subsequent risk for CVD later in life remains unclear. Here, we investigated the impact of maternal exposure to a high-fat/calorie diet (HFD) during pregnancy and early postnatal period on endothelial function of the offspring in a nonhuman primate model. METHODS: Offspring, naturally born to either a control (CTR) diet (14% fat calories) or a HFD (36% fat calories) consumption dam, were breast-fed until weaning at about 8 months of age. After weaning, the offspring were either maintained on the same diet (CTR/CTR, HFD/HFD), or underwent a diet switch (CTR/HFD, HFD/CTR). Blood samples and arterial tissues were collected at necropsy when the animals were about 13 months of age. RESULTS: HFD/HFD juveniles displayed an increased plasma insulin level and glucose-stimulated insulin secretion in comparison with CTR/CTR. In abdominal aorta, but not the renal artery, acetylcholine-induced vasorelaxation was decreased remarkably for HFD/HFD juveniles compared with CTR/CTR. HFD/HFD animals also showed a thicker intima wall and an abnormal vascular-morphology, concurrent with elevated expression levels of several markers related to vascular inflammation and fibrinolytic function. Diet-switching animals (HFD/CTR and CTR/HFD) displayed modest damage on the abdominal vessel. CONCLUSION: Our data indicate that maternal HFD exposure impairs offspring's endothelial function. Both early programming events and postweaning diet contribute to the abnormalities that could be reversed partially by diet intervention. Nature Publishing Group 2013-02 2012-03-27 /pmc/articles/PMC3468685/ /pubmed/22450853 http://dx.doi.org/10.1038/ijo.2012.42 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Fan, L Lindsley, S R Comstock, S M Takahashi, D L Evans, A E He, G-W Thornburg, K L Grove, K L Maternal high-fat diet impacts endothelial function in nonhuman primate offspring |
title | Maternal high-fat diet impacts endothelial function in nonhuman primate offspring |
title_full | Maternal high-fat diet impacts endothelial function in nonhuman primate offspring |
title_fullStr | Maternal high-fat diet impacts endothelial function in nonhuman primate offspring |
title_full_unstemmed | Maternal high-fat diet impacts endothelial function in nonhuman primate offspring |
title_short | Maternal high-fat diet impacts endothelial function in nonhuman primate offspring |
title_sort | maternal high-fat diet impacts endothelial function in nonhuman primate offspring |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3468685/ https://www.ncbi.nlm.nih.gov/pubmed/22450853 http://dx.doi.org/10.1038/ijo.2012.42 |
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