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Does Early Mismatched Nutrition Predispose to Hypertension and Atherosclerosis, in Male Mice?

BACKGROUND: A link between early mismatched nutritional environment and development of components of the metabolic syndrome later in life has been shown in epidemiological and animal data. The aim of this study was to investigate whether an early mismatched nutrition produced by catch-up growth afte...

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Autores principales: Bol, Vanesa, Desjardins, Fanny, Reusens, Brigitte, Balligand, Jen-Luc, Remacle, Claude
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936567/
https://www.ncbi.nlm.nih.gov/pubmed/20844591
http://dx.doi.org/10.1371/journal.pone.0012656
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author Bol, Vanesa
Desjardins, Fanny
Reusens, Brigitte
Balligand, Jen-Luc
Remacle, Claude
author_facet Bol, Vanesa
Desjardins, Fanny
Reusens, Brigitte
Balligand, Jen-Luc
Remacle, Claude
author_sort Bol, Vanesa
collection PubMed
description BACKGROUND: A link between early mismatched nutritional environment and development of components of the metabolic syndrome later in life has been shown in epidemiological and animal data. The aim of this study was to investigate whether an early mismatched nutrition produced by catch-up growth after fetal protein restriction could induce the appearance of hypertension and/or atherosclerosis in adult male mice. METHODOLOGY/PRINCIPAL FINDINGS: Wild-type C57BL6/J or LDLr−/− dams were fed a low protein (LP) or a control (C) diet during gestation. Catch-up growth was induced in LP offspring by feeding dams with a control diet and by culling the litter to 4 pups against 8 in controls. At weaning, male mice were fed either standard chow or an obesogenic diet (OB), leading to 4 experimental groups. Blood pressure (BP) and heart rate (HR) were assessed in conscious unrestrained wild-type mice by telemetry. Atherosclerosis plaque area was measured in aortic root sections of LDLr−/− mice. We found that: (1) postnatal OB diet increased significantly BP (P<0.0001) and HR (P<0.008) in 3-month old OB-C and OB-LP offspring, respectively; (2) that maternal LP diet induced a significant higher BP (P<0.009) and HR (P<0.004) and (3) an altered circadian rhythm in addition to higher plasma corticosterone concentration in 9 months-old LP offspring; (4) that, although LP offspring showed higher plasma total cholesterol than control offspring, atherosclerosis assessed in aortic roots of 6-mo old mice featured increased plaque area due to OB feeding but not due to early mismatched nutrition. CONCLUSIONS/SIGNIFICANCE: These results indicate a long-term effect of early mismatched nutrition on the appearance of hypertension independently of obesity, while no effect on atherosclerosis was noticed at this age.
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spelling pubmed-29365672010-09-15 Does Early Mismatched Nutrition Predispose to Hypertension and Atherosclerosis, in Male Mice? Bol, Vanesa Desjardins, Fanny Reusens, Brigitte Balligand, Jen-Luc Remacle, Claude PLoS One Research Article BACKGROUND: A link between early mismatched nutritional environment and development of components of the metabolic syndrome later in life has been shown in epidemiological and animal data. The aim of this study was to investigate whether an early mismatched nutrition produced by catch-up growth after fetal protein restriction could induce the appearance of hypertension and/or atherosclerosis in adult male mice. METHODOLOGY/PRINCIPAL FINDINGS: Wild-type C57BL6/J or LDLr−/− dams were fed a low protein (LP) or a control (C) diet during gestation. Catch-up growth was induced in LP offspring by feeding dams with a control diet and by culling the litter to 4 pups against 8 in controls. At weaning, male mice were fed either standard chow or an obesogenic diet (OB), leading to 4 experimental groups. Blood pressure (BP) and heart rate (HR) were assessed in conscious unrestrained wild-type mice by telemetry. Atherosclerosis plaque area was measured in aortic root sections of LDLr−/− mice. We found that: (1) postnatal OB diet increased significantly BP (P<0.0001) and HR (P<0.008) in 3-month old OB-C and OB-LP offspring, respectively; (2) that maternal LP diet induced a significant higher BP (P<0.009) and HR (P<0.004) and (3) an altered circadian rhythm in addition to higher plasma corticosterone concentration in 9 months-old LP offspring; (4) that, although LP offspring showed higher plasma total cholesterol than control offspring, atherosclerosis assessed in aortic roots of 6-mo old mice featured increased plaque area due to OB feeding but not due to early mismatched nutrition. CONCLUSIONS/SIGNIFICANCE: These results indicate a long-term effect of early mismatched nutrition on the appearance of hypertension independently of obesity, while no effect on atherosclerosis was noticed at this age. Public Library of Science 2010-09-09 /pmc/articles/PMC2936567/ /pubmed/20844591 http://dx.doi.org/10.1371/journal.pone.0012656 Text en Bol 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
Bol, Vanesa
Desjardins, Fanny
Reusens, Brigitte
Balligand, Jen-Luc
Remacle, Claude
Does Early Mismatched Nutrition Predispose to Hypertension and Atherosclerosis, in Male Mice?
title Does Early Mismatched Nutrition Predispose to Hypertension and Atherosclerosis, in Male Mice?
title_full Does Early Mismatched Nutrition Predispose to Hypertension and Atherosclerosis, in Male Mice?
title_fullStr Does Early Mismatched Nutrition Predispose to Hypertension and Atherosclerosis, in Male Mice?
title_full_unstemmed Does Early Mismatched Nutrition Predispose to Hypertension and Atherosclerosis, in Male Mice?
title_short Does Early Mismatched Nutrition Predispose to Hypertension and Atherosclerosis, in Male Mice?
title_sort does early mismatched nutrition predispose to hypertension and atherosclerosis, in male mice?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936567/
https://www.ncbi.nlm.nih.gov/pubmed/20844591
http://dx.doi.org/10.1371/journal.pone.0012656
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