The anti-hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice.

To demonstrate that p53 modulates endothelial function and the stress response to a high-fat western diet (WD).Three-month old p53+/+ wild type (WT) and p53+/- male mice were fed a regular or WD for 3 months. Plasma levels of total cholesterol (TC) and LDL-cholesterol were significantly elevated (p&...

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Main Authors: Francois Leblond, Steve Poirier, Carol Yu, Natacha Duquette, Gaetan Mayer, Eric Thorin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3960235?pdf=render
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author Francois Leblond
Steve Poirier
Carol Yu
Natacha Duquette
Gaetan Mayer
Eric Thorin
author_facet Francois Leblond
Steve Poirier
Carol Yu
Natacha Duquette
Gaetan Mayer
Eric Thorin
author_sort Francois Leblond
collection DOAJ
description To demonstrate that p53 modulates endothelial function and the stress response to a high-fat western diet (WD).Three-month old p53+/+ wild type (WT) and p53+/- male mice were fed a regular or WD for 3 months. Plasma levels of total cholesterol (TC) and LDL-cholesterol were significantly elevated (p<0.05) in WD-fed WT (from 2.1±0.2 mmol/L to 3.1±0.2, and from 0.64±0.09 mmol/L to 1.25±0.11, respectively) but not in p53+/- mice. The lack of cholesterol accumulation in WD-fed p53+/- mice was associated with high bile acid plasma concentrations (p53+/- =  4.7±0.9 vs. WT =  3.3±0.2 μmol/L, p<0.05) concomitant with an increased hepatic 7-alpha-hydroxylase mRNA expression. While the WD did not affect aortic endothelial relaxant function in p53+/- mice (WD =  83±5 and RD =  82±4% relaxation), it increased the maximal response to acetylcholine in WT mice (WD =  87±2 vs. RD =  62±5% relaxation, p<0.05) to levels of p53+/-. In WT mice, the rise in TC associated with higher (p<0.05) plasma levels of pro-inflammatory keratinocyte-derived chemokine, and an over-activation (p<0.05) of the relaxant non-nitric oxide/non-prostacyclin endothelial pathway. It is likely that in WT mice, activations of these pathways are adaptive and contributed to maintain endothelial function, while the WD neither promoted inflammation nor affected endothelial function in p53+/- mice.Our data demonstrate that low endogenous p53 expression prevents the rise in circulating levels of cholesterol when fed a WD. Consequently, the endothelial stress of hypercholesterolemia is absent in young p53+/- mice as evidenced by the absence of endothelial adaptive pathway over-activation to minimize stress-related damage.
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spelling doaj.art-507d74adf9894c22b6007f267de75e6f2022-12-22T01:59:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0193e9239410.1371/journal.pone.0092394The anti-hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice.Francois LeblondSteve PoirierCarol YuNatacha DuquetteGaetan MayerEric ThorinTo demonstrate that p53 modulates endothelial function and the stress response to a high-fat western diet (WD).Three-month old p53+/+ wild type (WT) and p53+/- male mice were fed a regular or WD for 3 months. Plasma levels of total cholesterol (TC) and LDL-cholesterol were significantly elevated (p<0.05) in WD-fed WT (from 2.1±0.2 mmol/L to 3.1±0.2, and from 0.64±0.09 mmol/L to 1.25±0.11, respectively) but not in p53+/- mice. The lack of cholesterol accumulation in WD-fed p53+/- mice was associated with high bile acid plasma concentrations (p53+/- =  4.7±0.9 vs. WT =  3.3±0.2 μmol/L, p<0.05) concomitant with an increased hepatic 7-alpha-hydroxylase mRNA expression. While the WD did not affect aortic endothelial relaxant function in p53+/- mice (WD =  83±5 and RD =  82±4% relaxation), it increased the maximal response to acetylcholine in WT mice (WD =  87±2 vs. RD =  62±5% relaxation, p<0.05) to levels of p53+/-. In WT mice, the rise in TC associated with higher (p<0.05) plasma levels of pro-inflammatory keratinocyte-derived chemokine, and an over-activation (p<0.05) of the relaxant non-nitric oxide/non-prostacyclin endothelial pathway. It is likely that in WT mice, activations of these pathways are adaptive and contributed to maintain endothelial function, while the WD neither promoted inflammation nor affected endothelial function in p53+/- mice.Our data demonstrate that low endogenous p53 expression prevents the rise in circulating levels of cholesterol when fed a WD. Consequently, the endothelial stress of hypercholesterolemia is absent in young p53+/- mice as evidenced by the absence of endothelial adaptive pathway over-activation to minimize stress-related damage.http://europepmc.org/articles/PMC3960235?pdf=render
spellingShingle Francois Leblond
Steve Poirier
Carol Yu
Natacha Duquette
Gaetan Mayer
Eric Thorin
The anti-hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice.
PLoS ONE
title The anti-hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice.
title_full The anti-hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice.
title_fullStr The anti-hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice.
title_full_unstemmed The anti-hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice.
title_short The anti-hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice.
title_sort anti hypercholesterolemic effect of low p53 expression protects vascular endothelial function in mice
url http://europepmc.org/articles/PMC3960235?pdf=render
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