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Fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction
High serum phosphorus (P) impairs endothelial function by increasing oxidative stress and decreasing nitric oxide production. Serum P levels fluctuate due to circadian rhythms or dietary P intake in healthy people and due to dialysis in end-stage chronic kidney disease patients. Here we examined whe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306666/ https://www.ncbi.nlm.nih.gov/pubmed/25678749 http://dx.doi.org/10.3164/jcbn.14-96 |
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author | Watari, Eriko Taketani, Yutaka Kitamura, Tomoyo Tanaka, Terumi Ohminami, Hirokazu Abuduli, Maerjianghan Harada, Nagakatsu Yamanaka-Okumura, Hisami Yamamoto, Hironori Takeda, Eiji |
author_facet | Watari, Eriko Taketani, Yutaka Kitamura, Tomoyo Tanaka, Terumi Ohminami, Hirokazu Abuduli, Maerjianghan Harada, Nagakatsu Yamanaka-Okumura, Hisami Yamamoto, Hironori Takeda, Eiji |
author_sort | Watari, Eriko |
collection | PubMed |
description | High serum phosphorus (P) impairs endothelial function by increasing oxidative stress and decreasing nitric oxide production. Serum P levels fluctuate due to circadian rhythms or dietary P intake in healthy people and due to dialysis in end-stage chronic kidney disease patients. Here we examined whether fluctuating plasma P caused by changes in dietary P intake may be involved in endothelial dysfunction, resulting in increased cardiovascular risk. Rats were fed a diet containing 0.6% P for 16 days (control group), or a diet alternating between 0.02% P and 1.2% P (LH group) or between 1.2% P and 0.02% P (HL group) every 2 days; the total amount of P intake among the groups during the feeding period was similar. In the LH and HL groups, endothelial-dependent vasodilation significantly decreased plasma 8-(OH)dG level significantly increased, and the expression of inflammatory factors such as MCP-1 increased in the endothelium as compared with the control group. These data indicate that repetitive fluctuations of plasma P caused by varying dietary P intake can impair endothelial function via increased oxidative stress and inflammatory response. Taken together, these results suggest that habitual fluctuation of dietary P intake might be a cause of cardiovascular disease through endothelial dysfunction, especially in chronic kidney disease patients. |
format | Online Article Text |
id | pubmed-4306666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-43066662015-02-12 Fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction Watari, Eriko Taketani, Yutaka Kitamura, Tomoyo Tanaka, Terumi Ohminami, Hirokazu Abuduli, Maerjianghan Harada, Nagakatsu Yamanaka-Okumura, Hisami Yamamoto, Hironori Takeda, Eiji J Clin Biochem Nutr Original Article High serum phosphorus (P) impairs endothelial function by increasing oxidative stress and decreasing nitric oxide production. Serum P levels fluctuate due to circadian rhythms or dietary P intake in healthy people and due to dialysis in end-stage chronic kidney disease patients. Here we examined whether fluctuating plasma P caused by changes in dietary P intake may be involved in endothelial dysfunction, resulting in increased cardiovascular risk. Rats were fed a diet containing 0.6% P for 16 days (control group), or a diet alternating between 0.02% P and 1.2% P (LH group) or between 1.2% P and 0.02% P (HL group) every 2 days; the total amount of P intake among the groups during the feeding period was similar. In the LH and HL groups, endothelial-dependent vasodilation significantly decreased plasma 8-(OH)dG level significantly increased, and the expression of inflammatory factors such as MCP-1 increased in the endothelium as compared with the control group. These data indicate that repetitive fluctuations of plasma P caused by varying dietary P intake can impair endothelial function via increased oxidative stress and inflammatory response. Taken together, these results suggest that habitual fluctuation of dietary P intake might be a cause of cardiovascular disease through endothelial dysfunction, especially in chronic kidney disease patients. the Society for Free Radical Research Japan 2015-01 2014-12-16 /pmc/articles/PMC4306666/ /pubmed/25678749 http://dx.doi.org/10.3164/jcbn.14-96 Text en Copyright © 2015 JCBN 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 work is properly cited. |
spellingShingle | Original Article Watari, Eriko Taketani, Yutaka Kitamura, Tomoyo Tanaka, Terumi Ohminami, Hirokazu Abuduli, Maerjianghan Harada, Nagakatsu Yamanaka-Okumura, Hisami Yamamoto, Hironori Takeda, Eiji Fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction |
title | Fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction |
title_full | Fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction |
title_fullStr | Fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction |
title_full_unstemmed | Fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction |
title_short | Fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction |
title_sort | fluctuating plasma phosphorus level by changes in dietary phosphorus intake induces endothelial dysfunction |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306666/ https://www.ncbi.nlm.nih.gov/pubmed/25678749 http://dx.doi.org/10.3164/jcbn.14-96 |
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