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Short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice
Members of the fibroblast growth factor (FGF) 19 subfamily, including FGF23, FGF15/19, and FGF21, have a role as endocrine factors which influence the metabolism of inorganic phosphate (Pi) and vitamin D, bile acid, and energy. It has been reported that dietary Pi regulates circulating FGF23. In thi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947966/ https://www.ncbi.nlm.nih.gov/pubmed/24688219 http://dx.doi.org/10.3164/jcbn.13-109 |
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author | Nakahashi, Otoki Yamamoto, Hironori Tanaka, Sarasa Kozai, Mina Takei, Yuichiro Masuda, Masashi Kaneko, Ichiro Taketani, Yutaka Iwano, Masayuki Miyamoto, Ken-ichi Takeda, Eiji |
author_facet | Nakahashi, Otoki Yamamoto, Hironori Tanaka, Sarasa Kozai, Mina Takei, Yuichiro Masuda, Masashi Kaneko, Ichiro Taketani, Yutaka Iwano, Masayuki Miyamoto, Ken-ichi Takeda, Eiji |
author_sort | Nakahashi, Otoki |
collection | PubMed |
description | Members of the fibroblast growth factor (FGF) 19 subfamily, including FGF23, FGF15/19, and FGF21, have a role as endocrine factors which influence the metabolism of inorganic phosphate (Pi) and vitamin D, bile acid, and energy. It has been reported that dietary Pi regulates circulating FGF23. In this study, the short-term effects of dietary Pi restriction on the expression of FGF19 subfamily members in mice were analyzed. An initial analysis confirmed plasma FGF23 levels positively correlated with the amount of dietary Pi. On the other hand, ileal Fgf15 gene expression, but not hepatic Fgf21 gene expression, was up-regulated by dietary Pi restriction. In addition, we observed the increase of plasma 1,25-dihydroxyvitamin D [1,25(OH)(2)D] levels by dietary Pi restriction, and the up-regulation of ileal Fgf15 mRNA expression by 1,25(OH)(2)D(3) and vitamin D receptor (VDR). Importantly, dietary Pi restriction-induced Fgf15 gene expression was prevented in VDR-knockout mice. Furthermore, diurnal variations of plasma triglyceride concentrations and hepatic mRNA expression of the bile acid synthesis enzyme Cyp7a1 as one of Fgf15 negative target genes was influenced by dietary Pi restriction. These results suggest that dietary Pi restriction up-regulates ileal Fgf15 gene expression through 1,25(OH)(2)D(3) and VDR, and may affect hepatic bile acid homeostasis. |
format | Online Article Text |
id | pubmed-3947966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-39479662014-03-31 Short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice Nakahashi, Otoki Yamamoto, Hironori Tanaka, Sarasa Kozai, Mina Takei, Yuichiro Masuda, Masashi Kaneko, Ichiro Taketani, Yutaka Iwano, Masayuki Miyamoto, Ken-ichi Takeda, Eiji J Clin Biochem Nutr Original Article Members of the fibroblast growth factor (FGF) 19 subfamily, including FGF23, FGF15/19, and FGF21, have a role as endocrine factors which influence the metabolism of inorganic phosphate (Pi) and vitamin D, bile acid, and energy. It has been reported that dietary Pi regulates circulating FGF23. In this study, the short-term effects of dietary Pi restriction on the expression of FGF19 subfamily members in mice were analyzed. An initial analysis confirmed plasma FGF23 levels positively correlated with the amount of dietary Pi. On the other hand, ileal Fgf15 gene expression, but not hepatic Fgf21 gene expression, was up-regulated by dietary Pi restriction. In addition, we observed the increase of plasma 1,25-dihydroxyvitamin D [1,25(OH)(2)D] levels by dietary Pi restriction, and the up-regulation of ileal Fgf15 mRNA expression by 1,25(OH)(2)D(3) and vitamin D receptor (VDR). Importantly, dietary Pi restriction-induced Fgf15 gene expression was prevented in VDR-knockout mice. Furthermore, diurnal variations of plasma triglyceride concentrations and hepatic mRNA expression of the bile acid synthesis enzyme Cyp7a1 as one of Fgf15 negative target genes was influenced by dietary Pi restriction. These results suggest that dietary Pi restriction up-regulates ileal Fgf15 gene expression through 1,25(OH)(2)D(3) and VDR, and may affect hepatic bile acid homeostasis. the Society for Free Radical Research Japan 2014-03 2014-03-01 /pmc/articles/PMC3947966/ /pubmed/24688219 http://dx.doi.org/10.3164/jcbn.13-109 Text en Copyright © 2014 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 Nakahashi, Otoki Yamamoto, Hironori Tanaka, Sarasa Kozai, Mina Takei, Yuichiro Masuda, Masashi Kaneko, Ichiro Taketani, Yutaka Iwano, Masayuki Miyamoto, Ken-ichi Takeda, Eiji Short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice |
title | Short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice |
title_full | Short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice |
title_fullStr | Short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice |
title_full_unstemmed | Short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice |
title_short | Short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice |
title_sort | short-term dietary phosphate restriction up-regulates ileal fibroblast growth factor 15 gene expression in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947966/ https://www.ncbi.nlm.nih.gov/pubmed/24688219 http://dx.doi.org/10.3164/jcbn.13-109 |
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