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Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells

BACKGROUND: Adequate folate status supports endothelial structure and function. Folic acid (FA), an oxidized synthetic folate, which is present in the plasma of patients consuming fortified food or FA supplements, may impair cellular uptake of physiological, reduced folates. We studied the effect of...

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Autores principales: Smith, Desiree, Hornstra, Jacqueline, Rocha, Monica, Jansen, Gerrit, Assaraf, Yehuda, Lasry, Inbal, Blom, Henk, Smulders, Yvo M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of Cardiovascular Pharmacology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642340/
https://www.ncbi.nlm.nih.gov/pubmed/28991880
http://dx.doi.org/10.1097/FJC.0000000000000514
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author Smith, Desiree
Hornstra, Jacqueline
Rocha, Monica
Jansen, Gerrit
Assaraf, Yehuda
Lasry, Inbal
Blom, Henk
Smulders, Yvo M.
author_facet Smith, Desiree
Hornstra, Jacqueline
Rocha, Monica
Jansen, Gerrit
Assaraf, Yehuda
Lasry, Inbal
Blom, Henk
Smulders, Yvo M.
author_sort Smith, Desiree
collection PubMed
description BACKGROUND: Adequate folate status supports endothelial structure and function. Folic acid (FA), an oxidized synthetic folate, which is present in the plasma of patients consuming fortified food or FA supplements, may impair cellular uptake of physiological, reduced folates. We studied the effect of FA on uptake of the dominant circulatory folate, 5-methyltetrahydrofolate (5MTHF) in endothelial cells. METHODS AND RESULTS: For short-term effects of FA, primary human umbilical vein endothelial cells (HUVECs) were maintained in growth medium containing 200 nM 5MTHF and preincubated with 20 nM FA 10 minutes before the 5MTHF uptake assessment. For long-term effects, HUVECs were cultured for 3 passages in growth medium containing either 200 nM 5MTHF, or a combination of 100 nM 5MTHF and 100 nM FA. 5MTHF uptake was assessed after exposing cells to 200 nM [(13)C(5)]-5MTHF, after which intracellular [(13)C(5)]-5MTHF was quantified using liquid chromatography/tandem mass spectrometry. Acute FA exposure caused a 57% reduction in 5MTHF uptake compared with control conditions (51 ± 12 vs. 22 ± 7 fmol·min(−1)·mg(−1) protein; P = 0.01). Long-term exposure to FA reduced 5MTHF uptake by 41% (51 ± 12 vs. 30 ± 11 fmol·min(−1)·mg(−1) protein; P = 0.05) and reduced total cellular 5MTHF levels by 47 ± 21% in HUVEC (P = 0.02). CONCLUSION: Unmetabolized FA, which appears in the plasma after consumption of fortified food or FA supplements, may impair uptake of 5MTHF, the dominant bioactive form of folate, in HUVEC.
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spelling pubmed-56423402017-10-24 Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells Smith, Desiree Hornstra, Jacqueline Rocha, Monica Jansen, Gerrit Assaraf, Yehuda Lasry, Inbal Blom, Henk Smulders, Yvo M. J Cardiovasc Pharmacol Original Article BACKGROUND: Adequate folate status supports endothelial structure and function. Folic acid (FA), an oxidized synthetic folate, which is present in the plasma of patients consuming fortified food or FA supplements, may impair cellular uptake of physiological, reduced folates. We studied the effect of FA on uptake of the dominant circulatory folate, 5-methyltetrahydrofolate (5MTHF) in endothelial cells. METHODS AND RESULTS: For short-term effects of FA, primary human umbilical vein endothelial cells (HUVECs) were maintained in growth medium containing 200 nM 5MTHF and preincubated with 20 nM FA 10 minutes before the 5MTHF uptake assessment. For long-term effects, HUVECs were cultured for 3 passages in growth medium containing either 200 nM 5MTHF, or a combination of 100 nM 5MTHF and 100 nM FA. 5MTHF uptake was assessed after exposing cells to 200 nM [(13)C(5)]-5MTHF, after which intracellular [(13)C(5)]-5MTHF was quantified using liquid chromatography/tandem mass spectrometry. Acute FA exposure caused a 57% reduction in 5MTHF uptake compared with control conditions (51 ± 12 vs. 22 ± 7 fmol·min(−1)·mg(−1) protein; P = 0.01). Long-term exposure to FA reduced 5MTHF uptake by 41% (51 ± 12 vs. 30 ± 11 fmol·min(−1)·mg(−1) protein; P = 0.05) and reduced total cellular 5MTHF levels by 47 ± 21% in HUVEC (P = 0.02). CONCLUSION: Unmetabolized FA, which appears in the plasma after consumption of fortified food or FA supplements, may impair uptake of 5MTHF, the dominant bioactive form of folate, in HUVEC. Journal of Cardiovascular Pharmacology 2017-10 2017-07-12 /pmc/articles/PMC5642340/ /pubmed/28991880 http://dx.doi.org/10.1097/FJC.0000000000000514 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Article
Smith, Desiree
Hornstra, Jacqueline
Rocha, Monica
Jansen, Gerrit
Assaraf, Yehuda
Lasry, Inbal
Blom, Henk
Smulders, Yvo M.
Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells
title Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells
title_full Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells
title_fullStr Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells
title_full_unstemmed Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells
title_short Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells
title_sort folic acid impairs the uptake of 5-methyltetrahydrofolate in human umbilical vascular endothelial cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642340/
https://www.ncbi.nlm.nih.gov/pubmed/28991880
http://dx.doi.org/10.1097/FJC.0000000000000514
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