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Nitric Oxide Modulation by Folic Acid Fortification

Folic acid (FA) can be protected the neural tube defects (NTDs) causing nitric oxide (NO) induction, but the alleviation mechanism of the detailed FA function against NO has not yet been clarified. This study focused on elucidation of the interaction of FA and NO. FA suppressed nitrite accumulation...

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Autores principales: Taira, Junsei, Ogi, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278735/
https://www.ncbi.nlm.nih.gov/pubmed/32392814
http://dx.doi.org/10.3390/antiox9050393
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author Taira, Junsei
Ogi, Takayuki
author_facet Taira, Junsei
Ogi, Takayuki
author_sort Taira, Junsei
collection PubMed
description Folic acid (FA) can be protected the neural tube defects (NTDs) causing nitric oxide (NO) induction, but the alleviation mechanism of the detailed FA function against NO has not yet been clarified. This study focused on elucidation of the interaction of FA and NO. FA suppressed nitrite accumulation as the NO indicator in lipopolysaccharide (LPS)-stimulated RAW264.7 cells, then the expression of the iNOS gene due to the LPS treatment was not inhibited by FA, suggesting that FA can modulate against NO or nitrogen radicals. NOR3 (4-ethyl-2-hydroxyamino-5-nitro-3-hexenamide) as the NO donor was used for evaluation of the NO scavenging activity of FA. FA suppressed the nitrite accumulation in a dose-dependent manner. To confirm the reaction product of FA and NO (FA-NO), liquid chromatography–mass spectrometry (LC/MS) was used to measure a similar system containing NOR3 and FA, and then detected the mass numbers of the FA-NO as m/z 470.9 (M + H)(+) and m/z 469.1 (M − H)(−). In addition, the adducts of the FA-NO derived from (14)NO and (15)NO gave individual mass numbers of the isotopic ratio of nitrogen for the following products: FA-(14)NO, m/z 471.14 (M + H)(+); m/z 469.17 (M − H)(−) and FA-(15)NO, m/z 472.16 (M + H)(+); m/z 470.12 (M − H)(–). To clarify the detailed NO scavenging action of FA, an electron spin resonance (ESR) study for radical detecting of the system containing carboxy-PTIO (2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) as an NO detection reagent in the presence of NOR3 and FA was performed. The carboxy-PTI (2-carboxyphenyl-4,4,5,5-tetramethylimidazoline-1-oxyl) radical produced from the reaction with NO reduced in the presence of FA showing that FA can directly scavenge NO. These results indicated that NO scavenging activity of FA reduced the accumulation of nitrite in the LPS-stimulated RAW264.7 cells. The NO modulation due to FA would be responsible for the alleviation from the failure in neural tube formation causing a high level of NO production.
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spelling pubmed-72787352020-06-12 Nitric Oxide Modulation by Folic Acid Fortification Taira, Junsei Ogi, Takayuki Antioxidants (Basel) Article Folic acid (FA) can be protected the neural tube defects (NTDs) causing nitric oxide (NO) induction, but the alleviation mechanism of the detailed FA function against NO has not yet been clarified. This study focused on elucidation of the interaction of FA and NO. FA suppressed nitrite accumulation as the NO indicator in lipopolysaccharide (LPS)-stimulated RAW264.7 cells, then the expression of the iNOS gene due to the LPS treatment was not inhibited by FA, suggesting that FA can modulate against NO or nitrogen radicals. NOR3 (4-ethyl-2-hydroxyamino-5-nitro-3-hexenamide) as the NO donor was used for evaluation of the NO scavenging activity of FA. FA suppressed the nitrite accumulation in a dose-dependent manner. To confirm the reaction product of FA and NO (FA-NO), liquid chromatography–mass spectrometry (LC/MS) was used to measure a similar system containing NOR3 and FA, and then detected the mass numbers of the FA-NO as m/z 470.9 (M + H)(+) and m/z 469.1 (M − H)(−). In addition, the adducts of the FA-NO derived from (14)NO and (15)NO gave individual mass numbers of the isotopic ratio of nitrogen for the following products: FA-(14)NO, m/z 471.14 (M + H)(+); m/z 469.17 (M − H)(−) and FA-(15)NO, m/z 472.16 (M + H)(+); m/z 470.12 (M − H)(–). To clarify the detailed NO scavenging action of FA, an electron spin resonance (ESR) study for radical detecting of the system containing carboxy-PTIO (2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) as an NO detection reagent in the presence of NOR3 and FA was performed. The carboxy-PTI (2-carboxyphenyl-4,4,5,5-tetramethylimidazoline-1-oxyl) radical produced from the reaction with NO reduced in the presence of FA showing that FA can directly scavenge NO. These results indicated that NO scavenging activity of FA reduced the accumulation of nitrite in the LPS-stimulated RAW264.7 cells. The NO modulation due to FA would be responsible for the alleviation from the failure in neural tube formation causing a high level of NO production. MDPI 2020-05-07 /pmc/articles/PMC7278735/ /pubmed/32392814 http://dx.doi.org/10.3390/antiox9050393 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Taira, Junsei
Ogi, Takayuki
Nitric Oxide Modulation by Folic Acid Fortification
title Nitric Oxide Modulation by Folic Acid Fortification
title_full Nitric Oxide Modulation by Folic Acid Fortification
title_fullStr Nitric Oxide Modulation by Folic Acid Fortification
title_full_unstemmed Nitric Oxide Modulation by Folic Acid Fortification
title_short Nitric Oxide Modulation by Folic Acid Fortification
title_sort nitric oxide modulation by folic acid fortification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278735/
https://www.ncbi.nlm.nih.gov/pubmed/32392814
http://dx.doi.org/10.3390/antiox9050393
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