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Evaluation of 10-Nitro Oleic Acid Bio-Elimination in Rats and Humans
Nitrated fatty acids are endogenously present in human and animal tissues, as well as in plant-derived oils. In particular, 10-nitro oleic acid (10-NO(2)-OA) potently induces Nrf2-dependent antioxidant gene expression and inhibits TLR4/NF-κB signaling, thus promoting an overall cyto-protective and a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215368/ https://www.ncbi.nlm.nih.gov/pubmed/28054588 http://dx.doi.org/10.1038/srep39900 |
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author | Salvatore, Sonia R. Vitturi, Dario A. Fazzari, Marco Jorkasky, Diane K. Schopfer, Francisco J. |
author_facet | Salvatore, Sonia R. Vitturi, Dario A. Fazzari, Marco Jorkasky, Diane K. Schopfer, Francisco J. |
author_sort | Salvatore, Sonia R. |
collection | PubMed |
description | Nitrated fatty acids are endogenously present in human and animal tissues, as well as in plant-derived oils. In particular, 10-nitro oleic acid (10-NO(2)-OA) potently induces Nrf2-dependent antioxidant gene expression and inhibits TLR4/NF-κB signaling, thus promoting an overall cyto-protective and anti-inflammatory response. 10-NO(2)-OA has been extensively tested in animal models and is currently undergoing clinical evaluation in humans. Bio-elimination pathways for 10-NO(2)-OA were evaluated in rats (30 mg/kg·day) and in humans (0.34 mg/kg) using samples obtained from a double-blind, dose-rising clinical trial. Quantitative radiochromatographic/MS analysis indicated that the renal and fecal pathways are the main routes for 10-NO(2)-OA excretion in rats, and allowed the identification of 4-nitro-octanedioic acid (NO(2)-8:0-diCOOH) as the most abundant metabolite in rat urine. In addition, high resolution LC-MS/MS analysis revealed the presence of a novel series of urinary metabolites including ω-carboxylation and β-oxidation products, as well as N-acetylcysteine, taurine and sulfo-conjugates in both rats and humans. Overall, the findings reported herein not only provide valuable tools for the experimental evaluation of 10-NO(2)-OA levels in vivo, but importantly they also set the basis for monitoring its metabolism during potential clinical interventions in humans. |
format | Online Article Text |
id | pubmed-5215368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52153682017-01-09 Evaluation of 10-Nitro Oleic Acid Bio-Elimination in Rats and Humans Salvatore, Sonia R. Vitturi, Dario A. Fazzari, Marco Jorkasky, Diane K. Schopfer, Francisco J. Sci Rep Article Nitrated fatty acids are endogenously present in human and animal tissues, as well as in plant-derived oils. In particular, 10-nitro oleic acid (10-NO(2)-OA) potently induces Nrf2-dependent antioxidant gene expression and inhibits TLR4/NF-κB signaling, thus promoting an overall cyto-protective and anti-inflammatory response. 10-NO(2)-OA has been extensively tested in animal models and is currently undergoing clinical evaluation in humans. Bio-elimination pathways for 10-NO(2)-OA were evaluated in rats (30 mg/kg·day) and in humans (0.34 mg/kg) using samples obtained from a double-blind, dose-rising clinical trial. Quantitative radiochromatographic/MS analysis indicated that the renal and fecal pathways are the main routes for 10-NO(2)-OA excretion in rats, and allowed the identification of 4-nitro-octanedioic acid (NO(2)-8:0-diCOOH) as the most abundant metabolite in rat urine. In addition, high resolution LC-MS/MS analysis revealed the presence of a novel series of urinary metabolites including ω-carboxylation and β-oxidation products, as well as N-acetylcysteine, taurine and sulfo-conjugates in both rats and humans. Overall, the findings reported herein not only provide valuable tools for the experimental evaluation of 10-NO(2)-OA levels in vivo, but importantly they also set the basis for monitoring its metabolism during potential clinical interventions in humans. Nature Publishing Group 2017-01-05 /pmc/articles/PMC5215368/ /pubmed/28054588 http://dx.doi.org/10.1038/srep39900 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Salvatore, Sonia R. Vitturi, Dario A. Fazzari, Marco Jorkasky, Diane K. Schopfer, Francisco J. Evaluation of 10-Nitro Oleic Acid Bio-Elimination in Rats and Humans |
title | Evaluation of 10-Nitro Oleic Acid Bio-Elimination in Rats and Humans |
title_full | Evaluation of 10-Nitro Oleic Acid Bio-Elimination in Rats and Humans |
title_fullStr | Evaluation of 10-Nitro Oleic Acid Bio-Elimination in Rats and Humans |
title_full_unstemmed | Evaluation of 10-Nitro Oleic Acid Bio-Elimination in Rats and Humans |
title_short | Evaluation of 10-Nitro Oleic Acid Bio-Elimination in Rats and Humans |
title_sort | evaluation of 10-nitro oleic acid bio-elimination in rats and humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215368/ https://www.ncbi.nlm.nih.gov/pubmed/28054588 http://dx.doi.org/10.1038/srep39900 |
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