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Fate of Pathologically Bound Oxygen Resulting from Inhalation of Labeled Ozone in Rats

Inhaled ozone (O(3)) reacts chemically with respiratory tract biomolecules where it forms covalently bound oxygen adducts. We investigated the fate of these adducts following inhalation exposure of rats to labeled ozone ((18)O(3), 2 ppm, 6 hr or 5 ppm, 2 hr). Increased (18)O was detected in blood pl...

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Detalles Bibliográficos
Autores principales: Hatch, Gary E., Slade, Ralph, McKee, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772903/
https://www.ncbi.nlm.nih.gov/pubmed/24052692
http://dx.doi.org/10.4137/EHI.S12673
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author Hatch, Gary E.
Slade, Ralph
McKee, John
author_facet Hatch, Gary E.
Slade, Ralph
McKee, John
author_sort Hatch, Gary E.
collection PubMed
description Inhaled ozone (O(3)) reacts chemically with respiratory tract biomolecules where it forms covalently bound oxygen adducts. We investigated the fate of these adducts following inhalation exposure of rats to labeled ozone ((18)O(3), 2 ppm, 6 hr or 5 ppm, 2 hr). Increased (18)O was detected in blood plasma at 7 hr post exposure and was continuously present in urine for 4 days. Total (18)O excreted was ~53% of the estimated amount of (18)O(3) retained by the rats during (18)O(3) exposure suggesting that only moderate recycling of the adduct material occurs. The time course of excretion, as well as properties of the excreted (18)O were determined to provide guidance to future searches for urinary oxidative stress markers. These results lend plausibility to published findings that O(3) inhalation could exert influences outside the lung, such as enhancement of atherosclerotic plaques.
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spelling pubmed-37729032013-09-19 Fate of Pathologically Bound Oxygen Resulting from Inhalation of Labeled Ozone in Rats Hatch, Gary E. Slade, Ralph McKee, John Environ Health Insights Original Research Inhaled ozone (O(3)) reacts chemically with respiratory tract biomolecules where it forms covalently bound oxygen adducts. We investigated the fate of these adducts following inhalation exposure of rats to labeled ozone ((18)O(3), 2 ppm, 6 hr or 5 ppm, 2 hr). Increased (18)O was detected in blood plasma at 7 hr post exposure and was continuously present in urine for 4 days. Total (18)O excreted was ~53% of the estimated amount of (18)O(3) retained by the rats during (18)O(3) exposure suggesting that only moderate recycling of the adduct material occurs. The time course of excretion, as well as properties of the excreted (18)O were determined to provide guidance to future searches for urinary oxidative stress markers. These results lend plausibility to published findings that O(3) inhalation could exert influences outside the lung, such as enhancement of atherosclerotic plaques. Libertas Academica 2013-09-04 /pmc/articles/PMC3772903/ /pubmed/24052692 http://dx.doi.org/10.4137/EHI.S12673 Text en © 2013 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article published under the Creative Commons CC-BY-NC 3.0 license.
spellingShingle Original Research
Hatch, Gary E.
Slade, Ralph
McKee, John
Fate of Pathologically Bound Oxygen Resulting from Inhalation of Labeled Ozone in Rats
title Fate of Pathologically Bound Oxygen Resulting from Inhalation of Labeled Ozone in Rats
title_full Fate of Pathologically Bound Oxygen Resulting from Inhalation of Labeled Ozone in Rats
title_fullStr Fate of Pathologically Bound Oxygen Resulting from Inhalation of Labeled Ozone in Rats
title_full_unstemmed Fate of Pathologically Bound Oxygen Resulting from Inhalation of Labeled Ozone in Rats
title_short Fate of Pathologically Bound Oxygen Resulting from Inhalation of Labeled Ozone in Rats
title_sort fate of pathologically bound oxygen resulting from inhalation of labeled ozone in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772903/
https://www.ncbi.nlm.nih.gov/pubmed/24052692
http://dx.doi.org/10.4137/EHI.S12673
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