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Exhaled Nitric Oxide and Pulmonary Oxygen Toxicity Susceptibility
Individual susceptibility to pulmonary oxygen toxicity (PO(2)tox) is highly variable and currently lacks a reliable biomarker for predicting pulmonary hyperoxic stress. As nitric oxide (NO) is involved in many respiratory system processes and functions, we aimed to determine if expired nitric oxide...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456729/ https://www.ncbi.nlm.nih.gov/pubmed/37623874 http://dx.doi.org/10.3390/metabo13080930 |
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author | Fothergill, David M. Gertner, Jeffery W. |
author_facet | Fothergill, David M. Gertner, Jeffery W. |
author_sort | Fothergill, David M. |
collection | PubMed |
description | Individual susceptibility to pulmonary oxygen toxicity (PO(2)tox) is highly variable and currently lacks a reliable biomarker for predicting pulmonary hyperoxic stress. As nitric oxide (NO) is involved in many respiratory system processes and functions, we aimed to determine if expired nitric oxide (F(E)NO) levels can provide an indication of PO(2)tox susceptibility in humans. Eight U.S. Navy-trained divers volunteered as subjects. The hyperoxic exposures consisted of six- and eight-hour hyperbaric chamber dives conducted on consecutive days in which subjects breathed 100% oxygen at 202.65 kPa. Subjects’ individual variability in pulmonary function and F(E)NO was measured twice daily over five days and compared with their post-dive values to assess susceptibility to PO(2)tox. Only subjects who showed no decrements in pulmonary function following the six-hour exposure conducted the eight-hour dive. F(E)NO decreased by 55% immediately following the six-hour oxygen exposure (n = 8, p < 0.0001) and by 63% following the eight-hour exposure (n = 4, p < 0.0001). Four subjects showed significant decreases in pulmonary function immediately following the six-hour exposure. These subjects had the lowest baseline F(E)NO, had the lowest post-dive F(E)NO, and had clinical symptoms of PO(2)tox. Individuals with low F(E)NO were the first to develop PO(2)tox symptoms and deficits in pulmonary function from the hyperoxic exposures. These data suggest that endogenous levels of NO in the lungs may protect against the development of PO(2)tox. |
format | Online Article Text |
id | pubmed-10456729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104567292023-08-26 Exhaled Nitric Oxide and Pulmonary Oxygen Toxicity Susceptibility Fothergill, David M. Gertner, Jeffery W. Metabolites Article Individual susceptibility to pulmonary oxygen toxicity (PO(2)tox) is highly variable and currently lacks a reliable biomarker for predicting pulmonary hyperoxic stress. As nitric oxide (NO) is involved in many respiratory system processes and functions, we aimed to determine if expired nitric oxide (F(E)NO) levels can provide an indication of PO(2)tox susceptibility in humans. Eight U.S. Navy-trained divers volunteered as subjects. The hyperoxic exposures consisted of six- and eight-hour hyperbaric chamber dives conducted on consecutive days in which subjects breathed 100% oxygen at 202.65 kPa. Subjects’ individual variability in pulmonary function and F(E)NO was measured twice daily over five days and compared with their post-dive values to assess susceptibility to PO(2)tox. Only subjects who showed no decrements in pulmonary function following the six-hour exposure conducted the eight-hour dive. F(E)NO decreased by 55% immediately following the six-hour oxygen exposure (n = 8, p < 0.0001) and by 63% following the eight-hour exposure (n = 4, p < 0.0001). Four subjects showed significant decreases in pulmonary function immediately following the six-hour exposure. These subjects had the lowest baseline F(E)NO, had the lowest post-dive F(E)NO, and had clinical symptoms of PO(2)tox. Individuals with low F(E)NO were the first to develop PO(2)tox symptoms and deficits in pulmonary function from the hyperoxic exposures. These data suggest that endogenous levels of NO in the lungs may protect against the development of PO(2)tox. MDPI 2023-08-08 /pmc/articles/PMC10456729/ /pubmed/37623874 http://dx.doi.org/10.3390/metabo13080930 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fothergill, David M. Gertner, Jeffery W. Exhaled Nitric Oxide and Pulmonary Oxygen Toxicity Susceptibility |
title | Exhaled Nitric Oxide and Pulmonary Oxygen Toxicity Susceptibility |
title_full | Exhaled Nitric Oxide and Pulmonary Oxygen Toxicity Susceptibility |
title_fullStr | Exhaled Nitric Oxide and Pulmonary Oxygen Toxicity Susceptibility |
title_full_unstemmed | Exhaled Nitric Oxide and Pulmonary Oxygen Toxicity Susceptibility |
title_short | Exhaled Nitric Oxide and Pulmonary Oxygen Toxicity Susceptibility |
title_sort | exhaled nitric oxide and pulmonary oxygen toxicity susceptibility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456729/ https://www.ncbi.nlm.nih.gov/pubmed/37623874 http://dx.doi.org/10.3390/metabo13080930 |
work_keys_str_mv | AT fothergilldavidm exhalednitricoxideandpulmonaryoxygentoxicitysusceptibility AT gertnerjefferyw exhalednitricoxideandpulmonaryoxygentoxicitysusceptibility |