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Controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function

BACKGROUND: Exposure to wood smoke is associated with respiratory symptoms, whereas knowledge on systemic effects is limited. We investigated effects on systemic inflammation, oxidative stress and microvascular function (MVF) after controlled wood smoke exposure. METHODS: In a randomised, double-bli...

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Autores principales: Forchhammer, Lykke, Møller, Peter, Riddervold, Ingunn Skogstad, Bønløkke, Jakob, Massling, Andreas, Sigsgaard, Torben, Loft, Steffen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369202/
https://www.ncbi.nlm.nih.gov/pubmed/22452928
http://dx.doi.org/10.1186/1743-8977-9-7
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author Forchhammer, Lykke
Møller, Peter
Riddervold, Ingunn Skogstad
Bønløkke, Jakob
Massling, Andreas
Sigsgaard, Torben
Loft, Steffen
author_facet Forchhammer, Lykke
Møller, Peter
Riddervold, Ingunn Skogstad
Bønløkke, Jakob
Massling, Andreas
Sigsgaard, Torben
Loft, Steffen
author_sort Forchhammer, Lykke
collection PubMed
description BACKGROUND: Exposure to wood smoke is associated with respiratory symptoms, whereas knowledge on systemic effects is limited. We investigated effects on systemic inflammation, oxidative stress and microvascular function (MVF) after controlled wood smoke exposure. METHODS: In a randomised, double-blinded, cross-over study 20 non-smoking atopic subjects were exposed at rest to 14, 220, or 354 μg/m(3 )of particles from a well-burning modern wood stove for 3 h in a climate controlled chamber with 2 week intervals. We investigated the level of oxidatively damaged DNA, inflammatory markers and adhesion molecules before and 0, 6 and 20 h after exposure. Six h after exposure we measured MVF non-invasively by digital peripheral artery tonometry following arm ischemia. RESULTS: The MVF score was unaltered after inhalation of clean air (1.58 ± 0.07; mean ± SEM), low (1.51 ± 0.07) or high (1.61 ± 0.09) concentrations of wood smoke particles in atopic subjects, whereas unexposed non-atopic subjects had higher score (1.91 ± 0.09). The level of oxidatively damaged DNA, mRNA of ITGAL, CCL2, TNF, IL6, IL8, HMOX1, and OGG1 and surface marker molecules ICAM1, ITGAL and L-selectin in peripheral blood mononuclear cells were not affected by inhalation of wood smoke particles. CONCLUSIONS: Exposure to wood smoke had no effect on markers of oxidative stress, DNA damage, cell adhesion, cytokines or MVF in atopic subjects.
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spelling pubmed-33692022012-06-07 Controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function Forchhammer, Lykke Møller, Peter Riddervold, Ingunn Skogstad Bønløkke, Jakob Massling, Andreas Sigsgaard, Torben Loft, Steffen Part Fibre Toxicol Research BACKGROUND: Exposure to wood smoke is associated with respiratory symptoms, whereas knowledge on systemic effects is limited. We investigated effects on systemic inflammation, oxidative stress and microvascular function (MVF) after controlled wood smoke exposure. METHODS: In a randomised, double-blinded, cross-over study 20 non-smoking atopic subjects were exposed at rest to 14, 220, or 354 μg/m(3 )of particles from a well-burning modern wood stove for 3 h in a climate controlled chamber with 2 week intervals. We investigated the level of oxidatively damaged DNA, inflammatory markers and adhesion molecules before and 0, 6 and 20 h after exposure. Six h after exposure we measured MVF non-invasively by digital peripheral artery tonometry following arm ischemia. RESULTS: The MVF score was unaltered after inhalation of clean air (1.58 ± 0.07; mean ± SEM), low (1.51 ± 0.07) or high (1.61 ± 0.09) concentrations of wood smoke particles in atopic subjects, whereas unexposed non-atopic subjects had higher score (1.91 ± 0.09). The level of oxidatively damaged DNA, mRNA of ITGAL, CCL2, TNF, IL6, IL8, HMOX1, and OGG1 and surface marker molecules ICAM1, ITGAL and L-selectin in peripheral blood mononuclear cells were not affected by inhalation of wood smoke particles. CONCLUSIONS: Exposure to wood smoke had no effect on markers of oxidative stress, DNA damage, cell adhesion, cytokines or MVF in atopic subjects. BioMed Central 2012-03-27 /pmc/articles/PMC3369202/ /pubmed/22452928 http://dx.doi.org/10.1186/1743-8977-9-7 Text en Copyright ©2012 Forchhammer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Forchhammer, Lykke
Møller, Peter
Riddervold, Ingunn Skogstad
Bønløkke, Jakob
Massling, Andreas
Sigsgaard, Torben
Loft, Steffen
Controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function
title Controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function
title_full Controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function
title_fullStr Controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function
title_full_unstemmed Controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function
title_short Controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function
title_sort controlled human wood smoke exposure: oxidative stress, inflammation and microvascular function
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369202/
https://www.ncbi.nlm.nih.gov/pubmed/22452928
http://dx.doi.org/10.1186/1743-8977-9-7
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