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Effects of elevated CO(2) levels on lung immune response to organic dust and lipopolysaccharide

Workplaces with elevated organic dust levels such as animal feed barns also commonly have elevated levels of gasses, such as CO(2). Workers exposed to such complex environments often experience respiratory effects that may be due to a combination of respirable factors. We examined the effects of CO(...

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Autores principales: Schneberger, David, Pandher, Upkardeep, Thompson, Brooke, Kirychuk, Shelley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033726/
https://www.ncbi.nlm.nih.gov/pubmed/33836776
http://dx.doi.org/10.1186/s12931-021-01700-4
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author Schneberger, David
Pandher, Upkardeep
Thompson, Brooke
Kirychuk, Shelley
author_facet Schneberger, David
Pandher, Upkardeep
Thompson, Brooke
Kirychuk, Shelley
author_sort Schneberger, David
collection PubMed
description Workplaces with elevated organic dust levels such as animal feed barns also commonly have elevated levels of gasses, such as CO(2). Workers exposed to such complex environments often experience respiratory effects that may be due to a combination of respirable factors. We examined the effects of CO(2) on lung innate immune responses in mice co-exposed to the inflammatory agents lipopolysaccharide (LPS) and organic dust. We evaluated CO(2) levels at the building recommended limit (1000 ppm) as well as the exposure limit (5000 ppm). Mice were nasally instilled with dust extracts or LPS and immediately put into chambers with a constant flow of room air (avg. 430 ppm CO(2)), 1000 ppm, or 5000 ppm CO(2) enriched air. Results reveal that organic dust exposures tended to show decreased inflammatory responses with 1000 ppm CO(2) and increased responses at 5000 ppm CO(2). Conversely, LPS with addition of CO(2) as low as 1000 ppm tended to inhibit several inflammatory markers. In most cases saline treated animals showed few changes with CO(2) exposure, though some changes in mRNA levels were present. This shows that CO(2) as low as 1000 ppm CO(2) was capable of altering innate immune responses to both LPS and organic dust extracts, but each response was altered in a different fashion.
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spelling pubmed-80337262021-04-09 Effects of elevated CO(2) levels on lung immune response to organic dust and lipopolysaccharide Schneberger, David Pandher, Upkardeep Thompson, Brooke Kirychuk, Shelley Respir Res Research Workplaces with elevated organic dust levels such as animal feed barns also commonly have elevated levels of gasses, such as CO(2). Workers exposed to such complex environments often experience respiratory effects that may be due to a combination of respirable factors. We examined the effects of CO(2) on lung innate immune responses in mice co-exposed to the inflammatory agents lipopolysaccharide (LPS) and organic dust. We evaluated CO(2) levels at the building recommended limit (1000 ppm) as well as the exposure limit (5000 ppm). Mice were nasally instilled with dust extracts or LPS and immediately put into chambers with a constant flow of room air (avg. 430 ppm CO(2)), 1000 ppm, or 5000 ppm CO(2) enriched air. Results reveal that organic dust exposures tended to show decreased inflammatory responses with 1000 ppm CO(2) and increased responses at 5000 ppm CO(2). Conversely, LPS with addition of CO(2) as low as 1000 ppm tended to inhibit several inflammatory markers. In most cases saline treated animals showed few changes with CO(2) exposure, though some changes in mRNA levels were present. This shows that CO(2) as low as 1000 ppm CO(2) was capable of altering innate immune responses to both LPS and organic dust extracts, but each response was altered in a different fashion. BioMed Central 2021-04-09 2021 /pmc/articles/PMC8033726/ /pubmed/33836776 http://dx.doi.org/10.1186/s12931-021-01700-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Schneberger, David
Pandher, Upkardeep
Thompson, Brooke
Kirychuk, Shelley
Effects of elevated CO(2) levels on lung immune response to organic dust and lipopolysaccharide
title Effects of elevated CO(2) levels on lung immune response to organic dust and lipopolysaccharide
title_full Effects of elevated CO(2) levels on lung immune response to organic dust and lipopolysaccharide
title_fullStr Effects of elevated CO(2) levels on lung immune response to organic dust and lipopolysaccharide
title_full_unstemmed Effects of elevated CO(2) levels on lung immune response to organic dust and lipopolysaccharide
title_short Effects of elevated CO(2) levels on lung immune response to organic dust and lipopolysaccharide
title_sort effects of elevated co(2) levels on lung immune response to organic dust and lipopolysaccharide
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033726/
https://www.ncbi.nlm.nih.gov/pubmed/33836776
http://dx.doi.org/10.1186/s12931-021-01700-4
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