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Biomarkers after Controlled Inhalation Exposure to Exhaust from Hydrogenated Vegetable Oil (HVO)
Hydrogenated vegetable oil (HVO) is a renewable diesel fuel used to replace petroleum diesel. The organic compounds in HVO are poorly characterized; therefore, toxicological properties could be different from petroleum diesel exhaust. The aim of this study was to evaluate the exposure and effective...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296316/ https://www.ncbi.nlm.nih.gov/pubmed/34208511 http://dx.doi.org/10.3390/ijerph18126492 |
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author | Krais, Annette M. Essig, Julie Y. Gren, Louise Vogs, Carolina Assarsson, Eva Dierschke, Katrin Nielsen, Jörn Strandberg, Bo Pagels, Joakim Broberg, Karin Lindh, Christian H. Gudmundsson, Anders Wierzbicka, Aneta |
author_facet | Krais, Annette M. Essig, Julie Y. Gren, Louise Vogs, Carolina Assarsson, Eva Dierschke, Katrin Nielsen, Jörn Strandberg, Bo Pagels, Joakim Broberg, Karin Lindh, Christian H. Gudmundsson, Anders Wierzbicka, Aneta |
author_sort | Krais, Annette M. |
collection | PubMed |
description | Hydrogenated vegetable oil (HVO) is a renewable diesel fuel used to replace petroleum diesel. The organic compounds in HVO are poorly characterized; therefore, toxicological properties could be different from petroleum diesel exhaust. The aim of this study was to evaluate the exposure and effective biomarkers in 18 individuals after short-term (3 h) exposure to HVO exhaust and petroleum diesel exhaust fumes. Liquid chromatography tandem mass spectrometry was used to analyze urinary biomarkers. A proximity extension assay was used for the measurement of inflammatory proteins in plasma samples. Short-term (3 h) exposure to HVO exhaust (PM(1) ~1 µg/m(3) and ~90 µg/m(3) for vehicles with and without exhaust aftertreatment systems, respectively) did not increase any exposure biomarker, whereas petroleum diesel exhaust (PM(1) ~300 µg/m(3)) increased urinary 4-MHA, a biomarker for p-xylene. HVO exhaust from the vehicle without exhaust aftertreatment system increased urinary 4-HNE-MA, a biomarker for lipid peroxidation, from 64 ng/mL urine (before exposure) to 141 ng/mL (24 h after exposure, p < 0.001). There was no differential expression of plasma inflammatory proteins between the HVO exhaust and control exposure group. In conclusion, short-term exposure to low concentrations of HVO exhaust did not increase urinary exposure biomarkers, but caused a slight increase in lipid peroxidation associated with the particle fraction. |
format | Online Article Text |
id | pubmed-8296316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82963162021-07-23 Biomarkers after Controlled Inhalation Exposure to Exhaust from Hydrogenated Vegetable Oil (HVO) Krais, Annette M. Essig, Julie Y. Gren, Louise Vogs, Carolina Assarsson, Eva Dierschke, Katrin Nielsen, Jörn Strandberg, Bo Pagels, Joakim Broberg, Karin Lindh, Christian H. Gudmundsson, Anders Wierzbicka, Aneta Int J Environ Res Public Health Article Hydrogenated vegetable oil (HVO) is a renewable diesel fuel used to replace petroleum diesel. The organic compounds in HVO are poorly characterized; therefore, toxicological properties could be different from petroleum diesel exhaust. The aim of this study was to evaluate the exposure and effective biomarkers in 18 individuals after short-term (3 h) exposure to HVO exhaust and petroleum diesel exhaust fumes. Liquid chromatography tandem mass spectrometry was used to analyze urinary biomarkers. A proximity extension assay was used for the measurement of inflammatory proteins in plasma samples. Short-term (3 h) exposure to HVO exhaust (PM(1) ~1 µg/m(3) and ~90 µg/m(3) for vehicles with and without exhaust aftertreatment systems, respectively) did not increase any exposure biomarker, whereas petroleum diesel exhaust (PM(1) ~300 µg/m(3)) increased urinary 4-MHA, a biomarker for p-xylene. HVO exhaust from the vehicle without exhaust aftertreatment system increased urinary 4-HNE-MA, a biomarker for lipid peroxidation, from 64 ng/mL urine (before exposure) to 141 ng/mL (24 h after exposure, p < 0.001). There was no differential expression of plasma inflammatory proteins between the HVO exhaust and control exposure group. In conclusion, short-term exposure to low concentrations of HVO exhaust did not increase urinary exposure biomarkers, but caused a slight increase in lipid peroxidation associated with the particle fraction. MDPI 2021-06-16 /pmc/articles/PMC8296316/ /pubmed/34208511 http://dx.doi.org/10.3390/ijerph18126492 Text en © 2021 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 Krais, Annette M. Essig, Julie Y. Gren, Louise Vogs, Carolina Assarsson, Eva Dierschke, Katrin Nielsen, Jörn Strandberg, Bo Pagels, Joakim Broberg, Karin Lindh, Christian H. Gudmundsson, Anders Wierzbicka, Aneta Biomarkers after Controlled Inhalation Exposure to Exhaust from Hydrogenated Vegetable Oil (HVO) |
title | Biomarkers after Controlled Inhalation Exposure to Exhaust from Hydrogenated Vegetable Oil (HVO) |
title_full | Biomarkers after Controlled Inhalation Exposure to Exhaust from Hydrogenated Vegetable Oil (HVO) |
title_fullStr | Biomarkers after Controlled Inhalation Exposure to Exhaust from Hydrogenated Vegetable Oil (HVO) |
title_full_unstemmed | Biomarkers after Controlled Inhalation Exposure to Exhaust from Hydrogenated Vegetable Oil (HVO) |
title_short | Biomarkers after Controlled Inhalation Exposure to Exhaust from Hydrogenated Vegetable Oil (HVO) |
title_sort | biomarkers after controlled inhalation exposure to exhaust from hydrogenated vegetable oil (hvo) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296316/ https://www.ncbi.nlm.nih.gov/pubmed/34208511 http://dx.doi.org/10.3390/ijerph18126492 |
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