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Transient and Persistent Metabolomic Changes in Plasma following Chronic Cigarette Smoke Exposure in a Mouse Model

Cigarette smoke exposure is linked to the development of a variety of chronic lung and systemic diseases in susceptible individuals. Metabolomics approaches may aid in defining disease phenotypes, may help predict responses to treatment, and could identify biomarkers of risk for developing disease....

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Autores principales: Cruickshank-Quinn, Charmion I., Mahaffey, Spencer, Justice, Matthew J., Hughes, Grant, Armstrong, Michael, Bowler, Russell P., Reisdorph, Richard, Petrache, Irina, Reisdorph, Nichole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090193/
https://www.ncbi.nlm.nih.gov/pubmed/25007263
http://dx.doi.org/10.1371/journal.pone.0101855
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author Cruickshank-Quinn, Charmion I.
Mahaffey, Spencer
Justice, Matthew J.
Hughes, Grant
Armstrong, Michael
Bowler, Russell P.
Reisdorph, Richard
Petrache, Irina
Reisdorph, Nichole
author_facet Cruickshank-Quinn, Charmion I.
Mahaffey, Spencer
Justice, Matthew J.
Hughes, Grant
Armstrong, Michael
Bowler, Russell P.
Reisdorph, Richard
Petrache, Irina
Reisdorph, Nichole
author_sort Cruickshank-Quinn, Charmion I.
collection PubMed
description Cigarette smoke exposure is linked to the development of a variety of chronic lung and systemic diseases in susceptible individuals. Metabolomics approaches may aid in defining disease phenotypes, may help predict responses to treatment, and could identify biomarkers of risk for developing disease. Using a mouse model of chronic cigarette smoke exposure sufficient to cause mild emphysema, we investigated whether cigarette smoke induces distinct metabolic profiles and determined their persistence following smoking cessation. Metabolites were extracted from plasma and fractionated based on chemical class using liquid-liquid and solid-phase extraction prior to performing liquid chromatography mass spectrometry-based metabolomics. Metabolites were evaluated for statistically significant differences among group means (p-value≤0.05) and fold change ≥1.5). Cigarette smoke exposure was associated with significant differences in amino acid, purine, lipid, fatty acid, and steroid metabolite levels compared to air exposed animals. Whereas 60% of the metabolite changes were reversible, 40% of metabolites remained persistently altered even following 2 months of smoking cessation, including nicotine metabolites. Validation of metabolite species and translation of these findings to human plasma metabolite signatures induced by cigarette smoking may lead to the discovery of biomarkers or pathogenic pathways of smoking-induced disease.
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spelling pubmed-40901932014-07-14 Transient and Persistent Metabolomic Changes in Plasma following Chronic Cigarette Smoke Exposure in a Mouse Model Cruickshank-Quinn, Charmion I. Mahaffey, Spencer Justice, Matthew J. Hughes, Grant Armstrong, Michael Bowler, Russell P. Reisdorph, Richard Petrache, Irina Reisdorph, Nichole PLoS One Research Article Cigarette smoke exposure is linked to the development of a variety of chronic lung and systemic diseases in susceptible individuals. Metabolomics approaches may aid in defining disease phenotypes, may help predict responses to treatment, and could identify biomarkers of risk for developing disease. Using a mouse model of chronic cigarette smoke exposure sufficient to cause mild emphysema, we investigated whether cigarette smoke induces distinct metabolic profiles and determined their persistence following smoking cessation. Metabolites were extracted from plasma and fractionated based on chemical class using liquid-liquid and solid-phase extraction prior to performing liquid chromatography mass spectrometry-based metabolomics. Metabolites were evaluated for statistically significant differences among group means (p-value≤0.05) and fold change ≥1.5). Cigarette smoke exposure was associated with significant differences in amino acid, purine, lipid, fatty acid, and steroid metabolite levels compared to air exposed animals. Whereas 60% of the metabolite changes were reversible, 40% of metabolites remained persistently altered even following 2 months of smoking cessation, including nicotine metabolites. Validation of metabolite species and translation of these findings to human plasma metabolite signatures induced by cigarette smoking may lead to the discovery of biomarkers or pathogenic pathways of smoking-induced disease. Public Library of Science 2014-07-09 /pmc/articles/PMC4090193/ /pubmed/25007263 http://dx.doi.org/10.1371/journal.pone.0101855 Text en © 2014 Cruickshank-Quinn et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cruickshank-Quinn, Charmion I.
Mahaffey, Spencer
Justice, Matthew J.
Hughes, Grant
Armstrong, Michael
Bowler, Russell P.
Reisdorph, Richard
Petrache, Irina
Reisdorph, Nichole
Transient and Persistent Metabolomic Changes in Plasma following Chronic Cigarette Smoke Exposure in a Mouse Model
title Transient and Persistent Metabolomic Changes in Plasma following Chronic Cigarette Smoke Exposure in a Mouse Model
title_full Transient and Persistent Metabolomic Changes in Plasma following Chronic Cigarette Smoke Exposure in a Mouse Model
title_fullStr Transient and Persistent Metabolomic Changes in Plasma following Chronic Cigarette Smoke Exposure in a Mouse Model
title_full_unstemmed Transient and Persistent Metabolomic Changes in Plasma following Chronic Cigarette Smoke Exposure in a Mouse Model
title_short Transient and Persistent Metabolomic Changes in Plasma following Chronic Cigarette Smoke Exposure in a Mouse Model
title_sort transient and persistent metabolomic changes in plasma following chronic cigarette smoke exposure in a mouse model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090193/
https://www.ncbi.nlm.nih.gov/pubmed/25007263
http://dx.doi.org/10.1371/journal.pone.0101855
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