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PM Source Apportionment for Short-Term Cardiac Function Changes in ApoE(−/−) Mice

Daily rates of cardiovascular mortality and morbidity are have been associated with daily variations in fine particulate matter (aerodynamic diameter ≤2.5 μm, PM(2.5)), but little is known about the influences of the individual source-related PM(2.5) categories or the temporal lags for the effects....

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Autores principales: Lippmann, Morton, Hwang, Jiang-Shiang, Maciejczyk, Polina, Chen, Lung-Chi
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1310921/
https://www.ncbi.nlm.nih.gov/pubmed/16263514
http://dx.doi.org/10.1289/ehp.8091
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author Lippmann, Morton
Hwang, Jiang-Shiang
Maciejczyk, Polina
Chen, Lung-Chi
author_facet Lippmann, Morton
Hwang, Jiang-Shiang
Maciejczyk, Polina
Chen, Lung-Chi
author_sort Lippmann, Morton
collection PubMed
description Daily rates of cardiovascular mortality and morbidity are have been associated with daily variations in fine particulate matter (aerodynamic diameter ≤2.5 μm, PM(2.5)), but little is known about the influences of the individual source-related PM(2.5) categories or the temporal lags for the effects. We investigated heart rate (HR) and HR variability (HRV) data collected during a 5-month study involving 6 hr/day, 5 day/week exposures of normal (C57) mice and a murine model for atherosclerotic disease (ApoE(−/−)) in Sterling Forest (Tuxedo, New York, USA). The mice were exposed to concentrated ambient particles (PM(2.5) concentrated 10-fold, producing an average of 113 μg/m3). Daily 6-hr PM(2.5) air samples were analyzed by X-ray fluorescence, permitting attribution to major PM source categories [secondary sulfate (SS), resuspended soil (RS), residual oil (RO) combustion, and other, largely due to motor vehicle traffic]. We examined associations between these PM(2.5) components and both HR and HRV for three different daily time periods: during exposure, the afternoon after exposure, and late at night. For HR there were significant transient associations for RS during exposure, and for SS in the afternoon after exposure. For HRV, there were comparable associations with RO in the afternoon after exposure and for both SS and RS late at night. The biologic bases for these associations and their temporal lags are not known but may be related to the differential solubility of the biologically active PM components at the respiratory epithelia and their access to cells that release mediators that reach the cardiovascular system. Clearly, further research to elucidate the underlying processes is needed.
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spelling pubmed-13109212005-12-12 PM Source Apportionment for Short-Term Cardiac Function Changes in ApoE(−/−) Mice Lippmann, Morton Hwang, Jiang-Shiang Maciejczyk, Polina Chen, Lung-Chi Environ Health Perspect Research Daily rates of cardiovascular mortality and morbidity are have been associated with daily variations in fine particulate matter (aerodynamic diameter ≤2.5 μm, PM(2.5)), but little is known about the influences of the individual source-related PM(2.5) categories or the temporal lags for the effects. We investigated heart rate (HR) and HR variability (HRV) data collected during a 5-month study involving 6 hr/day, 5 day/week exposures of normal (C57) mice and a murine model for atherosclerotic disease (ApoE(−/−)) in Sterling Forest (Tuxedo, New York, USA). The mice were exposed to concentrated ambient particles (PM(2.5) concentrated 10-fold, producing an average of 113 μg/m3). Daily 6-hr PM(2.5) air samples were analyzed by X-ray fluorescence, permitting attribution to major PM source categories [secondary sulfate (SS), resuspended soil (RS), residual oil (RO) combustion, and other, largely due to motor vehicle traffic]. We examined associations between these PM(2.5) components and both HR and HRV for three different daily time periods: during exposure, the afternoon after exposure, and late at night. For HR there were significant transient associations for RS during exposure, and for SS in the afternoon after exposure. For HRV, there were comparable associations with RO in the afternoon after exposure and for both SS and RS late at night. The biologic bases for these associations and their temporal lags are not known but may be related to the differential solubility of the biologically active PM components at the respiratory epithelia and their access to cells that release mediators that reach the cardiovascular system. Clearly, further research to elucidate the underlying processes is needed. National Institute of Environmental Health Sciences 2005-11 2005-07-05 /pmc/articles/PMC1310921/ /pubmed/16263514 http://dx.doi.org/10.1289/ehp.8091 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Lippmann, Morton
Hwang, Jiang-Shiang
Maciejczyk, Polina
Chen, Lung-Chi
PM Source Apportionment for Short-Term Cardiac Function Changes in ApoE(−/−) Mice
title PM Source Apportionment for Short-Term Cardiac Function Changes in ApoE(−/−) Mice
title_full PM Source Apportionment for Short-Term Cardiac Function Changes in ApoE(−/−) Mice
title_fullStr PM Source Apportionment for Short-Term Cardiac Function Changes in ApoE(−/−) Mice
title_full_unstemmed PM Source Apportionment for Short-Term Cardiac Function Changes in ApoE(−/−) Mice
title_short PM Source Apportionment for Short-Term Cardiac Function Changes in ApoE(−/−) Mice
title_sort pm source apportionment for short-term cardiac function changes in apoe(−/−) mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1310921/
https://www.ncbi.nlm.nih.gov/pubmed/16263514
http://dx.doi.org/10.1289/ehp.8091
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