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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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Detalles Bibliográficos
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
Descripción
Sumario: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.