| dc.contributor |
Kenneth Adler, Committee Chair |
|
| dc.contributor |
Philip Sannes, Committee Member |
|
| dc.contributor |
Damian Shea, Committee Member |
|
| dc.contributor |
Kevin Dreher, Committee Member |
|
| dc.creator |
Knuckles, Travis |
|
| dc.date |
2010-04-02T18:55:33Z |
|
| dc.date |
2010-04-02T18:55:33Z |
|
| dc.date |
2006-07-18 |
|
| dc.date.accessioned |
2023-02-28T17:08:38Z |
|
| dc.date.available |
2023-02-28T17:08:38Z |
|
| dc.identifier |
etd-06122005-112617 |
|
| dc.identifier |
http://www.lib.ncsu.edu/resolver/1840.16/4528 |
|
| dc.identifier.uri |
http://localhost:8080/xmlui/handle/CUHPOERS/265723 |
|
| dc.description |
Epidemiological studies have shown an association between air pollution particulate matter (PM) and adverse cardiovascular effects. Although numerous mechanisms have been proposed, the actual mechanism(s) as well as emission sources and associated causal properties by which PM affects the cardiovascular system remain elusive. At least some adverse PM health effects can be attributed to bioavailable constituents, most notably, the transition metal content of the particles. Toxicological studies in rats using residual oil fly ash (ROFA) combustion source particles show extrapulmonary effects ranging from thermo-regulatory alterations, myocardial necrotic lesions, to fatal cardiac arrhythmias. Exposure of rats to ROFA via intratracheal instillation shows a rapid and transient increase in plasma metal content as early as 15mins post-exposure, suggesting that PM constituents are bioavailable to both the systemic circulation and perfused organs. However, the impact of this systemic exposure on extrapulmonary organs at the cellular and molecular levels is unknown. In this study, cardiomyocytes derived from 1-day-old rat pups were exposed to determine the direct effects of a particle free residual oil fly ash leachate (ROFA-L). Using concentration of leachate relevant to amount that were found in the plasma of rats following pulmonary deposition, I have shown that ROFA bioavailable constituents cytotoxicity in cardiomyocyte cultures and alter cardiomyocyte gene expression and transcription factor activation profiles consistent with alteration in cardiomyocyte growth and function. |
|
| dc.rights |
I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to NC State University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
|
| dc.subject |
PM |
|
| dc.subject |
cardiac injury |
|
| dc.subject |
oxidative stress |
|
| dc.subject |
cardiac toxicity |
|
| dc.subject |
microarray analysis |
|
| dc.subject |
transcription factors |
|
| dc.title |
In Vitro Cardiotoxicity of Residual Oil Fly Ash. |
|