Ethane and n-pentane in exhaled breath are biomarkers of exposure not effect

被引:17
作者
Gorham, Katrine A. [1 ]
Andersen, Mads P. Sulbaek [1 ]
Meinardi, Simone [1 ]
Delfino, Ralph J. [2 ]
Staimer, Norbert [2 ]
Tjoa, Thomas [2 ]
Rowland, F. Sherwood [1 ]
Blake, Donald R. [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Sch Med, Dept Epidemiol, Irvine, CA 92717 USA
基金
美国国家卫生研究院;
关键词
Ethane; pentane; nitric oxide; carbonylated proteins; oxidative stress; exhaled breath analysis; LIPID-PEROXIDATION; PULMONARY-FUNCTION; OXIDATIVE STRESS; NITRIC-OXIDE; DISEASE; 8-ISOPROSTANE; ALKANES; PROTEIN; OZONE; AIR;
D O I
10.1080/13547500902730680
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The relationship of exhaled ethane and n-pentane to exhaled NO, carbonylated proteins, and indoor/outdoor atmospheric pollutants were examined in order to evaluate ethane and n-pentane as potential markers of airway inflammation and/or oxidative stress. Exhaled NO and carbonylated proteins were found to have no significant associations with either ethane (p = 0.96 and p = 0.81, respectively) or n-pentane (p = 0.44 and 0.28, respectively) when outliers were included. In the case where outliers were removed n-pentane was found to be inversely associated with carbonylated proteins. Exhaled hydrocarbons adjusted for indoor hydrocarbon concentrations were instead found to be positively associated with air pollutants (NO, NO2 and CO), suggesting pollutant exposure is driving exhaled hydrocarbon concentrations. Given these findings, ethane and n-pentane do not appear to be markers of airway inflammation or oxidative stress.
引用
收藏
页码:17 / 25
页数:9
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