Effect of age on the breath methylated alkane contour, a display of apparent new markers of oxidative stress

被引:127
作者
Phillips, M
Cataneo, RN
Greenberg, J
Gunawardena, R
Naidu, A
Rahbari-Oskoui, F
机构
[1] Menssana Res Inc, Ft Lee, NJ 07024 USA
[2] Sisters Char Med Ctr, Dept Med, Staten Isl, NY USA
[3] New York Med Coll, Dept Med, Valhalla, NY 10595 USA
来源
JOURNAL OF LABORATORY AND CLINICAL MEDICINE | 2000年 / 136卷 / 03期
关键词
D O I
10.1067/mlc.2000.108943
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Reactive oxygen species (ROS) are toxic byproducts of mitochondrial energy production that inflict oxidative stress, a constant barrage of damage to DNA, proteins, lipids, and other biologically important molecules. Oxidative stress has been implicated as a pathologic mechanism in aging and in several diseases. We developed a display of apparent new markers of oxidative stress in human beings, the breath methylated alkane contour (BMAC). The BMAC is a three-dimensional display of C4 to C20 alkanes and monomethylated alkanes in breath, with x-axis = carbon chain length, z-axis = methylation site, and y-axis = alveolar gradient (relative abundance in breath minus relative abundance in room air). In 102 normal human subjects of 9 to 89 years of age, alveolar gradients of components of the BMAC increased significantly with age. The mean alveolar gradient of all components of the BMAC varied from negative in the youngest quartile (ages 9 to 31 years) to positive in the oldest quartile (ages 74 to 89 years)(P < 2.10(-9)). These findings were consistent with an increase in oxidative stress with advancing age, although an age-related decline in clearance by cytochrome p450 may have contributed. The BMAC provides a display of apparent new markers of oxidative stress with potential applications in aging research, clinical diagnosis, pharmacology, and toxicology.
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页码:243 / 249
页数:7
相关论文
共 31 条
[1]   LIFE-SPAN OF DROSOPHILA-MELANOGASTER IN HIGHLY OXYGENATED ATMOSPHERES [J].
BARET, P ;
FOUARGE, A ;
BULLENS, P ;
LINTS, FA .
MECHANISMS OF AGEING AND DEVELOPMENT, 1994, 76 (01) :25-31
[2]   Structural and functional changes in proteins induced by free radical-mediated oxidative stress and protective action of the antioxidants N-tert-butyl-α-phenylnitrone and vitamin E [J].
Butterfield, DA ;
Koppal, T ;
Howard, B ;
Subramaniam, R ;
Hall, N ;
Hensley, K ;
Yatin, S ;
Allen, K ;
Aksenov, M ;
Aksenov, M ;
Carney, J .
TOWARDS PROLONGATION OF THE HEALTHY LIFE SPAN: PRACTICAL APPROACHES TO INTERVENTION, 1998, 854 :448-462
[3]  
Charpentier KP, 1997, BIOPHARM DRUG DISPOS, V18, P139, DOI 10.1002/(SICI)1099-081X(199703)18:2<139::AID-BDD7>3.0.CO
[4]  
2-Z
[5]  
Davies KJA, 1995, BIOCHEM SOC SYMP, P1, DOI 10.1042/bss0610001
[6]  
HIETANEN E, 1994, EUR J CLIN NUTR, V48, P575
[7]   SHORTENING OF THE INVITRO LIFESPAN OF HUMAN-DIPLOID FIBROBLASTS EXPOSED TO HYPERBARIC-OXYGEN [J].
HONDA, S ;
MATSUO, M .
EXPERIMENTAL GERONTOLOGY, 1983, 18 (05) :339-345
[8]   BREATH PENTANE EXCRETION AS A MARKER OF DISEASE-ACTIVITY IN RHEUMATOID-ARTHRITIS [J].
HUMAD, S ;
ZARLING, E ;
CLAPPER, M ;
SKOSEY, JL .
FREE RADICAL RESEARCH COMMUNICATIONS, 1988, 5 (02) :101-106
[9]  
Jones Martin, 1993, Biochemical Society Transactions, V21, p485S
[10]  
KNEEPKENS CMF, 1992, CLIN INVEST MED, V15, P163