Effect of low-dose aspirin on the markers of oxidative stress

被引:24
作者
Ristimäe, T
Zilmer, M
Zilmer, K
Kairane, C
Kullisaar, T
Teesalu, R
机构
[1] Tartu State Univ, Dept Cardiol, Fac Med, EE-51014 Tartu, Estonia
[2] Tartu State Univ, Dept Biochem, Fac Med, EE-51014 Tartu, Estonia
关键词
low-dose aspirin; healthy middle-aged subjects; oxidative stress;
D O I
10.1023/A:1007867402152
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The present study estimates effects of low-dose enteric coated aspirin (ECA) on oxidative stress (OS) markers in a group of middle-aged men (mean age 51.2 +/- 6.9 years) free of pre-existing ischemic heart disease. Methods. Serum products of lipid peroxidation, and measures of antioxidative status were detected in 25 healthy men in baseline and after two-week treatment period. Results. In respect to serum products of lipid peroxidation and markers of antioxidant status, no statistically significant differences between the pre- and after-treatment data were observed for any measures, with the exception of values of serum antioxidative capacity (39.0 +/- 2.5 and 42 +/- 4.6, respectively). Conclusions. Administration of ECA does not initiate the OS in blood and improves the general antioxidative potency of blood. This may imply towards certain antiatherogenic influence of low-dose ECA, exhibited even with a short-term treatment period. Regarding OS markers, a variety of individual responses observed in the selected subgroups should be investigated and possibly taken into account while treatment with ECA is initiated for primary prevention of cerebrovascular events.
引用
收藏
页码:485 / 490
页数:6
相关论文
共 28 条
[1]  
ARMSTRONG D, 1998, METHODS MOLB IOL
[2]   The role of oxidized lipoproteins in atherogenesis [J].
Berliner, JA ;
Heinecke, JW .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (05) :707-727
[3]  
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[4]  
CHARMA M, 1994, INT J CARDIOL, V43, P121
[5]  
CLEMETSON KJ, 1987, PLATELETS BIOL PATHO, V3, P1
[6]   Blood radicals - Reactive nitrogen species, reactive oxygen species, transition metal ions, and the vascular system [J].
DarleyUsmar, V ;
Halliwell, B .
PHARMACEUTICAL RESEARCH, 1996, 13 (05) :649-662
[7]  
DAVIDGE ST, 1994, AM J OBSTET GYNECOL, V170, P215
[8]  
DEGAETANO G, 1982, LANCET, V2, P974
[9]   Mechanisms of disease - Antioxidants and atherosclerotic heart disease [J].
Diaz, MN ;
Frei, B ;
Vita, JA ;
Keaney, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (06) :408-416
[10]   TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77