TY - JOUR
T1 - Antioxidant properties of aspirin
T2 - Characterization of the ability of aspirin to inhibit silica-induced lipid peroxidation, DNA damage, NF-κB activation, and TNF-α production
AU - Shi, Xianglin
AU - Ding, Min
AU - Dong, Zigang
AU - Chen, Fei
AU - Ye, Jiangping
AU - Wang, Suwei
AU - Leonard, Stephen S.
AU - Castranova, Vince
AU - Vallyathan, Val
N1 - Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.
PY - 1999
Y1 - 1999
N2 - Electron spin resonance (ESR) was used to investigate the reaction of aspirin toward reactive oxygen species, such as hydroxyl radicals (.OH), superoxide radicals (O2-) and H2O2. The Fenton reaction (Fe(II) + H2O2→FE(III) + .OH + OR) was used as a source of .OH radicals. The results show that aspirin is an efficient .OH radical scavenger with a reaction rate constant of k = 3.6 x 1010 M-1 sec-1, which is faster than several well established antioxidants, such as ascorbate, glutathione and cysteine. However, aspirin is not a good scavenger for O2- or H2O2. Through its antioxidant property, aspirin exhibited a protective effect against silica-induced lipid peroxidation and DNA strand breakage. Aspirin also inhibited the activation of nuclear transcription factor-κβ induced by silica, lipopolysaccharide or the transition metal, Fe(II), as demonstrated by electrophoretic mobility shift assay. The results show that aspirin functions as an antioxidant via its ability to scavenge .OH radicals. This antioxidant property may explain some of its various physiological and pharmacological actions.
AB - Electron spin resonance (ESR) was used to investigate the reaction of aspirin toward reactive oxygen species, such as hydroxyl radicals (.OH), superoxide radicals (O2-) and H2O2. The Fenton reaction (Fe(II) + H2O2→FE(III) + .OH + OR) was used as a source of .OH radicals. The results show that aspirin is an efficient .OH radical scavenger with a reaction rate constant of k = 3.6 x 1010 M-1 sec-1, which is faster than several well established antioxidants, such as ascorbate, glutathione and cysteine. However, aspirin is not a good scavenger for O2- or H2O2. Through its antioxidant property, aspirin exhibited a protective effect against silica-induced lipid peroxidation and DNA strand breakage. Aspirin also inhibited the activation of nuclear transcription factor-κβ induced by silica, lipopolysaccharide or the transition metal, Fe(II), as demonstrated by electrophoretic mobility shift assay. The results show that aspirin functions as an antioxidant via its ability to scavenge .OH radicals. This antioxidant property may explain some of its various physiological and pharmacological actions.
KW - Antioxidant properties
KW - Aspirin
KW - DNA damage
KW - Lipid peroxidation
KW - NF-κB
KW - Silica
KW - TNF-α
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U2 - 10.1023/A:1006934612368
DO - 10.1023/A:1006934612368
M3 - Article
C2 - 10544957
AN - SCOPUS:0032848467
SN - 0300-8177
VL - 199
SP - 93
EP - 102
JO - Molecular and cellular biochemistry
JF - Molecular and cellular biochemistry
IS - 1-2
ER -