Hydrogen peroxide scavenging activity by non-steroidal anti-inflammatory drugs

被引:63
作者
Costa, D [1 ]
Gomes, A [1 ]
Reis, S [1 ]
Lima, JLFC [1 ]
Fernandes, E [1 ]
机构
[1] Univ Porto, Fac Farm, Dept Quim Fis, REQUIMTE, P-4099030 Oporto, Portugal
关键词
NSAIDs; hydrogen peroxide scavenging activity; microplate chemiluminescence assay;
D O I
10.1016/j.lfs.2004.10.052
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hydrogen peroxide (H2O2) has been shown to be formed during inflammatory processes and is implicated in its pathophysiology. Thus, a putative scavenging activity against this reactive oxygen specie (ROS) by anti-inflammatory drugs may be of great therapeutical value. The present study was undertaken to evaluate the scavenging activity for H2O2 by several non-steroidal anti -inflammatory drugs (NSAIDs), namely indomethacin, acemetacin, etodolac, tolmetin, ketorolac, oxaprozin, sulindac and its metabolites sulindac sulfide and sulindac sulfone. The H2O2 scavenging assay was performed by measuring H2O2-elicited lucigenin chemiluminescence using a microplate reader. The specificity of the method was confirmed by the use of catalase, which completely prevented the H2O2-induced lucigenin chemiluminescence. The endogenous antioxidants melatonin and reduced glutathione (GSH) were used as positive controls. The obtained results demonstrated that all the studied NSAIDs display H2O2, scavenging activity, although in different extents. The ranking order of potency found was sulindac sulfeme > sulindac sulfide > GSH > sulindac > indomethacin > acemetacin > etodolac > oxaprozin > ketorolac approximate to melatonin > tolmetin. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:2841 / 2848
页数:8
相关论文
共 24 条
[1]   REACTIVE OXYGEN SPECIES AND AIRWAY INFLAMMATION [J].
BARNES, PJ .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 9 (03) :235-243
[2]   Inducing the cell cycle arrest and apoptosis of oral KB carcinoma cells by hydroxychavicol: roles of glutathione and reactive oxygen species [J].
Chang, MC ;
Uang, BJ ;
Wu, HL ;
Lee, JJ ;
Hahn, LJ ;
Jeng, JH .
BRITISH JOURNAL OF PHARMACOLOGY, 2002, 135 (03) :619-630
[3]   Reactive nitrogen species in the chemical biology of inflammation [J].
Dedon, PC ;
Tannenbaum, SR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2004, 423 (01) :12-22
[4]   THE ROLE OF PHYSIOLOGICAL OXYGEN PARTIAL PRESSURES IN LIPID-PEROXIDATION - THEORETICAL CONSIDERATIONS AND EXPERIMENTAL-EVIDENCE [J].
DEGROOT, H ;
NOLL, T .
CHEMISTRY AND PHYSICS OF LIPIDS, 1987, 44 (2-4) :209-226
[5]   In vitro scavenging activity for reactive oxygen and nitrogen species by nonsteroidal anti-inflammatory indole, pyrrole, and oxazole derivative drugs [J].
Fernandes, E ;
Costa, D ;
Toste, SA ;
Lima, JLFC ;
Reis, S .
FREE RADICAL BIOLOGY AND MEDICINE, 2004, 37 (11) :1895-1905
[6]   The metabolism of sulindac enhances its scavenging activity against reactive oxygen and nitrogen species [J].
Fernandes, E ;
Toste, SA ;
Lima, JLFC ;
Reis, S .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 35 (09) :1008-1017
[7]   ACIDIC NONSTEROID ANTI-INFLAMMATORY DRUGS ACCUMULATING IN INFLAMED TISSUE [J].
GRAF, P ;
GLATT, M ;
BRUNE, K .
EXPERIENTIA, 1975, 31 (08) :951-953
[8]  
Gulcin I, 2003, J PINEAL RES, V34, P278
[9]   THE IMPORTANCE OF FREE-RADICALS AND CATALYTIC METAL-IONS IN HUMAN-DISEASES [J].
HALLIWELL, B ;
GUTTERIDGE, JMC .
MOLECULAR ASPECTS OF MEDICINE, 1985, 8 (02) :89-+
[10]   Inside the neutrophil phagosome: Oxidants, myeloperoxidase, and bacterial killing [J].
Hampton, MB ;
Kettle, AJ ;
Winterbourn, CC .
BLOOD, 1998, 92 (09) :3007-3017