Gentisic acid, an aspirin metabolite, inhibits oxidation of low-density lipoprotein and the formation of cholesterol ester hydroperoxides in human plasma

被引:75
作者
Ashidate, K
Kawamura, M
Mimura, D
Tohda, H
Miyazaki, S
Teramoto, T
Yamamoto, Y
Hirata, Y
机构
[1] Tokyo Teishin Hosp, Dept Internal Med, Chiyoda Ku, Tokyo 1028798, Japan
[2] Kudanzaka Hosp, Dept Internal Med, Tokyo, Japan
[3] Univ Tokyo, Grad Sch Engn, Dept Chem & Biotechnol, Tokyo, Japan
[4] Univ Tokyo, Sch Med, Dept Internal Med, Tokyo 113, Japan
[5] Tokyo Univ Technol, Sch Bion, Tokyo, Japan
[6] Tokyo Med & Dent Univ, Dept Clin & Mol Endocrinol, Tokyo, Japan
关键词
gentisic acid; aspirin; antioxidant; LDL oxidation;
D O I
10.1016/j.ejphar.2005.03.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gentisic acid, an aspirin metabolite, has an antioxidant effect, although its detailed mechanism remains elusive. The present study was designed to determine whether it inhibits low-density lipoprotein (LDL) oxidation and the formation of lipid hydroperoxides in human plasma. The susceptibility of LDL oxidative modification was investigated by a method using 2,2'-azobis or Cu2+. To study the effect of gentisic acid on free radical-induced damage to plasma lipids, cholesterol ester hydroperoxides generated by incubating human fresh plasma with Cu2+ and gentisic acid was analyzed. Gentisic acid inhibited LDL oxidation in a concentration-dependent manner. It significantly inhibited the formation of cholesterol ester hydroperoxides in plasma, and was consumed after the depletion of ascorbic acid and reduced form of coenzyme Q-10 (CoQH(2)-10), whereas concentrations of other antioxidants remained unchanged. Gentisic acid had a potent free radical scavenging activity with a minimal chelating effect. The potent antioxidant property of gentisic acid may partly account for the anti-atherogenic effects of aspirin. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:173 / 179
页数:7
相关论文
共 26 条
[1]   Aspirin [J].
Awtry, EH ;
Loscalzo, J .
CIRCULATION, 2000, 101 (10) :1206-1218
[2]   ANTIOXIDANT DETERMINATIONS BY THE USE OF A STABLE FREE RADICAL [J].
BLOIS, MS .
NATURE, 1958, 181 (4617) :1199-1200
[3]  
CHUNG BH, 1980, J LIPID RES, V21, P284
[4]  
DAVIS WB, 1989, BIOCHEM PHARMACOL, V38, P4013
[5]   CONTINUOUS MONITORING OF INVITRO OXIDATION OF HUMAN LOW-DENSITY LIPOPROTEIN [J].
ESTERBAUER, H ;
STRIEGL, G ;
PUHL, H ;
ROTHENEDER, M .
FREE RADICAL RESEARCH COMMUNICATIONS, 1989, 6 (01) :67-75
[6]   The salicylate metabolite gentisic acid, but not the parent drug, inhibits glucose autoxidation-mediated atherogenic modification of low density lipoprotein [J].
Exner, M ;
Hermann, M ;
Hofbauer, R ;
Kapiotis, S ;
Speiser, W ;
Held, I ;
Seelos, C ;
Gmeiner, BMK .
FEBS LETTERS, 2000, 470 (01) :47-50
[7]  
Forth W., 1987, Allgemeine und spezielle Pharmakologie und Toxikologie, V5th
[8]   ANTIOXIDANT DEFENSES AND LIPID-PEROXIDATION IN HUMAN-BLOOD PLASMA [J].
FREI, B ;
STOCKER, R ;
AMES, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (24) :9748-9752
[9]   HUMAN (THP-1) MACROPHAGES OXIDIZE LDL BY A THIOL-DEPENDENT MECHANISM [J].
GRAHAM, A ;
WOOD, JL ;
OLEARY, VJ ;
STONE, D .
FREE RADICAL RESEARCH, 1994, 21 (05) :295-308
[10]   AROMATIC HYDROXYLATION AS A POTENTIAL MEASURE OF HYDROXYL-RADICAL FORMATION INVIVO - IDENTIFICATION OF HYDROXYLATED DERIVATIVES OF SALICYLATE IN HUMAN-BODY FLUIDS [J].
GROOTVELD, M ;
HALLIWELL, B .
BIOCHEMICAL JOURNAL, 1986, 237 (02) :499-504