Myeloperoxidase-induced lipid peroxidation of LDL in the presence of nitrite. Protection by cocoa flavanols

被引:20
作者
Schewe, T [1 ]
Sies, H [1 ]
机构
[1] Univ Dusseldorf, Inst Biochem & Mol Biol 1, D-40001 Dusseldorf, Germany
关键词
antioxidants; atherosclerosis; catechins; epicatechin; flavonoids; NO; peroxynitrite; polyphenols; protein tyrosine nitration;
D O I
10.1002/biof.5520240106
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid peroxidation (LPO) of low-density lipoprotein (LDL) is believed to be a pivotal process rendering this plasma lipoprotein atherogenic. Several endogenous factors have been proposed to mediate LPO of LDL, among them myeloperoxidase (MPO), which is active in atherosclerotic lesions, and the plasma level of which has been proposed to be a prognostic parameter for cardiac events. Nitrite, a major oxidation product of nitric oxide, is substrate of MPO and a cofactor of MPO-mediated LPO under physiological conditions. Dietary flavonoids including (-)-epicatechin, a major flavan-3-ol in cocoa products, grapes and wine, are substrates of MPO as well as potent inhibitors of LPO in LDL at micromolar concentrations. Moreover, they strongly suppress protein tyrosine nitration of LDL by MPO/nitrite or peroxynitrite. By blunting undesirable MPO-mediated actions of nitrite, presumably via scavenging of the strong prooxidant and nitrating NO2 radical, dietary flavonoids modulate NO metabolism in a favorable direction and thus counteract endothelial dysfunction. This article gives a survey on recent progress in this field with special reference to own recently published work.
引用
收藏
页码:49 / 58
页数:10
相关论文
共 42 条
[1]   Peroxidase-catalyzed formation of quercetin quinone methide-glutathione adducts [J].
Awad, HM ;
Boersma, MG ;
Vervoort, J ;
Rietjens, IMCM .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 378 (02) :224-233
[2]   Structure-activity study on the quinone/quinone methide chemistry of flavonoids [J].
Awad, HM ;
Boersma, MG ;
Boeren, S ;
van Bladeren, PJ ;
Vervoort, J ;
Rietjens, IMCM .
CHEMICAL RESEARCH IN TOXICOLOGY, 2001, 14 (04) :398-408
[3]  
Baldus S, 2001, J CLIN INVEST, V108, P1759
[4]   Prognostic value of myeloperoxidase in patients with chest pain [J].
Brennan, M ;
Penn, MS ;
Van Lente, F ;
Nambi, V ;
Shishehbor, MH ;
Aviles, RJ ;
Goormastic, M ;
Pepoy, ML ;
McErlean, ES ;
Topol, EJ ;
Nissen, SE ;
Hazen, SL .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (17) :1595-1604
[5]   A tale of two controversies -: Defining both the role of peroxidases in nitrotyrosine formation in vivo using eosinophil peroxidase and myeloperoxidase-deficient mice, and the nature of peroxidase-generated reactive nitrogen species [J].
Brennan, ML ;
Wu, WJ ;
Fu, XM ;
Shen, ZZ ;
Song, W ;
Frost, H ;
Vadseth, C ;
Narine, L ;
Lenkiewicz, E ;
Borchers, MT ;
Lusis, AJ ;
Lee, JJ ;
Lee, NA ;
Abu-Soud, HM ;
Ischiropoulos, H ;
Hazen, SL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (20) :17415-17427
[6]   Increased atherosclerosis in myeloperoxidase-deficient mice [J].
Brennan, ML ;
Anderson, MM ;
Shih, DM ;
Qu, XD ;
Wang, XP ;
Mehta, AC ;
Lim, LL ;
Shi, WB ;
Hazen, SL ;
Jacob, JS ;
Crowley, JR ;
Heinecke, JW ;
Lusis, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (04) :419-430
[7]   Mechanism of reaction of myeloperoxidase with nitrite [J].
Burner, U ;
Furtmüller, PG ;
Kettle, AJ ;
Koppenol, WH ;
Obinger, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (27) :20597-20601
[8]   Oxidation of hydroquinone, 2,3-dimethylhydroquinone and 2,3,5-trimethylhydroquinone by human myeloperoxidase [J].
Burner, U ;
Krapfenbauer, G ;
Furtmüller, PG ;
Regelsberger, G ;
Obinger, C .
REDOX REPORT, 2000, 5 (04) :185-190
[9]  
BUYN J, 1999, FEBS LETT, V455, P243
[10]   Myeloperoxidase binds to low-density lipoprotein: potential implications for atherosclerosis [J].
Carr, AC ;
Myzak, MC ;
Stocker, R ;
McCall, MR ;
Frei, B .
FEBS LETTERS, 2000, 487 (02) :176-180