Vascular NADPH oxidases as drug targets for novel antioxidant strategies

被引:171
作者
Guzik, Tomasz J. [1 ]
Harrison, David G.
机构
[1] Emory Univ, Sch Med, Div Cardiol, Atlanta, GA 30322 USA
[2] Jagiellonian Univ, Sch Med, Dept Pharmacol, PL-31101 Krakow, Poland
[3] Jagiellonian Univ, Sch Med, Dept Med, PL-31101 Krakow, Poland
关键词
D O I
10.1016/j.drudis.2006.04.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Reactive oxygen species (ROS) play important roles in the pathogenesis of cardiovascular disease. Surprisingly, large clinical trials have shown that ROS scavenging by antioxidant vitamins is ineffective or harmful. Therefore, prevention of ROS formation, by targeting specific sources of superoxide anion and other ROS, might prove beneficial. Potential targets include the NADPH oxidases (Nox enzymes), xanthine oxidase, endothelial nitric oxide synthase and mitochondrial oxidases. Nox enzymes play a central role because they can regulate other enzymatic sources of ROS. Statins, angiotensin-converting enzyme inhibitors and angiotensin receptor antagonists block upstream signaling of Nox activation, which contributes to their clinical effectiveness. Here, we discuss novel possibilities where drugs that directly inhibit Nox activation could successfully inhibit oxidative stress.
引用
收藏
页码:524 / 533
页数:10
相关论文
共 82 条
[41]   Vascular oxidative stress and endothelial dysfunction in patients with chronic heart failure - Role of xanthine-oxidase and extracellular superoxide dismutase [J].
Landmesser, U ;
Spiekermann, S ;
Dikalov, S ;
Tatge, H ;
Wilke, R ;
Kohler, C ;
Harrison, DG ;
Hornig, B ;
Drexler, H .
CIRCULATION, 2002, 106 (24) :3073-3078
[42]   Apocynin increases glutathione synthesis and activates AP-1 in alveolar epithelial cells [J].
Lapperre, TS ;
Jimenez, LA ;
Antonicelli, F ;
Drost, EM ;
Hiemstra, PS ;
Stolk, J ;
MacNee, W ;
Rahman, I .
FEBS LETTERS, 1999, 443 (02) :235-239
[43]   Novel gp91phox homologues in vascular smooth muscle cells -: Nox1 mediates angiotensin II-induced superoxide formation and redox-sensitive signaling pathways [J].
Lassègue, B ;
Sorescu, D ;
Szöcs, K ;
Yin, QQ ;
Akers, M ;
Zhang, Y ;
Grant, SL ;
Lambeth, JD ;
Griendling, KK .
CIRCULATION RESEARCH, 2001, 88 (09) :888-894
[44]   Role of superoxide in angiotensin II-induced but not catecholamine-induced hypertension [J].
Laursen, JB ;
Rajagopalan, S ;
Galis, Z ;
Tarpey, M ;
Freeman, BA ;
Harrison, DG .
CIRCULATION, 1997, 95 (03) :588-593
[45]  
Lonn E, 2005, JAMA-J AM MED ASSOC, V293, P1338, DOI 10.1001/jama.293.11.1338
[46]   Therapeutic control of free radicals [J].
McCord, JM .
DRUG DISCOVERY TODAY, 2004, 9 (18) :781-782
[47]   Role of xanthine oxidoreductase and NAD(P)H oxidase in endothelial superoxide production in response to oscillatory shear stress [J].
McNally, JS ;
Davis, ME ;
Giddens, DP ;
Saha, A ;
Hwang, JN ;
Dikalov, S ;
Jo, H ;
Harrison, DG .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (06) :H2290-H2297
[48]   Vitamin e supplementation in patients with carotid atherosclerosis - Reversal of altered oxidative stress status in plasma but not in plaque [J].
Micheletta, F ;
Natoli, S ;
Misuraca, M ;
Sbarigia, E ;
Diczfalusy, U ;
Iuliano, L .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (01) :136-140
[49]   Meta-analysis: High-dosage vitamin E supplementation may increase all-cause mortality [J].
Miller, ER ;
Pastor-Barriuso, R ;
Dalal, D ;
Riemersma, RA ;
Appel, LJ ;
Guallar, E .
ANNALS OF INTERNAL MEDICINE, 2005, 142 (01) :37-46
[50]   Effects of angiotensin II infusion on the expression and function of NAD(P)H oxidase and components of nitric Oxide/cGMP signaling [J].
Mollnau, H ;
Wendt, M ;
Szöcs, K ;
Lassègue, B ;
Schulz, E ;
Oelze, M ;
Li, HG ;
Bodenschatz, M ;
August, M ;
Kleschyov, AL ;
Tsilimingas, N ;
Walter, U ;
Förstermann, U ;
Meinertz, T ;
Griendling, K ;
Münzel, T .
CIRCULATION RESEARCH, 2002, 90 (04) :E58-E65