Depressed glutathione synthesis precedes oxidative stress and atherogenesis in Apo-E-/- mice

被引:58
作者
Biswas, SK
Newby, DE
Rahman, I
Megson, IL
机构
[1] Univ Edinburgh, Queens Med Res Inst, Ctr Cardiovasc Sci, Edinburgh EH16 4TJ, Midlothian, Scotland
[2] Univ Rochester, Ctr Med, Div Lung Biol, Dept Environm Med, Rochester, NY 14642 USA
关键词
Apo-e; atherosclerosis; glutathione; glutathione peroxidase; gamma-glutamylcysteine ligase; peroxidation;
D O I
10.1016/j.bbrc.2005.10.098
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
Glutathione is a vital intracellular antioxidant. The enzymes involved in its synthesis and utilisation are tightly regulated, but the importance Of glutathione regulation in atherogenesis is poorly understood. Here, we establish that glutathione is severely (similar to 80%) depleted very early (10 weeks) in the atheroma-prone aortic arch of male apoprotein E-deficient (Apo-E-/-) mice compared to age-matched wild-type controls. Importantly, this event pre-empts lipid peroxidation and detectable atheroma by several months. Depletion of glutathione was associated with excessive oxidant but-den and reduced transcription and activity of the rate-limiting enzyme for glutathione synthesis, gamma-glutamylcysteine ligase, together with the glutathione-dependent antioxidant enzyme, glutathione peroxidase. Depletion via reduced synthesis of glutathione precedes lipid peroxidation and atherogenesis in Apo-E-/- mice. We suggest that glutathione deficiency is central to the failure of the intracellular antioxidant defences and is causally implicated in the pathogenesis of atherosclerosis. Modification of the glutathione pathway may present a novel and important therapeutic target in the prevention and treatment of atherosclerosis. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1368 / 1373
页数:6
相关论文
共 35 条
[1]   ATHEROSCLEROSIS - BASIC MECHANISMS - OXIDATION, INFLAMMATION, AND GENETICS [J].
BERLINER, JA ;
NAVAB, M ;
FOGELMAN, AM ;
FRANK, JS ;
DEMER, LL ;
EDWARDS, PA ;
WATSON, AD ;
LUSIS, AJ .
CIRCULATION, 1995, 91 (09) :2488-2496
[2]  
COPPOLA L, 1992, DRUGS EXP CLIN RES, P18
[3]   AORTIC ANTIOXIDANT DEFENSE-MECHANISMS - TIME-RELATED CHANGES IN CHOLESTEROL-FED RABBITS [J].
DELBOCCIO, G ;
LAPENNA, D ;
PORRECA, E ;
PENNELLI, A ;
SAVINI, F ;
FELICIANI, P ;
RICCI, G ;
CUCCURULLO, F .
ATHEROSCLEROSIS, 1990, 81 (02) :127-135
[4]  
FLOHE W, 1979, TRACE METALS HLTH DI, P263
[5]   Heterozygous cellular glutathione peroxidase deficiency in the mouse - Abnormalities in vascular and cardiac function and structure [J].
Forgione, MA ;
Cap, A ;
Liao, R ;
Moldovan, NI ;
Eberhardt, RT ;
Lim, CC ;
Jones, J ;
Goldschmidt-Clermont, PJ ;
Loscalzo, J .
CIRCULATION, 2002, 106 (09) :1154-1158
[6]   Cellular glutathione peroxidase deficiency and endothelial dysfunction [J].
Forgione, MA ;
Weiss, N ;
Heydrick, S ;
Cap, A ;
Klings, ES ;
Bierl, C ;
Eberhardt, RT ;
Farber, HW ;
Loscalzo, J .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 282 (04) :H1255-H1261
[7]   Antioxidant defence mechanisms: From the beginning to the end (of the beginning) [J].
Halliwell, B .
FREE RADICAL RESEARCH, 1999, 31 (04) :261-272
[8]   Homocysteine down-regulates cellular glutathione peroxidase (GPx1) by decreasing translation [J].
Handy, DE ;
Zhang, YF ;
Loscalzo, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (16) :15518-15525
[9]   Mechanisms of disease - Inflammation, atherosclerosis, and coronary artery disease [J].
Hansson, GK .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (16) :1685-1695
[10]   Oxidants and antioxidants in the pathogenesis of atherosclerosis: implications for the oxidized low density lipoprotein hypothesis [J].
Heinecke, JW .
ATHEROSCLEROSIS, 1998, 141 (01) :1-15