Oxidative stress and diabetic cardiovascular complications

被引:351
作者
Jay, D [1 ]
Hitomi, H [1 ]
Griendling, KK [1 ]
机构
[1] Emory Univ, Dept Med, Div Cardiol, Atlanta, GA 30322 USA
关键词
free radicals;
D O I
10.1016/j.freeradbiomed.2005.06.018
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
Diabetes diagnoses are increasing at an alarming rate worldwide. The majority of diabetes-related deaths arise from cardiovascular complications such as myocardial infarction, stroke, and peripheral vascular disease. Oxidative stress has been demonstrated to be present in animal models as well as in patients with diabetes and has been Suggested as a possible contributor to the accelerated atherosclerosis seen in diabetics. The generation of reactive oxygen species in diabetes Occurs via several mechanisms and is initiated not only by glucose, but also by other substances that are found at elevated levels in diabetic patients. The resulting oxidative stress leads to a number of proatherogenic events. The elucidation of the mechanisms of oxidative stress in diabetes and their relationship with atherosclerosis could potentially identify molecular targets of therapy for this condition and its cardiovascular consequences. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:183 / 192
页数:10
相关论文
共 124 条
[81]   High glucose induces cell death of cultured human aortic smooth muscle cells through the formation of hydrogen peroxide [J].
Peiró, C ;
Lafuente, N ;
Matesanz, N ;
Cercas, E ;
Llergo, JL ;
Vallejo, S ;
Rodríguez-Mañas, L ;
Sánchez-Ferrer, CF .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 133 (07) :967-974
[82]   Oral administration of the antioxidant, N-acetylcysteine, abrogates diabetes-induced endothelial dysfunction [J].
Pieper, GM ;
Siebeneich, W .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1998, 32 (01) :101-105
[83]   FFA-induced endothelial dysfunction can be corrected by vitamin C [J].
Pleiner, J ;
Schaller, G ;
Mittermayer, F ;
Bayerle-Eder, M ;
Roden, M ;
Wolzt, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (06) :2913-2917
[84]   IRS1 degradation and increased serine phosphorylation cannot predict the degree of metabolic insulin resistance induced by oxidative stress [J].
Potashnik, R ;
Bloch-Damti, A ;
Bashan, N ;
Rudich, A .
DIABETOLOGIA, 2003, 46 (05) :639-648
[85]   Activation of nulcear factor-κB by hyperglycemia in vascular smooth muscle cells is regulated by aldose reductase [J].
Ramana, KV ;
Friedrich, B ;
Srivastava, S ;
Bhatnagar, A ;
Srivastava, SK .
DIABETES, 2004, 53 (11) :2910-2920
[86]   Nitric oxide regulates the polyol pathway of glucose metabolism in vascular smooth muscle cells [J].
Ramana, KV ;
Chandra, D ;
Srivastava, S ;
Bhatnagar, A ;
Srivastava, SK .
FASEB JOURNAL, 2003, 17 (03) :417-425
[87]   Modulation of oxidant stress in vivo in chronic cigarette smokers [J].
Reilly, M ;
Delanty, N ;
Lawson, JA ;
FitzGerald, GA .
CIRCULATION, 1996, 94 (01) :19-25
[88]   Plasma leptin levels are associated with coronary atherosclerosis in type 2 diabetes [J].
Reilly, MP ;
Iqbal, N ;
Schutta, M ;
Wolfe, ML ;
Scally, M ;
Localio, AR ;
Rader, DJ ;
Kimmel, SE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (08) :3872-3878
[89]   Endothelial dysfunction in small resistance arteries of patients with non-insulin-dependent diabetes mellitus [J].
Rizzoni, D ;
Porteri, E ;
Guelfi, D ;
Muiesan, ML ;
Piccoli, A ;
Valentini, U ;
Cimino, A ;
Girelli, A ;
Salvetti, M ;
De Ciuceis, C ;
Tiberio, GAM ;
Giulini, SM ;
Sleiman, I ;
Monteduro, C ;
Rosei, EA .
JOURNAL OF HYPERTENSION, 2001, 19 (05) :913-919
[90]   Mechanisms of disease - Atherosclerosis - An inflammatory disease [J].
Ross, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (02) :115-126