Oxidative stress and stress signaling: menace of diabetic cardiomyopathy

被引:157
作者
Wold, LE
Ceylan-Isik, AF
Ren, J [1 ]
机构
[1] Univ N Dakota, Dept Pharmacol Physiol & Therapeut, Grand Forks, ND 58203 USA
[2] Univ Wyoming, Ctr Cardiovasc Res & Alternat Med, Laramie, WY 82071 USA
关键词
diabetes; heart; cardiomyopathy; oxidative stress; signal transduction;
D O I
10.1111/j.1745-7254.2005.00146.x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cardiovascular disease is the most common cause of death in the diabetic population and is currently one of the leading causes of death in the United States and other industrialized countries. The health care expenses associated with cardiovascular disease are staggering, reaching more than US$350 billion in 2003. The risk factors for cardiovascular disease include high fat/cholesterol levels, alcoholism, smoking, genetics, environmental factors and hypertension, which are commonly used to gauge an individual's risk of cardiovascular disease and to track their progress during therapy. Most recently, these factors have become important in the early prevention of cardiovascular diseases. Oxidative stress, the imbalance between reactive oxygen species production and breakdown by endogenous antioxidants, has been implicated in the onset and progression of cardiovascular diseases such as congestive heart failure and diabetes-associated heart dysfunction (diabetic cardiomyopathy). Antioxidant therapy has shown promise in preventing the development of diabetic heart complications. This review focuses on recent advances in oxidative stress theory and antioxidant therapy in diabetic cardiomyopathy, with an emphasis on the stress signaling pathways hypothesized to be involved. Many of these stress signaling pathways lead to activation of reactive oxygen species, major players in the development and progression of diabetic cardiomyopathy.
引用
收藏
页码:908 / 917
页数:10
相关论文
共 109 条
[51]   Characterization and functional analysis of the promoter of RAGE, the receptor for advanced glycation end products [J].
Li, JF ;
Schmidt, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (26) :16498-16506
[52]   Benefit and risk of exercise on myocardial function in diabetes [J].
Li, SY ;
Culver, B ;
Ren, J .
PHARMACOLOGICAL RESEARCH, 2003, 48 (02) :127-132
[53]   The impact of diabetes on left ventricular filling pattern in normotensive and hypertensive adults: The strong heart study [J].
Liu, JE ;
Palmieri, V ;
Roman, NJ ;
Bella, JN ;
Fabsitz, R ;
Howard, BV ;
Welty, TK ;
Lee, ET ;
Devereux, RB .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (07) :1943-1949
[54]   Advanced glycation end products increase retinal vascular endothelial growth factor expression [J].
Lu, M ;
Kuroki, M ;
Amano, S ;
Tolentino, M ;
Keough, K ;
Kim, I ;
Bucala, R ;
Adamis, AP .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (06) :1219-1224
[55]   HEMOGLOBIN-AGE - A CIRCULATING MARKER OF ADVANCED GLYCOSYLATION [J].
MAKITA, Z ;
VLASSARA, H ;
RAYFIELD, E ;
CARTWRIGHT, K ;
FRIEDMAN, E ;
RODBY, R ;
CERAMI, A ;
BUCALA, R .
SCIENCE, 1992, 258 (5082) :651-653
[56]   The role of Jak/STAT signaling in heart tissue renin-angiotensin system [J].
Mascareno, E ;
Siddiqui, MAQ .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2000, 212 (1-2) :171-175
[57]   NF-κB as a primary regulator of the stress response [J].
Mercurio, F ;
Manning, AM .
ONCOGENE, 1999, 18 (45) :6163-6171
[58]   The role of oxidative stress and NF-κB activation in late diabetic complications [J].
Mohamed, AK ;
Bierhaus, A ;
Schiekofer, S ;
Tritschler, H ;
Ziegler, R ;
Nawroth, PP .
BIOFACTORS, 1999, 10 (2-3) :157-167
[59]   Progression of nephropathy in spontaneous diabetic rats is prevented by OPB-9195, a novel inhibitor of advanced glycation [J].
Nakamura, S ;
Makita, Z ;
Ishikawa, S ;
Yasumura, K ;
Fujii, W ;
Yanagisawa, K ;
Kawata, T ;
Koike, T .
DIABETES, 1997, 46 (05) :895-899
[60]   Angiotensin II signaling in vascular smooth muscle cells under high glucose conditions [J].
Natarajan, R ;
Scott, S ;
Bai, W ;
Yerneni, KKV ;
Nadler, J .
HYPERTENSION, 1999, 33 (01) :378-384