Cardiovascular effects and molecular targets of resveratrol

被引:297
作者
Li, Huige [1 ]
Xia, Ning [1 ]
Foerstermann, Ulrich [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Pharmacol, D-55131 Mainz, Germany
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2012年 / 26卷 / 02期
关键词
Resveratrol; Cardiovascular disease; Nitric oxide; Oxidative stress; Vascular inflammation; SMOOTH-MUSCLE-CELLS; NITRIC-OXIDE SYNTHASE; NF-KAPPA-B; E-DEFICIENT MICE; WINE POLYPHENOL RESVERATROL; INDUCED CARDIAC-HYPERTROPHY; ARTERIAL ENDOTHELIAL-CELLS; VASCULAR OXIDATIVE STRESS; ACTIVATED PROTEIN-KINASE; INDUCED DIABETIC-RATS;
D O I
10.1016/j.niox.2011.12.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Resveratrol (3,5,4'-trihydroxy-trans-stilbene) is a polyphenol phytoalexin present in a variety of plant species and has been implicated to explain the health benefits of red wine. A wide range of health beneficial effects have been demonstrated for resveratrol in animal studies. In this review, we summarize the cardiovascular effects of resveratrol with emphasis on the molecular targets of the compound. In this regard, resveratrol stimulates endothelial production of nitric oxide, reduces oxidative stress, inhibits vascular inflammation and prevents platelet aggregation. In animal models of cardiovascular disease, resveratrol protects the heart from ischemia-reperfusion injury, reduces blood pressure and cardiac hypertrophy in hypertensive animals, and slows the progression of atherosclerosis. A number of direct and indirect target molecules mediating the aforementioned cardiovascular effects of resveratrol have been identified. These include, among others, the estrogen receptor alpha, the adenosine receptors, the cyclooxygenase 1, the histone/protein deacetylase sirtuin 1, the AMP-activated protein kinase, the Akt kinase, the nuclear factor-E2-related factor-2, and NF-kappa B. Molecular mechanisms involved in the signal cascades are discussed. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:102 / 110
页数:9
相关论文
共 114 条
[1]
Resveratrol and life extension [J].
Agarwal, Beamon ;
Baur, Joseph A. .
RESVERATROL AND HEALTH, 2011, 1215 :138-143
[2]
Chronic resveratrol treatment restores vascular responsiveness of cerebral arterioles in type 1 diabetic rats [J].
Arrick, Denise M. ;
Sun, Hong ;
Patel, Kaushik P. ;
Mayhan, William G. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2011, 301 (03) :H696-H703
[3]
SIRT1 regulates oxidant- and cigarette smoke-induced eNOS acetylation in endothelial cells: Role of resveratrol [J].
Arunachalam, Gnanapragasam ;
Yao, Hongwei ;
Sundar, Isaac K. ;
Caito, Samuel ;
Rahman, Irfan .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 393 (01) :66-72
[4]
Therapeutic potential of resveratrol:: the in vivo evidence [J].
Baur, Joseph A. ;
Sinclair, David A. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (06) :493-506
[5]
AMPK activation, a preventive therapeutic target in the transition from cardiac injury to heart failure [J].
Beauloye, Christophe ;
Bertrand, Luc ;
Horman, Sandrine ;
Hue, Louis .
CARDIOVASCULAR RESEARCH, 2011, 90 (02) :224-233
[6]
Resveratrol is Not a Direct Activator of SIRT1 Enzyme Activity [J].
Beher, Dirk ;
Wu, John ;
Cumine, Suzanne ;
Kim, Ki Won ;
Lu, Shu-Chen ;
Atangan, Larissa ;
Wang, Minghan .
CHEMICAL BIOLOGY & DRUG DESIGN, 2009, 74 (06) :619-624
[7]
Resveratrol inhibits metal ion-dependent and independent peroxidation of porcine low-density lipoproteins [J].
Belguendouz, L ;
Fremont, L ;
Linard, A .
BIOCHEMICAL PHARMACOLOGY, 1997, 53 (09) :1347-1355
[8]
Mechanism of human SIRT1 activation by resveratrol [J].
Borra, MT ;
Smith, BC ;
Denu, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (17) :17187-17195
[9]
Bradamante S, 2004, CARDIOVASC DRUG REV, V22, P169
[10]
Resveratrol inhibits the mTOR mitogenic signaling evoked by oxidized LDL in smooth muscle cells [J].
Brito, Paula M. ;
Devillard, Raphael ;
Negre-Salvayre, Anne ;
Almeida, Leonor M. ;
Dinis, Teresa C. P. ;
Salvayre, Robert ;
Auge, Nathalie .
ATHEROSCLEROSIS, 2009, 205 (01) :126-134