Resveratrol, a polyphenolic compound found in wine, inhibits tissue factor expression in vascular cells - A possible mechanism for the cardiovascular benefits associated with moderate consumption of wine

被引:171
作者
Pendurthi, UR
Williams, JT
Rao, LVM
机构
[1] Univ Texas, Ctr Hlth, Dept Mol Biol, Tyler, TX 75708 USA
[2] Univ Texas, Ctr Hlth, Dept Biochem, Tyler, TX 75710 USA
关键词
tissue factor; resveratrol; endothelial cell; monocytes; cardioprotective effect;
D O I
10.1161/01.ATV.19.2.419
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A number of studies suggest that moderate consumption of red wine may be more effective than other alcoholic beverages in decreasing the risk of coronary heart disease mortality. The phytochemical resveratrol found in wine, derived from grapes, has been thought to be responsible for cardiovascular benefits associated with wine consumption because it was shown to have antioxidant and antiplatelet activities. In the present investigation, we examined the effect of resveratrol on induction of tissue factor (TF) expression in vascular cells that were exposed to pathophysiological stimuli. The data presented herein show that resveratrol, in a dose-dependent manner, inhibited the expression of TF in endothelial cells stimulated with a variety of agonists, including interleukin-1 beta (IL-I beta), tumor necrosis factor-alpha (TNF alpha) and lipopolysaccharide (LPS). A similar inhibition of TF induction was also seen in LPS stimulated monocytes that were pretreated with resveratrol before their stimulation with LPS. In addition, resveratrol was shown to inhibit the LPS-induced expression of TNF alpha mRNA in endothelial cells and of TNF alpha and IL-1 beta mRNA in monocytes. Nuclear run-on analysis in endothelial cells showed that resveratrol inhibited TF expression at the level of transcription. However, resveratrol did not significantly alter the binding of the transcription factors c-Fos/c-Jun and c-Rel/p65, the transcription factors required for the induction of TF promoter in both endothelial cells and monocytes, Similarly, resveratrol had no significant effect on the binding of NF-kappa B in endothelial cells stimulated with IL-1 beta, TNF alpha, and LPS. Overall, our data show that resveratrol could effectively suppress the aberrant expression of TF and cytokines in vascular cells, but it requires further investigation to understand how resveratrol exerts its inhibitory effect.
引用
收藏
页码:419 / 426
页数:8
相关论文
共 55 条
[1]   A SIMPLIFIED PROCEDURE FOR PURIFICATION OF HUMAN-PROTHROMBIN, FACTOR-IX AND FACTOR-X [J].
BAJAJ, SP ;
RAPAPORT, SI ;
PRODANOS, C .
PREPARATIVE BIOCHEMISTRY, 1981, 11 (04) :397-412
[2]  
BENSI G, 1990, CELL GROWTH DIFFER, V1, P491
[3]  
Bertelli AAE, 1996, DRUG EXP CLIN RES, V22, P61
[4]  
BERTELLI AAE, 1995, INT J TISSUE REACT, V17, P1
[5]   TISSUE FACTOR MESSENGER-RNA IN THP-1 MONOCYTIC CELLS IS REGULATED AT BOTH TRANSCRIPTIONAL AND POSTTRANSCRIPTIONAL LEVELS IN RESPONSE TO LIPOPOLYSACCHARIDE [J].
BRAND, K ;
FOWLER, BJ ;
EDGINGTON, TS ;
MACKMAN, N .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (09) :4732-4738
[6]   Alcohol, ischemic heart disease, and the French paradox [J].
Constant, J .
CORONARY ARTERY DISEASE, 1997, 8 (10) :645-649
[7]   The contribution of thrombosis to the clinical expression of coronary atherosclerosis [J].
Davies, MJ .
THROMBOSIS RESEARCH, 1996, 82 (01) :1-32
[8]  
DRAKE TA, 1989, AM J PATHOL, V134, P1087
[9]   ISCHEMIC-HEART-DISEASE AND PLATELET-AGGREGATION - THE CAERPHILLY COLLABORATIVE HEART-DISEASE STUDY [J].
ELWOOD, PC ;
RENAUD, S ;
SHARP, DS ;
BESWICK, AD ;
OBRIEN, JR ;
YARNELL, JWG .
CIRCULATION, 1991, 83 (01) :38-44
[10]  
Engstad CS, 1997, THROMB HAEMOSTASIS, V77, P690