Inhibitory effect of resveratrol on free radical generation in blood platelets

被引:77
作者
Olas, B
Zbikowska, HM
Wachowicz, B
Krajewski, T
Buczynski, A
Magnuszewska, A
机构
[1] Univ Lodz, Inst Biochem, Dept Gen Biochem, PL-90237 Lodz, Poland
[2] Mil Med Acad, Dept Prevent Med, Lodz, Poland
关键词
blood platelet; resveratrol; free radicals;
D O I
10.18388/abp.1999_4119
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
Resveratrol. (3,4',5-trihydroxystilbene), a compound found in many plants, has been shown to prevent coronary heart diseases and to exert a variety of antiinflammatory and anticancerogenic effects. It is effective in lowering the level of serum lipids and in inhibiting platelet aggregation. We evaluated the effect of trans-resveratrol on the production of free radicals in pig blood platelets and showed that resveratrol inhibited the production of different reactive oxygen species (O-2(radical anion), H2O2, singlet oxygen and organic radicals) measured by the luminol-dependent chemiluminescence in resting platelets (P < 0.05). Resveratrol inhibited also the generation of radicals in platelets activated by thrombin (P < 0.05). Treatment of platelets with resveratrol at concentrations of 6.25 and 12.5 mu g/ml caused a statistically insignificant increase in the production of O-2(radical anion) in these cells, as measured by reduction of cytochrome c; however, at higher doses (25, 50 and 100 mu g/ml) resveratrol distinctly reduced the generation of O-2(radical anion) in platelets (P < 0.05). We suggest that free radicals play an important role in the reduced reactivity of blood platelets induced by resveratrol.
引用
收藏
页码:961 / 966
页数:6
相关论文
共 30 条
[1]   MODULATION OF PLATELET-FUNCTION BY REACTIVE OXYGEN METABOLITES [J].
AMBROSIO, G ;
GOLINO, P ;
PASCUCCI, I ;
ROSOLOWSKY, M ;
CAMPBELL, WB ;
DECLERCK, F ;
TRITTO, I ;
CHIARIELLO, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (01) :H308-H318
[2]  
Bertelli AAE, 1996, DRUG EXP CLIN RES, V22, P61
[3]  
BERTELLI AAE, 1995, INT J TISSUE REACT, V17, P1
[4]   PLATELET ACTIVATION [J].
BLOCKMANS, D ;
DECKMYN, H ;
VERMYLEN, J .
BLOOD REVIEWS, 1995, 9 (03) :143-156
[5]   AN ANTIPLATELET PRINCIPLE OF VERATRUM-FORMOSANUM [J].
CHUNG, MI ;
TENG, CM ;
CHENG, KL ;
KO, FN ;
LIN, CN .
PLANTA MEDICA, 1992, 58 (03) :274-276
[6]   Selected phenolic compounds in cultivated plants: Ecologic functions, health implications, and modulation by pesticides [J].
Daniel, O ;
Meier, MS ;
Schlatter, J ;
Frischknecht, P .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1999, 107 :109-114
[7]   HYDROGEN-PEROXIDE IS AN INTERMEDIATE IN THE PLATELET ACTIVATION CASCADE TRIGGERED BY COLLAGEN, BUT NOT BY THROMBIN [J].
DELPRINCIPE, D ;
MENICHELLI, A ;
DEMATTEIS, W ;
DIGIULIO, S ;
GIORDANI, M ;
SAVINI, I ;
AGRO, AF .
THROMBOSIS RESEARCH, 1991, 62 (05) :365-375
[8]   HYDROGEN-PEROXIDE HAS A ROLE IN THE AGGREGATION OF HUMAN-PLATELETS [J].
DELPRINCIPE, D ;
MENICHELLI, A ;
DEMATTEIS, W ;
DICORPO, ML ;
DIGIULIO, S ;
FINAZZIAGRO, A .
FEBS LETTERS, 1985, 185 (01) :142-146
[9]  
Forde RC, 1997, CIRCULATION, V95, P787
[10]   INHIBITION OF OXIDATION OF HUMAN LOW-DENSITY-LIPOPROTEIN BY PHENOLIC SUBSTANCES IN RED WINE [J].
FRANKEL, EN ;
KANNER, J ;
GERMAN, JB ;
PARKS, E ;
KINSELLA, JE .
LANCET, 1993, 341 (8843) :454-457