Antioxidant effect of flavonoids after ascorbate/Fe2+-induced oxidative stress in cultured retinal cells

被引:93
作者
Areias, FM
Rego, AC
Oliveira, CR
Seabra, RM
机构
[1] Univ Porto, Fac Pharm, Lab Pharmacognosy, CEQUP, P-4050047 Porto, Portugal
[2] Univ Coimbra, Ctr Neurosci Coimbra, P-3004504 Coimbra, Portugal
[3] Univ Coimbra, Fac Med, P-3004504 Coimbra, Portugal
关键词
antioxidants; flavonoids; oxidative stress; retinal cells;
D O I
10.1016/S0006-2952(01)00621-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, we investigated the structure-activity relationship of four flavonoids, i.e. eriodictyol, luteolin, quercetin, and taxifolin, in cultured retinal cells after ascorbate/Fe2+-induced oxidative stress. The relative order of antioxidant efficacy, determined by the thiobarbituric acid method, was the following: eriodictyol > quercetin > luteolin > taxifolin. Upon preincubation, the flavonoids were also effective in reducing the extent of lipid peroxidation. Oxidative stress, determined by the changes in fluorescence of 2',7'-dichlorodihydrofluorescein, was also decreased in the presence of the flavonoids, showing the following order of antioxidant efficacy: eriodictyol > taxifolin approximate to quercetin > luteolin. Ascorbate/Fe2+-induced oxidative stress or incubation in the presence of the flavonoids did not significantly affect the viability of retinal cells. We also evaluated the degree of membrane partition of the flavonoids. In this system, the results strongly suggest that the higher antioxidant activity of the flavonoids is not correlated with the presence of a double bond at C-2-C-3 and/or a hydroxyl group at C-3 on the C ring, but rather may depend on the capacity to inhibit the production of reactive oxygen species to interact hydrophobically with membranes. Eriodictyol was shown to be the most efficient antioxidant in protecting against oxidative stress induced by ascorbate/Fe2+ in the retinal cells. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:111 / 118
页数:8
相关论文
共 45 条
[11]   Quercetin and myricetin protect against hydrogen peroxide-induced DNA damage (strand breaks and oxidised pyrimidines) in human lymphocytes [J].
Duthie, SJ ;
Collins, AR ;
Duthie, GG ;
Dodson, VL .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1997, 393 (03) :223-231
[12]   FLAVONOID INHIBITION OF ENZYMATIC AND NONENZYMIC LIPID-PEROXIDATION IN RAT-LIVER DIFFERS FROM ITS INFLUENCE ON THE GLUTATHIONE-RELATED ENZYMES [J].
GALVEZ, J ;
DELACRUZ, JP ;
ZARZUELO, A ;
DELACUESTA, FS .
PHARMACOLOGY, 1995, 51 (02) :127-133
[13]   ALTERED BRAIN METABOLISM OF IRON AS A CAUSE OF NEURODEGENERATIVE DISEASES [J].
GERLACH, M ;
BENSHACHAR, D ;
RIEDERER, P ;
YOUDIM, MBH .
JOURNAL OF NEUROCHEMISTRY, 1994, 63 (03) :793-807
[14]  
HALLIWELL B, 1990, METHOD ENZYMOL, V186, P1
[15]   REACTIVE OXYGEN SPECIES AND THE CENTRAL-NERVOUS-SYSTEM [J].
HALLIWELL, B .
JOURNAL OF NEUROCHEMISTRY, 1992, 59 (05) :1609-1623
[16]   OXYGEN RADICALS AND THE NERVOUS-SYSTEM [J].
HALLIWELL, B ;
GUTTERIDGE, JMC .
TRENDS IN NEUROSCIENCES, 1985, 8 (01) :22-26
[17]   THE DEFINITION AND MEASUREMENT OF ANTIOXIDANTS IN BIOLOGICAL-SYSTEMS [J].
HALLIWELL, B ;
GUTTERIDGE, JMC .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (01) :125-126
[18]   Antiperoxidative components in Thymus vulgaris [J].
Haraguchi, H ;
Saito, T ;
Ishikawa, H ;
Date, H ;
Kataoka, S ;
Tamura, Y ;
Mizutani, K .
PLANTA MEDICA, 1996, 62 (03) :217-221
[19]   IDENTIFICATION OF GABAERGIC AMACRINE CELL-LIKE NEURONS DEVELOPING IN CHICK RETINAL MONOLAYER-CULTURES [J].
HUBA, R ;
HOFMANN, HD .
NEUROSCIENCE LETTERS, 1990, 117 (1-2) :37-42
[20]  
Kolhir VK, 1996, PHYTOTHER RES, V10, P478, DOI 10.1002/(SICI)1099-1573(199609)10:6&lt