Flavonoids protect neuronal cells from oxidative stress by three distinct mechanisms

被引:704
作者
Ishige, K
Schubert, D
Sagara, Y
机构
[1] Salk Inst Biol Studies, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
关键词
flavonoids; oxidative stress; glutamate toxicity; vitamin E; reactive oxygen species; mitochondria; glutathione; neuronal cells; quercetin; buthionine sulfoximine; apoptosis; free radicals;
D O I
10.1016/S0891-5849(00)00498-6
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
Flavonoids are a family of antioxidants found in fruits and vegetables as well as in popular beverages such as red wine and tea. Although the physiological benefits of flavonoids have been largely attributed to their antioxidant properties in plasma, flavonoids may also protect cells from various insults. Nerve cell death from oxidative stress has been implicated in a variety of pathologies, including stroke, trauma, and diseases such as Alzheimer's and Parkinson's. To determine the potential protective mechanisms of flavonoids in cell death, the mouse hippocampal cell line HT-22, a model system for oxidative stress, was used. In this system, exogenous glutamate inhibits cystine uptake and depletes intracellular glutathione (GSH), leading to the accumulation of reactive oxygen species (ROS) and an increase in Ca2+ influx, which ultimately causes neuronal death. Many, but not all, flavonoids protect HT-22 cells and rat primary neurons from glutamate toxicity as well as from five other oxidative injuries. Three structural requirements of flavonoids for protection from glutamate are the hydroxylated C3, an unsaturated C ring, and hydrophobicity. We also found three distinct mechanisms of protection. These include increasing intracellular GSH, directly lowering levels of ROS, and preventing the influx of Ca2+ despite high levels of ROS. These data show that the mechanism of protection from oxidative insults by flavonoids is highly specific for each compound. (C) 2001 Elsevier Science Inc.
引用
收藏
页码:433 / 446
页数:14
相关论文
共 71 条
  • [1] Abe K, 1996, J NEUROCHEM, V67, P2074
  • [2] CHELATING AND FREE-RADICAL SCAVENGING MECHANISMS OF INHIBITORY-ACTION OF RUTIN AND QUERCETIN IN LIPID-PEROXIDATION
    AFANASEV, IB
    DOROZHKO, AI
    BRODSKII, AV
    KOSTYUK, VA
    POTAPOVITCH, AI
    [J]. BIOCHEMICAL PHARMACOLOGY, 1989, 38 (11) : 1763 - 1769
  • [3] DEPROTONATION INDUCED C-13 NMR SHIFTS IN PHENOLS AND FLAVONOIDS
    AGRAWAL, PK
    SCHNEIDER, HJ
    [J]. TETRAHEDRON LETTERS, 1983, 24 (02) : 177 - 180
  • [4] OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING
    AMES, BN
    SHIGENAGA, MK
    HAGEN, TM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) : 7915 - 7922
  • [5] [Anonymous], 1998, ANTIOX HEALTH DIS
  • [6] BASS DA, 1983, J IMMUNOL, V130, P1910
  • [7] Neuroprotection against oxidative stress by estrogens: Structure-activity relationship
    Behl, C
    Skutella, T
    Lezoualch, F
    Post, A
    Widmann, M
    Newton, CJ
    Holsboer, F
    [J]. MOLECULAR PHARMACOLOGY, 1997, 51 (04) : 535 - 541
  • [8] Vitamin nature of flavones
    Bentsath, A
    Rusznyak, S
    Gyorgyi, AS
    [J]. NATURE, 1936, 138 : 798 - 798
  • [9] THE DATA SUPPORT A ROLE FOR ANTIOXIDANTS IN REDUCING CANCER RISK
    BLOCK, G
    [J]. NUTRITION REVIEWS, 1992, 50 (07) : 207 - 213
  • [10] BORS W, 1990, METHOD ENZYMOL, V186, P343