Requirement for GSH in recycling of ascorbic acid in endothelial cells

被引:66
作者
May, JM [1 ]
Qu, ZC [1 ]
Li, X [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
ascorbic acid; GSH; ferricyanide; dehydroascorbic acid; bovine aortic endothelial cells;
D O I
10.1016/S0006-2952(01)00736-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ascorbic acid may be involved in the defense against oxidant stress in endothelial cells. Such a role requires that the cells effectively recycle the vitamin from its oxidized forms. In this work, we studied the ability of cultured bovine aortic endothelial cells (BAECs) to take up and reduce dehydroascorbic acid (DHA) to ascorbate, as well as the dependence of ascorbate recycling on intracellular GSH. BAECs took up and reduced DHA to ascorbate much more readily than they took up ascorbate. Although BAECs in culture did not contain ascorbate, ascorbate accumulated to concentrations of 2-3 mM in BAECs following incubation with 400 muM DHA. Extracellular ferricyanide oxidized intracellular ascorbate, which was recycled by the cells. Reduction of DHA, either when added to the cells or when generated in response to ferricyanide, caused significant decreases in intracellular GSH concentrations. Depletion of intracellular GSH with 1-chloro-2,4-dinitrobenzene, diethylmaleate, and diamide almost abolished the ability of the cells to reduce DHA to ascorbate. DHA reduction by thioredoxin reductase was evident in dialyzed cell extracts, but occurred at rates far lower than direct GSH reduction of DHA. These results suggest that maximal rates of DHA reduction, and thus recycling of ascorbate from DHA, are dependent upon GSH in these cells. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:873 / 881
页数:9
相关论文
共 56 条
[1]   A SENSITIVE AND SIMPLE METHOD FOR DETERMINATION OF FERROCYANIDE [J].
AVRON, M ;
SHAVIT, N .
ANALYTICAL BIOCHEMISTRY, 1963, 6 (06) :549-&
[2]   DETOXIFICATION OF XENOBIOTICS BY GLUTATHIONE S-TRANSFERASES IN ERYTHROCYTES - THE TRANSPORT OF THE CONJUGATE OF GLUTATHIONE AND 1-CHLORO-2,4-DINITROBENZENE [J].
AWASTHI, YC ;
MISRA, G ;
RASSIN, DK ;
SRIVASTAVA, SK .
BRITISH JOURNAL OF HAEMATOLOGY, 1983, 55 (03) :419-425
[3]  
AWASTHI YC, 1981, BLOOD, V58, P733
[4]  
Beckman JS, 1996, AM J PHYSIOL-CELL PH, V271, pC1424
[5]   HUMAN THIOREDOXIN REDUCTASE DIRECTLY REDUCES LIPID HYDROPEROXIDES BY NADPH AND SELENOCYSTINE STRONGLY STIMULATES THE REACTION VIA CATALYTICALLY GENERATED SELENOLS [J].
BJORNSTEDT, M ;
HAMBERG, M ;
KUMAR, S ;
XUE, J ;
HOLMGREN, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (20) :11761-11764
[6]   AN ENZYME FROM RAT LIVER CATALYSING CONJUGATIONS WITH GLUTATHIONE [J].
BOOTH, J ;
BOYLAND, E ;
SIMS, P .
BIOCHEMICAL JOURNAL, 1961, 79 (03) :516-&
[7]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]   Altered eicosanoid biosynthesis in selenium-deficient endothelial cells [J].
Cao, YZ ;
Reddy, CC ;
Sordillo, LM .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (03) :381-389
[9]   High glucose induces antioxidant enzymes in human endothelial cells in culture - Evidence linking hyperglycemia and oxidative stress [J].
Ceriello, A ;
delloRusso, P ;
Amstad, P ;
Cerutti, P .
DIABETES, 1996, 45 (04) :471-477
[10]   Protective role of glutathione synthesis in response to oxidized low density lipoprotein in human vascular endothelial cells [J].
Cho, SS ;
Hazama, M ;
Urata, Y ;
Goto, SJ ;
Horiuchi, S ;
Sumikawa, K ;
Kondo, T .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (5-6) :589-602