Ascorbic acid prevents increased endothelial permeability caused by oxidized low density lipoprotein

被引:30
作者
May, James M. [1 ]
Qu, Zhi-Chao [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, 7465 Med Res Bldg 4, Nashville, TN 37232 USA
关键词
Paracellular transport; oxidative stress; endothelial dysfunction; ALPHA-LIPOIC ACID; LIGHT-CHAIN PHOSPHATASE; IN-VITRO MODEL; LDL OXIDATION; BARRIER FUNCTION; OXIDANT STRESS; VITAMIN-C; CELL-LINE; ACTIVATION; TOCOPHEROL;
D O I
10.3109/10715762.2010.508496
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
Mildly oxidized low density lipoprotein (mLDL) acutely increases the permeability of the vascular endothelium to molecules that would not otherwise cross the barrier. This study has shown that ascorbic acid tightens the permeability barrier in the endothelial barrier in cells, so this work tested whether it might prevent the increase in endothelial permeability due to mLDL. Treatment of EA.hy926 endothelial cells with mLDL decreased intracellular GSH and activated the cells to further oxidize the mLDL. mLDL also increased endothelial permeability over 2 h to both inulin and ascorbate in cells cultured on semi-permeable filters. This effect was blocked by microtubule and microfilament inhibitors, but not by chelation of intracellular calcium. Intracellular ascorbate both prevented and reversed the mLDL-induced increase in endothelial permeability, an effect mimicked by other cell-penetrant antioxidants. These results suggest a role for endothelial cell ascorbate in ameliorating an important facet of endothelial dysfunction caused by mLDL.
引用
收藏
页码:1359 / 1368
页数:10
相关论文
共 42 条
[1]   INVITRO MODEL OF ANGIOGENESIS USING A HUMAN ENDOTHELIUM-DERIVED PERMANENT CELL-LINE - CONTRIBUTIONS OF INDUCED GENE-EXPRESSION, G-PROTEINS, AND INTEGRINS [J].
BAUER, J ;
MARGOLIS, M ;
SCHREINER, C ;
EDGELL, CJ ;
AZIZKHAN, J ;
LAZAROWSKI, E ;
JULIANO, RL .
JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 153 (03) :437-449
[2]   Oxidized lipoprotein induces the macrophage ascorbate transporter (SVCT2): Protection by intracellular ascorbate against oxidant stress and apoptosis [J].
Chi, Xiumei ;
May, James M. .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2009, 485 (02) :174-182
[3]   Efficient repair of protein radicals by ascorbate [J].
Domazou, Anastasia S. ;
Koppenol, Willem H. ;
Gebicki, Janusz M. .
FREE RADICAL BIOLOGY AND MEDICINE, 2009, 46 (08) :1049-1057
[4]  
Ehringer WD, 1996, J CELL PHYSIOL, V167, P562, DOI 10.1002/(SICI)1097-4652(199606)167:3<562::AID-JCP20>3.3.CO
[5]  
2-K
[6]   Mildly oxidized low density lipoprotein induces contraction of human endothelial cells through activation of Rho/Rho kinase and inhibition of myosin light chain phosphatase [J].
Essler, M ;
Retzer, M ;
Bauer, M ;
Heemskerk, JW ;
Aepfelbacher, M ;
Siess, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (43) :30361-30364
[7]   Thrombin inactivates myosin light chain phosphatase via Rho and its target Rho kinase in human endothelial cells [J].
Essler, M ;
Amano, M ;
Kruse, HJ ;
Kaibuchi, K ;
Weber, PC ;
Aepfelbacher, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) :21867-21874
[8]   ALPHA-LIPOIC ACID REDUCTION BY MAMMALIAN-CELLS TO THE DITHIOL FORM, AND RELEASE INTO THE CULTURE-MEDIUM [J].
HANDELMAN, GJ ;
HAN, D ;
TRITSCHLER, H ;
PACKER, L .
BIOCHEMICAL PHARMACOLOGY, 1994, 47 (10) :1725-1730
[9]   Advanced glycation end products increase endothelial permeability through the RAGE/Rho signaling pathway [J].
Hirose, Akiko ;
Tanikawa, Takahisa ;
Mori, Hiroko ;
Okada, Yosuke ;
Tanaka, Yoshiya .
FEBS LETTERS, 2010, 584 (01) :61-66
[10]   FLUOROMETRIC METHOD FOR DETERMINATION OF OXIDIZED AND REDUCED GLUTATHIONE IN TISSUES [J].
HISSIN, PJ ;
HILF, R .
ANALYTICAL BIOCHEMISTRY, 1976, 74 (01) :214-226