Diphenyl diselenide protects endothelial cells against oxidized low density lipoprotein-induced injury: Involvement of mitochondrial function

被引:26
|
作者
Hort, Mariana Appel [1 ,2 ]
Straliotto, Marcos Raniel [1 ]
de Oliveira, Jade [1 ]
Amoedo, Nivea Dias [3 ]
Teixeira da Rocha, Joao Batista [4 ]
Galina, Antonio [3 ]
Ribeiro-do-Valle, Rosa Maria [2 ]
de Bem, Andreza Fabro [1 ]
机构
[1] Univ Fed Santa Catarina, Ctr Ciencias Biol, Dept Bioquim, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Fed Santa Catarina, Ctr Ciencias Biol, Dept Farmacol, BR-88040900 Florianopolis, SC, Brazil
[3] Univ Fed Rio de Janeiro, Lab Bioquim & Biol Mol Canc, Ctr Ciancias Saude, Inst Bioquim Med, Rio De Janeiro, Brazil
[4] Univ Fed Santa Maria, Dept Quim, BR-97119900 Santa Maria, RS, Brazil
关键词
Diphenyl diselenide; Endothelial cells; Mitochondria; Oxidative stress; Oxidized LDL; ACTIVE ORGANOSELENIUM COMPOUND; E-DEFICIENT MICE; OXIDATIVE STRESS; GLUTATHIONE-PEROXIDASE; VASCULAR CELLS; PZ-51; EBSELEN; NITRIC-OXIDE; IN-VITRO; LDL; ATHEROSCLEROSIS;
D O I
10.1016/j.biochi.2014.07.004
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
Elevated levels of oxidized low density lipoprotein (oxLDL) are considered to be one of the major risk factors for atherosclerosis and cardiovascular morbidity. The early stages of atherosclerosis are initiated by the accumulation of oxLDL and the induction of toxic effects on endothelial cells, resulting in endothelial dysfunction. The aim of this study was to investigate how diphenyl diselenide (DD), an organoselenium compound, protect vascular endothelial cells against the toxic effects of oxLDL in vitro. Our data showed that the treatment of bovine endothelial aortic cells (BAEC) with DD (0.1-1 mu M) for 24 h protected from oxLDL-induced reactive species (RS) production and reduced glutathione (GSH) depletion. Moreover, DD (1 mu M) per se improved the maximal mitochondrial respiratory capacity and prevented oxLDL-induced mitochondrial damage. In addition, DD could prevent apoptosis induced by oxLDL in BAEC. Results from this study may provide insight into a possible molecular mechanism underlying DD suppression of oxLDL-mediated vascular endothelial dysfunction. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:172 / 181
页数:10
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