Hydrogen sulfide destroys lipid hydroperoxides in oxidized LDL

被引:46
|
作者
Muellner, Markus K. [1 ]
Schreier, Sabine M. [1 ]
Laggner, Hilde [1 ]
Hermann, Marcela [2 ]
Esterbauer, Harald [3 ]
Exner, Markus [4 ]
Gmeiner, Bernhard M. K. [1 ]
Kapiotis, Stylianos [3 ,5 ]
机构
[1] Med Univ Vienna, CPP, Dept Med Chem, Vienna, Austria
[2] Med Univ Vienna, MFPL, Dept Med Biochem, Vienna, Austria
[3] Med Univ Vienna, Clin Inst Med & Chem Lab Diagnost, Vienna, Austria
[4] Spitzauer & Partner, Labor Gruppenpraxis Bauer, Vienna, Austria
[5] Hosp Div Redeemer, Cent Lab, Vienna, Austria
关键词
atherosclerosis; hydrogen sulfide (H2S); low-densitylipoprotein (LDL) oxidation; lipid hydroperoxide; (9-S)-hydroxy-(10E; 12Z)-octadecadienoic acid (9-HODE); (9S)-hydroperoxy-(10E; 12Z)-octadecadienoic acid (9-HPODE); LOW-DENSITY-LIPOPROTEIN; HEME OXYGENASE-1; OXIDATIVE MODIFICATION; PEROXIDATION PRODUCTS; PARAOXONASE; CHOLESTEROL; INHIBITOR; INDUCTION; MECHANISM; IONS;
D O I
10.1042/BJ20082421
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
LOOHs (lipid hydroperoxides) in oxLDL oxidized LDL (low-density lipoprotein) are potentially atherogenic compounds. Recently, H2S was identified as the third endogenous gasotransmitter in the vasculature. H2O2 is known to be destroyed by H2S. Assuming that H2S may also react with LOOHs, the results show that H2S can destroy LOOHs in oxLDL. The ability of LOOH-enriched LDL to induce HO-1 (haem oxygenase 1) in endothelial cells was abolished by 1-I,S pretreatment. I-IPLC analysis showed that 9-HPODE [(9S)-hydroperoxy-(10E,12Z)octadecadienoic acid], a compound found in oxLDL, was reduced to 9-HODS [(9S)-hydroxy-(10E,12Z)-octadecadienoic acid] in the presence of H2S. Thus H2S may act its an antiatherogenic agent by reducing LOOHS to the less reactive LOHs and could abrogate the pathobiological activity of oxLDL.
引用
收藏
页码:277 / 281
页数:5
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