Propofol attenuation of hydrogen peroxide-mediated oxidative stress and apoptosis in cultured cardiomyocytes involves haeme oxygenase-1

被引:72
作者
Xu, J. -J. [1 ]
Wang, Y. -L. [2 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Anesthesiol, Anesthesiol Res Lab, Wuhan 430060, Peoples R China
[2] Wuhan Univ, Zhongnan Hosp, Dept Anesthesiol, Anesthesiol Res Lab, Wuhan 430072, Peoples R China
关键词
anaesthetics intravenous; propofol; hydrogen peroxide; haeme oxygenase-1; cardiac myocytes;
D O I
10.1017/S0265021508003542
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Background and objective: Our aim was to investigate the cytoprotective effect of propofol against hydrogen peroxide (H2O2)-mediated injury and the effects on the haeme oxygenase-1 system, which is a possible new cytoprotective pathway of propofol. Methods: Primary cultured newborn rat cardiomyocytes were divided into five groups: (1) untreated (Group control); (2) treated with 200 mu mol L-1 H2O2 (Group H) and treated with 200 mu mol L-1 H2O2 in the presence of propofol (25, 50 and 100 mu mol L-1, (3) Group 25P + H, (4) Group 50P + H and (5) Group 100P + H, respectively); added with zinc protoporphyrin IX (ZnPPIX) (10 mu mol L-1 a potent inhibitor of haeme oxygenase activity, or SC-3060 (0.2 mu L mL(-1)),a specific synthetic inhibitor of nuclear factor kappa B. All were incubated for 6 h. The protective effects of propofol were evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide cytotoxicity assay, the concentration of malondialdehyde, superoxide dismutase activity and cell apoptosis by enzyme-linked immunosorbent assay (ELISA). Reverse transcription polymerase chain reaction (RT-PCR) and western blot analysis were used to detect haeme oxygenase-1 expression. Results: Compared with H2O2, propofol concentrations (ranging from 50 to 100 mu mol L-1) significantly increased haeme oxygenase-1 expression and decreased cardiomyocytes apoptosis, accompanied with a decrease in malondialdehyde, but with an increase in superoxide dismutase activity and cell activity (P < 0.05 and P < 0.01, respectively). The protective effects of propofol were mitigated by the addition of ZnPPIX. The addition of SC-3060 reversed propofol-induced haeme oxygenase-1 expression. Conclusion: Propofol can protect cardiomyocytes against H2O2-mediated cytotoxicity in a dose-dependent manner and increase haeme oxygenase-1 expression, which may partly mediate the cytoprotective effects of propofol.
引用
收藏
页码:395 / 402
页数:8
相关论文
共 30 条
[1]
Acquaviva R, 2004, ANESTHESIOLOGY, V101, P1363
[2]
Involvement of JNKs and p38-MAPK/MSK1 pathways in H2O2-induced upregulation of heme oxygenase-1 mRNA in H9c2 cells [J].
Aggeli, Ioanna-Katerina S. ;
Gaitanaki, Catherine ;
Beis, Isidoros .
CELLULAR SIGNALLING, 2006, 18 (10) :1801-1812
[3]
SUPEROXIDE-DEPENDENT AND ASCORBATE-DEPENDENT FORMATION OF HYDROXYL RADICALS FROM HYDROGEN-PEROXIDE IN THE PRESENCE OF IRON - ARE LACTOFERRIN AND TRANSFERRIN PROMOTERS OF HYDROXYL-RADICAL GENERATION [J].
ARUOMA, OI ;
HALLIWELL, B .
BIOCHEMICAL JOURNAL, 1987, 241 (01) :273-278
[4]
Sevoflurane but not propofol preserves myocardial function during minimally invasive direct coronary artery bypass surgery [J].
Bein, B ;
Renner, J ;
Caliebe, D ;
Scholz, J ;
Paris, A ;
Fraund, S ;
Zaehle, W ;
Tonner, PH .
ANESTHESIA AND ANALGESIA, 2005, 100 (03) :610-616
[5]
Severity of oxidative stress generates different mechanisms of endothelial cell death [J].
Burlacu, A ;
Jinga, V ;
Gafencu, AV ;
Simionescu, M .
CELL AND TISSUE RESEARCH, 2001, 306 (03) :409-416
[6]
Study on changes of heme oxygenase-1 expression in patients with coronary heart disease [J].
Chen, SM ;
Li, YG ;
Wang, DM .
CLINICAL CARDIOLOGY, 2005, 28 (04) :197-201
[7]
Hemodynamics in elderly coronary artery disease patients undergoing propofol sedation [J].
Cillo, Joseph E., Jr. ;
Finn, Richard .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2006, 64 (09) :1338-1342
[8]
The effects of propofol on lipid peroxidation and inflammatory response in elective coronary artery bypass grafting [J].
Corcoran, TB ;
Engel, A ;
Sakamoto, H ;
O'Callaghan-Enright, S ;
O'Donnell, A ;
Heffron, JA ;
Shorten, G .
JOURNAL OF CARDIOTHORACIC AND VASCULAR ANESTHESIA, 2004, 18 (05) :592-604
[9]
Free radicals in the physiological control of cell function [J].
Dröge, W .
PHYSIOLOGICAL REVIEWS, 2002, 82 (01) :47-95
[10]
Cobalt induces heme oxygenase-1 expression by a hypoxia-inducible factor-independent mechanism in Chinese hamster ovary cells - Regulation by Nrf2 and MafG transcription factors [J].
Gong, PF ;
Hu, B ;
Stewart, D ;
Ellerbe, M ;
Figueroa, YG ;
Blank, V ;
Beckman, BS ;
Alam, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (29) :27018-27025