Inducible nitric oxide synthase and cyclooxgenase-2 mediate protection of hydrogen peroxide preconditioning against apoptosis induced by oxidative stress in PC12 cells

被引:26
作者
Tang, Xiao-qing
Yu, Hui-min
Zhi, Jun-li
Cui, Yu
Tang, Er-hu
Feng, Jian-qiang [1 ]
Chen, Pei-xi
机构
[1] Sun Yat Sen Univ, Zhongshan Med Coll, Dept Physiol, Guangzhou 510080, Peoples R China
[2] Nahua Univ, Coll Med, Dept Physiol, Hengyang City 421001, Hunan, Peoples R China
关键词
inducible nitric oxide synthase; cyclooxygenase; hydrogen superoxide; apoptosis; preconditioning;
D O I
10.1016/j.lfs.2006.03.010
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The induction of inducible nitric oxide synthase (iNOS) in response to different stress is associated with simultaneous induction of cyclooxygenase-2 (COX-2) in various cell types. Both NOS and COX-2 have been reported to mediate the late phase of cardioprotection induced by different preconditioning. However, whether both iNOS and COX-2 are mediators in the neuroprotection induced by preconditioning with hydrogen peroxide (H2O2) at low concentration is unknown. In this study, using the neurosecretory cell line-PC12 cells to set up the model of neuroprotection of preconditioning with H2O2 against apoptosis, we first investigate what changes in expression of NOS and COX-2 appear during H2O2 preconditioning, then determine if both NOS inhibitor and COX-2 inhibitor interfere with the neuroprotection elicited by preconditioning with H2O2. We found that preconditioning with H2O2 at 10 mu M significantly protected PC12 cells against apoptosis induced by lethal H2O2 (50 mu M) and increased the expression of NOS and COX-2 and that selective NOS inhibitor, aminoguanidine (AG) and COX-2 inhibitor, NS-398 obviously blocked the protective effects induced by preconditioning with 10 mu M H2O2. The results of this study suggest that both iNOS and COX-2 are mediators of the neuroprotection induced by preconditioning with oxidative stress (H2O2 at low concentration) in PC12 cells. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:870 / 876
页数:7
相关论文
共 28 条
[1]   Oxidative damage of cardiomyocytes is limited by extracellular regulated kinases 1/2-mediated induction of cyclooxygenase-2 [J].
Adderley, SR ;
Fitzgerald, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (08) :5038-5046
[2]   COX-2: an in vivo evidence of its participation in heat stress-induced myocardial preconditioning [J].
Arnaud, C ;
Joyeux-Faure, M ;
Godin-Ribuot, D ;
Ribuot, C .
CARDIOVASCULAR RESEARCH, 2003, 58 (03) :582-588
[3]   Free-radical production triggered by hyperthermia contributes to heat stress-induced cardioprotection in isolated rat hearts [J].
Arnaud, C ;
Joyeux, M ;
Garrel, C ;
Godin-Ribuot, D ;
Demenge, P ;
Ribuot, C .
BRITISH JOURNAL OF PHARMACOLOGY, 2002, 135 (07) :1776-1782
[4]  
Bell RM, 1999, CIRCULATION, V100, P242
[5]   The late phase of preconditioning [J].
Bolli, R .
CIRCULATION RESEARCH, 2000, 87 (11) :972-983
[7]   Delayed or second window preconditioning induced by adenosine al receptor activation is independent of early generation of nitric oxide or late induction of inducible nitric oxide synthase [J].
Dana, A ;
Baxter, GF ;
Yellon, DM .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2001, 38 (02) :278-287
[8]   Evidence for an essential role of cyclooxygenase-2 as a mediator of the late phase of ischemic preconditioning in mice [J].
Guo, Y ;
Bao, W ;
Wu, WJ ;
Shinmura, K ;
Tang, XL ;
Bolli, R .
BASIC RESEARCH IN CARDIOLOGY, 2000, 95 (06) :479-484
[9]   The late phase of ischemic preconditioning is abrogated by targeted disruption of the inducible NO synthase gene [J].
Guo, Y ;
Jones, WK ;
Xuan, YT ;
Tang, XL ;
Bao, W ;
Wu, WJ ;
Han, H ;
Laubach, VE ;
Ping, PP ;
Yang, ZQ ;
Qiu, YM ;
Bolli, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11507-11512
[10]  
Guo YR, 2000, CIRCULATION, V102, P121