Epsilon protein kinase C as a potential therapeutic target for the ischemic heart

被引:121
作者
Inagaki, Koichi [1 ]
Churchill, Enic [1 ]
Mochly-Rosen, Daria [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Mol Pharmacol, CCSR, Stanford, CA 94305 USA
关键词
preconditioniong; postconditioning; ischemia/reperfusion; PKC; ROS; K-ATP channel; cardiac transplant; signal transduction;
D O I
10.1016/j.cardiores.2006.02.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ischemic heart disease is the leading cause of morbidity and mortality in the western world. Ischemic damage can occur by acute myocardial infarction, stable angina, cardiac stunning, and myocardial hibernation. In addition, 'scheduled' ischemic events, occurring during cardiac surgery, heart transplantation, and elective angioplasty, can also result in cardiac damage. Ischemic or pharmacological preconditioning can decrease the extent of damage to the myocardium. Although the mechanism of preconditioning-mediated cardioprotection is not fully understood, epsilon PKC has been implicated as a critical mediator of this process in animal studies. The use of isozyme-specific pharmacological tools has permitted a better elucidation of the upstream stimuli and the downstream transducers of epsilon PKC in the pathways leading to cardioprotection. While little is known about the role of epsilon PKC in these pathways in humans, animal studies suggest a potential therapeutic role of epsilon PKC. This review will focus on the role of epsilon PKC in cardiac protection and on the signal transduction cascades that have been implicated in this protection. (c) 2006 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:222 / 230
页数:9
相关论文
共 112 条
  • [1] Protein kinase C-ε primes the cardiac sarcolemmal adenosine triphosphate-sensitive potassium channel to modulation by isoflurane
    Aizawa, K
    Turner, LA
    Weihrauch, D
    Bosnjak, ZJ
    Kwok, WM
    [J]. ANESTHESIOLOGY, 2004, 101 (02) : 381 - 389
  • [2] PROPERTIES AND FUNCTIONS OF ATP-SENSITIVE K-CHANNELS
    ASHCROFT, SJH
    ASHCROFT, FM
    [J]. CELLULAR SIGNALLING, 1990, 2 (03) : 197 - 214
  • [3] Mitochondrial PKCε and MAPK form signaling modules in the murine heart -: Enhanced mitochondrial PKCε-MAPK interactions and differential MAPK activation in PKCε-induced cardioprotection
    Baines, CP
    Zhang, J
    Wang, GW
    Zheng, YT
    Xiu, JX
    Cardwell, EM
    Bolli, R
    Ping, P
    [J]. CIRCULATION RESEARCH, 2002, 90 (04) : 390 - 397
  • [4] Protein kinase Cε interacts with and inhibits the permeability transition pore in cardiac mitochondria
    Baines, CP
    Song, CX
    Zheng, YT
    Wang, GW
    Zhang, J
    Wang, OL
    Guo, Y
    Bolli, R
    Cardwell, EM
    Ping, PP
    [J]. CIRCULATION RESEARCH, 2003, 92 (08) : 873 - 880
  • [5] Oxygen radicals released during ischemic preconditioning contribute to cardioprotection in the rabbit myocardium
    Baines, CP
    Goto, M
    Downey, JM
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (01) : 207 - 216
  • [6] Biodistribution of intracellularly acting peptides conjugated reversibly to Tat
    Begley, R
    Liron, T
    Baryza, J
    Mochly-Rosen, D
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 318 (04) : 949 - 954
  • [7] Belhomme D, 1999, CIRCULATION, V100, P340
  • [8] Pivotal role of NOX-2-containing NADPH oxidase in early ischemic preconditioning
    Bell, RM
    Cave, AC
    Johar, S
    Hearse, DJ
    Shah, AM
    Shattock, MJ
    [J]. FASEB JOURNAL, 2005, 19 (12) : 2037 - +
  • [9] BERGESE SD, 1995, AM J PATHOL, V147, P166
  • [10] Evidence that late preconditioning against myocardial stunning in conscious rabbits is triggered by the generation of nitric oxide
    Bolli, R
    Bhatti, ZA
    Tang, XL
    Qiu, YM
    Zhang, Q
    Guo, Y
    Jadoon, AK
    [J]. CIRCULATION RESEARCH, 1997, 81 (01) : 42 - 52