Mitochondrial ATP-sensitive potassium channel plays a dominant role in ischemic preconditioning of rabbit heart

被引:28
作者
Nakai, Y [1 ]
Horimoto, H [1 ]
Mieno, S [1 ]
Sasaki, S [1 ]
机构
[1] Osaka Med Coll, Dept Thorac & Cardiovasc Surg, Takatsuki, Osaka 5698686, Japan
关键词
preconditioning; mitochondria; ATP-sensitive; potassium channel; ischemia-reperfusion;
D O I
10.1159/000049695
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: The ATP-sensitive potassium (KATP) channel has been shown to be important in the ischemic preconditioning (IPC) response. Recently, the mitochondrial rather than the sarcolemmal KATP channel has been focused on due to its energy-modulating property. Hence, this study was undertaken to elucidate the role of the mitochondrial KATP channel in IPC by modulating the mitochondrial KATP channel in isolated perfused rabbit hearts. Methods: Seven hearts served as a control with no interventions. Seven hearts underwent IPC consisting of two 5-min cycles of global ischemia followed by 5 min of reperfusion, Seven hearts received the selective mitochondrial KATP channel blocker 5-dehydroxydecanoate (5-HD, 100 muM) for 5 min before IPC, and 7 hearts received the selective mitochondrial KATP channel opener diazoxide (50 muM) for 5 min. Then, all hearts were subjected to 1 h of left anterior descending coronary artery ischemia and 1 h of reperfusion. Left ventricular pressures, monophasic action potentials and coronary flow were measured throughout the experiment and infarct size was detected at the end of experiment. Results: (1) The mitochondria-selective K-ATP channel opener diazoxide reduced infarct size as com pa red to control (p < 0.05); (2) IPC reduced infarct size and preserved postischemic diastolic function as compared to control (p < 0.05), and (3) the mitochondria-selective KATP channel blocker 5-HD reversed these effects, Conclusion: The mitochondrial ATP-sensitive potassium channel may be a potential site of cardioprotection. Copyright <(c)> 2001 S. Karger AG. Basel.
引用
收藏
页码:57 / 63
页数:7
相关论文
共 33 条
[1]   PRESERVATION OF INTERVENTRICULAR SEPTAL FUNCTION IN PATIENTS HAVING CORONARY-ARTERY BYPASS GRAFTS WITHOUT CARDIOPULMONARY BYPASS [J].
AKINS, CW ;
BOUCHER, CA ;
POHOST, GM .
AMERICAN HEART JOURNAL, 1984, 107 (02) :304-309
[2]  
ASHCROFT FM, 1988, ANNU REV NEUROSCI, V11, P97, DOI 10.1146/annurev.ne.11.030188.000525
[3]   PROPERTIES AND FUNCTIONS OF ATP-SENSITIVE K-CHANNELS [J].
ASHCROFT, SJH ;
ASHCROFT, FM .
CELLULAR SIGNALLING, 1990, 2 (03) :197-214
[4]   BLOCKADE OF ISCHEMIC PRECONDITIONING IN DOGS BY THE NOVEL ATP DEPENDENT POTASSIUM CHANNEL ANTAGONIST SODIUM 5-HYDROXYDECANOATE [J].
AUCHAMPACH, JA ;
GROVER, GJ ;
GROSS, GJ .
CARDIOVASCULAR RESEARCH, 1992, 26 (11) :1054-1062
[5]   MECHANISM OF MYOCARDIAL STUNNING [J].
BOLLI, R .
CIRCULATION, 1990, 82 (03) :723-738
[6]   Coronary artery bypass grafting without cardiopulmonary bypass [J].
Buffolo, E ;
deAndrade, JCS ;
Branco, JNR ;
Teles, CA ;
Aguiar, LF ;
Gomes, WJ .
ANNALS OF THORACIC SURGERY, 1996, 61 (01) :63-66
[7]   Preconditioning during simulated MIDCABG attenuates blood flow defects and neutrophil accumulation [J].
Bufkin, BL ;
Shearer, ST ;
Vinten-Johansen, J ;
Duarte, IG ;
Thourani, VH ;
Nakamura, M ;
Zhao, ZQ ;
Guyton, RA .
ANNALS OF THORACIC SURGERY, 1998, 66 (03) :726-731
[8]   Ischemic preconditioning in human and rat ventricle [J].
Cleveland, JC ;
Wollmering, MM ;
Meldrum, DR ;
Rowland, RT ;
Rehring, TF ;
Sheridan, BC ;
Harken, AH ;
Banerjee, A .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 271 (05) :H1786-H1794
[9]   ATP-REGULATED K+ CHANNELS PROTECT THE MYOCARDIUM AGAINST ISCHEMIA REPERFUSION DAMAGE [J].
COLE, WC ;
MCPHERSON, CD ;
SONTAG, D .
CIRCULATION RESEARCH, 1991, 69 (03) :571-581
[10]  
FOBES RA, 1999, CIRCULATION, V100, P342