Sarcolemmal and mitochondrial adenosine triphosphate-dependent potassium channels - Mechanism of desflurane-induced cardioprotection

被引:127
作者
Toller, WG
Gross, ER
Kersten, JR
Pagel, PS
Gross, GJ
Warltier, DC
机构
[1] Med Coll Wisconsin, Dept Anesthesiol, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Pharmacol, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
[4] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
关键词
myocardial ischemia;
D O I
10.1097/00000542-200006000-00033
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background Volatile anesthetic-induced preconditioning is mediated by adenosine triphosphate-dependent potassium (K-ATP) channels; however, the subcellular location of these channels is unknown. The authors tested the hypothesis that desflurane reduces experimental myocardial infarct size by activation of specific sarcolemmal and mitochondrial K-ATP channels. Methods: Barbiturate-anesthetized dogs (n = 88) were acutely instrumented for measurement of aortic and left ventricular pressures. All dogs were subjected to a 60-min left anterior descending coronary artery occlusion followed by 3-h reperfusion. In four separate groups, dogs received vehicle (0.9% saline) or the nonselective K-ATP channel antagonist glyburide (0.1 mg/kg intravenously) in the presence or absence of 1 minimum alveolar concentration desflurane. In four additional groups, dogs received 45-min intracoronary infusions of the selective sarcolemmal (HMR 1098; 1 mu g . kg(-1) . min(-1)) or mitochondrial (5-hydroxydecanoate [5-HD]; 150 mu g . kg(-1) . min(-1)) K-ATP channel antagonists in the presence or absence of desflurane. Myocardial perfusion and infarct size were measured with radioactive microspheres and triphenyltetrazolium staining, respectively. Results: Desflurane significantly (P < 0.05) decreased infarct size to 10 +/- 2% (mean +/- SEM) of the area at risk as compared with control experiments (25 +/- 3% of area at risk). This beneficial effect of desflurane was abolished by glyburide (25 +/- 2%) of area at risk. Glyburide (24 +/- 12%), HMR 1098 (21 +/- 4%), and 5-HD (24 +/- 2% of area at risk) alone had no effects on myocardial infarct size. HMR 1098 and 5-HD abolished the protective effects of desflurane (19 +/- 3% and 22 +/- 2% of area at risk, respectively). Conclusion Desflurane reduces myocardial infarct size in vivo, and the results further suggest that both sarcolemmal and mitochondrial K-ATP channels could be involved.
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收藏
页码:1731 / 1739
页数:9
相关论文
共 43 条
[1]  
*AM PHYS SOC, 1991, GUID PRINC CAR US AN
[2]   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
[3]   Ischemic preconditioning depends on interaction between mitochondrial KATP channels and actin cytoskeleton [J].
Baines, CP ;
Liu, GS ;
Birincioglu, M ;
Critz, SD ;
Cohen, MV ;
Downey, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1999, 276 (04) :H1361-H1368
[4]  
Billman GE, 1998, J PHARMACOL EXP THER, V286, P1465
[5]   Anesthetic-induced preconditioning - Previous administration of isoflurane decreases myocardial infarct size in rabbits [J].
Cason, BA ;
Gamperl, AK ;
Slocum, RE ;
Hickey, RF .
ANESTHESIOLOGY, 1997, 87 (05) :1182-1190
[6]   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
[7]  
*COMM REV GUID CAR, 1996, GUID CAR US LAB AN
[8]   MAC OF I-653 IN BEAGLE DOGS AND NEW-ZEALAND WHITE-RABBITS [J].
DOORLEY, BM ;
WATERS, SJ ;
TERRELL, RC ;
ROBINSON, JL .
ANESTHESIOLOGY, 1988, 69 (01) :89-91
[9]  
Garlid KD, 1997, CIRC RES, V81, P1072
[10]   The mitochondrial K-ATP channel as a receptor for potassium channel openers [J].
Garlid, KD ;
Paucek, P ;
YarovYarovoy, V ;
Sun, XC ;
Schindler, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (15) :8796-8799