Ischemic preconditioning reduces unloaded myocardial oxygen consumption in an in-vivo sheep model

被引:15
作者
Tanoue, Y
Herijgers, P
Meuris, B
Verbeken, E
Leunens, V
Lox, M
Flameng, W
机构
[1] Katholieke Univ Leuven, Ctr Expt Surg & Anaesthesiol, CEHA, Cardiovasc Res Unit, Louvain, Belgium
[2] Katholieke Univ Leuven, Dept Pathol, Louvain, Belgium
关键词
ischemia; oxygen consumption; preconditioning; reperfusion; ventricular function;
D O I
10.1016/S0008-6363(02)00278-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Ischemic preconditioning (IP) describes the adaptation of the myocardium to ischemic stress preceded by short periods of ischemia and reperfusion. However, its cardioprotective mechanisms are not completely understood. We assessed the effect of IP on ventricular energetics in an in-vivo sheep model. Methods: IP was performed in six sheep by three 5 min aortic cross-clamping periods interspersed with 5 min of reperfusion during cardiopulmonary bypass and with six sheep as time-matched controls. Global myocardialy ischemia was subsequently achieved by 30 ruin aortic cross-clamping with left ventricular unloading during normothermic cardiopulmonary bypass. Weaning from cardiopulmonary bypass was performed 40 min after reperfusion. At baseline, after treatment (IP or time-matched cardiopulmonary bypass), and up to 100 min after reperfusion, left ventricular pressure-volume loops, were measured using a conductance catheter during a tight heart bypass preparation. Contractility, diastolic function, and ventruculo-arterial coupling were evaluated. Ventricular energetics [the relation between myocardial oxygen consumption (MVO2) and systolic pressure-volume area (PVA)] was also evaluated. A right heart bypass was instituted to control the preload and to decompress the right ventricle completely, thereby eliminating parallel conductance variation and minimizing the contribution of the right ventricle to MVO2 Results: IP reduced unloaded MVO2 (PVA-independent MVO2). Contractility, diastolic function, and ventriculo-arterial coupling in the IP group were better preserved than in the control group after ischemia-reperfusion. Conclusions: IP reduces unloaded NVO2, and preserves contractility, diastolic function, and ventriculo-arterial coupling after 30 min global myocardial ischemia in an in-vivo sheep model. (C) 2002 Elsevier Science BY All rights reserved.
引用
收藏
页码:633 / 641
页数:9
相关论文
共 26 条
[1]   CONTINUOUS MEASUREMENT OF LEFT-VENTRICULAR VOLUME IN ANIMALS AND HUMANS BY CONDUCTANCE CATHETER [J].
BAAN, J ;
VANDERVELDE, ET ;
DEBRUIN, HG ;
SMEENK, GJ ;
KOOPS, J ;
VANDIJK, AD ;
TEMMERMAN, D ;
SENDEN, J ;
BUIS, B .
CIRCULATION, 1984, 70 (05) :812-823
[2]   DOES CARDIOPULMONARY BYPASS ALONE ELICIT MYOPROTECTIVE PRECONDITIONING [J].
BURNS, PG ;
KRUKENKAMP, IB ;
CALDARONE, CA ;
GAUDETTE, GR ;
BUKHARI, EA ;
LEVITSKY, S .
CIRCULATION, 1995, 92 (09) :447-451
[3]   ISCHEMIC PRECONDITIONING AND CONTRACTILE FUNCTION - STUDIES WITH NORMOTHERMIC AND HYPOTHERMIC GLOBAL-ISCHEMIA [J].
CAVE, AC ;
HEARSE, DJ .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1992, 24 (10) :1113-1123
[4]   CARDIOPULMONARY BYPASS [J].
FERRARIS, VA ;
KLINGMAN, R ;
BUFO, A ;
SAIFI, J .
CURRENT OPINION IN CARDIOLOGY, 1991, 6 (02) :227-234
[5]   NEW STRATEGIES FOR INTRAOPERATIVE MYOCARDIAL PROTECTION [J].
FLAMENG, W .
CURRENT OPINION IN CARDIOLOGY, 1995, 10 (06) :577-583
[6]   Myocardial protection by brief ischemia in noncardiac tissue [J].
Gho, BCG ;
Schoemaker, RG ;
vandenDoel, MA ;
Duncker, DJ ;
Verdouw, PD .
CIRCULATION, 1996, 94 (09) :2193-2200
[7]   LINEARITY OF THE FRANK-STARLING RELATIONSHIP IN THE INTACT HEART - THE CONCEPT OF PRELOAD RECRUITABLE STROKE WORK [J].
GLOWER, DD ;
SPRATT, JA ;
SNOW, ND ;
KABAS, JS ;
DAVIS, JW ;
OLSEN, CO ;
TYSON, GS ;
SABISTON, DC ;
RANKIN, JS .
CIRCULATION, 1985, 71 (05) :994-1009
[8]   Preconditioning with ischaemia reduces both myocardial oxygen consumption and infarct size in a graded pattern [J].
Grund, F ;
Sommerschild, HT ;
Kirkeboen, KA ;
Ilebekk, A .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (11) :3067-3079
[9]   Localization and determination of infarct size by Gd-Mesoporphyrin enhanced MRI in dogs [J].
Herijgers, P ;
Laycock, SK ;
Ni, YC ;
Marchal, G ;
Bogaert, J ;
Bosmans, H ;
Petre, C ;
Flameng, W .
INTERNATIONAL JOURNAL OF CARDIAC IMAGING, 1997, 13 (06) :499-507
[10]   ISCHEMIC PRECONDITIONING IN A MODEL OF GLOBAL-ISCHEMIA - INFARCT SIZE LIMITATION, BUT NO REDUCTION OF STUNNING [J].
JENKINS, DP ;
PUGSLEY, WB ;
YELLON, DM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1995, 27 (08) :1623-1632