ENERGETIC DETERMINANTS OF STUNNING AND CELL-DAMAGE FOLLOWING REOXYGENATION OF RABBIT MYOCARDIUM

被引:5
作者
DIETRICH, DLL
ELZINGA, G
机构
[1] Laboratory for Physiology, Free University, Amsterdam
关键词
ANOXIA; ATP TURNOVER; STUNNING; CELL DAMAGE;
D O I
10.1016/0022-2828(92)93094-Z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The energetic conditions in anoxia which lead to stunning and cell damage upon reoxygenation of the myocardium are studied in isolated papillary muscles of rabbit contracting isometrically at 20°C. Before anoxia and thereafter the muscles are stimulated at 0.2 Hz, while during anoxia stimulation frequency is varied. Total creatine (CrT) content is taken as a measure of cell damage. The degree of stunning is estimated from the difference in force before anoxia and at the end of the recovery period when no creatine is lost. In anoxic rabbit papillary muscles glycogen is the substrate for lactate formation. The 'ATP reserve' of the muscle can then be calculated from: 2 ATP+PCr+ADP+3 (glycosyl units). In control muscles it equals 482.2 μmol.g-1 dw of ATP. By varying stimulus frequency (0, 0.2, 0.5, or 1 Hz) during and the length of the anoxic period (20 to 80 min), the fraction of the ATP reserve used in anoxia is varied. It is found that the degree of stunning depends on the degree of ATP reserve depletion. When the ATP reserve becomes virtually zero force recovers to only 67% of the preanoxic value. When anoxia continues after the ATP reserve is virtually zero, creatine in the muscle decreases during reoxygenation, indicating cell damage. Apparently a hierarchy of cellular ATPases exists in the myocardium when energy is short preserving cell integrity as long as possible. © 1992.
引用
收藏
页码:1277 / 1290
页数:14
相关论文
共 34 条
[1]   MYOCARDIAL CONTRACTILE FUNCTION DURING ISCHEMIA AND HYPOXIA [J].
ALLEN, DG ;
ORCHARD, CH .
CIRCULATION RESEARCH, 1987, 60 (02) :153-168
[2]   INTRACELLULAR CALCIUM-CONCENTRATION DURING HYPOXIA AND METABOLIC INHIBITION IN MAMMALIAN VENTRICULAR MUSCLE [J].
ALLEN, DG ;
ORCHARD, CH .
JOURNAL OF PHYSIOLOGY-LONDON, 1983, 339 (JUN) :107-122
[3]   THE CONSEQUENCES OF SIMULATED ISCHEMIA ON INTRACELLULAR CA2+ AND TENSION IN ISOLATED FERRET VENTRICULAR MUSCLE [J].
ALLEN, DG ;
LEE, JA ;
SMITH, GL .
JOURNAL OF PHYSIOLOGY-LONDON, 1989, 410 :297-323
[4]   MARKED REDUCTION OF FREE-RADICAL GENERATION AND CONTRACTILE DYSFUNCTION BY ANTIOXIDANT THERAPY BEGUN AT THE TIME OF REPERFUSION - EVIDENCE THAT MYOCARDIAL STUNNING IS A MANIFESTATION OF REPERFUSION INJURY [J].
BOLLI, R ;
JEROUDI, MO ;
PATEL, BS ;
ARUOMA, OI ;
HALLIWELL, B ;
LAI, EK ;
MCCAY, PB .
CIRCULATION RESEARCH, 1989, 65 (03) :607-622
[5]   MECHANISM OF MYOCARDIAL STUNNING [J].
BOLLI, R .
CIRCULATION, 1990, 82 (03) :723-738
[6]  
BRAUNWALD E, 1982, Circulation, V66, P1147
[7]   ENERGY DEMAND, SUPPLY, AND UTILIZATION IN HYPOXIA, AND FORCE RECOVERY AFTER REOXYGENATION IN RABBIT HEART-MUSCLE [J].
DIETRICH, DLL ;
MAST, F ;
ELZINGA, G .
CIRCULATION RESEARCH, 1990, 67 (05) :1089-1096
[8]   ATP FORMATION AND ENERGY DEMAND IN ANOXIC HEART-MUSCLE OF THE RABBIT [J].
DIETRICH, DLL ;
ELZINGA, G .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (02) :H526-H532
[9]   MECHANISMS OF ISCHEMIC MYOCARDIAL-CELL DAMAGE ASSESSED BY P-31 NUCLEAR MAGNETIC-RESONANCE [J].
FLAHERTY, JT ;
WEISFELDT, ML ;
BULKLEY, BH ;
GARDNER, TJ ;
GOTT, VL ;
JACOBUS, WE .
CIRCULATION, 1982, 65 (03) :561-571
[10]  
GENOTE CE, 1982, J MOL CELL CARDIOL, V14, P587