EFFECTS OF ISOFLURANE, HALOTHANE, AND ENFLURANE ON MYOCARDIAL FLOW AND ENERGY STORES IN THE PERFUSED RAT-HEART

被引:8
作者
BLAISE, GA [1 ]
NOEL, J [1 ]
VILLENEUVE, E [1 ]
HOLLMAN, C [1 ]
VINET, B [1 ]
BOULANGER, Y [1 ]
VINAY, P [1 ]
机构
[1] UNIV MONTREAL,HOP NOTRE DAME,DEPT NEPHROL,MONTREAL H2L 4M1,QUEBEC,CANADA
关键词
ANESTHETICS; VOLATILE; CORONARY FLOW; METABOLIC EQUILIBRIUM;
D O I
10.1139/y91-112
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of three volatile anesthetics (halothane, enflurane, and isoflurane) on coronary flow and metabolic state of isolated rat hearts was studied. These anesthetics are coronary dilators and their effects are dose dependent. At 2 MAC (minimum alveolar concentration), isoflurane, enflurane, and halothane increase coronary flow by 114 +/- 5.9, 93 +/- 6.1, and 77 +/- 6.4%, respectively (p < 0.001). At these concentrations, they also have a modest but significant metabolic effect causing a 30% reduction in myocardial ATP and phosphocreatine levels, with no significant modification in ADP and AMP concentrations. Energy charge and lactate/pyruvate ratio were also unaffected by these anesthetics. The vascular and metabolic effects were reversible within 2 and 30 min, respectively. Perfusion of the hearts with a Krebs-Henseleit solution without Pi did not interfere with the vascular and the metabolic effect of the anesthetics; however, in this case, ATP and phosphocreatine concentration did not return to control levels after their discontinuation despite full recovery of the vascular effect. These data suggest that the volatile anesthetics have direct coronary vascular and myocardial metabolic effects and that these effects occur independently.
引用
收藏
页码:752 / 760
页数:9
相关论文
共 40 条
[1]  
BECKER GL, 1986, ANESTH ANALG, V65, P1130
[2]   CONTRIBUTION OF INHIBITION OF NADH-DEHYDROGENASE TO CARDIOTOXIC EFFECTS OF HALOTHANE [J].
BERMAN, MC ;
KEWLEY, CF ;
KENCH, JE .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1974, 6 (01) :39-47
[3]  
BERNE RM, 1979, HDB PHYSL 2, V1, P873
[4]   ISOFLURANE CAUSES ENDOTHELIUM-DEPENDENT INHIBITION OF CONTRACTILE RESPONSES OF CANINE CORONARY-ARTERIES [J].
BLAISE, G ;
SILL, JC ;
NUGENT, M ;
VANDYKE, RA ;
VANHOUTTE, PM .
ANESTHESIOLOGY, 1987, 67 (04) :513-517
[5]  
BLAISE G, 1989, CLIN INVEST MED, V12, P254
[6]   BIOCHEMICAL-CHARACTERIZATION AND OSMOLYTES IN PAPILLARY COLLECTING DUCTS FROM PIG AND DOG KIDNEYS [J].
BOULANGER, Y ;
LEGAULT, P ;
TEJEDOR, A ;
VINAY, P ;
THERIAULT, Y .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1988, 66 (10) :1282-1290
[7]  
BOULIEU R, 1984, CLIN CHIM ACTA, V137, P184
[8]   RELEASE OF A CORONARY VASODILATOR METABOLITE FROM GUINEA-PIG ISOLATED PERFUSED HEART STIMULATED BY CATECHOLAMINES, HISTAMINE AND ELECTRICAL PACING AND BY EXPOSURE TO ANOXIA [J].
BROADLEY, KJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1976, 58 (01) :89-100
[9]  
CALVERLEY RK, 1972, ANESTH ANALG, V51, P247
[10]  
COTERALLARO M, 1983, THROMB HAEMOSTASIS, V50, P857