Myocardial substrate metabolism influences left ventricular energetics in vivo

被引:209
作者
Korvald, C [1 ]
Elvenes, OP [1 ]
Myrmel, T [1 ]
机构
[1] Univ Tromso Hosp, Dept Thorac & Cardiovasc Surg, N-9038 Tromso, Norway
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2000年 / 278卷 / 04期
关键词
left ventricle; cardiac energetics; pressure-volume area; glucose-insulin-potassium;
D O I
10.1152/ajpheart.2000.278.4.H1345
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The myocardial oxygen consumption (MVo(2)) to left ventricular pressure-volume area (PVA) relationship is assumed unaltered by substrates, despite varying phosphate-to-oxygen ratios and possible excess MVo(2) associated with fatty acid consumption. The validity of this assumption was tested in vivo. Left ventricular volumes and pressures were assessed with a combined conductance-pressure catheter in eight anesthetized pigs. MVo(2) was calculated from coronary flow and arterial-coronary sinus O-2 differences. Metabolism was altered by glucose-insulin-potassium (GIK) or Intralipid-heparin (IH) infusions in random order and monitored with [C-14]glucose and [H-3]oleate tracers. Profound shifts in glucose and fatty acid oxidation were observed. Contractility, coronary flow, and slope of the MVo(2)-PVA relationship were unchanged during GIK and IH infusions, MVo(2) at zero PVA (unloaded MVo(2)) was 0.16 +/- 0.13 J . beat(-1) . 100 g-(1) higher during IH compared with GIK infusion (P = 0.001), a 48% increase. The study demonstrates a marked energetic advantage of glucose oxidation in the myocardium, profoundly affecting the MVo(2)-PVA relationship. This may in part explain the "oxygen-wasting" effect of lipid-enhancing interventions such as adrenergic drugs and ischemia.
引用
收藏
页码:H1345 / H1351
页数:7
相关论文
共 40 条
[11]   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
[12]   IMPROVED CARDIAC-FUNCTION WITH GLUCOSE-INSULIN-POTASSIUM AFTER AORTOCORONARY BYPASS-GRAFTING [J].
GRADINAC, S ;
COLEMAN, GM ;
TAEGTMEYER, H ;
SWEENEY, MS ;
FRAZIER, OH .
ANNALS OF THORACIC SURGERY, 1989, 48 (04) :484-489
[13]   Alteration in energetics in patients with left ventricular dysfunction after myocardial infarction: Increased oxygen cost of contractility [J].
Hayashi, Y ;
Takeuchi, M ;
Takaoka, H ;
Hata, K ;
Mori, M ;
Yokoyama, M .
CIRCULATION, 1996, 93 (05) :932-939
[14]   LONG-CHAIN FATTY-ACIDS ACTIVATE CALCIUM CHANNELS IN VENTRICULAR MYOCYTES [J].
HUANG, JMC ;
XIAN, H ;
BACANER, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6452-6456
[15]   DETERMINATION OF LEFT-VENTRICULAR END-SYSTOLIC PRESSURE-VOLUME RELATIONSHIPS BY THE CONDUCTANCE (VOLUME) CATHETER TECHNIQUE [J].
KASS, DA ;
YAMAZAKI, T ;
BURKHOFF, D ;
MAUGHAN, WL ;
SAGAWA, K .
CIRCULATION, 1986, 73 (03) :586-595
[16]  
Kleinbaum D., 1988, APPLIED REGRESSION A, P260
[17]   Myocardial substrate oxidation during warm continuous blood cardioplegia [J].
Larsen, TS ;
Irtun, O ;
Steigen, TK ;
Andreasen, TV ;
Sorlie, D .
ANNALS OF THORACIC SURGERY, 1996, 62 (03) :762-768
[18]   CHANGES IN SUBSTRATE METABOLISM AND EFFECTS OF EXCESS FATTY-ACIDS IN REPERFUSED MYOCARDIUM [J].
LIEDTKE, AJ ;
DEMAISON, L ;
EGGLESTON, AM ;
COHEN, LM ;
NELLIS, SH .
CIRCULATION RESEARCH, 1988, 62 (03) :535-542
[19]   ACETYL-COA CARBOXYLASE - AN IMPORTANT REGULATOR OF FATTY-ACID OXIDATION IN THE HEART [J].
LOPASCHUK, GD ;
GAMBLE, J .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1994, 72 (10) :1101-1109
[20]   REPEATED MEASUREMENTS AND MULTIPLE COMPARISONS IN CARDIOVASCULAR RESEARCH [J].
LUDBROOK, J .
CARDIOVASCULAR RESEARCH, 1994, 28 (03) :303-311