Glucose and glycogen utilisation in myocardial ischemia - Changes in metabolism and consequences for the myocyte

被引:83
作者
King, LM [1 ]
Opie, LH [1 ]
机构
[1] Univ Cape Town, Sch Med, MRC UCT Ischaem Heart Dis Res Unit, ZA-7925 Cape Town, South Africa
关键词
glycolysis; glycogenolysis; high energy phosphate stores; glycolytic flux; cardiomyocytes; myocardial ischemia;
D O I
10.1023/A:1006870419309
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Experimentally, enhanced glycolytic flux has been shown to confer many benefits to the ischemic heart, including maintenance of membrane activity, inhibition of contracture, reduced arrhythmias, and improved functional recovery. While at moderate low coronary flows, the benefits of glycolysis appear extensive, the controversy arises at very low flow rates, in the absence of flow; or when glycolytic substrate may be present in excess, such that high glucose concentrations with or without insulin overload the cell with deleterious metabolites. Under conditions of total global ischemia, glycogen is the only substrate for glycolytic flux. Glycogenolysis may only be protective until the accumulation of metabolites (lactate, H+, NADH, sugar phosphates and Pi) outweighs the benefit of the ATP produced. The possible deleterious effects associated with increased glycolysis cannot be ignored, and may explain some of the controversial findings reported in the literature. However, an optimal balance between the rate of ATP production and rate of accumulation of metabolites (determined by the glycolytic flux rate and the rate of coronary washout), may ensure optimal recovery. In addition, the effects of glucose utilisation must be distinguished from those of glycogen, differences which may be explained by functional compartmentation within the cell.
引用
收藏
页码:3 / 26
页数:24
相关论文
共 233 条
  • [1] Regulation of fatty acid oxidation by acetyl-CoA generated from glucose utilization in isolated myocytes
    Abdelaleem, S
    Nada, MA
    SayedAhmed, M
    Hendrickson, SC
    StLouis, J
    Walthall, HP
    Lowe, JE
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1996, 28 (05) : 825 - 833
  • [2] PREISCHEMIC GLYCOGEN REDUCTION OR GLYCOLYTIC INHIBITION IMPROVES POSTISCHEMIC RECOVERY OF HYPERTROPHIED RAT HEARTS
    ALLARD, MF
    EMANUEL, PG
    RUSSELL, JA
    BISHOP, SP
    DIGERNESS, SB
    ANDERSON, PG
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (01): : H66 - H74
  • [3] A NUCLEAR MAGNETIC-RESONANCE STUDY OF METABOLISM IN THE FERRET HEART DURING HYPOXIA AND INHIBITION OF GLYCOLYSIS
    ALLEN, DG
    MORRIS, PG
    ORCHARD, CH
    PIROLO, JS
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1985, 361 (APR): : 185 - 204
  • [4] MYOCARDIAL CONTRACTILE FUNCTION DURING ISCHEMIA AND HYPOXIA
    ALLEN, DG
    ORCHARD, CH
    [J]. CIRCULATION RESEARCH, 1987, 60 (02) : 153 - 168
  • [5] ALLSHIRE AP, 1990, PATHOPHYSIOLOGY SEVE
  • [6] A NEW LOOK AT THE BIOGENESIS OF GLYCOGEN
    ALONSO, MD
    LOMAKO, J
    LOMAKO, WM
    WHELAN, WJ
    [J]. FASEB JOURNAL, 1995, 9 (12) : 1126 - 1137
  • [7] ADENOSINE AND INSULIN MEDIATE GLUCOSE-UPTAKE IN NORMOXIC RAT HEARTS BY DIFFERENT MECHANISMS
    ANGELLO, DA
    BERNE, RM
    CODDINGTON, NM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (03): : H880 - H885
  • [8] ANNESLEY TM, 1980, J BIOL CHEM, V255, P3924
  • [9] DETERMINANTS OF A PROTECTIVE EFFECT OF GLUCOSE AND INSULIN ON THE ISCHEMIC MYOCARDIUM - EFFECTS ON CONTRACTILE FUNCTION, DIASTOLIC COMPLIANCE, METABOLISM, AND ULTRASTRUCTURE DURING ISCHEMIA AND REPERFUSION
    APSTEIN, CS
    GRAVINO, FN
    HAUDENSCHILD, CC
    [J]. CIRCULATION RESEARCH, 1983, 52 (05) : 515 - 526
  • [10] APSTEIN CS, 1994, DIASTOLIC RELAXATION