Electrophysiologic Changes in Ischemic Ventricular Myocardium: I. Influence of Ionic, Metabolic, and Energetic Changes

Myocardial Ischemia. Myocardial ischemia leads to significant changes in the intracellular and extracellular ionic milieu, high‐energy phosphate compounds, and accumulation of metabolic by‐products. Changes are measured in extracellular pH and K+ and intracellular pH, Ca2+, Na+ Mg2+, ATP, ADP, and inorganic phosphate. Alterations of membrane currents occur as a consequence of these ionic changes, adrenergic receptor stimulation, and accumulation of lactate, amphipathic compounds, and adenosine. Changes in the volume of the extracellular and intracellular spaces contribute further to the ultimate perturbations of active and passive membrane properties that underlie alterations in excitability, abnormal automaticity, refractoriness, and conduction. These characteristic changes of electrophysiologic properties culminate in loss of excitability and failure of impulse propagation and form the substrate for ventricular arrhythmias mediated through abnormal impulse formation and reentry. The ability to detail the changes in ions, metabolites, and high‐energy phosphate compounds in both the extracellular and intracellular spaces and to correlate them directly with the simultaneously occurring electrophysiologic changes have greatly enhanced our understanding of the electrical events that characterize the ischemic process and hold promise for permitting studies aimed at developing interventions that may lessen the lethal consequences of ischemia.

[1]  D. Hearse Myocardial ischaemia: can we agree on a definition for the 21st century? , 1994, Cardiovascular research.

[2]  P. Poole‐Wilson,et al.  Effects of ischaemia and reperfusion on calcium exchange and mechanical function in isolated rabbit myocardium. , 1981, Cardiovascular research.

[3]  K. Hermsmeyer Angiotensin II Increases Electrical Coupling in Mammalian Ventricular Myocardium , 1980, Circulation research.

[4]  W. Nayler,et al.  Ischemia and reperfusion increase 125I-labeled endothelin-1 binding in rat cardiac membranes. , 1990, The American journal of physiology.

[5]  A. Noma,et al.  Dependence of junctional conductance on proton, calcium and magnesium ions in cardiac paired cells of guinea‐pig. , 1987, The Journal of physiology.

[6]  R. London,et al.  Mechanism of preconditioning. Ionic alterations. , 1993, Circulation research.

[7]  A. Vleugels,et al.  Ionic Currents during Hypoxia in Voltage‐Clamped Cat Ventricular Muscle , 1980, Circulation research.

[8]  E. Braunwald,et al.  Preservation of high-energy phosphates by verapamil in reperfused myocardium. , 1984, Circulation.

[9]  H. Fozzard,et al.  Influence of Extracellular K+ Concentration on Cable Properties and Excitability of Sheep Cardiac Purkinje Fibers , 1970, Circulation research.

[10]  堀江 稔 Voltage-dependent magnesium block of adenosine-triphosphate-sensitive potassium channel in guinea-pig ventricular cells , 1988 .

[11]  H. Hirche,et al.  Myocardial extracellular K+ and H+ increase and noradrenaline release as possible cause of early arrhythmias following acute coronary artery occlusion in pigs. , 1980, Journal of molecular and cellular cardiology.

[12]  J. Doeller,et al.  Gap junctional conductance between pairs of ventricular myocytes is modulated synergistically by H+ and Ca++ , 1990, The Journal of general physiology.

[13]  E Jüngling,et al.  Free energy change of ATP-hydrolysis: a causal factor of early hypoxic failure of the myocardium? , 1982, Journal of molecular and cellular cardiology.

[14]  P. Corr,et al.  Recent Insights Pertaining to Sarcolemmal Phospholipid Alterations Underlying Arrhythmogenesis in the Ischemic Heart , 1993, Journal of cardiovascular electrophysiology.

[15]  W. Cascio,et al.  Early changes in extracellular potassium in ischemic rabbit myocardium. The role of extracellular carbon dioxide accumulation and diffusion. , 1992, Circulation research.

[16]  J W Fiolet,et al.  Transmural inhomogeneity of energy metabolism during acute global ischemia in the isolated rat heart: dependence on environmental conditions. , 1985, Journal of molecular and cellular cardiology.

[17]  C Lenfant,et al.  NHLBI funding policies. Enhancing stability, predictability, and cost control. , 1994, Circulation.

[18]  A. Kleber,et al.  The “Border Zone” in Myocardial Ischemia: An Electrophysiological, Metabolic, and Histochemical Correlation in the Pig Heart , 1979, Circulation research.

[19]  M M Pike,et al.  Quantification of [Ca2+]i in perfused hearts. Critical evaluation of the 5F-BAPTA and nuclear magnetic resonance method as applied to the study of ischemia and reperfusion. , 1990, Circulation research.

[20]  T. Opthof,et al.  Injury current and gradients of diastolic stimulation threshold, TQ potential, and extracellular potassium concentration during acute regional ischemia in the isolated perfused pig heart. , 1991, Circulation research.

[21]  K. Blackburn,et al.  Endothelin and calcium dynamics in vascular smooth muscle. , 1992, Annual review of physiology.

[22]  H. C. Hartzell,et al.  Effects of intracellular free magnesium on calcium current in isolated cardiac myocytes. , 1988, Science.

[23]  J Tranum-Jensen,et al.  The subendocardial border zone during acute ischemia of the rabbit heart: an electrophysiologic, metabolic, and morphologic correlative study. , 1986, Circulation.

[24]  L. Gettes,et al.  Effect of Rate on Changes in Conduction Velocity and Extracellular Potassium Concentration During Acute Ischemia in the In Situ Pig Heart , 1993, Journal of cardiovascular electrophysiology.

[25]  H. Tan,et al.  R 56865 delays cellular electrical uncoupling in ischemic rabbit papillary muscle. , 1993, Journal of molecular and cellular cardiology.

[26]  貝原 宗重 Inhibition of the calcium channel by intracellular protons in single ventricular myocytes of the guinea-pig , 1991 .

[27]  P. Corr,et al.  Pathophysiological concentrations of lysophosphatides and the slow response. , 1982, The American journal of physiology.

[28]  A. Kleber,et al.  Electrical uncoupling and increase of extracellular resistance after induction of ischemia in isolated, arterially perfused rabbit papillary muscle. , 1987, Circulation research.

[29]  J. Weiss,et al.  Sulfonylureas, ATP-sensitive K+ channels, and cellular K+ loss during hypoxia, ischemia, and metabolic inhibition in mammalian ventricle. , 1991, Circulation research.

[30]  M. Janse,et al.  Electrophysiological mechanisms of ventricular arrhythmias resulting from myocardial ischemia and infarction. , 1989, Physiological reviews.

[31]  P. Poole‐Wilson,et al.  Myocardial potassium loss after acute coronary occlusion in humans. , 1987, Journal of the American College of Cardiology.

[32]  M. Rosen,et al.  Abnormal Automatic Rhythms in Ischemic Purkinje Fibers Are Modulated by a Specific α1‐Adrenergic Receptor Subtype , 1991, Circulation.

[33]  R. Case,et al.  Phosphate loss during reversible myocardial ischemia. , 1973, Journal of molecular and cellular cardiology.

[34]  P. Corr,et al.  Alpha1adrenergic system and arrhythmias in ischaemic heart disease , 1991 .

[35]  I. Leusen,et al.  Acidification and intracellular sodium ion activity during stimulated myocardial ischemia. , 1990, The American journal of physiology.

[36]  M. Kameyama,et al.  Inhibition of the calcium channel by intracellular protons in single ventricular myocytes of the guinea‐pig. , 1988, The Journal of physiology.

[37]  M. Karmazyn,et al.  Role of Na(+)-H+ exchange in mediating effects of endothelin-1 on normal and ischemic/reperfused hearts. , 1994, Circulation research.

[38]  G. Kabell Modulation of conduction slowing in ischemic rabbit myocardium by calcium-channel activation and blockade. , 1988, Circulation.

[39]  L. Gettes,et al.  Effects of verapamil on ischemia-induced changes in extracellular K+, pH, and local activation in the pig. , 1986, Circulation.

[40]  A. Terzic,et al.  Cardiac alpha 1-adrenoceptors: an overview. , 1993, Pharmacological reviews.

[41]  P. Corr,et al.  Increased lysophosphatidylcholine content induced by thrombin receptor stimulation in adult rabbit cardiac ventricular myocytes. , 1994, Cardiovascular research.

[42]  W. Lederer,et al.  Nucleotide modulation of the activity of rat heart ATP‐sensitive K+ channels in isolated membrane patches. , 1989, The Journal of physiology.

[43]  Michèle Bernier,et al.  R56865, a Potent New Antiarrhythmic Agent, Effective During Ischemia and Reperfusion in the Rat Heart , 1990, Journal of cardiovascular pharmacology.

[44]  V. Wiegand,et al.  Early Mortality Due to Ventricular Fibrillation, and the Vulnerability of the Heart Following Acute Experimental Coronary Occlusion: Possible Mechanisms and Pharmacological Prophylaxis , 1978 .

[45]  G. Yan,et al.  Changes in extracellular and intracellular pH in ischemic rabbit papillary muscle. , 1992, Circulation research.

[46]  P. Corr,et al.  Electrophysiological Effects of Amphiphiles on Canine Purkinje Fibers , 1981, Circulation research.

[47]  P. Corr,et al.  Long‐Chain Acylcarnitines Mediate the Hypoxia‐Induced Increase in α1‐Adrenergic Receptors on Adult Canine Myocytes , 1987, Circulation research.

[48]  R. London,et al.  Correlation between cytosolic free calcium, contracture, ATP, and irreversible ischemic injury in perfused rat heart. , 1990, Circulation research.

[49]  R. Harvey,et al.  On the role of sodium ions in the regulation of the inward-rectifying potassium conductance in cat ventricular myocytes , 1989, The Journal of general physiology.

[50]  E. Michelson,et al.  Instantaneous and Delayed Ventricular Arrhythmias After Reperfusion of Acutely Ischemic Myocardium: Evidence for Multiple Mechanisms , 1981, Circulation.

[51]  L. Gettes,et al.  Magnitude and time course of extracellular potassium inhomogeneities during acute ischemia in pigs. Effect of verapamil. , 1991, Circulation.

[52]  A. Noma,et al.  Membrane current through adenosine‐triphosphate‐regulated potassium channels in guinea‐pig ventricular cells. , 1985, The Journal of physiology.

[53]  A. Kleber Extracellular potassium accumulation in acute myocardial ischemia. , 1984, Journal of molecular and cellular cardiology.

[54]  D. Kunze,et al.  Changes in Extracellular Potassium Activity in Response to Decreased pH in Rabbit Atrial Muscle , 1976, Circulation research.

[55]  J. Délèze,et al.  The recovery of resting potential and input resistance in sheep heart injured by knife or laser , 1970, The Journal of physiology.

[56]  H Kusuoka,et al.  Intracellular free calcium concentration measured with 19F NMR spectroscopy in intact ferret hearts. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[57]  A. Bardají,et al.  Low incidence of ventricular arrhythmias induced by ischaemia at the borders of a chronic infarct in a model with local postinfarction denervation. , 1994, Cardiovascular research.

[58]  A. Kleber,et al.  Flow of “Injury” Current and Patterns of Excitation during Early Ventricular Arrhythmias in Acute Regional Myocardial Ischemia in Isolated Porcine and Canine Hearts: Evidence for Two Different Arrhythmogenic Mechanisms , 1980, Circulation research.

[59]  M R Franz,et al.  Effect of ischemia on calcium-dependent fluorescence transients in rabbit hearts containing indo 1. Correlation with monophasic action potentials and contraction. , 1988, Circulation.

[60]  W. Cascio,et al.  Passive electrical properties, mechanical activity, and extracellular potassium in arterially perfused and ischemic rabbit ventricular muscle. Effects of calcium entry blockade or hypocalcemia. , 1990, Circulation research.

[61]  G. Tseng Cell swelling increases membrane conductance of canine cardiac cells: evidence for a volume-sensitive Cl channel. , 1992, The American journal of physiology.

[62]  S. Lamp,et al.  ATP‐sensitive K+ channels and cellular K+ loss in hypoxic and ischaemic mammalian ventricle. , 1992, The Journal of physiology.

[63]  J. Lowe,et al.  Relation between high energy phosphate and lethal injury in myocardial ischemia in the dog. , 1978, The American journal of pathology.

[64]  K I Shine,et al.  Effects of heart rate on extracellular [K+] accumulation during myocardial ischemia. , 1986, The American journal of physiology.

[65]  Jean Charles Gilbert,et al.  Inhibition of sodium pump by l-palmitoylcarnitine in single guinea-pig ventricular myocytes. , 1992, Journal of molecular and cellular cardiology.

[66]  J. Makielski,et al.  Intracellular H+ and Ca2+ modulation of trypsin-modified ATP-sensitive K+ channels in rabbit ventricular myocytes. , 1993, Circulation research.

[67]  R. Myerburg,et al.  Electrophysiological properties and responses to simulated ischemia in cat ventricular myocytes of endocardial and epicardial origin. , 1990, Circulation research.

[68]  H. Irisawa,et al.  Intra‐ and Extracellular Actions of Proton on the Calcium Current of Isolated Guinea Pig Ventricular Cells , 1986, Circulation research.

[69]  D Durrer,et al.  Mechanism and Time Course of S‐T and T‐Q Segment Changes during Acute Regional Myocardial Ischemia in the Pig Heart Determined by Extracellular and Intracellular Recordings , 1978, Circulation research.

[70]  R. Coronel,et al.  The change of the free energy of ATP hydrolysis during global ischemia and anoxia in the rat heart. Its possible role in the regulation of transsarcolemmal sodium and potassium gradients. , 1984, Journal of molecular and cellular cardiology.

[71]  P. Corr,et al.  Inhibition of gap junctional conductance by long-chain acylcarnitines and their preferential accumulation in junctional sarcolemma during hypoxia. , 1993, Circulation research.

[72]  M. Morad,et al.  Cytosolic magnesium modulates calcium channel activity in mammalian ventricular cells. , 1989, The American journal of physiology.

[73]  H. Reuter,et al.  Slow recovery from inactivation of inward currents in mammalian myocardial fibres , 1974, The Journal of physiology.

[74]  S. Matsuoka,et al.  Chloride‐sensitive nature of the adrenaline‐induced current in guinea‐pig cardiac myocytes. , 1990, The Journal of physiology.

[75]  D. Allen,et al.  Changes in intracellular free calcium concentration during long exposures to simulated ischemia in isolated mammalian ventricular muscle. , 1992, Circulation research.

[76]  C Antzelevitch,et al.  A subpopulation of cells with unique electrophysiological properties in the deep subepicardium of the canine ventricle. The M cell. , 1991, Circulation research.

[77]  R. London,et al.  Elevation in Cytosolic Free Calcium Concentration Early in Myocardial Ischemia in Perfused Rat Heart , 1987, Circulation research.

[78]  V. Breu,et al.  Role of endothelin during reperfusion after ischemia in isolated perfused rat heart. , 1994, Journal of cardiovascular pharmacology.

[79]  J. Weiss,et al.  Lactate transport in mammalian ventricle. General properties and relation to K+ fluxes. , 1994, Circulation research.

[80]  C W Balke,et al.  Two Periods of Early Ventricular Arrhythmia in the Canine Acute Myocardial Infarction Model , 1979, Circulation.

[81]  H. Matsuura,et al.  Measurement of Na(+)-K+ pump current in isolated rabbit ventricular myocytes using the whole-cell voltage-clamp technique. Inhibition of the pump by oxidant stress. , 1993, Circulation research.

[82]  W. Clusin,et al.  Endothelin activates voltage‐dependent Ca2+ current by a G protein‐dependent mechanism in rabbit cardiac myocytes. , 1992, The Journal of physiology.

[83]  R. Myerburg,et al.  Simultaneous recording of action potentials from endocardium and epicardium during ischemia in the isolated cat ventricle: relation of temporal electrophysiologic heterogeneities to arrhythmias. , 1986, Circulation.

[84]  R. Haworth,et al.  Inhibition of ATP-Sensitive Potassium Channels of Adult Rat Heart Cells by Antiarrhythmic Drugs , 1989, Circulation research.

[85]  L. Sorbera,et al.  Atrionatriuretic peptide transforms cardiac sodium channels into calcium-conducting channels. , 1990, Science.

[86]  J. L. Hill,et al.  Interaction of Acidosis and Increased Extracellular Potassium on Action Potential Characteristics and Conduction in Guinea Pig Ventricular Muscle , 1982, Circulation research.

[87]  G. Billman Effect of α1-Adrenergic Receptor Antagonists on Susceptibility to Malignant Arrhythmias: Protection from Ventricular Fibrillation , 1994, Journal of Cardiovascular Pharmacology.

[88]  S. Pogwizd,et al.  Induction of Delayed Afterdepolarizations and Triggered Activity in Canine Purkinje Fibers by Lysophosphoglycerides , 1986, Circulation research.

[89]  L. Gettes,et al.  Influence of rate-dependent cellular uncoupling on conduction change during simulated ischemia in guinea pig papillary muscles: effect of verapamil. , 1989, Circulation research.

[90]  A. Wilde,et al.  Effect of norepinephrine and heart rate on intracellular sodium activity and membrane potential in beating guinea pig ventricular muscle. , 1991, Circulation research.

[91]  M. Sanguinetti,et al.  Influence of ATP-sensitive potassium channel modulators on ischemia-induced fibrillation in isolated rat hearts. , 1989, Journal of molecular and cellular cardiology.

[92]  R. Myerburg,et al.  Effect of H+ on ATP-regulated K+ channels in feline ventricular myocytes. , 1991, American Journal of Physiology.

[93]  A. Noma,et al.  Voltage‐dependent magnesium block of adenosine‐triphosphate‐sensitive potassium channel in guinea‐pig ventricular cells. , 1987, The Journal of physiology.

[94]  H. Fozzard,et al.  Increase in Intracellular Sodium Ion Activity during Stimulation in Mammalian Cardiac Muscle , 1982, Circulation research.

[95]  I. Findlay Calcium-dependent inactivation of the ATP-sensitive K+ channel of rat ventricular myocytes. , 1988, Biochimica et biophysica acta.

[96]  P. Corr,et al.  Increased alpha-adrenergic receptors in ischemic cat myocardium. A potential mediator of electrophysiological derangements. , 1981, The Journal of clinical investigation.

[97]  M. Lewis,et al.  Antiarrhythmic and electrophysiological effects of alpha adrenoceptor blockade during myocardial ischaemia and reperfusion in isolated guinea-pig heart. , 1985, Journal of molecular and cellular cardiology.

[98]  A. Kléber,et al.  Resting Membrane Potential, Extracellular Potassium Activity, and Intracellular Sodium Activity during Acute Global Ischemia in Isolated Perfused Guinea Pig Hearts , 1983, Circulation research.

[99]  M. Shattock,et al.  Role of Na-activated K channel, Na-K-Cl cotransport, and Na-K pump in [K]e changes during ischemia in rat heart. , 1992, American Journal of Physiology.

[100]  I. Watanabe,et al.  Effects of verapamil and propranolol on changes in extracellular K+, pH, and local activation during graded coronary flow in the pig. , 1989, Circulation.

[101]  H. Tan,et al.  Ischaemic preconditioning delays ischaemia induced cellular electrical uncoupling in rabbit myocardium by activation of ATP sensitive potassium channels. , 1993, Cardiovascular research.

[102]  J. Burt,et al.  Block of intercellular communication: interaction of intracellular H+ and Ca2+. , 1987, The American journal of physiology.

[103]  R. Myerburg,et al.  Verapamil diminishes action potential changes during metabolic inhibition by blocking ATP-regulated potassium currents. , 1992, Circulation research.

[104]  A. Bardají,et al.  Ventricular arrhythmias and local electrograms after chronic regional denervation of the ischemic area in the pig heart. , 1989, Journal of the American College of Cardiology.

[105]  C J van Echteld,et al.  Intracellular sodium during ischemia and calcium-free perfusion: a 23Na NMR study. , 1991, Journal of molecular and cellular cardiology.

[106]  D. Clapham,et al.  Potassium channels in cardiac cells activated by arachidonic acid and phospholipids. , 1989, Science.

[107]  M. Lieberman,et al.  Na-K pump site density and ouabain binding affinity in cultured chick heart cells. , 1987, The American journal of physiology.

[108]  C. January,et al.  The Effects of Membrane Potential, Extracellular Potassium, and Tetrodotoxin on the Intracellular Sodium Ion Activity of Sheep Cardiac Muscle , 1984, Circulation research.

[109]  H. Irisawa,et al.  Intracellular Na+ activates a K+ channel in mammalian cardiac cells , 1984, Nature.

[110]  F. Verdonck,et al.  Consequences of CO2 acidosis for transmembrane Na+ transport and membrane current in rabbit cardiac Purkinje fibres. , 1990, The Journal of physiology.

[111]  J. Hume,et al.  Unitary chloride channels activated by protein kinase C in guinea pig ventricular myocytes. , 1995, Circulation research.

[112]  E. Weiss,et al.  Separation of hexose-transporting from nontransporting LLC-PK1 cells on density gradients. , 1986, The American journal of physiology.

[113]  W. Lederer,et al.  The regulation of ATP‐sensitive K+ channel activity in intact and permeabilized rat ventricular myocytes. , 1990, The Journal of physiology.

[114]  Liedtke Aj Lipid burden in ischemic myocardium , 1988 .

[115]  L. Opie,et al.  Protons in ischemia: where do they come from; where do they go to? , 1991, Journal of molecular and cellular cardiology.

[116]  P B Corr,et al.  Dissociation between cellular K+ loss, reduction in repolarization time, and tissue ATP levels during myocardial hypoxia and ischemia. , 1993, Circulation research.

[117]  I. Fleidervish,et al.  Inward sodium current at resting potentials in single cardiac myocytes induced by the ischemic metabolite lysophosphatidylcholine. , 1992, Circulation research.

[118]  E. Marbán,et al.  Mechanism of the increase in intracellular sodium during metabolic inhibition: direct evidence against mediation by voltage-dependent sodium channels. , 1992, Journal of molecular and cellular cardiology.

[119]  W. Lederer,et al.  ATP-sensitive potassium channel modulation of the guinea pig ventricular action potential and contraction. , 1991, Circulation research.

[120]  P. Corr,et al.  Cellular uncoupling induced by accumulation of long-chain acylcarnitine during ischemia. , 1994, Circulation research.

[121]  M. Lieberman,et al.  (Na + K + 2Cl) cotransport in cultured embryonic chick heart cells. , 1987, The American journal of physiology.

[122]  A. Kleber,et al.  Propagation of Electrical Activity in Ischemic and Infarcted Myocardium as the Basis of Ventricular Arrhythmias , 1992 .

[123]  M. Kameyama,et al.  Involvement of Na(+)-H+ antiporter in regulation of L-type Ca2+ channel current by angiotensin II in rabbit ventricular myocytes. , 1994, Circulation research.

[124]  A. Zygmunt,et al.  Calcium-activated chloride current in rabbit ventricular myocytes. , 1991, Circulation research.

[125]  D Durrer,et al.  Combined effects of hypoxia, hyperkalemia and acidosis on membrane action potential and excitability of guinea-pig ventricular muscle. , 1984, Journal of molecular and cellular cardiology.

[126]  R. Weingart,et al.  Ungulate cardiac Purkinje fibres: the influence of intracellular pH on the electrical cell‐to‐cell coupling , 1982, The Journal of physiology.

[127]  A. Wilde,et al.  The Combined Effects of Hypoxia, High K+, and Acidosis on the Intracellular Sodium Activity and Resting Potential in Guinea Pig Papillary Muscle , 1986, Circulation research.

[128]  A. Noma,et al.  ATP-regulated K+ channels in cardiac muscle , 1983, Nature.

[129]  A. Wilde,et al.  Changes in conduction velocity during acute ischemia in ventricular myocardium of the isolated porcine heart. , 1986, Circulation.

[130]  J. Burt,et al.  Uncoupling of cardiac cells by fatty acids: structure-activity relationships. , 1991, The American journal of physiology.

[131]  W. Moore,et al.  The role of protons in nerve conduction , 1973 .

[132]  A. Brown,et al.  Angiotensin II Modulates Cardiac Na+ Channels in Neonatal Rat , 1989, Circulation research.

[133]  M J Janse,et al.  Potassium accumulation in the globally ischemic mammalian heart. A role for the ATP-sensitive potassium channel. , 1990, Circulation research.

[134]  D. Garfinkel,et al.  Magnesium in cardiac energy metabolism. , 1986, Journal of molecular and cellular cardiology.

[135]  J. L. Hill,et al.  Effect of Acute Coronary Artery Occlusion on Local Myocardial Extracellular K+ Activity in Swine , 1980, Circulation.

[136]  E. Marbán,et al.  Oscillations of membrane current and excitability driven by metabolic oscillations in heart cells. , 1994, Science.

[137]  R. London,et al.  Amiloride delays the ischemia-induced rise in cytosolic free calcium. , 1991, Circulation research.

[138]  W. Cascio,et al.  Hypercapnic acidosis and dimethyl amiloride reduce reperfusion induced cell death in ischaemic ventricular myocardium. , 1995, Cardiovascular research.

[139]  R. London,et al.  Cytosolic free magnesium levels in ischemic rat heart. , 1989, The Journal of biological chemistry.

[140]  A. Liedtke Lipid burden in ischemic myocardium. , 1988, Journal of molecular and cellular cardiology.

[141]  P. Jynge,et al.  Magnesium and reperfusion of ischemic rat heart as assessed by 31P-NMR. , 1989, The American journal of physiology.

[142]  I. Leusen,et al.  Simulated ischemia and intracellular pH in isolated ventricular muscle. , 1989, The American journal of physiology.

[143]  P. Corr,et al.  Activation of thrombin receptor increases intracellular Na+ during myocardial ischemia. , 1995, The American journal of physiology.

[144]  G. Gintant,et al.  Beta-adrenergic modulation of fast inward sodium current in canine myocardium. Syncytial preparations versus isolated myocytes. , 1992, Circulation research.

[145]  E. Marbán,et al.  Mechanism of ischemic contracture in ferret hearts: relative roles of [Ca2+]i elevation and ATP depletion. , 1990, The American journal of physiology.