Frequency, amplitude, and propagation velocity of spontaneous Ca++-dependent contractile waves in intact adult rat cardiac muscle and isolated myocytes.

Spontaneous contractile waves due to spontaneous calcium cycling by the sarcoplasmic reticulum occur in unstimulated bulk rat papillary muscle and single rat cardiac myocytes with intact sarcolemmal function. We used video analytic techniques to quantify the wave characteristics in both bulk muscle and myocytes; laser-light scattering techniques were also employed in muscle. In muscle bathed in physiological concentrations of calcium, the true periodicity of these waves was a fraction of 1 Hz and increased up to several hertz with increases in cell calcium. This was paralleled by an increase in the frequency of scattered laser light intensity fluctuations. In myocytes, a range of spontaneous contractile wave frequencies similar to that which occurred in the muscle was observed; it could be demonstrated that an increase in superfusate calcium concentrations (2-15 mM at 23 degrees C) increases the oscillation frequency but not amplitude. In both myocytes and muscle, low concentrations of caffeine (0.5 mM) and higher temperature increased the oscillation frequency but diminished their amplitude. However, the scattered light fluctuations did not change with temperature and decreased with caffeine. These results demonstrate that (1) the true frequency of spontaneous sarcoplasmic reticulum oscillations in the unstimulated rat muscle and single myocytes with intact sarcolemmal function is low, i.e., a fraction of a hertz; (2) with cell calcium loading, the oscillation frequency accelerates to those frequencies measured previously in the "calcium overload" state; (3) while scattered light fluctuations which sample myofilament motion are a sensitive, noninvasive method of detecting the oscillations in bulk muscle, they can be insensitive to the divergent changes in oscillation amplitude and frequency.

[1]  E. Lakatta,et al.  Fluctuations in intracellular calcium concentration and their effect on tonic tension in canine cardiac Purkinje fibres. , 1985, The Journal of physiology.

[2]  E. Lakatta,et al.  Frequency modulation and synchronization of spontaneous oscillations in cardiac cells. , 1985, The American journal of physiology.

[3]  A. Fabiato,et al.  Rapid ionic modifications during the aequorin-detected calcium transient in a skinned canine cardiac Purkinje cell , 1985, The Journal of general physiology.

[4]  E. Lakatta,et al.  Probability of occurrence and frequency distribution of spontaneous contractile waves in unstimulated, Ca2+ tolerant, adult rat myocytes , 1985 .

[5]  H. Spurgeon,et al.  Twitch characteristics in rat cardiac myocytes depend on spontaneous contractile waves in the absence of stimulation , 1985 .

[6]  S. Banerjee,et al.  Measurement of Cytosolic Free Calcium Concentration in Isolated Rat Ventricular Myocytes with Quin 2 , 1984, Circulation research.

[7]  P. Tatham,et al.  Cytoplasmic free calcium measured by quin2 fluorescence in isolated ventricular myocytes at rest and during potassium-depolarization. , 1984, Biochemical and biophysical research communications.

[8]  E. Lakatta,et al.  Calcium‐Dependent Mechanical Oscillations Occur Spontaneously in Unstimulated Mammalian Cardiac Tissues , 1984, Circulation research.

[9]  C. Baumgarten,et al.  Methods for Detecting Calcium Release from the Sarcoplasmic Reticulum of Skinned Cardiac Cells and the Relationships Between Calculated Transsarcolemmal Calcium Movements and Calcium Release , 1984 .

[10]  E. Lakatta,et al.  Effect of sodium on calcium-dependent force in unstimulated rat cardiac muscle. , 1984, The American journal of physiology.

[11]  P. Cobbold,et al.  Aequorin measurements of free calcium in single heart cells , 1984, Nature.

[12]  E. Lakatta,et al.  Cellular calcium fluctuations in mammalian heart: direct evidence from noise analysis of aequorin signals in Purkinje fibers. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[13]  S. Houser,et al.  Isolation and morphology of calcium-tolerant feline ventricular myocytes. , 1983, The American journal of physiology.

[14]  D. Allen,et al.  Oscillations of intracellular Ca2+ in mammalian cardiac muscle , 1983, Nature.

[15]  E. Lakatta,et al.  Scattered-light intensity fluctuations in diastolic rat cardiac muscle caused by spontaneous Ca++-dependent cellular mechanical oscillations , 1983, The Journal of general physiology.

[16]  A. Fabiato,et al.  Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum. , 1983, The American journal of physiology.

[17]  W. Clusin Caffeine induces a transient inward current in cultured cardiac cells , 1983, Nature.

[18]  A. Noma,et al.  Transient Depolarization and Spontaneous Voltage Fluctuations in Isolated Single Cells from Guinea Pig Ventricles: Calcium‐Mediated Membrane Potential Fluctuations , 1982, Circulation research.

[19]  B. R. Jewell,et al.  Calcium‐ and length‐dependent force production in rat ventricular muscle , 1982, The Journal of physiology.

[20]  R. Tsien,et al.  Fluctuations in membrane current driven by intracellular calcium in cardiac Purkinje fibers. , 1982, Biophysical journal.

[21]  W. Wier,et al.  Measurement of Ca2+ concentrations in living cells. , 1982, Progress in biophysics and molecular biology.

[22]  E. Neher,et al.  Inward current channels activated by intracellular Ca in cultured cardiac cells , 1981, Nature.

[23]  A. Somlyo,et al.  Primary role of sarcoplasmic reticulum in phasic contractile activation of cardiac myocytes with shunted myolemma , 1981, The Journal of cell biology.

[24]  D. Lappé,et al.  Diastolic scattered light fluctuation, resting force and twitch force in mammalian cardiac muscle , 1981, The Journal of physiology.

[25]  D. Lappé,et al.  Intensity fluctuation spectroscopy monitors contractile activation in "resting" cardiac muscle , 1980, Science.

[26]  A. Cittadini,et al.  Calcium transport and contractile activity in dissociated mammalian heart cells. , 1979, The American journal of physiology.

[27]  R. Solaro,et al.  Modification of calcium requirement for activation of cardiac myofibrillar ATPase by cyclic AMP dependent phosphorylation , 1979 .

[28]  R. Tsien,et al.  Cellular and subcellular mechanisms of cardiac pacemaker oscillations. , 1979, The Journal of experimental biology.

[29]  G. Inesi,et al.  Sarcomere motion in isolated cardiac cells. , 1979, The American journal of physiology.

[30]  R. Tsien,et al.  Ionic basis of transient inward current induced by strophanthidin in cardiac Purkinje fibres. , 1978, The Journal of physiology.

[31]  R Weingart,et al.  Role of calcium ions in transient inward currents and aftercontractions induced by strophanthidin in cardiac Purkinje fibres. , 1978, The Journal of physiology.

[32]  A. Fabiato,et al.  Effects of pH on the myofilaments and the sarcoplasmic reticulum of skinned cells from cardiace and skeletal muscles. , 1978, The Journal of physiology.

[33]  A. Fabiato,et al.  Contractions induced by a calcium‐triggered release of calcium from the sarcoplasmic reticulum of single skinned cardiac cells. , 1975, The Journal of physiology.

[34]  A. Fabiato,et al.  Effects of magnesium ion on activation of skinned cardiac cells , 1974 .

[35]  A. Fabiato,et al.  Excitation‐Contraction Coupling of Isolated Cardiac Fibers with Disrupted or Closed Sarcolemmas: CALCIUM‐DEPENDENT CYCLIC AND TONIC CONTRACTIONS , 1972, Circulation research.

[36]  A. Fabiato,et al.  Excitation-Contraction Coupling of Isolated Cardiac Fibers with Disrupted or Closed Sarcolemmas , 1972 .