Cooperative activation in cardiac muscle: impact of sarcomere length.

This study was undertaken to determine the impact of sarcomere length (SL) on the level of cooperative activation of the cardiac myofilament at physiological [Mg2+]. Active force development was measured in skinned rat cardiac trabeculae as a function of free [Ca2+] at five SLs (1.85-2.25 microm; 1 mM free [Mg2+]; 15 degrees C). Only muscle preparations with minimal force rundown during the entire protocol were included in the analysis (average 7.2 +/- 1.7%). Median SL was measured by on-line computer video micrometry and controlled within 0.01 microm. Care was taken to ensure a sufficient number of data points in the steep portion of the [Ca2+]-force relationship at every SL to allow for accurate fit of the data to a modified Hill equation. Multiple linear regression analysis of the fit parameters revealed that both maximum, Ca2+-saturated force and Ca2+ sensitivity were a significant function of SL (P < 0.001), whereas the level of cooperativity did not depend on SL (P = 0.2). Further analysis of the [Ca2+]-force relationships revealed a marked asymmetry that, also, was not affected by SL (P = 0.2-0.6). Finally, we found that the level of cooperativity in isolated skinned myocardium was comparable to that reported for intact, nonskinned myocardium. Our results suggest that an increase in SL induces an increase in the Ca2+ responsiveness of the cardiac sarcomere without affecting the level of cooperativity.

[1]  R. Moss,et al.  Calcium alone does not fully activate the thin filament for S1 binding to rigor myofibrils. , 1996, Biophysical journal.

[2]  J. Shiner,et al.  Activation of thin-filament-regulated muscle by calcium ion: considerations based on nearest-neighbor lattice statistics. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[3]  M. Geeves,et al.  Dynamics of the muscle thin filament regulatory switch: the size of the cooperative unit. , 1994, Biophysical journal.

[4]  B. Brenner,et al.  Equatorial x-ray diffraction from single skinned rabbit psoas fibers at various degrees of activation. Changes in intensities and lattice spacing. , 1985, Biophysical journal.

[5]  A. Weber,et al.  Cooperation within actin filament in vertebrate skeletal muscle. , 1972, Nature: New biology.

[6]  H. T. ter Keurs,et al.  Tension Development and Sarcomere Length in Rat Cardiac Trabeculae: Evidence of Length‐Dependent Activation , 1980, Circulation research.

[7]  E. Marbán,et al.  Relationship between force and intracellular [Ca2+] in tetanized mammalian heart muscle , 1986, The Journal of general physiology.

[8]  P. D. de Tombe,et al.  Protein kinase A does not alter economy of force maintenance in skinned rat cardiac trabeculae. , 1995, Circulation research.

[9]  R. Moss,et al.  Calcium-sensitive cross-bridge transitions in mammalian fast and slow skeletal muscle fibers. , 1990, Science.

[10]  E. Marbán,et al.  Myofilament Ca2+ sensitivity in intact versus skinned rat ventricular muscle. , 1994, Circulation research.

[11]  R. van Heuningen,et al.  Tension development and sarcomere length in rat cardiac trabeculae. Evidence of length-dependent activation. , 1980 .

[12]  D. Trentham,et al.  Relationships between chemical and mechanical events during muscular contraction. , 1986, Annual review of biophysics and biophysical chemistry.

[13]  R. Moss Ca2+ regulation of mechanical properties of striated muscle. Mechanistic studies using extraction and replacement of regulatory proteins. , 1992, Circulation research.

[14]  D. Allen,et al.  The cellular basis of the length-tension relation in cardiac muscle. , 1985, Journal of molecular and cellular cardiology.

[15]  R. Moss,et al.  Alterations in the Ca2+ sensitivity of tension development by single skeletal muscle fibers at stretched lengths. , 1983, Biophysical journal.

[16]  R. Solaro,et al.  The hill coefficient for the Ca2+-activation of striated muscle contraction. , 1984, Biophysical journal.

[17]  K Sagawa,et al.  Contractility-dependent curvilinearity of end-systolic pressure-volume relations. , 1987, The American journal of physiology.

[18]  E. Rome,et al.  X-ray diffraction studies of the filament lattice of striated muscle in various bathing media. , 1968, Journal of molecular biology.

[19]  K S McDonald,et al.  Rate of tension development in cardiac muscle varies with level of activator calcium. , 1995, Circulation research.

[20]  R. Gupta,et al.  Intracellular free magnesium and high energy phosphates in the perfused normotensive and spontaneously hypertensive rat heart. A 31P NMR study. , 1991, American journal of hypertension.

[21]  D. Maughan,et al.  On the composition of the cytosol of relaxed skeletal muscle of the frog. , 1988, The American journal of physiology.

[22]  S. Kurihara,et al.  Length dependence of Ca(2+)-tension relationship in aequorin-injected ferret papillary muscles. , 1997, The American journal of physiology.

[23]  K S McDonald,et al.  Osmotic compression of single cardiac myocytes eliminates the reduction in Ca2+ sensitivity of tension at short sarcomere length. , 1995, Circulation research.

[24]  F. Fuchs,et al.  Sarcomere length versus interfilament spacing as determinants of cardiac myofilament Ca2+ sensitivity and Ca2+ binding. , 1996, Journal of molecular and cellular cardiology.

[25]  P. D. de Tombe,et al.  Right ventricular contractile protein function in rats with left ventricular myocardial infarction. , 1996, The American journal of physiology.

[26]  K S McDonald,et al.  Sarcomere length dependence of the rate of tension redevelopment and submaximal tension in rat and rabbit skinned skeletal muscle fibres , 1997, The Journal of physiology.

[27]  A. Fabiato,et al.  Dependence of the contractile activation of skinned cardiac cells on the sarcomere length , 1975, Nature.

[28]  J. Potter,et al.  The calcium and magnesium binding sites on cardiac troponin and their role in the regulation of myofibrillar adenosine triphosphatase. , 1980, The Journal of biological chemistry.

[29]  K. Campbell,et al.  Rate constant of muscle force redevelopment reflects cooperative activation as well as cross-bridge kinetics. , 1997, Biophysical journal.

[30]  P. D. de Tombe,et al.  Decreased myocyte tension development and calcium responsiveness in rat right ventricular pressure overload. , 1997, Circulation.

[31]  J W Krueger,et al.  Myocardial sarcomere dynamics during isometric contraction. , 1975, The Journal of physiology.

[32]  N. Yagi,et al.  Lateral filamentary spacing in chemically skinned murine muscles during contraction. , 1985, The Journal of physiology.

[33]  M. Greaser,et al.  Substitution of cardiac troponin C into rabbit muscle does not alter the length dependence of Ca2+ sensitivity of tension. , 1991, The Journal of physiology.

[34]  R. Moss,et al.  Influence of a strong-binding myosin analogue on calcium-sensitive mechanical properties of skinned skeletal muscle fibers. , 1992, The Journal of biological chemistry.

[35]  J. Potter,et al.  The calcium and magnesium binding sites on troponin and their role in the regulation of myofibrillar adenosine triphosphatase. , 1975, The Journal of biological chemistry.

[36]  R Craig,et al.  Tropomyosin and actin isoforms modulate the localization of tropomyosin strands on actin filaments. , 2000, Journal of molecular biology.

[37]  P. D. de Tombe,et al.  Protein kinase A does not alter unloaded velocity of sarcomere shortening in skinned rat cardiac trabeculae. , 1997, American journal of physiology. Heart and circulatory physiology.

[38]  H. T. ter Keurs,et al.  Comparison between the Sarcomere Length‐Force Relations of Intact and Skinned Trabeculae from Rat Right Ventricle: Influence of Calcium Concentrations on These Relations , 1986, Circulation research.

[39]  A. Fabiato,et al.  Computer programs for calculating total from specified free or free from specified total ionic concentrations in aqueous solutions containing multiple metals and ligands. , 1988, Methods in enzymology.

[40]  D. Maughan,et al.  Influence of osmotic compression on calcium activation and tension in skinned muscle fibers of the rabbit , 1981, Pflügers Archiv.

[41]  Stephen H. Smith,et al.  Calcium, cross-bridges, and the Frank-Starling relationship. , 2001, News in physiological sciences : an international journal of physiology produced jointly by the International Union of Physiological Sciences and the American Physiological Society.

[42]  M. Geeves,et al.  The muscle thin filament as a classical cooperative/allosteric regulatory system. , 1998, Journal of molecular biology.

[43]  I. Ohtsuki,et al.  Role of troponin C in determining the Ca(2+)-sensitivity and cooperativity of the tension development in rabbit skeletal and cardiac muscles. , 1994, Journal of biochemistry.

[44]  J. Murray,et al.  Molecular control mechanisms in muscle contraction. , 1973, Physiological reviews.

[45]  T. Irving,et al.  Myofilament lattice spacing as a function of sarcomere length in isolated rat myocardium. , 2000, American journal of physiology. Heart and circulatory physiology.