Myocardial cross-bridge kinetics in transition to failure in Dahl salt-sensitive rats.

The role of altered cross-bridge kinetics during the transition from cardiac hypertrophy to failure is poorly defined. We examined this in Dahl salt-sensitive (DS) rats, which develop hypertrophy and failure when fed a high-salt diet (HS). DS rats fed a low-salt diet were controls. Serial echocardiography disclosed compensated hypertrophy at 6 wk of HS, followed by progressive dilatation and impaired function. Mechanical properties of skinned left ventricular papillary muscle strips were analyzed at 6 wk of HS and then during failure (12 wk HS) by applying small amplitude (0.125%) length perturbations over a range of calcium concentrations. No differences in isometric tension-calcium relations or cross-bridge cycling kinetics or mechanical function were found at 6 wk. In contrast, 12 wk HS strips exhibited increased calcium sensitivity of isometric tension, decreased frequency of minimal dynamic stiffness, and a decreased range of frequencies over which cross bridges produce work and power. Thus the transition from hypertrophy to heart failure in DS rats is characterized by major changes in cross-bridge cycling kinetics and mechanical performance.

[1]  F. Eberli,et al.  Altered β-adrenergic signal transduction in nonfailing hypertrophied myocytes from Dahl salt-sensitive rats , 2000 .

[2]  P. Burton,et al.  Effect of protein kinase A on calcium sensitivity of force and its sarcomere length dependence in human cardiomyocytes. , 2000, Cardiovascular research.

[3]  J. Seidman,et al.  Altered crossbridge kinetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy. , 1999, Circulation research.

[4]  R. Schwinger,et al.  Reduced Ca2+-Sensitivity of SERCA 2a in Failing Human Myocardium due to Reduced Serin-16 Phospholamban Phoshorylation , 1999 .

[5]  D. Maughan,et al.  Mechanoenergetic alterations during the transition from cardiac hypertrophy to failure in Dahl salt-sensitive rats. , 1998, Circulation.

[6]  J. Lüdemann,et al.  Alterations of cross-bridge kinetics in human atrial and ventricular myocardium. , 1998, Cardiovascular research.

[7]  D. Reda,et al.  Effect of single-drug therapy on reduction of left atrial size in mild to moderate hypertension: comparison of six antihypertensive agents. , 1997, Circulation.

[8]  M. Böhm,et al.  Changes in essential myosin light chain isoform expression provide a molecular basis for isometric force regulation in the failing human heart. , 1997, Journal of molecular and cellular cardiology.

[9]  R. Moss,et al.  Calcium sensitivity of isometric tension is increased in canine experimental heart failure. , 1995, Circulation research.

[10]  Y. Kihara,et al.  Neurohumoral factors during transition from left ventricular hypertrophy to failure in Dahl salt-sensitive rats. , 1995, Biochemical and biophysical research communications.

[11]  S Sasayama,et al.  Transition from compensatory hypertrophy to dilated, failing left ventricles in Dahl salt-sensitive rats. , 1994, The American journal of physiology.

[12]  E Erdmann,et al.  The failing human heart is unable to use the Frank-Starling mechanism. , 1994, Circulation research.

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

[14]  M. Böhm,et al.  Cardiac adenylyl cyclase, beta-adrenergic receptors, and G proteins in salt-sensitive hypertension. , 1993, Hypertension.

[15]  M. Geeves,et al.  Regulation of the interaction between actin and myosin subfragment 1: evidence for three states of the thin filament. , 1993, Biophysical journal.

[16]  M Kawai,et al.  Crossbridge scheme and the kinetic constants of elementary steps deduced from chemically skinned papillary and trabecular muscles of the ferret. , 1993, Circulation research.

[17]  R. Hajjar,et al.  Cross‐Bridge Dynamics in Human Ventricular Myocardium: Regulation of Contractility in the Failing Heart , 1992, Circulation.

[18]  N. Alpert,et al.  Altered Myocardial Force‐Frequency Relation in Human Heart Failure , 1992, Circulation.

[19]  G. M. Briggs,et al.  Role of intracellular calcium handling in force-interval relationships of human ventricular myocardium. , 1990, The Journal of clinical investigation.

[20]  M. Feldman,et al.  Depression of systolic and diastolic myocardial reserve during atrial pacing tachycardia in patients with dilated cardiomyopathy. , 1988, The Journal of clinical investigation.

[21]  W. Hunter,et al.  Effect of isoproterenol on force transient time course and on stiffness spectra in rabbit papillary muscle in barium contracture. , 1988, Journal of molecular and cellular cardiology.

[22]  K Sagawa,et al.  Dynamic Stiffness of Barium‐Contractured Cardiac Muscles With Different Speeds of Contraction , 1987, Circulation research.

[23]  R. Godt,et al.  Influence of temperature upon contractile activation and isometric force production in mechanically skinned muscle fibers of the frog , 1982, The Journal of general physiology.

[24]  L K DAHL,et al.  Effects of chronia excess salt ingestion. Evidence that genetic factors play an important role in susceptibility to experimental hypertension. , 1962, The Journal of experimental medicine.

[25]  J. Metzger,et al.  Development in Single Adult Cardiac Myocytes-Activated Tension 2 + Effects of Myosin Heavy Chain Isoform Switching on Ca , 1999 .

[26]  J. Seidman,et al.  Altered Crossbridge Kinetics in the a MHC 403 / 1 Mouse Model of Familial Hypertrophic Cardiomyopathy , 1999 .

[27]  J. Moore,et al.  Work production and work absorption in muscle strips from vertebrate cardiac and insect flight muscle fibers. , 1998, Advances in experimental medicine and biology.

[28]  J. Ross Jr. Adrenergic regulation of the force-frequency effect , 1998 .

[29]  M. Heine,et al.  Effects of Chronic Excess Salt Ingestion: Modification Of Experimental Hypertension In The Rat By Variations In The Diet , 1968, Circulation research.