1. Positive inotropic effects of low dATP/ATP ratios on mechanics and kinetics of porcine cardiac muscle.
- Author
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Schoffstall B, Clark A, and Chase PB
- Subjects
- Actins chemistry, Actins physiology, Actomyosin physiology, Animals, Biomechanical Phenomena, Hydrolysis, In Vitro Techniques, Kinetics, Male, Muscle, Skeletal chemistry, Myosins physiology, Rabbits, Swine, Adenosine Triphosphate metabolism, Calcium physiology, Deoxyadenine Nucleotides metabolism, Myocardial Contraction, Myocardium metabolism
- Abstract
Substitution of 2'-deoxy ATP (dATP) for ATP as substrate for actomyosin results in significant enhancement of in vitro parameters of cardiac contraction. To determine the minimal ratio of dATP/ATP (constant total NTP) that significantly enhances cardiac contractility and obtain greater understanding of how dATP substitution results in contractile enhancement, we varied dATP/ATP ratio in porcine cardiac muscle preparations. At maximum Ca(2+) (pCa 4.5), isometric force increased linearly with dATP/ATP ratio, but at submaximal Ca(2+) (pCa 5.5) this relationship was nonlinear, with the nonlinearity evident at 2-20% dATP; force increased significantly with only 10% of substrate as dATP. The rate of tension redevelopment (k(TR)) increased with dATP at all Ca(2+) levels. k(TR) increased linearly with dATP/ATP ratio at pCa 4.5 and 5.5. Unregulated actin-activated Mg-NTPase rates and actin sliding speed linearly increased with the dATP/ATP ratio (p < 0.01 at 10% dATP). Together these data suggest cardiac contractility is enhanced when only 10% of the contractile substrate is dATP. Our results imply that relatively small (but supraphysiological) levels of dATP increase the number of strongly attached, force-producing actomyosin cross-bridges, resulting in an increase in overall contractility through both thin filament activation and kinetic shortening of the actomyosin cross-bridge cycle.
- Published
- 2006
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