The aims of the program project are to study the mechanism of contraction of cardiac muscle. The focus is on fundamental properties, i.e., on the manner in which force is generated and regulated. The investigators come from various disciplines including physiology, bioengineering, biochemistry, biostructure and pharmacology. The majority of them are senior investigators with considerable experience and a history of collaboration. Their areas of expertise will be combined in a multidisciplinary, highly interactive effort to study the fundamentals of contraction in the heart. Several specific issues are to be investigated using complementary methodologies. In Project I, the phenomenon of stepwise sarcomere shortening will be pursued using several optical and mechanical techniques. The question of whether stepwise shortening is associated with thick filament shortening is investigated in Project II, using both the freeze-fracture method and optical imaging of the striations. In Project III, myofilament activation will be studied using a new fluorescent probe to measure bound calcium. This is closely related to Project IV, in which activation and other factors are considered as possible mechanisms underlying Starling's Law of the Heart; skinned and intact preparations will be studied. In Project V, the effect of history on contractile performance is considered with methods including those in each of the first four projects. Finally, in Project VI, the subcellular disposition of calcium in various compartments of heart cells will be investigated using the X-ray microanalysis method. There will be four core facilities in support of these research activities: Core A - Administrative; Core B - Computer Programming; Core C - Electron Microscopy; and Core D - Instrumentation. These facilities will be used broadly by the investigators, thereby serving as an additional focal point of interaction.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL031962-02
Application #
3098243
Study Section
Heart, Lung, and Blood Research Review Committee A (HLBA)
Project Start
1984-04-01
Project End
1989-03-31
Budget Start
1985-04-01
Budget End
1986-03-31
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Chase, P B; Denkinger, T M; Kushmerick, M J (1998) Effect of viscosity on mechanics of single, skinned fibers from rabbit psoas muscle. Biophys J 74:1428-38
deBeer, E L; Sontrop, A M; Kellermayer, M S et al. (1997) Actin-filament motion in the in vitro motility assay has a periodic component. Cell Motil Cytoskeleton 38:341-50
Wiseman, R W; Beck, T W; Chase, P B (1996) Effect of intracellular pH on force development depends on temperature in intact skeletal muscle from mouse. Am J Physiol 271:C878-86
Kellermayer, M S; Pollack, G H (1996) Rescue of in vitro actin motility halted at high ionic strength by reduction of ATP to submicromolar levels. Biochim Biophys Acta 1277:107-14
Hancock, W O; Martyn, D A; Huntsman, L L et al. (1996) Influence of Ca2+ on force redevelopment kinetics in skinned rat myocardium. Biophys J 70:2819-29
Kellermayer Jr, M S; Hinds, T R; Pollack, G H (1995) Persisting in vitro actin motility at nanomolar adenosine triphosphate levels: comparison of skeletal and cardiac myosins. Physiol Chem Phys Med NMR 27:167-78
Martyn, D A; Chase, P B (1995) Faster force transient kinetics at submaximal Ca2+ activation of skinned psoas fibers from rabbit. Biophys J 68:235-42
Chase, P B; Kushmerick, M J (1995) Effect of physiological ADP concentrations on contraction of single skinned fibers from rabbit fast and slow muscles. Am J Physiol 268:C480-9
Chase, P B; Martyn, D A; Hannon, J D (1994) Isometric force redevelopment of skinned muscle fibers from rabbit activated with and without Ca2+. Biophys J 67:1994-2001
Chase, P B; Martyn, D A; Hannon, J D (1994) Activation dependence and kinetics of force and stiffness inhibition by aluminiofluoride, a slowly dissociating analogue of inorganic phosphate, in chemically skinned fibres from rabbit psoas muscle. J Muscle Res Cell Motil 15:119-29

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