The determinants of work capacity (i.e., power output) will be examined by measuring power-load curves in single permeabilized rat cardiac myocytes. The role of myosin heavy chain (MHC) will be assessed by examining power-load curves in myocytes with varying mixtures of alpha (a) and beta (b) myosin heavy chain. The applicant expects that these studies on the mixtures will provide insight on the role of force generating or detachment in determining the power output. The contribution (direct effect on the cross-bridge transitions or an indirect effect of thin filament activation) of Ca2+ to power output will be evaluated using varying concentrations of calcium in the experiments or changing the sensitivity of the thin filament system to calcium by extracting TnC or using calcium sensitizing agents. The role of titin on shortening dependence of power output will be assessed by studying myocytes with and without titin, while the effect of the extracellular matrix will be evaluated by using multicellular preparations and comparing them with the single myocyte data. The effect of sarcomere length and interfillament spacing on power output will also be evaluated. The alterations in sarcomere length will also be used to ascertain if attachment rates and detachment rates are the determinants of the power output. Finally, some experiments will be carried out on rat skeletal fibers for the purpose of comparison and validation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL057852-01
Application #
2031072
Study Section
Cardiovascular and Pulmonary Research A Study Section (CVA)
Project Start
1997-09-01
Project End
1997-10-31
Budget Start
1997-09-01
Budget End
1997-10-31
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Physiology
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Hanft, Laurin M; Emter, Craig A; McDonald, Kerry S (2017) Cardiac myofibrillar contractile properties during the progression from hypertension to decompensated heart failure. Am J Physiol Heart Circ Physiol 313:H103-H113
Hanft, Laurin M; Cornell, Timothy D; McDonald, Colin A et al. (2016) Molecule specific effects of PKA-mediated phosphorylation on rat isolated heart and cardiac myofibrillar function. Arch Biochem Biophys 601:22-31
Nance, Michael E; Whitfield, Justin T; Zhu, Yi et al. (2015) Attenuated sarcomere lengthening of the aged murine left ventricle observed using two-photon fluorescence microscopy. Am J Physiol Heart Circ Physiol 309:H918-25
Domeier, Timothy L; Roberts, Cale J; Gibson, Anne K et al. (2014) Dantrolene suppresses spontaneous Ca2+ release without altering excitation-contraction coupling in cardiomyocytes of aged mice. Am J Physiol Heart Circ Physiol 307:H818-29
Hanft, Laurin M; Greaser, Marion L; McDonald, Kerry S (2014) Titin-mediated control of cardiac myofibrillar function. Arch Biochem Biophys 552-553:83-91
Marshall, Kurt D; Muller, Brittany N; Krenz, Maike et al. (2013) Heart failure with preserved ejection fraction: chronic low-intensity interval exercise training preserves myocardial O2 balance and diastolic function. J Appl Physiol (1985) 114:131-47
Hanft, Laurin M; Biesiadecki, Brandon J; McDonald, Kerry S (2013) Length dependence of striated muscle force generation is controlled by phosphorylation of cTnI at serines 23/24. J Physiol 591:4535-47
Hinken, Aaron C; Hanft, Laurin M; Scruggs, Sarah B et al. (2012) Protein kinase C depresses cardiac myocyte power output and attenuates myofilament responses induced by protein kinase A. J Muscle Res Cell Motil 33:439-48
McDonald, Kerry S; Hanft, Laurin M; Domeier, Timothy L et al. (2012) Length and PKA Dependence of Force Generation and Loaded Shortening in Porcine Cardiac Myocytes. Biochem Res Int 2012:371415
Hanft, Laurin M; McDonald, Kerry S (2010) Length dependence of force generation exhibit similarities between rat cardiac myocytes and skeletal muscle fibres. J Physiol 588:2891-903

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