This proposal focuses on the regulation of energy balance in fast and slow skeletal muscles in order to determine mechanisms of regulation of oxidative phosphorylation that presumably operate in all cell types. The premise for this work is that kinetic expressions for existing data are phenomenological rather than mechanistic. In order ultimately to develop a detailed kinetic equation for oxidative phosphorylation, the applicant proposes to undertake a detailed thermodynamic analysis of forces and flows in muscles. Flows in this system are the rates of ATP synthesis and oxygen consumption, while forces are the cytoplasmic chemical potential of ATP (GP) and the redox potential of NADH (Gredox). Both slow and fast muscles will be studied since terms for GP predominate in fast muscles, while a composite of GP and Gredox operate in slow muscles. Experiments will address three fundamental questions: 1. What is the scope of regulation in cellular respiration? The range of normal operation for oxidative phosphorylation and energy balance will determined in order to assess physiological fluxes (J) as a fraction of maximal flux (Jmax). 2. Are the physiological functional ranges of these fluxes also the maximum? This idea will be tested by extending the thermodynamic analysis beyond the physiologically accessible range, which will involve manipulating GP and Gredox. 3. What is the kinetic equation(s) for regulation? This question will be addressed by defining and testing the rate equation for mitochondrial ATP synthesis applicable to each muscle type.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR036281-14
Application #
2769563
Study Section
Special Emphasis Panel (ZRG2-PHY (03))
Project Start
1988-10-01
Project End
2000-03-31
Budget Start
1998-09-01
Budget End
2000-03-31
Support Year
14
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Washington
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Vinnakota, Kalyan C; Rusk, Joshua; Palmer, Lauren et al. (2010) Common phenotype of resting mouse extensor digitorum longus and soleus muscles: equal ATPase and glycolytic flux during transient anoxia. J Physiol 588:1961-83
Amara, Catherine E; Marcinek, David J; Shankland, Eric G et al. (2008) Mitochondrial function in vivo: spectroscopy provides window on cellular energetics. Methods 46:312-8
Arakaki, Lorilee S L; Burns, David H; Kushmerick, Martin J (2007) Accurate myoglobin oxygen saturation by optical spectroscopy measured in blood-perfused rat muscle. Appl Spectrosc 61:978-85
Conley, Kevin E; Jubrias, Sharon A; Amara, Catherine E et al. (2007) Mitochondrial dysfunction: impact on exercise performance and cellular aging. Exerc Sport Sci Rev 35:43-9
Conley, Kevin E; Amara, Catherine E; Jubrias, Sharon A et al. (2007) Mitochondrial function, fibre types and ageing: new insights from human muscle in vivo. Exp Physiol 92:333-9
Amara, Catherine E; Shankland, Eric G; Jubrias, Sharon A et al. (2007) Mild mitochondrial uncoupling impacts cellular aging in human muscles in vivo. Proc Natl Acad Sci U S A 104:1057-62
Vinnakota, Kalyan; Kemp, Melissa L; Kushmerick, Martin J (2006) Dynamics of muscle glycogenolysis modeled with pH time course computation and pH-dependent reaction equilibria and enzyme kinetics. Biophys J 91:1264-87
Dash, Ranjan K; Bell, Bradley M; Kushmerick, Martin J et al. (2005) Estimating in vitro mitochondrial oxygen consumption during muscle contraction and recovery: a novel approach that accounts for diffusion. Ann Biomed Eng 33:343-55
Kushmerick, Martin J (2005) From crossbridges to metabolism: system biology for energetics. Adv Exp Med Biol 565:171-80; discussion 180-2, 379-9
Marcinek, David J; Schenkman, Kenneth A; Ciesielski, Wayne A et al. (2005) Reduced mitochondrial coupling in vivo alters cellular energetics in aged mouse skeletal muscle. J Physiol 569:467-73

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