Effects of altered pyruvate dehydrogenase activity on contracting skeletal muscle bioenergetics

• Published in: American journal of physiology. Regulatory, integrative and comparative physiology Vol. 316; no. 1; p. R76
• Main Authors: Kasper, Jonathan D, Meyer, Ronald A, Beard, Daniel A, Wiseman, Robert W
• Format: Journal Article
• Language: English
• Published: United States 01-01-2019
• Subjects: Adenosine Triphosphate - metabolism; Animals; Energy Metabolism - drug effects; Male; Muscle Contraction - drug effects; Muscle, Skeletal - drug effects; Muscle, Skeletal - enzymology; Oxidation-Reduction - drug effects; Oxidoreductases - drug effects; Oxygen Consumption - drug effects; Oxygen Consumption - physiology; Pyruvate Dehydrogenase Complex - metabolism; Pyruvate Dehydrogenase Complex - pharmacology; Rats, Wistar; pyruvate dehydrogenase; phosphate potential; magnetic resonance; substrate disposal; mitochondria
• ISSN: 1522-1490
• DOI: 10.1152/ajpregu.00321.2018

During aerobic exercise (>65% of maximum oxygen consumption), the primary source of acetyl-CoA to fuel oxidative ATP synthesis in muscle is the pyruvate dehydrogenase (PDH) reaction. This study investigated how regulation of PDH activity affects muscle energetics by determining whether activation of PDH with dichloroacetate (DCA) alters the dynamics of the phosphate potential of rat gastrocnemius muscle during contraction. Twitch contractions were induced in vivo over a broad range of intensities to sample submaximal and maximal aerobic workloads. Muscle phosphorus metabolites were measured in vivo before and after DCA treatment by phosphorus nuclear magnetic resonance spectroscopy. At rest, DCA increased PDH activation compared with control (90 ± 12% vs. 23 ± 3%, P < 0.05), with parallel decreases in inorganic phosphate (P
) of 17% (1.4 ± 0.2 vs. 1.7 ± 0.1 mM, P < 0.05) and an increase in the free energy of ATP hydrolysis (ΔG
) (-66.2 ± 0.3 vs. -65.6 ± 0.2 kJ/mol, P < 0.05). During stimulation DCA increased steady-state phosphocreatine (PCr) and the magnitude of ΔG
, with concomitant reduction in P
and ADP concentrations. These effects were not due to kinetic alterations in PCr hydrolysis, resynthesis, or glycolytic ATP production and altered the flow-force relationship between mitochondrial ATP synthesis rate and ΔG
. DCA had no significant effect at 1.0- to 2.0-Hz stimulation because physiological mechanisms at these high stimulation levels cause maximal activation of PDH. These data support a role of PDH activation in the regulation of the energetic steady state by altering the phosphate potential (ΔG
) at rest and during contraction.