Subsarcolemmal and intermyofibrillar mitochondria play distinct roles in regulating skeletal muscle fatty acid metabolism

Am J Physiol Cell Physiol. 2005 May;288(5):C1074-82. doi: 10.1152/ajpcell.00391.2004. Epub 2005 Jan 12.

Abstract

Skeletal muscle contains two populations of mitochondria that appear to be differentially affected by disease and exercise training. It remains unclear how these mitochondrial subpopulations contribute to fiber type-related and/or training-induced changes in fatty acid oxidation and regulation of carnitine palmitoyltransferase-1beta (CPT1beta), the enzyme that controls mitochondrial fatty acid uptake in skeletal muscle. To this end, we found that fatty acid oxidation rates were 8.9-fold higher in subsarcolemmal mitochondria (SS) and 5.3-fold higher in intermyofibrillar mitochondria (IMF) that were isolated from red gastrocnemius (RG) compared with white gastrocnemius (WG) muscle, respectively. Malonyl-CoA (10 muM), a potent inhibitor of CPT1beta, completely abolished fatty acid oxidation in SS and IMF mitochondria from WG, whereas oxidation rates in the corresponding fractions from RG were inhibited only 89% and 60%, respectively. Endurance training also elicited mitochondrial adaptations that resulted in enhanced fatty acid oxidation capacity. Ten weeks of treadmill running differentially increased palmitate oxidation rates 100% and 46% in SS and IMF mitochondria, respectively. In SS mitochondria, elevated fatty acid oxidation rates were accompanied by a 48% increase in citrate synthase activity but no change in CPT1 activity. Nonlinear regression analyses of mitochondrial fatty acid oxidation rates in the presence of 0-100 muM malonyl-CoA indicated that IC(50) values were neither dependent on mitochondrial subpopulation nor affected by exercise training. However, in IMF mitochondria, training reduced the Hill coefficient (P < 0.05), suggesting altered CPT1beta kinetics. These results demonstrate that endurance exercise provokes subpopulation-specific changes in mitochondrial function that are characterized by enhanced fatty acid oxidation and modified CPT1beta-malonyl-CoA dynamics.

MeSH terms

  • Animals
  • Carnitine O-Palmitoyltransferase / isolation & purification
  • Carnitine O-Palmitoyltransferase / metabolism*
  • Citrate (si)-Synthase / metabolism
  • Enzyme Activation / drug effects
  • Enzyme Activation / physiology
  • Male
  • Malonyl Coenzyme A / pharmacology
  • Mitochondria, Muscle / drug effects
  • Mitochondria, Muscle / metabolism*
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism*
  • Myofibrils / drug effects
  • Myofibrils / metabolism
  • Oxidation-Reduction / drug effects
  • Palmitates / metabolism*
  • Physical Endurance / physiology
  • Physical Exertion / physiology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Palmitates
  • Malonyl Coenzyme A
  • Carnitine O-Palmitoyltransferase
  • Citrate (si)-Synthase