Compartmentalized acyl-CoA metabolism in skeletal muscle regulates systemic glucose homeostasis

Research output: Contribution to journalJournal articleResearchpeer-review

  • Lei O Li
  • Grevengoed, Trisha Jean
  • David S Paul
  • Olga Ilkayeva
  • Timothy R Koves
  • Florencia Pascual
  • Christopher B Newgard
  • Deborah M Muoio
  • Rosalind A Coleman

The impaired capacity of skeletal muscle to switch between the oxidation of fatty acid (FA) and glucose is linked to disordered metabolic homeostasis. To understand how muscle FA oxidation affects systemic glucose, we studied mice with a skeletal muscle-specific deficiency of long-chain acyl-CoA synthetase (ACSL)1. ACSL1 deficiency caused a 91% loss of ACSL-specific activity and a 60-85% decrease in muscle FA oxidation. Acsl1(M-/-) mice were more insulin sensitive, and, during an overnight fast, their respiratory exchange ratio was higher, indicating greater glucose use. During endurance exercise, Acsl1(M-/-) mice ran only 48% as far as controls. At the time that Acsl1(M-/-) mice were exhausted but control mice continued to run, liver and muscle glycogen and triacylglycerol stores were similar in both genotypes; however, plasma glucose concentrations in Acsl1(M-/-) mice were ∼40 mg/dL, whereas glucose concentrations in controls were ∼90 mg/dL. Excess use of glucose and the likely use of amino acids for fuel within muscle depleted glucose reserves and diminished substrate availability for hepatic gluconeogenesis. Surprisingly, the content of muscle acyl-CoA at exhaustion was markedly elevated, indicating that acyl-CoAs synthesized by other ACSL isoforms were not available for β-oxidation. This compartmentalization of acyl-CoAs resulted in both an excessive glucose requirement and severely compromised systemic glucose homeostasis.

Original languageEnglish
Issue number1
Pages (from-to)23-35
Number of pages13
Publication statusPublished - Jan 2015
Externally publishedYes

    Research areas

  • Animals, Blood Glucose, Cell Compartmentation, Cerebral Cortex, Coenzyme A, Coenzyme A Ligases, Fasting, Fatty Acids, Female, Gluconeogenesis, Homeostasis, Hypoglycemia, Liver, Male, Metabolomics, Mice, Knockout, Muscle, Skeletal, Oxidation-Reduction, Physical Endurance, Pregnancy, Signal Transduction

ID: 146698721