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Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control.

Publication ,  Journal Article
Noland, RC; Koves, TR; Seiler, SE; Lum, H; Lust, RM; Ilkayeva, O; Stevens, RD; Hegardt, FG; Muoio, DM
Published in: J Biol Chem
August 21, 2009

In addition to its essential role in permitting mitochondrial import and oxidation of long chain fatty acids, carnitine also functions as an acyl group acceptor that facilitates mitochondrial export of excess carbons in the form of acylcarnitines. Recent evidence suggests carnitine requirements increase under conditions of sustained metabolic stress. Accordingly, we hypothesized that carnitine insufficiency might contribute to mitochondrial dysfunction and obesity-related impairments in glucose tolerance. Consistent with this prediction whole body carnitine diminution was identified as a common feature of insulin-resistant states such as advanced age, genetic diabetes, and diet-induced obesity. In rodents fed a lifelong (12 month) high fat diet, compromised carnitine status corresponded with increased skeletal muscle accumulation of acylcarnitine esters and diminished hepatic expression of carnitine biosynthetic genes. Diminished carnitine reserves in muscle of obese rats was accompanied by marked perturbations in mitochondrial fuel metabolism, including low rates of complete fatty acid oxidation, elevated incomplete beta-oxidation, and impaired substrate switching from fatty acid to pyruvate. These mitochondrial abnormalities were reversed by 8 weeks of oral carnitine supplementation, in concert with increased tissue efflux and urinary excretion of acetylcarnitine and improvement of whole body glucose tolerance. Acetylcarnitine is produced by the mitochondrial matrix enzyme, carnitine acetyltransferase (CrAT). A role for this enzyme in combating glucose intolerance was further supported by the finding that CrAT overexpression in primary human skeletal myocytes increased glucose uptake and attenuated lipid-induced suppression of glucose oxidation. These results implicate carnitine insufficiency and reduced CrAT activity as reversible components of the metabolic syndrome.

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Published In

J Biol Chem

DOI

EISSN

1083-351X

Publication Date

August 21, 2009

Volume

284

Issue

34

Start / End Page

22840 / 22852

Location

United States

Related Subject Headings

  • gamma-Butyrobetaine Dioxygenase
  • Vitamin B Complex
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rats, Wistar
  • Rats
  • Random Allocation
  • Oxidative Phosphorylation
  • Overnutrition
  • Mixed Function Oxygenases
  • Mitochondria, Muscle
 

Citation

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Noland, R. C., Koves, T. R., Seiler, S. E., Lum, H., Lust, R. M., Ilkayeva, O., … Muoio, D. M. (2009). Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control. J Biol Chem, 284(34), 22840–22852. https://doi.org/10.1074/jbc.M109.032888
Noland, Robert C., Timothy R. Koves, Sarah E. Seiler, Helen Lum, Robert M. Lust, Olga Ilkayeva, Robert D. Stevens, Fausto G. Hegardt, and Deborah M. Muoio. “Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control.J Biol Chem 284, no. 34 (August 21, 2009): 22840–52. https://doi.org/10.1074/jbc.M109.032888.
Noland RC, Koves TR, Seiler SE, Lum H, Lust RM, Ilkayeva O, et al. Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control. J Biol Chem. 2009 Aug 21;284(34):22840–52.
Noland, Robert C., et al. “Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control.J Biol Chem, vol. 284, no. 34, Aug. 2009, pp. 22840–52. Pubmed, doi:10.1074/jbc.M109.032888.
Noland RC, Koves TR, Seiler SE, Lum H, Lust RM, Ilkayeva O, Stevens RD, Hegardt FG, Muoio DM. Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control. J Biol Chem. 2009 Aug 21;284(34):22840–22852.

Published In

J Biol Chem

DOI

EISSN

1083-351X

Publication Date

August 21, 2009

Volume

284

Issue

34

Start / End Page

22840 / 22852

Location

United States

Related Subject Headings

  • gamma-Butyrobetaine Dioxygenase
  • Vitamin B Complex
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rats, Wistar
  • Rats
  • Random Allocation
  • Oxidative Phosphorylation
  • Overnutrition
  • Mixed Function Oxygenases
  • Mitochondria, Muscle