The influence of a chronic L-carnitine administration on the plasma metabolome of male Fischer 344 rats

Mol Nutr Food Res. 2017 May;61(5). doi: 10.1002/mnfr.201600651. Epub 2017 Feb 10.

Abstract

Scope: L-carnitine has been advertised as a fat-lowering and performance-enhancing supplement, although scientific evidence for its effectiveness is lacking. The uptake of about 1-2 g of L-carnitine per day may result in the formation of metabolites like trimethylamine-N-oxide (TMAO), which in turn may be converted to potential carcinogens or promote the development of cardiovascular diseases.

Methods and results: To assess whether an L-carnitine supplementation changes overall metabolism or causes the formation of previously unknown metabolites, we analyzed plasma samples from Fischer 344 rats originating from a previous study using a multi-platform metabolomics approach comprising LC-MS/MS and GC×GC-MS methods. Despite an intake of up to 352 mg L-carnitine/kg body weight/day for 1 year, plasma concentrations of only 29 out of 359 metabolites were significantly influenced, the induced concentration changes being often comparatively small. Nevertheless, a clear dose-response relationship and a substantial concentration increase were observed for TMAO, i.e. a tenfold higher TMAO level was measured in the high-dose group when compared to the control (2.5 versus 25.0 μM).

Conclusion: Although L-carnitine supplementation did not cause large changes in the plasma metabolome, a higher risk for cardiovascular disease due to chronically elevated TMAO plasma concentrations cannot be excluded.

Keywords: Fischer 344 rat; Food safety; L-carnitine; Trimethylamine-N-oxide; Untargeted multi-platform metabolomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carcinogens / metabolism
  • Cardiovascular Diseases / blood
  • Cardiovascular Diseases / etiology
  • Carnitine / administration & dosage*
  • Carnitine / adverse effects*
  • Carnitine / blood
  • Dietary Supplements
  • Dose-Response Relationship, Drug
  • Male
  • Metabolome*
  • Metabolomics
  • Methylamines / blood
  • Rats
  • Rats, Inbred F344
  • Tandem Mass Spectrometry

Substances

  • Carcinogens
  • Methylamines
  • trimethyloxamine
  • Carnitine