Lean-seafood intake decreases urinary markers of mitochondrial lipid and energy metabolism in healthy subjects: Metabolomics results from a randomized crossover intervention study

Mol Nutr Food Res. 2016 Jul;60(7):1661-72. doi: 10.1002/mnfr.201500785. Epub 2016 May 4.

Abstract

Scope: Proteins constitute an important part of the human diet, but understanding of the effects of different dietary protein sources on human metabolism is sparse. We aimed to elucidate diet-induced metabolic changes through untargeted urinary metabolomics after four weeks of intervention with lean-seafood or nonseafood diets. It is shown that lean-seafood intake reduces urinary excretion of metabolites involved in mitochondrial lipid and energy metabolism possibly facilitating a higher lipid catabolism in healthy subjects.

Methods: In a randomized controlled trial with crossover design, 20 healthy subjects consumed two balanced diets that varied in main protein sources for 4 weeks. Morning spot urine samples were collected before and after each intervention period. Untargeted metabolomics based on (1) H NMR spectroscopy and LC-MS analyses were applied to characterize the urinary metabolic response to the interventions.

Results: The lean-seafood diet period reduced the urinary level of l-carnitine, 2,6-dimethylheptanoylcarnitine, and N-methyl-2-pyridone-5-carboxamide, relative to the nonseafood period. The dietary analysis revealed that the higher urinary level of trimethylamine-N-oxide after the lean-seafood diet period and guanidinoacetate and 3-methylhistidine after the nonseafood diet period was related to the endogenous content of these compounds in the diets.

Conclusions: Our data reveal that 4 weeks of lean-seafood intake reduces urinary excretion of metabolites involved in mitochondrial lipid and energy metabolism possibly facilitating a higher lipid catabolism in healthy subjects after the lean-seafood intake.

Keywords: Biomarkers; Dietary protein; Lipid metabolism; Metabolism; Urine.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Biomarkers / urine*
  • Carnitine / urine
  • Cross-Over Studies
  • Diet
  • Dietary Proteins / administration & dosage
  • Energy Metabolism*
  • Female
  • Glycine / analogs & derivatives
  • Glycine / urine
  • Healthy Volunteers
  • Humans
  • Lipid Metabolism*
  • Male
  • Metabolomics
  • Methylamines / urine
  • Methylhistidines / urine
  • Middle Aged
  • Mitochondria / metabolism*
  • Pyridones / urine
  • Seafood*
  • Young Adult

Substances

  • Biomarkers
  • Dietary Proteins
  • Methylamines
  • Methylhistidines
  • N-methyl-2-pyridone-5-carboxamide
  • Pyridones
  • trimethyloxamine
  • glycocyamine
  • 3-methylhistidine
  • Carnitine
  • Glycine