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Urinary metabolome dynamics in 13C-labeled mice.

Annelaure Damont1, Anaïs Legrand2, Kathleen Rousseau2

  • 1Paris-Saclay University, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), MetaboHUB, F-91191, Gif sur Yvette, France. annelaure.damont@cea.fr.

Metabolomics : Official Journal of the Metabolomic Society
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Summary

Mice tolerated a whole-body carbon-13 (13C) labeled diet for six weeks, revealing variable 13C incorporation kinetics across metabolites. This study offers broad insights into mammalian metabolome dynamics using isotope tracing.

Keywords:
13C-metabolomicsIn vivoIsotope tracingMammal labelingMass spectrometry

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Area of Science:

  • Metabolomics
  • Systems Biology
  • Isotope Tracing

Background:

  • Metabolic flux analysis typically uses specific labeled precursors and LC-HRMS.
  • Targeted approaches limit the scope of metabolic pathway investigation.

Purpose of the Study:

  • To investigate whole metabolome dynamics using a novel approach of a fully 13C-enriched diet in mice.
  • To assess the feasibility and outcomes of long-term whole-body isotope labeling.

Main Methods:

  • Mice were fed a diet fully enriched in 13C for six weeks.
  • Urine samples were collected daily and analyzed using LC-HRMS and isotope tracing.
  • Comparative analysis was performed against control mice fed an unenriched diet.

Main Results:

  • Mice tolerated the 13C-enriched diet, showing normal growth.
  • LC-HRMS identified 238 metabolites, with 13C labeling profiles monitored over 39 days.
  • Urine labeling reached >90% 13C after 22 days, but incorporation kinetics varied significantly between metabolites.

Conclusions:

  • A diet fully labeled with 13C is well-tolerated by mice over six weeks.
  • This whole-body labeling approach reveals dynamic metabolome information in mammals via urine analysis.
  • The study provides comprehensive metabolic pathway insights, surpassing limitations of targeted fluxomic studies.