Metabolic signature of 13C-labeled wheat bran consumption related to gut fermentation in humans: a pilot study.

Purpose: The aim of this pilot study was to analyze concomitantly the kinetics of production of 13C-labeled gut-derived metabolites from 13C-labeled wheat bran in three biological matrices (breath, plasma, stools), in order to assess differential fermentation profiles among subjects. Methods: Six he...

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Publicado en:European Journal of Nutrition Vol. 62; no. 6; pp. 2633 - 2649
Autores principales: Meiller, Laure, Sauvinet, Valérie, Breyton, Anne-Esther, Ranaivo, Harimalala, Machon, Christelle, Mialon, Anne, Meynier, Alexandra, Bischoff, Stephan C., Walter, Jens, Neyrinck, Audrey M., Laville, Martine, Delzenne, Nathalie M., Vinoy, Sophie, Nazare, Julie-Anne
Formato: research tables/charts Journal Article
Publicado: Springer Nature Sep2023
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Sep2023
      vid: 62
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s00394-023-03161-5
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        atl: Metabolic signature of 13C-labeled wheat bran consumption related to gut fermentation in humans: a pilot study.
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          Meiller, Laure
          Sauvinet, Valérie
          Breyton, Anne-Esther
          Ranaivo, Harimalala
          Machon, Christelle
          Mialon, Anne
          Meynier, Alexandra
          Bischoff, Stephan C.
          Walter, Jens
          Neyrinck, Audrey M.
          Laville, Martine
          Delzenne, Nathalie M.
          Vinoy, Sophie
          Nazare, Julie-Anne
        affil: Centre de Recherche en Nutrition Humaine Rhône-Alpes, Univ-Lyon, INSERM, INRAe, Claude Bernard Lyon1 University, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre Bénite, France
      sug:
        subj:
          Dietary Fiber Metabolism
          Wheat Metabolism
          Fermentation
          Gut Microbiota Metabolism
          Breakfast
          Metabolites
          Kinetics
          Fatty Acids, Volatile
          Human
          Pilot Studies
          Female
          Adult
          Gas Chromatography-Mass Spectrometry
          Butyric Acids
          Gene Expression
          RNA
          Adult: 19-44 years
          Female
      ab: Purpose: The aim of this pilot study was to analyze concomitantly the kinetics of production of 13C-labeled gut-derived metabolites from 13C-labeled wheat bran in three biological matrices (breath, plasma, stools), in order to assess differential fermentation profiles among subjects. Methods: Six healthy women consumed a controlled breakfast containing 13C-labeled wheat bran biscuits. H2, CH4 and 13CO2, 13CH4 24 h-concentrations in breath were measured, respectively, by gas chromatography (GC) and GC-isotope ratio mass spectrometry (GC-IRMS). Plasma and fecal concentrations of 13C-short-chain fatty acids (linear SCFAs: acetate, propionate, butyrate, valerate; branched SCFAs: isobutyrate, isovalerate) were quantified using GC-combustion-IRMS. Gut microbiota composition was assessed by16S rRNA gene sequencing analysis. Results: H2 and CH4 24 h-kinetics distinguished two groups in terms of fermentation-related gas excretion: high-CH4 producers vs low-CH4 producers (fasting concentrations: 45.3 ± 13.6 ppm vs 6.5 ± 3.6 ppm). Expired 13CH4 was enhanced and prolonged in high-CH4 producers compared to low-CH4 producers. The proportion of plasma and stool 13C-butyrate tended to be higher in low-CH4 producers, and inversely for 13C-acetate. Plasma branched SCFAs revealed different kinetics of apparition compared to linear SCFAs. Conclusion: This pilot study allowed to consider novel procedures for the development of biomarkers revealing dietary fiber-gut microbiota interactions. The non-invasive assessment of exhaled gas following 13C-labeled fibers ingestion enabled to decipher distinct fermentation profiles: high-CH4 producers vs low-CH4 producers. The isotope labeling permits a specific in vivo characterisation of the dietary fiber impact consumption on microbiota metabolite production. Clinical trial registration: The study has been registered under the number NCT03717311 at ClinicalTrials.gov on October 24, 2018.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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