Phenylalanine stable isotope tracer labeling of cow milk and meat and human experimental applications to study dietary protein-derived amino acid availability.


Journal

Clinical nutrition (Edinburgh, Scotland)
ISSN: 1532-1983
Titre abrégé: Clin Nutr
Pays: England
ID NLM: 8309603

Informations de publication

Date de publication:
12 2020
Historique:
received: 21 02 2019
revised: 25 02 2020
accepted: 20 03 2020
pubmed: 27 4 2020
medline: 20 8 2021
entrez: 27 4 2020
Statut: ppublish

Résumé

Availability of dietary protein-derived amino acids (AA) is an important determinant for their utilization in metabolism and for protein synthesis. Intrinsic labeling of protein is the only method to directly trace availability and utilization. The purpose of the present study was to produce labeled milk and meat proteins and investigate how dietary protein-derived AA availability is affected by the protein-meal matrix. Four lactating cows were infused with L-[ring-d Whey and caseinate acquired label to 15-20 mol percent excess (MPE), and the meat proteins reached 0.41-0.73 MPE. The [d Phenylalanine stable isotope-labeled milk and meat were produced and proved a valuable tool to investigate AA absorption characteristics. Dietary protein in food-matrices showed delayed postprandial plasma AA availability as compared to whey protein alone and meat hydrolysate.

Sections du résumé

BACKGROUND & AIMS
Availability of dietary protein-derived amino acids (AA) is an important determinant for their utilization in metabolism and for protein synthesis. Intrinsic labeling of protein is the only method to directly trace availability and utilization. The purpose of the present study was to produce labeled milk and meat proteins and investigate how dietary protein-derived AA availability is affected by the protein-meal matrix.
METHODS
Four lactating cows were infused with L-[ring-d
RESULTS
Whey and caseinate acquired label to 15-20 mol percent excess (MPE), and the meat proteins reached 0.41-0.73 MPE. The [d
CONCLUSIONS
Phenylalanine stable isotope-labeled milk and meat were produced and proved a valuable tool to investigate AA absorption characteristics. Dietary protein in food-matrices showed delayed postprandial plasma AA availability as compared to whey protein alone and meat hydrolysate.

Identifiants

pubmed: 32334880
pii: S0261-5614(20)30134-5
doi: 10.1016/j.clnu.2020.03.017
pii:
doi:

Substances chimiques

Amino Acids 0
Carbon Isotopes 0
Dietary Proteins 0
Whey Proteins 0
Phenylalanine 47E5O17Y3R

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3652-3662

Informations de copyright

Copyright © 2020 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest Søren Reitelseder and Lars Holm have received funding from The Danish Dairy Research Foundation, Arla Foods Ingredients Group P/S and DC Ingredients. Peter Lund has received funding from The Danish Dairy Research Foundation. Kristian Raaby Poulsen is employee at Arla Foods Ingredients Group P/S, and Erik T. Hansen is employee at DC Ingredients. Otherwise, the authors declare no conflicts of interest.

Auteurs

Søren Reitelseder (S)

Institute of Sports Medicine Copenhagen, Department of Orthopedic Surgery M, Bispebjerg Hospital, Copenhagen, Denmark; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. Electronic address: s.reitelseder@gmail.com.

Britt Tranberg (B)

Institute of Sports Medicine Copenhagen, Department of Orthopedic Surgery M, Bispebjerg Hospital, Copenhagen, Denmark. Electronic address: britt.tranberg@gmail.com.

Jakob Agergaard (J)

Institute of Sports Medicine Copenhagen, Department of Orthopedic Surgery M, Bispebjerg Hospital, Copenhagen, Denmark. Electronic address: jakobagergaard@hotmail.com.

Kasper Dideriksen (K)

Institute of Sports Medicine Copenhagen, Department of Orthopedic Surgery M, Bispebjerg Hospital, Copenhagen, Denmark. Electronic address: kasperjuel@hotmail.com.

Grith Højfeldt (G)

Institute of Sports Medicine Copenhagen, Department of Orthopedic Surgery M, Bispebjerg Hospital, Copenhagen, Denmark. Electronic address: grithwh@gmail.com.

Marie Emily Merry (ME)

Institute of Sports Medicine Copenhagen, Department of Orthopedic Surgery M, Bispebjerg Hospital, Copenhagen, Denmark. Electronic address: gr3v@kk.dk.

Adam C Storm (AC)

Department of Animal Science, Aarhus University Foulum, Aarhus University, Aarhus, Denmark. Electronic address: achs@novozymes.com.

Kristian R Poulsen (KR)

Arla Foods Ingredients Group P/S, Nr. Vium, Denmark. Electronic address: kristian.raaby.poulsen@arlafoods.com.

Erik T Hansen (ET)

DC Ingredients, Copenhagen, Denmark. Electronic address: eth@dat-schaub.dk.

Gerrit van Hall (G)

Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Clinical Metabolomics Core Facility, Clinical Biochemistry, Rigshospitalet. Electronic address: gerrit.van.hall@regionh.dk.

Peter Lund (P)

Department of Animal Science, Aarhus University Foulum, Aarhus University, Aarhus, Denmark. Electronic address: peter.lund@anis.au.dk.

Lars Holm (L)

Institute of Sports Medicine Copenhagen, Department of Orthopedic Surgery M, Bispebjerg Hospital, Copenhagen, Denmark; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, UK. Electronic address: L.Holm@bham.ac.uk.

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Classifications MeSH