Professor KENNETH SMITH KEN.SMITH@NOTTINGHAM.AC.UK
PROFESSOR OF METABOLIC MASS SPECTROMETRY
Internal comparison between deuterium oxide (D2O) and L-[ring-13C6] phenylalanine for acute measurement of muscle protein synthesis in humans
Smith, Ken; Cegielski, Jessica; Wilkinson, Daniel; Phillips, Bethan; Boereboom, Catherine; Lund, Jonathan; Atherton, Philip
Authors
Jessica Cegielski
Dr DANIEL WILKINSON DANIEL.WILKINSON@NOTTINGHAM.AC.UK
PRINCIPAL RESEARCH FELLOW
Professor BETH PHILLIPS beth.phillips@nottingham.ac.uk
PROFESSOR OF TRANSLATIONAL PHYSIOLOGY
Catherine Boereboom
Mr Jonathan LundEDIT JON.LUND@NOTTINGHAM.AC.UK
CLINICAL ASSOCIATE PROFESSOR
Professor PHILIP ATHERTON philip.atherton@nottingham.ac.uk
PROFESSOR OF CLINICAL, METABOLIC & MOLECULAR PHYSIOLOGY
Abstract
Stable isotope tracer methodologies are becoming increasingly widespread in metabolic research; yet a number of factors restrict their implementation, such as, i.v infusions, multiple cannulae, tissue samples, and significant cost. We recently validated the sensitivity of the orally administered stable isotope tracer deuterium oxide (D2O) for quantifying day‐to‐day changes in muscle protein synthesis (MPS). This method is less invasive, restrictive, and more cost‐effective than traditional amino acid (AA) tracer techniques. In the present study, we hypothesized the sensitivity of our analytical techniques (GC‐Pyrolysis‐IRMS) would permit D2O‐derived measurements of MPS over much shorter periods (i.e., hours) usually only possible using AA‐tracer techniques. We recruited nine males (24 ± 3 year, BMI: 25 ± 3 kg·m−²) into an internally controlled comparison of D2O versus 13C AA‐tracers. The day before the acute study subjects consumed 400 mL D2O, and on the study day, received a primed (0.3 mg·kg−1) continuous (0.6 mg·kg·h−1) i.v infusion of L‐[ring‐13C6]‐phenylalanine to quantify MPS under both: (1) basal [postabsorptive] and; (2) stimulated [postprandial] that is, consumption of 20 g EAA, conditions. Measures of MPS yielded indistinguishable technique differences with respect to EAA, 13C: 0.065 ± 0.004 to 0.089 ± 0.006%·h−1 (P < 0.05) and D2O: 0.050 ± 0.007 to 0.088 ± 0.008%·h−1 (P < 0.05) with qualitatively similar increases. Our findings reveal that acute measurement of MPS, usually only possible using AA‐tracers, are feasible over shorter periods with orally administered D2O when used in tandem with GC‐Pyrolysis‐IRMS. We conclude that this D2O approach provides a less invasive, cost‐effective, and flexible means by which to quantify MPS acutely over several hours.
Citation
Smith, K., Cegielski, J., Wilkinson, D., Phillips, B., Boereboom, C., Lund, J., & Atherton, P. (2015). Internal comparison between deuterium oxide (D2O) and L-[ring-13C6] phenylalanine for acute measurement of muscle protein synthesis in humans. Physiological Reports, 3(7), Article e12433. https://doi.org/10.14814/phy2.12433
Journal Article Type | Article |
---|---|
Acceptance Date | May 25, 2015 |
Publication Date | Jul 1, 2015 |
Deposit Date | Sep 6, 2018 |
Publicly Available Date | Feb 7, 2019 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 3 |
Issue | 7 |
Article Number | e12433 |
DOI | https://doi.org/10.14814/phy2.12433 |
Public URL | https://nottingham-repository.worktribe.com/output/1104550 |
Publisher URL | https://physoc.onlinelibrary.wiley.com/doi/full/10.14814/phy2.12433 |
PMID | 26149278 |
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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