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dc.contributor.authorPavis, GF
dc.contributor.authorAbdelrahman, DR
dc.contributor.authorMurton, AJ
dc.contributor.authorWall, BT
dc.contributor.authorStephens, FB
dc.contributor.authorDirks, ML
dc.date.accessioned2023-08-21T10:12:12Z
dc.date.issued2023-07-11
dc.date.updated2023-08-21T06:53:25Z
dc.description.abstractBACKGROUND: The decline in postabsorptive and postprandial muscle protein fractional synthesis rates (FSR) does not quantitatively account for muscle atrophy during uncomplicated, short-term disuse, when atrophy rates are the highest. We sought to determine whether 2 days of unilateral knee immobilization affects mixed muscle protein fractional breakdown rates (FBR) during postabsorptive and simulated postprandial conditions. METHODS: Twenty-three healthy, male participants (age: 22 ± 1 year; height: 179 ± 1 cm; body mass: 73.4 ± 1.5 kg; body mass index 22.8 ± 0.5 kg·m-2 ) took part in this randomized, controlled study. After 48 h of unilateral knee immobilization, primed continuous intravenous l-[15 N]-phenylalanine and l-[ring-2 H5 ]-phenylalanine infusions were used for parallel determinations of FBR and FSR, respectively, in a postabsorptive (saline infusion; FAST) or simulated postprandial state (67.5 mg·kg body mass-1 ·h-1 amino acid infusion; FED). Bilateral m. vastus lateralis biopsies from the control (CON) and immobilized (IMM) legs, and arterialized-venous blood samples, were collected throughout. RESULTS: Amino acid infusion rapidly increased plasma phenylalanine (59 ± 9%), leucine (76 ± 5%), isoleucine (109 ± 7%) and valine (42 ± 4%) concentrations in FED only (all P < 0.001), which was sustained for the remainder of infusion. Serum insulin concentrations peaked at 21.8 ± 2.2 mU·L-1 at 15 min in FED only (P < 0.001) and were 60% greater in FED than FAST (P < 0.01). Immobilization did not influence FBR in either FAST (CON: 0.150 ± 0.018; IMM: 0.143 ± 0.017%·h-1 ) or FED (CON: 0.134 ± 0.012; IMM: 0.160 ± 0.018%·h-1 ; all effects P > 0.05). However, immobilization decreased FSR (P < 0.05) in both FAST (0.071 ± 0.004 vs. 0.086 ± 0.007%·h-1 ; IMM vs CON, respectively) and FED (0.066 ± 0.016 vs. 0.119 ± 0.016%·h-1 ; IMM vs CON, respectively). Consequently, immobilization decreased net muscle protein balance (P < 0.05) and to a greater extent in FED (CON: -0.012 ± 0.025; IMM: -0.095 ± 0.023%·h-1 ; P < 0.05) than FAST (CON: -0.064 ± 0.020; IMM: -0.072 ± 0.017%·h-1 ). CONCLUSIONS: We conclude that merely 2 days of leg immobilization does not modulate postabsorptive and simulated postprandial muscle protein breakdown rates. Instead, under these conditions the muscle negative muscle protein balance associated with brief periods of experimental disuse is driven near exclusively by reduced basal muscle protein synthesis rates and anabolic resistance to amino acid administration.en_GB
dc.description.sponsorshipNutricia Research Foundationen_GB
dc.description.sponsorshipUniversity of Exeteren_GB
dc.description.sponsorshipBeachbody LLCen_GB
dc.description.sponsorshipNational Institute of Agingen_GB
dc.format.mediumPrint-Electronic
dc.identifier.citationPublished online 11 July 2023en_GB
dc.identifier.doihttps://doi.org/10.1002/jcsm.13284
dc.identifier.grantnumber2019-30en_GB
dc.identifier.grantnumberP30-AG024832en_GB
dc.identifier.urihttp://hdl.handle.net/10871/133820
dc.identifierORCID: 0000-0002-6019-6709 (Wall, Benjamin T)
dc.identifierORCID: 0000-0001-6312-5351 (Stephens, Francis B)
dc.identifierScopusID: 12779890700 (Stephens, Francis B)
dc.identifierORCID: 0000-0002-9189-1042 (Dirks, Marlou L)
dc.identifierResearcherID: G-5813-2011 (Dirks, Marlou L)
dc.language.isoenen_GB
dc.publisherWiley / Society on Sarcopenia, Cachexia and Wasting Disordersen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/37431714en_GB
dc.rights© 2023 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectAmino acidsen_GB
dc.subjectImmobilizationen_GB
dc.subjectMuscle disuse atrophyen_GB
dc.subjectMuscle protein breakdownen_GB
dc.subjectProtein synthesisen_GB
dc.titleShort-term disuse does not affect postabsorptive or postprandial muscle protein fractional breakdown ratesen_GB
dc.typeArticleen_GB
dc.date.available2023-08-21T10:12:12Z
dc.identifier.issn2190-5991
exeter.place-of-publicationGermany
dc.descriptionThis is the final version. Available on open access from Wiley via the DOI in this recorden_GB
dc.identifier.eissn2190-6009
dc.identifier.journalJ Cachexia Sarcopenia Muscleen_GB
dc.relation.ispartofJ Cachexia Sarcopenia Muscle
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2023-05-22
dc.rights.licenseCC BY
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2023-07-11
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2023-08-21T10:10:04Z
refterms.versionFCDVoR
refterms.dateFOA2023-08-21T10:12:16Z
refterms.panelAen_GB
refterms.dateFirstOnline2023-07-11


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© 2023 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the
original work is properly cited.
Except where otherwise noted, this item's licence is described as © 2023 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.