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dc.contributor.authorWest, S
dc.contributor.authorMonteyne, AJ
dc.contributor.authorWhelehan, G
dc.contributor.authorvan der Heijden, I
dc.contributor.authorAbdelrahman, DR
dc.contributor.authorMurton, AJ
dc.contributor.authorFinnigan, TJA
dc.contributor.authorStephens, FB
dc.contributor.authorWall, BT
dc.date.accessioned2023-10-11T15:22:50Z
dc.date.issued2023-08-25
dc.date.updated2023-10-11T14:58:17Z
dc.description.abstractPea protein is an attractive nonanimal-derived protein source to support dietary protein requirements. However, although high in leucine, a low methionine content has been suggested to limit its anabolic potential. Mycoprotein has a complete amino acid profile which, at least in part, may explain its ability to robustly stimulate myofibrillar protein synthesis (MyoPS) rates. We hypothesized that an inferior postexercise MyoPS response would be seen following ingestion of pea protein compared with mycoprotein, which would be (partially) rescued by blending the two sources. Thirty-three healthy, young [age: 21 ± 1 yr, body mass index (BMI): 24 ± 1 kg·m-2] and resistance-trained participants received primed, continuous infusions of l-[ring-2H5]phenylalanine and completed a bout of whole body resistance exercise before ingesting 25 g of protein from mycoprotein (MYC, n = 11), pea protein (PEA, n = 11), or a blend (39% MYC, 61% PEA) of the two (BLEND, n = 11). Blood and muscle samples were taken pre-, 2 h, and 4 h postexercise/protein ingestion to assess postabsorptive and postprandial postexercise myofibrillar protein fractional synthetic rates (FSRs). Protein ingestion increased plasma essential amino acid and leucine concentrations (time effect; P < 0.0001), but more rapidly in BLEND and PEA compared with MYC (time × condition interaction; P < 0.0001). From similar postabsorptive values (MYC, 0.026 ± 0.008%·h-1; PEA, 0.028 ± 0.007%·h-1; BLEND, 0.026 ± 0.006%·h-1), resistance exercise and protein ingestion increased myofibrillar FSRs (time effect; P < 0.0001) over a 4-h postprandial period (MYC, 0.076 ± 0.004%·h-1; PEA, 0.087 ± 0.01%·h-1; BLEND, 0.085 ± 0.01%·h-1), with no differences between groups (all; P > 0.05). These data show that all three nonanimal-derived protein sources have utility in supporting postexercise muscle reconditioning.NEW & NOTEWORTHY This study provides evidence that pea protein (PEA), mycoprotein (MYC), and their blend (BLEND) can support postexercise myofibrillar protein synthesis rates following a bout of whole body resistance exercise. Furthermore, these data suggest that a methionine deficiency in pea may not limit its capacity to stimulate an acute increase in muscle protein synthesis (MPS).en_GB
dc.description.sponsorshipNational Institute of Agingen_GB
dc.description.sponsorshipMarlow Foods Ltd.en_GB
dc.format.extentE267-E279
dc.identifier.citationVol. 325, No. 3, pp. E267-E279en_GB
dc.identifier.doihttps://doi.org/10.1152/ajpendo.00166.2023
dc.identifier.grantnumberP30- AG024832en_GB
dc.identifier.urihttp://hdl.handle.net/10871/134216
dc.identifierORCID: 0000-0001-6312-5351 (Stephens, Francis B)
dc.identifierORCID: 0000-0002-6019-6709 (Wall, Benjamin T)
dc.language.isoenen_GB
dc.publisherAmerican Physiological Societyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/37529834en_GB
dc.rights© 2023 The Authors. Open access. Licensed under Creative Commons Attribution CC-BY 4.0.en_GB
dc.subjectmuscle protein synthesisen_GB
dc.subjectmycoproteinen_GB
dc.subjectpea proteinen_GB
dc.subjectprotein blenden_GB
dc.subjectresistance exerciseen_GB
dc.titleIngestion of mycoprotein, pea protein, and their blend support comparable postexercise myofibrillar protein synthesis rates in resistance-trained individuals.en_GB
dc.typeArticleen_GB
dc.date.available2023-10-11T15:22:50Z
dc.identifier.issn0193-1849
exeter.place-of-publicationUnited States
dc.descriptionThis is the final version. Available on open access from the American Physiological Society via the DOI in this record. en_GB
dc.descriptionData availability: Data described in the manuscript may be made available upon request, pending application.en_GB
dc.identifier.eissn1522-1555
dc.identifier.journalAmerican Journal of Physiology Endocrinology and Metabolismen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2023-07-26
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2023-07-26
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2023-10-11T15:18:37Z
refterms.versionFCDVoR
refterms.dateFOA2023-10-11T15:22:51Z
refterms.panelAen_GB


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© 2023 The Authors. Open access. Licensed under Creative Commons Attribution CC-BY 4.0.
Except where otherwise noted, this item's licence is described as © 2023 The Authors. Open access. Licensed under Creative Commons Attribution CC-BY 4.0.