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dc.contributor.authorCivil, Rita
dc.contributor.authorBrook, Matthew S.
dc.contributor.authorSantos, Lívia
dc.contributor.authorVarley, Ian
dc.contributor.authorElliott-Sale, Kirsty J.
dc.contributor.authorLensu, Sanna
dc.contributor.authorAhtiainen, Juha P.
dc.contributor.authorKainulainen, Heikki
dc.contributor.authorKoch, Lauren G.
dc.contributor.authorBritton, Steven L.
dc.contributor.authorWilkinson, Daniel J.
dc.contributor.authorSmith, Kenneth
dc.contributor.authorAtherton, Philip J.
dc.contributor.authorSale, Craig
dc.date.accessioned2024-09-24T09:08:27Z
dc.date.available2024-09-24T09:08:27Z
dc.date.issued2024
dc.identifier.citationCivil, R., Brook, M. S., Santos, L., Varley, I., Elliott-Sale, K. J., Lensu, S., Ahtiainen, J. P., Kainulainen, H., Koch, L. G., Britton, S. L., Wilkinson, D. J., Smith, K., Atherton, P. J., & Sale, C. (2024). The effects of endurance trainability phenotype, sex, and interval running training on bone collagen synthesis in adult rats. <i>Bone</i>, <i>189</i>, Article 117257. <a href="https://doi.org/10.1016/j.bone.2024.117257" target="_blank">https://doi.org/10.1016/j.bone.2024.117257</a>
dc.identifier.otherCONVID_243148853
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/97181
dc.description.abstractBone is influenced by many factors such as genetics and mechanical loading, but the short-term physiological effects of these factors on bone (re)modelling are not well characterised. This study investigated the effects of endurance trainability phenotype, sex, and interval running training (7-week intervention) on bone collagen formation in rats using a deuterium oxide stable isotope tracer method. Bone samples of the femur diaphysis, proximal tibia, mid-shaft tibia, and distal tibia were collected after necropsy from forty-six 9 ± 3-month male and female rats selectively bred for yielding low (LRT) or high (HRT) responses to endurance training. Bone collagen proteins were isolated and hydrolysed, and fractional synthetic rates (FSRs) were determined by the incorporation of deuterium into protein-bound alanine via GC-pyrolysis-IRMS. There was a significant large main effect of phenotype at the femur site (p < 0.001; η2g = 0.473) with HRT rats showing greater bone collagen FSRs than LRT rats. There was a significant large main effect of phenotype (p = 0.008; η2g = 0.178) and a significant large main effect of sex (p = 0.005; η2g = 0.196) at the proximal site of the tibia with HRT rats showing greater bone collagen FSRs than LRT rats, and male rats showing greater bone collagen FSRs compared to female rats. There was a significant large main effect of training at the mid-shaft site of the tibia (p = 0.012; η2g = 0.159), with rats that underwent interval running training having greater bone collagen FSRs than control rats. Similarly, there was a significant large main effect of training at the distal site of the tibia (p = 0.050; η2g = 0.156), with rats in the interval running training group having greater bone collagen FSRs compared to rats in the control group. Collectively, this evidence highlights that bone responses to physiological effects are site-specific, indicating that interval running training has positive effects on bone collagen synthesis at the tibial mid-shaft and distal sites, whilst genetic factors affect bone collagen synthesis at the femur diaphysis (phenotype) and proximal tibia (phenotype and sex) in rats.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesBone
dc.rightsCC BY-NC 4.0
dc.subject.otherbone
dc.subject.othercollagen
dc.subject.otherexercise
dc.subject.othersex differences
dc.subject.otherdeuterium oxide tracer
dc.subject.othergene expression
dc.titleThe effects of endurance trainability phenotype, sex, and interval running training on bone collagen synthesis in adult rats
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202409246059
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosPsykologian laitosfi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.laitosDepartment of Psychologyen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn8756-3282
dc.relation.volume189
dc.type.versionpublishedVersion
dc.rights.copyright© 2024 The Authors. Published by Elsevier Inc.
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber355392
dc.relation.grantnumber321522
dc.subject.ysoluu
dc.subject.ysogeneettiset tekijät
dc.subject.ysosukupuolierot
dc.subject.ysokollageenit
dc.subject.ysoympäristötekijät
dc.subject.ysogeeniekspressio
dc.subject.ysointervalliharjoittelu
dc.subject.ysokestävyysharjoittelu
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p24244
jyx.subject.urihttp://www.yso.fi/onto/yso/p21661
jyx.subject.urihttp://www.yso.fi/onto/yso/p5290
jyx.subject.urihttp://www.yso.fi/onto/yso/p8590
jyx.subject.urihttp://www.yso.fi/onto/yso/p6194
jyx.subject.urihttp://www.yso.fi/onto/yso/p25831
jyx.subject.urihttp://www.yso.fi/onto/yso/p27766
jyx.subject.urihttp://www.yso.fi/onto/yso/p7676
dc.rights.urlhttps://creativecommons.org/licenses/by-nc/4.0/
dc.relation.doi10.1016/j.bone.2024.117257
dc.relation.funderResearch Council of Finlanden
dc.relation.funderResearch Council of Finlanden
dc.relation.funderSuomen Akatemiafi
dc.relation.funderSuomen Akatemiafi
jyx.fundingprogramAcademy Project, AoFen
jyx.fundingprogramAcademy Project, AoFen
jyx.fundingprogramAkatemiahanke, SAfi
jyx.fundingprogramAkatemiahanke, SAfi
jyx.fundinginformationThis work was completed as part of the PhD programme of work for RC, for which she received funding from the Nottingham Trent University Vice Chancellors Studentship Scheme. SL has received funding from the Academy of Finland, and currently the Research Council of Finland (decisions 321522 and 355392). Animal samples used in this analysis were a gift from the University of Michigan. This work was also supported by the UK MRC (grant no. MR/P021220/1) as part of the MRC-ARUK Centre for Musculoskeletal Ageing Research awarded to the Universities of Nottingham and Birmingham and supported by the National Institute of Health Research (NIHR) Nottingham Biomedical Research Centre.
dc.type.okmA1


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