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Characterising 24-h skeletal muscle gene expression alongside metabolic & endocrine responses under diurnal conditions.

cris.virtualsource.author-orcid19ea78ef-67c8-4518-83f3-3cff5e094637
datacite.rightsopen.access
dc.contributor.authorSmith, Harry A
dc.contributor.authorTempleman, Iain
dc.contributor.authorDavis, Max
dc.contributor.authorSlater, Tommy
dc.contributor.authorClayton, David J
dc.contributor.authorVarley, Ian
dc.contributor.authorJames, Lewis J
dc.contributor.authorMiddleton, Benita
dc.contributor.authorJohnston, Jonathan D
dc.contributor.authorKaragounis, Leonidas
dc.contributor.authorTsintzas, Kostas
dc.contributor.authorThompson, Dylan
dc.contributor.authorGonzalez, Javier T
dc.contributor.authorWalhin, Jean-Philippe
dc.contributor.authorBetts, James A
dc.date.accessioned2024-10-26T18:08:02Z
dc.date.available2024-10-26T18:08:02Z
dc.date.issued2025-03-17
dc.description.abstractCONTEXT Skeletal muscle plays a central role in the storage, synthesis, and breakdown of nutrients, yet little research has explored temporal responses of this human tissue, especially with concurrent measures of systemic biomarkers of metabolism. OBJECTIVE To characterise temporal profiles in skeletal muscle expression of genes involved in carbohydrate metabolism, lipid metabolism, circadian clocks, and autophagy and descriptively relate them to systemic metabolites and hormones during a controlled laboratory protocol. METHODS Ten healthy adults (9M/1F, mean ± SD: age: 30 ± 10 y; BMI: 24.1 ± 2.7 kg·m-2) rested in the laboratory for 37 hours with all data collected during the final 24 hours of this period (i.e., 0800-0800 h). Participants ingested hourly isocaloric liquid meal replacements alongside appetite assessments during waking before a sleep opportunity from 2200-0700 h. Blood samples were collected hourly for endocrine and metabolite analyses, with muscle biopsies occurring every 4 h from 1200 h to 0800 h the following day to quantify gene expression. RESULTS Plasma insulin displayed diurnal rhythmicity peaking at 1804 h. Expression of skeletal muscle genes involved in carbohydrate metabolism (Name - Acrophase; GLUT4 - 1440 h; PPARGC1A -1613 h; HK2 - 1824 h) and lipid metabolism (FABP3 - 1237 h; PDK4 - 0530 h; CPT1B - 1258 h) displayed 24 h rhythmicity that reflected the temporal rhythm of insulin. Equally, circulating glucose (0019 h), NEFA (0456 h), glycerol (0432 h), triglyceride (2314 h), urea (0046 h), CTX (0507 h) and cortisol concentrations (2250 h) also all displayed diurnal rhythmicity. CONCLUSION Diurnal rhythms were present in human skeletal muscle gene expression as well systemic metabolites and hormones under controlled diurnal conditions. The temporal patterns of genes relating to carbohydrate and lipid metabolism alongside circulating insulin are consistent with diurnal rhythms being driven in part by the diurnal influence of cyclic feeding and fasting.
dc.description.numberOfPages14
dc.description.sponsorshipInstitut für Sozial- und Präventivmedizin (ISPM)
dc.identifier.doi10.48350/197040
dc.identifier.pmid38779872
dc.identifier.publisherDOI10.1210/clinem/dgae350
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/177610
dc.language.isoen
dc.publisherOxford University Press
dc.relation.ispartofThe Journal of Clinical Endocrinology & Metabolism
dc.relation.issn0021-972X
dc.relation.organizationDCD5A442BECFE17DE0405C82790C4DE2
dc.subjectCircadian rhythms Diurnal Gene expression Glucose Lipids Skeletal muscle
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc300 - Social sciences, sociology & anthropology::360 - Social problems & social services
dc.titleCharacterising 24-h skeletal muscle gene expression alongside metabolic & endocrine responses under diurnal conditions.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
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oaire.citation.endPagee1030
oaire.citation.issue4
oaire.citation.startPagee1017
oaire.citation.volume110
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
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unibe.date.licenseChanged2024-05-24 18:53:23
unibe.description.ispublishedpub
unibe.eprints.legacyId197040
unibe.journal.abbrevTitleJ CLIN ENDOCR METAB
unibe.refereedtrue
unibe.subtype.articlejournal

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