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dc.contributor.authorAllan, Robert
dc.contributor.authorMorton, James P.
dc.contributor.authorClose, Graeme L.
dc.contributor.authorDrust, Barry
dc.contributor.authorGregson, Warren
dc.contributor.authorSharples, Adam
dc.date.accessioned2021-01-29T09:58:48Z
dc.date.available2021-01-29T09:58:48Z
dc.date.created2020-10-14T11:57:34Z
dc.date.issued2020
dc.identifier.citationEuropean Journal of Applied Physiology. 2020, 120(11), 2487-2493.en_US
dc.identifier.issn1439-6319
dc.identifier.urihttps://hdl.handle.net/11250/2725309
dc.descriptionOpen Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.description.abstractThis investigation sought to determine whether post-exercise cold water immersion and low glycogen availability, separately and in combination, would preferentially activate either the Exon 1a or Exon 1b Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) promoter. Through a reanalysis of sample design, we identified that the systemic cold-induced augmentation of total PGC-1α gene expression observed previously (Allan et al. in J Appl Physiol 123(2):451–459, 2017) was largely a result of increased expression from the alternative promoter (Exon 1b), rather than canonical promoter (Exon 1a). Low glycogen availability in combination with local cooling of the muscle (Allan et al. in Physiol Rep 7(11):e14082, 2019) demonstrated that PGC-1α alternative promoter (Exon 1b) expression continued to rise at 3 h post-exercise in all conditions; whilst, expression from the canonical promoter (Exon 1a) decreased between the same time points (post-exercise–3 h post-exercise). Importantly, this increase in PGC-1α Exon 1b expression was reduced compared to the response of low glycogen or cold water immersion alone, suggesting that the combination of prior low glycogen and CWI post-exercise impaired the response in gene expression versus these conditions individually. Data herein emphasise the influence of post-exercise cooling and low glycogen availability on Exon-specific control of total PGC-1 α gene expression and highlight the need for future research to assess Exon-specific regulation of PGC-1α.en_US
dc.language.isoengen_US
dc.subjectCWIen_US
dc.subjectPGC-1αen_US
dc.subjectexonen_US
dc.titlePGC-1α alternative promoter (Exon 1b) controls augmentation of total PGC-1α gene expression in response to cold water immersion and low glycogen availabilityen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber2487-2493en_US
dc.source.volume120en_US
dc.source.journalEuropean Journal of Applied Physiologyen_US
dc.source.issue11en_US
dc.identifier.doi10.1007/s00421-020-04467-6
dc.identifier.cristin1839484
dc.description.localcodeInstitutt for fysisk prestasjonsevne / Department of Physical Performanceen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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