Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/12468
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dc.contributor.authorShepherd, Sam Oen_UK
dc.contributor.authorCocks, Matthewen_UK
dc.contributor.authorTipton, Kevinen_UK
dc.contributor.authorRanasinghe, Aaron Men_UK
dc.contributor.authorBarker, Thomas Aen_UK
dc.contributor.authorBurniston, Jatin Gen_UK
dc.contributor.authorWagenmakers, Anton J Men_UK
dc.contributor.authorShaw, Christopher Sen_UK
dc.date.accessioned2016-08-30T00:02:02Z-
dc.date.available2016-08-30T00:02:02Zen_UK
dc.date.issued2012-08en_UK
dc.identifier.urihttp://hdl.handle.net/1893/12468-
dc.description.abstractThe lipid droplet (LD)-associated protein perilipin 2 (PLIN2) appears to colocalize with LDs in human skeletal muscle fibres, although the function of PLIN2 in the regulation of intramuscular triglyceride (IMTG) metabolism is currently unknown. Here we investigated the hypothesis that the presence of PLIN2 in skeletal muscle LDs is related to IMTG utilisation during exercise. We therefore measured exercise-induced changes in IMTG and PLIN2 distribution and changes in their colocalization. Muscle biopsies from the vastus lateralis were obtained from seven lean, untrained men (22±2 years old, body mass index 24.2±0.9 kgm-2 and peak oxygen uptake 3.35±0.13 l min-1) before and after 1 h of moderate-intensity cycling at ∼65% peak oxygen uptake. Cryosections were stained for perilipin 2, IMTG and myosin heavy chain type I and viewed using wide-field and confocal fluorescence microscopy. Exercise induced a 50±7% decrease in IMTG content in type I fibres only (P less than 0.05), but no change in PLIN2 content. Colocalization analysis showed that the fraction of PLIN2 associated with IMTG was 0.67±0.03 before exercise, which was reduced to 0.51±0.01 postexercise (P less than 0.05). Further analysis revealed that the number of PLIN2-associated LDs was reduced by 31±10% after exercise (P less than 0.05), whereas the number of PLIN2-null LDs was unchanged. No such changes were seen in type II fibres. In conclusion, this study shows that PLIN2 content in skeletal muscle is unchanged in response to a single bout of endurance exercise. Furthermore, the PLIN2 and IMTG association is reduced postexercise, apparently due to preferential utilization of PLIN2- associated LDs. These results confirm the hypothesis that the PLIN2 association with IMTG is related to the utilization of IMTG as a fuel during exercise.en_UK
dc.language.isoenen_UK
dc.publisherWiley-Blackwell for the Physiological Societyen_UK
dc.relationShepherd SO, Cocks M, Tipton K, Ranasinghe AM, Barker TA, Burniston JG, Wagenmakers AJM & Shaw CS (2012) Preferential utilization of perilipin 2-associated intramuscular triglycerides during 1 h of moderate-intensity endurance-type exercise. Experimental Physiology, 97 (8), pp. 970-980. https://doi.org/10.1113/expphysiol.2012.064592en_UK
dc.rightsThe publisher does not allow this work to be made publicly available in this Repository. Please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study.en_UK
dc.rights.urihttp://www.rioxx.net/licenses/under-embargo-all-rights-reserveden_UK
dc.subjectFatigue Case studiesen_UK
dc.titlePreferential utilization of perilipin 2-associated intramuscular triglycerides during 1 h of moderate-intensity endurance-type exerciseen_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate3000-01-01en_UK
dc.rights.embargoreason[Tipton_2012_Preferential_utilization_of_perilipin_2.pdf] The publisher does not allow this work to be made publicly available in this Repository therefore there is an embargo on the full text of the work.en_UK
dc.identifier.doi10.1113/expphysiol.2012.064592en_UK
dc.citation.jtitleExperimental Physiologyen_UK
dc.citation.issn1469-445Xen_UK
dc.citation.issn0958-0670en_UK
dc.citation.volume97en_UK
dc.citation.issue8en_UK
dc.citation.spage970en_UK
dc.citation.epage980en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.author.emailk.d.tipton@stir.ac.uken_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationSporten_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationLiverpool John Moores Universityen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.identifier.isiWOS:000306788000008en_UK
dc.identifier.scopusid2-s2.0-84864292963en_UK
dc.identifier.wtid709682en_UK
dc.contributor.orcid0000-0002-6545-8122en_UK
dcterms.dateAccepted2012-08-31en_UK
dc.date.filedepositdate2013-05-01en_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorShepherd, Sam O|en_UK
local.rioxx.authorCocks, Matthew|en_UK
local.rioxx.authorTipton, Kevin|0000-0002-6545-8122en_UK
local.rioxx.authorRanasinghe, Aaron M|en_UK
local.rioxx.authorBarker, Thomas A|en_UK
local.rioxx.authorBurniston, Jatin G|en_UK
local.rioxx.authorWagenmakers, Anton J M|en_UK
local.rioxx.authorShaw, Christopher S|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate3000-01-01en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved||en_UK
local.rioxx.filenameTipton_2012_Preferential_utilization_of_perilipin_2.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source0958-0670en_UK
Appears in Collections:Faculty of Health Sciences and Sport Journal Articles

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