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dc.contributor.authorLautridou, Jacky
dc.contributor.authorPichereau, Vianney
dc.contributor.authorArtigaud, Sébastien
dc.contributor.authorBernay, Benoit
dc.contributor.authorBarak, Otto
dc.contributor.authorHoiland, Ryan
dc.contributor.authorLovering, Andrew T
dc.contributor.authorEftedal, Ingrid
dc.contributor.authorDujic, Zeljko
dc.contributor.authorGuerrero, François
dc.date.accessioned2017-06-06T07:48:57Z
dc.date.available2017-06-06T07:48:57Z
dc.date.created2017-04-20T15:03:02Z
dc.date.issued2017
dc.identifier.issn1862-8354
dc.identifier.urihttp://hdl.handle.net/11250/2444376
dc.description.abstractPurpose: Decompression sickness (DCS) is a poorly understood and complex systemic disease caused by inadequate desaturation following a reduction of ambient pressure. A previous proteomic study of ours showed that DCS occurrence but not diving was associated with changes in the plasma proteome in rats, including a dramatic decrease of abundance of the tetrameric form of Transthyretin (TTR). The present study aims to assess the impact on the human blood proteome of a dive inducing significant decompression stress but without inducing DCS symptoms. Experimental design: Twelve healthy male divers were subjected to a single dive at a depth of 18m of sea water (msw) with a 47-min bottom time followed by a direct ascent to the surface at a rate of 9msw/min. Venous blood was collected before the dive as well as 30mn and 2h following the dive. The plasma proteomes from four individuals were then analyzed by using a two-dimensional electrophoresis-based proteomic strategy. Results: No protein spot showed a significantly changed abundance (fdr< 0.1) between the tested times. Conclusion: These results strengthen the hypothesis according to which significant changes of the plasma proteome measurable with two-dimensional electrophoresis may only occur along with DCS symptoms.nb_NO
dc.language.isoengnb_NO
dc.publisherWileynb_NO
dc.titleEvolution of the plasma proteome of divers before and after a single SCUBA divenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.source.journalPROTEOMICS - Clinical Applicationsnb_NO
dc.identifier.doi10.1002/prca.201700016
dc.identifier.cristin1465755
dc.description.localcode© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the authors' accepted and refereed manuscript to the article. Locked until 12 May 2018 due to copyright restrictionsnb_NO
cristin.unitcode194,65,25,0
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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