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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/32566

Title: Resolvin E1 (RvE1) attenuates LPS induced inflammation and subsequent atrophy in C2C12 myotubes
Authors: Baker, Luke
Martin, Neil R.W.
Kimber, Marc C.
Pritchard, Gareth J.
Lindley, Martin R.
Lewis, Mark P.
Keywords: Specialised pro-resolving mediators
Skeletal muscle
Muscle ageing
Cytokines
Resolution
Omega-3 Fatty Acids
Issue Date: 2018
Publisher: © Wiley
Citation: BAKER, L. ...et al., 2018. Resolvin E1 (RvE1) attenuates LPS induced inflammation and subsequent atrophy in C2C12 myotubes. Journal of Cellular Biochemistry, 119 (7), pp.6094-6103.
Abstract: Resolution of inflammation is now known to be an active process which in part is instigated and controlled by specialised pro-resolving lipid mediators (SPM’s) derived from dietary omega-3 fatty acids. Resolvin E1 (RvE1) is one of these SPM’s derived from the omega-3 fatty acid eicosapentaenoic acid. Using both molecular and phenotypic functional measures we report that in a model of Lipopolysaccharide (LPS) induced inflammation, RvE1 attenuated mRNA gene expression levels of both interlukin-6 and monocyte chemoattractant protein-1 whilst having no effect on tumour necrosis factor-α or Interlukin-1β in C2C12 skeletal muscle myotubes. Findings at the molecular level were transferred into similar changes in extracellular protein levels of the corresponding genes with the greatest attenuation being noted in IL-6 protein concentrations. RvE1 instigated beneficial morphological changes through the prevention of endotoxin induced skeletal muscle atrophy, thus resulting in a rescue of endotoxin force losses in tissue engineered skeletal muscle. These findings demonstrate, in our model of endotoxin induced inflammation in skeletal muscle, that RvE1 has pro-resolving properties in this cell type. Our data provides rationale for further investigation into the mechanistic action of RvE1 in skeletal muscle, with the vision of having potential benefits for the prevention/resolution of in vivo skeletal muscle atrophy.
Description: This paper is in closed access until 25th Mar 2019.
Version: Accepted for publication
DOI: 10.1002/jcb.26807
URI: https://dspace.lboro.ac.uk/2134/32566
Publisher Link: https://doi.org/10.1002/jcb.26807
ISSN: 0730-2312
Appears in Collections:Closed Access (Sport, Exercise and Health Sciences)
Closed Access (Chemistry)

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