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dc.contributor.authorArmengol López, Sandra
dc.contributor.authorBotham, Kathleen M.
dc.contributor.authorLawson, Charlotte
dc.date.accessioned2012-04-17T18:05:12Z
dc.date.available2012-04-17T18:05:12Z
dc.date.issued2012
dc.identifier.citationInternational Journal of Vascular Medicine 2012 : (2012) // Article ID 942512es
dc.identifier.issn2090-2824 (Print)
dc.identifier.issn2090-2832 (Online)
dc.identifier.urihttp://hdl.handle.net/10810/7354
dc.description8 p.es
dc.description.abstractChylomicron remnants (CMRs) contribute directly to human monocyte activation in vitro, by increasing reactive oxygen species (ROS) production and cell migration. In this study, the effects of the oxidative state of CMR on the degree of monocyte activation was investigated. CMR-like particles (CRLPs) were prepared in three different oxidative states, normal (CRLPs), protected from oxidation by incorporation of the antioxidant, probucol (pCRLPs), or oxidised with CuSO4 (oxCRLPs). Lipid accumulation and ROS production were significantly increased in primary human monocytes incubated with CRLPs, whilst secretion on monocyte chemoattractant protein-1 was reduced, but oxCRLPs had no additional effect. In contrast, pCRLPs were taken up by monocytes to a lesser extent and had no significant effect on ROS or MCP-1 secretion. These studies suggest that the oxidative state of CMRs modulates their stimulation of the activation of peripheral blood human monocytes and that dietary antioxidants may provide some protection against these atherogenic effects.es
dc.language.isoenges
dc.publisherHindawi Publishing Corporationes
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.titleThe Oxidative State of Chylomicron Remnants Influences Their Modulation of Human Monocyte Activationes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holderCopyright © 2012 Sandra Armengol Lopez et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.es
dc.relation.publisherversionhttp://www.hindawi.com/journals/ijvm/2012/942512/es
dc.identifier.doi10.1155/2012/942512
dc.departamentoesFisiologíaes_ES
dc.departamentoeuFisiologiaes_ES
dc.subject.categoriaCARDIOLOGY AND CARDIOVASCULAR MEDICINE


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