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dc.contributor.authorHarrington, L.S.
dc.contributor.authorLundberg, M.H.
dc.contributor.authorWaight, M.
dc.contributor.authorRozario, A.
dc.contributor.authorMitchell, J.A.
dc.date.accessioned2013-04-24T14:55:03Z
dc.date.available2013-04-24T14:55:03Z
dc.date.issued2011-05-20
dc.identifier.citationHarrington , L S , Lundberg , M H , Waight , M , Rozario , A & Mitchell , J A 2011 , ' Reduced endothelial dependent vasodilation in vessels from TLR4 mice is associated with increased superoxide generation ' , Biochemical and Biophysical Research Communications , vol. 408 , no. 4 , pp. 511-515 . https://doi.org/10.1016/j.bbrc.2011.04.024
dc.identifier.issn0006-291X
dc.identifier.otherPURE: 1744570
dc.identifier.otherPURE UUID: fdf0a817-02d8-49bb-93b1-d49898c9133f
dc.identifier.otherScopus: 79956201256
dc.identifier.urihttp://hdl.handle.net/2299/10518
dc.descriptionMEDLINE® is the source for the MeSH terms of this document.
dc.description.abstractToll like receptor (TLR)4 is a pattern recognition receptor expressed in endothelial and other cells, responsible for the sensing of endotoxin and host derived ligands. Our group has shown previously that the absence of TLR4 is associated with reduced endothelial dependent vasodilator responses and left heart hypertrophy in animal models. However, the mechanism behind reduced endothelial cell function in TLR4 mice is not known. We have used en face confocal imaging of mesenteric arteries from mice deficient in the TLR4 receptor stained with dihydroethidium (DHE) to measure superoxide production. Using the isometric wire myograph, mesenteric artery vasodilator responses to acetylcholine and MnCl (a superoxide dismutase mimetic) were measured. Mesenteric arteries from TLR4 mice had a reduced endothelial dependent relaxant response and increased superoxide levels when stimulated with acetylcholine. Increased levels of superoxide, as detected by DHE staining, were seen in vessels from TLR4 mice, which were reduced to control levels in the presence of MnCl. Our observations suggest that loss of TLR4 increases superoxide generation which reduces the biological activity of endothelial derived nitric oxide and thereby explains the endothelial dysfunction and associated cardiovascular phenotype in TLR4 mice. These data implicate a novel cardio-protective role for TLR4 in vascular homeostasis.en
dc.format.extent5
dc.language.isoeng
dc.relation.ispartofBiochemical and Biophysical Research Communications
dc.titleReduced endothelial dependent vasodilation in vessels from TLR4 mice is associated with increased superoxide generationen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.contributor.institutionDepartment of Human and Environmental Sciences
dc.contributor.institutionPharmacology and Clinical Science Research
dc.contributor.institutionAgriculture, Veterinary and Food Sciences
dc.contributor.institutionCardiovascular Pathologies
dc.contributor.institutionDiabetic neuropathies
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=79956201256&partnerID=8YFLogxK
rioxxterms.versionVoR
rioxxterms.versionofrecordhttps://doi.org/10.1016/j.bbrc.2011.04.024
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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