Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/13184
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dc.contributor.authorLiu, J Jen
dc.contributor.authorChen, J Ren
dc.contributor.authorBradley, C Jen
dc.contributor.authorXie, Ben
dc.contributor.authorJohnston, Colin Ien
dc.contributor.authorBuxton, Brian Fen
dc.date.accessioned2015-05-16T02:58:36Z
dc.date.available2015-05-16T02:58:36Z
dc.date.issued1994-09-01en
dc.identifier.citationCardiovascular Research; 28(9): 1353-9en
dc.identifier.govdoc7954645en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/13184en
dc.description.abstractSpasm of internal mammary artery is a problem during coronary artery bypass grafting. The mechanism is unknown. The aim of this study was to determine whether supernatants derived from neutrophils affected endothelium dependent relaxation of human internal mammary artery.The studies involved use of an organ chamber, measurement of cytosolic Ca2+, electron microscopy, and chemical characterisation.Autologous neutrophils and internal mammary artery were obtained from patients undergoing the bypass grafting. Supernatants derived from the neutrophils were used to treat the patients' internal mammary artery rings. The results showed that the supernatants derived from 1 x 10(3)-5 x 10(6) cells.ml-1 neutrophils produced a potent concentration dependent inhibition of the endothelium dependent relaxation to ATP, acetylcholine, and the calcium ionophore A23187, but not the endothelium independent relaxation to sodium nitroprusside. In cultured human endothelial cells, the neutrophil derived supernatants induced an increase in cytosolic calcium ([Ca2+]i), caused calcium oscillations, and desensitised the ATP induced increase in [Ca2+]i. The increased [Ca2+]i resulted from a calcium influx. The supernatants also induced an increase in vesicle formation and possibly exocytosis in the internal mammary artery endothelium. Chemical characterisation showed that the effect of the supernatants was caused by a factor that is stable to heat, extreme pH and protease, is negatively charged and weakly hydrophobic, and has a molecular weight under 500 Dalton.Autologous neutrophils release a stable non-protein small molecule that disturbs internal mammary artery endothelial function. Since it raises [Ca2+]i and causes possible exocytosis, it may have functions beyond its inhibition of vascular relaxation. This factor could be one of the contributors to internal mammary artery spasm and late atherosclerosis.en
dc.language.isoenen
dc.subject.otherAcetylcholine.pharmacologyen
dc.subject.otherAdenosine Triphosphate.pharmacologyen
dc.subject.otherBiological Factors.isolation & purification.pharmacology.secretionen
dc.subject.otherCalcimycin.pharmacologyen
dc.subject.otherCalcium.metabolismen
dc.subject.otherCells, Cultureden
dc.subject.otherCoronary Artery Bypassen
dc.subject.otherCytosol.drug effects.metabolismen
dc.subject.otherDose-Response Relationship, Drugen
dc.subject.otherEndothelium, Vascular.cytology.drug effectsen
dc.subject.otherExocytosis.drug effectsen
dc.subject.otherHumansen
dc.subject.otherIn Vitro Techniquesen
dc.subject.otherMammary Arteries.drug effectsen
dc.subject.otherNeutrophils.secretionen
dc.subject.otherNitroprusside.pharmacologyen
dc.titleAutologous neutrophil derived supernatants inhibit endothelium dependent relaxation in human coronary bypass graft.en
dc.typeJournal Articleen
dc.identifier.journaltitleCardiovascular researchen
dc.identifier.affiliationDepartment of Cardiac Surgery, University of Melbourne Austin Hospital, Heidelberg, Victoria, Australiaen
dc.description.pages1353-9en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/7954645en
dc.type.austinJournal Articleen
item.languageiso639-1en-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
crisitem.author.deptCardiac Surgery-
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