Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10884
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dc.contributor.authorRai, Sudarshan-
dc.contributor.authorHare, David L-
dc.contributor.authorZulli, Anthony-
dc.date.accessioned2015-05-16T00:27:42Z
dc.date.available2015-05-16T00:27:42Z
dc.date.issued2009-09-15en
dc.identifier.citationInternational Journal of Experimental Pathology 2009; 90(6): 598-604en
dc.identifier.govdoc19758419en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/10884en
dc.description.abstractA physiological atherogenic human diet consists of 0.1% cholesterol, fat, as well as high levels of methionine, which is the precursor to homocysteine. The pathological effects of a diet enriched with physiologically high levels of cholesterol, methionine and fat over a short period on the aorta are unknown. In this regard, we sought to determine the effects of a 0.1% cholesterol diet in combination with a 1% methionine over a 4-week period on endothelial function and artery pathology and the expression of endothelial nitric oxide synthase as well as nitrosative stress by nitrotyrosine (NT), oxidative stress by heat shock protein 70 (HSP70) and endoplasmic reticulum stress by glucose regulated protein 78 (GRP78). Rabbits were fed for 4 weeks a diet supplemented with 1% methionine + 0.1% cholesterol + 5% peanut oil (MC). The endothelial function of the abdominal aorta was examined using organ bath techniques, atherosclerosis determined in each artery by microscopy and eNOS, NT, GRP78 and HSP70 by standard immunohistochemistry. Endothelium dependent relaxation in response to acetylcholine significantly decreased by 63% at 1 muM acetylcholine (P < 0.001) compared with control arteries. There was no evidence of atherosclerosis formation in any artery studied, however, eNOS, NT and GRP78 was clearly present in all arteries studied but HSP70 was not easily detectable. Severe endothelial dysfunction is present in the abdominal aorta of rabbits within 4 weeks of physiological dietary manipulation, possibly due to NT formation and endoplasmic reticulum stress. This model could be used to study the early onset of endothelial dysfunction prior to the initiation of atherosclerosis.en
dc.language.isoenen
dc.subject.otherAcetylcholine.administration & dosageen
dc.subject.otherAnimalsen
dc.subject.otherAorta, Abdominal.pathology.physiopathologyen
dc.subject.otherAortic Diseases.etiology.pathology.physiopathologyen
dc.subject.otherCholesterol.blooden
dc.subject.otherCholesterol, Dietaryen
dc.subject.otherDiet, Atherogenicen
dc.subject.otherDose-Response Relationship, Drugen
dc.subject.otherEndoplasmic Reticulum.metabolismen
dc.subject.otherEndothelium, Vascular.drug effects.pathology.physiopathologyen
dc.subject.otherHSP70 Heat-Shock Proteins.metabolismen
dc.subject.otherHeat-Shock Proteins.metabolismen
dc.subject.otherMaleen
dc.subject.otherMethionine.administration & dosageen
dc.subject.otherNitric Oxide Synthase Type III.metabolismen
dc.subject.otherRabbitsen
dc.subject.otherSeverity of Illness Indexen
dc.subject.otherTime Factorsen
dc.subject.otherTyrosine.analogs & derivatives.metabolismen
dc.subject.otherVasodilator Agents.administration & dosageen
dc.titleA physiologically relevant atherogenic diet causes severe endothelial dysfunction within 4 weeks in rabbit.en
dc.typeJournal Articleen
dc.identifier.journaltitleInternational journal of experimental pathologyen
dc.identifier.affiliationDepartments of Cardiology and Medicine, University of Melbourne, Austin Health, Australiaen
dc.identifier.doi10.1111/j.1365-2613.2009.00668.xen
dc.description.pages598-604en
dc.identifier.orcid0000-0001-9554-6556-
dc.identifier.pubmedid19758419-
dc.type.austinJournal Articleen
local.name.researcherHare, David L
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
crisitem.author.deptCardiology-
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