Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/13580
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dc.contributor.authorGilbert, Richard Een
dc.contributor.authorCox, Allison Jen
dc.contributor.authorWu, L Len
dc.contributor.authorAllen, Terri Jen
dc.contributor.authorHulthen, U Len
dc.contributor.authorJerums, Georgeen
dc.contributor.authorCooper, Mark Een
dc.date.accessioned2015-05-16T03:27:44Z
dc.date.available2015-05-16T03:27:44Z
dc.date.issued1998-03-01en
dc.identifier.citationDiabetes; 47(3): 414-22en
dc.identifier.govdoc9519748en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/13580en
dc.description.abstractTransforming growth factor-beta (TGF-beta) and the renin-angiotensin system (RAS) have both been implicated in the pathogenesis of glomerulosclerosis in diabetic kidney disease. However, tubulointerstitial pathology may also be an important determinant of progressive renal dysfunction in diabetic nephropathy. In the present study, we investigated tubulointerstitial injury, TGF-beta1 expression, and the effect of blocking the RAS by inhibition of ACE. We randomized 36 male SD rats to control and diabetic groups. Diabetes was induced in 24 rats by administration of streptozotocin; 12 diabetic rats were further randomized to receive the ACE inhibitor ramipril (3 mg/l drinking water). At 6 months, experimental diabetes was associated with tubulointerstitial damage, a 70% increase in expression of TGF-beta1 (P < 0.05 vs. control), and a 120% increase in alpha1 (IV) collagen gene expression (P < 0.01 vs. control). In situ hybridization demonstrated a diffuse increase in both TGF-beta1 and alpha1 (IV) collagen mRNA in renal tubules. In addition, intense expression of both transcripts was noted in regions of focal tubular dilatation. Administration of the ACE inhibitor ramipril prevented tubulointerstitial injury and the overexpression of TGF-beta1 and alpha1 (IV) collagen mRNA. Changes in gene expression were accompanied by parallel changes in immunostaining for TGF-beta1 and type IV collagen. The observed beneficial effects of ramipril on the tubulointerstitium in experimental diabetes suggest that this mechanism may contribute to the therapeutic effect of ACE inhibitors in diabetic nephropathy.en
dc.language.isoenen
dc.subject.otherAngiotensin-Converting Enzyme Inhibitors.pharmacology.therapeutic useen
dc.subject.otherAnimalsen
dc.subject.otherCohort Studiesen
dc.subject.otherCollagen.biosynthesis.classification.geneticsen
dc.subject.otherDiabetes Mellitus, Experimental.complicationsen
dc.subject.otherDiabetic Nephropathies.drug therapy.pathologyen
dc.subject.otherGene Expression Regulation, Developmental.geneticsen
dc.subject.otherImmunohistochemistryen
dc.subject.otherIn Situ Hybridizationen
dc.subject.otherKidney Tubules.chemistry.drug effects.pathologyen
dc.subject.otherMaleen
dc.subject.otherRNA, Messenger.analysis.geneticsen
dc.subject.otherRamipril.pharmacology.therapeutic useen
dc.subject.otherRandom Allocationen
dc.subject.otherRatsen
dc.subject.otherRats, Sprague-Dawleyen
dc.subject.otherRenin-Angiotensin System.drug effectsen
dc.subject.otherTransforming Growth Factor beta.biosynthesis.geneticsen
dc.titleExpression of transforming growth factor-beta1 and type IV collagen in the renal tubulointerstitium in experimental diabetes: effects of ACE inhibition.en
dc.typeJournal Articleen
dc.identifier.journaltitleDiabetesen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Austin and Repatriation Medical Centre, Heidelberg, Victoria, Australiaen
dc.description.pages414-22en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/9519748en
dc.type.austinJournal Articleen
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.languageiso639-1en-
crisitem.author.deptEndocrinology-
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