Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11407
Full metadata record
DC FieldValueLanguage
dc.contributor.authorBurrell, Louise Men
dc.contributor.authorBurchill, Luke Jen
dc.contributor.authorDean, Rachael Gen
dc.contributor.authorGriggs, Karenen
dc.contributor.authorPatel, Sheila Ken
dc.contributor.authorVelkoska, Elenaen
dc.date.accessioned2015-05-16T00:59:53Z
dc.date.available2015-05-16T00:59:53Z
dc.date.issued2011-12-23en
dc.identifier.citationExperimental Physiology 2011; 97(4): 477-85en
dc.identifier.govdoc22198016en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/11407en
dc.description.abstractRenin-angiotensin system blockade slows but does not prevent the cardiovascular complications of chronic kidney disease (CKD). Angiotensin-converting enzyme (ACE) 2 is differentially regulated in acute kidney injury, with increased cardiac ACE2 but decreased kidney ACE2 levels. This study investigated the effect of long-term ACE inhibition on cardiac and renal ACE2 in rats with CKD induced by subtotal nephrectomy (STNx). Sprague-Dawley rats had sham (control) or STNx surgery. Control rats received vehicle (n = 9) and STNx rats ramipril (1 mg kg(-1) day(-1); n = 10) or vehicle (n = 10) for 28 days. Subtotal nephrectomy resulted in impaired creatinine clearance (P < 0.05), proteinuria (P < 0.05), renal fibrosis (P < 0.05) and reduced renal cortical ACE2 mRNA (P < 0.05) and activity (P < 0.05). In rats with CKD, ramipril improved creatinine clearance (P < 0.05) and was associated with an increase in cortical but not medullary ACE2 activity (P < 0.05). Compared with control rats, STNx rats were hypertensive (P < 0.01), with increased left ventricular end-diastolic pressure (LVEDP; P < 0.01), left ventricular hypertrophy (LVH; P < 0.05) and interstitial (P < 0.05) and perivascular fibrosis (P < 0.01). In rats with CKD, ramipril decreased blood pressure (P < 0.001) and reduced LVEDP (P < 0.01), LVH (P < 0.01) and perivascular fibrosis (P < 0.05) but did not significantly reduce interstitial fibrosis. There was no change in cardiac ACE2 in rats with CKD compared with control rats. In rats with CKD, ACE inhibition had major benefits to reduce blood pressure and cardiac hypertrophy and to improve creatinine clearance, but did not significantly impact on cardiac ACE2, cardiac interstitial fibrosis, renal fibrosis or proteinuria. Thus, in rats with CKD, renal ACE2 deficiency and lack of activation of cardiac ACE2 may contribute to the progression of cardiac and renal tissue injury. As long-term ACE inhibition only partly ameliorated the adverse cardio-renal effects of CKD, adjunctive therapies that lead to further increases in ACE2 activity may be needed to combat the cardio-renal complications of CKD.en
dc.language.isoenen
dc.subject.otherAngiotensin-Converting Enzyme Inhibitors.pharmacology.therapeutic useen
dc.subject.otherAnimalsen
dc.subject.otherGene Expression Regulation, Enzymologicen
dc.subject.otherHypertension.drug therapy.enzymologyen
dc.subject.otherHypertrophy, Left Ventricular.drug therapy.enzymologyen
dc.subject.otherKidney Failure, Chronic.drug therapy.enzymologyen
dc.subject.otherMyocardium.metabolism.pathologyen
dc.subject.otherNephrectomyen
dc.subject.otherPeptidyl-Dipeptidase A.biosynthesis.deficiency.geneticsen
dc.subject.otherRamipril.pharmacology.therapeutic useen
dc.subject.otherRatsen
dc.subject.otherRats, Sprague-Dawleyen
dc.subject.otherTreatment Outcomeen
dc.titleChronic kidney disease: cardiac and renal angiotensin-converting enzyme (ACE) 2 expression in rats after subtotal nephrectomy and the effect of ACE inhibition.en
dc.typeJournal Articleen
dc.identifier.journaltitleExperimental physiologyen
dc.identifier.affiliationDepartment of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1113/expphysiol.2011.063156en
dc.description.pages477-85en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/22198016en
dc.type.austinJournal Articleen
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
crisitem.author.deptCardiology-
crisitem.author.deptGeneral Medicine-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptMedicine (University of Melbourne)-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

4
checked on Jan 26, 2023

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.