Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9494
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dc.contributor.authorKubota, Eijien
dc.contributor.authorDean, Rachael Gen
dc.contributor.authorHubner, Richard Aen
dc.contributor.authorCasley, David Jen
dc.contributor.authorJohnston, Colin Ien
dc.contributor.authorBurrell, Louise Men
dc.date.accessioned2015-05-15T22:36:34Z
dc.date.available2015-05-15T22:36:34Z
dc.date.issued2003-09-01en
dc.identifier.citationClinical Science 2003; 105(3): 339-45en
dc.identifier.govdoc12741953en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9494en
dc.description.abstractVasopeptidase inhibitors simultaneously inhibit angiotensin-converting enzyme (ACE) and neutral endopeptidase (NEP). The present study characterized the tissue distributions of ACE and NEP, and assessed the effects of the vasopeptidase inhibitor omapatrilat on ACE and NEP in rat tissues. In vivo ACE and NEP inhibition was studied by in vitro autoradiography and using the ACE inhibitor radioligand (125)I-MK351A and the NEP inhibitor radioligand (125)I-RB104 in rats that received oral omapatrilat (40 mg x day(-1) x kg(-1)) for 3 days. In vitro autoradiography was used to examine the distribution of ACE and NEP in the kidney, aorta, heart, adrenal gland, lung, intestine, liver, spleen and brain, and to assess enzyme inhibition after oral omapatrilat. Omapatrilat inhibited plasma ACE and increased plasma renin activity (P <0.01). Tissue ACE was inhibited by 70-95% (P <0.01), except in the brain, where ACE was not inhibited. NEP was inhibited by 87% in the kidney and by 20-40% in atria, aorta, adrenal gland, lung, liver and intestine; it was not inhibited in the brain, the ventricle or the spleen. Omapatrilat is a potent vasopeptidase inhibitor that significantly inhibits tissue ACE and NEP, with the degree of inhibition varying according to the enzyme and the tissue under assessment. The degree and site of tissue enzyme inhibition by vasopeptidase inhibitors may be relevant to end-organ protection as well as to the side-effect profiles of these agents.en
dc.language.isoenen
dc.subject.otherAdministration, Oralen
dc.subject.otherAdrenal Glands.enzymologyen
dc.subject.otherAngiotensin-Converting Enzyme Inhibitors.pharmacologyen
dc.subject.otherAnimalsen
dc.subject.otherAorta.enzymologyen
dc.subject.otherAutoradiographyen
dc.subject.otherBrain.enzymologyen
dc.subject.otherHeart Atria.enzymologyen
dc.subject.otherIntestines.enzymologyen
dc.subject.otherIodine Radioisotopes.diagnostic useen
dc.subject.otherKidney.enzymologyen
dc.subject.otherLiver.enzymologyen
dc.subject.otherLung.enzymologyen
dc.subject.otherMaleen
dc.subject.otherNeprilysin.analysis.antagonists & inhibitorsen
dc.subject.otherPeptidyl-Dipeptidase A.analysis.blooden
dc.subject.otherPyridines.pharmacologyen
dc.subject.otherRatsen
dc.subject.otherRats, Sprague-Dawleyen
dc.subject.otherRenin.blooden
dc.subject.otherThiazepines.pharmacologyen
dc.titleDifferential tissue and enzyme inhibitory effects of the vasopeptidase inhibitor omapatrilat in the rat.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical Scienceen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Austin, Victoria 3084, Australiaen
dc.identifier.doi10.1042/CS20030097en
dc.description.pages339-45en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/12741953en
dc.type.austinJournal Articleen
local.name.researcherBurrell, Louise M
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptCardiology-
crisitem.author.deptGeneral Medicine-
crisitem.author.deptMedicine (University of Melbourne)-
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