Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/13550
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dc.contributor.authorDean, Rachael Gen
dc.contributor.authorMurone, Carmelen
dc.contributor.authorLew, R Aen
dc.contributor.authorZhuo, Jen
dc.contributor.authorCasley, David Jen
dc.contributor.authorMüller-Esterl, Wen
dc.contributor.authorAlcorn, Den
dc.contributor.authorMendelsohn, Frederick AOen
dc.date.accessioned2015-05-16T03:25:38Z
dc.date.available2015-05-16T03:25:38Z
dc.date.issued1997-11-01en
dc.identifier.citationKidney International; 52(5): 1261-70en
dc.identifier.govdoc9350649en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/13550en
dc.description.abstractBradykinin exerts important influences on renal hemodynamics and tubular function by acting on renal bradykinin B2 receptors. However, the precise sites and mechanisms of its actions on the kidney are not known. To help elucidate the mechanisms of renal actions of bradykinin in vivo, we have employed high resolution electron microscopic autoradiography to localize bradykinin B2 binding sites in the rat kidney following intravenous administration of a radiolabeled ligand, 125I-HPP-Hoe140 (3-4-Hydroxyphenyl-propionyl-DArg0-[Hyp3-Thi5-D-Tic 7-Oic8]-bradykinin), a derivative of the highly selective bradykinin B2 receptor antagonist, Hoe140. In non-treated rats, bradykinin B2 binding sites were localized to the cell bodies and the luminal brush border of the proximal convoluted tubules in the cortex. In the medulla (except for the outer stripe of the outer medulla), binding occurred in the distal tubules, thin limbs of the loop of Henle, collecting ducts, peritubular capillary endothelium and renomedullary interstitial cells. To exclude the possibility that the radioligand may bind to angiotensin converting enzyme, rats were pretreated with the angiotensin converting enzyme inhibitor, perindopril. In these rats, binding to the cell bodies and the luminal brush border of the proximal convoluted tubules in the cortex was completely abolished, while binding remained unaltered in the medulla. Further studies using high performance liquid chromatography revealed that while the radioligand was degraded following systemic administration in nontreated rats, the degradation was significantly reduced in the rats pretreated chronically with perindopril. These results indicate that binding detected in the proximal tubules in the normal rats is due primarily to the tubular uptake of the degraded radioligand, and that bradykinin B2 binding sites occur predominantly in the renal tubules, vascular endothelium, and renomedullary interstitial cells of the renal medulla.en
dc.language.isoenen
dc.subject.otherAngiotensin-Converting Enzyme Inhibitors.pharmacologyen
dc.subject.otherAnimalsen
dc.subject.otherAutoradiographyen
dc.subject.otherBinding Sitesen
dc.subject.otherBradykinin.analogs & derivatives.metabolismen
dc.subject.otherIodine Radioisotopes.diagnostic useen
dc.subject.otherKidney.chemistryen
dc.subject.otherMaleen
dc.subject.otherRatsen
dc.subject.otherRats, Sprague-Dawleyen
dc.subject.otherReceptor, Bradykinin B2en
dc.subject.otherReceptors, Bradykinin.analysisen
dc.titleLocalization of bradykinin B2 binding sites in rat kidney following chronic ACE inhibitor treatment.en
dc.typeJournal Articleen
dc.identifier.journaltitleKidney Internationalen
dc.identifier.affiliationUniversity of Melbourne, Department of Medicine, Austin, Heidelberg, Australiaen
dc.description.pages1261-70en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/9350649en
dc.type.austinJournal Articleen
local.name.researcherMurone, Carmel
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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