Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12931
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dc.contributor.authorShulkes, Arthuren
dc.contributor.authorEnglin, Ien
dc.contributor.authorRead, D Men
dc.contributor.authorHardy, Kenneth Johnen
dc.date.accessioned2015-05-16T02:41:39Z
dc.date.available2015-05-16T02:41:39Z
dc.date.issued1987-11-12en
dc.identifier.citationPeptides; 8(6): 961-5en
dc.identifier.govdoc3126491en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12931en
dc.description.abstractThe kidney plays a key role in the metabolism of neurotensin (NT). We have examined the renal mechanisms of NT clearance by measuring plasma NT basally and after 45 min infusion of NT(1-13) in intact rats, anephric rats (no glomerular filtration, no peritubular metabolism) and ureteral ligated rats (reduced filtration). Plasma NT was measured by radioimmunoassay with both C (biologically active end) and N terminal directed antisera. In anephric and ureteral ligated rats, basal plasma NT like immunoreactivity measured with either antisera was increased 3-fold compared with unoperated rats. C terminal concentrations were higher than N indicating that a C terminal variant of NT was present in basal plasma. Infusion of NT(1-13) increased N terminal NT from 36 +/- 3 to 249 +/- 35 pmol/l (p less than 0.01) in unoperated rats with significantly larger increases in the renally compromised groups. This was reflected in the reduced metabolic clearance rates (measured with the N terminal directed antisera) in the anephric (16 +/- 1 ml/kg/min) and ureteral ligated (17 +/- 3 ml/kg/min) rats when compared with the control rats (26 +/- 4 ml/kg/min). The similar reductions in the anephric and ureteral ligated rats suggested that the decrease in N terminal NT metabolism was from the absence of filtration. Infusion of NT did not increase C terminal NT immunoreactivity in intact, anephric and ureteral ligated rats showing that the C terminal end was extremely labile. However when endogenous converting enzyme activity was blocked by captopril administration there was a significant increase in C terminal immunoreactivity suggesting a role for converting enzyme like proteases in the clearance of the biologically active end of NT.(ABSTRACT TRUNCATED AT 250 WORDS)en
dc.language.isoenen
dc.subject.otherAnimalsen
dc.subject.otherChromatography, High Pressure Liquiden
dc.subject.otherFemaleen
dc.subject.otherKidney.metabolismen
dc.subject.otherNeurotensin.immunology.metabolismen
dc.subject.otherPepsin A.pharmacologyen
dc.subject.otherRatsen
dc.subject.otherRats, Inbred Strainsen
dc.titleNeurotensin metabolism in the rat: contribution of the kidney.en
dc.typeJournal Articleen
dc.identifier.journaltitlePeptidesen
dc.identifier.affiliationDepartment of Surgery, University of Melbourne, Austin Hospital, Victoria, Australiaen
dc.description.pages961-5en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/3126491en
dc.type.austinJournal Articleen
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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