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DC Field | Value | Language |
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dc.contributor.author | Shulkes, Arthur | en |
dc.contributor.author | Englin, I | en |
dc.contributor.author | Read, D M | en |
dc.contributor.author | Hardy, Kenneth John | en |
dc.date.accessioned | 2015-05-16T02:41:39Z | |
dc.date.available | 2015-05-16T02:41:39Z | |
dc.date.issued | 1987-11-12 | en |
dc.identifier.citation | Peptides; 8(6): 961-5 | en |
dc.identifier.govdoc | 3126491 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/12931 | en |
dc.description.abstract | The 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.iso | en | en |
dc.subject.other | Animals | en |
dc.subject.other | Chromatography, High Pressure Liquid | en |
dc.subject.other | Female | en |
dc.subject.other | Kidney.metabolism | en |
dc.subject.other | Neurotensin.immunology.metabolism | en |
dc.subject.other | Pepsin A.pharmacology | en |
dc.subject.other | Rats | en |
dc.subject.other | Rats, Inbred Strains | en |
dc.title | Neurotensin metabolism in the rat: contribution of the kidney. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Peptides | en |
dc.identifier.affiliation | Department of Surgery, University of Melbourne, Austin Hospital, Victoria, Australia | en |
dc.description.pages | 961-5 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/3126491 | en |
dc.type.austin | Journal Article | en |
item.fulltext | No Fulltext | - |
item.openairetype | Journal Article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
Appears in Collections: | Journal articles |
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