Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/13620
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dc.contributor.authorWookey, Peter Jen
dc.contributor.authorCooper, Mark Een
dc.date.accessioned2015-05-16T03:30:33Z
dc.date.available2015-05-16T03:30:33Z
dc.date.issued1998-09-01en
dc.identifier.citationClinical and Experimental Pharmacology & Physiology; 25(9): 653-60en
dc.identifier.govdoc9750952en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/13620en
dc.description.abstract1. There are high-affinity binding sites for amylin in the renal cortex associated with proximal tubules. These appear to represent seven transmembrane (heptatopic) receptors that are known to form ternary complexes with G-proteins and activate second messenger systems. 2. Amylin stimulates sodium/water reabsorption from the basolateral side of the proximal tubules and plays a role in sodium homeostasis. 3. The transient expression of amylin-like mRNA has been detected perinatally, using in situ hybridization, in the subnephrogenic zone of the metanephros and is associated with proximal tubules of the developing nephron. There it is thought to play a role as a growth factor for brush border epithelial cells in the developing kidney and in renal regrowth in the adult kidney. 4. In two models of hypertension, the spontaneously hypertensive rat (SHR) and one created surgically by subtotal nephrectomy, renal amylin receptors are activated. In the SHR, activation precedes the rise in blood pressure and suggests that activation of the amylin system may be an important event in the development of hypertension.en
dc.language.isoenen
dc.subject.otherAmyloid.biosynthesis.physiologyen
dc.subject.otherAnimalsen
dc.subject.otherHumansen
dc.subject.otherHypertension, Renal.metabolism.physiopathologyen
dc.subject.otherIslet Amyloid Polypeptideen
dc.subject.otherKidney.metabolism.physiologyen
dc.subject.otherRatsen
dc.subject.otherRats, Inbred SHRen
dc.titleAmylin: physiological roles in the kidney and a hypothesis for its role in hypertension.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical and Experimental Pharmacology & Physiologyen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Austin & Repatriation Medical Centre, West Heidelberg, Victoria, Australiaen
dc.description.pages653-60en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/9750952en
dc.type.austinJournal Articleen
local.name.researcherWookey, Peter J
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptMedicine (University of Melbourne)-
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