Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/11223
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jackson, B | - |
dc.contributor.author | Fabris, Bruno | - |
dc.contributor.author | Paxton, D | - |
dc.contributor.author | Franze, L | - |
dc.contributor.author | Johnston, Colin I | - |
dc.date.accessioned | 2015-05-16T00:48:42Z | |
dc.date.available | 2015-05-16T00:48:42Z | |
dc.date.issued | 1990-03-01 | - |
dc.identifier.citation | Clinical and Experimental Pharmacology & Physiology; 17(3): 229-34 | en_US |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/11223 | en |
dc.description.abstract | 1. To dissociate the effects on the development of diabetic renal injury of angiotensin converting enzyme (ACE) inhibition per se, and a reduction in systemic blood pressure, we have studied the effects of chronic ramapril treatment in streptozotocin diabetic spontaneously hypertensive rats, with modulation of the hypotensive effect by a high salt diet. 2. Three weeks following uninephrectomy and induction of diabetes with streptozotocin, spontaneously hypertensive rats were allocated to three treatment groups. Groups 1 and 2 received 1% sodium chloride and Group 3 water as drinking solution. Groups 2 and 3 received 0.4 mg/kg per day ramapril in drinking solution over the subsequent 2 month study period. 3. Sodium chloride drinking solution (1%) completely prevented any hypotensive effect of ramapril. Blood pressure was reduced in Group 3 rats over the entire period of study, when compared with Group 2 rats (P less than 0.001). 4. Urinary protein excretion progressively increased in Group 1 and 2 rats, and was significantly reduced (P less than 0.001) in Group 3. After 2 months treatment, urinary protein (expressed as mean and s.e.m.) was 160 +/- 30 mg/day in Group 1, 240 +/- 50 mg/day in Group 2, and 60 +/- 11 mg/day in Group 3. 5. Angiotensin converting enzyme inhibition per se was not associated with a reduced protein excretion in diabetic nephropathy, requiring concomitant control of systemic blood pressure to become renoprotective. | en_US |
dc.language.iso | en | en |
dc.subject.other | Animals | en |
dc.subject.other | Bicyclo Compounds.pharmacology | en |
dc.subject.other | Blood Pressure.drug effects | en |
dc.subject.other | Bridged Compounds.pharmacology | en |
dc.subject.other | Diabetes Mellitus, Experimental.physiopathology | en |
dc.subject.other | Glomerular Filtration Rate.drug effects | en |
dc.subject.other | Male | en |
dc.subject.other | Proteinuria.etiology | en |
dc.subject.other | Ramipril | en |
dc.subject.other | Rats | en |
dc.subject.other | Rats, Inbred SHR | en |
dc.subject.other | Sodium, Dietary.pharmacology | en |
dc.subject.other | Streptozocin | en |
dc.subject.other | Time Factors | en |
dc.title | High salt diet ameliorates effects of angiotensin converting enzyme inhibition in spontaneously hypertensive streptozotocin diabetic rats. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Clinical and Experimental Pharmacology & Physiology | en_US |
dc.identifier.affiliation | Medicine (University of Melbourne) | en_US |
dc.description.pages | 229-34 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/2140303 | en |
dc.type.content | Text | en_US |
dc.type.austin | Journal Article | en |
local.name.researcher | Jackson, Belinda D | |
item.fulltext | No Fulltext | - |
item.openairetype | Journal Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Gastroenterology and Hepatology | - |
Appears in Collections: | Journal articles |
Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.