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https://ahro.austin.org.au/austinjspui/handle/1/12084
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Jackson, B | - |
dc.contributor.author | Cubela, R B | - |
dc.contributor.author | Debrevi, L | - |
dc.contributor.author | Whitty, M | - |
dc.contributor.author | Johnston, Colin I | - |
dc.date.accessioned | 2015-05-16T01:43:51Z | |
dc.date.available | 2015-05-16T01:43:51Z | |
dc.date.issued | 1987-05-16 | - |
dc.identifier.citation | Journal of Cardiovascular Pharmacology; 10 Suppl 10(): S167-9 | en_US |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/12084 | en |
dc.description.abstract | Sprague-Dawley rats subjected to subtotal (1 7/8) nephrectomy or streptozotocin diabetes were treated with an angiotensin converting enzyme inhibitor or a calcium channel blocker and their course compared with untreated control animals. Subtotal nephrectomy led to hypertension, proteinuria, reduced creatinine clearance, and glomerulosclerosis over 6 weeks. Enalapril treatment (5 mg/kg/day, n = 11) or felodipine (30 mg/kg/day, n = 11) reduced systolic blood pressure to a comparable degree. Plasma creatinine (mumol/l) was lower after enalapril treatment (110 +/- 8, p less than 0.05) than with felodipine treatment (153 +/- 27) or no treatment (173 +/- 19, n = 18). Proteinuria (mg/24 h) was lower with enalapril treatment (15 +/- 3, p less than 0.001) than with no treatment (85 +/- 22) and increased with felodipine (221 +/- 35). Glomerulosclerosis was reduced with enalapril but not felodipine treatment. Diabetic rats were treated with enalapril (5 mg/kg/day, n = 17), verapamil (5 mg/kg/day, n = 17), or untreated. Diabetic rats had increased creatinine clearance (ml/min) compared with nondiabetic controls (1.52 +/- 0.06 vs. 1.15 +/- 0.05, n = 11, p less than 0.01). Enalapril and verapamil treatment reduced blood pressure equally. Enalapril but not verapamil reduced the elevated creatinine clearance of diabetic rats (enalapril, 1.37 +/- 0.04 ml/min, p less than 0.01; verapamil, 1.49 +/- 0.5 ml/min). Proteinuria (mg/24 h) was lower (p less than 0.05) with enalapril treatment (36 +/- 3) but not with verapamil treatment (58 +/- 10) in comparison to that in untreated diabetes (71 +/- 18).(ABSTRACT TRUNCATED AT 250 WORDS) | en_US |
dc.language.iso | en | en |
dc.subject.other | Angiotensin-Converting Enzyme Inhibitors.pharmacology | en |
dc.subject.other | Animals | en |
dc.subject.other | Calcium Channel Blockers.therapeutic use | en |
dc.subject.other | Diabetes Mellitus, Experimental.complications | en |
dc.subject.other | Diabetic Nephropathies.drug therapy.etiology | en |
dc.subject.other | Enalapril.pharmacology | en |
dc.subject.other | Felodipine | en |
dc.subject.other | Hypertension.drug therapy.etiology | en |
dc.subject.other | Kidney Failure, Chronic.drug therapy.etiology | en |
dc.subject.other | Nephrectomy | en |
dc.subject.other | Nitrendipine.analogs & derivatives.pharmacology | en |
dc.subject.other | Proteinuria.etiology | en |
dc.subject.other | Rats | en |
dc.subject.other | Rats, Inbred Strains | en |
dc.subject.other | Verapamil.pharmacology | en |
dc.title | Disparate effects of angiotensin converting enzyme inhibitor and calcium blocker treatment on the preservation of renal structure and function following subtotal nephrectomy or streptozotocin-induced diabetes in the rat. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Journal of Cardiovascular Pharmacology | en_US |
dc.identifier.affiliation | Medicine (University of Melbourne) | en_US |
dc.description.pages | S167-9 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/2455124 | en |
dc.type.content | Text | en_US |
dc.type.austin | Journal Article | en |
local.name.researcher | Jackson, Belinda D | |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Gastroenterology and Hepatology | - |
Appears in Collections: | Journal articles |
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