Comparison of nephron-protective effects of enalapril and glp analogues (exenatide) in diabetic nephropathy
dc.contributor.author | Çavusoglu T. | |
dc.contributor.author | Erbas O. | |
dc.contributor.author | Karadeniz T. | |
dc.contributor.author | Akdemir O. | |
dc.contributor.author | Acikgoz E. | |
dc.contributor.author | Karadeniz M. | |
dc.contributor.author | Tuglu M.I. | |
dc.contributor.author | Ates U. | |
dc.date.accessioned | 2024-07-22T08:17:17Z | |
dc.date.available | 2024-07-22T08:17:17Z | |
dc.date.issued | 2014 | |
dc.description.abstract | Background: One of the major concerns is a nephropathy in diabetes, which applies many different kinds of medicines. However, required level of the treatment of renal disease has not been achieved. Aim: To investigate and compare the effect of the enalapril and the exenatide on diabetic nephropathy in rats developed diabetes by streptozosin. Material and Methods: 32 male Sprague Dawley rats were divided into 4 groups: (1) Control, (2) Diabetic (DM), (3) DM+ Enalapril, and (4) DM+ exenatide groups. Then, the animals were euthanized and their blood samples were collected by cardiac puncture for blood glucose; blood urea nitrogen (BUN), creatinin, and nephrectomy were performed for histopathologic examination, and urine samples were taken on stick for proteinuria. Results: Administration of the enalapril or the exenatide in diabetic rats resulted in a significant reduction both fibronectin, induced nitric oxide synthase (i-NOS) expression in glomerular area and urine protein levels. It was shown that both of enalapril and exenatide protected the renal glomerulus more than diabetic group in the nephropathy histopathologically. Conclusion: The beneficial effects of enalapril and exenatide which reduces fibronectin, i-NOS expression and urine protein levels or increases recovery of glomerules, might be used for preventing the harmful effects of diabetic nephropathy. © 2014 Georg Thieme Verlag KG Stuttgart New York. | |
dc.identifier.DOI-ID | 10.1055/s-0034-1372584 | |
dc.identifier.issn | 09477349 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/17018 | |
dc.language.iso | English | |
dc.publisher | Georg Thieme Verlag | |
dc.subject | Animals | |
dc.subject | Antihypertensive Agents | |
dc.subject | Diabetes Mellitus, Experimental | |
dc.subject | Diabetic Nephropathies | |
dc.subject | Enalapril | |
dc.subject | Gene Expression Regulation, Enzymologic | |
dc.subject | Hypoglycemic Agents | |
dc.subject | Male | |
dc.subject | Nephrons | |
dc.subject | Nitric Oxide Synthase Type II | |
dc.subject | Peptides | |
dc.subject | Rats | |
dc.subject | Rats, Sprague-Dawley | |
dc.subject | Venoms | |
dc.subject | creatinine | |
dc.subject | enalapril | |
dc.subject | exendin 4 | |
dc.subject | fibronectin | |
dc.subject | glucagon like peptide 1 | |
dc.subject | glucose | |
dc.subject | inducible nitric oxide synthase | |
dc.subject | servier | |
dc.subject | unclassified drug | |
dc.subject | antidiabetic agent | |
dc.subject | antihypertensive agent | |
dc.subject | enalapril | |
dc.subject | exendin 4 | |
dc.subject | inducible nitric oxide synthase | |
dc.subject | Nos2 protein, rat | |
dc.subject | peptide | |
dc.subject | venom | |
dc.subject | analytical equipment | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | animal tissue | |
dc.subject | article | |
dc.subject | autoanalyzer | |
dc.subject | brush border | |
dc.subject | comparative study | |
dc.subject | controlled study | |
dc.subject | creatinine blood level | |
dc.subject | diabetic nephropathy | |
dc.subject | dilatation | |
dc.subject | dissociation | |
dc.subject | drug effect | |
dc.subject | glomerular structure | |
dc.subject | glomerulus | |
dc.subject | glucose blood level | |
dc.subject | histopathology | |
dc.subject | immunity | |
dc.subject | immunohistochemistry | |
dc.subject | immunoreactivity | |
dc.subject | investigative procedures | |
dc.subject | kidney parenchyma | |
dc.subject | kidney tubule epithelium | |
dc.subject | male | |
dc.subject | nephrectomy | |
dc.subject | nonhuman | |
dc.subject | priority journal | |
dc.subject | protein depletion | |
dc.subject | protein determination | |
dc.subject | protein expression | |
dc.subject | protein urine level | |
dc.subject | proteinuria | |
dc.subject | rat | |
dc.subject | renal protection | |
dc.subject | treatment response | |
dc.subject | tubular dilatation | |
dc.subject | urea nitrogen blood level | |
dc.subject | urinalysis | |
dc.subject | urine dipstick | |
dc.subject | animal | |
dc.subject | biosynthesis | |
dc.subject | Diabetes Mellitus, Experimental | |
dc.subject | Diabetic Nephropathies | |
dc.subject | drug effects | |
dc.subject | gene expression regulation | |
dc.subject | metabolism | |
dc.subject | nephron | |
dc.subject | pathology | |
dc.subject | Sprague Dawley rat | |
dc.title | Comparison of nephron-protective effects of enalapril and glp analogues (exenatide) in diabetic nephropathy | |
dc.type | Article |