Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats

The current study evaluates the impact of high fructose feeding in rat model of gentamicin induced nephrotoxicity. Sprague-Dawley rats weighing 180-200 g were randomized into four groups; (C) received standard rodents chow with free access to ad libitum drinking water for 8 weeks and was considered...

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Published in:BioMed Research International
Main Author: Ibraheem Z.O.; Basir R.; Aljobory A.K.; Ibrahim O.E.; Alsumaidaee A.; Yam M.F.
Format: Article
Language:English
Published: Hindawi Publishing Corporation 2014
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84904121391&doi=10.1155%2f2014%2f823879&partnerID=40&md5=9dbe1f1607993f933ab18db00f0127d4
id 2-s2.0-84904121391
spelling 2-s2.0-84904121391
Ibraheem Z.O.; Basir R.; Aljobory A.K.; Ibrahim O.E.; Alsumaidaee A.; Yam M.F.
Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats
2014
BioMed Research International
2014

10.1155/2014/823879
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84904121391&doi=10.1155%2f2014%2f823879&partnerID=40&md5=9dbe1f1607993f933ab18db00f0127d4
The current study evaluates the impact of high fructose feeding in rat model of gentamicin induced nephrotoxicity. Sprague-Dawley rats weighing 180-200 g were randomized into four groups; (C) received standard rodents chow with free access to ad libitum drinking water for 8 weeks and was considered as control, (F) received standard rodents chow with free access to drinking water supplemented with 20% (W/V) fructose for the same abovementioned period, (FG) was fed as group F and was given 80 mg/kg (body weight)/day gentamicin sulphate intraperitoneally during the last 20 days of the feeding period, and (G) was given gentamicin as above and fed as group C. Renal function was assessed at the end of the treatment period through measuring serum creatinine, uric acid and albumin, creatinine clearance, absolute and fractional excretion of both sodium and potassium, twenty-four-hour urinary excretion of albumin, and renal histology. For metabolic syndrome assessment, fasting plasma glucose and insulin were measured and oral glucose tolerance test was performed throughout the treatment period. Results showed that gentamicin enhances progression of fructose induced metabolic syndrome. On the other hand, fructose pretreatment before gentamicin injection produced a comparable degree of renal dysfunction to those which were given fructose-free water but the picture of nephrotoxicity was somewhat altered as it was characterized by higher extent of glomerular congestion and protein urea. Overall, more vigilance is required when nephrotoxic drugs are prescribed for patients with fructose induced metabolic syndrome. © 2014 Zaid O. Ibraheem et al.
Hindawi Publishing Corporation
23146133
English
Article
All Open Access; Gold Open Access
author Ibraheem Z.O.; Basir R.; Aljobory A.K.; Ibrahim O.E.; Alsumaidaee A.; Yam M.F.
spellingShingle Ibraheem Z.O.; Basir R.; Aljobory A.K.; Ibrahim O.E.; Alsumaidaee A.; Yam M.F.
Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats
author_facet Ibraheem Z.O.; Basir R.; Aljobory A.K.; Ibrahim O.E.; Alsumaidaee A.; Yam M.F.
author_sort Ibraheem Z.O.; Basir R.; Aljobory A.K.; Ibrahim O.E.; Alsumaidaee A.; Yam M.F.
title Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats
title_short Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats
title_full Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats
title_fullStr Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats
title_full_unstemmed Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats
title_sort Impact of gentamicin coadministration along with high fructose feeding on progression of renal failure and metabolic syndrome in sprague-dawley rats
publishDate 2014
container_title BioMed Research International
container_volume 2014
container_issue
doi_str_mv 10.1155/2014/823879
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-84904121391&doi=10.1155%2f2014%2f823879&partnerID=40&md5=9dbe1f1607993f933ab18db00f0127d4
description The current study evaluates the impact of high fructose feeding in rat model of gentamicin induced nephrotoxicity. Sprague-Dawley rats weighing 180-200 g were randomized into four groups; (C) received standard rodents chow with free access to ad libitum drinking water for 8 weeks and was considered as control, (F) received standard rodents chow with free access to drinking water supplemented with 20% (W/V) fructose for the same abovementioned period, (FG) was fed as group F and was given 80 mg/kg (body weight)/day gentamicin sulphate intraperitoneally during the last 20 days of the feeding period, and (G) was given gentamicin as above and fed as group C. Renal function was assessed at the end of the treatment period through measuring serum creatinine, uric acid and albumin, creatinine clearance, absolute and fractional excretion of both sodium and potassium, twenty-four-hour urinary excretion of albumin, and renal histology. For metabolic syndrome assessment, fasting plasma glucose and insulin were measured and oral glucose tolerance test was performed throughout the treatment period. Results showed that gentamicin enhances progression of fructose induced metabolic syndrome. On the other hand, fructose pretreatment before gentamicin injection produced a comparable degree of renal dysfunction to those which were given fructose-free water but the picture of nephrotoxicity was somewhat altered as it was characterized by higher extent of glomerular congestion and protein urea. Overall, more vigilance is required when nephrotoxic drugs are prescribed for patients with fructose induced metabolic syndrome. © 2014 Zaid O. Ibraheem et al.
publisher Hindawi Publishing Corporation
issn 23146133
language English
format Article
accesstype All Open Access; Gold Open Access
record_format scopus
collection Scopus
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