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Comparison of the Species-Sensitive Effects of Different Dosages of Calcium and Verapamil on Gentamicin-Induced Nephrotoxicity in Rats and Rabbits
AIM: To compare the effects of different dosages of calcium and verapamil on gentamicin-induced nephrotoxicity in rats and rabbits. MATERIALS AND METHODS: Rabbits and rats of either sex in weight range of 1.5–2.5 kg and 175–225 g, respectively were used in study. Gentamicin 80 mg/kg i.m., calcium ca...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413402/ https://www.ncbi.nlm.nih.gov/pubmed/25948958 http://dx.doi.org/10.4103/0971-6580.155320 |
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author | Patil, Amol N. Arora, Tarun Desai, Amrita Tripathi, Chakra Dhar |
author_facet | Patil, Amol N. Arora, Tarun Desai, Amrita Tripathi, Chakra Dhar |
author_sort | Patil, Amol N. |
collection | PubMed |
description | AIM: To compare the effects of different dosages of calcium and verapamil on gentamicin-induced nephrotoxicity in rats and rabbits. MATERIALS AND METHODS: Rabbits and rats of either sex in weight range of 1.5–2.5 kg and 175–225 g, respectively were used in study. Gentamicin 80 mg/kg i.m., calcium carbonate 0.5 g/kg/day oral, calcium carbonate 1.0 g/kg/day oral, and verapamil 7 mg/kg/day i.m. were administered for 6 days in either species containing 7 groups. Blood urea nitrogen (BUN), serum creatinine and, urine protein levels were assessed on day 0 and day 7 for kidney function. The animals were sacrificed on day 7 for histopathplogical examination and kidney superoxide dismutase levels (SOD) were measured. Statistical analysis was done using student's unpaired t-test, analysis of variance (ANOVA) and Wilcoxon Rank Sum test. P-value less than 0.05 was considered significant. RESULTS: The results showed that calcium was able to reverse significantly increased BUN, serum creatinine, urine protein, and reduced kidney SOD levels in gentamicin-treated nephrotoxic rats or rabbits in a dose-dependent manner while verapamil had no protective or nephrotoxic effect. CONCLUSION: Calcium 0.5 g/kg/day and 1.0 g/kg/day were able to reverse tubular necrosis and mesangial proliferation in gentamicin-treated nephrotoxic animals. There was no species-sensitive variation in reversal of nephrotoxicity by calcium in rats and rabbits. |
format | Online Article Text |
id | pubmed-4413402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44134022015-05-06 Comparison of the Species-Sensitive Effects of Different Dosages of Calcium and Verapamil on Gentamicin-Induced Nephrotoxicity in Rats and Rabbits Patil, Amol N. Arora, Tarun Desai, Amrita Tripathi, Chakra Dhar Toxicol Int Original Article AIM: To compare the effects of different dosages of calcium and verapamil on gentamicin-induced nephrotoxicity in rats and rabbits. MATERIALS AND METHODS: Rabbits and rats of either sex in weight range of 1.5–2.5 kg and 175–225 g, respectively were used in study. Gentamicin 80 mg/kg i.m., calcium carbonate 0.5 g/kg/day oral, calcium carbonate 1.0 g/kg/day oral, and verapamil 7 mg/kg/day i.m. were administered for 6 days in either species containing 7 groups. Blood urea nitrogen (BUN), serum creatinine and, urine protein levels were assessed on day 0 and day 7 for kidney function. The animals were sacrificed on day 7 for histopathplogical examination and kidney superoxide dismutase levels (SOD) were measured. Statistical analysis was done using student's unpaired t-test, analysis of variance (ANOVA) and Wilcoxon Rank Sum test. P-value less than 0.05 was considered significant. RESULTS: The results showed that calcium was able to reverse significantly increased BUN, serum creatinine, urine protein, and reduced kidney SOD levels in gentamicin-treated nephrotoxic rats or rabbits in a dose-dependent manner while verapamil had no protective or nephrotoxic effect. CONCLUSION: Calcium 0.5 g/kg/day and 1.0 g/kg/day were able to reverse tubular necrosis and mesangial proliferation in gentamicin-treated nephrotoxic animals. There was no species-sensitive variation in reversal of nephrotoxicity by calcium in rats and rabbits. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4413402/ /pubmed/25948958 http://dx.doi.org/10.4103/0971-6580.155320 Text en Copyright: © Toxicology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Patil, Amol N. Arora, Tarun Desai, Amrita Tripathi, Chakra Dhar Comparison of the Species-Sensitive Effects of Different Dosages of Calcium and Verapamil on Gentamicin-Induced Nephrotoxicity in Rats and Rabbits |
title | Comparison of the Species-Sensitive Effects of Different Dosages of Calcium and Verapamil on Gentamicin-Induced Nephrotoxicity in Rats and Rabbits |
title_full | Comparison of the Species-Sensitive Effects of Different Dosages of Calcium and Verapamil on Gentamicin-Induced Nephrotoxicity in Rats and Rabbits |
title_fullStr | Comparison of the Species-Sensitive Effects of Different Dosages of Calcium and Verapamil on Gentamicin-Induced Nephrotoxicity in Rats and Rabbits |
title_full_unstemmed | Comparison of the Species-Sensitive Effects of Different Dosages of Calcium and Verapamil on Gentamicin-Induced Nephrotoxicity in Rats and Rabbits |
title_short | Comparison of the Species-Sensitive Effects of Different Dosages of Calcium and Verapamil on Gentamicin-Induced Nephrotoxicity in Rats and Rabbits |
title_sort | comparison of the species-sensitive effects of different dosages of calcium and verapamil on gentamicin-induced nephrotoxicity in rats and rabbits |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413402/ https://www.ncbi.nlm.nih.gov/pubmed/25948958 http://dx.doi.org/10.4103/0971-6580.155320 |
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