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Antioxidant properties of repaglinide and its protections against cyclosporine A-induced renal tubular injury
OBJECTIVE(S): Repaglinide (RG) is an antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus. It has a good safety and efficacy profile in diabetic patients with complications in renal impairment and is an appropriate treatment choice, even for individuals with more...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010847/ https://www.ncbi.nlm.nih.gov/pubmed/27635199 |
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author | Li, Dao Li, Jin Li, Hui Wu, Qiong Li, Qi-Xiong |
author_facet | Li, Dao Li, Jin Li, Hui Wu, Qiong Li, Qi-Xiong |
author_sort | Li, Dao |
collection | PubMed |
description | OBJECTIVE(S): Repaglinide (RG) is an antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus. It has a good safety and efficacy profile in diabetic patients with complications in renal impairment and is an appropriate treatment choice, even for individuals with more severe degrees of renal malfunctions. The aim of the present study was to examine the protective effect of RG on cyclosporine A (CsA)-induced rat renal impairment and to evaluate the antioxidant mechanisms by which RG exerts its protective actions. MATERIALS AND METHODS: Fifty male Sprague-Dawley rats weighing 250–300 g were randomly divided into five groups: administrations of olive oil (control, PO), RG (0.4 mg/kg, PO), CsA (30 mg/kg in olive oil, SC), RG (0.2 or 0.4 mg/kg, PO) plus CsA (30 mg/kg in olive oil SC) every day for 15 days. RESULTS: SC administration of CsA (30 mg/kg) to rats produced marked elevations in the levels of renal impairment parameters such as urinary protein, N-acetyl-beta-D-glucosaminidase (NAG), serum creatinine (SCr), and blood urea nitrogen (BUN). It also caused histologic injury to the kidneys. Oral administration of RG (0.2 and 0.4 mg/kg) markedly decreased all the aforementioned changes. In addition, CsA caused increases in the levels of malondialdehyde (MDA) and decreases in superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), glutathione reductase (GSR), glutathione-S-transferase (GST), and glutathione in kidney homogenate, which were reversed significantly by both doses of RG. CONCLUSION: The findings of our study indicate that RG may play an important role in protecting the kidney from oxidative insult. |
format | Online Article Text |
id | pubmed-5010847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-50108472016-09-15 Antioxidant properties of repaglinide and its protections against cyclosporine A-induced renal tubular injury Li, Dao Li, Jin Li, Hui Wu, Qiong Li, Qi-Xiong Iran J Basic Med Sci Original Article OBJECTIVE(S): Repaglinide (RG) is an antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus. It has a good safety and efficacy profile in diabetic patients with complications in renal impairment and is an appropriate treatment choice, even for individuals with more severe degrees of renal malfunctions. The aim of the present study was to examine the protective effect of RG on cyclosporine A (CsA)-induced rat renal impairment and to evaluate the antioxidant mechanisms by which RG exerts its protective actions. MATERIALS AND METHODS: Fifty male Sprague-Dawley rats weighing 250–300 g were randomly divided into five groups: administrations of olive oil (control, PO), RG (0.4 mg/kg, PO), CsA (30 mg/kg in olive oil, SC), RG (0.2 or 0.4 mg/kg, PO) plus CsA (30 mg/kg in olive oil SC) every day for 15 days. RESULTS: SC administration of CsA (30 mg/kg) to rats produced marked elevations in the levels of renal impairment parameters such as urinary protein, N-acetyl-beta-D-glucosaminidase (NAG), serum creatinine (SCr), and blood urea nitrogen (BUN). It also caused histologic injury to the kidneys. Oral administration of RG (0.2 and 0.4 mg/kg) markedly decreased all the aforementioned changes. In addition, CsA caused increases in the levels of malondialdehyde (MDA) and decreases in superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), glutathione reductase (GSR), glutathione-S-transferase (GST), and glutathione in kidney homogenate, which were reversed significantly by both doses of RG. CONCLUSION: The findings of our study indicate that RG may play an important role in protecting the kidney from oxidative insult. Mashhad University of Medical Sciences 2016-07 /pmc/articles/PMC5010847/ /pubmed/27635199 Text en Copyright: © Iranian Journal of Basic Medical Sciences 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 Li, Dao Li, Jin Li, Hui Wu, Qiong Li, Qi-Xiong Antioxidant properties of repaglinide and its protections against cyclosporine A-induced renal tubular injury |
title | Antioxidant properties of repaglinide and its protections against cyclosporine A-induced renal tubular injury |
title_full | Antioxidant properties of repaglinide and its protections against cyclosporine A-induced renal tubular injury |
title_fullStr | Antioxidant properties of repaglinide and its protections against cyclosporine A-induced renal tubular injury |
title_full_unstemmed | Antioxidant properties of repaglinide and its protections against cyclosporine A-induced renal tubular injury |
title_short | Antioxidant properties of repaglinide and its protections against cyclosporine A-induced renal tubular injury |
title_sort | antioxidant properties of repaglinide and its protections against cyclosporine a-induced renal tubular injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010847/ https://www.ncbi.nlm.nih.gov/pubmed/27635199 |
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