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Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats

This study evaluated the possible protective effect of Crocus sativus L. (saffron) in the treatment of renal calculi. Aqueous extract of saffron (25, 50 and 100 mg/kg, daily) was administered intraperitoneally in two regimens of protective or curative, using male Wistar rats. Urolithiasis was induce...

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Autores principales: Amin, Bahareh, Feriz, Hanieh Moghri, Hariri, Alireza Timcheh, Meybodi, Naser Tayyebi, Hosseinzadeh, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616248/
https://www.ncbi.nlm.nih.gov/pubmed/26535035
http://dx.doi.org/10.17179/excli2014-510
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author Amin, Bahareh
Feriz, Hanieh Moghri
Hariri, Alireza Timcheh
Meybodi, Naser Tayyebi
Hosseinzadeh, Hossein
author_facet Amin, Bahareh
Feriz, Hanieh Moghri
Hariri, Alireza Timcheh
Meybodi, Naser Tayyebi
Hosseinzadeh, Hossein
author_sort Amin, Bahareh
collection PubMed
description This study evaluated the possible protective effect of Crocus sativus L. (saffron) in the treatment of renal calculi. Aqueous extract of saffron (25, 50 and 100 mg/kg, daily) was administered intraperitoneally in two regimens of protective or curative, using male Wistar rats. Urolithiasis was induced by ethylene glycol (% 0.75) in drinking water. Urine was collected for biochemical analysis and the kidneys were prepared for total lipid peroxide and histological evaluation. Ethylene glycol feeding resulted in an increased urine output, renal excretion of oxalate and decreased excretion of citrate and magnesium. Saffron did not show diuretic effect; however, it significantly reduced the elevated urinary oxalate in prophylactic (50 and 100 mg/kg) and curative (100 mg/kg) studies. Only the high dose of prophylactic regimen restored citrate concentration of urine. Increased number of calcium oxalate crystals deposits in the kidney tissue of calculogenic rats was significantly reverted by the prophylactic and high dose of curative saffron treatment. Malondialdehyde (MDA, a lipid peroxidation product) in the kidneys was increased following the lithogenic treatment; however, prophylactic (50, 100 mg/kg) and curative (100 mg/kg) regimens with saffron reduced the elevated levels of MDA. Results in the current study indicate that saffron can protect against ethylene glycol induced calcium oxalate (CaOx) nephrolithiasis. The mechanisms underlying this effect are mediated possibly through effect on the urinary concentration of stone-forming constituents and an antioxidant effect.
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spelling pubmed-46162482015-11-03 Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats Amin, Bahareh Feriz, Hanieh Moghri Hariri, Alireza Timcheh Meybodi, Naser Tayyebi Hosseinzadeh, Hossein EXCLI J Original Article This study evaluated the possible protective effect of Crocus sativus L. (saffron) in the treatment of renal calculi. Aqueous extract of saffron (25, 50 and 100 mg/kg, daily) was administered intraperitoneally in two regimens of protective or curative, using male Wistar rats. Urolithiasis was induced by ethylene glycol (% 0.75) in drinking water. Urine was collected for biochemical analysis and the kidneys were prepared for total lipid peroxide and histological evaluation. Ethylene glycol feeding resulted in an increased urine output, renal excretion of oxalate and decreased excretion of citrate and magnesium. Saffron did not show diuretic effect; however, it significantly reduced the elevated urinary oxalate in prophylactic (50 and 100 mg/kg) and curative (100 mg/kg) studies. Only the high dose of prophylactic regimen restored citrate concentration of urine. Increased number of calcium oxalate crystals deposits in the kidney tissue of calculogenic rats was significantly reverted by the prophylactic and high dose of curative saffron treatment. Malondialdehyde (MDA, a lipid peroxidation product) in the kidneys was increased following the lithogenic treatment; however, prophylactic (50, 100 mg/kg) and curative (100 mg/kg) regimens with saffron reduced the elevated levels of MDA. Results in the current study indicate that saffron can protect against ethylene glycol induced calcium oxalate (CaOx) nephrolithiasis. The mechanisms underlying this effect are mediated possibly through effect on the urinary concentration of stone-forming constituents and an antioxidant effect. Leibniz Research Centre for Working Environment and Human Factors 2015-03-12 /pmc/articles/PMC4616248/ /pubmed/26535035 http://dx.doi.org/10.17179/excli2014-510 Text en Copyright © 2015 Amin et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Amin, Bahareh
Feriz, Hanieh Moghri
Hariri, Alireza Timcheh
Meybodi, Naser Tayyebi
Hosseinzadeh, Hossein
Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats
title Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats
title_full Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats
title_fullStr Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats
title_full_unstemmed Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats
title_short Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats
title_sort protective effects of the aqueous extract of crocus sativus against ethylene glycol induced nephrolithiasis in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616248/
https://www.ncbi.nlm.nih.gov/pubmed/26535035
http://dx.doi.org/10.17179/excli2014-510
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