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Thymoquinone protects the rat kidneys against renal fibrosis

Thymoquinone (TQ) is the main active ingredient of Nigella sativa seeds with various pharmacological effects. The aim of this study was to investigate the effect of TQ on renal fibrosis and permeability and oxidative stress status in lipopolysaccharide (LPS)-induced inflammation in male rats. Eighty...

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Autores principales: Bargi, Rahimeh, Asgharzadeh, Fereshteh, Beheshti, Farimah, Hosseini, Mahmoud, Farzadnia, Mehdi, Khazaei, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691574/
https://www.ncbi.nlm.nih.gov/pubmed/29204176
http://dx.doi.org/10.4103/1735-5362.217428
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author Bargi, Rahimeh
Asgharzadeh, Fereshteh
Beheshti, Farimah
Hosseini, Mahmoud
Farzadnia, Mehdi
Khazaei, Majid
author_facet Bargi, Rahimeh
Asgharzadeh, Fereshteh
Beheshti, Farimah
Hosseini, Mahmoud
Farzadnia, Mehdi
Khazaei, Majid
author_sort Bargi, Rahimeh
collection PubMed
description Thymoquinone (TQ) is the main active ingredient of Nigella sativa seeds with various pharmacological effects. The aim of this study was to investigate the effect of TQ on renal fibrosis and permeability and oxidative stress status in lipopolysaccharide (LPS)-induced inflammation in male rats. Eighty male Wistar rats were divided into 5 groups as follow: control (received normal saline), LPS (1 mg/kg/day), and LPS+TQ (by doses of 2, 5 and 10 mg/kg/day). After three weeks, the biochemical parameters such as blood urea nitrogen (BUN) and creatinine in serum samples, oxidative stress markers including malondialdehyde (MDA), total thiol groups, superoxide dismutase (SOD) and catalase (CAT) activities in renal tissue homogenate and renal permeability (evaluated by Evan’s blue dye method) were measured and renal fibrosis was evaluated, histologically using Masson’s trichrome staining. LPS administration induced renal fibrosis (1.49 ± 0.08 vs. 7.15 ± 0.18%) and significantly increased renal permeability (6.03 ± 1.05 vs. 13.5 ± 1.04 μg evans blue(EB)/g tissue), serum BUN and creatinine levels and oxidative stress marker (MDA) (P < 0.05), while, it reduced anti-oxidative markers including total thiol group, SOD and CAT activities (P < 0.05). Administration of TQ significantly improved these alterations which were dose-dependent in oxidative stress markers, renal permeability (TQ 2, 5 and 10 mg/kg: 10.7 ± 0.3, 9.2 ± 1.4 and 11.5 ± 0.6 μg EB/g tissue; respectively) and fibrosis (TQ 2, 5 and 10 mg/kg: 6.09 ± 0.7, 4.26 ± 0.14 and 2.52 ± 0.08%; respectively). In conclusion, administration of TQ reduced renal fibrosis and permeability and improved oxidative stress status. Thus, TQ can be considered in conditions accompanied with chronic inflammation at least as a part of treatment strategy.
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spelling pubmed-56915742017-12-05 Thymoquinone protects the rat kidneys against renal fibrosis Bargi, Rahimeh Asgharzadeh, Fereshteh Beheshti, Farimah Hosseini, Mahmoud Farzadnia, Mehdi Khazaei, Majid Res Pharm Sci Original Article Thymoquinone (TQ) is the main active ingredient of Nigella sativa seeds with various pharmacological effects. The aim of this study was to investigate the effect of TQ on renal fibrosis and permeability and oxidative stress status in lipopolysaccharide (LPS)-induced inflammation in male rats. Eighty male Wistar rats were divided into 5 groups as follow: control (received normal saline), LPS (1 mg/kg/day), and LPS+TQ (by doses of 2, 5 and 10 mg/kg/day). After three weeks, the biochemical parameters such as blood urea nitrogen (BUN) and creatinine in serum samples, oxidative stress markers including malondialdehyde (MDA), total thiol groups, superoxide dismutase (SOD) and catalase (CAT) activities in renal tissue homogenate and renal permeability (evaluated by Evan’s blue dye method) were measured and renal fibrosis was evaluated, histologically using Masson’s trichrome staining. LPS administration induced renal fibrosis (1.49 ± 0.08 vs. 7.15 ± 0.18%) and significantly increased renal permeability (6.03 ± 1.05 vs. 13.5 ± 1.04 μg evans blue(EB)/g tissue), serum BUN and creatinine levels and oxidative stress marker (MDA) (P < 0.05), while, it reduced anti-oxidative markers including total thiol group, SOD and CAT activities (P < 0.05). Administration of TQ significantly improved these alterations which were dose-dependent in oxidative stress markers, renal permeability (TQ 2, 5 and 10 mg/kg: 10.7 ± 0.3, 9.2 ± 1.4 and 11.5 ± 0.6 μg EB/g tissue; respectively) and fibrosis (TQ 2, 5 and 10 mg/kg: 6.09 ± 0.7, 4.26 ± 0.14 and 2.52 ± 0.08%; respectively). In conclusion, administration of TQ reduced renal fibrosis and permeability and improved oxidative stress status. Thus, TQ can be considered in conditions accompanied with chronic inflammation at least as a part of treatment strategy. Medknow Publications & Media Pvt Ltd 2017-12 /pmc/articles/PMC5691574/ /pubmed/29204176 http://dx.doi.org/10.4103/1735-5362.217428 Text en Copyright: © 2017 Research in Pharmaceutical 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Bargi, Rahimeh
Asgharzadeh, Fereshteh
Beheshti, Farimah
Hosseini, Mahmoud
Farzadnia, Mehdi
Khazaei, Majid
Thymoquinone protects the rat kidneys against renal fibrosis
title Thymoquinone protects the rat kidneys against renal fibrosis
title_full Thymoquinone protects the rat kidneys against renal fibrosis
title_fullStr Thymoquinone protects the rat kidneys against renal fibrosis
title_full_unstemmed Thymoquinone protects the rat kidneys against renal fibrosis
title_short Thymoquinone protects the rat kidneys against renal fibrosis
title_sort thymoquinone protects the rat kidneys against renal fibrosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691574/
https://www.ncbi.nlm.nih.gov/pubmed/29204176
http://dx.doi.org/10.4103/1735-5362.217428
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