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Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats

OBJECTIVE: Studies have demonstrated that carbon tetrachloride (CCl(4)) increases the generation of reactive oxygen species (ROS) in many tissues including the kidney, heart, lung, brain, and liver. The major aim of the present study was to evaluate the protective activity of Tanacetum parthenium ex...

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Autores principales: Mazani, Mohammad, Mahmoodzadeh, Yavar, Chinifroush Asl, Mir Mehdi, Banaei, Shokofeh, Rezagholizadeh, Lotfollah, Mohammadnia, Alireza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204152/
https://www.ncbi.nlm.nih.gov/pubmed/30377595
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author Mazani, Mohammad
Mahmoodzadeh, Yavar
Chinifroush Asl, Mir Mehdi
Banaei, Shokofeh
Rezagholizadeh, Lotfollah
Mohammadnia, Alireza
author_facet Mazani, Mohammad
Mahmoodzadeh, Yavar
Chinifroush Asl, Mir Mehdi
Banaei, Shokofeh
Rezagholizadeh, Lotfollah
Mohammadnia, Alireza
author_sort Mazani, Mohammad
collection PubMed
description OBJECTIVE: Studies have demonstrated that carbon tetrachloride (CCl(4)) increases the generation of reactive oxygen species (ROS) in many tissues including the kidney, heart, lung, brain, and liver. The major aim of the present study was to evaluate the protective activity of Tanacetum parthenium extract (TPE) in renal tissues of CCl(4)-intoxicated rats. MATERIALS AND METHODS: Animals were divided into seven groups of six rats. Group 1 was the control group that was not treated with CCl(4). The rats in the other groups were intraperitoneally injected with CCl(4) (1.5 ml/kg, 1:1 in olive oil) on day 14. Rats in the groups bTPE40, bTPE80, and bTPE120 were gavaged with 40, 80, and 120 mg/kg of TPE, respectively for 14 constitutive days on a daily basis, before CCl(4) administration. Rats in groups aTPE80 and aTPE120 were gavaged with 80 and 120 mg/kg of TPE, respectively, 2, 6, 24 and 48 hr after receiving CCl(4). Blood samples were collected at the end of the 16(th) day through an intracardiac puncture and then serums were separated. RESULTS: CCl(4) increased urea, creatinine, uric acid and creatinine: albumin (C/A) ratio level in serum and decreased total antioxidant and antioxidant enzymes (SOD and GPx) when compared to the control group (p<0.001). But administration of TPE to rats either before or after exposure to CCl(4), attenuated these changes when compared with CCl(4) control group (p<0.05 – p<0.001). CONCLUSION: TPE had potent nephroprotective effects against oxygen free radicals produced through CCl(4) metabolism.
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spelling pubmed-62041522018-10-30 Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats Mazani, Mohammad Mahmoodzadeh, Yavar Chinifroush Asl, Mir Mehdi Banaei, Shokofeh Rezagholizadeh, Lotfollah Mohammadnia, Alireza Avicenna J Phytomed Original Research Article OBJECTIVE: Studies have demonstrated that carbon tetrachloride (CCl(4)) increases the generation of reactive oxygen species (ROS) in many tissues including the kidney, heart, lung, brain, and liver. The major aim of the present study was to evaluate the protective activity of Tanacetum parthenium extract (TPE) in renal tissues of CCl(4)-intoxicated rats. MATERIALS AND METHODS: Animals were divided into seven groups of six rats. Group 1 was the control group that was not treated with CCl(4). The rats in the other groups were intraperitoneally injected with CCl(4) (1.5 ml/kg, 1:1 in olive oil) on day 14. Rats in the groups bTPE40, bTPE80, and bTPE120 were gavaged with 40, 80, and 120 mg/kg of TPE, respectively for 14 constitutive days on a daily basis, before CCl(4) administration. Rats in groups aTPE80 and aTPE120 were gavaged with 80 and 120 mg/kg of TPE, respectively, 2, 6, 24 and 48 hr after receiving CCl(4). Blood samples were collected at the end of the 16(th) day through an intracardiac puncture and then serums were separated. RESULTS: CCl(4) increased urea, creatinine, uric acid and creatinine: albumin (C/A) ratio level in serum and decreased total antioxidant and antioxidant enzymes (SOD and GPx) when compared to the control group (p<0.001). But administration of TPE to rats either before or after exposure to CCl(4), attenuated these changes when compared with CCl(4) control group (p<0.05 – p<0.001). CONCLUSION: TPE had potent nephroprotective effects against oxygen free radicals produced through CCl(4) metabolism. Mashhad University of Medical Sciences 2018 /pmc/articles/PMC6204152/ /pubmed/30377595 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Mazani, Mohammad
Mahmoodzadeh, Yavar
Chinifroush Asl, Mir Mehdi
Banaei, Shokofeh
Rezagholizadeh, Lotfollah
Mohammadnia, Alireza
Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats
title Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats
title_full Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats
title_fullStr Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats
title_full_unstemmed Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats
title_short Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats
title_sort renoprotective effects of the methanolic extract of tanacetum parthenium against carbon tetrachloride-induced renal injury in rats
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204152/
https://www.ncbi.nlm.nih.gov/pubmed/30377595
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