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Can crocin play a preventive role in Wistar rats with carbon tetrachloride-induced nephrotoxicity?
OBJECTIVE(S): To investigate protective role of crocin by attempting to create nephrotoxicity with carbon tetrachloride. MATERIALS AND METHODS: Ethics committee approval was obtained and 50 male Wistar rats were randomly divided into 5 groups that included 10 rats each: Control, Corn oil, Crocin, Ca...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960754/ https://www.ncbi.nlm.nih.gov/pubmed/29796221 http://dx.doi.org/10.22038/IJBMS.2018.26101.6412 |
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author | Erdemli, Mehmet Erman Gul, Mehmet Altinoz, Eyup Aksungur, Zeynep Gul, Semir Bag, Harika Gozukara |
author_facet | Erdemli, Mehmet Erman Gul, Mehmet Altinoz, Eyup Aksungur, Zeynep Gul, Semir Bag, Harika Gozukara |
author_sort | Erdemli, Mehmet Erman |
collection | PubMed |
description | OBJECTIVE(S): To investigate protective role of crocin by attempting to create nephrotoxicity with carbon tetrachloride. MATERIALS AND METHODS: Ethics committee approval was obtained and 50 male Wistar rats were randomly divided into 5 groups that included 10 rats each: Control, Corn oil, Crocin, Carbon tetrachloride (CCl4), and Crocin + Carbon tetrachloride. Following the experiments, the rats were decapitated under anesthesia and incised kidney tissues were subjected to biochemical and histological examinations. RESULTS: In the CCl(4) administered group, MDA, TOS, Bun, and creatinine levels increased, GSH, SOD, CAT, and TAS levels decreased (P≤0.05), glomerular collapse in kidney sections, narrowing and local occlusion in Bowman’s space in certain glomeruli, inflammatory cell infiltration and congestion were observed when compared to all other groups. There was a significant decrease in increased MDA, TOS, Bun, and creatinine levels, and a significant increase in decreased GSH, SOD, CAT, and TAS levels in CCl(4) + crocin administered group compared to the CCl(4) group (P≤0.05), local minimal glomerular damage, tubular damage, inflammatory infiltration, and vascular collagen symptoms were observed in kidney sections, however significant improvement was observed in damage findings when compared to the CCl(4) group. CONCLUSION: At this dose and time interval, against a highly toxic chemical such as CCl(4), crocin was able to suppress oxidative stress by playing a protective role in the kidney tissue. |
format | Online Article Text |
id | pubmed-5960754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-59607542018-05-24 Can crocin play a preventive role in Wistar rats with carbon tetrachloride-induced nephrotoxicity? Erdemli, Mehmet Erman Gul, Mehmet Altinoz, Eyup Aksungur, Zeynep Gul, Semir Bag, Harika Gozukara Iran J Basic Med Sci Original Article OBJECTIVE(S): To investigate protective role of crocin by attempting to create nephrotoxicity with carbon tetrachloride. MATERIALS AND METHODS: Ethics committee approval was obtained and 50 male Wistar rats were randomly divided into 5 groups that included 10 rats each: Control, Corn oil, Crocin, Carbon tetrachloride (CCl4), and Crocin + Carbon tetrachloride. Following the experiments, the rats were decapitated under anesthesia and incised kidney tissues were subjected to biochemical and histological examinations. RESULTS: In the CCl(4) administered group, MDA, TOS, Bun, and creatinine levels increased, GSH, SOD, CAT, and TAS levels decreased (P≤0.05), glomerular collapse in kidney sections, narrowing and local occlusion in Bowman’s space in certain glomeruli, inflammatory cell infiltration and congestion were observed when compared to all other groups. There was a significant decrease in increased MDA, TOS, Bun, and creatinine levels, and a significant increase in decreased GSH, SOD, CAT, and TAS levels in CCl(4) + crocin administered group compared to the CCl(4) group (P≤0.05), local minimal glomerular damage, tubular damage, inflammatory infiltration, and vascular collagen symptoms were observed in kidney sections, however significant improvement was observed in damage findings when compared to the CCl(4) group. CONCLUSION: At this dose and time interval, against a highly toxic chemical such as CCl(4), crocin was able to suppress oxidative stress by playing a protective role in the kidney tissue. Mashhad University of Medical Sciences 2018-04 /pmc/articles/PMC5960754/ /pubmed/29796221 http://dx.doi.org/10.22038/IJBMS.2018.26101.6412 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 Erdemli, Mehmet Erman Gul, Mehmet Altinoz, Eyup Aksungur, Zeynep Gul, Semir Bag, Harika Gozukara Can crocin play a preventive role in Wistar rats with carbon tetrachloride-induced nephrotoxicity? |
title | Can crocin play a preventive role in Wistar rats with carbon tetrachloride-induced nephrotoxicity? |
title_full | Can crocin play a preventive role in Wistar rats with carbon tetrachloride-induced nephrotoxicity? |
title_fullStr | Can crocin play a preventive role in Wistar rats with carbon tetrachloride-induced nephrotoxicity? |
title_full_unstemmed | Can crocin play a preventive role in Wistar rats with carbon tetrachloride-induced nephrotoxicity? |
title_short | Can crocin play a preventive role in Wistar rats with carbon tetrachloride-induced nephrotoxicity? |
title_sort | can crocin play a preventive role in wistar rats with carbon tetrachloride-induced nephrotoxicity? |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960754/ https://www.ncbi.nlm.nih.gov/pubmed/29796221 http://dx.doi.org/10.22038/IJBMS.2018.26101.6412 |
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