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Renoprotective effect of crocin following liver ischemia/ reperfusion injury in Wistar rats
OBJECTIVE(S): The objectives of the current study were to evaluate the effects of hepatic ischemia/reperfusion (IR) injury on the activity of antioxidant enzymes, biochemical factors, and histopathological changes in rat kidney, and to investigate the effect of crocin on IR-related changes. MATERIAL...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673703/ https://www.ncbi.nlm.nih.gov/pubmed/29147494 http://dx.doi.org/10.22038/IJBMS.2017.9450 |
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author | Mard, Seyyed Ali Akbari, Ghaidafeh Mansouri, Esrafil Parsanahad, Mahdi |
author_facet | Mard, Seyyed Ali Akbari, Ghaidafeh Mansouri, Esrafil Parsanahad, Mahdi |
author_sort | Mard, Seyyed Ali |
collection | PubMed |
description | OBJECTIVE(S): The objectives of the current study were to evaluate the effects of hepatic ischemia/reperfusion (IR) injury on the activity of antioxidant enzymes, biochemical factors, and histopathological changes in rat kidney, and to investigate the effect of crocin on IR-related changes. MATERIALS AND METHODS: Thirty-two male Wistar rats were randomly allocated into four groups (n=8). They were sham-operated, IR, crocin pre-treatment, and crocin pretreatment+IR groups. Sham-operated and Crocin pre-treatment groups received normal saline (N/S, 2 ml/day) and crocin (200 mg/kg) for seven consecutive days intraperitoneally (IP), respectively, then rats underwent laparotomy, only. IR and crocin pretreatment+IR groups received N/S and crocin with the same dose, time, and route, respectively, then rats underwent partial (70%) ischemia for 45 min that was followed by reperfusion for 60 min. At the end of the experiment, kidney specimens were taken for histopathological and antioxidant evaluations and also blood samples were obtained for biochemical analysis. RESULTS: The results of the present study showed that crocin pre-treatment significantly increased the activity of antioxidants, decreased the serum levels of liver enzymes and blood urea nitrogen following IR-induced hepatic injury. Crocin also ameliorated kidney’s histopathological disturbance beyond IR-induced hepatic injury. CONCLUSION: Crocin as an antioxidant agent protected renal insult following liver IR injury by increasing the activity of antioxidant enzymes, reducing serum levels of liver enzymes, and improving histopathological changes. |
format | Online Article Text |
id | pubmed-5673703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-56737032017-11-16 Renoprotective effect of crocin following liver ischemia/ reperfusion injury in Wistar rats Mard, Seyyed Ali Akbari, Ghaidafeh Mansouri, Esrafil Parsanahad, Mahdi Iran J Basic Med Sci Original Article OBJECTIVE(S): The objectives of the current study were to evaluate the effects of hepatic ischemia/reperfusion (IR) injury on the activity of antioxidant enzymes, biochemical factors, and histopathological changes in rat kidney, and to investigate the effect of crocin on IR-related changes. MATERIALS AND METHODS: Thirty-two male Wistar rats were randomly allocated into four groups (n=8). They were sham-operated, IR, crocin pre-treatment, and crocin pretreatment+IR groups. Sham-operated and Crocin pre-treatment groups received normal saline (N/S, 2 ml/day) and crocin (200 mg/kg) for seven consecutive days intraperitoneally (IP), respectively, then rats underwent laparotomy, only. IR and crocin pretreatment+IR groups received N/S and crocin with the same dose, time, and route, respectively, then rats underwent partial (70%) ischemia for 45 min that was followed by reperfusion for 60 min. At the end of the experiment, kidney specimens were taken for histopathological and antioxidant evaluations and also blood samples were obtained for biochemical analysis. RESULTS: The results of the present study showed that crocin pre-treatment significantly increased the activity of antioxidants, decreased the serum levels of liver enzymes and blood urea nitrogen following IR-induced hepatic injury. Crocin also ameliorated kidney’s histopathological disturbance beyond IR-induced hepatic injury. CONCLUSION: Crocin as an antioxidant agent protected renal insult following liver IR injury by increasing the activity of antioxidant enzymes, reducing serum levels of liver enzymes, and improving histopathological changes. Mashhad University of Medical Sciences 2017-10 /pmc/articles/PMC5673703/ /pubmed/29147494 http://dx.doi.org/10.22038/IJBMS.2017.9450 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 Mard, Seyyed Ali Akbari, Ghaidafeh Mansouri, Esrafil Parsanahad, Mahdi Renoprotective effect of crocin following liver ischemia/ reperfusion injury in Wistar rats |
title | Renoprotective effect of crocin following liver ischemia/ reperfusion injury in Wistar rats |
title_full | Renoprotective effect of crocin following liver ischemia/ reperfusion injury in Wistar rats |
title_fullStr | Renoprotective effect of crocin following liver ischemia/ reperfusion injury in Wistar rats |
title_full_unstemmed | Renoprotective effect of crocin following liver ischemia/ reperfusion injury in Wistar rats |
title_short | Renoprotective effect of crocin following liver ischemia/ reperfusion injury in Wistar rats |
title_sort | renoprotective effect of crocin following liver ischemia/ reperfusion injury in wistar rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673703/ https://www.ncbi.nlm.nih.gov/pubmed/29147494 http://dx.doi.org/10.22038/IJBMS.2017.9450 |
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