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The hepatoprotective effect of Aloe vera on ischemia-reperfusion injury in rats
OBJECTIVE: Aloe vera is known for its antioxidant properties. In this experimental study, we aimed to investigate the efficacy of Aloe vera in ischemia-reperfusion (I/R) liver injury in rats. METHODS: Male Wistar Albino rats were divided into three groups, where the sham group (n=7) underwent no med...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790936/ https://www.ncbi.nlm.nih.gov/pubmed/31650105 http://dx.doi.org/10.14744/nci.2018.82957 |
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author | Sehitoglu, Muserref Hilal Karaboga, Ihsan Kiraz, Asli Kiraz, Hasan Ali |
author_facet | Sehitoglu, Muserref Hilal Karaboga, Ihsan Kiraz, Asli Kiraz, Hasan Ali |
author_sort | Sehitoglu, Muserref Hilal |
collection | PubMed |
description | OBJECTIVE: Aloe vera is known for its antioxidant properties. In this experimental study, we aimed to investigate the efficacy of Aloe vera in ischemia-reperfusion (I/R) liver injury in rats. METHODS: Male Wistar Albino rats were divided into three groups, where the sham group (n=7) underwent no medication or surgical procedures, the I/R group (n=7) was the control group that received 45 minutes of applied abdominal aorta ischemia and rats were sacrificed 24 hours after reperfusion, and the I/R+AV group (n=7) was the treatment group that was given Aloe vera (30 mg/kg) every day followed by gastric lavage for a month before applying ischemia and performing sacrifice as in the previous group. Before sacrifice, all the liver tissues were removed. Tissues were examined for histopathological investigation, iNOS immunoreactivity and tissue biochemistry, malondialdehyde (MDA), catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) activities. RESULTS: The SOD, CAT, and GSH-Px levels of the I/R+AV group were not significantly different from the sham group (p>0.05) but were significantly higher when compared to the I/R group. MDA levels of liver tissues were significantly lower (p<0.05) in the I/R+AV group as compared to the I/R group. Disrupted hepatic cords, sinusoidal dilatation, hemorrhage, cytoplasmic vacuolization of hepatocytes, and intensive iNOS immunoreactivity were detected in the I/R group. Decreased histopathological change score and iNOS immunoreactivity score were noticed in the I/R+AV group as compared to the I/R group. CONCLUSION: It was found that Aloe vera showed a hepatoprotective effect against I/R injury. Further research is required to determine the effective dose, administration method, and effects of Aloe vera for liver transplantation. |
format | Online Article Text |
id | pubmed-6790936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-67909362019-10-24 The hepatoprotective effect of Aloe vera on ischemia-reperfusion injury in rats Sehitoglu, Muserref Hilal Karaboga, Ihsan Kiraz, Asli Kiraz, Hasan Ali North Clin Istanb Original Article OBJECTIVE: Aloe vera is known for its antioxidant properties. In this experimental study, we aimed to investigate the efficacy of Aloe vera in ischemia-reperfusion (I/R) liver injury in rats. METHODS: Male Wistar Albino rats were divided into three groups, where the sham group (n=7) underwent no medication or surgical procedures, the I/R group (n=7) was the control group that received 45 minutes of applied abdominal aorta ischemia and rats were sacrificed 24 hours after reperfusion, and the I/R+AV group (n=7) was the treatment group that was given Aloe vera (30 mg/kg) every day followed by gastric lavage for a month before applying ischemia and performing sacrifice as in the previous group. Before sacrifice, all the liver tissues were removed. Tissues were examined for histopathological investigation, iNOS immunoreactivity and tissue biochemistry, malondialdehyde (MDA), catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) activities. RESULTS: The SOD, CAT, and GSH-Px levels of the I/R+AV group were not significantly different from the sham group (p>0.05) but were significantly higher when compared to the I/R group. MDA levels of liver tissues were significantly lower (p<0.05) in the I/R+AV group as compared to the I/R group. Disrupted hepatic cords, sinusoidal dilatation, hemorrhage, cytoplasmic vacuolization of hepatocytes, and intensive iNOS immunoreactivity were detected in the I/R group. Decreased histopathological change score and iNOS immunoreactivity score were noticed in the I/R+AV group as compared to the I/R group. CONCLUSION: It was found that Aloe vera showed a hepatoprotective effect against I/R injury. Further research is required to determine the effective dose, administration method, and effects of Aloe vera for liver transplantation. Kare Publishing 2018-10-10 /pmc/articles/PMC6790936/ /pubmed/31650105 http://dx.doi.org/10.14744/nci.2018.82957 Text en Copyright: © 2019 by Istanbul Northern Anatolian Association of Public Hospitals http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License |
spellingShingle | Original Article Sehitoglu, Muserref Hilal Karaboga, Ihsan Kiraz, Asli Kiraz, Hasan Ali The hepatoprotective effect of Aloe vera on ischemia-reperfusion injury in rats |
title | The hepatoprotective effect of Aloe vera on ischemia-reperfusion injury in rats |
title_full | The hepatoprotective effect of Aloe vera on ischemia-reperfusion injury in rats |
title_fullStr | The hepatoprotective effect of Aloe vera on ischemia-reperfusion injury in rats |
title_full_unstemmed | The hepatoprotective effect of Aloe vera on ischemia-reperfusion injury in rats |
title_short | The hepatoprotective effect of Aloe vera on ischemia-reperfusion injury in rats |
title_sort | hepatoprotective effect of aloe vera on ischemia-reperfusion injury in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790936/ https://www.ncbi.nlm.nih.gov/pubmed/31650105 http://dx.doi.org/10.14744/nci.2018.82957 |
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