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Morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model
Liver diseases are among the most serious health issues nowadays. Hepatocellular carcinoma, one of the most lethal types of cancer worldwide, can be caused by chemically-induced oxidative stress. In the present study, we aimed to evaluate the protective effects of morin hydrate (MH) against acrylami...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4564079/ https://www.ncbi.nlm.nih.gov/pubmed/26252199 http://dx.doi.org/10.3892/ijmm.2015.2306 |
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author | SINGH, MAHENDRA PAL JAKHAR, REKHA KANG, SUN CHUL |
author_facet | SINGH, MAHENDRA PAL JAKHAR, REKHA KANG, SUN CHUL |
author_sort | SINGH, MAHENDRA PAL |
collection | PubMed |
description | Liver diseases are among the most serious health issues nowadays. Hepatocellular carcinoma, one of the most lethal types of cancer worldwide, can be caused by chemically-induced oxidative stress. In the present study, we aimed to evaluate the protective effects of morin hydrate (MH) against acrylamide (AA)-induced hepatotoxicity in male ICR mice. The mice were randomly allocated into 4 groups [the control, the group subcutaneously injected with AA alone (50 mg/kg body weight), the group subcutaneously injected with AA (50 mg/kg body weight) and MH (5 mg/kg body weight) and the group subcutaneously injected with AA (50 mg/kg body weight) and MH (15 mg/kg body weight) for 5 consecutive days]. Histopathological evaluations were performed and the levels of serum hepatic enzymes were analyzed to determine initial liver injury, and the mice in the AA-treated groups were compared with the mice receiving no treatment and with the mice administered MH in combination with AA. Furthermore, oxidative stress, hepatic inflammation and the levels of DNA damage-related markers were evaluated to determine the extent of liver damage induced by AA within a short-term period. The subcutaneous administration of AA induced severe hepatic injury, and combined treatment with AA and MH resulted in a significant improvement in all evaluated parameters. This recovery was most obvious in the group receiving AA and 15 mg/kg body weight dose of MH. The findings of our study demonstrated that MH protected mice from severe hepatic injury induced by AA. Moreover, MH is a natural polyphenolic compound, and thus it has potential for use in the treatment of severe liver diseases, in place of many synthetic drugs. |
format | Online Article Text |
id | pubmed-4564079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-45640792015-11-30 Morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model SINGH, MAHENDRA PAL JAKHAR, REKHA KANG, SUN CHUL Int J Mol Med Articles Liver diseases are among the most serious health issues nowadays. Hepatocellular carcinoma, one of the most lethal types of cancer worldwide, can be caused by chemically-induced oxidative stress. In the present study, we aimed to evaluate the protective effects of morin hydrate (MH) against acrylamide (AA)-induced hepatotoxicity in male ICR mice. The mice were randomly allocated into 4 groups [the control, the group subcutaneously injected with AA alone (50 mg/kg body weight), the group subcutaneously injected with AA (50 mg/kg body weight) and MH (5 mg/kg body weight) and the group subcutaneously injected with AA (50 mg/kg body weight) and MH (15 mg/kg body weight) for 5 consecutive days]. Histopathological evaluations were performed and the levels of serum hepatic enzymes were analyzed to determine initial liver injury, and the mice in the AA-treated groups were compared with the mice receiving no treatment and with the mice administered MH in combination with AA. Furthermore, oxidative stress, hepatic inflammation and the levels of DNA damage-related markers were evaluated to determine the extent of liver damage induced by AA within a short-term period. The subcutaneous administration of AA induced severe hepatic injury, and combined treatment with AA and MH resulted in a significant improvement in all evaluated parameters. This recovery was most obvious in the group receiving AA and 15 mg/kg body weight dose of MH. The findings of our study demonstrated that MH protected mice from severe hepatic injury induced by AA. Moreover, MH is a natural polyphenolic compound, and thus it has potential for use in the treatment of severe liver diseases, in place of many synthetic drugs. D.A. Spandidos 2015-10 2015-08-07 /pmc/articles/PMC4564079/ /pubmed/26252199 http://dx.doi.org/10.3892/ijmm.2015.2306 Text en Copyright: © Singh et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles SINGH, MAHENDRA PAL JAKHAR, REKHA KANG, SUN CHUL Morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model |
title | Morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model |
title_full | Morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model |
title_fullStr | Morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model |
title_full_unstemmed | Morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model |
title_short | Morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model |
title_sort | morin hydrate attenuates the acrylamide-induced imbalance in antioxidant enzymes in a murine model |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4564079/ https://www.ncbi.nlm.nih.gov/pubmed/26252199 http://dx.doi.org/10.3892/ijmm.2015.2306 |
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