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Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice

Ellagic acid, a natural polyphenolic compound commonly present in vegetables, fruits, nuts, and other edible plants, exerts many pharmacological activities. The present project was designed to explore the hepatoprotective effect of ellagic acid against alcohol-induced liver disease (ALD) and the cor...

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Autores principales: Zhao, Liang, Mehmood, Arshad, Soliman, Mohamed Mohamed, Iftikhar, Asra, Iftikhar, Maryam, Aboelenin, Salama Mostafa, Wang, Chengtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478122/
https://www.ncbi.nlm.nih.gov/pubmed/34595202
http://dx.doi.org/10.3389/fnut.2021.744520
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author Zhao, Liang
Mehmood, Arshad
Soliman, Mohamed Mohamed
Iftikhar, Asra
Iftikhar, Maryam
Aboelenin, Salama Mostafa
Wang, Chengtao
author_facet Zhao, Liang
Mehmood, Arshad
Soliman, Mohamed Mohamed
Iftikhar, Asra
Iftikhar, Maryam
Aboelenin, Salama Mostafa
Wang, Chengtao
author_sort Zhao, Liang
collection PubMed
description Ellagic acid, a natural polyphenolic compound commonly present in vegetables, fruits, nuts, and other edible plants, exerts many pharmacological activities. The present project was designed to explore the hepatoprotective effect of ellagic acid against alcohol-induced liver disease (ALD) and the correlation among alcohol, oxidative stress, inflammation, and gut microbiota. Fifty percent (v/v) alcohol (10 mL/kg bw daily) was orally administrated for 4 weeks in mice along with ellagic acid (50 and 100 mg/kg bw). Alcohol administration significantly (p < 0.05) increased the activities of alanine aminotransferase and serum aspartate aminotransferase, levels of triglyceride, low density lipoprotein, free fatty acid, and total cholesterol, and decreased contents of the high-density lipoprotein in model group compared with the control group, which were further improved by ellagic acid (50 or 100 mg/kg bw). Furthermore, daily supplementation of ellagic acid alleviated hepatic antioxidant activities (glutathione peroxidase, catalase, malondialdehyde, superoxide dismutase, and glutathione), proinflammatory cytokines levels (IL-6, IL-1β, and TNF-α), genes expressions (Tlr4, Myd88, Cd14, Cox2, Nos2, and Nfκb1), and histopathological features in alcohol-induced liver injured mice. Additionally, results also revealed that ellagic acid supplementation improved alcohol-induced gut microbiota dysbiosis. In conclusion, ellagic acid mitigated oxidative stress, inflammatory response, steatosis, and gut microbiota dysbiosis in ALD mice. Our results suggested that ellagic acid could be applied as an ideal dietary therapy against ALD.
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spelling pubmed-84781222021-09-29 Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice Zhao, Liang Mehmood, Arshad Soliman, Mohamed Mohamed Iftikhar, Asra Iftikhar, Maryam Aboelenin, Salama Mostafa Wang, Chengtao Front Nutr Nutrition Ellagic acid, a natural polyphenolic compound commonly present in vegetables, fruits, nuts, and other edible plants, exerts many pharmacological activities. The present project was designed to explore the hepatoprotective effect of ellagic acid against alcohol-induced liver disease (ALD) and the correlation among alcohol, oxidative stress, inflammation, and gut microbiota. Fifty percent (v/v) alcohol (10 mL/kg bw daily) was orally administrated for 4 weeks in mice along with ellagic acid (50 and 100 mg/kg bw). Alcohol administration significantly (p < 0.05) increased the activities of alanine aminotransferase and serum aspartate aminotransferase, levels of triglyceride, low density lipoprotein, free fatty acid, and total cholesterol, and decreased contents of the high-density lipoprotein in model group compared with the control group, which were further improved by ellagic acid (50 or 100 mg/kg bw). Furthermore, daily supplementation of ellagic acid alleviated hepatic antioxidant activities (glutathione peroxidase, catalase, malondialdehyde, superoxide dismutase, and glutathione), proinflammatory cytokines levels (IL-6, IL-1β, and TNF-α), genes expressions (Tlr4, Myd88, Cd14, Cox2, Nos2, and Nfκb1), and histopathological features in alcohol-induced liver injured mice. Additionally, results also revealed that ellagic acid supplementation improved alcohol-induced gut microbiota dysbiosis. In conclusion, ellagic acid mitigated oxidative stress, inflammatory response, steatosis, and gut microbiota dysbiosis in ALD mice. Our results suggested that ellagic acid could be applied as an ideal dietary therapy against ALD. Frontiers Media S.A. 2021-09-14 /pmc/articles/PMC8478122/ /pubmed/34595202 http://dx.doi.org/10.3389/fnut.2021.744520 Text en Copyright © 2021 Zhao, Mehmood, Soliman, Iftikhar, Iftikhar, Aboelenin and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Zhao, Liang
Mehmood, Arshad
Soliman, Mohamed Mohamed
Iftikhar, Asra
Iftikhar, Maryam
Aboelenin, Salama Mostafa
Wang, Chengtao
Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice
title Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice
title_full Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice
title_fullStr Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice
title_full_unstemmed Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice
title_short Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice
title_sort protective effects of ellagic acid against alcoholic liver disease in mice
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478122/
https://www.ncbi.nlm.nih.gov/pubmed/34595202
http://dx.doi.org/10.3389/fnut.2021.744520
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