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Ellagic Acid Prevents Binge Alcohol-Induced Leaky Gut and Liver Injury through Inhibiting Gut Dysbiosis and Oxidative Stress

Alcoholic liver disease (ALD) is a major liver disease worldwide and can range from simple steatosis or inflammation to fibrosis/cirrhosis, possibly through leaky gut and systemic endotoxemia. Many patients with alcoholic steatohepatitis (ASH) die within 60 days after clinical diagnosis due to the l...

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Autores principales: Kim, Dong-ha, Sim, Yejin, Hwang, Jin-hyeon, Kwun, In-Sook, Lim, Jae-Hwan, Kim, Jihoon, Kim, Jee-In, Baek, Moon-Chang, Akbar, Mohammed, Seo, Wonhyo, Kim, Do-Kyun, Song, Byoung-Joon, Cho, Young-Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465052/
https://www.ncbi.nlm.nih.gov/pubmed/34573017
http://dx.doi.org/10.3390/antiox10091386
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author Kim, Dong-ha
Sim, Yejin
Hwang, Jin-hyeon
Kwun, In-Sook
Lim, Jae-Hwan
Kim, Jihoon
Kim, Jee-In
Baek, Moon-Chang
Akbar, Mohammed
Seo, Wonhyo
Kim, Do-Kyun
Song, Byoung-Joon
Cho, Young-Eun
author_facet Kim, Dong-ha
Sim, Yejin
Hwang, Jin-hyeon
Kwun, In-Sook
Lim, Jae-Hwan
Kim, Jihoon
Kim, Jee-In
Baek, Moon-Chang
Akbar, Mohammed
Seo, Wonhyo
Kim, Do-Kyun
Song, Byoung-Joon
Cho, Young-Eun
author_sort Kim, Dong-ha
collection PubMed
description Alcoholic liver disease (ALD) is a major liver disease worldwide and can range from simple steatosis or inflammation to fibrosis/cirrhosis, possibly through leaky gut and systemic endotoxemia. Many patients with alcoholic steatohepatitis (ASH) die within 60 days after clinical diagnosis due to the lack of an approved drug, and thus, synthetic and/or dietary agents to prevent ASH and premature deaths are urgently needed. We recently reported that a pharmacologically high dose of pomegranate extract prevented binge alcohol-induced gut leakiness and hepatic inflammation by suppressing oxidative and nitrative stress. Herein, we investigate whether a dietary antioxidant ellagic acid (EA) contained in many fruits, including pomegranate and vegetables, can protect against binge alcohol-induced leaky gut, endotoxemia, and liver inflammation. Pretreatment with a physiologically-relevant dose of EA for 14 days significantly reduced the binge alcohol-induced gut barrier dysfunction, endotoxemia, and inflammatory liver injury in mice by inhibiting gut dysbiosis and the elevated oxidative stress and apoptosis marker proteins. Pretreatment with EA significantly prevented the decreased amounts of gut tight junction/adherent junction proteins and the elevated gut leakiness in alcohol-exposed mice. Taken together, our results suggest that EA could be used as a dietary supplement for alcoholic hepatitis patients.
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spelling pubmed-84650522021-09-27 Ellagic Acid Prevents Binge Alcohol-Induced Leaky Gut and Liver Injury through Inhibiting Gut Dysbiosis and Oxidative Stress Kim, Dong-ha Sim, Yejin Hwang, Jin-hyeon Kwun, In-Sook Lim, Jae-Hwan Kim, Jihoon Kim, Jee-In Baek, Moon-Chang Akbar, Mohammed Seo, Wonhyo Kim, Do-Kyun Song, Byoung-Joon Cho, Young-Eun Antioxidants (Basel) Article Alcoholic liver disease (ALD) is a major liver disease worldwide and can range from simple steatosis or inflammation to fibrosis/cirrhosis, possibly through leaky gut and systemic endotoxemia. Many patients with alcoholic steatohepatitis (ASH) die within 60 days after clinical diagnosis due to the lack of an approved drug, and thus, synthetic and/or dietary agents to prevent ASH and premature deaths are urgently needed. We recently reported that a pharmacologically high dose of pomegranate extract prevented binge alcohol-induced gut leakiness and hepatic inflammation by suppressing oxidative and nitrative stress. Herein, we investigate whether a dietary antioxidant ellagic acid (EA) contained in many fruits, including pomegranate and vegetables, can protect against binge alcohol-induced leaky gut, endotoxemia, and liver inflammation. Pretreatment with a physiologically-relevant dose of EA for 14 days significantly reduced the binge alcohol-induced gut barrier dysfunction, endotoxemia, and inflammatory liver injury in mice by inhibiting gut dysbiosis and the elevated oxidative stress and apoptosis marker proteins. Pretreatment with EA significantly prevented the decreased amounts of gut tight junction/adherent junction proteins and the elevated gut leakiness in alcohol-exposed mice. Taken together, our results suggest that EA could be used as a dietary supplement for alcoholic hepatitis patients. MDPI 2021-08-30 /pmc/articles/PMC8465052/ /pubmed/34573017 http://dx.doi.org/10.3390/antiox10091386 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Dong-ha
Sim, Yejin
Hwang, Jin-hyeon
Kwun, In-Sook
Lim, Jae-Hwan
Kim, Jihoon
Kim, Jee-In
Baek, Moon-Chang
Akbar, Mohammed
Seo, Wonhyo
Kim, Do-Kyun
Song, Byoung-Joon
Cho, Young-Eun
Ellagic Acid Prevents Binge Alcohol-Induced Leaky Gut and Liver Injury through Inhibiting Gut Dysbiosis and Oxidative Stress
title Ellagic Acid Prevents Binge Alcohol-Induced Leaky Gut and Liver Injury through Inhibiting Gut Dysbiosis and Oxidative Stress
title_full Ellagic Acid Prevents Binge Alcohol-Induced Leaky Gut and Liver Injury through Inhibiting Gut Dysbiosis and Oxidative Stress
title_fullStr Ellagic Acid Prevents Binge Alcohol-Induced Leaky Gut and Liver Injury through Inhibiting Gut Dysbiosis and Oxidative Stress
title_full_unstemmed Ellagic Acid Prevents Binge Alcohol-Induced Leaky Gut and Liver Injury through Inhibiting Gut Dysbiosis and Oxidative Stress
title_short Ellagic Acid Prevents Binge Alcohol-Induced Leaky Gut and Liver Injury through Inhibiting Gut Dysbiosis and Oxidative Stress
title_sort ellagic acid prevents binge alcohol-induced leaky gut and liver injury through inhibiting gut dysbiosis and oxidative stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465052/
https://www.ncbi.nlm.nih.gov/pubmed/34573017
http://dx.doi.org/10.3390/antiox10091386
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