4.6 Article

Protective Effects of Ellagic Acid Against Alcoholic Liver Disease in Mice

Journal

FRONTIERS IN NUTRITION
Volume 8, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnut.2021.744520

Keywords

alcoholic liver disease; polyphenolic compound; ellagic acid; inflammation; gut microbiota

Funding

  1. China Postdoctoral Science Foundation [2019TQ0011]
  2. Beijing Postdoctoral Research Foundation, Technological Innovation Service Capacity Building-Basic Scientific Research Expenses [PXM2020-014213-000017]
  3. Taif University Researchers Supporting Project [TURSP-2020/105]

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The study demonstrated that ellagic acid significantly alleviated oxidative stress, inflammatory response, steatosis, and gut microbiota dysbiosis in alcohol-induced liver disease (ALD) mice. This suggests that ellagic acid could be a promising dietary therapy for ALD.
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-1 beta, and TNF-alpha), genes expressions (Tlr4, Myd88, Cd14, Cox2, Nos2, and Nf kappa b1), 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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