Anti-inflammatory and antioxidant effects of umbelliferone in chronic alcohol-fed rats.
- Author:
Mi Ok SIM
1
;
Hae In LEE
;
Ju Ri HAM
;
Kwon Il SEO
;
Myung Joo KIM
;
Mi Kyung LEE
Author Information
- Publication Type:Original Article
- Keywords: Alcohol; antioxidant; inflammation; TLR4 signaling; umbelliferone
- MeSH: Animals; Antioxidants*; Carrier Proteins; Catalase; Cytokines; Diet; Fibrosis; Gene Expression; Hydrogen Peroxide; Inflammation; Interleukin-10; Interleukin-6; Liver; Liver Diseases; NF-kappa B; Rats*; RNA, Messenger; Superoxide Dismutase; Toll-Like Receptor 4; Tumor Necrosis Factor-alpha
- From:Nutrition Research and Practice 2015;9(4):364-369
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND/OBJECTIVES: Inflammation is associated with various types of acute and chronic alcohol liver diseases. In this study, we examined whether umbelliferone (7-hydroxycoumarin, UF) ameliorates chronic alcohol-induced liver damage by modulating inflammatory response and the antioxidant system. METHODS: Rats were fed a Liber-Decarli liquid diet containing 5% alcohol with or without UF (0.05 g/L) for 8 weeks, while normal rats received an isocaloric carbohydrate liquid diet. RESULTS: Chronic alcohol intake significantly increased serum tumor necrosis factor-alpha (TNF-alpha) and interleukin 6 levels and decreased interleukin 10 level; however, UF supplementation reversed the cytokines related to liver damage. UF significantly suppressed hepatic lipopolysaccharide binding protein, toll-like receptor 4 (TLR4), nuclear factor kappa B, and TNF-alpha gene expression increases in response to chronic alcohol intake. Masson's trichrome staining revealed that UF improved mild hepatic fibrosis caused by alcohol, and UF also significantly increased the mRNA expressions and activities of superoxide dismutase and catalase in liver, and thus, decreased lipid peroxide and mitochondrial hydrogen peroxide levels. CONCLUSIONS: The findings of this study indicate that UF protects against alcohol-induced liver damage by inhibiting the TLR4 signaling pathway and activating the antioxidant system.
